Literature DB >> 32133986

ALIXE: a phase-combination tool for fragment-based molecular replacement.

Claudia Millán1, Elisabet Jiménez1, Antonia Schuster2, Kay Diederichs2, Isabel Usón1.   

Abstract

Fragment-based molecular replacement exploits the use of very accurate yet incomplete search models. In the case of the ARCIMBOLDO programs, consistent phase sets produced from the placement and refinement of fragments with Phaser can be combined in order to increase their signal before proceeding to the step of density modification and autotracing with SHELXE. The program ALIXE compares multiple phase sets, evaluating mean phase differences to determine their common origin, and subsequently produces sets of combined phases that group consistent solutions. In this work, its use on different scenarios of very partial molecular-replacement solutions and its performance after the development of a much-optimized set of algorithms are described. The program is available both standalone and integrated within the ARCIMBOLDO programs. ALIXE has been analysed to identify its rate-limiting steps while exploring the best parameterization to improve its performance and make this software efficient enough to work on modest hardware. The algorithm has been parallelized and redesigned to meet the typical landscape of solutions. Analysis of pairwise correlation between the phase sets has also been explored to test whether this would provide additional insight. ALIXE can be used to exhaustively analyse all partial solutions produced or to complement those already selected for expansion, and also to reduce the number of redundant solutions, which is particularly relevant to the case of coiled coils, or to combine partial solutions from different programs. In each case parallelization and optimization to provide speedup makes its use amenable to typical hardware found in crystallography. ARCIMBOLDO_BORGES and ARCIMBOLDO_SHREDDER now call on ALIXE by default. open access.

Entities:  

Keywords:  ALIXE; ARCIMBOLDO; combination; fragment-based molecular replacement; phasing

Year:  2020        PMID: 32133986     DOI: 10.1107/S205979832000056X

Source DB:  PubMed          Journal:  Acta Crystallogr D Struct Biol        ISSN: 2059-7983            Impact factor:   7.652


  3 in total

1.  Helical ensembles outperform ideal helices in molecular replacement.

Authors:  Filomeno Sánchez Rodríguez; Adam J Simpkin; Owen R Davies; Ronan M Keegan; Daniel J Rigden
Journal:  Acta Crystallogr D Struct Biol       Date:  2020-09-16       Impact factor: 7.652

2.  SPACA6 ectodomain structure reveals a conserved superfamily of gamete fusion-associated proteins.

Authors:  Tyler D R Vance; Patrick Yip; Elisabet Jiménez; Sheng Li; Diana Gawol; James Byrnes; Isabel Usón; Ahmed Ziyyat; Jeffrey E Lee
Journal:  Commun Biol       Date:  2022-09-17

3.  Fragment-based determination of a proteinase K structure from MicroED data using ARCIMBOLDO_SHREDDER.

Authors:  Logan S Richards; Claudia Millán; Jennifer Miao; Michael W Martynowycz; Michael R Sawaya; Tamir Gonen; Rafael J Borges; Isabel Usón; Jose A Rodriguez
Journal:  Acta Crystallogr D Struct Biol       Date:  2020-07-27       Impact factor: 7.652

  3 in total

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