3HL7
Crystal Structure of Human p38alpha complexed with SD-0006
Summary for 3HL7
Entry DOI | 10.2210/pdb3hl7/pdb |
Related | 3HLL |
Descriptor | Mitogen-activated protein kinase 14, 2-{4-[5-(4-chlorophenyl)-4-pyrimidin-4-yl-1H-pyrazol-3-yl]piperidin-1-yl}-2-oxoethanol, 2-fluoro-4-[4-(4-fluorophenyl)-1H-pyrazol-3-yl]pyridine, ... (4 entities in total) |
Functional Keywords | atp-binding, kinase, nucleotide-binding, nucleus, phosphoprotein, serine/threonine-protein kinase, transferase |
Biological source | Homo sapiens (human) |
Cellular location | Cytoplasm : Q16539 |
Total number of polymer chains | 1 |
Total formula weight | 41998.29 |
Authors | Shieh, H.-S.,Kurumbail, R.G.,Stegeman, R.A.,Williams, J.M. (deposition date: 2009-05-26, release date: 2009-07-14, Last modification date: 2024-02-21) |
Primary citation | Xing, L.,Shieh, H.S.,Selness, S.R.,Devraj, R.V.,Walker, J.K.,Devadas, B.,Hope, H.R.,Compton, R.P.,Schindler, J.F.,Hirsch, J.L.,Benson, A.G.,Kurumbail, R.G.,Stegeman, R.A.,Williams, J.M.,Broadus, R.M.,Walden, Z.,Monahan, J.B. Structural bioinformatics-based prediction of exceptional selectivity of p38 MAP kinase inhibitor PH-797804. Biochemistry, 48:6402-6411, 2009 Cited by PubMed: 19496616DOI: 10.1021/bi900655f PDB entries with the same primary citation |
Experimental method |
Structure validation
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