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1.
Acta Crystallogr D Biol Crystallogr ; 56(Pt 10): 1223-32, 2000 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-10998618

RESUMEN

If only native amplitudes are used for structure determination, then additional 'theoretical' information is necessary to determine their phases. For use in a phasing procedure, this information can be formulated as a selection criterion (figure of merit) which assigns a reliability weight to every trial phase set and distinguishes the closest ones to the true phase set. Different types of additional information may be tested as a selection criterion: electron-density histograms, connectivity properties, statistical likelihood, atomicity etc. A common feature of such criteria is that they do not unambiguously judge the phase quality at low resolution. Nevertheless, the selection of the phase sets with best criterion values increases the ratio of good phase sets in the ensemble considered. An approximate solution of the phase problem may then be found by averaging the selected phase sets. Cluster analysis of the selected phase sets and averaging within clusters allow further improvement of this solution.


Asunto(s)
Conformación Proteica , Proteínas/química , Ribonucleasas/química , Ribosomas/ultraestructura , Análisis por Conglomerados , Simulación por Computador , Cristalografía , Análisis de Fourier , Procesamiento de Imagen Asistido por Computador , Modelos Moleculares , Análisis de Activación de Neutrones , Conformación de Ácido Nucleico , ARN de Transferencia de Aspártico/química , Thermus thermophilus/ultraestructura
2.
Acta Crystallogr D Biol Crystallogr ; 56(Pt 10): 1233-44, 2000 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-10998619

RESUMEN

Direct phasing needs additional information of a non-specific kind in order to select the correct phase set from all possible ones. This paper analyses the use of constraints which can be formulated in terms of electron-density values. One- and multi-dimensional histograms and connectivity properties are implemented as such constraints in density-modification procedures. These approaches usually cannot unambiguously select the best solution from a set of alternative phase variants. Nevertheless, they do allow the rejection of wrong solutions and the use of cluster analysis and averaging on the remaining variants provide a good starting point for further phase-refinement procedures.


Asunto(s)
Cristalografía por Rayos X/métodos , Isoenzimas/química , Conformación Molecular , Conformación Proteica , Ribonucleasas/química , Electrones , Análisis de Fourier , Modelos Moleculares
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