6mzc | pdb_00006mzc
From Proteopedia
Human TFIID BC core
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Structural highlights
DiseaseTAF2_HUMAN Microcephaly-thin corpus callosum-intellectual disability syndrome. The disease is caused by mutations affecting the gene represented in this entry. FunctionTAF2_HUMAN Transcription factor TFIID is one of the general factors required for accurate and regulated initiation by RNA polymerase II. TFIID is a multimeric protein complex that plays a central role in mediating promoter responses to various activators and repressors. It requires core promoter-specific cofactors for productive transcription stimulation. TAF2 stabilizes TFIID binding to core promoter.[1] [2] See AlsoReferences
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This page was last modified 14:45, 13 March 2024.