Structure of PDB 3uzt Chain A Binding Site BS01
Receptor Information
>3uzt Chain A (length=586) Species:
9913
(Bos taurus) [
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KKILLPEPSIRSVMQKYLEDRGEVTFEKIFSQKLGYLLFRDFCLKHLEEA
KPLVEFYEEIKKYEKLETEEERLVCSREIFDTYIMKELLACSHPFSKSAI
EHVQGHLVKKQVPPDLFQPYIEEICQNLRGDVFQKFIESDKFTRFCQWKN
VELNIHLTMNDFSVHRIIGRGGFGEVYGCRKADTGKMYAMKCLDKKRIKM
KQGETLALNERIMLSLVSTGDCPFIVCMSYAFHTPDKLSFILDLMNGGDL
HYHLSQHGVFSEADMRFYAAEIILGLEHMHNRFVVYRDLKPANILLDEHG
HVRISDLGLACDFSKKKPHASVGTHGYMAPEVLQKGVAYDSSADWFSLGC
MLFKLLRGHSPFRQHKTKDVELPDSFSPELRSLLEGLLQRDVNRRLGCLG
RGAQEVKESPFFRSLDWQMVFLQKYPPPLIPPRGDTKGIKLLDSDQELYR
NFPLTISERWQQEVAETVFDTINAETDRLEARKKTKNKDYALGKDCIMHG
YMSKMWQRRYFYLFPNRLEWRGEGEAPQSLLTMEEIQSVEETQIKERKCL
LLKIRGGKQFVLQCDSDPELVQWKKELRDAYREAQQ
Ligand information
>3uzt Chain B (length=7) [
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ccauacg
.......
Receptor-Ligand Complex Structure
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PDB
3uzt
Molecular mechanism for inhibition of g protein-coupled receptor kinase 2 by a selective RNA aptamer.
Resolution
3.51 Å
Binding residue
(original residue number in PDB)
I197 R199 G200 V205 A218 M274 H280 A321 L324 D335
Binding residue
(residue number reindexed from 1)
I168 R170 G171 V176 A189 M245 H251 A292 L295 D306
Binding affinity
PDBbind-CN
: Kd=35nM
Enzymatic activity
Catalytic site (original residue number in PDB)
D317 K319 N322 D335 K344 T353
Catalytic site (residue number reindexed from 1)
D288 K290 N293 D306 K315 T324
Enzyme Commision number
2.7.11.15
: [beta-adrenergic-receptor] kinase.
Gene Ontology
Molecular Function
GO:0001664
G protein-coupled receptor binding
GO:0004672
protein kinase activity
GO:0004674
protein serine/threonine kinase activity
GO:0004703
G protein-coupled receptor kinase activity
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0031694
alpha-2A adrenergic receptor binding
GO:0031755
Edg-2 lysophosphatidic acid receptor binding
GO:0047696
beta-adrenergic receptor kinase activity
Biological Process
GO:0002026
regulation of the force of heart contraction
GO:0002029
desensitization of G protein-coupled receptor signaling pathway
GO:0002031
G protein-coupled receptor internalization
GO:0003108
negative regulation of the force of heart contraction by chemical signal
GO:0006468
protein phosphorylation
GO:0006886
intracellular protein transport
GO:0007165
signal transduction
GO:0007186
G protein-coupled receptor signaling pathway
GO:0007213
G protein-coupled acetylcholine receptor signaling pathway
GO:0009966
regulation of signal transduction
GO:0016310
phosphorylation
GO:0018105
peptidyl-serine phosphorylation
GO:0045880
positive regulation of smoothened signaling pathway
GO:0045988
negative regulation of striated muscle contraction
GO:0060048
cardiac muscle contraction
GO:1901081
negative regulation of relaxation of smooth muscle
GO:1903566
positive regulation of protein localization to cilium
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0005886
plasma membrane
GO:0016020
membrane
GO:0042995
cell projection
GO:0045202
synapse
GO:0098793
presynapse
GO:0098794
postsynapse
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3uzt
,
PDBe:3uzt
,
PDBj:3uzt
PDBsum
3uzt
PubMed
22727813
UniProt
P21146
|ARBK1_BOVIN Beta-adrenergic receptor kinase 1 (Gene Name=GRK2)
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