Beta-adrenergic receptor kinase

(Difference between revisions)

Revision as of 08:51, 3 April 2019

↑ Benovic JL, Strasser RH, Caron MG, Lefkowitz RJ. Beta-adrenergic receptor kinase: identification of a novel protein kinase that phosphorylates the agonist-occupied form of the receptor. Proc Natl Acad Sci U S A. 1986 May;83(9):2797-801. PMID:2871555
↑ Tesmer VM, Lennarz S, Mayer G, Tesmer JJ. Molecular Mechanism for Inhibition of G Protein-Coupled Receptor Kinase 2 by a Selective RNA Aptamer. Structure. 2012 Jun 21. PMID:22727813 doi:10.1016/j.str.2012.05.002

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 </StructureSection>
-== 3D Structures of β adrenergic receptor kinase ==
-Updated on {{REVISIONDAY2}}-{{MONTHNAME|{{REVISIONMONTH}}}}-{{REVISIONYEAR}}
-[[1ym7]] – bBARK1 (mutant) - bovine  <BR />
-[[5uvc]], [[5uuu]] – hBARK1 + inhibitor - human  <BR />
-[[4pnk]], [[3cik]], [[5he3]] – hBARK1 + guanine-nucleotide binding protein G β,γ subunits <BR />
-[[3psc]], [[5he0]], [[5he1]], [[5he2]], [[6c2y]] – hBARK1 (mutant) + guanine-nucleotide binding protein G β,γ subunits  <BR />
-[[4mk0]], [[3v5w]] – hBARK1 + guanine-nucleotide binding protein G β,γ subunits + paroxetine derivative<BR />
-[[3uzs]] – hBARK1 (mutant) + guanine-nucleotide binding protein G β,γ subunits + RNA  <BR />
-[[3uzt]] – hBARK1 (mutant) + RNA  <BR />
-[[3krw]], [[3krx]], [[5wg3]], [[5wg4]], [[5wg5]], [[5ukk]], [[5ukl]], [[5he3]] – hBARK1 + guanine-nucleotide binding protein G β,γ subunits + inhibitor<BR />
-[[3pvu]], [[3pvw]], [[5ukm]], [[5he0]], [[5he1]], [[5he2]] – bBARK1 (mutant) + guanine-nucleotide binding protein G β,γ subunits + inhibitor  <BR />
-[[2bcj]] – bBARK1 (mutant) + guanine-nucleotide binding protein G α,β,γ subunits  <BR />
-[[1omw]] – bBARK1 (mutant) + guanine-nucleotide binding protein G β,γ subunits  <BR />
 == References ==
 <references/>
 [[Category:Topic Page]]