Evidence map›Paper›PMID 24515886›Full record

ArticleJournal of biomolecular NMR2014

Spectral density mapping protocols for analysis of molecular motions in disordered proteins.

Pavel Kadeřávek, Vojtěch Zapletal, Alžbeta Rabatinová, Libor Krásný, Vladimír Sklenář, Lukáš Žídek

Abstract read
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In one paragraph

Article in Journal of biomolecular NMR, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
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  5. Review
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  7. Article
  8. Boosting the resolution of low-fieldJournal of biomolecular NMR · 2020
    Article
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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

6 authors.

Pavel KadeřávekCentral European Institute of Technology, Masaryk University, Kamenice 5, 625 00, Brno, Czech Republic.
Vojtěch Zapletal
Alžbeta Rabatinová
Libor Krásný
Vladimír Sklenář
Lukáš Žídek

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spectral density mapping represents the method of choice for investigations of molecular motions of intrinsically disordered proteins (IDPs). However, the current methodology has been developed for well-folded proteins. In order to find conditions for a reliable analysis of relaxation of IDPs, accuracy of the current reduced spectral density mapping protocols applied to IDPs was examined and new spectral density mapping methods employing cross-correlated relaxation rates have been designed. Various sources of possible systematic errors were analyzed theoretically and the presented approaches were tested on a partially disordered protein, delta subunit of bacterial RNA polymerase. Results showed that the proposed protocols provide unbiased description of molecular motions of IDPs and allow to separate slow exchange from fast dynamics.

Indexed as

Intrinsically Disordered ProteinsModels, MolecularNuclear Magnetic Resonance, BiomolecularProtein ConformationProtein FoldingIntrinsically Disordered Proteins

Identifiers

What OpenQuestion holds

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Registered trials

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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.