6.1.1.22: asparagine-tRNA ligase
This is an abbreviated version!
For detailed information about asparagine-tRNA ligase, go to the full flat file.
Word Map on EC 6.1.1.22
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6.1.1.22
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aminoacyl-trna
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asnrs
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aspartyl-trna
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malayi
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brugia
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aminoacylation
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amidotransferase
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asparaginylation
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asp-trnaasn
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glutaminyl-trna
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gatcabs
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filariasis
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transamidation
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nondiscriminating
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glu-trnagln
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mischarged
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misacylated
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asn-trna
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nd-asprs
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ammonia-dependent
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anti-ks
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lysyl-trna
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trnaasp
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histidyl-trna
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medicine
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drug development
- 6.1.1.22
- aminoacyl-trna
- asnrs
- aspartyl-trna
- malayi
- brugia
- aminoacylation
-
amidotransferase
-
asparaginylation
- asp-trnaasn
- glutaminyl-trna
- gatcabs
- filariasis
-
transamidation
-
nondiscriminating
- glu-trnagln
-
mischarged
-
misacylated
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asn-trna
- nd-asprs
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ammonia-dependent
-
anti-ks
- lysyl-trna
- trnaasp
-
histidyl-trna
- medicine
- drug development
Reaction
Synonyms
AS-AR, AsnRS, Asparagine synthetase A, Asparagine translase, asparagine tRNA synthetase, Asparagine--tRNA ligase, Asparaginyl transfer ribonucleic acid synthetase, Asparaginyl transfer RNA synthetase, asparaginyl tRNA synthetase, Asparaginyl-transfer ribonucleate synthetase, asparaginyl-transfer RNA synthetase, Asparaginyl-tRNA synthetase, Asparagyl-transfer RNA synthetase, class IIb asparaginyl-tRNA synthetase, More, NARS, NARS2, NRS, Potentially protective 63 kDa antigen, PYRAB02460, Synthetase, asparaginyl-transfer ribonucleate
ECTree
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Application
Application on EC 6.1.1.22 - asparagine-tRNA ligase
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drug development
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Brugia malayi asparaginyl-tRNA synthetase, a target for anti-parasitic drug design
medicine
filariasis caused by the nematode, Brugia malayi, is an important worldwide tropical disease in which parasites disappear from the bloodstream during daylight hours, thus hampering standard microscopic diagnostic methods
medicine
homozygous missense mutation c.822G>C affects the 3 splice site of exon 7, leading to skipping of the whole exon 7 and a part of exon 8 in the NARS2 mRNA. Upon expression in fibroblasts a specific decrease in the amount of charged mt-tRNAAsn is found. Mutation was found in in two siblings born to consanguineous parents, one presenting with mild intellectual disability and epilepsy in childhood, whereas the other had severe myopathy