Contribution of structural biology to clinically validated target proteins

Masumi Mori, Naoko Ogawa, Kunihiro Tanikawa, Sanae Dodo, Sotaro Shibayama, Shigeyuki Yokoyama, Akiko Tanaka

Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskriftPeer review

Sammanfattning

We identified six groups of diseases expected to cause serious future health issues on the basis of a WHO report. Approved drugs for these diseases were associated with 409 target proteins; however, the percentage of selected proteins with full-length structural information deposited in the Protein Data Bank (PDB) was only 9.8%. The reason for the low percentage may be as a result of a disproportionate number of intractable proteins with multiple transmembrane regions and variable, or undefined glycosylation patterns, which impede protein preparation and crystallization, in such druggable proteins. We stress the importance of structural analysis of proteins, especially approved-drug target proteins, and the development of new methods to enable structural analyses of presently intractable proteins. In addition, we present an overview of large structural biology projects.

Originalspråkengelska
Sidor (från-till)469-472
Antal sidor4
TidskriftDrug Discovery Today
Volym13
Nummer11-12
DOI
StatusPublished - 2008 juni
Externt publiceradJa

Ämnesklassifikation (UKÄ)

  • Farmaceutisk vetenskap

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