<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Antika TR</submitter><funding>Ministry of Science and Technology, Taiwan</funding><pagination>10015-10025</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9508852</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>50(17)</volume><pubmed_abstract>tRNAHis guanylyltransferase (Thg1) catalyzes the 3'-5' incorporation of guanosine into position -1 (G-1) of tRNAHis. G-1 is unique to tRNAHis and is crucial for recognition by histidyl-tRNA synthetase (HisRS). Yeast Thg1 requires ATP for G-1 addition to tRNAHis opposite A73, whereas archaeal Thg1 requires either ATP or GTP for G-1 addition to tRNAHis opposite C73. Paradoxically, human Thg1 (HsThg1) can add G-1 to tRNAsHis with A73 (cytoplasmic) and C73 (mitochondrial). As N73 is immediately followed by a CCA end (positions 74-76), how HsThg1 prevents successive 3'-5' incorporation of G-1/G-2/G-3 into mitochondrial tRNAHis (tRNAmHis) through a template-dependent mechanism remains a puzzle. We showed herein that mature native human tRNAmHis indeed contains only G-1. ATP was absolutely requir</pubmed_abstract><journal>Nucleic acids research</journal><pubmed_title>Human Thg1 displays tRNA-inducible GTPase activity.</pubmed_title><pmcid>PMC9508852</pmcid><funding_grant_id>110-2311-B-008-001</funding_grant_id><pubmed_authors>Yeh FL</pubmed_authors><pubmed_authors>Wang TL</pubmed_authors><pubmed_authors>Chang TH</pubmed_authors><pubmed_authors>Antika TR</pubmed_authors><pubmed_authors>Nazilah KR</pubmed_authors><pubmed_authors>Lo YT</pubmed_authors><pubmed_authors>Yeh CS</pubmed_authors><pubmed_authors>Wang CC</pubmed_authors><pubmed_authors>Lee YH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Human Thg1 displays tRNA-inducible GTPase activity.</name><description>tRNAHis guanylyltransferase (Thg1) catalyzes the 3'-5' incorporation of guanosine into position -1 (G-1) of tRNAHis. G-1 is unique to tRNAHis and is crucial for recognition by histidyl-tRNA synthetase (HisRS). Yeast Thg1 requires ATP for G-1 addition to tRNAHis opposite A73, whereas archaeal Thg1 requires either ATP or GTP for G-1 addition to tRNAHis opposite C73. Paradoxically, human Thg1 (HsThg1) can add G-1 to tRNAsHis with A73 (cytoplasmic) and C73 (mitochondrial). As N73 is immediately followed by a CCA end (positions 74-76), how HsThg1 prevents successive 3'-5' incorporation of G-1/G-2/G-3 into mitochondrial tRNAHis (tRNAmHis) through a template-dependent mechanism remains a puzzle. We showed herein that mature native human tRNAmHis indeed contains only G-1. ATP was absolutely requir</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2026-05-28T01:08:32.123Z</modification><creation>2025-04-19T22:47:07.055Z</creation></dates><accession>S-EPMC9508852</accession><cross_references><pubmed>36107775</pubmed><doi>10.1093/nar/gkac768</doi></cross_references></HashMap>