PDB ID: 5HE3
Hetero Atom Contents
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Color scheme of protein:
Code | Name | Style | Show | Link | |
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FF1 | (4~{S})-4-[3-[2-(2,6-dimethylphenyl)ethylcarbamoyl]-4-fluoranyl-phenyl]-~{N}-(1~{H}-indazol-5-yl)-6-methyl-2-oxidanylidene-3,4-dihydro-1~{H}-pyrimidine-5-carboxamide | PoSSuM | |||
MG | Magnesium ion | PoSSuM |
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Download interaction data: 5HE3
Structure summary
Code : | 5HE3 PDBj RCSB PDB PDBe | ||||||||||||||||||||||||||||||||||||
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Header : | TRANSFERASE/TRANSFERASE INHIBITOR | ||||||||||||||||||||||||||||||||||||
Title : | Bovine GRK2 in complex with Gbetagamma subunits and CCG224411 | ||||||||||||||||||||||||||||||||||||
Release Data : | 2016-05-11 | ||||||||||||||||||||||||||||||||||||
Compound : |
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Source : |
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Authors : | Cato, M.C., Tesmer, J.J.G. | ||||||||||||||||||||||||||||||||||||
Keywords : | RGS, kinase, PH, WD-40, inhibitor complex, TRANSFERASE-TRANSFERASE INHIBITOR complex | ||||||||||||||||||||||||||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 2.7400 Å ) | ||||||||||||||||||||||||||||||||||||
Citation : |
Structure-Based Design, Synthesis, and Biological Evaluation of Highly Selective and Potent G Protein-Coupled Receptor Kinase 2 Inhibitors.
Waldschmidt, H.V.,Homan, K.T.,Cruz-Rodriguez, O.
et al.
PubMed: 27050625 |
Reaction
Chain : | A | ||||||||
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UniProt : | P21146 (ARBK1_BOVIN) | ||||||||
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Chain : | B |
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UniProt : | P62873 (GBB1_HUMAN) |
Reaction : | - |
Chain : | G |
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UniProt : | P59768 (GBG2_HUMAN) |
Reaction : | - |