4l9c
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Crystal structure of the FP domain of human F-box protein Fbxo7 (native)
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Structural highlights
DiseaseFBX7_HUMAN Parkinsonian-pyramidal syndrome. The disease is caused by mutations affecting the gene represented in this entry. FunctionFBX7_HUMAN Substrate recognition component of a SCF (SKP1-CUL1-F-box protein) E3 ubiquitin-protein ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Recognizes BIRC2 and DLGAP5.[1] [2] References
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This page was last modified 12:18, 1 March 2024.