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4ANL

Structure of G1269A Mutant Anaplastic Lymphoma Kinase

Summary for 4ANL
Entry DOI10.2210/pdb4anl/pdb
Related4ANQ 4ANS 4AOI
DescriptorALK TYROSINE KINASE RECEPTOR (2 entities in total)
Functional Keywordstransferase, crizotinib
Biological sourceHOMO SAPIENS (HUMAN)
Total number of polymer chains1
Total formula weight38610.15
Authors
McTigue, M.,Deng, Y.,Liu, W.,Brooun, A. (deposition date: 2012-03-20, release date: 2013-03-27, Last modification date: 2023-12-20)
Primary citationHuang, Q.,Johnson, T.W.,Bailey, S.,Brooun, A.,Bunker, K.D.,Burke, B.J.,Collins, M.R.,Cook, A.S.,Cui, J.J.,Dack, K.N.,Deal, J.G.,Deng, Y.,Dinh, D.,Engstrom, L.D.,He, M.,Hoffman, J.,Hoffman, R.L.,Johnson, P.S.,Kania, R.S.,Lam, H.,Lam, J.L.,Le, P.T.,Li, Q.,Lingardo, L.,Liu, W.,Lu, M.W.,Mctigue, M.,Palmer, C.L.,Richardson, P.F.,Sach, N.W.,Shen, H.,Smeal, T.,Smith, G.L.,Stewart, A.E.,Timofeevski, S.,Tsaparikos, K.,Wang, H.,Zhu, H.,Zhu, J.,Zou, H.Y.,Edwards, M.P.
Design of Potent and Selective Inhibitors to Overcome Clinical Anaplastic Lymphoma Kinase Mutations Resistant to Crizotinib.
J.Med.Chem., 57:1170-, 2014
Cited by
PubMed: 24432909
DOI: 10.1021/JM401805H
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.7 Å)
Structure validation

218500

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