Structure of PDB 3hzw Chain B Binding Site BS01
Receptor Information
>3hzw Chain B (length=121) Species:
8726
(Bothrops jararacussu) [
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SLFELGKMILQETGKNPAKSYGAYGCNCGVLGRGKPKDATDRCCYVHKCC
YKKLTGCDPKKDRYSYSWKDKTIVCGENNPCLKELCECDKAVAICLRENL
GTYNKKYRYHLKPFCKKADPC
Ligand information
Ligand ID
PBP
InChI
InChI=1S/C8H6Br2O/c9-5-8(11)6-1-3-7(10)4-2-6/h1-4H,5H2
InChIKey
FKJSFKCZZIXQIP-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
BrCC(=O)c1ccc(Br)cc1
OpenEye OEToolkits 2.0.7
c1cc(ccc1C(=O)CBr)Br
ACDLabs 12.01
C(C(c1ccc(cc1)Br)=O)Br
Formula
C8 H6 Br2 O
Name
p-Bromophenacyl bromide
ChEMBL
CHEMBL142826
DrugBank
ZINC
ZINC000000028146
PDB chain
3hzw Chain B Residue 201 [
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Receptor-Ligand Complex Structure
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PDB
3hzw
Comparison between apo and complexed structures of bothropstoxin-I reveals the role of Lys122 and Ca(2+)-binding loop region for the catalytically inactive Lys49-PLA(2)s.
Resolution
2.28 Å
Binding residue
(original residue number in PDB)
G30 C45 H48
Binding residue
(residue number reindexed from 1)
G29 C44 H47
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
N28 G30 L32 H48 K49 Y52 Y73 D99
Catalytic site (residue number reindexed from 1)
N27 G29 L31 H47 K48 Y51 Y64 D89
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0004623
phospholipase A2 activity
GO:0005509
calcium ion binding
GO:0005543
phospholipid binding
GO:0008201
heparin 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:0042130
negative regulation of T cell proliferation
GO:0042742
defense response to bacterium
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:3hzw
,
PDBe:3hzw
,
PDBj:3hzw
PDBsum
3hzw
PubMed
20371382
UniProt
Q90249
|PA2H1_BOTJR Basic phospholipase A2 homolog bothropstoxin-I
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