Structure of PDB 5xd3 Chain A Binding Site BS03
Receptor Information
>5xd3 Chain A (length=291) Species:
246196
(Mycolicibacterium smegmatis MC2 155) [
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KHTVRAAGAVLWRDATVEVAVIHRPRYDDWSLPKGKLDQGETEPVAAARE
IHEETGHTAVLGRRLGRVTYPIPQGTKRVWYWAAKSTGGDFSPNDEVDKL
VWLPVDAAMDQLQYPDDRKVLRRFVKRPVDTKTVLVVRHGTAGRRSRYKG
DDRKRPLDKRGRAQAEALVAQLMAFGATTLYAADRVRCHQTIEPLAQELD
QLIHNEPLLTEEAYAADHKAARKRLLEIAGRPGNPVICTQGKVIPGLIEW
WCERAKVRPETTGNRKGSTWVLSLSDGELVGADYLSPPDEK
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
5xd3 Chain A Residue 404 [
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Receptor-Ligand Complex Structure
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PDB
5xd3
Hydrolysis of diadenosine polyphosphates. Exploration of an additional role of Mycobacterium smegmatis MutT1
Resolution
1.78 Å
Binding residue
(original residue number in PDB)
K65 E85
Binding residue
(residue number reindexed from 1)
K34 E54
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T23 A29
Catalytic site (residue number reindexed from 1)
T3 A9
Enzyme Commision number
3.6.1.58
: 8-oxo-dGDP phosphatase.
3.6.1.61
: diadenosine hexaphosphate hydrolase (ATP-forming).
3.6.1.69
: 8-oxo-(d)GTP phosphatase.
Gene Ontology
Molecular Function
GO:0008413
8-oxo-7,8-dihydroguanosine triphosphate pyrophosphatase activity
GO:0016787
hydrolase activity
GO:0044715
8-oxo-dGDP phosphatase activity
GO:0044716
8-oxo-GDP phosphatase activity
GO:0046872
metal ion binding
Biological Process
GO:0006260
DNA replication
GO:0006281
DNA repair
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:5xd3
,
PDBe:5xd3
,
PDBj:5xd3
PDBsum
5xd3
PubMed
28705712
UniProt
A0QUZ2
|MUTT1_MYCS2 8-oxo-(d)GTP phosphatase (Gene Name=mutT1)
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