Beta-adrenergic receptor kinase
From Proteopedia
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[[1ym7]] – bBARK1 (mutant) - bovine <BR /> | [[1ym7]] – bBARK1 (mutant) - bovine <BR /> | ||
| - | [[4pnk]], [[3cik]], [[5he3]] – hBARK1 + guanine-nucleotide binding protein G β,γ subunits | + | [[5uvc]], [[5uuu]] – hBARK1 + inhibitor - human <BR /> |
| + | [[4pnk]], [[3cik]], [[5he3]] – hBARK1 + guanine-nucleotide binding protein G β,γ subunits <BR /> | ||
[[3psc]], [[5he0]], [[5he1]], [[5he2]] – hBARK1 (mutant) + guanine-nucleotide binding protein G β,γ subunits <BR /> | [[3psc]], [[5he0]], [[5he1]], [[5he2]] – 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 /> | [[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 /> | [[3uzs]] – hBARK1 (mutant) + guanine-nucleotide binding protein G β,γ subunits + RNA <BR /> | ||
[[3uzt]] – hBARK1 (mutant) + RNA <BR /> | [[3uzt]] – hBARK1 (mutant) + RNA <BR /> | ||
| - | [[3krw]], [[3krx]] – hBARK1 + guanine-nucleotide binding protein G β,γ subunits + inhibitor<BR /> | + | [[3krw]], [[3krx]], [[5wg3]], [[5wg4]], [[5wg5]], [[5ukk]], [[5ukl]], [[5he3]] – hBARK1 + guanine-nucleotide binding protein G β,γ subunits + inhibitor<BR /> |
| - | [[3pvu]], [[3pvw]] – bBARK1 (mutant) + 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 /> | [[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 /> | [[1omw]] – bBARK1 (mutant) + guanine-nucleotide binding protein G β,γ subunits <BR /> | ||
Revision as of 08:40, 28 March 2018
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3D Structures of β adrenergic receptor kinase
Updated on 28-March-2018
1ym7 – bBARK1 (mutant) - bovine
5uvc, 5uuu – hBARK1 + inhibitor - human
4pnk, 3cik, 5he3 – hBARK1 + guanine-nucleotide binding protein G β,γ subunits
3psc, 5he0, 5he1, 5he2 – hBARK1 (mutant) + guanine-nucleotide binding protein G β,γ subunits
4mk0, 3v5w – hBARK1 + guanine-nucleotide binding protein G β,γ subunits + paroxetine derivative
3uzs – hBARK1 (mutant) + guanine-nucleotide binding protein G β,γ subunits + RNA
3uzt – hBARK1 (mutant) + RNA
3krw, 3krx, 5wg3, 5wg4, 5wg5, 5ukk, 5ukl, 5he3 – hBARK1 + guanine-nucleotide binding protein G β,γ subunits + inhibitor
3pvu, 3pvw, 5ukm, 5he0, 5he1, 5he2 – bBARK1 (mutant) + guanine-nucleotide binding protein G β,γ subunits + inhibitor
2bcj – bBARK1 (mutant) + guanine-nucleotide binding protein G α,β,γ subunits
1omw – bBARK1 (mutant) + guanine-nucleotide binding protein G β,γ subunits
References
- ↑ 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
Proteopedia Page Contributors and Editors (what is this?)
Michal Harel, Alexander Berchansky, Cristina Murga, Joel L. Sussman
