Structure of PDB 6jsu Chain A Binding Site BS02
Receptor Information
>6jsu Chain A (length=323) Species:
235909
(Geobacillus kaustophilus HTA426) [
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EMVETVCGPVPVEQLGKTLIHEHFLFGYPGFQGDVTRGTFREDESLRVAV
EAAEKMKRHGIQTVVDPTPNDCGRNPAFLRRVAEETGLNIICATGYCYEG
EGAPPYFQFRRLLGTAEDDIYDMFMAELTEGIADTGIKAGVIKLASSKGR
ITEYEKMFFRAAARAQKETGAVIITHTQEGTMGPEQAAYLLEHGADPKKI
VIGHMCGNTDPDYHRKTLAYGVYIAFDRFGIQGMVGAPTDEERVRTLLAL
LRDGYEKQIMLSHNTVNVWLGRPFTLPEPFAEMMKNWHVEHLFVNIIPAL
KNEGIRDEVLEQMFIGNPAALFS
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
6jsu Chain A Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
6jsu
Directed Computational Evolution of Quorum-Quenching Lactonases from the Amidohydrolase Superfamily.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
K145 H178 H206
Binding residue
(residue number reindexed from 1)
K143 H176 H204
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
H23 H25 K145 H178 H206 G209 R230 N266
Catalytic site (residue number reindexed from 1)
H21 H23 K143 H176 H204 G207 R228 N264
Enzyme Commision number
3.5.-.-
Gene Ontology
Molecular Function
GO:0008270
zinc ion binding
GO:0016787
hydrolase activity
GO:0046872
metal ion binding
Biological Process
GO:0009056
catabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:6jsu
,
PDBe:6jsu
,
PDBj:6jsu
PDBsum
6jsu
PubMed
32320671
UniProt
Q5KZU5
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