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Exploiting distant homologues for phasing through the generation of compact fragments, local fold refinement and partial solution combination

Macromolecular structures can be solved by molecular replacement provided that suitable search models are available. Models from distant homologues may deviate too much from the target structure to succeed, notwithstanding an overall similar fold or even their featuring areas of very close geometry....

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Autores principales: Millán, Claudia, Sammito, Massimo Domenico, McCoy, Airlie J., Nascimento, Andrey F. Ziem, Petrillo, Giovanna, Oeffner, Robert D., Domínguez-Gil, Teresa, Hermoso, Juan A., Read, Randy J., Usón, Isabel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5892878/
https://www.ncbi.nlm.nih.gov/pubmed/29652256
http://dx.doi.org/10.1107/S2059798318001365
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author Millán, Claudia
Sammito, Massimo Domenico
McCoy, Airlie J.
Nascimento, Andrey F. Ziem
Petrillo, Giovanna
Oeffner, Robert D.
Domínguez-Gil, Teresa
Hermoso, Juan A.
Read, Randy J.
Usón, Isabel
author_facet Millán, Claudia
Sammito, Massimo Domenico
McCoy, Airlie J.
Nascimento, Andrey F. Ziem
Petrillo, Giovanna
Oeffner, Robert D.
Domínguez-Gil, Teresa
Hermoso, Juan A.
Read, Randy J.
Usón, Isabel
author_sort Millán, Claudia
collection PubMed
description Macromolecular structures can be solved by molecular replacement provided that suitable search models are available. Models from distant homologues may deviate too much from the target structure to succeed, notwithstanding an overall similar fold or even their featuring areas of very close geometry. Successful methods to make the most of such templates usually rely on the degree of conservation to select and improve search models. ARCIMBOLDO_SHREDDER uses fragments derived from distant homologues in a brute-force approach driven by the experimental data, instead of by sequence similarity. The new algorithms implemented in ARCIMBOLDO_SHREDDER are described in detail, illustrating its characteristic aspects in the solution of new and test structures. In an advance from the previously published algorithm, which was based on omitting or extracting contiguous polypeptide spans, model generation now uses three-dimensional volumes respecting structural units. The optimal fragment size is estimated from the expected log-likelihood gain (LLG) values computed assuming that a substructure can be found with a level of accuracy near that required for successful extension of the structure, typically below 0.6 Å root-mean-square deviation (r.m.s.d.) from the target. Better sampling is attempted through model trimming or decomposition into rigid groups and optimization through Phaser’s gyre refinement. Also, after model translation, packing filtering and refinement, models are either disassembled into predetermined rigid groups and refined (gimble refinement) or Phaser’s LLG-guided pruning is used to trim the model of residues that are not contributing signal to the LLG at the target r.m.s.d. value. Phase combination among consistent partial solutions is performed in reciprocal space with ALIXE. Finally, density modification and main-chain autotracing in SHELXE serve to expand to the full structure and identify successful solutions. The performance on test data and the solution of new structures are described.
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spelling pubmed-58928782018-04-13 Exploiting distant homologues for phasing through the generation of compact fragments, local fold refinement and partial solution combination Millán, Claudia Sammito, Massimo Domenico McCoy, Airlie J. Nascimento, Andrey F. Ziem Petrillo, Giovanna Oeffner, Robert D. Domínguez-Gil, Teresa Hermoso, Juan A. Read, Randy J. Usón, Isabel Acta Crystallogr D Struct Biol Research Papers Macromolecular structures can be solved by molecular replacement provided that suitable search models are available. Models from distant homologues may deviate too much from the target structure to succeed, notwithstanding an overall similar fold or even their featuring areas of very close geometry. Successful methods to make the most of such templates usually rely on the degree of conservation to select and improve search models. ARCIMBOLDO_SHREDDER uses fragments derived from distant homologues in a brute-force approach driven by the experimental data, instead of by sequence similarity. The new algorithms implemented in ARCIMBOLDO_SHREDDER are described in detail, illustrating its characteristic aspects in the solution of new and test structures. In an advance from the previously published algorithm, which was based on omitting or extracting contiguous polypeptide spans, model generation now uses three-dimensional volumes respecting structural units. The optimal fragment size is estimated from the expected log-likelihood gain (LLG) values computed assuming that a substructure can be found with a level of accuracy near that required for successful extension of the structure, typically below 0.6 Å root-mean-square deviation (r.m.s.d.) from the target. Better sampling is attempted through model trimming or decomposition into rigid groups and optimization through Phaser’s gyre refinement. Also, after model translation, packing filtering and refinement, models are either disassembled into predetermined rigid groups and refined (gimble refinement) or Phaser’s LLG-guided pruning is used to trim the model of residues that are not contributing signal to the LLG at the target r.m.s.d. value. Phase combination among consistent partial solutions is performed in reciprocal space with ALIXE. Finally, density modification and main-chain autotracing in SHELXE serve to expand to the full structure and identify successful solutions. The performance on test data and the solution of new structures are described. International Union of Crystallography 2018-04-03 /pmc/articles/PMC5892878/ /pubmed/29652256 http://dx.doi.org/10.1107/S2059798318001365 Text en © Millán et al. 2018 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.http://creativecommons.org/licenses/by/2.0/uk/
spellingShingle Research Papers
Millán, Claudia
Sammito, Massimo Domenico
McCoy, Airlie J.
Nascimento, Andrey F. Ziem
Petrillo, Giovanna
Oeffner, Robert D.
Domínguez-Gil, Teresa
Hermoso, Juan A.
Read, Randy J.
Usón, Isabel
Exploiting distant homologues for phasing through the generation of compact fragments, local fold refinement and partial solution combination
title Exploiting distant homologues for phasing through the generation of compact fragments, local fold refinement and partial solution combination
title_full Exploiting distant homologues for phasing through the generation of compact fragments, local fold refinement and partial solution combination
title_fullStr Exploiting distant homologues for phasing through the generation of compact fragments, local fold refinement and partial solution combination
title_full_unstemmed Exploiting distant homologues for phasing through the generation of compact fragments, local fold refinement and partial solution combination
title_short Exploiting distant homologues for phasing through the generation of compact fragments, local fold refinement and partial solution combination
title_sort exploiting distant homologues for phasing through the generation of compact fragments, local fold refinement and partial solution combination
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5892878/
https://www.ncbi.nlm.nih.gov/pubmed/29652256
http://dx.doi.org/10.1107/S2059798318001365
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