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  Nucleotide based covalent inhibitors of KRas can only be efficient in vivo if they bind reversibly with GTP-like affinity

Müller, M., Jeganathan, S., Heidrich, A., Campos, J., & Goody, R. S. (2017). Nucleotide based covalent inhibitors of KRas can only be efficient in vivo if they bind reversibly with GTP-like affinity. Scientific Reports, 7: 3687, pp. 1-11. doi:10.1038/s41598-017-03973-6.

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 Creators:
Müller, Matthias1, Author           
Jeganathan, Sadasivam1, Author           
Heidrich, Angelika1, Author           
Campos, Jeremy1, Author           
Goody, Roger S.1, Author           
Affiliations:
1Abt. III: Strukturbiochemie, Max Planck Institute of Molecular Physiology, Max Planck Society, ou_2040307              

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Language(s): eng - English
 Dates: 2017-06-17
 Publication Status: Published online
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1038/s41598-017-03973-6
 Degree: -

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Title: Scientific Reports
  Abbreviation : Sci. Rep.
Source Genre: Journal
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Affiliations:
Publ. Info: London, UK : Nature Publishing Group
Pages: - Volume / Issue: 7 Sequence Number: 3687 Start / End Page: 1 - 11 Identifier: ISSN: 2045-2322
CoNE: https://pure.mpg.de/cone/journals/resource/2045-2322