Structure of PDB 7tu6 Chain D Binding Site BS04
Receptor Information
>7tu6 Chain D (length=430) Species:
398720
(Leeuwenhoekiella blandensis MED217) [
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NWEHLLSLKRQGDTAKRLRIEQDDTRLGFEVDYDRIIFSAPFRSLQDKTQ
VIPLDFVHTRLTHSLEVSVVGRSLGRMVGKKLLEKYPHLEQVYGYKFNDF
GAIVAAAALAHDIGNPPFGHSGEKAIGEFFKNGYGKRYKDSLTAKEYQDL
IKFEGNANGFKVLSQSKPGAQGGLRLSYATLGAFMKYPKESLPHKPSDHI
ADKKYGFFQSERALFEDVAQELGLLKRSDVSWSRHPLAYLVEAADDICYT
IIDFEDGINLGLIPEEYALEYMVKLVGQTIDRNKYNALQETSDRVSYLRA
LAIGTLINESVDTFMKYEEEILAGTFDQSLIDKSNYQAQITDIINLSIER
IYNSREVIEKEIAGYEILSTLLEARCRALDNNDTHYNQLIQQLLAPNEKS
LYENLIQICAEVSTMTDGKALRNYKKIKGL
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
7tu6 Chain D Residue 503 [
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Receptor-Ligand Complex Structure
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PDB
7tu6
High-resolution structures of the SAMHD1 dGTPase homolog from Leeuwenhoekiella blandensis reveal a novel mechanism of allosteric activation by dATP.
Resolution
2.7 Å
Binding residue
(original residue number in PDB)
H68 H116 D117 D253
Binding residue
(residue number reindexed from 1)
H63 H111 D112 D245
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.1.5.1
: dGTPase.
Gene Ontology
Molecular Function
GO:0008832
dGTPase activity
GO:0016787
hydrolase activity
GO:0016793
triphosphoric monoester hydrolase activity
GO:0046872
metal ion binding
Biological Process
GO:0006203
dGTP catabolic process
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Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:7tu6
,
PDBe:7tu6
,
PDBj:7tu6
PDBsum
7tu6
PubMed
35643313
UniProt
A3XHN1
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