Structure of PDB 4g5q Chain B Binding Site BS02
Receptor Information
>4g5q Chain B (length=316) Species:
9606
(Homo sapiens) [
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REVKLLLLGAGESGKSTIVKQMKIIHEAGYSEEECKQYKAVVYSNTIQSI
IAIIRAMGRLKIDFGDSARADDARQLFVLAGAAEEGFMTAELAGVIKRLW
KDSGVQACFNRSREYQLNDSAAYYLNDLDRIAQPNYIPTQQDVLRTRVKT
TGIVETHFTFKDLHFKMFDVGGSERKKWIHCFEGVTAIIFCVALSDYDLV
LAEDEEMNRMHESMKLFDSICNNKWFTDTSIILFLNKKDLFEEKIKKSPL
TICYPEYAGSNTYEEAAAYIQCQFEDLNKRKDTKEIYTHFTCATDTKNVQ
FVFDAVTDVIIKNNLK
Ligand information
Ligand ID
GDP
InChI
InChI=1S/C10H15N5O11P2/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(25-9)1-24-28(22,23)26-27(19,20)21/h2-3,5-6,9,16-17H,1H2,(H,22,23)(H2,19,20,21)(H3,11,13,14,18)/t3-,5-,6-,9-/m1/s1
InChIKey
QGWNDRXFNXRZMB-UUOKFMHZSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
c1nc2c(n1C3C(C(C(O3)COP(=O)(O)OP(=O)(O)O)O)O)N=C(NC2=O)N
CACTVS 3.385
NC1=Nc2n(cnc2C(=O)N1)[C@@H]3O[C@H](CO[P](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
CACTVS 3.385
NC1=Nc2n(cnc2C(=O)N1)[CH]3O[CH](CO[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 12.01
O=P(O)(O)OP(=O)(O)OCC3OC(n2cnc1c2N=C(N)NC1=O)C(O)C3O
OpenEye OEToolkits 1.7.6
c1nc2c(n1[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)OP(=O)(O)O)O)O)N=C(NC2=O)N
Formula
C10 H15 N5 O11 P2
Name
GUANOSINE-5'-DIPHOSPHATE
ChEMBL
CHEMBL384759
DrugBank
DB04315
ZINC
ZINC000008215481
PDB chain
4g5q Chain B Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
4g5q
Crystal Structures of the scaffolding protein LGN reveal the general mechanism by which GoLoco binding motifs inhibit the release of GDP from Galphai subunits in G-coupled heterotrimeric proteins
Resolution
2.9 Å
Binding residue
(original residue number in PDB)
E43 G45 K46 S47 T48 S151 R176 R178 N269 K270 D272 L273 C325 A326 T327
Binding residue
(residue number reindexed from 1)
E12 G14 K15 S16 T17 S120 R145 R147 N236 K237 D239 L240 C292 A293 T294
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
E43 T48 R178 D200
Catalytic site (residue number reindexed from 1)
E12 T17 R147 D169
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0001664
G protein-coupled receptor binding
GO:0003924
GTPase activity
GO:0003925
G protein activity
GO:0005515
protein binding
GO:0005525
GTP binding
GO:0010854
adenylate cyclase regulator activity
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: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:0007193
adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway
GO:0007198
adenylate cyclase-inhibiting serotonin receptor signaling pathway
GO:0034695
response to prostaglandin E
GO:0043434
response to peptide hormone
GO:0043949
regulation of cAMP-mediated signaling
GO:0045542
positive regulation of cholesterol biosynthetic process
GO:0051301
cell division
GO:0060236
regulation of mitotic spindle organization
GO:0072678
T cell migration
GO:1904322
cellular response to forskolin
GO:1904778
positive regulation of protein localization to cell cortex
Cellular Component
GO:0005634
nucleus
GO:0005654
nucleoplasm
GO:0005730
nucleolus
GO:0005737
cytoplasm
GO:0005765
lysosomal membrane
GO:0005813
centrosome
GO:0005829
cytosol
GO:0005834
heterotrimeric G-protein complex
GO:0005856
cytoskeleton
GO:0005886
plasma membrane
GO:0005938
cell cortex
GO:0030496
midbody
GO:0070062
extracellular exosome
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4g5q
,
PDBe:4g5q
,
PDBj:4g5q
PDBsum
4g5q
PubMed
UniProt
P63096
|GNAI1_HUMAN Guanine nucleotide-binding protein G(i) subunit alpha-1 (Gene Name=GNAI1)
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