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胱天蛋白酶2

胱天蛋白酶2
已知的结构
PDB直系同源搜索: PDBe RCSB
识别号
别名CASP2;, CASP-2, ICH1, NEDD-2, NEDD2, PPP1R57, caspase 2
外部IDOMIM600639 MGI97295 HomoloGene:7254 GeneCardsCASP2
为以下药物的标靶
emricasan[1]
基因位置(人类
7号染色体
染色体7号染色体[2]
7号染色体
胱天蛋白酶2的基因位置
胱天蛋白酶2的基因位置
基因座7q34起始143,288,215 bp[2]
终止143,307,696 bp[2]
RNA表达模式




查阅更多表达数据
直系同源
物种人类小鼠
Entrez
Ensembl
UniProt
mRNA​序列

NM_032983
​NM_001224
​NM_032982
​NM_032984

NM_007610

蛋白序列

NP_001215
​NP_116764
​NP_116765

NP_031636

基因位置​(UCSC)Chr 7: 143.29 – 143.31 MbChr 6: 42.24 – 42.26 Mb
PubMed​查找[4][5]
维基数据
查看/编辑人类查看/编辑小鼠

胱天蛋白酶2是一种在人类中由CASP2基因编码的[6]几乎所有可获得完整基因组数据的哺乳动物中都已鉴定出CASP2直向同源物[7]鸟类蜥蜴滑体动物真骨类中也存在独特的直系同源物。

功能

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胱天蛋白酶的连续激活在细胞凋亡的执行阶段发挥着核心作用。胱天蛋白酶以无活性的酶原形式存在,在保守的天冬氨酸残基上进行蛋白酶解加工,产生两个亚基,分别为大的和小的,它们二聚化形成活性酶。该蛋白质的蛋白酶解裂解是由多种细胞凋亡刺激诱导的。[8]

胱天蛋白酶2通过蛋白酶解裂解其他蛋白质。它属于称为胱天蛋白酶的半胱氨酸蛋白酶家族,仅在天冬氨酸残基后的氨基酸处切割蛋白质。在该家族中,胱天蛋白酶2属于Ich-1亚家族。它是不同物种动物中最保守的胱天蛋白酶之一。胱天蛋白酶2与起始胱天蛋白酶具有相似的氨基酸序列,包括胱天蛋白酶1胱天蛋白酶4胱天蛋白酶5胱天蛋白酶9。它作为酶原产生,包含一个与胱天蛋白酶9相似的长前结构域,并包含称为CARD结构域的蛋白质相互作用结构域。胱天蛋白酶原2包含两个亚基:p19和p12。

它已被证明与使用其CARD结构域参与细胞凋亡的多种蛋白质相关,包括具有死亡结构域的RIP相关Ich-1/Ced-3同源蛋白(RAIDD)、具有胱天蛋白酶募集结构域(ARC)的细胞凋亡抑制蛋白,以及死亡效应丝形成 Ced-4 样凋亡蛋白(DEFCAP)。[9]胱天蛋白酶2与RAIDD和带有死亡结构域(PIDD或LRDD)的p53诱导蛋白一起形成所谓的PIDDosome,[10]它可以作为蛋白酶的激活平台,尽管它也可能是在没有PIDD的情况下激活。[11]总体而言,胱天蛋白酶2似乎是一种用途广泛的胱天蛋白酶,除了诱导细胞死亡外还具有多种功能。[12][13]

相互作用

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胱天蛋白酶2已被证明可以与以下物质相互作用:

参见

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参考资料

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  1. ^ 對Caspase 2起作用的藥物;在維基數據上查看/編輯參考. 
  2. ^ 2.0 2.1 2.2 GRCh38: Ensembl release 89: ENSG00000106144 - Ensembl, May 2017
  3. ^ 3.0 3.1 3.2 GRCm38: Ensembl release 89: ENSMUSG00000029863 - Ensembl, May 2017
  4. ^ Human PubMed Reference:. National Center for Biotechnology Information, U.S. National Library of Medicine. 
  5. ^ Mouse PubMed Reference:. National Center for Biotechnology Information, U.S. National Library of Medicine. 
  6. ^ Kumar S, White DL, Takai S, Turczynowicz S, Juttner CA, Hughes TP. Apoptosis regulatory gene NEDD2 maps to human chromosome segment 7q34-35, a region frequently affected in haematological neoplasms. Hum. Genet. June 1995, 95 (6): 641–4. PMID 7789948. S2CID 22813779. doi:10.1007/bf00209480. 
  7. ^ OrthoMaM phylogenetic marker: CASP2 coding sequence. [20 December 2009]. (原始内容存档于24 September 2015). 
  8. ^ Entrez Gene: CASP2. 
  9. ^ Zhivotovsky B, Orrenius S. Caspase-2 function in response to DNA damage. Biochem. Biophys. Res. Commun. 2005, 331 (3): 859–67. PMID 15865942. doi:10.1016/j.bbrc.2005.03.191可免费查阅. 
  10. ^ 10.0 10.1 Tinel A, Tschopp J. The PIDDosome, a protein complex implicated in activation of caspase-2 in response to genotoxic stress. Science. May 2004, 304 (5672): 843–6. Bibcode:2004Sci...304..843T. PMID 15073321. S2CID 6583298. doi:10.1126/science.1095432. 
  11. ^ Manzl C, Krumschnabel G, Bock F, Sohm B, Labi V, Baumgartner F, Logette E, Tschopp J, Villunger A. Caspase-2 activation in the absence of PIDDosome formation. J. Cell Biol. April 2009, 185 (2): 291–303 [2024-01-20]. PMC 2700374可免费查阅. PMID 19364921. doi:10.1083/jcb.200811105. (原始内容存档于2023-03-28). 
  12. ^ Krumschnabel G, Manzl C, Villunger A. Caspase-2: killer, savior and safeguard--emerging versatile roles for an ill-defined caspase. Oncogene. September 2009, 28 (35): 3093–6. PMC 3272399可免费查阅. PMID 19581929. doi:10.1038/onc.2009.173. 
  13. ^ Krumschnabel G, Sohm B, Bock F, Manzl C, Villunger A. The enigma of caspase-2: the laymen's view. Cell Death Differ. February 2009, 16 (2): 195–207. PMC 3272397可免费查阅. PMID 19023332. doi:10.1038/cdd.2008.170. 
  14. ^ 14.0 14.1 Guo Y, Srinivasula SM, Druilhe A, Fernandes-Alnemri T, Alnemri ES. Caspase-2 induces apoptosis by releasing proapoptotic proteins from mitochondria. J. Biol. Chem. April 2002, 277 (16): 13430–7. PMID 11832478. doi:10.1074/jbc.M108029200可免费查阅. 
  15. ^ Paroni G, Henderson C, Schneider C, Brancolini C. Caspase-2-induced apoptosis is dependent on caspase-9, but its processing during UV- or tumor necrosis factor-dependent cell death requires caspase-3. J. Biol. Chem. June 2001, 276 (24): 21907–15. PMID 11399776. doi:10.1074/jbc.M011565200可免费查阅. 
  16. ^ Droin N, Beauchemin M, Solary E, Bertrand R. Identification of a caspase-2 isoform that behaves as an endogenous inhibitor of the caspase cascade. Cancer Res. December 2000, 60 (24): 7039–47. PMID 11156409. 
  17. ^ Duan H, Dixit VM. RAIDD is a new 'death' adaptor molecule (PDF). Nature. January 1997, 385 (6611): 86–9. Bibcode:1997Natur.385...86D. PMID 8985253. S2CID 4317538. doi:10.1038/385086a0. hdl:2027.42/62739可免费查阅. 
  18. ^ Srinivasula SM, Ahmad M, Fernandes-Alnemri T, Litwack G, Alnemri ES. Molecular ordering of the Fas-apoptotic pathway: the Fas/APO-1 protease Mch5 is a CrmA-inhibitable protease that activates multiple Ced-3/ICE-like cysteine proteases. Proc. Natl. Acad. Sci. U.S.A. December 1996, 93 (25): 14486–91. Bibcode:1996PNAS...9314486S. PMC 26159可免费查阅. PMID 8962078. doi:10.1073/pnas.93.25.14486可免费查阅. 

外部链接

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胱天蛋白酶2引用了美国国家医学图书馆提供的数据,这些数据属于公共领域


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胱天蛋白酶2
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