The molecular replacement method.

By Michael G. Rossmann. 1990

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Citations in the corpus

Implementation of molecular replacement in AMoRe. (2001, methodology): “The rotational NCS, determined with the help of the selfrotation function, may be used to enhance the signal-to-noise ratio of cross-rotation functions (Rossmann et al., 1972; Tong & Rossmann, 1990).”
Increasing the Radius of Convergence of Molecular Replacement by Density and Energy Guided Protein Structure Optimization (2011, unknown): “the Patterson map, we compute equation (1) once, sum over all the symmetric”
Model morphing and sequence assignment after molecular replacement (2013, background): “2244 doi:10.1107/S0907444913017770 Acta Cryst.”
Pushing the boundaries of molecular replacement with maximum likelihood. (2001, background): “…has been carried out with a divide-and-conquer approach, in which the dimensionality of the problem is reduced by separating the search for one molecule into two separate three-dimensional searches: a rotation search for orientation and a translation search for position (Rossmann, 1972).”
Structures of bovine, equine and leporine serum albumin. (2012, methodology): “The structure of BSA was solved at 2.47 Å resolution by molecular replacement (Rossmann, 1990) with the program Phaser (McCoy et al., 2007) using the HSA data set with PDB code 1ao6 (Sugio et al., 1999) as a model.”
Crystal structure determination and refinement via SIR2014 (2015, methodology): “…methods are implemented, based on the simulated annealing (SA) approach (to be used when the molecular geometry is known; see Altomare et al., 2009) and molecularreplacement techniques (MR; see Rossmann, 1972; Navaza, 1994; Vagin & Teplyakov, 1997; Caliandro et al., 2006, 2009; McCoy et al., 2007).”
Spherical polar Fourier assembly of protein complexes with arbitrary point group symmetry (2016, background): “…it would be useful to be able to generate high-quality candidate complex structures for use as templates in molecular replacement (MR) techniques (Rossmann, 1990; Navaza, 2001), to provide angular parameters for locked MR search functions (Tong, 2001) or to dock high-resolution structural…”
Using iterative fragment assembly and progressive sequence truncation to facilitate phasing and crystal structure determination of distantly related proteins. (2016, background): “One solution to the phase problem is molecular replacement (MR), which estimates the phase of each diffraction amplitude by placing one or more homologous search models in the unit cell of the crystal (Rossmann, 1990; Navaza, 1994).”