NFS1

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

Cysteine desulfurase, mitochondrial is an enzyme that in humans is encoded by the NFS1 gene.[5][6][7]

AliasesNFS1, IscS, NIFS, HUSSY-08, NFS1 cysteine desulfurase, cysteine desulfurase, COXPD52
End35,699,355 bp[1]
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NFS1
Identifiers
AliasesNFS1, IscS, NIFS, HUSSY-08, NFS1 cysteine desulfurase, cysteine desulfurase, COXPD52
External IDsOMIM: 603485; MGI: 1316706; HomoloGene: 5463; GeneCards: NFS1; OMA:NFS1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001198989
NM_021100
NM_181679

NM_010911

RefSeq (protein)

NP_001185918
NP_066923

NP_035041

Location (UCSC)Chr 20: 35.67 – 35.7 MbChr 2: 155.97 – 155.99 Mb
PubMed search[3][4]
Wikidata
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Iron-sulfur clusters are required for the function of many cellular enzymes. The protein encoded by this gene supplies inorganic sulfur to these clusters by removing the sulfur from cysteine, creating alanine in the process. This gene uses alternate in-frame translation initiation sites to generate mitochondrial forms and cytoplasmic/nuclear forms. Selection of the alternative initiation sites is determined by the cytosolic pH. The encoded protein belongs to the class-V family of pyridoxal phosphate-dependent aminotransferases.[7]

References

Further reading

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