Structure of PDB 1as0 Chain A Binding Site BS02
Receptor Information
>1as0 Chain A (length=313) Species:
10116
(Rattus norvegicus) [
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REVKLLLLGAVESGKSTIVKQMKIIHEAGYSEEECKQYKAVVYSNTIQSI
IAIIRAMGRLKIDFGDAARADDARQLFVLAGAAEEGFMTAELAGVIKRLW
KDSGVQACFNRSREYQLNDSAAYYLNDLDRIAQPNYIPTQQDVLRTRVKT
TGIVETHFTFKDLHFKMFDVGGQRSERKKWIHCFEGVTAIIFCVALSDYD
LVLAEDEEMNRMHESMKLFDSICNNKWFTDTSIILFLNKKDLFEEKIKKS
PLTICYPEYAGSNTYEEAAAYIQCQFEDLNKRKDTKEIYTHFTCATDTKN
VQFVFDAVTDVII
Ligand information
Ligand ID
GSP
InChI
InChI=1S/C10H16N5O13P3S/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(26-9)1-25-29(19,20)27-30(21,22)28-31(23,24)32/h2-3,5-6,9,16-17H,1H2,(H,19,20)(H,21,22)(H2,23,24,32)(H3,11,13,14,18)/t3-,5-,6-,9-/m1/s1
InChIKey
XOFLBQFBSOEHOG-UUOKFMHZSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc2c(n1C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OP(=S)(O)O)O)O)N=C(NC2=O)N
CACTVS 3.341
NC1=Nc2n(cnc2C(=O)N1)[C@@H]3O[C@H](CO[P@@](O)(=O)O[P@@](O)(=O)O[P](O)(O)=S)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.5.0
c1nc2c(n1[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@](=O)(O)OP(=S)(O)O)O)O)N=C(NC2=O)N
CACTVS 3.341
NC1=Nc2n(cnc2C(=O)N1)[CH]3O[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=S)[CH](O)[CH]3O
ACDLabs 10.04
S=P(O)(O)OP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c2N=C(N)NC1=O)C(O)C3O
Formula
C10 H16 N5 O13 P3 S
Name
5'-GUANOSINE-DIPHOSPHATE-MONOTHIOPHOSPHATE
ChEMBL
CHEMBL1204628
DrugBank
DB01864
ZINC
ZINC000008217391
PDB chain
1as0 Chain A Residue 355 [
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Receptor-Ligand Complex Structure
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PDB
1as0
Structural and biochemical characterization of the GTPgammaS-, GDP.Pi-, and GDP-bound forms of a GTPase-deficient Gly42 --> Val mutant of Gialpha1.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
E43 S44 G45 K46 S47 T48 D150 L175 R176 T177 K180 T181 G202 G203 N269 K270 D272 L273 C325 A326
Binding residue
(residue number reindexed from 1)
E12 S13 G14 K15 S16 T17 D119 L144 R145 T146 K149 T150 G171 G172 N238 K239 D241 L242 C294 A295
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
E43 T48 R178 D200 Q204
Catalytic site (residue number reindexed from 1)
E12 T17 R147 D169 Q173
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0001664
G protein-coupled receptor binding
GO:0003924
GTPase activity
GO:0005515
protein binding
GO:0005525
GTP binding
GO:0016787
hydrolase activity
GO:0019001
guanyl nucleotide binding
GO:0019003
GDP binding
GO:0031683
G-protein beta/gamma-subunit complex binding
GO:0031749
D2 dopamine receptor binding
GO:0031821
G protein-coupled serotonin receptor binding
GO:0032794
GTPase activating protein binding
GO:0046872
metal ion 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
GO:0043949
regulation of cAMP-mediated signaling
GO:0050805
negative regulation of synaptic transmission
GO:0051301
cell division
GO:0060236
regulation of mitotic spindle organization
GO:0099645
neurotransmitter receptor localization to postsynaptic specialization membrane
GO:1904322
cellular response to forskolin
GO:1904778
positive regulation of protein localization to cell cortex
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005813
centrosome
GO:0005834
heterotrimeric G-protein complex
GO:0005856
cytoskeleton
GO:0005886
plasma membrane
GO:0005938
cell cortex
GO:0030496
midbody
GO:0032991
protein-containing complex
GO:0098794
postsynapse
GO:0098978
glutamatergic synapse
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1as0
,
PDBe:1as0
,
PDBj:1as0
PDBsum
1as0
PubMed
9398294
UniProt
P10824
|GNAI1_RAT Guanine nucleotide-binding protein G(i) subunit alpha-1 (Gene Name=Gnai1)
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