Aggregation studies in crystals of apolar helical peptides: Boc-Aib-Val-Ala-Leu-Aib-Val-Ala-Leu-Aib-OMe


Autoria(s): Karle, IL; Flippen-Anderson, JL; Uma, K; Balaram, Padmanabhan
Data(s)

01/12/1988

Resumo

In the crystal, the backbone of Boc-(Aib-Val-Ala-Leu)2-Aib-OMe adopts a helical form with four alpha-type hydrogen bonds in the middle, flanked by 3(10)-type hydrogen bonds at either end. The helical molecules stack in columns with head-to-tail hydrogen bonds, either directly between NH and CO, or bridged by solvent molecules. The packing of the helices is parallel, even in space group P2(1). Cell parameters are a = 9.837(2) A, b = 15.565(3) A, c = 20.087(5) A, beta = 96.42(2) degrees, dcalc = 1.091 g/cm3 for C46H83N9O12.1.5H2O.0.67CH3OH. There appears to be some hydration of the backbone in this apolar helix.

Formato

application/pdf

Identificador

http://eprints.iisc.ernet.in/27231/1/4.pdf

Karle, IL and Flippen-Anderson, JL and Uma, K and Balaram, Padmanabhan (1988) Aggregation studies in crystals of apolar helical peptides: Boc-Aib-Val-Ala-Leu-Aib-Val-Ala-Leu-Aib-OMe. In: International Journal of Peptide & Protein Research Int J Pept Protein Res, 32 (6). pp. 536-543.

Publicador

National Center for Biotechnology Information

Relação

http://www.ncbi.nlm.nih.gov/pubmed/3246478

http://eprints.iisc.ernet.in/27231/

Palavras-Chave #Molecular Biophysics Unit
Tipo

Journal Article

PeerReviewed