Structure of PDB 5fwa Chain A Binding Site BS02
Receptor Information
>5fwa Chain A (length=339) Species:
10090
(Mus musculus) [
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DTWQDEEYFDSYGTLKLHLEMLADQPRTTKYHSVILQNKESLKDKVILDV
GCGTGIISLFCAHHARPKAVYAVEASDMAQHTSQLVLQNGFADTITVFQQ
KVEDVVLPEKVDVLVSEWMGTCLLFEFMIESILYARDTWLKGDGIIWPTT
AALHLVPCSAEKDYHSKVLFWDNAYEFNLSALKSLAIKEFFSRPKSNHIL
KPEDCLSEPCTILQLDMRTVQVPDLETMRGELRFDIQKAGTLHGFTAWFS
VYFQSLEEGQPQQVLSTGPLHPTTHWKQTLFMMDDPVPVHTGDVVTGSVV
LQRNPVWRRHMSVSLSWVVTSALDPTSQRVGEKVFPIWW
Ligand information
Ligand ID
CA
InChI
InChI=1S/Ca/q+2
InChIKey
BHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
Formula
Ca
Name
CALCIUM ION
ChEMBL
DrugBank
DB14577
ZINC
PDB chain
5fwa Chain A Residue 1452 [
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Receptor-Ligand Complex Structure
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PDB
5fwa
Structural studies of protein arginine methyltransferase 2 reveal its interactions with potential substrates and inhibitors.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
G196 D199
Binding residue
(residue number reindexed from 1)
G90 D93
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D130 E223 E232 H381
Catalytic site (residue number reindexed from 1)
D24 E117 E126 H275
Enzyme Commision number
2.1.1.125
: Transferred entry: 2.1.1.319, 2.1.1.320, 2.1.1.321 and 2.1.1.322.
Gene Ontology
Molecular Function
GO:0008168
methyltransferase activity
GO:0016274
protein-arginine N-methyltransferase activity
GO:0046872
metal ion binding
Biological Process
GO:0018216
peptidyl-arginine methylation
GO:0032259
methylation
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:5fwa
,
PDBe:5fwa
,
PDBj:5fwa
PDBsum
5fwa
PubMed
27879050
UniProt
Q3UKX1
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