Structure of PDB 6loj Chain B Binding Site BS01
Receptor Information
>6loj Chain B (length=571) Species:
9606
(Homo sapiens) [
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SEIHMTGPMCLIENTNGRLMANPEALKILSAITQPMVVVAIVGLYRTGKS
YLMNKLAGKKKGFSLGSTVQSHTKGIWMWCVPHPKKPGHILVLLDTEGLG
DVEKGDNQNDSWIFALAVLLSSTFVYNSIGTINQQAMDQLYYVTELTHRI
RSKSSPDSADFVSFFPDFVWTLRDFSLDLEALTPDEYLTYSLKLKKGTSQ
KDETFNLPRLCIRKFFPKKKCFVFDRPVHRRKLAQLEKLQDEELDPEFVQ
QVADFCSYIFSNSKTKTLSGGIQVNGPRLESLVLTYVNAISSGDLPCMEN
AVLALAQIENSAAVQKAIAHYEQQMGQKVQLPTETLQELLDLHRDSEREA
IEVFIRSSFKDVDHLFQKELAAQLEKKRDDFCKQNQEASSDRCSALLQVI
FSPLEEEVKAGIYSKPGGYRLFVQKLQDLKKKYYEEPRKGIQAEEILQTY
LKSKESMTDAILQTDQTLTEKEKEIEVERVKAESAQASAKMLHEMQRKNE
QMMEQKERSYQEHLKQLTEKMENDRVQLLKEQERTLALKLQEQEQLLKEG
FQKESRIMKNEIQDLQTKMRR
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
6loj Chain B Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
6loj
Substrate-binding destabilizes the hydrophobic cluster to relieve the autoinhibition of bacterial ubiquitin ligase IpaH9.8.
Resolution
3.72 Å
Binding residue
(original residue number in PDB)
R48 G50 K51 S52 E99 D184 A248
Binding residue
(residue number reindexed from 1)
R46 G48 K49 S50 E97 D174 A234
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
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6loj
,
PDBe:6loj
,
PDBj:6loj
PDBsum
6loj
PubMed
33303953
UniProt
P32455
|GBP1_HUMAN Guanylate-binding protein 1 (Gene Name=GBP1)
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