• Official Full Name
  • arginyl-tRNA synthetase 2, mitochondrial
  • Synonyms
Source (Host):Mammalian CellsSpecies:Chicken
Product nameRecombinant Chicken RARS2
Source (Host):Mammalian CellsSpecies:Zebrafish
Product nameRecombinant Zebrafish RARS2
Source (Host):Species:Human
Product nameRecombinant Human RARS2 cell lysate

Involved Pathway

Rars2 involved in several pathways and played different roles in them. We selected most pathways Rars2 participated on our site, such as Aminoacyl-tRNA biosynthesis, which may be useful for your reference. Also, other proteins which involved in the same pathway with Rars2 were listed below. Creative Biomart supplied nearly all the proteins listed, you can search them on our site.
Pathway Name
Pathway Related Protein
Aminoacyl-tRNA biosynthesis

Protein Function

Rars2 has several biochemical functions, for example, ATP binding, arginine-tRNA ligase activity, poly(A) RNA binding. Some of the functions are cooperated with other proteins, some of the functions could acted by Rars2 itself. We selected most functions Rars2 had, and list some proteins which have the same functions with Rars2. You can find most of the proteins on our site.
Related Protein
Function ATP binding
Related Protein LATS2; TRPM4; DNA2; GART; PAPSS1; NOD1; TTLL13; CCT5; MVD; ABCF2A
Function arginine-tRNA ligase activity
Related Protein DALRD3; RARS; RARS2
Function poly(A) RNA binding
Related Protein DCAF13; RPL30; CCT3; NOP16; RPL18A; CRKL; RPS11; C3orf26; MRPL3; NGDN

Interacting Protein

Rars2 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with Rars2 here. Most of them are supplied by our site. Hope this information will be useful for your research of Rars2.
TRMT10C; PHLDA3; dppD; ssdna_dtdc; ICT1; Rhoa; SIRT4

Rars2 Related Articles

Joseph, JT; Innes, AM; et al. Neuropathologic Features of Pontocerebellar Hypoplasia Type 6. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY 73:1009-1025(2014).
Eggens, VRC; Barth, PG; et al. EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations. ORPHANET JOURNAL OF RARE DISEASES 9:-(2014).