Conformational preferences induced by cyclization in orbitides: a vibrational CD study-Reference-Cited by-同舟云学术

Conformational preferences induced by cyclization in orbitides: a vibrational CD study

Published:2022 Issue:6 Volume:20 Page:1306-1314
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Yokomichi Maria A. S.¹,Silva Hanyeny R. L.²,Brandao Lorenza E. V. N.³,Vicente Eduardo F.³,Batista Jr. Joao M.¹^ORCID

Affiliation:

1. Institute of Science and Technology, Federal University of Sao Paulo (Unifesp), Rua Talim 330, Sao Jose dos Campos, SP 12231-280, Brazil

2. Sao Paulo State University (Unesp), School of Agricultural and Veterinarian Sciences, Via de Acesso Professor Paulo Donato Castelane Castellane S/N, Jaboticabal, SP 14884-900, Brazil

3. Sao Paulo State University (Unesp), School of Sciences and Engineering, Rua Domingos da Costa Lopes, 780, Tupa, SP 17602-496, Brazil

Abstract

Vibrational CD and DFT calculations reveal solution-state conformational preferences of orbitides following cyclization.

Funder

Fundação de Amparo à Pesquisa do Estado de São Paulo

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/OB/D1OB02170B

Reference32 articles.

1. Ribosomally synthesized and post-translationally modified peptide natural products: overview and recommendations for a universal nomenclature

2. An Orbitide from Ratibida columnifera Seed Containing 16 Amino Acid Residues

3. Biologically Active Orbitides from the Euphorbiaceae Family

4. Strategies for Fine-Tuning the Conformations of Cyclic Peptides

5. Characterization of the macrocyclase involved in the biosynthesis of RiPP cyclic peptides in plants

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