Structure of PDB 8i67 Chain A Binding Site BS01
Receptor Information
>8i67 Chain A (length=228) Species:
83332
(Mycobacterium tuberculosis H37Rv) [
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SMTARPLSELVERGWAAALEPVADQVAHMGQFLRAEIAAGRRYLPAGSNV
LRAFTFPFDNVRVLIVGQDPYPTPGHAVGLSFSVAPDVRPWPRSLANIFD
EYTADLGYPLPSNGDLTPWAQRGVLLLNRVLTVRPSNPASHRGKGWEAVT
ECAIRALAARAAPLVAILWGRDASTLKPMLAAGNCVAIESPHPSPLSASR
GFFGSRPFSRANELLVGMGAEPIDWRLP
Ligand information
Ligand ID
OD3
InChI
InChI=1S/C3H3NO2S/c5-2-1-7-3(6)4-2/h1H2,(H,4,5,6)
InChIKey
ZOBPZXTWZATXDG-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.7
C1C(=O)NC(=O)S1
CACTVS 3.385
O=C1CSC(=O)N1
Formula
C3 H3 N O2 S
Name
1,3-thiazolidine-2,4-dione;
2,4-Thiazolidinedione
ChEMBL
CHEMBL85398
DrugBank
DB11898
ZINC
ZINC000008554292
PDB chain
8i67 Chain A Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
8i67
Structural plasticity in Mycobacterium tuberculosis uracil-DNA glycosylase (MtUng) and its functional implications.
Resolution
1.72 Å
Binding residue
(original residue number in PDB)
G66 Q67 D68 Y70 F81 N127 H191
Binding residue
(residue number reindexed from 1)
G67 Q68 D69 Y71 F82 N128 H192
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.2.2.27
: uracil-DNA glycosylase.
Gene Ontology
Molecular Function
GO:0004844
uracil DNA N-glycosylase activity
GO:0016787
hydrolase activity
GO:0016799
hydrolase activity, hydrolyzing N-glycosyl compounds
Biological Process
GO:0006281
DNA repair
GO:0006284
base-excision repair
GO:0097510
base-excision repair, AP site formation via deaminated base removal
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:8i67
,
PDBe:8i67
,
PDBj:8i67
PDBsum
8i67
PubMed
37399710
UniProt
P9WFQ9
|UNG_MYCTU Uracil-DNA glycosylase (Gene Name=ung)
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