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Histidine–tRNA ligase, cytoplasmic

From Wikipedia, the free encyclopedia
(Redirected from HARS)
HARS1
Identifiers
AliasesHARS1, HRS, USH3B, CMT2W, histidyl-tRNA synthetase, HARS, histidyl-tRNA synthetase 1
External IDsOMIM: 142810; MGI: 108087; GeneCards: HARS1
Available structures
PDBOrtholog search: PDBe RCSB
Enzyme activity
EC #BRENDAExPASyKEGGMetaCyc
6.1.1.21↗↗↗↗
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_008214

RefSeq (protein)

NP_032240

Location (UCSC)Chr 5: 140.67 – 140.69 MbChr 18: 36.9 – 36.92 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Histidine–tRNA ligase, cytoplasmic, also called histidyl-tRNA synthetase 1, is an enzyme which in humans is encoded by the HARS1 gene (previously HARS).[5][6] As a histidine–tRNA ligase, this enzyme functions to attach the amino acid histidine to its corresponding (cognate) transfer RNA (tRNAHis), which is required for RNA-to-protein translation.[5]

Function

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Aminoacyl-tRNA synthetases are a class of enzymes that charge tRNAs with their cognate amino acids. The protein encoded by this gene is a cytoplasmic enzyme which belongs to the class II family of aminoacyl tRNA synthetases. The enzyme is responsible for the synthesis of histidyl-transfer RNA, which is essential for the incorporation of histidine into proteins.[7] The gene is located in a head-to-head orientation with HARS2 on chromosome five, where the homologous genes share a bidirectional promoter.[5]

Clinical significance

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The gene product is a frequent target of autoantibodies in the human autoimmune disease polymyositis/dermatomyositis.[7] Pathogenic mutations in HARS1 are the cause of Type IIIB usher syndrome (USH3B), which is associated with progressive hearing and vision loss.[8]

Interactions

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HARS has been shown to interact with EEF1B2[9] and EEF1G.[9]

See also

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References

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  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000170445 – Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000001380 – Ensembl, May 2017
  3. ↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. 1 2 3 "Entrez Gene: HARS histidyl-tRNA synthetase".
  6. ↑ Wasmuth JJ, Carlock LR (1986). "Chromosomal localization of human gene for histidyl-tRNA synthetase: clustering of genes encoding aminoacyl-tRNA synthetases on human chromosome 5". Somat. Cell Mol. Genet. 12 (5): 513–7. doi:10.1007/BF01539922. PMID 3464104. S2CID 28520231.
  7. 1 2 Freist W, Verhey JF, Rühlmann A, Gauss DH, Arnez JG (1999). "Histidyl-tRNA synthetase". Biol. Chem. 380 (6): 623–46. doi:10.1515/BC.1999.079. PMID 10430027.
  8. ↑ "USHER SYNDROME, TYPE IIIB; USH3B". Online Mendelian Inheritance in Man. Johns Hopkins University. Retrieved 2026-09-27.
  9. 1 2 Sang Lee J, Gyu Park S, Park H, Seol W, Lee S, Kim S (2002). "Interaction network of human aminoacyl-tRNA synthetases and subunits of elongation factor 1 complex". Biochem. Biophys. Res. Commun. 291 (1): 158–64. doi:10.1006/bbrc.2002.6398. PMID 11829477.

Further reading

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