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Research at St Andrews

Characterization of a dual function macrocyclase enables design and use of efficient 2 macrocyclization substrates (dataset)

Dataset

Associated persons

  • Clarissa Melo Czekster (Creator)
  • Hannes Ludewig (Creator)
  • Stephen Andrew McMahon (Creator)
  • James Henderson Naismith Biotherapy Centre, Sichuan University, Chengdu, China, RCaH, Rutherford Appleton Laboratory , Harwell Oxford, Didcot OX11 0FA, U.K., Division of Structural Biology, University of Oxford , Henry Wellcome Building for Genomic Medicine, Old Road Campus, Roosevelt Drive, Headington, Oxford OX3 7BN, U.K. (Creator)

Associated organisations

  • Biotherapy Centre, Sichuan University, Chengdu, China
  • RCaH, Rutherford Appleton Laboratory , Harwell Oxford, Didcot OX11 0FA, U.K.
  • Division of Structural Biology, University of Oxford , Henry Wellcome Building for Genomic Medicine, Old Road Campus, Roosevelt Drive, Headington, Oxford OX3 7BN, U.K.

Description

Accession codes 5N4B (S577A 473 mutant bound to 25mer peptide), 5N4C (S577A mutant bound to 35mer peptide), 5N4D (D661A 474 mutant bound to 25mer peptide), 5N4E (H698A mutant bound to 35mer peptide) and 5N4F 475 (apoGmPOPB).
Date made available1 Nov 2017
PublisherProtein Data Bank (PDB)

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