Structure of PDB 7rsf Chain A Binding Site BS01
Receptor Information
>7rsf Chain A (length=380) Species:
511145
(Escherichia coli str. K-12 substr. MG1655) [
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KLPPFIEIYRALIATPSISATEEALDQSNADLITLLADWFKDLGFNVEVQ
PVPGTRNKFNMLASTGQGAGGLLLAGHTDTVPFDDGRWTRDPFTLTEHDG
KLYGLGTADMKGFFAFILDALRDVDVTKLKKPLYILATADEETSMAGARY
FAETTALRPDCAIIGEPTSLQPVRAHKGHISNAIRIQGQSGHSSDPARGV
NAIELMHDAIGHILQLRDNLKERYHYEAFTVPYPTLNLGHIHGGDASNRI
CAWCELHMDIRPLPGMTLNELNGLLNDALAPVSERWPGRLTVDELHPPIP
GYECPPNHQLVEVVEKLLGAKTEVVNYCTEAPFIQTLCPTLVLGPGSINQ
AHQPDEYLETRFIKPTRELITQVIHHFCWH
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
7rsf Chain A Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
7rsf
Acetylornithine deacetylase from Escherichia coli
Resolution
2.13 Å
Binding residue
(original residue number in PDB)
H80 D112 E169
Binding residue
(residue number reindexed from 1)
H77 D109 E166
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.5.1.16
: acetylornithine deacetylase.
Gene Ontology
Molecular Function
GO:0008270
zinc ion binding
GO:0008777
acetylornithine deacetylase activity
GO:0016787
hydrolase activity
GO:0019213
deacetylase activity
GO:0046872
metal ion binding
GO:0050897
cobalt ion binding
Biological Process
GO:0006526
L-arginine biosynthetic process
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:7rsf
,
PDBe:7rsf
,
PDBj:7rsf
PDBsum
7rsf
PubMed
UniProt
P23908
|ARGE_ECOLI Acetylornithine deacetylase (Gene Name=argE)
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