8p2p
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Polymeric form of the BTB domain of human ZBTB18
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Structural highlights
DiseaseZBT18_HUMAN Distal deletion 1q. The disease is caused by variants affecting the gene represented in this entry. FunctionZBT18_HUMAN Transcriptional repressor that plays a role in various developmental processes such as myogenesis and brain development. Plays a key role in myogenesis by directly repressing the expression of ID2 and ID3, 2 inhibitors of skeletal myogenesis. Also involved in controlling cell division of progenitor cells and regulating the survival of postmitotic cortical neurons. Specifically binds the consensus DNA sequence 5'-[AC]ACATCTG[GT][AC]-3' which contains the E box core, and acts by recruiting chromatin remodeling multiprotein complexes. May also play a role in the organization of chromosomes in the nucleus.[1] References
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This page was last modified 05:17, 5 June 2024.