8exf | pdb_00008exf
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Crystal structure of human FAM46A-BCCIPa complex at 3.2 angstrom resolution
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Structural highlights
DiseaseTET5A_HUMAN Osteogenesis imperfecta type 3. The disease is caused by variants affecting the gene represented in this entry. FunctionTET5A_HUMAN Cytoplasmic non-canonical poly(A) RNA polymerase that catalyzes the transfer of one adenosine molecule from an ATP to an mRNA poly(A) tail bearing a 3'-OH terminal group and participates in the cytoplasmic polyadenylation (PubMed:33882302). Polyadenylates mRNA encoding extracellular matrix constituents and other genes crucial for bone mineralization and during osteoblast mineralization, mainly focuses on ER-targeted mRNAs (By similarity).[UniProtKB:D3Z5S8][1] References
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This page was last modified 10:25, 25 October 2023.