3FHR
High resolution crystal structure of mitogen-activated protein kinase-activated protein kinase 3 (MK3)-inhibitor complex
Summary for 3FHR
Entry DOI | 10.2210/pdb3fhr/pdb |
Descriptor | MAP kinase-activated protein kinase 3, 2-(2-QUINOLIN-3-YLPYRIDIN-4-YL)-1,5,6,7-TETRAHYDRO-4H-PYRROLO[3,2-C]PYRIDIN-4-ONE (3 entities in total) |
Functional Keywords | kinase-inhibitor complex, atp-binding, kinase, nucleotide-binding, nucleus, phosphoprotein, serine/threonine-protein kinase, transferase |
Biological source | Homo sapiens (human) |
Cellular location | Nucleus: Q16644 |
Total number of polymer chains | 1 |
Total formula weight | 38915.36 |
Authors | Cheng, R.K.Y.,Barker, J.,Palan, S.,Felicetti, B.,Whittaker, M.,Hesterkamp, T. (deposition date: 2008-12-10, release date: 2009-12-15, Last modification date: 2024-03-20) |
Primary citation | Cheng, R.,Felicetti, B.,Palan, S.,Toogood-Johnson, I.,Scheich, C.,Barker, J.,Whittaker, M.,Hesterkamp, T. High-resolution crystal structure of human Mapkap kinase 3 in complex with a high affinity ligand Protein Sci., 19:168-173, 2010 Cited by PubMed: 19937655DOI: 10.1002/pro.294 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.9 Å) |
Structure validation
Download full validation report