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ALA1 alanine--tRNA ligase [ Saccharomyces cerevisiae S288C ]

Gene ID: 854513, updated on 5-May-2024

Summary

Gene symbol
ALA1
Gene description
alanine--tRNA ligase
Primary source
SGD:S000005862
Locus tag
YOR335C
See related
AllianceGenome:SGD:S000005862
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Saccharomyces cerevisiae S288C (strain: S288C)
Lineage
Eukaryota; Fungi; Dikarya; Ascomycota; Saccharomycotina; Saccharomycetes; Saccharomycetales; Saccharomycetaceae; Saccharomyces
Also known as
CDC64
Summary
Enables alanine-tRNA ligase activity. Involved in alanyl-tRNA aminoacylation. Located in mitochondrion. Used to study Charcot-Marie-Tooth disease; axonal neuropathy; cerebellar ataxia; and dermatomyositis. Human ortholog(s) of this gene implicated in Charcot-Marie-Tooth disease axonal type 2N; combined oxidative phosphorylation deficiency 8; and developmental and epileptic encephalopathy 29. Orthologous to several human genes including AARS1 (alanyl-tRNA synthetase 1). [provided by Alliance of Genome Resources, Apr 2022]
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Genomic context

Location:
chromosome: XV
Exon count:
1
Sequence:
Chromosome: XV; NC_001147.6 (946233..949109, complement)

Chromosome XV - NC_001147.6Genomic Context describing neighboring genes Neighboring gene H(+)-transporting V1 sector ATPase subunit E Neighboring gene Mrs2p Neighboring gene Kre5p Neighboring gene Tea1p

Bibliography

Pathways from PubChem

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Gene Ontology Provided by SGD

Function Evidence Code Pubs
enables ATP binding IEA
Inferred from Electronic Annotation
more info
 
enables alanine-tRNA ligase activity IBA
Inferred from Biological aspect of Ancestor
more info
 
enables alanine-tRNA ligase activity IEA
Inferred from Electronic Annotation
more info
 
enables alanine-tRNA ligase activity IMP
Inferred from Mutant Phenotype
more info
PubMed 
enables aminoacyl-tRNA editing activity IBA
Inferred from Biological aspect of Ancestor
more info
 
enables aminoacyl-tRNA ligase activity IEA
Inferred from Electronic Annotation
more info
 
enables metal ion binding IEA
Inferred from Electronic Annotation
more info
 
enables nucleic acid binding IEA
Inferred from Electronic Annotation
more info
 
enables sequence-specific mRNA binding IDA
Inferred from Direct Assay
more info
PubMed 
enables tRNA binding IEA
Inferred from Electronic Annotation
more info
 
enables zinc ion binding IEA
Inferred from Electronic Annotation
more info
 
enables zinc ion binding RCA
inferred from Reviewed Computational Analysis
more info
PubMed 
Process Evidence Code Pubs
involved_in alanyl-tRNA aminoacylation IBA
Inferred from Biological aspect of Ancestor
more info
 
involved_in alanyl-tRNA aminoacylation IEA
Inferred from Electronic Annotation
more info
 
involved_in alanyl-tRNA aminoacylation IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in aminoacyl-tRNA metabolism involved in translational fidelity IEA
Inferred from Electronic Annotation
more info
 
involved_in mitochondrial alanyl-tRNA aminoacylation IEA
Inferred from Electronic Annotation
more info
 
involved_in protein metabolic process IEA
Inferred from Electronic Annotation
more info
 
involved_in translation IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
located_in cytoplasm HDA PubMed 
located_in cytoplasm IDA
Inferred from Direct Assay
more info
PubMed 
located_in cytoplasm IEA
Inferred from Electronic Annotation
more info
 
located_in mitochondrion HDA PubMed 
is_active_in mitochondrion IBA
Inferred from Biological aspect of Ancestor
more info
 
located_in mitochondrion IDA
Inferred from Direct Assay
more info
PubMed 
located_in mitochondrion IEA
Inferred from Electronic Annotation
more info
 

General protein information

Preferred Names
alanine--tRNA ligase
NP_014980.3
  • Cytoplasmic and mitochondrial alanyl-tRNA synthetase; required for protein synthesis; point mutation (cdc64-1 allele) causes cell cycle arrest at G1; lethality of null mutation is functionally complemented by human homolog AARS; mutations in human homolog AARS are associated with autoimmune disease polymyositis/dermatomyositis and with hereditary peripheral neuropathy, Charcot-Marie-Tooth (CMT) disease

NCBI Reference Sequences (RefSeq)

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Genome Annotation

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference assembly

Genomic

  1. NC_001147.6 Reference assembly

    Range
    946233..949109 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. NM_001183755.3NP_014980.3  TPA: alanine--tRNA ligase [Saccharomyces cerevisiae S288C]

    See identical proteins and their annotated locations for NP_014980.3

    Status: REVIEWED

    UniProtKB/TrEMBL
    A0A8H4BW42, B3LJZ4, B5VSL3, C8ZH87, N1NW84
    Conserved Domains (1) summary
    PLN02900
    Location:7946
    PLN02900; alanyl-tRNA synthetase