Structure of PDB 6umq Chain A Binding Site BS01
Receptor Information
>6umq Chain A (length=415) Species:
9606
(Homo sapiens) [
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VPASLSGQDVGSFAYLTIKDRIPQILTKVIDTLHRHKSEFFEKHGEEGVE
AEKKAISLLSKLRNELQTDKPFIPLVEKFVDTDIWNQYLEYQQSLLNESD
GKSRWFYSPWLLVECYMYRRIHEAIIQSPPIDYFDVFKESKEQNFYGSQE
SIIALCTHLQQLIRTIEDLDENQLKDEFFKLLQISLWLEDLKPFILLNDM
EHLWSLLSNCKKTREKASATRVYIVLDNSGFELVTDLILADFLLSSELAT
EVHFYGKTIPWFVSDTTIHDFNWLIEQVKHSNHKWMSKCGADWEEYIKMG
KWVYHNHIFWTLPHEYCAMPQVAPDLYAELQKAHLILFKGDLNYRKLTGD
RKWEFSVPFHQALNGFHPAPLCTIRTLKAEIQVGLQPGQGEQLLASEPSW
WTTGKYGIFQYDGPL
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
6umq Chain A Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
6umq
Human ARMT1 structure and substrate specificity indicates that it is a DUF89 family damage-control phosphatase.
Resolution
1.85 Å
Binding residue
(original residue number in PDB)
D253 N254 D291
Binding residue
(residue number reindexed from 1)
D227 N228 D265
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.1.1.-
3.1.3.-
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0008168
methyltransferase activity
GO:0008757
S-adenosylmethionine-dependent methyltransferase activity
GO:0008983
protein-glutamate O-methyltransferase activity
GO:0016787
hydrolase activity
GO:0016791
phosphatase activity
GO:0019899
enzyme binding
GO:0046872
metal ion binding
GO:0051998
protein carboxyl O-methyltransferase activity
GO:0097023
fructose 6-phosphate aldolase activity
GO:0103026
fructose-1-phosphatase activity
Biological Process
GO:0006974
DNA damage response
GO:0032259
methylation
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:6umq
,
PDBe:6umq
,
PDBj:6umq
PDBsum
6umq
PubMed
32682077
UniProt
Q9H993
|ARMT1_HUMAN Damage-control phosphatase ARMT1 (Gene Name=ARMT1)
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