Structure of PDB 8r1a Chain F Binding Site BS01
Receptor Information
>8r1a Chain F (length=587) Species:
9606
(Homo sapiens) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
IHMTGPMCLIENTNGRLMANPEALKILSAITQPMVVVAIVGLYRTGKSYL
MNKLAGKKKGFSLGSTVQSHTKGIWMWCVPHPKKPGHILVLLDTEGLGDV
EKGDNQNDSWIFALAVLLSSTFVYNSIGTINQQAMDQLYYVTELTHRIRS
KSSPDENENEVEDSADFVSFFPDFVWTLRDFSLDLEADGQPLTPDEYLTY
SLKLKKGTSQKDETFNLPRLCIRKFFPKKKCFVFDRPVHRRKLAQLEKLQ
DEELDPEFVQQVADFCSYIFSNSKTKTLSGGIQVNGPRLESLVLTYVNAI
SSGDLPCMENAVLALAQIENSAAVQKAIAHYEQQMGQKVQLPTESLQELL
DLHRDSEREAIEVFIRSSFKDVDHLFQKELAAQLEKKRDDFCKQNQEASS
DRCSGLLQVIFSPLEEEVKAGIYSKPGGYRLFVQKLQDLKKKYYEEPRKG
IQAEEILQTYLKSKESMTDAILQTDQTLTEKEKEIEVERVKAESAQASAK
MLQEMQRKNEQMMEQKERSYQEHLKQLTEKMENDRVQLLKEQERTLALKL
QEQEQLLKEGFQKESRIMKNEIQDLQTKMRRRKACTI
Ligand information
Ligand ID
AF3
InChI
InChI=1S/Al.3FH/h;3*1H/q+3;;;/p-3
InChIKey
KLZUFWVZNOTSEM-UHFFFAOYSA-K
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
F[Al](F)F
Formula
Al F3
Name
ALUMINUM FLUORIDE
ChEMBL
DrugBank
ZINC
PDB chain
8r1a Chain F Residue 600 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
8r1a
Elucidating the activation mechanism for GBP1 oligomerization
Resolution
26.8 Å
Binding residue
(original residue number in PDB)
Y47 R48 K51 T75 G100
Binding residue
(residue number reindexed from 1)
Y43 R44 K47 T71 G96
Annotation score
1
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
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:8r1a
,
PDBe:8r1a
,
PDBj:8r1a
PDBsum
8r1a
PubMed
38267655
UniProt
P32455
|GBP1_HUMAN Guanylate-binding protein 1 (Gene Name=GBP1)
[
Back to BioLiP
]