Evidence map›Paper›PMID 24878423›Full record

ReviewProgress in biophysics and molecular biology

Prediction and redesign of protein-protein interactions.

Rhonald C Lua, David C Marciano, Panagiotis Katsonis, Anbu K Adikesavan, Angela D Wilkins, Olivier Lichtarge

Open access · greenAbstract readReview
In one paragraph

Review in Progress in biophysics and molecular biology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
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

12 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Challenges in structural approaches to cell modeling.Journal of molecular biology · 2016
    Review
  8. Article
  9. Article
  10. A hybrid method for protein-protein interface prediction.Protein science : a publication of the Protein Society · 2016
    Article
  11. Article
  12. Paradoxes of early stages of evolution of life and biological complexity.Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life · 2015
    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

6 authors at 1 institution in 1 country.

Rhonald C LuaDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
David C MarcianoDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Panagiotis KatsonisDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Anbu K AdikesavanDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Angela D WilkinsDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Computational and Integrative Biomedical Research Center, Baylor College of Medicine, Houston, TX 77030, USA.
Olivier LichtargeDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Verna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, TX 77030, USA; Computational and Integrative Biomedical Research Center, Baylor College of Medicine, Houston, TX 77030, USA. Electronic address: lichtarge@bcm.edu.
Baylor College of Medicine · US

Funding

TRAINING PROGRAM IN COMPUTATIONAL BIOLOGY AND MEDICINET15LM007093 · NLM · RICE UNIVERSITY · PI Lydia E. Kavraki · 1992 to 2026
$20.8M
Functional Determinnats in G Protein-coupled ReceptorsR01GM066099 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI LICHTARGE, OLIVIER · 2003 to 2022
$7.5M
Comparative genomics of protein structure and functionR01GM079656 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI LICHTARGE, OLIVIER · 2007 to 2019
$4.3M
NIGMS NIH HHS GM066099NIGMS NIH HHS GM079656NIGMS NIH HHS R01 GM066099NIGMS NIH HHS R01 GM079656NLM NIH HHS 5T15LM07093NLM NIH HHS T15 LM007093
6 · The paper itself

Abstract

Understanding the molecular basis of protein function remains a central goal of biology, with the hope to elucidate the role of human genes in health and in disease, and to rationally design therapies through targeted molecular perturbations. We review here some of the computational techniques and resources available for characterizing a critical aspect of protein function - those mediated by protein-protein interactions (PPI). We describe several applications and recent successes of the Evolutionary Trace (ET) in identifying molecular events and shapes that underlie protein function and specificity in both eukaryotes and prokaryotes. ET is a part of analytical approaches based on the successes and failures of evolution that enable the rational control of PPI.

Indexed as

Computational BiologyHumansProtein Interaction MappingProteinsSubstrate SpecificityProteinsEvolutionary traceFunctional annotationFunctional sitesMolecular evolutionProtein designProtein–protein interaction networks

Identifiers

PMID24878423
PMCPMC4246023
OpenAlexW2070331825

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.