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Showing metabocard for PC(18:3(9Z,12Z,15Z)/14:1(9Z)) (HMDB0008197)

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enzymes (77)transporters (1) Show 78 proteins
Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2008-09-12 01:32:59 UTC
Update Date2022-11-30 19:03:09 UTC
HMDB IDHMDB0008197
Secondary Accession Numbers
  • HMDB08197
Metabolite Identification
Common NamePC(18:3(9Z,12Z,15Z)/14:1(9Z))
DescriptionPC(18:3(9Z,12Z,15Z)/14:1(9Z)) is a phosphatidylcholine (PC or GPCho). It is a glycerophospholipid in which a phosphorylcholine moiety occupies a glycerol substitution site. As is the case with diacylglycerols, glycerophosphocholines can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. Fatty acids containing 16, 18 and 20 carbons are the most common. PC(18:3(9Z,12Z,15Z)/14:1(9Z)), in particular, consists of one chain of a-linolenic acid at the C-1 position and one chain of myristoleic acid at the C-2 position. The a-linolenic acid moiety is derived from seed oils, especially canola and soybean oil, while the myristoleic acid moiety is derived from milk fats. Phospholipids, are ubiquitous in nature and are key components of the lipid bilayer of cells, as well as being involved in metabolism and signaling.While most phospholipids have a saturated fatty acid on C-1 and an unsaturated fatty acid on C-2 of the glycerol backbone, the fatty acid distribution at the C-1 and C-2 positions of glycerol within phospholipids is continually in flux, owing to phospholipid degradation and the continuous phospholipid remodeling that occurs while these molecules are in membranes. PCs can be synthesized via three different routes. In one route, choline is activated first by phosphorylation and then by coupling to CDP prior to attachment to phosphatidic acid. PCs can also synthesized by the addition of choline to CDP-activated 1,2-diacylglycerol. A third route to PC synthesis involves the conversion of either PS or PE to PC.
Structure
Data?1582752548
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0008197 (PC(18:3(9Z,12Z,15Z)/14:1(9Z)))


  Mrv0541 02231222102D          

 51 50  0  0  1  0            999 V2000
   25.2065   -6.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.5013   -7.4050    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   23.7961   -6.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.9117   -7.4050    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.0910   -7.4050    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.5013   -8.2193    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.6168   -6.9979    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   27.0240   -7.7031    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   26.2097   -6.2927    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.3220   -6.5908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.0272   -6.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.7324   -6.5908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.4376   -6.9979    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   29.0304   -7.7031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0902   -6.1454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.1427   -7.4050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2304   -6.9925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9449   -7.4051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6593   -6.9925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3738   -6.9926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0883   -7.4051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8028   -6.9926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5173   -6.9925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2317   -7.4050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9462   -6.9925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.6607   -6.9926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.3752   -7.4051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.0896   -6.9926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.8042   -7.4051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.5186   -6.9926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.2331   -7.4051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.9476   -6.9926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   22.3765   -6.9926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.3765   -6.1675    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.4986   -8.6318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2131   -8.2193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9275   -8.6318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.6420   -8.2193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.3565   -8.6318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.0710   -8.6318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.7855   -8.2193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.4999   -8.6318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.2144   -8.2193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.9289   -8.6318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.6434   -8.2193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.3578   -8.6318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.0724   -8.2193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.7868   -8.6318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.7868   -9.4568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.3297   -8.2599    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  1  4  1  0  0  0  0
  3  5  1  0  0  0  0
  2  6  1  6  0  0  0
  4  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 13 16  1  0  0  0  0
 18 17  1  0  0  0  0
 19 18  1  0  0  0  0
 20 19  2  0  0  0  0
 21 20  1  0  0  0  0
 22 21  1  0  0  0  0
 23 22  2  0  0  0  0
 24 23  1  0  0  0  0
 25 24  1  0  0  0  0
 26 25  2  0  0  0  0
 27 26  1  0  0  0  0
 28 27  1  0  0  0  0
 29 28  1  0  0  0  0
 30 29  1  0  0  0  0
 31 30  1  0  0  0  0
 32 31  1  0  0  0  0
 33 32  1  0  0  0  0
 34 33  1  0  0  0  0
 35 34  2  0  0  0  0
  5 34  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49  6  1  0  0  0  0
 49 50  2  0  0  0  0
  2 51  1  1  0  0  0
M  CHG  2   8  -1  13   1
M  END
Download

3D MOL for HMDB0008197 (PC(18:3(9Z,12Z,15Z)/14:1(9Z)))

HMDB0008197
     RDKit          3D
PC(18:3(9Z,12Z,15Z)/14:1(9Z))
122121  0  0  0  0  0  0  0  0999 V2000
   -1.3486   -9.4260   -0.5565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5145   -8.4139   -1.3778 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7638   -8.2757   -0.7015 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1985   -7.1463   -0.2173 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4519   -5.8429   -0.2871 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3240   -4.9162   -1.0169 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8051   -3.7900   -0.6149 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6196   -3.1139    0.6637 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7363   -3.6344    1.6852 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1603   -4.0344    2.8744 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5192   -4.0316    3.3717 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6724   -3.2626    4.6418 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3824   -1.8342    4.7088 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0145   -1.3504    4.4000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9118    0.1643    4.6184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4829    0.6489    4.2837 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8072    0.4188    2.8197 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1409    1.2149    1.9786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2314    2.3412    1.4946 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8302    1.6707 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3480    1.5188    0.9043 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0554    1.7331   -0.5373 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2263    2.6290   -1.0376 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1674    3.8332   -0.3383 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3508    4.9285   -0.7557 P   0  0  0  0  0  5  0  0  0  0  0  0
    5.7459    4.3643   -0.5422 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1829    5.3036   -2.3925 O   0  0  0  0  0  1  0  0  0  0  0  0
    4.1645    6.3759    0.1252 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9176    7.4558   -0.7106 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7523    8.7471    0.0140 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6653    8.7467    0.9464 N   0  0  0  0  0  4  0  0  0  0  0  0
    1.5075    8.0230    0.4546 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1264    8.1788    2.1950 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2359   10.0972    1.2195 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8621    2.4078   -0.8221 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0422    1.8040   -1.6877 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2616    0.6653   -2.1786 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3436    2.3890   -2.0833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0660    1.4245   -2.9641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4120    1.8921   -3.4200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3448    2.1696   -2.2607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5385    0.9337   -1.4159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4843    1.2729   -0.2833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7058    0.0627    0.6189 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2602   -0.9940   -0.2071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6922   -2.1679   -0.3951 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4418   -2.5433    0.2041 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3012   -2.8969   -0.6735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3917   -4.0112   -1.6143 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4216   -3.9757   -2.6713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1506   -9.2296    0.5386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4197   -9.3017   -0.7413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9819  -10.4227   -0.7824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4004   -8.9546   -2.3730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0633   -7.5241   -1.5805 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3884   -9.1828   -0.6045 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1733   -7.1381    0.2769 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0797   -5.5716    0.6845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4370   -5.9983   -0.9278 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.4586   -3.2722   -1.3821 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6677   -2.9785    1.0852 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3267   -2.0087    0.4433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3894   -3.6558    1.4992 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3397   -4.4164    3.5506 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3137   -3.6726    2.6870 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8390   -5.1192    3.5758 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7353   -3.4853    4.9954 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0706   -3.7825    5.4647 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6105   -1.5006    5.7778 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1734   -1.2827    4.1260 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6816   -1.5038    3.3784 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2938   -1.8564    5.0859 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0983    0.3963    5.6819 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7015    0.6201    4.0192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5009    1.7301    4.4839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1943    0.1098    4.9029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8202    0.8800    2.6663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9059   -0.6196    2.5422 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6430    2.5079    1.3265 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3129    0.9244    0.9424 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1074    0.7837   -1.0761 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1416    2.1002   -0.7145 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2351    2.7194   -2.1196 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0198    7.2216   -1.3421 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7790    7.5231   -1.3983 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6872    8.9449    0.5980 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5807    9.5496   -0.7341 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7330    8.0704    1.2690 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7267    6.9659    0.2833 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1695    8.4779   -0.4851 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8855    7.1131    2.1771 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2072    8.3853    2.3811 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5436    8.6347    3.0422 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7982   10.4836    2.0857 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1642   10.0320    1.5733 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2917   10.7500    0.3459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0739    3.3391   -2.6373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9122    2.6238   -1.1637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4209    1.2331   -3.8707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1152    0.4553   -2.4432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3288    2.7810   -4.0752 H   0  0  0  0  0  0  0  0  0  0  0  0
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 50122  1  0
M  CHG  2  27  -1  31   1
M  END
Download

3D SDF for HMDB0008197 (PC(18:3(9Z,12Z,15Z)/14:1(9Z)))


  Mrv0541 02231222102D          

 51 50  0  0  1  0            999 V2000
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   24.5013   -7.4050    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   23.7961   -6.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.9117   -7.4050    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.0910   -7.4050    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.5013   -8.2193    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.6168   -6.9979    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   27.0240   -7.7031    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   26.2097   -6.2927    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.3220   -6.5908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.0272   -6.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.7324   -6.5908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.4376   -6.9979    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   29.0304   -7.7031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  5 34  1  0  0  0  0
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 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49  6  1  0  0  0  0
 49 50  2  0  0  0  0
  2 51  1  1  0  0  0
M  CHG  2   8  -1  13   1
M  END
> <DATABASE_ID>
HMDB0008197

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCC\C=C/CCCCCCCC(=O)O[C@]([H])(COC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC)COP([O-])(=O)OCC[N+](C)(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C40H72NO8P/c1-6-8-10-12-14-16-18-19-20-21-23-24-26-28-30-32-39(42)46-36-38(37-48-50(44,45)47-35-34-41(3,4)5)49-40(43)33-31-29-27-25-22-17-15-13-11-9-7-2/h8,10,13-16,19-20,38H,6-7,9,11-12,17-18,21-37H2,1-5H3/b10-8-,15-13-,16-14-,20-19-/t38-/m1/s1

> <INCHI_KEY>
VMDDNEGQBQWKEU-RPHNJZPISA-N

> <FORMULA>
C40H72NO8P

> <MOLECULAR_WEIGHT>
725.9753

> <EXACT_MASS>
725.499554797

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
84.85099550928697

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
trimethyl(2-{[(2R)-3-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]-2-[(9Z)-tetradec-9-enoyloxy]propyl phosphonato]oxy}ethyl)azanium

> <ALOGPS_LOGP>
4.87

> <JCHEM_LOGP>
6.666109752528257

> <ALOGPS_LOGS>
-7.35

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8550572064469137

> <JCHEM_PKA_STRONGEST_BASIC>
-6.744159309169755

> <JCHEM_POLAR_SURFACE_AREA>
111.19

> <JCHEM_REFRACTIVITY>
220.3315000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
36

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.50e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
lecithin

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0008197 (PC(18:3(9Z,12Z,15Z)/14:1(9Z)))

HMDB0008197
     RDKit          3D
PC(18:3(9Z,12Z,15Z)/14:1(9Z))
122121  0  0  0  0  0  0  0  0999 V2000
   -1.3486   -9.4260   -0.5565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5145   -8.4139   -1.3778 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7638   -8.2757   -0.7015 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1985   -7.1463   -0.2173 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4519   -5.8429   -0.2871 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3240   -4.9162   -1.0169 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8051   -3.7900   -0.6149 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6196   -3.1139    0.6637 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7363   -3.6344    1.6852 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1603   -4.0344    2.8744 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5192   -4.0316    3.3717 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6724   -3.2626    4.6418 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3824   -1.8342    4.7088 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0145   -1.3504    4.4000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9118    0.1643    4.6184 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.8072    0.4188    2.8197 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1409    1.2149    1.9786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2314    2.3412    1.4946 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8302    1.6707 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3480    1.5188    0.9043 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0554    1.7331   -0.5373 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2263    2.6290   -1.0376 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1674    3.8332   -0.3383 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3508    4.9285   -0.7557 P   0  0  0  0  0  5  0  0  0  0  0  0
    5.7459    4.3643   -0.5422 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1829    5.3036   -2.3925 O   0  0  0  0  0  1  0  0  0  0  0  0
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    3.7523    8.7471    0.0140 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6653    8.7467    0.9464 N   0  0  0  0  0  4  0  0  0  0  0  0
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    0.2616    0.6653   -2.1786 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3436    2.3890   -2.0833 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.4418   -2.5433    0.2041 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3012   -2.8969   -0.6735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3917   -4.0112   -1.6143 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4216   -3.9757   -2.6713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1506   -9.2296    0.5386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4197   -9.3017   -0.7413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9819  -10.4227   -0.7824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4004   -8.9546   -2.3730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0633   -7.5241   -1.5805 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3884   -9.1828   -0.6045 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1733   -7.1381    0.2769 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0797   -5.5716    0.6845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4370   -5.9983   -0.9278 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5865   -5.2600   -2.0460 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4586   -3.2722   -1.3821 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6677   -2.9785    1.0852 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3267   -2.0087    0.4433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3894   -3.6558    1.4992 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3397   -4.4164    3.5506 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3137   -3.6726    2.6870 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8390   -5.1192    3.5758 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7353   -3.4853    4.9954 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0706   -3.7825    5.4647 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6105   -1.5006    5.7778 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1734   -1.2827    4.1260 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6816   -1.5038    3.3784 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2938   -1.8564    5.0859 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0983    0.3963    5.6819 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7015    0.6201    4.0192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5009    1.7301    4.4839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1943    0.1098    4.9029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8202    0.8800    2.6663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9059   -0.6196    2.5422 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6430    2.5079    1.3265 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3129    0.9244    0.9424 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1074    0.7837   -1.0761 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1416    2.1002   -0.7145 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2351    2.7194   -2.1196 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0198    7.2216   -1.3421 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7790    7.5231   -1.3983 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6872    8.9449    0.5980 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5807    9.5496   -0.7341 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7330    8.0704    1.2690 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7267    6.9659    0.2833 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1695    8.4779   -0.4851 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8855    7.1131    2.1771 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2072    8.3853    2.3811 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5436    8.6347    3.0422 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7982   10.4836    2.0857 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1642   10.0320    1.5733 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2917   10.7500    0.3459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0739    3.3391   -2.6373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9122    2.6238   -1.1637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4209    1.2331   -3.8707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1152    0.4553   -2.4432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3288    2.7810   -4.0752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8755    1.0754   -4.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0131    3.0020   -1.6316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3456    2.4360   -2.6819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9957    0.1557   -2.0735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5904    0.5159   -1.0615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1020    2.1440    0.2848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4428    1.5848   -0.7435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8863   -0.1349    1.2774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5537    0.4053    1.2987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2352   -0.7473   -0.6951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2491   -2.8450   -1.0471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6429   -3.4771    0.8335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0433   -1.8453    0.9638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4178   -3.0670   -0.0139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0054   -1.9614   -1.2385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5212   -4.9951   -1.0634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3919   -4.1373   -2.1199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0152   -4.5644   -3.5516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6398   -2.9766   -3.0966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3287   -4.5639   -2.4015 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  2  0
 25 27  1  0
 25 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 31 33  1  0
 31 34  1  0
 22 35  1  0
 35 36  1  0
 36 37  2  0
 36 38  1  0
 38 39  1  0
 39 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
 43 44  1  0
 44 45  1  0
 45 46  2  0
 46 47  1  0
 47 48  1  0
 48 49  1  0
 49 50  1  0
  1 51  1  0
  1 52  1  0
  1 53  1  0
  2 54  1  0
  2 55  1  0
  3 56  1  0
  4 57  1  0
  5 58  1  0
  5 59  1  0
  6 60  1  0
  7 61  1  0
  8 62  1  0
  8 63  1  0
  9 64  1  0
 10 65  1  0
 11 66  1  0
 11 67  1  0
 12 68  1  0
 12 69  1  0
 13 70  1  0
 13 71  1  0
 14 72  1  0
 14 73  1  0
 15 74  1  0
 15 75  1  0
 16 76  1  0
 16 77  1  0
 17 78  1  0
 17 79  1  0
 21 80  1  0
 21 81  1  0
 22 82  1  6
 23 83  1  0
 23 84  1  0
 29 85  1  0
 29 86  1  0
 30 87  1  0
 30 88  1  0
 32 89  1  0
 32 90  1  0
 32 91  1  0
 33 92  1  0
 33 93  1  0
 33 94  1  0
 34 95  1  0
 34 96  1  0
 34 97  1  0
 38 98  1  0
 38 99  1  0
 39100  1  0
 39101  1  0
 40102  1  0
 40103  1  0
 41104  1  0
 41105  1  0
 42106  1  0
 42107  1  0
 43108  1  0
 43109  1  0
 44110  1  0
 44111  1  0
 45112  1  0
 46113  1  0
 47114  1  0
 47115  1  0
 48116  1  0
 48117  1  0
 49118  1  0
 49119  1  0
 50120  1  0
 50121  1  0
 50122  1  0
M  CHG  2  27  -1  31   1
M  END
Download

PDB for HMDB0008197 (PC(18:3(9Z,12Z,15Z)/14:1(9Z)))

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  C   UNK     0      47.052 -13.063   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      45.736 -13.823   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      44.419 -13.063   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      48.369 -13.823   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      43.103 -13.823   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      45.736 -15.343   0.000  0.00  0.00           O+0
HETATM    7  P   UNK     0      49.685 -13.063   0.000  0.00  0.00           P+0
HETATM    8  O   UNK     0      50.445 -14.379   0.000  0.00  0.00           O-1
HETATM    9  O   UNK     0      48.925 -11.746   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      51.001 -12.303   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      52.317 -13.063   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      53.634 -12.303   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      54.950 -13.063   0.000  0.00  0.00           N+1
HETATM   14  C   UNK     0      54.190 -14.379   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      56.168 -11.471   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      56.266 -13.823   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      19.097 -13.053   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      20.430 -13.823   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      21.764 -13.053   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      23.098 -13.053   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      24.431 -13.823   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      25.765 -13.053   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      27.099 -13.053   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      28.433 -13.823   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      29.766 -13.053   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      31.100 -13.053   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      32.434 -13.823   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      33.767 -13.053   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      35.101 -13.823   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      36.435 -13.053   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      37.768 -13.823   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      39.102 -13.053   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      40.436 -13.823   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      41.769 -13.053   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      41.769 -11.513   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      27.064 -16.113   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      28.398 -15.343   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      29.731 -16.113   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      31.065 -15.343   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      32.399 -16.113   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      33.733 -16.113   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      35.066 -15.343   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      36.400 -16.113   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      37.734 -15.343   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      39.067 -16.113   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      40.401 -15.343   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      41.735 -16.113   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      43.068 -15.343   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      44.402 -16.113   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      44.402 -17.653   0.000  0.00  0.00           O+0
HETATM   51  H   UNK     0      47.282 -15.418   0.000  0.00  0.00           H+0
CONECT    1    2    4                                                       
CONECT    2    1    3    6   51                                             
CONECT    3    2    5                                                       
CONECT    4    1    7                                                       
CONECT    5    3   34                                                       
CONECT    6    2   49                                                       
CONECT    7    4    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15   16                                             
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   13                                                            
CONECT   17   18                                                            
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35    5                                                  
CONECT   35   34                                                            
CONECT   36   37                                                            
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48    6   50                                                  
CONECT   50   49                                                            
CONECT   51    2                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  100    0
END
Download

3D PDB for HMDB0008197 (PC(18:3(9Z,12Z,15Z)/14:1(9Z)))

COMPND    HMDB0008197
HETATM    1  C1  UNL     1      -1.349  -9.426  -0.556  1.00  0.00           C  
HETATM    2  C2  UNL     1      -0.514  -8.414  -1.378  1.00  0.00           C  
HETATM    3  C3  UNL     1       0.764  -8.276  -0.701  1.00  0.00           C  
HETATM    4  C4  UNL     1       1.198  -7.146  -0.217  1.00  0.00           C  
HETATM    5  C5  UNL     1       0.452  -5.843  -0.287  1.00  0.00           C  
HETATM    6  C6  UNL     1       1.324  -4.916  -1.017  1.00  0.00           C  
HETATM    7  C7  UNL     1       1.805  -3.790  -0.615  1.00  0.00           C  
HETATM    8  C8  UNL     1       1.620  -3.114   0.664  1.00  0.00           C  
HETATM    9  C9  UNL     1       0.736  -3.634   1.685  1.00  0.00           C  
HETATM   10  C10 UNL     1       1.160  -4.034   2.874  1.00  0.00           C  
HETATM   11  C11 UNL     1       2.519  -4.032   3.372  1.00  0.00           C  
HETATM   12  C12 UNL     1       2.672  -3.263   4.642  1.00  0.00           C  
HETATM   13  C13 UNL     1       2.382  -1.834   4.709  1.00  0.00           C  
HETATM   14  C14 UNL     1       1.015  -1.350   4.400  1.00  0.00           C  
HETATM   15  C15 UNL     1       0.912   0.164   4.618  1.00  0.00           C  
HETATM   16  C16 UNL     1      -0.483   0.649   4.284  1.00  0.00           C  
HETATM   17  C17 UNL     1      -0.807   0.419   2.820  1.00  0.00           C  
HETATM   18  C18 UNL     1       0.141   1.215   1.979  1.00  0.00           C  
HETATM   19  O1  UNL     1      -0.231   2.341   1.495  1.00  0.00           O  
HETATM   20  O2  UNL     1       1.429   0.830   1.671  1.00  0.00           O  
HETATM   21  C19 UNL     1       2.348   1.519   0.904  1.00  0.00           C  
HETATM   22  C20 UNL     1       2.055   1.733  -0.537  1.00  0.00           C  
HETATM   23  C21 UNL     1       3.226   2.629  -1.038  1.00  0.00           C  
HETATM   24  O3  UNL     1       3.167   3.833  -0.338  1.00  0.00           O  
HETATM   25  P1  UNL     1       4.351   4.929  -0.756  1.00  0.00           P  
HETATM   26  O4  UNL     1       5.746   4.364  -0.542  1.00  0.00           O  
HETATM   27  O5  UNL     1       4.183   5.304  -2.393  1.00  0.00           O1-
HETATM   28  O6  UNL     1       4.164   6.376   0.125  1.00  0.00           O  
HETATM   29  C22 UNL     1       3.918   7.456  -0.711  1.00  0.00           C  
HETATM   30  C23 UNL     1       3.752   8.747   0.014  1.00  0.00           C  
HETATM   31  N1  UNL     1       2.665   8.747   0.946  1.00  0.00           N1+
HETATM   32  C24 UNL     1       1.508   8.023   0.455  1.00  0.00           C  
HETATM   33  C25 UNL     1       3.126   8.179   2.195  1.00  0.00           C  
HETATM   34  C26 UNL     1       2.236  10.097   1.219  1.00  0.00           C  
HETATM   35  O7  UNL     1       0.862   2.408  -0.822  1.00  0.00           O  
HETATM   36  C27 UNL     1      -0.042   1.804  -1.688  1.00  0.00           C  
HETATM   37  O8  UNL     1       0.262   0.665  -2.179  1.00  0.00           O  
HETATM   38  C28 UNL     1      -1.344   2.389  -2.083  1.00  0.00           C  
HETATM   39  C29 UNL     1      -2.066   1.425  -2.964  1.00  0.00           C  
HETATM   40  C30 UNL     1      -3.412   1.892  -3.420  1.00  0.00           C  
HETATM   41  C31 UNL     1      -4.345   2.170  -2.261  1.00  0.00           C  
HETATM   42  C32 UNL     1      -4.538   0.934  -1.416  1.00  0.00           C  
HETATM   43  C33 UNL     1      -5.484   1.273  -0.283  1.00  0.00           C  
HETATM   44  C34 UNL     1      -5.706   0.063   0.619  1.00  0.00           C  
HETATM   45  C35 UNL     1      -6.260  -0.994  -0.207  1.00  0.00           C  
HETATM   46  C36 UNL     1      -5.692  -2.168  -0.395  1.00  0.00           C  
HETATM   47  C37 UNL     1      -4.442  -2.543   0.204  1.00  0.00           C  
HETATM   48  C38 UNL     1      -3.301  -2.897  -0.674  1.00  0.00           C  
HETATM   49  C39 UNL     1      -3.392  -4.011  -1.614  1.00  0.00           C  
HETATM   50  C40 UNL     1      -4.422  -3.976  -2.671  1.00  0.00           C  
HETATM   51  H1  UNL     1      -1.151  -9.230   0.539  1.00  0.00           H  
HETATM   52  H2  UNL     1      -2.420  -9.302  -0.741  1.00  0.00           H  
HETATM   53  H3  UNL     1      -0.982 -10.423  -0.782  1.00  0.00           H  
HETATM   54  H4  UNL     1      -0.400  -8.955  -2.373  1.00  0.00           H  
HETATM   55  H5  UNL     1      -1.063  -7.524  -1.581  1.00  0.00           H  
HETATM   56  H6  UNL     1       1.388  -9.183  -0.605  1.00  0.00           H  
HETATM   57  H7  UNL     1       2.173  -7.138   0.277  1.00  0.00           H  
HETATM   58  H8  UNL     1       0.080  -5.572   0.684  1.00  0.00           H  
HETATM   59  H9  UNL     1      -0.437  -5.998  -0.928  1.00  0.00           H  
HETATM   60  H10 UNL     1       1.587  -5.260  -2.046  1.00  0.00           H  
HETATM   61  H11 UNL     1       2.459  -3.272  -1.382  1.00  0.00           H  
HETATM   62  H12 UNL     1       2.668  -2.978   1.085  1.00  0.00           H  
HETATM   63  H13 UNL     1       1.327  -2.009   0.443  1.00  0.00           H  
HETATM   64  H14 UNL     1      -0.389  -3.656   1.499  1.00  0.00           H  
HETATM   65  H15 UNL     1       0.340  -4.416   3.551  1.00  0.00           H  
HETATM   66  H16 UNL     1       3.314  -3.673   2.687  1.00  0.00           H  
HETATM   67  H17 UNL     1       2.839  -5.119   3.576  1.00  0.00           H  
HETATM   68  H18 UNL     1       3.735  -3.485   4.995  1.00  0.00           H  
HETATM   69  H19 UNL     1       2.071  -3.782   5.465  1.00  0.00           H  
HETATM   70  H20 UNL     1       2.611  -1.501   5.778  1.00  0.00           H  
HETATM   71  H21 UNL     1       3.173  -1.283   4.126  1.00  0.00           H  
HETATM   72  H22 UNL     1       0.682  -1.504   3.378  1.00  0.00           H  
HETATM   73  H23 UNL     1       0.294  -1.856   5.086  1.00  0.00           H  
HETATM   74  H24 UNL     1       1.098   0.396   5.682  1.00  0.00           H  
HETATM   75  H25 UNL     1       1.701   0.620   4.019  1.00  0.00           H  
HETATM   76  H26 UNL     1      -0.501   1.730   4.484  1.00  0.00           H  
HETATM   77  H27 UNL     1      -1.194   0.110   4.903  1.00  0.00           H  
HETATM   78  H28 UNL     1      -1.820   0.880   2.666  1.00  0.00           H  
HETATM   79  H29 UNL     1      -0.906  -0.620   2.542  1.00  0.00           H  
HETATM   80  H30 UNL     1       2.643   2.508   1.326  1.00  0.00           H  
HETATM   81  H31 UNL     1       3.313   0.924   0.942  1.00  0.00           H  
HETATM   82  H32 UNL     1       2.107   0.784  -1.076  1.00  0.00           H  
HETATM   83  H33 UNL     1       4.142   2.100  -0.714  1.00  0.00           H  
HETATM   84  H34 UNL     1       3.235   2.719  -2.120  1.00  0.00           H  
HETATM   85  H35 UNL     1       3.020   7.222  -1.342  1.00  0.00           H  
HETATM   86  H36 UNL     1       4.779   7.523  -1.398  1.00  0.00           H  
HETATM   87  H37 UNL     1       4.687   8.945   0.598  1.00  0.00           H  
HETATM   88  H38 UNL     1       3.581   9.550  -0.734  1.00  0.00           H  
HETATM   89  H39 UNL     1       0.733   8.070   1.269  1.00  0.00           H  
HETATM   90  H40 UNL     1       1.727   6.966   0.283  1.00  0.00           H  
HETATM   91  H41 UNL     1       1.169   8.478  -0.485  1.00  0.00           H  
HETATM   92  H42 UNL     1       2.885   7.113   2.177  1.00  0.00           H  
HETATM   93  H43 UNL     1       4.207   8.385   2.381  1.00  0.00           H  
HETATM   94  H44 UNL     1       2.544   8.635   3.042  1.00  0.00           H  
HETATM   95  H45 UNL     1       2.798  10.484   2.086  1.00  0.00           H  
HETATM   96  H46 UNL     1       1.164  10.032   1.573  1.00  0.00           H  
HETATM   97  H47 UNL     1       2.292  10.750   0.346  1.00  0.00           H  
HETATM   98  H48 UNL     1      -1.074   3.339  -2.637  1.00  0.00           H  
HETATM   99  H49 UNL     1      -1.912   2.624  -1.164  1.00  0.00           H  
HETATM  100  H50 UNL     1      -1.421   1.233  -3.871  1.00  0.00           H  
HETATM  101  H51 UNL     1      -2.115   0.455  -2.443  1.00  0.00           H  
HETATM  102  H52 UNL     1      -3.329   2.781  -4.075  1.00  0.00           H  
HETATM  103  H53 UNL     1      -3.876   1.075  -4.030  1.00  0.00           H  
HETATM  104  H54 UNL     1      -4.013   3.002  -1.632  1.00  0.00           H  
HETATM  105  H55 UNL     1      -5.346   2.436  -2.682  1.00  0.00           H  
HETATM  106  H56 UNL     1      -4.996   0.156  -2.073  1.00  0.00           H  
HETATM  107  H57 UNL     1      -3.590   0.516  -1.062  1.00  0.00           H  
HETATM  108  H58 UNL     1      -5.102   2.144   0.285  1.00  0.00           H  
HETATM  109  H59 UNL     1      -6.443   1.585  -0.744  1.00  0.00           H  
HETATM  110  H60 UNL     1      -4.886  -0.135   1.277  1.00  0.00           H  
HETATM  111  H61 UNL     1      -6.554   0.405   1.299  1.00  0.00           H  
HETATM  112  H62 UNL     1      -7.235  -0.747  -0.695  1.00  0.00           H  
HETATM  113  H63 UNL     1      -6.249  -2.845  -1.047  1.00  0.00           H  
HETATM  114  H64 UNL     1      -4.643  -3.477   0.833  1.00  0.00           H  
HETATM  115  H65 UNL     1      -4.043  -1.845   0.964  1.00  0.00           H  
HETATM  116  H66 UNL     1      -2.418  -3.067  -0.014  1.00  0.00           H  
HETATM  117  H67 UNL     1      -3.005  -1.961  -1.239  1.00  0.00           H  
HETATM  118  H68 UNL     1      -3.521  -4.995  -1.063  1.00  0.00           H  
HETATM  119  H69 UNL     1      -2.392  -4.137  -2.120  1.00  0.00           H  
HETATM  120  H70 UNL     1      -4.015  -4.564  -3.552  1.00  0.00           H  
HETATM  121  H71 UNL     1      -4.640  -2.977  -3.097  1.00  0.00           H  
HETATM  122  H72 UNL     1      -5.329  -4.564  -2.402  1.00  0.00           H  
CONECT    1    2   51   52   53
CONECT    2    3   54   55
CONECT    3    4    4   56
CONECT    4    5   57
CONECT    5    6   58   59
CONECT    6    7    7   60
CONECT    7    8   61
CONECT    8    9   62   63
CONECT    9   10   10   64
CONECT   10   11   65
CONECT   11   12   66   67
CONECT   12   13   68   69
CONECT   13   14   70   71
CONECT   14   15   72   73
CONECT   15   16   74   75
CONECT   16   17   76   77
CONECT   17   18   78   79
CONECT   18   19   19   20
CONECT   20   21
CONECT   21   22   80   81
CONECT   22   23   35   82
CONECT   23   24   83   84
CONECT   24   25
CONECT   25   26   26   27   28
CONECT   28   29
CONECT   29   30   85   86
CONECT   30   31   87   88
CONECT   31   32   33   34
CONECT   32   89   90   91
CONECT   33   92   93   94
CONECT   34   95   96   97
CONECT   35   36
CONECT   36   37   37   38
CONECT   38   39   98   99
CONECT   39   40  100  101
CONECT   40   41  102  103
CONECT   41   42  104  105
CONECT   42   43  106  107
CONECT   43   44  108  109
CONECT   44   45  110  111
CONECT   45   46   46  112
CONECT   46   47  113
CONECT   47   48  114  115
CONECT   48   49  116  117
CONECT   49   50  118  119
CONECT   50  120  121  122
END
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SMILES for HMDB0008197 (PC(18:3(9Z,12Z,15Z)/14:1(9Z)))

CCCC\C=C/CCCCCCCC(=O)O[C@]([H])(COC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC)COP([O-])(=O)OCC[N+](C)(C)C
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INCHI for HMDB0008197 (PC(18:3(9Z,12Z,15Z)/14:1(9Z)))

InChI=1S/C40H72NO8P/c1-6-8-10-12-14-16-18-19-20-21-23-24-26-28-30-32-39(42)46-36-38(37-48-50(44,45)47-35-34-41(3,4)5)49-40(43)33-31-29-27-25-22-17-15-13-11-9-7-2/h8,10,13-16,19-20,38H,6-7,9,11-12,17-18,21-37H2,1-5H3/b10-8-,15-13-,16-14-,20-19-/t38-/m1/s1
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View in JSmolView Stereo Labels
Synonyms
ValueSource
Phosphatidylcholine(18:3/14:1)HMDB
GPCho(32:4)HMDB
PC(32:4)HMDB
GPCho(18:3/14:1)HMDB
LecithinHMDB
PC(18:3/14:1)HMDB
1-a-Linolenoyl-2-myristoleoyl-sn-glycero-3-phosphocholineHMDB
1-(9Z,12Z,15Z-Octadeatrienoyl)-2-(9Z-tetradecenoyl)-sn-glycero-3-phosphocholineHMDB
Phosphatidylcholine(32:4)HMDB
PC(18:3(9Z,12Z,15Z)/14:1(9Z))Lipid Annotator
Chemical FormulaC40H72NO8P
Average Molecular Weight725.9753
Monoisotopic Molecular Weight725.499554797
IUPAC Nametrimethyl(2-{[(2R)-3-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]-2-[(9Z)-tetradec-9-enoyloxy]propyl phosphonato]oxy}ethyl)azanium
Traditional Namelecithin
CAS Registry NumberNot Available
SMILES
CCCC\C=C/CCCCCCCC(=O)O[C@]([H])(COC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC)COP([O-])(=O)OCC[N+](C)(C)C
InChI Identifier
InChI=1S/C40H72NO8P/c1-6-8-10-12-14-16-18-19-20-21-23-24-26-28-30-32-39(42)46-36-38(37-48-50(44,45)47-35-34-41(3,4)5)49-40(43)33-31-29-27-25-22-17-15-13-11-9-7-2/h8,10,13-16,19-20,38H,6-7,9,11-12,17-18,21-37H2,1-5H3/b10-8-,15-13-,16-14-,20-19-/t38-/m1/s1
InChI KeyVMDDNEGQBQWKEU-RPHNJZPISA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as phosphatidylcholines. These are glycerophosphocholines in which the two free -OH are attached to one fatty acid each through an ester linkage.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassGlycerophospholipids
Sub ClassGlycerophosphocholines
Direct ParentPhosphatidylcholines
Alternative Parents
Substituents
  • Diacylglycero-3-phosphocholine
  • Phosphocholine
  • Fatty acid ester
  • Dialkyl phosphate
  • Dicarboxylic acid or derivatives
  • Organic phosphoric acid derivative
  • Phosphoric acid ester
  • Alkyl phosphate
  • Fatty acyl
  • Quaternary ammonium salt
  • Tetraalkylammonium salt
  • Carboxylic acid ester
  • Carboxylic acid derivative
  • Organic oxygen compound
  • Organic nitrogen compound
  • Carbonyl group
  • Organooxygen compound
  • Organonitrogen compound
  • Organic oxide
  • Organopnictogen compound
  • Amine
  • Organic salt
  • Hydrocarbon derivative
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Ontology
Physiological effect
Health effect
Disposition
Biological locationSource
Process
Naturally occurring process
Role
Biological roleIndustrial application
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility3.5e-05 g/LALOGPS
logP4.87ALOGPS
logP6.67ChemAxon
logS-7.4ALOGPS
pKa (Strongest Acidic)1.86ChemAxon
pKa (Strongest Basic)-6.7ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area111.19 ŲChemAxon
Rotatable Bond Count36ChemAxon
Refractivity220.33 m³·mol⁻¹ChemAxon
Polarizability84.85 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+269.78830932474
DeepCCS[M-H]-267.55230932474
DeepCCS[M-2H]-300.79230932474
DeepCCS[M+Na]+275.52830932474
AllCCS[M+H]+277.832859911
AllCCS[M+H-H2O]+277.532859911
AllCCS[M+NH4]+278.032859911
AllCCS[M+Na]+278.132859911
AllCCS[M-H]-263.132859911
AllCCS[M+Na-2H]-268.032859911
AllCCS[M+HCOO]-273.432859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
PC(18:3(9Z,12Z,15Z)/14:1(9Z))CCCC\C=C/CCCCCCCC(=O)O[C@]([H])(COC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC)COP([O-])(=O)OCC[N+](C)(C)C5079.0Standard polar33892256
PC(18:3(9Z,12Z,15Z)/14:1(9Z))CCCC\C=C/CCCCCCCC(=O)O[C@]([H])(COC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC)COP([O-])(=O)OCC[N+](C)(C)C4119.6Standard non polar33892256
PC(18:3(9Z,12Z,15Z)/14:1(9Z))CCCC\C=C/CCCCCCCC(=O)O[C@]([H])(COC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC)COP([O-])(=O)OCC[N+](C)(C)C4682.2Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - PC(18:3(9Z,12Z,15Z)/14:1(9Z)) GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(18:3(9Z,12Z,15Z)/14:1(9Z)) 10V, Positive-QTOFsplash10-004i-0000000900-baec86d99ec4c07a56992017-10-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(18:3(9Z,12Z,15Z)/14:1(9Z)) 20V, Positive-QTOFsplash10-0059-0600000900-19d8c67a8529ad20a7c92017-10-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(18:3(9Z,12Z,15Z)/14:1(9Z)) 40V, Positive-QTOFsplash10-00lr-1900231200-b28c785be4cd49eead392017-10-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(18:3(9Z,12Z,15Z)/14:1(9Z)) 10V, Positive-QTOFsplash10-001i-0000000900-e68e4f1bf436a4e43ef52021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(18:3(9Z,12Z,15Z)/14:1(9Z)) 20V, Positive-QTOFsplash10-001i-0000001900-f8fd657606f78ed862e12021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(18:3(9Z,12Z,15Z)/14:1(9Z)) 40V, Positive-QTOFsplash10-006t-0101491100-63fb47762a20c3159d8f2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(18:3(9Z,12Z,15Z)/14:1(9Z)) 10V, Negative-QTOFsplash10-00di-0000000900-63fe5d31f4ed259959872021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(18:3(9Z,12Z,15Z)/14:1(9Z)) 20V, Negative-QTOFsplash10-00fr-0091043700-b13e705e53fe5ba1b2352021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(18:3(9Z,12Z,15Z)/14:1(9Z)) 40V, Negative-QTOFsplash10-004i-5390300000-e32fb706502d828f85782021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(18:3(9Z,12Z,15Z)/14:1(9Z)) 10V, Positive-QTOFsplash10-004i-0000000900-34163778ef8ac8b44b922021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(18:3(9Z,12Z,15Z)/14:1(9Z)) 20V, Positive-QTOFsplash10-0059-0600000900-70c3e066fe3ad93c46112021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(18:3(9Z,12Z,15Z)/14:1(9Z)) 40V, Positive-QTOFsplash10-00lr-1900231200-dcd3f268a0e7ffb683582021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(18:3(9Z,12Z,15Z)/14:1(9Z)) 10V, Positive-QTOFsplash10-0002-0000000900-56bb2ae10a5ae49857d92021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(18:3(9Z,12Z,15Z)/14:1(9Z)) 20V, Positive-QTOFsplash10-0002-0000001900-753ed6acbe5cfbb86c252021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(18:3(9Z,12Z,15Z)/14:1(9Z)) 40V, Positive-QTOFsplash10-00kb-0600491100-9ba5d98dfe814b5e65732021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(18:3(9Z,12Z,15Z)/14:1(9Z)) 10V, Negative-QTOFsplash10-03di-0000000900-41581ec16564771253832021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(18:3(9Z,12Z,15Z)/14:1(9Z)) 20V, Negative-QTOFsplash10-03di-0030000900-d5811d1e1b08b219a7872021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(18:3(9Z,12Z,15Z)/14:1(9Z)) 40V, Negative-QTOFsplash10-01t9-0090000400-df5d3b23244e6be924042021-09-25Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Extracellular
  • Membrane
Biospecimen Locations
  • Feces
Tissue Locations
  • All Tissues
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
FecesDetected but not QuantifiedNot QuantifiedNewborn (0-30 days old)Not Specified
Premature neonates		 details
Predicted Concentrations
BiospecimenValueOriginal ageOriginal sexOriginal conditionComments
Blood0.001 +/- 0.001 uMAdult (>18 years old)BothNormal (Most Probable)Calculated using MetaboAnalyst
Blood0.733 +/- 0.451 uMAdult (>18 years old)BothNormal (Upper Limit)Calculated using MetaboAnalyst
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound52922827
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available

Only showing the first 10 proteins. There are 78 proteins in total.

Show all enzymes and transporters

Enzymes

Enzyme Details
1. Acyl-protein thioesterase 1
General function:
Involved in hydrolase activity
Specific function:
Hydrolyzes fatty acids from S-acylated cysteine residues in proteins such as trimeric G alpha proteins or HRAS. Has depalmitoylating activity and also low lysophospholipase activity.
Gene Name:
LYPLA1
Uniprot ID:
O75608
Molecular weight:
24669.355
Enzyme Details
2. Group XV phospholipase A2
General function:
Involved in phosphatidylcholine-sterol O-acyltransferase activity
Specific function:
Has transacylase and calcium-independent phospholipase A2 activity. Catalyzes the formation of 1-O-acyl-N-acetylsphingosine and the concomitant release of a lyso-phospholipid (By similarity). May have weak lysophospholipase activity.
Gene Name:
PLA2G15
Uniprot ID:
Q8NCC3
Molecular weight:
Not Available
Enzyme Details
3. Calcium-dependent phospholipase A2
General function:
Involved in phospholipase A2 activity
Specific function:
PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides. This isozyme hydrolyzes more efficiently L-alpha-1-palmitoyl-2-oleoyl phosphatidylcholine than L-alpha-1-palmitoyl-2-arachidonyl phosphatidylcholine, L-alpha-1-palmitoyl-2-arachidonyl phosphatidylethanolamine, or L-alpha-1-stearoyl-2-arachidonyl phosphatidylinositol. May be involved in the production of lung surfactant, the remodeling or regulation of cardiac muscle.
Gene Name:
PLA2G5
Uniprot ID:
P39877
Molecular weight:
15674.065
Enzyme Details
4. Group IIF secretory phospholipase A2
General function:
Involved in phospholipase A2 activity
Specific function:
PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides. Hydrolyzes phosphatidylglycerol versus phosphatidylcholine with a 15-fold preference.
Gene Name:
PLA2G2F
Uniprot ID:
Q9BZM2
Molecular weight:
23256.29
Enzyme Details
5. Cytosolic phospholipase A2
General function:
Involved in metabolic process
Specific function:
Selectively hydrolyzes arachidonyl phospholipids in the sn-2 position releasing arachidonic acid. Together with its lysophospholipid activity, it is implicated in the initiation of the inflammatory response.
Gene Name:
PLA2G4A
Uniprot ID:
P47712
Molecular weight:
85210.19
Enzyme Details
6. Phospholipase A2
General function:
Involved in phospholipase A2 activity
Specific function:
PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides.
Gene Name:
PLA2G1B
Uniprot ID:
P04054
Molecular weight:
16359.535
Enzyme Details
7. Group XIIB secretory phospholipase A2-like protein
General function:
Involved in phospholipase A2 activity
Specific function:
Not known; does not seem to have catalytic activity.
Gene Name:
PLA2G12B
Uniprot ID:
Q9BX93
Molecular weight:
Not Available
Enzyme Details
8. Group 10 secretory phospholipase A2
General function:
Involved in phospholipase A2 activity
Specific function:
PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides. Has a powerful potency for releasing arachidonic acid from cell membrane phospholipids. Prefers phosphatidylethanolamine and phosphatidylcholine liposomes to those of phosphatidylserine.
Gene Name:
PLA2G10
Uniprot ID:
O15496
Molecular weight:
18153.04
Enzyme Details
9. Group IIE secretory phospholipase A2
General function:
Involved in phospholipase A2 activity
Specific function:
PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides. Has a preference for arachidonic-containing phospholipids.
Gene Name:
PLA2G2E
Uniprot ID:
Q9NZK7
Molecular weight:
15988.525
Enzyme Details
10. Acyl-protein thioesterase 2
General function:
Involved in hydrolase activity
Specific function:
May hydrolyze fatty acids from S-acylated cysteine residues in proteins such as trimeric G alpha proteins or HRAS. Has lysophospholipase activity (By similarity). Deacylates GAP43.
Gene Name:
LYPLA2
Uniprot ID:
O95372
Molecular weight:
24736.71

Transporters

Enzyme Details
1. Multidrug resistance protein 3
General function:
Involved in ATP binding
Specific function:
Mediates ATP-dependent export of organic anions and drugs from the cytoplasm. Hydrolyzes ATP with low efficiency. Human MDR3 is not capable of conferring drug resistance. Mediates the translocation of phosphatidylcholine across the canalicular membrane of the hepatocyte
Gene Name:
ABCB4
Uniprot ID:
P21439
Molecular weight:
141521.8

Only showing the first 10 proteins. There are 78 proteins in total.

Show all enzymes and transporters