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  Unusual intramolecular hydrogen bonding in cycloamanide A, cyclic (LPro‐LVal‐LPhe‐LPhe‐LAla‐Gly)

Chiang, C. C., Karle, I. L., & Wieland, T. (1982). Unusual intramolecular hydrogen bonding in cycloamanide A, cyclic (LPro‐LVal‐LPhe‐LPhe‐LAla‐Gly). International journal of peptide and protein research, 20(5), 414-420. doi:10.1111/j.1399-3011.1982.tb03061.x.

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IntJPeptProtRes_20_1982_414.pdf (Any fulltext), 378KB
 
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 Creators:
Chiang, Chian Chian, Author
Karle, Isabella L., Author
Wieland, Theodor1, Author           
Affiliations:
1Max Planck Institute for Medical Research, Max Planck Society, ou_1125545              

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Free keywords: β‐bend; bond lengths and angles; crystal packing; hydrogen bonds; natural cyclic hexapeptide; torsional angles
 Abstract: The naturally occurring cyclic hexapeptide, cycloamanide A, has only one intramolecular hydrogen bond. It is a 4 leads to 1 type that encompasses the L Phe-L Ala sequence in which the experimentally determined phi, psi values are +54 degrees, -118 degrees and -88 degrees, -4 degrees, respectively. Even though the chirality is L, L, the phi, psi values are characteristic for a D, L beta-bend, Type II'. The conformation of the molecule was established by a crystal structure determination using X-ray diffraction analysis. Cycloamanide A (C33H42N6O6 . 4H2O) crystallizes in space group P2(1)2(1)2(1) with cell parameters a = 13.307(2) A, b = 24.820(4)A and c = 11.231(1)A.

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Language(s): eng - English
 Dates: 1982-03-221982-04-272009-01-121982-11
 Publication Status: Issued
 Pages: 7
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 Table of Contents: -
 Rev. Type: Peer
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Title: International journal of peptide and protein research
Source Genre: Journal
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Publ. Info: Denmark : Copenhagen, Munksgaard
Pages: - Volume / Issue: 20 (5) Sequence Number: - Start / End Page: 414 - 420 Identifier: ISSN: 0367-8377 (Print)