1OKH
Viscotoxin A3 from Viscum album L.
Summary for 1OKH
Entry DOI | 10.2210/pdb1okh/pdb |
Descriptor | VISCOTOXIN A3, PHOSPHATE ION, SULFATE ION, ... (4 entities in total) |
Functional Keywords | thionin, toxin, plant defense |
Biological source | VISCUM ALBUM (EUROPEAN MISTLETOE) |
Total number of polymer chains | 2 |
Total formula weight | 9971.26 |
Authors | Debreczeni, J.E.,Girmann, B.,Zeeck, A.,Sheldrick, G.M. (deposition date: 2003-07-24, release date: 2003-12-04, Last modification date: 2019-07-24) |
Primary citation | Debreczeni, J.E.,Girmann, B.,Zeeck, A.,Kratzner, R.,Sheldrick, G.M. Structure of Viscotoxin A3: Disulfide Location from Weak Sad Data Acta Crystallogr.,Sect.D, 59:2125-, 2003 Cited by PubMed Abstract: The crystal structure of viscotoxin A3 (VT A3) extracted from European mistletoe (Viscum album L.) has been solved using the anomalous diffraction of the native S atoms measured in-house with Cu Kalpha radiation to a resolution of 2.2 A and truncated to 2.5 A. A 1.75 A resolution synchrotron data set was used for phase expansion and refinement. An innovation in the dual-space substructure-solution program SHELXD enabled the individual S atoms of the disulfide bonds to be located using the Cu Kalpha data; this resulted in a marked improvement in the phasing compared with the use of super-S atoms. The VT A3 monomer consists of 46 amino acids with three disulfide bridges and has an overall fold resembling the canonical architecture of the alpha- and beta-thionins, a capital letter L. The asymmetric unit consists of two monomers related by a local twofold axis and held together by hydrophobic interactions between the monomer units. One phosphate anion (confirmed by 31P-NMR and MS) is associated with each monomer. PubMed: 14646070DOI: 10.1107/S0907444903018973 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.75 Å) |
Structure validation
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