Structure of PDB 1cjy Chain A Binding Site BS02
Receptor Information
>1cjy Chain A (length=633) Species:
9606
(Homo sapiens) [
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EHQYSHKFTVVVLRATKVTKGAFGDMLDTPDPYVELFISTTPDSRKRTRH
FNNDINPVWNETFEFILDPNQENVLEITLMDANYVMDETLGTATFTVSSM
KVGEKKEVPFIFNQVTEMVLEMSLEVCSCPDLRFSMALCDQEKTFRQQRK
EHIRESMKKLLGPKNSEGLHSARDVPVVAILGSGGGFRAMVGFSGVMKAL
YESGILDCATYVAGLSGSTWYMSTLYSHPDFPEKGPEEINEELMKNVSHN
PLLLLTPQKVKRYVESLWKKKSSGQPVTFTDIFGMLIGETLIHNRMNTTL
SSLKEKVNTAQCPLPLFTCLHVKPDVSELMFADWVEFSPYEIGMAKYGTF
MAPDLFGSKFFMGTVVKKYEENPLHFLMGVWGSAFSILFNRVLSTMEEEL
ENITTKHIVSNNQASWIHRMIMALVSDSALFNTREGRAGKVHNFMLGLNL
DVKSKKIHVVDSGLTFNLPYPLILRPQRGVDLIISFDFSARPSDSSPPFK
ELLLAEKWAKMNKLPFPKIDPYVFDREGLKECYVFKPKNPDMEKDCPTII
HFVLANINFRKYKAPGVPRETEEEKEIADFDIFDDPESPFSTFNFQYPNQ
AFKRLHDLMHFNTLNNIDVIKEAMVESIEYRRQ
Ligand information
Ligand ID
CA
InChI
InChI=1S/Ca/q+2
InChIKey
BHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
Formula
Ca
Name
CALCIUM ION
ChEMBL
DrugBank
DB14577
ZINC
PDB chain
1cjy Chain A Residue 951 [
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Receptor-Ligand Complex Structure
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PDB
1cjy
Crystal structure of human cytosolic phospholipase A2 reveals a novel topology and catalytic mechanism.
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
D40 D43 D93 A94 N95
Binding residue
(residue number reindexed from 1)
D28 D31 D81 A82 N83
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
G197 G198 R200 S228 D549
Catalytic site (residue number reindexed from 1)
G185 G186 R188 S216 D461
Enzyme Commision number
3.1.1.4
: phospholipase A2.
3.1.1.5
: lysophospholipase.
Gene Ontology
Molecular Function
GO:0004620
phospholipase activity
GO:0004622
lysophospholipase activity
GO:0004623
phospholipase A2 activity
GO:0005509
calcium ion binding
GO:0005544
calcium-dependent phospholipid binding
GO:0008289
lipid binding
GO:0008374
O-acyltransferase activity
GO:0010314
phosphatidylinositol-5-phosphate binding
GO:0016787
hydrolase activity
GO:0032266
phosphatidylinositol-3-phosphate binding
GO:0046872
metal ion binding
GO:0047498
calcium-dependent phospholipase A2 activity
GO:0047499
calcium-independent phospholipase A2 activity
GO:0070273
phosphatidylinositol-4-phosphate binding
GO:1902387
ceramide 1-phosphate binding
Biological Process
GO:0001516
prostaglandin biosynthetic process
GO:0002827
positive regulation of T-helper 1 type immune response
GO:0006071
glycerol metabolic process
GO:0006640
monoacylglycerol biosynthetic process
GO:0006650
glycerophospholipid metabolic process
GO:0006663
platelet activating factor biosynthetic process
GO:0006690
icosanoid metabolic process
GO:0009395
phospholipid catabolic process
GO:0010572
positive regulation of platelet activation
GO:0019369
arachidonate metabolic process
GO:0019370
leukotriene biosynthetic process
GO:0032308
positive regulation of prostaglandin secretion
GO:0034478
phosphatidylglycerol catabolic process
GO:0034638
phosphatidylcholine catabolic process
GO:0036151
phosphatidylcholine acyl-chain remodeling
GO:0042127
regulation of cell population proliferation
GO:0043032
positive regulation of macrophage activation
GO:0046456
icosanoid biosynthetic process
GO:0046475
glycerophospholipid catabolic process
GO:0050482
arachidonate secretion
GO:0051649
establishment of localization in cell
GO:0071236
cellular response to antibiotic
Cellular Component
GO:0000139
Golgi membrane
GO:0005634
nucleus
GO:0005635
nuclear envelope
GO:0005737
cytoplasm
GO:0005743
mitochondrial inner membrane
GO:0005783
endoplasmic reticulum
GO:0005789
endoplasmic reticulum membrane
GO:0005794
Golgi apparatus
GO:0005829
cytosol
GO:0016020
membrane
GO:0043231
intracellular membrane-bounded organelle
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1cjy
,
PDBe:1cjy
,
PDBj:1cjy
PDBsum
1cjy
PubMed
10319815
UniProt
P47712
|PA24A_HUMAN Cytosolic phospholipase A2 (Gene Name=PLA2G4A)
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