Type II' beta-bend conformation of tert. -butyloxycarbonyl-L-amino-succinyl-L-alanyl-glycine methyl ester in the solid state(539 views) Capasso S, Mazzarella L, Sica F, Zagari A
Int J Pept Protein Res (ISSN: 0367-8377, 0367-8377print), 1984; 24(6): 588-596.
Keywords: Formic Acid Derivative, Oligopeptide, T Butyloxycarbonyl Group, T-Butyloxycarbonyl Group, Article, Protein Conformation, Solution And Solubility, Formic Acid Esters, Support, Non-U S Gov,
Affiliations: Not available.
References: Not available.
Type II' beta-bend conformation of tert. -butyloxycarbonyl-L-amino-succinyl-L-alanyl-glycine methyl ester in the solid state
Boc-L-Asu-L-Ala-Gly-OMe crystallizes in the monoclinic space group P2(1) with cell dimensions a = 14.315 (3) A, b = 9.280 (2) A, c = 14.358(3) A, beta = 103.63(1) A, V= 1853.4 (9) A3, with two molecules in the asymmetric unit. The conformation of the two molecules is characterized by a type II' beta-bend, similar to that predicted earlier by potential energy calculations, stabilized by an intramolecular hydrogen bond. I.r. and 1H-n.m.r. data show that the folded conformation is also stable in chloroform solution.
Type II' beta-bend conformation of tert. -butyloxycarbonyl-L-amino-succinyl-L-alanyl-glycine methyl ester in the solid state
No results.
Type II' beta-bend conformation of tert. -butyloxycarbonyl-L-amino-succinyl-L-alanyl-glycine methyl ester in the solid state