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3OG7

B-Raf Kinase V600E oncogenic mutant in complex with PLX4032

Summary for 3OG7
Entry DOI10.2210/pdb3og7/pdb
DescriptorAKAP9-BRAF fusion protein, N-(3-{[5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]carbonyl}-2,4-difluorophenyl)propane-1-sulfonamide (3 entities in total)
Functional Keywordsb-raf, braf, proto-oncogene, v600e, kinase, transferase, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight66445.41
Authors
Zhang, Y.,Zhang, K.Y.,Zhang, C. (deposition date: 2010-08-16, release date: 2010-09-22, Last modification date: 2024-02-21)
Primary citationBollag, G.,Hirth, P.,Tsai, J.,Zhang, J.,Ibrahim, P.N.,Cho, H.,Spevak, W.,Zhang, C.,Zhang, Y.,Habets, G.,Burton, E.A.,Wong, B.,Tsang, G.,West, B.L.,Powell, B.,Shellooe, R.,Marimuthu, A.,Nguyen, H.,Zhang, K.Y.,Artis, D.R.,Schlessinger, J.,Su, F.,Higgins, B.,Iyer, R.,D'Andrea, K.,Koehler, A.,Stumm, M.,Lin, P.S.,Lee, R.J.,Grippo, J.,Puzanov, I.,Kim, K.B.,Ribas, A.,McArthur, G.A.,Sosman, J.A.,Chapman, P.B.,Flaherty, K.T.,Xu, X.,Nathanson, K.L.,Nolop, K.
Clinical efficacy of a RAF inhibitor needs broad target blockade in BRAF-mutant melanoma.
Nature, 467:596-599, 2010
Cited by
PubMed: 20823850
DOI: 10.1038/nature09454
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.45 Å)
Structure validation

218500

數據於2024-04-17公開中

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