Ambidexterity and Left-Handedness Induced by Geminally Disubstituted γ Amino Acid Residues in Chiral 3<sub>10</sub> Helices-Reference-Cited by-同舟云学术

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Ambidexterity and Left-Handedness Induced by Geminally Disubstituted γ Amino Acid Residues in Chiral 3₁₀ Helices

Published:2023-09-21 Issue:39 Volume:8 Page:36370-36385
ISSN:2470-1343
Container-title:ACS Omega
language:en
Short-container-title:ACS Omega

Author:

Debnath Swapna¹,Rajalakshmi Vignesh Shanmugam²,Kumar Dinesh³^ORCID,Das Babulal¹,Vasudev Prema G.³,Satpati Priyadarshi²^ORCID,Chatterjee Sunanda¹^ORCID

Affiliation:

1. Department of Chemistry, Indian Institute of Technology, Guwahati, Guwahati, Assam 781039, India

2. Biosciences and Bioengineering, Indian Institute of Technology, Guwahati, Guwahati, Assam 781039, India

3. Plant Biotechnology Division, CSIR-Central Institute of Medicinal and Aromatic Plants Lucknow, Uttar Pradesh 226015, India

Funder

Council of Scientific and Industrial Research, India

Indian Institute of Technology Guwahati

Science and Engineering Research Board

Department of Science and Technology, Ministry of Science and Technology, India

Publisher

American Chemical Society (ACS)

Subject

General Chemical Engineering,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acsomega.3c05124

Reference53 articles.

1. A Survey of Left-handed Helices in Protein Structures

2. A left-handed α-helix containing both L- and D-amino acids: The solution structure of the antimicrobial lipodepsipeptide tolaasin

3. Crystallographic Characterization of 12-Helical Secondary Structure in β-Peptides Containing Side Chain Groups

4. De Novo Left‐Handed Synthetic Peptidomimetic Foldamers

5. Ambidextrous molecules: Cylindrical peptide structures formed by fusing left- and right-handed helices

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