Structure of PDB 1muy Chain A Binding Site BS01
Receptor Information
>1muy Chain A (length=225) Species:
562
(Escherichia coli) [
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MQASQFSAQVLDWYDKYGRKTLPWQIDKTPYKVWLSEVMLQQTQVATVIP
YFERFMARFPTVTDLANAPLDEVLHLWTGLGYYARARNLHKAAQQVATLH
GGKFPETFEEVAALPGVGRSTAGAILSLSLGKHFPILDGNVKRVLARCYA
VSGWPGKKEVENKLWSLSEQVTPAVGVERFNQAMMDLGAMICTRSKPKCS
LCPLQNGCIAAANNSWALYPGKKPK
Ligand information
Ligand ID
SF4
InChI
InChI=1S/4Fe.4S
InChIKey
LJBDFODJNLIPKO-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.7
[S]12[Fe]3[S]4[Fe]1[S]5[Fe]2[S]3[Fe]45
CACTVS 3.385
S1[Fe]S[Fe]1.S2[Fe]S[Fe]2
Formula
Fe4 S4
Name
IRON/SULFUR CLUSTER
ChEMBL
DrugBank
ZINC
PDB chain
1muy Chain A Residue 300 [
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Receptor-Ligand Complex Structure
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PDB
1muy
MutY catalytic core, mutant and bound adenine structures define specificity for DNA repair enzyme superfamily.
Resolution
1.4 Å
Binding residue
(original residue number in PDB)
R147 C192 P197 C199 C202 Q205 C208
Binding residue
(residue number reindexed from 1)
R147 C192 P197 C199 C202 Q205 C208
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
E37 S120 D138
Catalytic site (residue number reindexed from 1)
E37 S120 D138
Enzyme Commision number
3.2.2.31
: adenine glycosylase.
Gene Ontology
Molecular Function
GO:0003677
DNA binding
GO:0003824
catalytic activity
GO:0016798
hydrolase activity, acting on glycosyl bonds
GO:0019104
DNA N-glycosylase activity
GO:0051539
4 iron, 4 sulfur cluster binding
Biological Process
GO:0006281
DNA repair
GO:0006284
base-excision repair
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:1muy
,
PDBe:1muy
,
PDBj:1muy
PDBsum
1muy
PubMed
9846876
UniProt
P17802
|MUTY_ECOLI Adenine DNA glycosylase (Gene Name=mutY)
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