Structure of PDB 5he2 Chain A
Receptor sequence
>5he2A (length=628) Species:
9913
(Bos taurus) [
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KKILLPEPSIRSVMQKYLEDRGEVTFEKIFSQKLGYLLFRDFCLKHLEEA
KPLVEFYEEIKKYEKLETEEERLVCSREIFDTYIMKELLACSHPFSKSAI
EHVQGHLVKKQVPPDLFQPYIEEICQNLRGDVFQKFIESDKFTRFCQWKN
VELNIHLTMNDFSVHRIIGRGGFGEVYGCRKADTGKMYAMKCLDKKRIKM
KQGETLALNERIMLSLVSTGDCPFIVCMSYAFHTPDKLSFILDLMNGGDL
HYHLSQHGVFSEADMRFYAAEIILGLEHMHNRFVVYRDLKPANILLDEHG
HVRISDLGLACDFSKKKPHASVGTHGYMAPEVLQKGVAYDSSADWFSLGC
MLFKLLRGHSPFRQHKTKDKHEIDRMTLTMAVELPDSFSPELRSLLEGLL
QRDVNRRLGCLGRGAQEVKESPFFRSLDWQMVFLQKYPPPLIPPRGSFDE
EDTKGIKLLDSDQELYRNFPLTISERWQQEVAETVFDTINAETDRLEARK
KTKNKQLGHEEDYALGKDCIMHGYMSKMGNPFLTQWQRRYFYLFPNRLEW
RGEGEAPQSLLTMEEIQSVEETQIKERKCLLLKIRGGKQFVLQCDSDPEL
VQWKKELRDAYREAQQLVQRVPKMKNKP
3D structure
PDB
5he2
Structure-Based Design, Synthesis, and Biological Evaluation of Highly Selective and Potent G Protein-Coupled Receptor Kinase 2 Inhibitors.
Chain
A
Resolution
2.79 Å
3D
structure
Catalytic site residues are labeled in the structure
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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.
Interaction with ligand
Site
#
Ligand
Ligand
chain
Binding residues on receptor
(original residue number in PDB)
Binding residues on receptor
(residue number reindexed from 1)
Binding affinity
BS01
F0S
A
I197 R199 G200 F202 G203 A218 L222 M274 L324 S334 D335 G337 L338
I168 R170 G171 F173 G174 A189 L193 M245 L295 S305 D306 G308 L309
PDBbind-CN
: -logKd/Ki=6.89,IC50=0.13uM
BindingDB: IC50=130nM
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
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:5he2
,
PDBe:5he2
,
PDBj:5he2
PDBsum
5he2
PubMed
27050625
UniProt
P21146
|ARBK1_BOVIN Beta-adrenergic receptor kinase 1 (Gene Name=GRK2)
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