Evidence map›Paper›PMID 27159634›Full record

ArticleJournal of computational biology : a journal of computational molecular cell biology2016

Predicting Designability of Small Proteins from Graph Features of Contact Maps.

Sumudu P Leelananda, Robert L Jernigan, Andrzej Kloczkowski

Abstract read
In one paragraph

Article in Journal of computational biology : a journal of computational molecular cell biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. A generic framework for hierarchical de novo protein design.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  2. 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

3 authors.

Sumudu P Leelananda1 Nationwide Children's Hospital , Columbus, Ohio.
Robert L Jernigan2 Iowa State University , Ames, Iowa.
Andrzej Kloczkowski1 Nationwide Children's Hospital , Columbus, Ohio.

Funding

Coarse-Grained Models of ProteinsR01GM072014 · NIGMS · IOWA STATE UNIVERSITY · PI JERNIGAN, ROBERT L · 2004 to 2012
$2.3M
High-Accuracy Protein Models Derived from Lower Resolution DataR01GM081680 · NIGMS · IOWA STATE UNIVERSITY · PI KLOCZKOWSKI, ANDRZEJ · 2007 to 2009
$763k
NIGMS NIH HHS R01 GM072014NIGMS NIH HHS R01 GM081680
6 · The paper itself

Abstract

Highly designable structures can be distinguished based on certain geometric graphical features of the interactions, confirming the fact that the topology of a protein structure and its residue-residue interaction network are important determinants of its designability. The most designable structures and least designable structures obtained for sets of proteins having the same number of residues are compared. It is shown that the most designable structures predicted by the graph features of the contact diagrams are more densely packed, whereas the poorly designable structures are more open structures or structures that are loosely packed. Interestingly enough, it can also be seen that the highly designable identified are also common structural motifs found in nature.

Indexed as

Computational BiologyComputer SimulationModels, MolecularProtein BindingProtein ConformationProtein FoldingProteinsProteinscontact mapsdesignabilitygraph featuresinteraction networklattice modelsmachine learningnetworkpredictionstructure

Identifiers

PMID27159634
PMCPMC4876523

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.