Structure of PDB 1m8t Chain C Binding Site BS01
Receptor Information
>1m8t Chain C (length=119) Species:
8665
(Ophiophagus hannah) [
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HLVQFNGMIRCTIPGSIPWWDYSDYGCYCGSGGSGTPVDELDRCCQVHDN
CYTQAQQLTECSPYSKRYSYDCSEGTLTCKADNDECAAFVCDCDRVAAIC
FAGAPYNKENINIDTTTRC
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
1m8t Chain C Residue 1003 [
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Receptor-Ligand Complex Structure
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PDB
1m8t
Structure of a king cobra phospholipase A2 determined from a hemihedrally twinned crystal.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
Y28 G30 G32 D49
Binding residue
(residue number reindexed from 1)
Y28 G30 G32 D49
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y28 G30 G32 H48 D49 Y52 Y73 D99
Catalytic site (residue number reindexed from 1)
Y28 G30 G32 H48 D49 Y52 Y68 D94
Enzyme Commision number
3.1.1.4
: phospholipase A2.
Gene Ontology
Molecular Function
GO:0004623
phospholipase A2 activity
GO:0005102
signaling receptor binding
GO:0005509
calcium ion binding
GO:0005543
phospholipid binding
GO:0016787
hydrolase activity
GO:0046872
metal ion binding
GO:0047498
calcium-dependent phospholipase A2 activity
GO:0090729
toxin activity
Biological Process
GO:0006633
fatty acid biosynthetic process
GO:0006644
phospholipid metabolic process
GO:0016042
lipid catabolic process
GO:0035821
modulation of process of another organism
GO:0048146
positive regulation of fibroblast proliferation
GO:0050482
arachidonate secretion
Cellular Component
GO:0005576
extracellular region
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1m8t
,
PDBe:1m8t
,
PDBj:1m8t
PDBsum
1m8t
PubMed
12925787
UniProt
Q9DF33
|PA2A2_OPHHA Acidic phospholipase A2 2
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