4esr | pdb_00004esr
From Proteopedia
Molecular and Structural Characterization of the SH3 Domain of AHI-1 in Regulation of Cellular Resistance of BCR-ABL+ Chronic Myeloid Leukemia Cells to Tyrosine Kinase Inhibitors
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Structural highlights
DiseaseAHI1_HUMAN Joubert syndrome;Joubert syndrome with ocular defect. The disease is caused by mutations affecting the gene represented in this entry. FunctionAHI1_HUMAN Component of the tectonic-like complex, a complex localized at the transition zone of primary cilia and acting as a barrier that prevents diffusion of transmembrane proteins between the cilia and plasma membranes. Contents | ||||||||||||||||||||
This page was last modified 11:05, 1 March 2024.