We report the observation of a number of unexpected isolated beta -turns wi
th a proline in the third position. These beta -turns are mainly, either ty
pe VIa1, type VIb or type IV although 3 examples of type I, 4 examples of t
ype II' and 5 examples of type VIa2 beta -turns were also observed in a rep
resentative protein data set, Nearly a third of these turns are located in
the loop regions and the rest are situated at ends of either helices or bet
a -strands, The formation of double beta -turns, where proline in the third
position in the first beta -turn corresponds to proline in second position
in the second overlapping beta -turn has earlier been suggested to stabili
ze the otherwise unfavourable proline in the third position. We observed a
number of multiple beta -turns, mainly of the type VIb or type IV, with pro
line in the third position that did not correspond to proline in second pos
ition in the overlapping beta -turn, Although these beta -turns may also be
stabilized due to the formation of multiple turns, the isolated beta -turn
s with proline residue in the third position are mainly surrounded by water
molecules which are likely to stabilize these turns. The phi, psi dihedral
angle values for proline residue in isolated and multiple beta -turns show
distinct preferences in the Ramachandran plot.