1RRU
The influence of a chiral amino acid on the helical handedness of PNA in solution and in crystals
Summary for 1RRU
Entry DOI | 10.2210/pdb1rru/pdb |
Related | 1HZS 1PUP 1QPY |
Descriptor | Peptide Nucleic Acid, (H-P(*CPN*GPN*TPN*APN*CPN*GPN)-LYS-NH2) (2 entities in total) |
Functional Keywords | pna, peptide nucleic acid, l-lysine, helical handedness, p-form, molecular mechanics |
Total number of polymer chains | 2 |
Total formula weight | 3429.63 |
Authors | Rasmussen, H.,Liljefors, T.,Petersson, B.,Nielsen, P.E.,Kastrup, J.S. (deposition date: 2003-12-09, release date: 2004-01-13, Last modification date: 2023-11-15) |
Primary citation | Rasmussen, H.,Liljefors, T.,Petersson, B.,Nielsen, P.E.,Kastrup, J.S. The Influence of a Chiral Amino Acid on the Helical Handedness of PNA in Solution and in Crystals J.Biomol.Struct.Dyn., 21:495-502, 2004 Cited by PubMed Abstract: The X-ray structure of a self-complementary PNA hexamer (H-CGTACG-L-Lys-NH(2)) has been determined to 2.35 A resolution. The introduction of an L-lysine moiety has previously been shown to induce a preferred left-handedness of the PNA double helices in aqueous solution. However, in the crystal structure an equal amount of interchanging right- and left-handed helices is observed. The lysine moieties are pointing into large solvent channels and no significant interactions between this moiety and the remaining PNA molecule are observed. In contrast, molecular mechanics calculations show a preference for the left-handed helix of this hexameric PNA in aqueous solution as expected. The calculations indicate that the difference in the free energy of solvation between the left-handed and the right-handed helix is the determining factor for the preference of the left-handed helix in aqueous solution. PubMed: 14692794PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.35 Å) |
Structure validation
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