Structure of PDB 6iux Chain A Binding Site BS01
Receptor Information
>6iux Chain A (length=358) Species:
9606
(Homo sapiens) [
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GSEKYVAAMVLSAAGDALGYYNGKWEFLQDGEKIHRQLAQLGGLDALDVG
RWRVSDDTVMHLATAEALVEAGKAPKLTQLYYLLAKHYQDCMEDMDGRAP
GGASVHNAMQLKPGKPNGWRIPFNSHEGGCGAAMRAMCIGLRFPHHSQLD
TLIQVSIESGRMTHHHPTGYLGALASALFTAYAVNSRPPLQWGKGLMELL
PEAKKYIVQSGYFVEENLQHWSYFQTKWENYLKLRGILDGESAPTFPESF
GVKERDQFYTSLSYSGWGGSSGHDAPMIAYDAVLAAGDSWKELAHRAFFH
GGDSDSTAAIAGCWWGVMYGFKGVSPSNYEKLEYRNRLEETARALYSLGS
KEDTVISL
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
6iux Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
6iux
Crystal structure of protein
Resolution
1.195 Å
Binding residue
(original residue number in PDB)
S54 D55 D56 D304
Binding residue
(residue number reindexed from 1)
S55 D56 D57 D305
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.2.2.19
: [protein ADP-ribosylarginine] hydrolase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003875
ADP-ribosylarginine hydrolase activity
GO:0005515
protein binding
GO:0016787
hydrolase activity
GO:0016799
hydrolase activity, hydrolyzing N-glycosyl compounds
GO:0030955
potassium ion binding
GO:0046872
metal ion binding
Biological Process
GO:0036211
protein modification process
GO:0051725
protein de-ADP-ribosylation
Cellular Component
GO:0005615
extracellular space
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6iux
,
PDBe:6iux
,
PDBj:6iux
PDBsum
6iux
PubMed
UniProt
P54922
|ADPRH_HUMAN ADP-ribosylhydrolase ARH1 (Gene Name=ADPRH)
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