3VQH
Bromine SAD partially resolves multiple binding modes for PKA inhibitor H-89
Summary for 3VQH
Entry DOI | 10.2210/pdb3vqh/pdb |
Related | 1YDT |
Descriptor | cAMP-dependent protein kinase catalytic subunit alpha, cAMP-dependent protein kinase inhibitor alpha, N-[2-(4-BROMOCINNAMYLAMINO)ETHYL]-5-ISOQUINOLINE SULFONAMIDE, ... (5 entities in total) |
Functional Keywords | protein-inhibitor complex, transferase-transferase inhibitor complex, transferase/transferase inhibitor |
Biological source | Homo sapiens (human) More |
Cellular location | Cytoplasm. Isoform 2: Cell projection, cilium, flagellum: P17612 |
Total number of polymer chains | 2 |
Total formula weight | 43679.49 |
Authors | Pflug, A.,Johnson, K.A.,Engh, R.A. (deposition date: 2012-03-23, release date: 2012-08-15, Last modification date: 2023-11-08) |
Primary citation | Pflug, A.,Johnson, K.A.,Engh, R.A. Anomalous dispersion analysis of inhibitor flexibility: a case study of the kinase inhibitor H-89 Acta Crystallogr.,Sect.F, 68:873-877, 2012 Cited by PubMed: 22869112DOI: 10.1107/S1744309112028655 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.95 Å) |
Structure validation
Download full validation report