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4I22

Structure of the monomeric (V948R)gefitinib/erlotinib resistant double mutant (L858R+T790M) EGFR kinase domain co-crystallized with gefitinib

Summary for 4I22
Entry DOI10.2210/pdb4i22/pdb
Related4I1Z 4I20 4I21 4I23 4I24
DescriptorEpidermal growth factor receptor, Gefitinib, SULFATE ION, ... (4 entities in total)
Functional Keywordskinase domain, phosphotrasfer, atp binding, transferase
Biological sourceHomo sapiens (human)
Cellular locationCell membrane; Single-pass type I membrane protein. Isoform 2: Secreted: P00533
Total number of polymer chains1
Total formula weight38219.48
Authors
Gajiwala, K.S.,Feng, J.,Ferre, R.,Ryan, K.,Brodsky, O.,Stewart, A. (deposition date: 2012-11-21, release date: 2013-01-16, Last modification date: 2024-03-27)
Primary citationGajiwala, K.S.,Feng, J.,Ferre, R.,Ryan, K.,Brodsky, O.,Weinrich, S.,Kath, J.C.,Stewart, A.
Insights into the Aberrant Activity of Mutant EGFR Kinase Domain and Drug Recognition.
Structure, 21:209-219, 2013
Cited by
PubMed: 23273428
DOI: 10.1016/j.str.2012.11.014
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.71 Å)
Structure validation

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