| http://purl.uniprot.org/citations/26272616 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
| http://purl.uniprot.org/citations/26272616 | http://www.w3.org/2000/01/rdf-schema#comment | "The connective polypeptide 1 (CP1) editing domain of leucyl-tRNA synthetase (LeuRS) from various species either harbors a conserved active site to exclude tRNA mis-charging with noncognate amino acids or is evolutionarily truncated or lost because there is no requirement for high translational fidelity. However, human mitochondrial LeuRS (hmtLeuRS) contains a full-length but degenerate CP1 domain that has mutations in some residues important for post-transfer editing. The significance of such an inactive CP1 domain and a translational accuracy mechanism with different noncognate amino acids are not completely understood. Here, we identified the essential role of the evolutionarily divergent CP1 domain in facilitating hmtLeuRS's catalytic efficiency and endowing enzyme with resistance to AN2690, a broad-spectrum drug acting on LeuRSs. In addition, the canonical core of hmtLeuRS is not stringent for noncognate norvaline (Nva) and valine (Val). hmtLeuRS has a very weak tRNA-independent pre-transfer editing activity for Nva, which is insufficient to remove mis-activated Nva. Moreover, hmtLeuRS chimeras fused with a functional CP1 domain from LeuRSs of other species, regardless of origin, showed restored post-transfer editing activity and acquired fidelity during aminoacylation. This work offers a novel perspective on the role of the CP1 domain in optimizing aminoacylation efficiency."xsd:string |
| http://purl.uniprot.org/citations/26272616 | http://purl.org/dc/terms/identifier | "doi:10.1074/jbc.m115.672824"xsd:string |
| http://purl.uniprot.org/citations/26272616 | http://purl.uniprot.org/core/author | "Wang M."xsd:string |
| http://purl.uniprot.org/citations/26272616 | http://purl.uniprot.org/core/author | "Ye Q."xsd:string |
| http://purl.uniprot.org/citations/26272616 | http://purl.uniprot.org/core/author | "Wang E.D."xsd:string |
| http://purl.uniprot.org/citations/26272616 | http://purl.uniprot.org/core/author | "Zhou X.L."xsd:string |
| http://purl.uniprot.org/citations/26272616 | http://purl.uniprot.org/core/author | "Ji Q.Q."xsd:string |
| http://purl.uniprot.org/citations/26272616 | http://purl.uniprot.org/core/author | "Fang Z.P."xsd:string |
| http://purl.uniprot.org/citations/26272616 | http://purl.uniprot.org/core/author | "Ruan Z.R."xsd:string |
| http://purl.uniprot.org/citations/26272616 | http://purl.uniprot.org/core/date | "2015"xsd:gYear |
| http://purl.uniprot.org/citations/26272616 | http://purl.uniprot.org/core/name | "J Biol Chem"xsd:string |
| http://purl.uniprot.org/citations/26272616 | http://purl.uniprot.org/core/pages | "24391-24402"xsd:string |
| http://purl.uniprot.org/citations/26272616 | http://purl.uniprot.org/core/title | "Degenerate connective polypeptide 1 (CP1) domain from human mitochondrial leucyl-tRNA synthetase."xsd:string |
| http://purl.uniprot.org/citations/26272616 | http://purl.uniprot.org/core/volume | "290"xsd:string |
| http://purl.uniprot.org/citations/26272616 | http://www.w3.org/2004/02/skos/core#exactMatch | http://purl.uniprot.org/pubmed/26272616 |
| http://purl.uniprot.org/citations/26272616 | http://xmlns.com/foaf/0.1/primaryTopicOf | https://pubmed.ncbi.nlm.nih.gov/26272616 |
| http://purl.uniprot.org/uniprot/#_Q15031-mappedCitation-26272616 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/26272616 |
| http://purl.uniprot.org/uniprot/#_Q9BQR0-mappedCitation-26272616 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/26272616 |
| http://purl.uniprot.org/uniprot/Q15031 | http://purl.uniprot.org/core/mappedCitation | http://purl.uniprot.org/citations/26272616 |
| http://purl.uniprot.org/uniprot/Q9BQR0 | http://purl.uniprot.org/core/mappedCitation | http://purl.uniprot.org/citations/26272616 |