Structure of PDB 6fv4 Chain A Binding Site BS01
Receptor Information
>6fv4 Chain A (length=381) Species:
246196
(Mycolicibacterium smegmatis MC2 155) [
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GSHMLLTADTVLTGTELLRPGWLEIASDRVVAVGAGAPPAQADRNLGAAT
VVPGFVDTHLHGGGGGNFSAATDDETARAVALHRAHGSTTLVASLVTAGP
EDLLRQVSGLARQVRAGLIDGIHLEGPWLSTLRCGAHQPVLMRDPDPGEI
GRVLDAGEGTVRMVTIAPERDGALAAIAQLVNAGVVAAVGHTEATYDQTR
AAIDAGATVGTHLFNAMRPIDRREPGPAVALTEDSRVTVEMIVDGVHVAP
AIYRHITQTVGPERLSLITAAMAATGMSDGVYRLGPLDIDVVAGVARVAG
TDTIAGSTATMEQVFRLAVAHCGLPRDDALSLAVRQACVNPARALGLPAA
GLAAGARADLVVLDHDLAVTAVMRAGEWVVT
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
6fv4 Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
6fv4
Structural and functional determination of homologs of theMycobacterium tuberculosis N-acetylglucosamine-6-phosphate deacetylase (NagA).
Resolution
1.974 Å
Binding residue
(original residue number in PDB)
H56 H58 E122
Binding residue
(residue number reindexed from 1)
H59 H61 E125
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
GO:0047419
N-acetylgalactosamine-6-phosphate deacetylase activity
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:6fv4
,
PDBe:6fv4
,
PDBj:6fv4
PDBsum
6fv4
PubMed
29728457
UniProt
A0QU89
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