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5UKK

Human GRK2 in complex with human G-beta-gamma subunits and CCG211998 (14ak)

Summary for 5UKK
Entry DOI10.2210/pdb5ukk/pdb
Related5UKL
DescriptorBeta-adrenergic receptor kinase 1, Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2, ... (6 entities in total)
Functional Keywordskinase, inhibitor complex, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceHomo sapiens (Human)
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Total number of polymer chains3
Total formula weight118920.83
Authors
Cato, M.C.,Homan, K.T.,Tesmer, J.J.G. (deposition date: 2017-01-23, release date: 2017-04-05, Last modification date: 2023-10-04)
Primary citationWaldschmidt, H.V.,Homan, K.T.,Cato, M.C.,Cruz-Rodriguez, O.,Cannavo, A.,Wilson, M.W.,Song, J.,Cheung, J.Y.,Koch, W.J.,Tesmer, J.J.,Larsen, S.D.
Structure-Based Design of Highly Selective and Potent G Protein-Coupled Receptor Kinase 2 Inhibitors Based on Paroxetine.
J. Med. Chem., 60:3052-3069, 2017
Cited by
PubMed: 28323425
DOI: 10.1021/acs.jmedchem.7b00112
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.6 Å)
Structure validation

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