6.1.1.7: alanine-tRNA ligase
This is an abbreviated version!
For detailed information about alanine-tRNA ligase, go to the full flat file.
Word Map on EC 6.1.1.7
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6.1.1.7
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aminoacylation
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synthetases
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aminoacyl-trna
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leukodystrophy
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alanylation
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mischarged
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aarss
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leukoencephalopathy
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mistranslation
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tmrnas
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charcot-marie-tooth
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noncognate
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thrrs
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threonyl-trna
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minihelix
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seryl-trna
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anti-pl-12
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valrs
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misactivation
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microhelix
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ilers
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trans-translation
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molecular biology
- 6.1.1.7
- aminoacylation
- synthetases
- aminoacyl-trna
- leukodystrophy
-
alanylation
-
mischarged
-
aarss
- leukoencephalopathy
-
mistranslation
- tmrnas
- charcot-marie-tooth
-
noncognate
- thrrs
- threonyl-trna
- minihelix
- seryl-trna
-
anti-pl-12
- valrs
-
misactivation
- microhelix
- ilers
-
trans-translation
- molecular biology
Reaction
Synonyms
AARS2, Ala-tRNA synthetase, ALA1, ALA2, Alanine transfer RNA synthetase, Alanine translase, Alanine tRNA synthetase, Alanine--tRNA ligase, Alanine-transfer RNA ligase, alanine-tRNA ligase, alanyl tRNA ligase, Alanyl-transfer ribonucleate synthetase, Alanyl-transfer ribonucleic acid synthetase, Alanyl-transfer RNA synthetase, alanyl-tRNA ligase, alanyl-tRNA synthase, Alanyl-tRNA synthetase, alanyltRNA synthetase, AlaRS, mitochondrial alanyl-tRNA synthetase, More, mtAlaRS, MurM, MurN, Synthase, alanyl-transfer ribonucleate
ECTree
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Localization
Localization on EC 6.1.1.7 - alanine-tRNA ligase
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additional information
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very poor mitochondrial targeting activity of the ALA1 leader peptide, mapping of the mitochondrial targeting signal, overview
an isolated 23 kDa appended C-terminal domain (C-Ala), consisting of the C-terminal 757968 amino acids, locates in the nucleus
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additional information
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an isolated 23 kDa appended C-terminal domain (C-Ala), consisting of the C-terminal 757968 amino acids, locates in the nucleus
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additional information
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isozyme pattern of expression and localization, overview
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additional information
the yeast Tetrapisispora phaffii possesses two significantly diverged AlaRS gene homologues, one encoding the cytoplasmic form and the other its mitochondrial counterpart
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additional information
the yeast Tetrapisispora phaffii possesses two significantly diverged AlaRS gene homologues, one encoding the cytoplasmic form and the other its mitochondrial counterpart
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additional information
the yeast Vanderwaltozyma polyspora possesses two significantly diverged AlaRS gene homologues, one encoding the cytoplasmic form and the other its mitochondrial counterpart. Clever selection of transcription and translation initiation sites enables the two isoforms to be localized and thus functional in their respective cellular compartments. But the two isoforms can also be stably expressed and function in the reciprocal compartments by insertion or removal of a mitochondrial targeting signal
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additional information
the yeast Vanderwaltozyma polyspora possesses two significantly diverged AlaRS gene homologues, one encoding the cytoplasmic form and the other its mitochondrial counterpart. Clever selection of transcription and translation initiation sites enables the two isoforms to be localized and thus functional in their respective cellular compartments. But the two isoforms can also be stably expressed and function in the reciprocal compartments by insertion or removal of a mitochondrial targeting signal
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additional information
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the yeast Vanderwaltozyma polyspora possesses two significantly diverged AlaRS gene homologues, one encoding the cytoplasmic form and the other its mitochondrial counterpart. Clever selection of transcription and translation initiation sites enables the two isoforms to be localized and thus functional in their respective cellular compartments. But the two isoforms can also be stably expressed and function in the reciprocal compartments by insertion or removal of a mitochondrial targeting signal
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additional information
Vanderwaltozyma polyspora ATCC 22028 / DSM 70294
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the yeast Vanderwaltozyma polyspora possesses two significantly diverged AlaRS gene homologues, one encoding the cytoplasmic form and the other its mitochondrial counterpart. Clever selection of transcription and translation initiation sites enables the two isoforms to be localized and thus functional in their respective cellular compartments. But the two isoforms can also be stably expressed and function in the reciprocal compartments by insertion or removal of a mitochondrial targeting signal
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