Structure of PDB 4zwo Chain B Binding Site BS02
Receptor Information
>4zwo Chain B (length=434) Species:
232
(Alteromonas sp.) [
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KLAVLYAEHIATLQKRTREIIERENLDGVVFHSGQAKRQFLDDMYYPFKV
NPQFKAWLPVIDNPHCWIVANGTDKPKLIFYRPVDFWHKVNEYWADYFDI
ELLVKPDQVEKLLPYDKARFAYIGEYLEVAQALGFELMNPEPVMNFYHYH
RAYKTQYELACMREANKIAVQGHKAARDAFFQGKSEFEIQQAYLLATQHS
ENDTPFGNIVALNENCAILHYTHFDRVAPATHRSFLIDAGANFNGYAADI
TRTYDFTGEGEFAELVATMKQHQIALCNQLAPGKLYGELHLDCHQRVAQT
LSDFNIVNLSADEIVAKGITSTFFPHGLGHHIGLQVHDVGGFMADEQGAH
QEPPEGHPFLRCTRKIEANQVFTIEPGLYFIDSLLGDLAATDNNQHINWD
KVAELKPFGGIRIEDNIIVHEDSLENMTRELELD
Ligand information
Ligand ID
MN
InChI
InChI=1S/Mn/q+2
InChIKey
WAEMQWOKJMHJLA-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mn+2]
CACTVS 3.341
[Mn++]
Formula
Mn
Name
MANGANESE (II) ION
ChEMBL
DrugBank
DB06757
ZINC
PDB chain
4zwo Chain B Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
4zwo
Engineering the Organophosphorus Acid Anhydrolase Enzyme for Increased Catalytic Efficiency and Broadened Stereospecificity on Russian VX.
Resolution
2.141 Å
Binding residue
(original residue number in PDB)
D255 H336 T379 E381 E420
Binding residue
(residue number reindexed from 1)
D249 H330 T373 E375 E414
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D45 H226 D244 D255 H332 H336 H343 E381 Y385 R418 E420
Catalytic site (residue number reindexed from 1)
D43 H220 D238 D249 H326 H330 H337 E375 Y379 R412 E414
Enzyme Commision number
3.1.8.1
: aryldialkylphosphatase.
3.4.13.9
: Xaa-Pro dipeptidase.
3.8.2.2
: diisopropyl-fluorophosphatase.
Gene Ontology
Molecular Function
GO:0016795
phosphoric triester hydrolase activity
View graph for
Molecular Function
External links
PDB
RCSB:4zwo
,
PDBe:4zwo
,
PDBj:4zwo
PDBsum
4zwo
PubMed
26418828
UniProt
Q44238
|PEPQ_ALTSX Xaa-Pro dipeptidase (Gene Name=pepQ)
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