Structure of PDB 4zwp Chain B Binding Site BS01
Receptor Information
>4zwp Chain B (length=428) Species:
232
(Alteromonas sp.) [
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NKLAVLYAEHIATLQKRTREIIERENLDGVVFHSGQAKRQFLDDMYYPFK
VNPQFKAWLPVIDNPHCWIVANGTDKPKLIFYRPVDFWHPNEYWADYFDI
ELLVKPDQVEKLLPYDKARFAYIGEYLEVAQALGFELMNPEPVMNFYHYH
RAYKTQYELACMREANKIAVQGHKAARDAFFQGKSEFEIQQAYLLATQHS
ENDTPFGNIVALNENCAILHYTHFDRVAPATHRSFLIDAGANFNGYAADI
TRTYDFTGEGEFAELVATMKQHQIALCNQLAPGKLYGELHLDCHQRVAQT
LSDFNIVNLSADEIVAKGITSTFFPHGLGHHIGLQVHDVGGFMADEQGAH
QEPPRCTRKIEANQVFTIEPGLYFIDSLLGDLAATDNNQHINWDKVAELK
PFGGIRIEDNIIVHEDSLENMTRELELD
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
4zwp Chain B Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
4zwp
Engineering the Organophosphorus Acid Anhydrolase Enzyme for Increased Catalytic Efficiency and Broadened Stereospecificity on Russian VX.
Resolution
2.397 Å
Binding residue
(original residue number in PDB)
D244 D255 E420
Binding residue
(residue number reindexed from 1)
D238 D249 E408
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)
D44 H220 D238 D249 H326 H330 H337 E369 Y373 R406 E408
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:4zwp
,
PDBe:4zwp
,
PDBj:4zwp
PDBsum
4zwp
PubMed
26418828
UniProt
Q44238
|PEPQ_ALTSX Xaa-Pro dipeptidase (Gene Name=pepQ)
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