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Rars2

Official Full Name

arginyl-tRNA synthetase 2, mitochondrial

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

Involved Pathway
Protein Function
Interacting Protein
Rars2 Related Articles

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	QARS;SEPSECS;IARS2;EPRS;PARS2;AARS2;MADD;HARS2;LARS2

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
ATP binding	ACLY;TAOK1;ATP1A1B;RET;TOR1L3;AK8;QARS;MYH9;KATNAL1
arginine-tRNA ligase activity	RARS2;DALRD3;RARS
poly(A) RNA binding	NME1;GPATCH8;UBE2I;NOL6;EIF3G;RPS15A;PCBP3;CD3EAP;DQX1

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

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).