Structure of PDB 1ppx Chain A Binding Site BS01
Receptor Information
>1ppx Chain A (length=129) Species:
562
(Escherichia coli) [
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MKKLQIAVGIIRNENNEIFITRRAADAHMANKLEFPGGKIEMGETPEQAV
VRELQEEVGITPQHFSLFEKLEYEFPDRHITLWFWLVERWEGEPWGKEGQ
PGEWMSLVGLNADDFPPANEPVIAKLKRL
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
1ppx Chain A Residue 130 [
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Receptor-Ligand Complex Structure
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PDB
1ppx
Solution structure and NH exchange studies of the MutT pyrophosphohydrolase complexed with Mg(2+) and 8-oxo-dGMP, a tightly bound product.
Resolution
N/A
Binding residue
(original residue number in PDB)
G38 E53 E56 E57
Binding residue
(residue number reindexed from 1)
G38 E53 E56 E57
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.6.1.55
: 8-oxo-dGTP diphosphatase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0005515
protein binding
GO:0008413
8-oxo-7,8-dihydroguanosine triphosphate pyrophosphatase activity
GO:0016787
hydrolase activity
GO:0030145
manganese ion binding
GO:0035539
8-oxo-7,8-dihydrodeoxyguanosine triphosphate pyrophosphatase activity
GO:0044715
8-oxo-dGDP phosphatase activity
GO:0044716
8-oxo-GDP phosphatase activity
GO:0046872
metal ion binding
GO:0047693
ATP diphosphatase activity
Biological Process
GO:0006203
dGTP catabolic process
GO:0006260
DNA replication
GO:0006281
DNA repair
GO:0006289
nucleotide-excision repair
GO:0046067
dGDP catabolic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:1ppx
,
PDBe:1ppx
,
PDBj:1ppx
PDBsum
1ppx
PubMed
12939141
UniProt
P08337
|MUTT_ECOLI 8-oxo-dGTP diphosphatase (Gene Name=mutT)
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