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Improving the Selectivity of Engineered Protease Inhibitors: Optimizing the P2 Prime Residue Using a Versatile Cyclic Peptide Library.
de Veer, Simon J; Wang, Conan K; Harris, Jonathan M; Craik, David J; Swedberg, Joakim E.
Affiliation
  • de Veer SJ; Institute of Health and Biomedical Innovation, Queensland University of Technology , Brisbane, Queensland QLD 4059, Australia.
  • Wang CK; Institute for Molecular Bioscience, The University of Queensland , 306 Carmody Road, Building 80, Queensland Bioscience Presinct, Brisbane, Queensland, QLD 4072, Australia.
  • Harris JM; Institute of Health and Biomedical Innovation, Queensland University of Technology , Brisbane, Queensland QLD 4059, Australia.
  • Craik DJ; Institute for Molecular Bioscience, The University of Queensland , 306 Carmody Road, Building 80, Queensland Bioscience Presinct, Brisbane, Queensland, QLD 4072, Australia.
  • Swedberg JE; Institute for Molecular Bioscience, The University of Queensland , 306 Carmody Road, Building 80, Queensland Bioscience Presinct, Brisbane, Queensland, QLD 4072, Australia.
J Med Chem ; 58(20): 8257-68, 2015 Oct 22.
Article in En | MEDLINE | ID: mdl-26393374
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Full text: 1 Database: MEDLINE Main subject: Peptides, Cyclic / Serine Proteinase Inhibitors Type of study: Prognostic_studies Language: En Journal: J Med Chem Year: 2015 Type: Article Affiliation country: Australia
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Full text: 1 Database: MEDLINE Main subject: Peptides, Cyclic / Serine Proteinase Inhibitors Type of study: Prognostic_studies Language: En Journal: J Med Chem Year: 2015 Type: Article Affiliation country: Australia