Structure of PDB 7tu2 Chain A Binding Site BS01
Receptor Information
>7tu2 Chain A (length=434) Species:
398720
(Leeuwenhoekiella blandensis MED217) [
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ANWEHLLSLKRQGDTAKRLRIEQDDTRLGFEVDYDAIIFSAPFRSLQDKT
QVIPLSKTDFVHTRLTHSLEVSVVGRSLGRMVGKKLLEKYPHLEQVYGYK
FNDFGAIVAAAALAHDIGNPPFGHSGEKAIGEFFKNGYGKRYKDSLTAKE
YQDLIKFEGNANGFKVLSQSKPGAQGGLRLSYATLGAFMKYPKESLPHKP
SDHIADKKYGFFQSERALFEDVAQELGLLKRSTTDDVSWSRHPLAYLVEA
ADDICYTIIDFEDGINLGLIPEEYALEYMVKLVGQTIDRNKYNALQETSD
RVSYLRALAIGTLINESVDTFMKYEEEILAGTFDQSLIDKSNYQAQITDI
INLSIERIYNSREVIEKEIAGYEILSTLLEARCRALDNNDTHYNQLIQQL
LAPSLYENLIQICAEVSTMTDGKALRNYKKIKGL
Ligand information
Ligand ID
MN
InChI
InChI=1S/Mn/q+2
InChIKey
WAEMQWOKJMHJLA-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mn+2]
CACTVS 3.341
[Mn++]
Formula
Mn
Name
MANGANESE (II) ION
ChEMBL
DrugBank
DB06757
ZINC
PDB chain
7tu2 Chain A Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
7tu2
High-resolution structures of the SAMHD1 dGTPase homolog from Leeuwenhoekiella blandensis reveal a novel mechanism of allosteric activation by dATP.
Resolution
2.13 Å
Binding residue
(original residue number in PDB)
H68 H116 D117 D253
Binding residue
(residue number reindexed from 1)
H67 H115 D116 D252
Annotation score
1
Enzymatic activity
Enzyme Commision number
?
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
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Biological Process
External links
PDB
RCSB:7tu2
,
PDBe:7tu2
,
PDBj:7tu2
PDBsum
7tu2
PubMed
35643313
UniProt
A3XHN1
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