Structure of PDB 5a65 Chain B Binding Site BS02
Receptor Information
>5a65 Chain B (length=197) Species:
10090
(Mus musculus) [
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GAMTQGLIEVERKFAPGPDTEERLQELGATLEHRVTFRDTYYDTSELSLM
LSDHWLRQREGSGWELKCPHNEYVEVTSEAAIVAQLFELLPAGVAAVLGS
LKLQEVASFITTRSSWKLALSEPQLTIDLDSADFGYAVGEVEAMVHEKAE
VPAALEKIITVSSMLGVPAQEEAPAKLMVYLQRFRPLDYQRLLEAAS
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
5a65 Chain B Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
5a65
Structural Determinants for Substrate Binding and Catalysis in Triphosphate Tunnel Metalloenzymes.
Resolution
1.98 Å
Binding residue
(original residue number in PDB)
D145 E159
Binding residue
(residue number reindexed from 1)
D128 E142
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.6.1.28
: thiamine-triphosphatase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0016462
pyrophosphatase activity
GO:0016787
hydrolase activity
GO:0046872
metal ion binding
GO:0050333
thiamine triphosphate phosphatase activity
Biological Process
GO:0006772
thiamine metabolic process
GO:0009229
thiamine diphosphate biosynthetic process
GO:0016311
dephosphorylation
GO:0042357
thiamine diphosphate metabolic process
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Cellular Component
External links
PDB
RCSB:5a65
,
PDBe:5a65
,
PDBj:5a65
PDBsum
5a65
PubMed
26221030
UniProt
Q8JZL3
|THTPA_MOUSE Thiamine-triphosphatase (Gene Name=Thtpa)
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