ISSN:
0006-3525
Keywords:
Chemistry
;
Polymer and Materials Science
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
Notes:
The peptide N-Boc-L-Pro-dehydro-Leu-OCH3 was synthesized by coupling dehydroleucine methyl ester with Boc-Pro-OH. It was crystallized from its solution in a methanol-water mixture at 4°C and the crystals belong to the orthorhombic space group P212121 with a = 10.239(1) Ă
, b = 19.276(4) Ă
, c = 20.319(3) Ă
, V = 4010(1) Ă
3, and Z = 8. The structure was solved by direct methods using MULTAN 80. The structure was refined to an R value of 0.095 for 1871 observed reflections. There are two crystallographically independent molecules in the unit cell. The molecular dimensions of the two molecules are very similar. The backbone conformation angles of these molecules are as follows: Ξ1 = -176(1)°, Ï0 = -2(2)°, Ï1 = -72(1)°, Ï1 = 141(1)°, Ï1 = 169(1)°, Ï2 = -98(1)°, Ï2 = -179(1)°, ΞT = 179(1)°, Ξ11 = 174(1)°, Ï10 = -3cm-1, Ï11 = -64(1)°, Ï11 = 148(1)°, Ï11 = 167(1)°, Ï12 = -67(1)°, Ï12 = 175(1)°, and Ξ1T = 172(1)°, respectively. Other torsion angles such as ΞâČ2 = 86(1)°, Ï2 = -5(2)°, âČ12 = 131(1)°, and Ï12 = -16(2)° are interesting to define the backbone conformation together with the dehydro-Leu side chain as a conformation similar to that of the ÎČ-bend type II. The central amide bond of Pro-dehydro-Leu segment is deviated from the planarity. The Boc group adopts a trans-cis conformation. The side-chain torsion angles Ï1, Ï2, Ï3, Ï4, and Ï0 for Pro-residue in the two molecules are 11(2)°, -11(2)°, 6(2)°, 2(1)°, -9(1)° and -18(1)°, 31(1)°, -31(1)°, 21(1)°, and -1(1)° respectively. The side chain of the Pro residue of molecule A is in the flattened CÎł-endo conformation while the pyrrolidine ring in miolecule B adopts the well-known CÎł-exo conformation. The side-chain torsion angles Ï, Ï2,1, and Ï2,2 in the leucyl residues of molecules A and B are -5(2)°, -111(2)°, 126(2)° and -16(2)°, -110(2)°, and 133(2)°, respectively. The molecular packing is stabilized by intermolecular hydrogen bonds and van der Waals interactions.
Additional Material:
3 Ill.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1002/bip.360271005
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