Structure of PDB 4h9u Chain B Binding Site BS01
Receptor Information
>4h9u Chain B (length=323) Species:
235909
(Geobacillus kaustophilus HTA426) [
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EMVETVCGPVPVEQLGKTLIHEHFLFGYPGFQGDVTRGTFREDESLRVAV
EAAEKMKRHGIQTVVDPTPNDCGRNPAFLRRVAEETGLNIICATGYYYEG
EGAPPYFQFRRLLGTAEDDIYDMFMAELTEGIADTGIKAGVIKLASSKGR
ITEYEKMFFRAAARAQKETGAVIITHTQEGTMGPEQAAYLLEHGADPKKI
VIGHMCGNTDPDYHRKTLAYGVYIAFDRFGIQGMVGAPTDEERVRTLLAL
LRDGYEKQIMLSHDTVNVWLGRPFTLPEPFAEMMKNWHVEHLFVNIIPAL
KNEGIRDEVLEQMFIGNPAALFS
Ligand information
Ligand ID
FE
InChI
InChI=1S/Fe/q+3
InChIKey
VTLYFUHAOXGGBS-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[Fe+3]
Formula
Fe
Name
FE (III) ION
ChEMBL
DrugBank
DB13949
ZINC
PDB chain
4h9u Chain B Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
4h9u
Structural evidence of a productive active site architecture for an evolved quorum-quenching GKL lactonase.
Resolution
2.099 Å
Binding residue
(original residue number in PDB)
H23 H25 K145 D266
Binding residue
(residue number reindexed from 1)
H21 H23 K143 D264
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
H23 H25 K145 H178 H206 G209 R230 D266
Catalytic site (residue number reindexed from 1)
H21 H23 K143 H176 H204 G207 R228 D264
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:4h9u
,
PDBe:4h9u
,
PDBj:4h9u
PDBsum
4h9u
PubMed
23461395
UniProt
Q5KZU5
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