Structure of PDB 5xd5 Chain B Binding Site BS05
Receptor Information
>5xd5 Chain B (length=289) Species:
246196
(Mycolicibacterium smegmatis MC2 155) [
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HTVRAAGAVLWRDATVEVAVIHRPRYDDWSLPKGKLDQGETEPVAAAREI
HEETGHTAVLGRRLGRVTYPIPQGTKRVWYWAAKSTGGDFSPNDEVDKLV
WLPVDAAMDQLQYPDDRKVLRRFVKRPVDTKTVLVVRHGTAGRRSRYKGD
DRKRPLDKRGRAQAEALVAQLMAFGATTLYAADRVRCHQTIEPLAQELDQ
LIHNEPLLTEEAYAADHKAARKRLLEIAGRPGNPVICTQGKVIPGLIEWW
CERAKVRPETTGNRKGSTWVLSLSDGELVGADYLSPPDE
Ligand information
Ligand ID
F
InChI
InChI=1S/FH/h1H/p-1
InChIKey
KRHYYFGTRYWZRS-UHFFFAOYSA-M
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[F-]
Formula
F
Name
FLUORIDE ION
ChEMBL
DrugBank
DB11257
ZINC
PDB chain
5xd5 Chain B Residue 411 [
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Receptor-Ligand Complex Structure
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PDB
5xd5
Hydrolysis of diadenosine polyphosphates. Exploration of an additional role of Mycobacterium smegmatis MutT1
Resolution
1.75 Å
Binding residue
(original residue number in PDB)
E81 E127
Binding residue
(residue number reindexed from 1)
E49 E95
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T23 A29
Catalytic site (residue number reindexed from 1)
T2 A8
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:5xd5
,
PDBe:5xd5
,
PDBj:5xd5
PDBsum
5xd5
PubMed
28705712
UniProt
A0QUZ2
|MUTT1_MYCS2 8-oxo-(d)GTP phosphatase (Gene Name=mutT1)
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