Structure of PDB 4ewl Chain B Binding Site BS02
Receptor Information
>4ewl Chain B (length=290) Species:
1773
(Mycobacterium tuberculosis) [
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MSETPRLLFVHAHPDDESLSNGATIAHYTSRGAQVHVVTCTLGEEGEVIG
DRWAQLTADHADQLGGYRIGELTAALRALGVSAPIYLGGAGRWRDSGMAG
TDQRSQRRFVDADPRQTVGALVAIIRELRPHVVVTYDPNGGYGHPDHVHT
HTVTTAAVAAAGVGDPWTVPKFYWTVLGLSALISGARALVPDDLRPEWVL
PRADEIAFGYSDDGIDAVVEADEQARAAKVAALAAHATQVVVGPTGRAAA
LSNNLALPILADEHYVLAGGSAGARDERGWETDLLAGLGF
Ligand information
Ligand ID
ACT
InChI
InChI=1S/C2H4O2/c1-2(3)4/h1H3,(H,3,4)/p-1
InChIKey
QTBSBXVTEAMEQO-UHFFFAOYSA-M
SMILES
Software
SMILES
ACDLabs 10.04
[O-]C(=O)C
OpenEye OEToolkits 1.5.0
CC(=O)[O-]
CACTVS 3.341
CC([O-])=O
Formula
C2 H3 O2
Name
ACETATE ION
ChEMBL
DrugBank
DB14511
ZINC
PDB chain
4ewl Chain B Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
4ewl
A new crystal form of MshB from Mycobacterium tuberculosis with glycerol and acetate in the active site suggests the catalytic mechanism.
Resolution
1.85 Å
Binding residue
(original residue number in PDB)
H13 D15 D16 Y142 H147
Binding residue
(residue number reindexed from 1)
H13 D15 D16 Y142 H147
Annotation score
5
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:4ewl
,
PDBe:4ewl
,
PDBj:4ewl
PDBsum
4ewl
PubMed
23090394
UniProt
P9WJN3
|MSHB_MYCTU 1D-myo-inositol 2-acetamido-2-deoxy-alpha-D-glucopyranoside deacetylase (Gene Name=mshB)
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