2kkr
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Solution structure of SCA7 zinc finger domain from human ataxin-7 protein
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Structural highlights
DiseaseATX7_HUMAN Spinocerebellar ataxia type 7. The disease is caused by mutations affecting the gene represented in this entry. FunctionATX7_HUMAN Acts as component of the STAGA transcription coactivator-HAT complex. Mediates the interaction of STAGA complex with the CRX and is involved in CRX-dependent gene activation. Necessary for microtubule cytoskeleton stabilization.[1] Evolutionary Conservation![]() Check, as determined by ConSurfDB. You may read the explanation of the method and the full data available from ConSurf. References
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This page was last modified 06:46, 1 May 2024.