The crystal structure of a tripeptide, glycyl-D, L-leucyl-L, D-alanine
has been determined by X-ray methods and refined to a final R-index o
f 0.079. There are two crystallographically independent molecules in a
monoclinic unit cell with a = 17.817(2), b = 10.276(2), c = 18.451 (3
)angstrom, beta = 116.95 (3), Z = 8 and space group P2(1)/n. Both the
molecules exist as zwitterions and adopt essentially similar conformat
ion, with the backbone folding characteristic of a type II reverse tur
n. Even the leucyl side chains assume essentially similar conformation
in the two independent molecules. The packing of the molecules involv
es spatial segregation of the leucyl side chains.