PAPSS2

PAPSS2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
Aliases PAPSS2, ATPSK2, BCYM4, SK2, 3'-phosphoadenosine 5'-phosphosulfate synthase 2
External IDs MGI: 1330223 HomoloGene: 55840 GeneCards: PAPSS2
RNA expression pattern




More reference expression data
Orthologs
Species Human Mouse
Entrez

9060

23972

Ensembl

ENSG00000198682

ENSMUSG00000024899

UniProt

O95340
Q5TB52

O88428

RefSeq (mRNA)

NM_004670
NM_001015880

NM_001201470
NM_011864

RefSeq (protein)

NP_001015880.1
NP_004661.2
NP_004661.2

NP_035994.2

Location (UCSC) Chr 10: 87.66 – 87.75 Mb Chr 19: 32.62 – 32.67 Mb
PubMed search [1] [2]
Wikidata
View/Edit HumanView/Edit Mouse

Bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthetase 2 is an enzyme that in humans is encoded by the PAPSS2 gene.[3][4]

Sulfation is a common modification of endogenous (lipids, proteins, and carbohydrates) and exogenous (xenobiotics and drugs) compounds. In mammals, the sulfate source is 3'-phosphoadenosine 5'-phosphosulfate (PAPS), created from ATP and inorganic sulfate. Two different tissue isoforms encoded by different genes synthesize PAPS. This gene encodes one of the two PAPS synthetases. Defects in this gene cause the Pakistani type of spondyloepimetaphyseal dysplasia. Two alternatively spliced transcript variants that encode different isoforms have been described for this gene.[4]

References

  1. "Human PubMed Reference:".
  2. "Mouse PubMed Reference:".
  3. ul Haque MF, King LM, Krakow D, Cantor RM, Rusiniak ME, Swank RT, Superti-Furga A, Haque S, Abbas H, Ahmad W, Ahmad M, Cohn DH (Oct 1998). "Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouse". Nat Genet. 20 (2): 157–62. doi:10.1038/2458. PMID 9771708.
  4. 1 2 "Entrez Gene: PAPSS2 3'-phosphoadenosine 5'-phosphosulfate synthase 2".

Further reading


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