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YARS2 encodes a mitochondrial protein that catalyzes the attachment of tyrosine to tRNA(Tyr). Additionally we are shipping tyrosyl-tRNA Synthetase 2, Mitochondrial Proteins (5) and many more products for this protein.
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Human Polyclonal YARS2 Primary Antibody for IHC (p), WB - ABIN1882153
Bonnefond, Frugier, Touzé, Lorber, Florentz, Giegé, Sauter, Rudinger-Thirion: Crystal structure of human mitochondrial tyrosyl-tRNA synthetase reveals common and idiosyncratic features. in Structure (London, England : 1993) 2007
Show all 3 references for ABIN1882153
Data identified novel YARS2 mutations and noted marked phenotypic variability among YARS2 MLASA patients, with phenotypes ranging from mild to lethal, suggesting that the background mtDNA haplotype may be contributing to the phenotypic variability.
The study confirms mutations in YARS2 as a cause of MLASA and shows that, like some of the cytoplasmic ARSs, mitochondrial ARSs occur in high-molecular-weight complexes.
first example of a TyrRS (show Yars Antibodies) lacking specificity toward N1-N72 and thus of a TyrRS (show Yars Antibodies) disobeying the identity rules
The YARS2 mutation reported here is an alternative cause of MLASA.
The gene for mitochondrial tyrosyl-tRNA synthetase (show Yars Antibodies) is described and the initial characterization of the enzyme is reported. Genes for the remaining missing synthetases have also been found with the exception of human glutaminyl-tRNA synthetase (show EPRS Antibodies).
the structure of a strictly mitochondrial human synthetase, namely tyrosyl-tRNA synthetase (mt-TyrRS), in complex with an adenylate analog at 2.2 A resolution
This gene encodes a mitochondrial protein that catalyzes the attachment of tyrosine to tRNA(Tyr). Mutations in this gene are associated with myopathy with lactic acidosis and sideroblastic anemia type 2 (MLASA2).
tyrosine--tRNA ligase, mitochondrial
, tyrosyl-tRNA synthetase, mitochondrial
, tyrosine tRNA ligase 2, mitochondrial