Structure of PDB 8e50 Chain A Binding Site BS01
Receptor Information
>8e50 Chain A (length=651) Species:
9606
(Homo sapiens) [
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GLRNVIYINETHTRHRGWLARRLSYVLFIQERDVHKGMFATNVTENVLNS
SRVQEAIAEVAAELNPQSKAVNKVKKKAKRILQEMVATVSPAMIRLTGWV
LLKLFNSFFWNIQIHKGQLEMVKAATETNLPLLFLPVHRSHIDYLLLTFI
LFCHNIKAPYIASGNNLNIPIFSTLIHKLGGFFIRRRLDETPDGRKDVLY
RALLHGHIVELLRQQQFLEIFLEGTRSRSGKTSCARAGLLSVVVDTLSTN
VIPDILIIPVGISYDRIIEGHYNGEQLGWSVARGVIRMLRKNYGCVRVDF
AQPFSLKEYLESQSQKPVSALLSLEQALLPAILPTDESLRRRLIANLAEH
ILFTASKSCAIMSTHIVACLLLYRHRQGIDLSTLVEDFFVMKEEVLARDF
DLGFSGNSEDVVMHAIQLLGNCVTITHTSRNDEFFITPSTTVPSVFELNF
YSNGVLHVFIMEAIIACSLYAVLNLISQEQLVRKAASLCYLLSNEGTISL
PCQTFYQVCHETVGKFIQYGILTVADCYLKVSQSKEHQQFITFLQRLLGP
LLEAYSSAAIFVHNFSGPVPEPEYLQKLHKYLITRTERNVAVYAESATYC
LVKNAVKMFKDIGVFKETKQKRVSVLELSSTFLPQCNRQKLLEYILSFVV
L
Ligand information
Ligand ID
COA
InChI
InChI=1S/C21H36N7O16P3S/c1-21(2,16(31)19(32)24-4-3-12(29)23-5-6-48)8-41-47(38,39)44-46(36,37)40-7-11-15(43-45(33,34)35)14(30)20(42-11)28-10-27-13-17(22)25-9-26-18(13)28/h9-11,14-16,20,30-31,48H,3-8H2,1-2H3,(H,23,29)(H,24,32)(H,36,37)(H,38,39)(H2,22,25,26)(H2,33,34,35)/t11-,14-,15-,16+,20-/m1/s1
InChIKey
RGJOEKWQDUBAIZ-IBOSZNHHSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC(C)(COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)C(C(=O)NCCC(=O)NCCS)O
CACTVS 3.341
CC(C)(CO[P@@](O)(=O)O[P@](O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O[P](O)(O)=O)n2cnc3c(N)ncnc23)[C@@H](O)C(=O)NCCC(=O)NCCS
OpenEye OEToolkits 1.5.0
CC(C)(CO[P@](=O)(O)O[P@@](=O)(O)OC[C@@H]1[C@H]([C@H]([C@@H](O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)[C@H](C(=O)NCCC(=O)NCCS)O
CACTVS 3.341
CC(C)(CO[P](O)(=O)O[P](O)(=O)OC[CH]1O[CH]([CH](O)[CH]1O[P](O)(O)=O)n2cnc3c(N)ncnc23)[CH](O)C(=O)NCCC(=O)NCCS
ACDLabs 10.04
O=C(NCCS)CCNC(=O)C(O)C(C)(C)COP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3OP(=O)(O)O
Formula
C21 H36 N7 O16 P3 S
Name
COENZYME A
ChEMBL
CHEMBL1213327
DrugBank
DB01992
ZINC
ZINC000008551087
PDB chain
8e50 Chain A Residue 901 [
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Receptor-Ligand Complex Structure
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PDB
8e50
Structural basis of the acyl-transfer mechanism of human GPAT1.
Resolution
3.67 Å
Binding residue
(original residue number in PDB)
R278 L280 K288 F313 R328 A329 G330 R462
Binding residue
(residue number reindexed from 1)
R186 L188 K196 F221 R236 A237 G238 R341
Annotation score
3
Enzymatic activity
Enzyme Commision number
2.3.1.15
: glycerol-3-phosphate 1-O-acyltransferase.
Gene Ontology
Molecular Function
GO:0004366
glycerol-3-phosphate O-acyltransferase activity
GO:0005515
protein binding
GO:0008374
O-acyltransferase activity
GO:0016746
acyltransferase activity
Biological Process
GO:0001817
regulation of cytokine production
GO:0006072
glycerol-3-phosphate metabolic process
GO:0006631
fatty acid metabolic process
GO:0006637
acyl-CoA metabolic process
GO:0006641
triglyceride metabolic process
GO:0006650
glycerophospholipid metabolic process
GO:0006651
diacylglycerol biosynthetic process
GO:0006654
phosphatidic acid biosynthetic process
GO:0006655
phosphatidylglycerol biosynthetic process
GO:0006924
activation-induced cell death of T cells
GO:0008654
phospholipid biosynthetic process
GO:0009749
response to glucose
GO:0016024
CDP-diacylglycerol biosynthetic process
GO:0019432
triglyceride biosynthetic process
GO:0040018
positive regulation of multicellular organism growth
GO:0042104
positive regulation of activated T cell proliferation
GO:0044255
cellular lipid metabolic process
GO:0050798
activated T cell proliferation
GO:0051607
defense response to virus
GO:0055089
fatty acid homeostasis
GO:0055091
phospholipid homeostasis
GO:0070236
negative regulation of activation-induced cell death of T cells
Cellular Component
GO:0005739
mitochondrion
GO:0005741
mitochondrial outer membrane
GO:0005886
plasma membrane
GO:0031966
mitochondrial membrane
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:8e50
,
PDBe:8e50
,
PDBj:8e50
PDBsum
8e50
PubMed
36522428
UniProt
Q9HCL2
|GPAT1_HUMAN Glycerol-3-phosphate acyltransferase 1, mitochondrial (Gene Name=GPAM)
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