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PDBsum entry 1ddl

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Virus/RNA PDB id
1ddl
Contents
Protein chains
188 a.a. *
175 a.a. *
DNA/RNA
Ligands
__U-__U
Waters ×285
* Residue conservation analysis

References listed in PDB file
Key reference
Title Refined structure of desmodium yellow mottle tymovirus at 2.7 a resolution.
Authors S.B.Larson, J.Day, M.A.Canady, A.Greenwood, A.Mcpherson.
Ref. J Mol Biol, 2000, 301, 625-642. [DOI no: 10.1006/jmbi.2000.3983]
PubMed id 10966774
Abstract
Desmodium yellow mottle virus is a 28 nm diameter, T=3 icosahedral plant virus of the tymovirus group. Its structure has been solved to a resolution of 2.7 A using X-ray diffraction analysis based on molecular replacement and phase extension methods. The final R value was 0.151 (R(free)=0.159) for 134,454 independent reflections. The folding of the polypeptide backbone is nearly identical with that of turnip yellow mosaic virus, as is the arrangement of subunits in the virus capsid. However, a major difference in the disposition of the amino-terminal ends of the subunits was observed. In turnip yellow mosaic virus, those from the B and C subunits comprising the hexameric capsomeres formed an annulus about the interior of the capsomere, while the corresponding N termini of the pentameric capsomere A subunits were not visible at all in electron density maps. In Desmodium yellow mottle tymovirus, amino termini from the A and B subunits combine to form the annuli, thereby resulting in a much strengthened association between the two types of capsomeres and an, apparently, more stable capsid. The first 13 residues of the C subunit were invisible in electron density maps. Two ordered fragments of single-stranded RNA, seven and two nucleotides in length, were observed. The ordered water structure of the virus particle was delineated and required 95 solvent molecules per protein subunit.
Figure 5.
Figure 5. The N termini of (a) DYMV and (b) TYMV are viewed along the quasi 3-fold axis of the respective ABC trimers superimposed on the density of an (F[o] - F[c]) exp ia[c] omit map with residues 15 to 26 of all subunits omitted from the models. These maps demonstrate the validity of the differences seen in the dispositions of the N termini of the two viruses. The maps in (a) are contoured at 1.2s (cyan) and 0.8s (light blue). The map in (b) is contoured at 2s.
Figure 10.
Figure 10. (a) The location of the RNA fragments with respect to the ABC trimer and (b), the location of RNA-A inside the hexameric cavity. RNA-A is shown as white, RNA-B as cyan. RNA-A lies along the inner surface between the annulus and the quasi 3-fold axis.
The above figures are reprinted by permission from Elsevier: J Mol Biol (2000, 301, 625-642) copyright 2000.
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