414D
5'-D(*GP*GP*GP*GP*CP*GP*CP*CP*CP*C)-3'
Summary for 414D
Entry DOI | 10.2210/pdb414d/pdb |
Descriptor | DNA (5'-D(*GP*GP*GP*GP*CP*GP*CP*CP*CP*C)-3') (2 entities in total) |
Functional Keywords | a-dna, double helix, dna |
Total number of polymer chains | 4 |
Total formula weight | 12187.92 |
Authors | Savitha, G.,Viswamitra, M.A. (deposition date: 1998-07-13, release date: 1999-06-14, Last modification date: 2024-02-28) |
Primary citation | Savitha, G.,Viswamitra, M.A. An A-DNA structure with two independent duplexes in the asymmetric unit. Acta Crystallogr.,Sect.D, 55:1136-1143, 1999 Cited by PubMed Abstract: The crystal and molecular structure of the self-complementary A-DNA decamer sequence d(G4CGC4) was solved at 1.9 A resolution. The decamer crystallizes in space group P21 with two independent duplexes in the asymmetric unit. Duplex 1 has interactions which are distributed symmetrically about its length compared with duplex 2. The two end base pairs of duplex 1 have a similar NH.O hydrogen-bond pattern involving GGC segments of duplex 2 and a symmetry-related neighbour, while the end base pairs of duplex 2 interact with the GCC and GGG segments of its symmetry-related neighbours through NH.O and NH.N hydrogen bonds and a water-mediated hydrogen bond between the carboxyl groups of C40 and C8. In addition to the C4'-C5' torsion angle gamma assuming the trans conformation in certain steps, this angle also adopts the gauche- conformation at C37 as opposed to the preferred gauche+ conformation, with a concomitant change in phosphodiester P-O5' (alpha) in the opposite sense. This facilitates stacking between adjacent bases. The study suggests that the structural alterations in the two molecules in the asymmetric unit originate from an inherent propensity of the d(G4CGC4) base sequence for varied intermolecular interactions and malleability. PubMed: 10329775DOI: 10.1107/S0907444999003182 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.9 Å) |
Structure validation
Download full validation report