| Standard Name | Msr1p 1 |
|---|---|
| Systematic Name | Yhr091cp |
| ORF Classification | Verified |
| Description | Mitochondrial arginyl-tRNA synthetase; mutations in human ortholog are associated with pontocerebellar hypoplasia type 6; MSR1 has a paralog, YDR341C, that arose from the whole genome duplication (1, 2, 3) |
| Name Description | Mitochondrial tRNA Synthetase aRginine 1 |
| Gene Product | mitochondrial arginyl-tRNA synthetase 1 |
| Click on image for expanded interactive view |
|---|
| Post-translational Modifications | PhosphoGRID | PhosphoPep Database |
|---|---|
| Domains/motifs | See the graphical view and list of proteins that share domains/motifs in common with Msr1p (InterPro) |
| Physical Interactions | There are 3 total physical interactions (BioGRID) |
| Homologs | PDB Homologs | BLASTP | BLASTP v. fungi | Fungal Alignment | Synteny Viewer |
| External Sequence Databases |
EBI: UPI0000168345 | P38714 MIPS: YHR091C NCBI: 1174539 | 308153546 | 487937 | 6321883 | 633022 | NP_011959.1 GenBank/EMBL/DDBJ: DAA06787.1 | L39019 | U00060 |
| External Classifications | EC: 6.1.1.19 [Arginine--tRNA ligase] |
external links for Msr1p
| Homologs | Interaction Resources | Protein databases/Other | Localization Resources |
|---|---|---|---|
| BLASTP (NCBI) | BioGRID | SCOP Superfamily | YPL+ |
| Ashbya (AGD) | BOND | GPMdb (Mass Spec.) | YeastGFP |
| YGOB | BioPIXIE | MIPS | |
| YOGY | CYC2008 (complexes) | Pfam domains | |
| Complexome | YeastRC Structure Prediction (Seattle) | ||
| DIP | |||
| GeneMANIA |
References cited on this page View Complete Literature Guide for Msr1p
| 1) | Tzagoloff A and Shtanko A (1995) Mitochondrial and cytoplasmic isoleucyl-, glutamyl- and arginyl-tRNA synthetases of yeast are encoded by separate genes. Eur J Biochem 230(2):582-6 |
| 2) | Byrne KP and Wolfe KH (2005) The Yeast Gene Order Browser: combining curated homology and syntenic context reveals gene fate in polyploid species. Genome Res 15(10):1456-61 |
| 3) | Cassandrini D, et al. (2013) Pontocerebellar hypoplasia type 6 caused by mutations in RARS2: definition of the clinical spectrum and molecular findings in five patients. J Inherit Metab Dis 36(1):43-53 |



