Structure of PDB 8cqb Chain B Binding Site BS01
Receptor Information
>8cqb Chain B (length=478) Species:
9606
(Homo sapiens) [
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HMTGPMCLIENTNGRLMANPEALKILSAITQPMVVVAIVGLYRTGKSYLM
NKLAGKKKGFSLGSTVQSHTKGIWMWCVPHPKKPGHILVLLDTEGLGDVE
KGDNQNDSWIFALAVLLSSTFVYNSIGTINQQAMDQLYYVTELTHRIRSK
SSPDENENEVEDSADFVSFFPDFVWTLRDFSLDLEADGQPLTPDEYLTYS
LKLKKGTSQKDETFNLPRLCIRKFFPKKKCFVFDRPVHRRKLAQLEKLQD
EELDPEFVQQVADFCSYIFSNSKTKTLSGGIQVNGPRLESLVLTYVNAIS
SGDLPCMENAVLALAQIENSAAVQKAIAHYEQQMGQKVQLPTETLQELLD
LHRDSEREAIEVFIRSSFKDVDHLFQKELAAQLEKKRDDFCKQNQEASSD
RCSALLQVIFSPLEEEVKAGIYSKPGGYRLFVQKLQDLKKKYYEEPRKGI
QAEEILQTYLKSKESMTDAILQTDQTLT
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
8cqb Chain B Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
8cqb
Cryo-EM structure of the human GBP1 dimer bound to GDP-AlF3
Resolution
3.7 Å
Binding residue
(original residue number in PDB)
R48 G50 K51 S52 Y53 L67 G68 R183 D184 P241 L247
Binding residue
(residue number reindexed from 1)
R43 G45 K46 S47 Y48 L62 G63 R178 D179 P236 L242
Annotation score
4
Enzymatic activity
Enzyme Commision number
3.6.1.-
3.6.5.-
Gene Ontology
Molecular Function
GO:0001530
lipopolysaccharide binding
GO:0003779
actin binding
GO:0003924
GTPase activity
GO:0003925
G protein activity
GO:0004382
GDP phosphatase activity
GO:0005515
protein binding
GO:0005525
GTP binding
GO:0016787
hydrolase activity
GO:0019003
GDP binding
GO:0019899
enzyme binding
GO:0019955
cytokine binding
GO:0030507
spectrin binding
GO:0042802
identical protein binding
GO:0042803
protein homodimerization activity
GO:0051879
Hsp90 protein binding
Biological Process
GO:0032703
negative regulation of interleukin-2 production
GO:0042742
defense response to bacterium
GO:0042832
defense response to protozoan
GO:0045087
innate immune response
GO:0050848
regulation of calcium-mediated signaling
GO:0050860
negative regulation of T cell receptor signaling pathway
GO:0051607
defense response to virus
GO:0051715
cytolysis in another organism
GO:0070373
negative regulation of ERK1 and ERK2 cascade
GO:0071346
cellular response to type II interferon
GO:0071347
cellular response to interleukin-1
GO:0071356
cellular response to tumor necrosis factor
GO:0072665
protein localization to vacuole
GO:0140639
positive regulation of pyroptotic inflammatory response
GO:0160075
non-canonical inflammasome complex assembly
GO:1900025
negative regulation of substrate adhesion-dependent cell spreading
GO:1903076
regulation of protein localization to plasma membrane
GO:1903077
negative regulation of protein localization to plasma membrane
Cellular Component
GO:0000139
Golgi membrane
GO:0005576
extracellular region
GO:0005737
cytoplasm
GO:0005794
Golgi apparatus
GO:0005829
cytosol
GO:0005886
plasma membrane
GO:0012506
vesicle membrane
GO:0015629
actin cytoskeleton
GO:0030659
cytoplasmic vesicle membrane
GO:0031410
cytoplasmic vesicle
GO:0106139
symbiont cell surface
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:8cqb
,
PDBe:8cqb
,
PDBj:8cqb
PDBsum
8cqb
PubMed
UniProt
P32455
|GBP1_HUMAN Guanylate-binding protein 1 (Gene Name=GBP1)
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