7FD0
Crystal Structure of human RIPK1 kinase domain in complex with a novel inhibitor
Summary for 7FD0
Entry DOI | 10.2210/pdb7fd0/pdb |
Descriptor | Receptor-interacting serine/threonine-protein kinase 1, N-[(3S)-5-methyl-7-[2-(oxan-4-yl)ethynyl]-4-oxidanylidene-2,3-dihydro-1,5-benzoxazepin-3-yl]-5-(phenylmethyl)-4H-1,2,4-triazole-3-carboxamide (3 entities in total) |
Functional Keywords | immune system-inhibitor complex, immune system/inhibitor |
Biological source | Homo sapiens (Human) |
Total number of polymer chains | 2 |
Total formula weight | 68338.93 |
Authors | |
Primary citation | Yang, X.,Lu, H.,Xie, H.,Zhang, B.,Nie, T.,Fan, C.,Yang, T.,Xu, Y.,Su, H.,Tang, W.,Zhou, B. Potent and Selective RIPK1 Inhibitors Targeting Dual-Pockets for the Treatment of Systemic Inflammatory Response Syndrome and Sepsis. Angew.Chem.Int.Ed.Engl., 61:e202114922-e202114922, 2022 Cited by PubMed: 34851543DOI: 10.1002/anie.202114922 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2 Å) |
Structure validation
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