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Membrane-bound transcription factor site-2 protease

Membrane-bound transcription factor site-2 protease, also known as S2P endopeptidase or site-2 protease (S2P), is an enzyme (EC 3.4.24.85) encoded by the MBTPS2 gene which liberates the N-terminal fragment of sterol regulatory element-binding protein (SREBP) transcription factors from membranes.[1][2] S2P cleaves the transmembrane domain of SREPB, making it a member of the class of intramembrane proteases.[3]

membrane-bound transcription factor peptidase, site 2
Identifiers
SymbolMBTPS2
Alt. symbolsS2P
NCBI gene51360
HGNC15455
OMIM300294
RefSeqNM_015884
UniProtO43462
Other data
EC number3.4.24.85
LocusChr. X p22.1-p22.2
Search for
StructuresSwiss-model
DomainsInterPro
S2P endopeptidase
Identifiers
EC no.3.4.24.85
CAS no.752251-31-3
Databases
IntEnzIntEnz view
BRENDABRENDA entry
ExPASyNiceZyme view
KEGGKEGG entry
MetaCycmetabolic pathway
PRIAMprofile
PDB structuresRCSB PDB PDBe PDBsum
Search
PMCarticles
PubMedarticles
NCBIproteins

S2P catalyses the following chemical reaction

Cleaves several transcription factors that are type-2 transmembrane proteins within membrane-spanning domains. Known substrates include sterol regulatory element-binding protein (SREBP)-1, SREBP-2 and forms of the transcriptional activator ATF6.

This enzyme belongs to the peptidase family M50.

Function edit

This gene encodes an intramembrane zinc metalloprotease, which is essential in development. This protease functions in the signal protein activation involved in sterol control of transcription and the ER stress response. Mutations in this gene have been associated with ichthyosis follicularis with atrichia and photophobia (IFAP syndrome); IFAP syndrome has been quantitatively linked to a reduction in cholesterol homeostasis and ER stress response.[provided by RefSeq, Aug 2009].

See also edit

References edit

  1. ^ Brown MS, Goldstein JL (September 1999). "A proteolytic pathway that controls the cholesterol content of membranes, cells, and blood". Proceedings of the National Academy of Sciences of the United States of America. 96 (20): 11041–8. Bibcode:1999PNAS...9611041B. doi:10.1073/pnas.96.20.11041. PMC 34238. PMID 10500120.
  2. ^ Rawson RB, Zelenski NG, Nijhawan D, Ye J, Sakai J, Hasan MT, et al. (December 1997). "Complementation cloning of S2P, a gene encoding a putative metalloprotease required for intramembrane cleavage of SREBPs". Molecular Cell. 1 (1): 47–57. doi:10.1016/S1097-2765(00)80006-4. PMID 9659902.
  3. ^ Brown MS, Ye J, Rawson RB, Goldstein JL (February 2000). "Regulated intramembrane proteolysis: a control mechanism conserved from bacteria to humans". Cell. 100 (4): 391–8. doi:10.1016/S0092-8674(00)80675-3. PMID 10693756.

External links edit


membrane, bound, transcription, factor, site, protease, also, known, endopeptidase, site, protease, enzyme, encoded, mbtps2, gene, which, liberates, terminal, fragment, sterol, regulatory, element, binding, protein, srebp, transcription, factors, from, membran. Membrane bound transcription factor site 2 protease also known as S2P endopeptidase or site 2 protease S2P is an enzyme EC 3 4 24 85 encoded by the MBTPS2 gene which liberates the N terminal fragment of sterol regulatory element binding protein SREBP transcription factors from membranes 1 2 S2P cleaves the transmembrane domain of SREPB making it a member of the class of intramembrane proteases 3 membrane bound transcription factor peptidase site 2IdentifiersSymbolMBTPS2Alt symbolsS2PNCBI gene51360HGNC15455OMIM300294RefSeqNM 015884UniProtO43462Other dataEC number3 4 24 85LocusChr X p22 1 p22 2Search forStructuresSwiss modelDomainsInterPro S2P endopeptidaseIdentifiersEC no 3 4 24 85CAS no 752251 31 3DatabasesIntEnzIntEnz viewBRENDABRENDA entryExPASyNiceZyme viewKEGGKEGG entryMetaCycmetabolic pathwayPRIAMprofilePDB structuresRCSB PDB PDBe PDBsumSearchPMCarticlesPubMedarticlesNCBIproteins S2P catalyses the following chemical reaction Cleaves several transcription factors that are type 2 transmembrane proteins within membrane spanning domains Known substrates include sterol regulatory element binding protein SREBP 1 SREBP 2 and forms of the transcriptional activator ATF6 This enzyme belongs to the peptidase family M50 Contents 1 Function 2 See also 3 References 4 External linksFunction editThis gene encodes an intramembrane zinc metalloprotease which is essential in development This protease functions in the signal protein activation involved in sterol control of transcription and the ER stress response Mutations in this gene have been associated with ichthyosis follicularis with atrichia and photophobia IFAP syndrome IFAP syndrome has been quantitatively linked to a reduction in cholesterol homeostasis and ER stress response provided by RefSeq Aug 2009 See also editMembrane bound transcription factor site 1 proteaseReferences edit Brown MS Goldstein JL September 1999 A proteolytic pathway that controls the cholesterol content of membranes cells and blood Proceedings of the National Academy of Sciences of the United States of America 96 20 11041 8 Bibcode 1999PNAS 9611041B doi 10 1073 pnas 96 20 11041 PMC 34238 PMID 10500120 Rawson RB Zelenski NG Nijhawan D Ye J Sakai J Hasan MT et al December 1997 Complementation cloning of S2P a gene encoding a putative metalloprotease required for intramembrane cleavage of SREBPs Molecular Cell 1 1 47 57 doi 10 1016 S1097 2765 00 80006 4 PMID 9659902 Brown MS Ye J Rawson RB Goldstein JL February 2000 Regulated intramembrane proteolysis a control mechanism conserved from bacteria to humans Cell 100 4 391 8 doi 10 1016 S0092 8674 00 80675 3 PMID 10693756 External links editSREBP site 2 protease at the U S National Library of Medicine Medical Subject Headings MeSH S2P endopeptidase at the U S National Library of Medicine Medical Subject Headings MeSH Portal nbsp Biology nbsp This article on a gene on the human X chromosome and or its associated protein is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Membrane bound transcription factor site 2 protease amp oldid 1172353101, wikipedia, wiki, book, books, library,

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