Evidence map›Paper›PMID 29968670›Full record

ArticleActa crystallographica. Section D, Structural biology2018

SIMBAD: a sequence-independent molecular-replacement pipeline.

Adam J Simpkin, Felix Simkovic, Jens M H Thomas, Martin Savko, Andrey Lebedev, Ville Uski, Charles Ballard, Marcin Wojdyr, Rui Wu, Ruslan Sanishvili and 6 more

Abstract read
In one paragraph

Article in Acta crystallographica. Section D, Structural biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed.

  1. Article
  2. Scotty: lattice coincidences for macromolecular crystallographic phasing.Acta crystallographica. Section D, Structural biology · 2026
    Article
  3. Crystal structure and functional characterization of an Asp49 phospholipase AActa crystallographica. Section F, Structural biology communications · 2026
    Article
  4. Article
  5. Project automation in CCP4 Cloud: Enabling customization and high-throughput efficiency.Protein science : a publication of the Protein Society · 2025
    Article
  6. Serendipitous high-resolution structure of Escherichia coli carbonic anhydrase 2.Acta crystallographica. Section F, Structural biology communications · 2025
    Article
  7. Structural Analysis ofMicroorganisms · 2023
    Article
  8. Article
  9. Article
  10. IUCrJ · 2022
    Article
  11. Predicting the performance of automated crystallographic model-building pipelines.Acta crystallographica. Section D, Structural biology · 2021
    Article
  12. Article
  13. Article
  14. Phasertng: directed acyclic graphs for crystallographic phasing.Acta crystallographica. Section D, Structural biology · 2021
    Article
  15. Shift-field refinement of macromolecular atomic models.Acta crystallographica. Section D, Structural biology · 2020
    Article
  16. Contamination or serendipity - doing the wrong thing by chance.Acta crystallographica. Section F, Structural biology communications · 2020
    Article
  17. Crystal structure of the Escherichia coli transcription termination factor Rho.Acta crystallographica. Section F, Structural biology communications · 2020
    Article
  18. Detecting the nature and solving the crystal structure of a contaminant protein from an opportunistic pathogen.Acta crystallographica. Section F, Structural biology communications · 2020
    Article
  19. Article
  20. Using Phaser and ensembles to improve the performance of SIMBAD.Acta crystallographica. Section D, Structural biology · 2020
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Adam J SimpkinInstitute of Integrative Biology, University of Liverpool, Liverpool L69 7ZB, England.
Felix SimkovicInstitute of Integrative Biology, University of Liverpool, Liverpool L69 7ZB, England.ORCID 0000-0003-3430-6828
Jens M H ThomasInstitute of Integrative Biology, University of Liverpool, Liverpool L69 7ZB, England.ORCID 0000-0003-0277-8505
Martin SavkoSynchrotron SOLEIL, L'Orme des Merisiers, Saint Aubin, BP 48, 91192 Gif-sur-Yvette, France.
Andrey LebedevSTFC, Rutherford Appleton Laboratory, Harwell Oxford, Didcot OX11 0FA, England.
Ville UskiSTFC, Rutherford Appleton Laboratory, Harwell Oxford, Didcot OX11 0FA, England.
Charles BallardSTFC, Rutherford Appleton Laboratory, Harwell Oxford, Didcot OX11 0FA, England.
Marcin WojdyrSTFC, Rutherford Appleton Laboratory, Harwell Oxford, Didcot OX11 0FA, England.ORCID 0000-0003-3980-4092
Rui WuFeil Family Brain and Mind Institute, Weill Cornell Medicine, New York, NY 10021, USA.
Ruslan SanishviliGM/CA@APS, The X-Ray Science Division, The Advanced Photon Source, Argonne National Laboratory, Lemont, IL 60439, USA.
Yibin XuDivision of Structural Biology, Walter and Eliza Hall Institute of Medical Research, Parkville, VIC 3052, Australia.
María Natalia LisaLaboratory of Molecular and Structural Microbiology, Institut Pasteur de Montevideo, Mataojo 2020, 11400 Montevideo, Uruguay.ORCID 0000-0001-9630-8090
Alejandro BuschiazzoLaboratory of Molecular and Structural Microbiology, Institut Pasteur de Montevideo, Mataojo 2020, 11400 Montevideo, Uruguay.ORCID 0000-0002-2509-6526
William ShepardSynchrotron SOLEIL, L'Orme des Merisiers, Saint Aubin, BP 48, 91192 Gif-sur-Yvette, France.
Daniel J RigdenInstitute of Integrative Biology, University of Liverpool, Liverpool L69 7ZB, England.ORCID 0000-0002-7565-8937
Ronan M KeeganInstitute of Integrative Biology, University of Liverpool, Liverpool L69 7ZB, England.

Funding

BBSRC BB/L009544/1National Health and Medical Research Council APP1004945NCI NIH HHS ACB-12002NIGMS NIH HHS AGM-12006U.S. Department of Energy, Office of Science DE-AC02-06CH11357
6 · The paper itself

Abstract

The conventional approach to finding structurally similar search models for use in molecular replacement (MR) is to use the sequence of the target to search against those of a set of known structures. Sequence similarity often correlates with structure similarity. Given sufficient similarity, a known structure correctly positioned in the target cell by the MR process can provide an approximation to the unknown phases of the target. An alternative approach to identifying homologous structures suitable for MR is to exploit the measured data directly, comparing the lattice parameters or the experimentally derived structure-factor amplitudes with those of known structures. Here, SIMBAD, a new sequence-independent MR pipeline which implements these approaches, is presented. SIMBAD can identify cases of contaminant crystallization and other mishaps such as mistaken identity (swapped crystallization trays), as well as solving unsequenced targets and providing a brute-force approach where sequence-dependent search-model identification may be nontrivial, for example because of conformational diversity among identifiable homologues. The program implements a three-step pipeline to efficiently identify a suitable search model in a database of known structures. The first step performs a lattice-parameter search against the entire Protein Data Bank (PDB), rapidly determining whether or not a homologue exists in the same crystal form. The second step is designed to screen the target data for the presence of a crystallized contaminant, a not uncommon occurrence in macromolecular crystallography. Solving structures with MR in such cases can remain problematic for many years, since the search models, which are assumed to be similar to the structure of interest, are not necessarily related to the structures that have actually crystallized. To cater for this eventuality, SIMBAD rapidly screens the data against a database of known contaminant structures. Where the first two steps fail to yield a solution, a final step in SIMBAD can be invoked to perform a brute-force search of a nonredundant PDB database provided by the MoRDa MR software. Through early-access usage of SIMBAD, this approach has solved novel cases that have otherwise proved difficult to solve.

Indexed as

Databases, ProteinSoftwareAlgorithmsAmino Acid SequenceCrystallizationCrystallography, X-RayModels, Molecularcontaminantlattice searchmolecular replacement pipelineSIMBADstructure solution

Identifiers

PMID29968670
PMCPMC6038384

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.