All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

Structural properties of CYP2D6: requirements for substrates and inhibitors

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F14%3A33150428" target="_blank" >RIV/61989592:15310/14:33150428 - isvavai.cz</a>

  • Alternative codes found

    RIV/61989592:15110/14:33150428

  • Result on the web

    <a href="http://www.futuremedicine.com/doi/pdf/10.2217/fmeb2013.13.91" target="_blank" >http://www.futuremedicine.com/doi/pdf/10.2217/fmeb2013.13.91</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.2217/9781780844626" target="_blank" >10.2217/9781780844626</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Structural properties of CYP2D6: requirements for substrates and inhibitors

  • Original language description

    CYP450 2D6 is a relatively flexible protein with plastic active site structure, allowing binding with high specificity of many different substrates of various sizes. Presence of a basic nitrogen atom at a distance of 5-7 ? from the site of metabolism isoften found in the structure of typical substrates. After substrate binding, the active site structure is changed, embracing the substrate and fixing it in the optimal position for enzyme reaction. The alleles found in the human population that correspond to CYP450 2D6 variants with decreased enzymatic activity possess changed amino acids which, interestingly, do not directly participate in forming the active site. Instead, they probably take part in maintaining other properties of the enzyme, for example in the formation of solvent or substrate access channels.

  • Czech name

  • Czech description

Classification

  • Type

    C - Chapter in a specialist book

  • CEP classification

    FR - Pharmacology and apothecary chemistry

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/GPP303%2F12%2FP019" target="_blank" >GPP303/12/P019: Mechanism of ligand access/egress to/from active site of microsomal drug-metabolising cytochromes P450</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2014

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Book/collection name

    CYP2D6: Genetics, Pharmacology and Clinical Relevance

  • ISBN

    978-1-78084-462-6

  • Number of pages of the result

    10

  • Pages from-to

    69-78

  • Number of pages of the book

    153

  • Publisher name

    Future Medicine Ltd.

  • Place of publication

    London

  • UT code for WoS chapter