Structure of PDB 1q74 Chain C Binding Site BS01
Receptor Information
>1q74 Chain C (length=279) Species:
1773
(Mycobacterium tuberculosis) [
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SETPRLLFVHAHPDDESLSNGATIAHYTSRGAQVHVVTCTLGEEGEVIGD
RWAQLTADHADQLGGYRIGELTAALRALGVSAPIYLGGAGRWRDSRSQRR
FVDADPRQTVGALVAIIRELRPHVVVTYDPNGGYGHPDHVHTHTVTTAAV
AAAGADHPGDPWTVPKFYWTVLGLSALISGARALVPDDLRPEWVLPRGYS
DDGIDAVVEADEQARAAKVAALAAHATQVVVGPTGRAAALSNNLALPILA
DEHYVLAGGSAGARDERGWETDLLAGLGF
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
1q74 Chain C Residue 304 [
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Receptor-Ligand Complex Structure
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PDB
1q74
The Crystal Structure of 1-D-myo-Inositol 2-Acetamido-2-deoxy-alpha-D-glucopyranoside Deacetylase (MshB) from Mycobacterium tuberculosis Reveals a Zinc Hydrolase with a Lactate Dehydrogenase Fold.
Resolution
1.7 Å
Binding residue
(original residue number in PDB)
H13 D16 H147
Binding residue
(residue number reindexed from 1)
H12 D15 H139
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.5.1.103
: N-acetyl-1-D-myo-inositol-2-amino-2-deoxy-alpha-D-glucopyranoside deacetylase.
Gene Ontology
Molecular Function
GO:0008270
zinc ion binding
GO:0016787
hydrolase activity
GO:0016811
hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides
GO:0019213
deacetylase activity
GO:0035595
N-acetylglucosaminylinositol deacetylase activity
GO:0046872
metal ion binding
Biological Process
GO:0010125
mycothiol biosynthetic process
GO:0016137
glycoside metabolic process
Cellular Component
GO:0005886
plasma membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1q74
,
PDBe:1q74
,
PDBj:1q74
PDBsum
1q74
PubMed
12958317
UniProt
P9WJN3
|MSHB_MYCTU 1D-myo-inositol 2-acetamido-2-deoxy-alpha-D-glucopyranoside deacetylase (Gene Name=mshB)
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