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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. Questions
  9. Schema
  10. External Links
  11. Analytics And Tracking
  12. Libraries
  13. CDN Services

We are analyzing https://link.springer.com/chapter/10.1007/978-94-017-8881-6_6.

Title:
Structural Biology of the Membrane Attack Complex | SpringerLink
Description:
The complement system is an intricate network of serum proteins that mediates humoral innate immunity through an amplification cascade that ultimately leads to recruitment of inflammatory cells or opsonisation or killing of pathogens. One effector arm of this network...
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {๐Ÿ“š}

  • Education
  • Business & Finance
  • Science

Content Management System {๐Ÿ“}

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 {๐Ÿ“ˆ}

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

๐ŸŒ  Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
However, some sources were not loaded, we suggest to reload the page to get complete results.

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How Does Link.springer.com Make Money? {๐Ÿ’ธ}

We can't tell how the site generates income.

The purpose of some websites isn't monetary gain; they're meant to inform, educate, or foster collaboration. Everyone has unique reasons for building websites. This could be an example. Link.springer.com might be cashing in, but we can't detect the method they're using.

Keywords {๐Ÿ”}

pubmed, google, scholar, cas, complement, membrane, central, complex, immunol, human, biol, attack, chem, component, structure, protein, podack, proteins, formation, cell, structural, tschopp, sci, mรผllereberhard, binding, assembly, mol, domain, usa, biochemistry, pore, nature, sodetz, proc, natl, acad, discipio, med, function, molecular, mechanism, factor, exp, tweten, analysis, chapter, components, membranes, poreforming, morgan,

Topics {โœ’๏ธ}

cytotoxic t-lymphocyte-mediated cytolysis perforin-mediated target-cell death mammalian membrane-attack complex/perforin month download article/chapter pore-forming toxin intermedilysin intersubunit beta-strand alignment beta-sheet transition identified multiple protease-resistant polypeptides ฮฒ-strand tilt angle mediates neuron-astroglial interactions species-selective recognition conferred cytotoxic t-cell granules serum-sensitive escherichia coli x-ray solution scattering cytolytic pore-forming protein thiol-activated cytolysin restrict perforin-mediated lysis high-affinity c5 convertases mac-phospholipid vesicle recombinants membrane attack complex/perforin membrane-attack complex/perforin c8alpha-macpf reveals mechanism trans-membrane complement channel alternative-pathway c5 convertase c8/c9 binding required complement poly-c9 determined complement-mediated bacterial killing pore-forming toxin cholesterol-dependent cytolysin privacy choices/manage cookies mac-constituting complement components macpf/cdc proteins bacterial protein toxin intermedilysin-receptor interactions poly-c9 formation generates cholesterol dependent cytolysins cholesterol-dependent cytolysins preissner kt pore-forming protein cd59-c9 binding interaction macpf/cdc family device instant download discipio rg pore-forming toxins cytolysin prepore moves laursen ns escherichia coli j5 schreck sf 2ย รฅ resolution reveals 13c resonance assignment

Questions {โ“}

  • Bamford DH, Grimes JM, Stuart DI (2005) What does structure tell us about virus evolution?
  • Markiewski MM, Nilsson B, Ekdahl KN, Mollnes TE, Lambris JD (2007) Complement and coagulation: strangers or partners in crime?
  • Nabholz M, Tschopp J (1989) CTL-mediated cytolysis: perforin and alternative pathways?

Schema {๐Ÿ—บ๏ธ}

ScholarlyArticle:
      headline:Structural Biology of the Membrane Attack Complex
      pageEnd:116
      pageStart:83
      image:https://media.springernature.com/w153/springer-static/cover/book/978-94-017-8881-6.jpg
      genre:
         Biomedical and Life Sciences
         Biomedical and Life Sciences (R0)
      isPartOf:
         name:MACPF/CDC Proteins - Agents of Defence, Attack and Invasion
         isbn:
            978-94-017-8881-6
            978-94-017-8880-9
         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:Andreas F.-P. Sonnen
            affiliation:
                  name:University Medical Center Freiburg
                  address:
                     name:Center for Chronic Immunodeficiency, University Medical Center Freiburg, Freiburg, Germany
                     type:PostalAddress
                  type:Organization
            email:[email protected]
            type:Person
            name:Philipp Henneke
            affiliation:
                  name:University Medical Center Freiburg
                  address:
                     name:Center for Chronic Immunodeficiency, University Medical Center Freiburg, Freiburg, Germany
                     type:PostalAddress
                  type:Organization
            type:Person
      keywords:Complememt system, Lipid membrane pore, Membrane attack complex, Pore-forming proteins, Structural biology
      description:The complement system is an intricate network of serum proteins that mediates humoral innate immunity through an amplification cascade that ultimately leads to recruitment of inflammatory cells or opsonisation or killing of pathogens. One effector arm of this network is the terminal pathway of complement, which leads to the formation of the membrane attack complex (MAC) composed of complement components C5b, C6, C7, C8 and C9. Upon formation of C5 convertases via the classical or alternative pathways of complement activation, C5b is generated from C5 by proteolytic cleavage, nucleating a series of association and polymerisation reactions of the MAC-constituting complement components that culminate in pore formation of pathogenic membranes. Recent structures of MAC components and homologous proteins significantly increased our understanding of oligomerisation, membrane association and integration, shedding light onto the molecular mechanism of this important branch of the innate immune system.
      datePublished:2014
      isAccessibleForFree:
      hasPart:
         isAccessibleForFree:
         cssSelector:.main-content
         type:WebPageElement
      context:https://schema.org
Book:
      name:MACPF/CDC Proteins - Agents of Defence, Attack and Invasion
      isbn:
         978-94-017-8881-6
         978-94-017-8880-9
Organization:
      name:Springer Netherlands
      logo:
         url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
         type:ImageObject
      name:University Medical Center Freiburg
      address:
         name:Center for Chronic Immunodeficiency, University Medical Center Freiburg, Freiburg, Germany
         type:PostalAddress
      name:University Medical Center Freiburg
      address:
         name:Center for Chronic Immunodeficiency, University Medical Center Freiburg, Freiburg, Germany
         type:PostalAddress
ImageObject:
      url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
Person:
      name:Andreas F.-P. Sonnen
      affiliation:
            name:University Medical Center Freiburg
            address:
               name:Center for Chronic Immunodeficiency, University Medical Center Freiburg, Freiburg, Germany
               type:PostalAddress
            type:Organization
      email:[email protected]
      name:Philipp Henneke
      affiliation:
            name:University Medical Center Freiburg
            address:
               name:Center for Chronic Immunodeficiency, University Medical Center Freiburg, Freiburg, Germany
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Center for Chronic Immunodeficiency, University Medical Center Freiburg, Freiburg, Germany
      name:Center for Chronic Immunodeficiency, University Medical Center Freiburg, Freiburg, Germany
WebPageElement:
      isAccessibleForFree:
      cssSelector:.main-content

External Links {๐Ÿ”—}(454)

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