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3HL7

Crystal Structure of Human p38alpha complexed with SD-0006

Summary for 3HL7
Entry DOI10.2210/pdb3hl7/pdb
Related3HLL
DescriptorMitogen-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 Keywordsatp-binding, kinase, nucleotide-binding, nucleus, phosphoprotein, serine/threonine-protein kinase, transferase
Biological sourceHomo sapiens (human)
Cellular locationCytoplasm : Q16539
Total number of polymer chains1
Total formula weight41998.29
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 citationXing, 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: 19496616
DOI: 10.1021/bi900655f
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.88 Å)
Structure validation

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