Structure of PDB 6jku Chain D Binding Site BS01
Receptor Information
>6jku Chain D (length=379) Species:
747
(Pasteurella multocida) [
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FMYAFVNAVIYTAKDVLYGKALVVDGDKISAILPVEDVPENLQKIDLQGN
NLTAGFIDLQLNGCGGVMFNEDISVKTLEIMQETNLKSGTTSYLPTFITS
PDEGMKDAVKVMREYLTQYKNQALGLHFEGPYLSVEKKGVHREEYIRAIS
PEMKTFLCDNADVITKITLAAENPTAQYIPDFVEKGIIVSLGHSNATYDV
AQQAIEKGASFATHLHNAMSPISSGRAMGVVGAVLDSDIYTGIIVDGLHV
DYGNIRLDKKVKGDKLCIVTDATAAAGADIDSFVFVGKTVYVRDGKCYDS
NGTLGGAAITMIESVKNAVQEVGIPLDETLRMCNYYPAKAIGVDHKLGSI
EVGKIANLTAFTNDFNVLGTAVNGEWKAN
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
6jku Chain D Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
6jku
Quaternary variations in the structural assembly of N-acetylglucosamine-6-phosphate deacetylase from Pasteurella multocida.
Resolution
1.95 Å
Binding residue
(original residue number in PDB)
E128 H192 H213
Binding residue
(residue number reindexed from 1)
E129 H193 H214
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.5.1.25
: N-acetylglucosamine-6-phosphate deacetylase.
Gene Ontology
Molecular Function
GO:0008448
N-acetylglucosamine-6-phosphate deacetylase activity
GO:0016787
hydrolase activity
GO:0016810
hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds
GO:0046872
metal ion binding
Biological Process
GO:0006040
amino sugar metabolic process
GO:0006044
N-acetylglucosamine metabolic process
GO:0006046
N-acetylglucosamine catabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:6jku
,
PDBe:6jku
,
PDBj:6jku
PDBsum
6jku
PubMed
32865821
UniProt
Q9CMF5
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