Structure of PDB 1fe5 Chain A Binding Site BS01
Receptor Information
>1fe5 Chain A (length=118) Species:
132961
(Bungarus caeruleus) [
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NLIQFKNMIQCAGTRPWTAYVNYGCYCGKGGSGTPVDELDRCCYTHDNCY
NEAEKIPGCNPNIKTYSYTCTEPNLTCTDTADTCARFLCNCDRTAAICFA
SAPYNSNNVMISSSTNCQ
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
1fe5 Chain A Residue 150 [
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Receptor-Ligand Complex Structure
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PDB
1fe5
Sequence and crystal structure determination of a basic phospholipase A2 from common krait (Bungarus caeruleus) at 2.4 A resolution: identification and characterization of its pharmacological sites.
Resolution
2.45 Å
Binding residue
(original residue number in PDB)
Y28 G30 G32 D49
Binding residue
(residue number reindexed from 1)
Y26 G28 G30 D47
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y28 G30 G32 H48 D49 Y52 Y68 D94
Catalytic site (residue number reindexed from 1)
Y26 G28 G30 H46 D47 Y50 Y66 D92
Enzyme Commision number
3.1.1.4
: phospholipase A2.
Gene Ontology
Molecular Function
GO:0004623
phospholipase A2 activity
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:0006644
phospholipid metabolic process
GO:0016042
lipid catabolic process
GO:0035821
modulation of process of another organism
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:1fe5
,
PDBe:1fe5
,
PDBj:1fe5
PDBsum
1fe5
PubMed
11286555
UniProt
Q9DF52
|PA2B_BUNCE Basic phospholipase A2 KPA2
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