4cpc
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Crystal structure of human synaptonemal complex protein SYCP3
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Structural highlights
DiseaseSYCP3_HUMAN Male infertility with normal virilization due to meiosis defect. The disease is caused by mutations affecting the gene represented in this entry. FunctionSYCP3_HUMAN Component of the transverse filaments of synaptonemal complexes (SCS), formed between homologous chromosomes during meiotic prophase. Has an essential meiotic function in spermatogenesis. May be important for testis development. Required for efficient phosphorylation of HORMAD1 and HORMAD2 (By similarity).[1] References
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This page was last modified 07:18, 1 May 2024.