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4TT7

Crystal structure of human ALK with a covalent modification

Summary for 4TT7
Entry DOI10.2210/pdb4tt7/pdb
DescriptorALK tyrosine kinase receptor, 1-THIOETHANESULFONIC ACID, 1,2-ETHANEDIOL, ... (4 entities in total)
Functional Keywordsatp-binding, receptor, transferase
Biological sourceHomo sapiens (Human)
Cellular locationCell membrane ; Single-pass type I membrane protein : Q9UM73
Total number of polymer chains1
Total formula weight37240.79
Authors
Badger, J.,Sridhar, V.,Chie-Leon, B.,Nienaber, V.L.,Hausheer, F.H. (deposition date: 2014-06-19, release date: 2015-02-11, Last modification date: 2023-09-27)
Primary citationParker, A.R.,Petluru, P.N.,Nienaber, V.L.,Zhao, M.,Ayala, P.Y.,Badger, J.,Chie-Leon, B.,Sridhar, V.,Logan, C.,Kochat, H.,Hausheer, F.H.
Novel covalent modification of human anaplastic lymphoma kinase (ALK) and potentiation of crizotinib-mediated inhibition of ALK activity by BNP7787.
Onco Targets Ther, 8:375-383, 2015
Cited by
PubMed: 25678804
DOI: 10.2147/OTT.S73690
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

218853

數據於2024-04-24公開中

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