HM13
HM13 (Histocompatibility minor 13) هوَ بروتين يُشَفر بواسطة جين HM13 في الإنسان.[1][2][3]
المراجع
- "Entrez Gene: HM13 histocompatibility (minor) 13"، مؤرشف من الأصل في 05 ديسمبر 2010.
- "Identification of signal peptide peptidase, a presenilin-type aspartic protease"، Science، 296 (5576): 2215–8، يونيو 2002، doi:10.1126/science.1070925، PMID 12077416.
- "Signal peptide peptidase forms a homodimer that is labeled by an active site-directed gamma-secretase inhibitor"، J Biol Chem، 279 (15): 15153–60، أبريل 2004، doi:10.1074/jbc.M309305200، PMID 14704149.
قراءة متعمقة
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- "Intramembrane proteolysis promotes trafficking of hepatitis C virus core protein to lipid droplets"، EMBO J.، 21 (15): 3980–8، 2002، doi:10.1093/emboj/cdf414، PMC 126158، PMID 12145199.
- "Requirements for signal peptide peptidase-catalyzed intramembrane proteolysis"، Mol. Cell، 10 (4): 735–44، 2002، doi:10.1016/S1097-2765(02)00655-X، PMID 12419218.
- "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences"، Proc. Natl. Acad. Sci. U.S.A.، 99 (26): 16899–903، 2003، doi:10.1073/pnas.242603899، PMC 139241، PMID 12477932.
- "Expression of the presenilin-like signal peptide peptidase (SPP) in mouse adult brain and during development"، Gene Expr. Patterns، 3 (5): 685–91، 2004، doi:10.1016/S1567-133X(03)00094-2، PMID 12972007.
- "Analysis of a high-throughput yeast two-hybrid system and its use to predict the function of intracellular proteins encoded within the human MHC class III region"، Genomics، 83 (1): 153–67، 2004، doi:10.1016/S0888-7543(03)00235-0، PMID 14667819.
- "Complete sequencing and characterization of 21,243 full-length human cDNAs"، Nat. Genet.، 36 (1): 40–5، 2004، doi:10.1038/ng1285، PMID 14702039.
- "Impas 1 possesses endoproteolytic activity against multipass membrane protein substrate cleaving the presenilin 1 holoprotein"، FEBS Lett.، 557 (1–3): 185–92، 2004، doi:10.1016/S0014-5793(03)01489-3، PMID 14741365.
- "Correlation between conformation and antibody binding: NMR structure of cross-reactive peptides from T. cruzi, human and L. braziliensis"، FEBS Lett.، 560 (1–3): 134–40، 2004، doi:10.1016/S0014-5793(04)00088-2، PMID 14988012.
- "Consensus analysis of signal peptide peptidase and homologous human aspartic proteases reveals opposite topology of catalytic domains compared with presenilins"، J. Biol. Chem.، 279 (49): 50790–8، 2005، doi:10.1074/jbc.M407898200، PMID 15385547.
- "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)"، Genome Res.، 14 (10B): 2121–7، 2004، doi:10.1101/gr.2596504، PMC 528928، PMID 15489334.
- "Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries"، DNA Res.، 12 (2): 117–26، 2007، doi:10.1093/dnares/12.2.117، PMID 16303743.
- "Cell-surface expression of a new splice variant of the mouse signal peptide peptidase"، Biochim. Biophys. Acta، 1759 (3–4): 159–65، 2006، doi:10.1016/j.bbaexp.2006.02.007، PMID 16730383.
- "Signal peptide peptidase is required for dislocation from the endoplasmic reticulum"، Nature، 441 (7095): 894–7، 2006، doi:10.1038/nature04830، PMID 16738546.
- "Signal peptide peptidase: biochemical properties and modulation by nonsteroidal antiinflammatory drugs"، Biochemistry، 45 (28): 8649–56، 2006، doi:10.1021/bi060597g، PMID 16834339.
- بوابة الكيمياء الحيوية
- بوابة علم الأحياء الخلوي والجزيئي
- بوابة طب
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