SCYE1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Aminoacyl tRNA synthetase complex-interacting multifunctional protein 1 is a protein that in humans is encoded by the AIMP1 gene.[5][6][7]

PDBOrtholog search: PDBe RCSB
AliasesAIMP1, EMAP2, EMAPII, HLD3, SCYE1, p43, aminoacyl tRNA synthetase complex interacting multifunctional protein 1
Quick facts AIMP1, Available structures ...
AIMP1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesAIMP1, EMAP2, EMAPII, HLD3, SCYE1, p43, aminoacyl tRNA synthetase complex interacting multifunctional protein 1
External IDsOMIM: 603605; MGI: 102774; HomoloGene: 31260; GeneCards: AIMP1; OMA:AIMP1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004757
NM_001142415
NM_001142416

NM_007926
NM_001368626

RefSeq (protein)

NP_001135887
NP_001135888
NP_004748

NP_001355555
NP_031952

Location (UCSC)Chr 4: 106.32 – 106.35 MbChr 3: 132.37 – 132.39 Mb
PubMed search[3][4]
Wikidata
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The protein encoded by this gene is a cytokine that may be induced by apoptosis and is also released from professional antigen-presenting cells such as dendritic cells. The release of this cytokine renders the tumor-associated vasculature sensitive to tumor necrosis factor. The precursor of SCYE1 (pro-SCYE1) is identical to the p43 subunit, which is associated with the multiaminoacyl-tRNA synthetase complex (mARS). Pro-SCYE1 may function in binding RNA as part of the tRNA synthetase complex in normal cells and in stimulating inflammatory responses after proteolytic cleavage in tumor cells.[7] As an inflammatory cytokine, AIMp1/p43 has demonstrated the ability to skew T-helper polarization in the direction of Th-1, and its homozygous deletion leads to a hyper-polarized Th-2 phenotype.

Interactions

SCYE1 has been shown to interact with SMURF2.[8]

References

Further reading

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