Structure of PDB 1shz Chain A Binding Site BS01
Receptor Information
>1shz Chain A (length=326) Species:
10090,10116
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AREVKLLLLGAGESGKSTFLKQMRIIHGQDFDQRAREEFRPTIYSNVIKG
MRVLVDAREKLHIPWGDNKNQLHGDKLMAFDTRAPMAAQGMVETRVFLQY
LPAIRALWEDSGIQNAYDRRREFQLGESVKYFLDNLDKLGVPDYIPSQQD
ILLARRPTKGIHETHFTFKDLHFKMFDVGGQRSERKKWFECFEGVTAIIF
CVALSDYDQVLMEDRQTNRMHESMKLFDSICNNKWFTDTSIILFLNKKDL
FEEKIKKSPLTICYPEYAGSNTYEEAAAYIQCQFEDLNKRKDTKEIYTHF
TCATDTKNVQFVFDAVTDVIIKNNLK
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
1shz Chain A Residue 377 [
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Receptor-Ligand Complex Structure
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PDB
1shz
Structure of the p115RhoGEF rgRGS domain-Galpha13/i1 chimera complex suggests convergent evolution of a GTPase activator.
Resolution
2.85 Å
Binding residue
(original residue number in PDB)
S62 T203
Binding residue
(residue number reindexed from 1)
S17 T158
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
E58 T63 R200 D222 Q226
Catalytic site (residue number reindexed from 1)
E13 T18 R155 D177 Q181
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0003924
GTPase activity
GO:0005525
GTP binding
GO:0019001
guanyl nucleotide binding
GO:0031683
G-protein beta/gamma-subunit complex binding
Biological Process
GO:0007165
signal transduction
GO:0007186
G protein-coupled receptor signaling pathway
GO:0007188
adenylate cyclase-modulating G protein-coupled receptor signaling pathway
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Molecular Function
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Biological Process
External links
PDB
RCSB:1shz
,
PDBe:1shz
,
PDBj:1shz
PDBsum
1shz
PubMed
15665872
UniProt
P10824
|GNAI1_RAT Guanine nucleotide-binding protein G(i) subunit alpha-1 (Gene Name=Gnai1);
P27601
|GNA13_MOUSE Guanine nucleotide-binding protein subunit alpha-13 (Gene Name=Gna13)
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