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LINK . SPRINGER . COM {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Schema
  9. External Links
  10. Analytics And Tracking
  11. Libraries
  12. CDN Services

We are analyzing https://link.springer.com/chapter/10.1007/978-1-4020-6554-5_2.

Title:
Caspase Mechanisms | SpringerLink
Description:
The main effectors of apoptosis encompass proteases from the caspase family, which reside as latent precursors in most nucleated animal cells. The apoptotic caspases constitute a minimal two-step signaling pathway. The apical (initiator) caspases are activated within...
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Telecommunications
  • Books & Literature

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,016 visitors per month in the current month.

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How Does Link.springer.com Make Money? {💸}

We can't see how the site brings in money.

While many websites aim to make money, others are created to share knowledge or showcase creativity. People build websites for various reasons. This could be one of them. Link.springer.com might have a hidden revenue stream, but it's not something we can detect.

Keywords {🔍}

google, scholar, pubmed, cas, article, cell, caspase, death, activation, salvesen, caspases, apoptosis, chapter, biol, mol, inhibition, structure, chem, mechanisms, riedl, apoptotic, signaling, protease, privacy, cookies, content, publish, activity, substrates, download, science, human, sci, usa, differ, procaspase, basis, springer, information, research, search, programmed, mechanism, proteolytic, preview, dixit, biochem, stennicke, structural, proteins,

Topics {✒️}

month download article/chapter interleukin-1-beta converting enzyme mort1/fadd-interacting protease apoptotic mammalian ced-3/ice apaf-1/caspase-9 complex initiates conserved xiap-interaction motif iap family proteins–suppressors privacy choices/manage cookies cytochrome c-dependent activation device instant download state equilibrium process ice-interacting protease programmed cell death proximity-induced clustering developing mammalian neurons datp-dependent formation apoptotic protease cascade induced proximity model death receptor recruitment download preview pdf european economic area nucleated animal cells altered cytokine export dimer formation drives conditions privacy policy dimeric active forms death receptor signaling conditional cell ablation step signaling pathway oligomeric signaling complexes lymphocyte serine proteases chapter cite apoptotic cell death peptide thioester substrates substrates article 12 accepting optional cookies dimeric procaspase-3 unfolds torrey pines road human protein homologous shape caspase activity dual function regulator riedl rights apoptotic caspases constitute apoptosis repeat proteins medical research cd95-mediated apoptosis journal finder publish flip-mediated inhibition main content log chapter usd 29

Schema {🗺️}

ScholarlyArticle:
      headline:Caspase Mechanisms
      pageEnd:23
      pageStart:13
      image:https://media.springernature.com/w153/springer-static/cover/book/978-1-4020-6554-5.jpg
      genre:
         Biomedical and Life Sciences
         Biomedical and Life Sciences (R0)
      isPartOf:
         name:Programmed Cell Death in Cancer Progression and Therapy
         isbn:
            978-1-4020-6554-5
            978-1-4020-6553-8
         type:Book
      publisher:
         name:Springer Netherlands
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:Guy S. Salvesen
            affiliation:
                  name:Burnham Institute for Medical Research
                  address:
                     name:Program on Apoptosis and Cell Death, Burnham Institute for Medical Research, La Jolla, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Stefan J. Riedl
            affiliation:
                  name:Burnham Institute for Medical Research
                  address:
                     name:Program on Apoptosis and Cell Death, Burnham Institute for Medical Research, La Jolla, USA
                     type:PostalAddress
                  type:Organization
            type:Person
      keywords:apoptosome, caspase, DISC, IAP, inhibition, protease, zymogen
      description:The main effectors of apoptosis encompass proteases from the caspase family, which reside as latent precursors in most nucleated animal cells. The apoptotic caspases constitute a minimal two-step signaling pathway. The apical (initiator) caspases are activated within oligomeric signaling complexes in response to apoptotic stimuli. Their mechanism of activation probably results from proximity-induced clustering to the dimeric active forms. Once activated, the apical caspases directly activate the executioner (effector) caspases by limited proteolytic cleavage. The distinct activation mechanisms explain how an apoptotic stimulus is converted to proteolytic activity, and how this activity is amplified to allow for limited proteolysis of the dozens of protein substrates whose cleavage is required for efficient apoptosis.
      datePublished:2008
      isAccessibleForFree:
      hasPart:
         isAccessibleForFree:
         cssSelector:.main-content
         type:WebPageElement
      context:https://schema.org
Book:
      name:Programmed Cell Death in Cancer Progression and Therapy
      isbn:
         978-1-4020-6554-5
         978-1-4020-6553-8
Organization:
      name:Springer Netherlands
      logo:
         url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
         type:ImageObject
      name:Burnham Institute for Medical Research
      address:
         name:Program on Apoptosis and Cell Death, Burnham Institute for Medical Research, La Jolla, USA
         type:PostalAddress
      name:Burnham Institute for Medical Research
      address:
         name:Program on Apoptosis and Cell Death, Burnham Institute for Medical Research, La Jolla, USA
         type:PostalAddress
ImageObject:
      url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
Person:
      name:Guy S. Salvesen
      affiliation:
            name:Burnham Institute for Medical Research
            address:
               name:Program on Apoptosis and Cell Death, Burnham Institute for Medical Research, La Jolla, USA
               type:PostalAddress
            type:Organization
      name:Stefan J. Riedl
      affiliation:
            name:Burnham Institute for Medical Research
            address:
               name:Program on Apoptosis and Cell Death, Burnham Institute for Medical Research, La Jolla, USA
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Program on Apoptosis and Cell Death, Burnham Institute for Medical Research, La Jolla, USA
      name:Program on Apoptosis and Cell Death, Burnham Institute for Medical Research, La Jolla, USA
WebPageElement:
      isAccessibleForFree:
      cssSelector:.main-content

External Links {🔗}(198)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js

CDN Services {📦}

  • Pbgrd

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