7a6h | pdb_00007a6h
From Proteopedia
Cryo-EM structure of human apo RNA Polymerase III
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Structural highlights
DiseaseRPAC1_HUMAN Treacher-Collins syndrome;Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry. FunctionRPAC1_HUMAN DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates. Common component of RNA polymerases I and III which synthesize ribosomal RNA precursors and small RNAs, such as 5S rRNA and tRNAs, respectively. RPAC1 is part of the Pol core element with the central large cleft and probably a clamp element that moves to open and close the cleft (By similarity).[UniProtKB:P07703][1] See AlsoReferences
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This page was last modified 07:43, 1 May 2024.