8a43 | pdb_00008a43
From Proteopedia
Structural highlights
DiseaseRPA2_HUMAN Treacher-Collins syndrome. The disease is caused by variants affecting the gene represented in this entry. FunctionRPA2_HUMAN DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates. Second largest core component of RNA polymerase I which synthesizes ribosomal RNA precursors. Proposed to contribute to the polymerase catalytic activity and forms the polymerase active center together with the largest subunit. Pol I is composed of mobile elements and RPA2 is part of the core element with the central large cleft and probably a clamp element that moves to open and close the cleft.[1] References
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This page was last modified 07:36, 3 November 2022.