7szb
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Crystal Structure Analysis of human PRPK complex with a compound
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Structural highlights
DiseasePRPK_HUMAN Galloway-Mowat syndrome. The disease is caused by variants affecting the gene represented in this entry. FunctionPRPK_HUMAN Component of the EKC/KEOPS complex that is required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine (PubMed:22912744, PubMed:27903914). The complex is probably involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37 (PubMed:22912744, PubMed:27903914). TP53RK has ATPase activity in the context of the EKC/KEOPS complex and likely plays a supporting role to the catalytic subunit OSGEP (By similarity). Atypical protein kinase that phosphorylates 'Ser-15' of p53/TP53 protein and may therefore participate in its activation (PubMed:11546806).[UniProtKB:P53323][UniProtKB:Q9UYB9][1] [2] [3] References
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This page was last modified 09:41, 25 October 2023.