Rars2

  • Official Full Name

    arginyl-tRNA synthetase 2, mitochondrial
Cat.# Product name Source (Host) Species Tag Protein Length Price
RARS2-10892Z Recombinant Zebrafish RARS2 Mammalian Cell Zebrafish His
RARS2-5301C Recombinant Chicken RARS2 Mammalian Cell Chicken His
RARS2-1473HCL Recombinant Human RARS2 cell lysate Human Non
Rars2-2011R Recombinant Rat Rars2 Protein, His-tagged E.coli Rat His Val313-Cys578

    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 WARS,MADD,EPRS,CARS,VARS2,TARSL2,PET112L,RARS,AARS,MTFMT

    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.

    Function Related Protein
    arginine-tRNA ligase activity DALRD3,RARS
    ATP binding MCM8,ATP2B4,STK16,LIMK2,PRKCHA,VSIG8B,RRM1,PAK3,P2RX8,FYN
    poly(A) RNA binding DDX18,RPL35,ZFP579,ZFP346,MAZ,ZFP207,DQX1,RBM22,RPL5,FAM120A

    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

    Resources

    References

    • 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).

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