Kaspaza-7, apoptozno vezana cisteinska peptidaza, znana i kao CASP7, jest protein koji je kod ljudi kodiran genom CASP7 sa hromosoma 10.

Kaspaza-7
Dostupne strukture
PDBPretraga ortologa: PDBe RCSB
Spisak PDB ID kodova

1F1J, 1GQF, 1I4O, 1I51, 1K86, 1K88, 1KMC, 1SHJ, 1SHL, 2QL5, 2QL7, 2QL9, 2QLB, 2QLF, 2QLJ, 3EDR, 3H1P, 3IBC, 3IBF, 3R5K, 4FDL, 4FEA, 4HQ0, 4HQR, 4JB8, 4JJ8, 4JR1, 4JR2, 4LSZ, 4ZVR, 4ZVQ, 4ZVO, 4ZVU, 4ZVT, 4ZVS, 4ZVP, 5IC6

Identifikatori
AliasiCASP7
Vanjski ID-jeviOMIM: 601761 MGI: 109383 HomoloGene: 11168 GeneCards: CASP7
Lokacija gena (čovjek)
Hromosom 10 (čovjek)
Hrom.Hromosom 10 (čovjek)[1]
Hromosom 10 (čovjek)
Genomska lokacija za Kaspaza-7
Genomska lokacija za Kaspaza-7
Bend10q25.3Početak113,679,162 bp[1]
Kraj113,730,907 bp[1]
Lokacija gena (miš)
Hromosom 19 (miš)
Hrom.Hromosom 19 (miš)[2]
Hromosom 19 (miš)
Genomska lokacija za Kaspaza-7
Genomska lokacija za Kaspaza-7
Bend19 D2|19 51.84 cMPočetak56,385,561 bp[2]
Kraj56,430,776 bp[2]
Obrazac RNK ekspresije
Više referentnih podataka o ekspresiji
Ontologija gena
Molekularna funkcija cysteine-type peptidase activity
cysteine-type endopeptidase activity
GO:0001948, GO:0016582 vezivanje za proteine
hydrolase activity
GO:0070122 peptidase activity
cysteine-type endopeptidase activity involved in execution phase of apoptosis
cysteine-type endopeptidase activity involved in apoptotic process
Ćelijska komponenta citoplazma
citosol
jedro
nukleoplazma
Biološki proces Proteoliza
cellular response to staurosporine
execution phase of apoptosis
GO:0097285 apoptoza
Izvori:Amigo / QuickGO
Ortolozi
VrsteČovjekMiš
Entrez
Ensembl
UniProt
RefSeq (mRNK)
NM_001227
NM_001267056
NM_001267057
NM_001267058
NM_033338

NM_033339
NM_033340
NM_001320911

NM_007611

RefSeq (bjelančevina)
NP_001218
NP_001253985
NP_001253986
NP_001253987
NP_001307840

NP_203124
NP_203125
NP_203126

NP_031637

Lokacija (UCSC)Chr 10: 113.68 – 113.73 MbChr 19: 56.39 – 56.43 Mb
PubMed pretraga[3][4]
Wikipodaci
Pogledaj/uredi – čovjekPogledaj/uredi – miš

Ortolozi CASP7[5] identificirani su kod gotovo svih sisara za koje su dostupni potpuni podaci o genomu. Jedinstveni ortolozi su također prisutni u ptica, gušterova, Lissamphibia i Teleostea.

Aminokiselinska sekvenca uredi

Dužina polipeptidnog lanca je 303 aminokiseline, a molekulska težina 34.277 Da.[5]

1020304050
MADDQGCIEEQGVEDSANEDSVDAKPDRSSFVPSLFSKKKKNVTMRSIKT
TRDRVPTYQYNMNFEKLGKCIIINNKNFDKVTGMGVRNGTDKDAEALFKC
FRSLGFDVIVYNDCSCAKMQDLLKKASEEDHTNAACFACILLSHGEENVI
YGKDGVTPIKDLTAHFRGDRCKTLLEKPKLFFIQACRGTELDDGIQADSG
PINDTDANPRYKIPVEADFLFAYSTVPGYYSWRSPGRGSWFVQALCSILE
EHGKDLEIMQILTRVNDRVARHFESQSDDPHFHEKKQIPCVVSMLTKELY
FSQ

Funkcija uredi

Kaspaza-7 je član porodice proteina kaspaza (cistein [[asparaginska kiselinas|aspartat proteaza) i pokazalo se da je stražarski protein apoptoza. Sekvencijalna aktivacija kaspaza igra centralnu ulogu u fazi izvršenja ćelije apoptoza. Kaspaze postoje kao neaktivni proenzimi koji se podvrgavaju proteolitskoj obradi uzvodnim kaspazama (kapaza-8,9) na konzerviranim asparaginskim ostacima, kako bi se dobile dvije podjedinice, velika i mala, koje se dimeriziraju i formiraju aktivni enzim u obliku heterotetramer. Prekursor ove kaspaze cepaju kapazu-3, kapazu-10 i kapazu-9. Aktivira se na podražaje ćelijske smrti i inducira apoptozu. Alternativna prerada RNK rezultira u četiri varijante transkripta, kodirajući tri različite izoforme.[6]

Interakcije uredi

Pokazalo se da kaspaza 7 u interakciji sa:

Također pogledajte uredi

Reference uredi

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000165806 - Ensembl, maj 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000025076 - Ensembl, maj 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b "OrthoMaM phylogenetic marker: CASP7 coding sequence". Arhivirano s originala, 4. 3. 2016. Pristupljeno 20. 12. 2009.
  6. ^ "Entrez Gene: CASP7 caspase 7, apoptosis-related cysteine peptidase".
  7. ^ Guo Y, Srinivasula SM, Druilhe A, Fernandes-Alnemri T, Alnemri ES (Apr 2002). "Caspase-2 induces apoptosis by releasing proapoptotic proteins from mitochondria". J. Biol. Chem. 277 (16): 13430–7. doi:10.1074/jbc.M108029200. PMID 11832478.
  8. ^ Srinivasula SM, Ahmad M, Fernandes-Alnemri T, Litwack G, Alnemri ES (Dec 1996). "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. 93 (25): 14486–91. Bibcode:1996PNAS...9314486S. doi:10.1073/pnas.93.25.14486. PMC 26159. PMID 8962078.
  9. ^ Tamm I, Wang Y, Sausville E, Scudiero DA, Vigna N, Oltersdorf T, Reed JC (Dec 1998). "IAP-family protein survivin inhibits caspase activity and apoptosis induced by Fas (CD95), Bax, caspases, and anticancer drugs". Cancer Res. 58 (23): 5315–20. PMID 9850056.
  10. ^ Shin S, Sung BJ, Cho YS, Kim HJ, Ha NC, Hwang JI, Chung CW, Jung YK, Oh BH (Jan 2001). "An anti-apoptotic protein human survivin is a direct inhibitor of caspase-3 and -7". Biochemistry. 40 (4): 1117–23. doi:10.1021/bi001603q. PMID 11170436.
  11. ^ Riedl SJ, Renatus M, Schwarzenbacher R, Zhou Q, Sun C, Fesik SW, Liddington RC, Salvesen GS (Mar 2001). "Structural basis for the inhibition of caspase-3 by XIAP". Cell. 104 (5): 791–800. doi:10.1016/S0092-8674(01)00274-4. PMID 11257232. S2CID 17915093.
  12. ^ Roy N, Deveraux QL, Takahashi R, Salvesen GS, Reed JC (Dec 1997). "The c-IAP-1 and c-IAP-2 proteins are direct inhibitors of specific caspases". EMBO J. 16 (23): 6914–25. doi:10.1093/emboj/16.23.6914. PMC 1170295. PMID 9384571.
  13. ^ Deveraux QL, Takahashi R, Salvesen GS, Reed JC (Jul 1997). "X-linked IAP is a direct inhibitor of cell-death proteases". Nature. 388 (6639): 300–4. Bibcode:1997Natur.388..300D. doi:10.1038/40901. PMID 9230442. S2CID 4395885.
  14. ^ Suzuki Y, Nakabayashi Y, Nakata K, Reed JC, Takahashi R (Jul 2001). "X-linked inhibitor of apoptosis protein (XIAP) inhibits caspase-3 and -7 in distinct modes". J. Biol. Chem. 276 (29): 27058–63. doi:10.1074/jbc.M102415200. PMID 11359776.

Dopunska literatura uredi

Vanjski linkovi uredi