Evidence map›Paper›PMID 26969117›Full record

ArticleBMC systems biology2016

Systems biology of the structural proteome.

Elizabeth Brunk, Nathan Mih, Jonathan Monk, Zhen Zhang, Edward J O'Brien, Spencer E Bliven, Ke Chen, Roger L Chang, Philip E Bourne, Bernhard O Palsson

Abstract read
In one paragraph

Article in BMC systems biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

  1. Review
  2. Review
  3. Genome-scale metabolic models consistently predictFrontiers in bioinformatics · 2023
    Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Structural Biology in the Multi-Omics Era.Journal of chemical information and modeling · 2020
    Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. ssbio: a Python framework for structural systems biology.Bioinformatics (Oxford, England) · 2018
    Article
  19. Article
  20. 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

10 authors.

Elizabeth BrunkDepartment of Bioengineering, University of California, La Jolla, San Diego, CA, 92093, USA.
Nathan MihBioinformatics and Systems Biology Program, University of California, La Jolla, San Diego, CA, 92093, USA.
Jonathan MonkDepartment of Bioengineering, University of California, La Jolla, San Diego, CA, 92093, USA.
Zhen ZhangDepartment of Bioengineering, University of California, La Jolla, San Diego, CA, 92093, USA.
Edward J O'BrienDepartment of Bioengineering, University of California, La Jolla, San Diego, CA, 92093, USA.
Spencer E BlivenBioinformatics and Systems Biology Program, University of California, La Jolla, San Diego, CA, 92093, USA.
Ke ChenDepartment of Bioengineering, University of California, La Jolla, San Diego, CA, 92093, USA.
Roger L ChangDepartment of Systems Biology, Harvard Medical School, Boston, MA, 02115, USA.
Philip E BourneOffice of the Director, National Institutes of Health, Bethesda, MD, 20894, USA.
Bernhard O PalssonDepartment of Bioengineering, University of California, La Jolla, San Diego, CA, 92093, USA. palsson@eng.ucsd.edu.

Funding

GENOMICALLY BASED MODELS FOR ANTIBIOTIC DEVELOPMENTR01GM057089 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI PALSSON, BERNHARD O · 1998 to 2021
$6.9M
Structural Bioinformatics, Systems Pharmacology and Scholarly CommunicationZIALM000928 · NLM · NATIONAL LIBRARY OF MEDICINE · PI BOURNE, PHILIP · 2015 to 2016
$1.3M
Intramural NIH HHSNIGMS NIH HHS GM057089NIGMS NIH HHS R01 GM057089
6 · The paper itself

Abstract

backgroundThe success of genome-scale models (GEMs) can be attributed to the high-quality, bottom-up reconstructions of metabolic, protein synthesis, and transcriptional regulatory networks on an organism-specific basis. Such reconstructions are biochemically, genetically, and genomically structured knowledge bases that can be converted into a mathematical format to enable a myriad of computational biological studies. In recent years, genome-scale reconstructions have been extended to include protein structural information, which has opened up new vistas in systems biology research and empowered applications in structural systems biology and systems pharmacology.

resultsHere, we present the generation, application, and dissemination of genome-scale models with protein structures (GEM-PRO) for Escherichia coli and Thermotoga maritima. We show the utility of integrating molecular scale analyses with systems biology approaches by discussing several comparative analyses on the temperature dependence of growth, the distribution of protein fold families, substrate specificity, and characteristic features of whole cell proteomes. Finally, to aid in the grand challenge of big data to knowledge, we provide several explicit tutorials of how protein-related information can be linked to genome-scale models in a public GitHub repository ( https://github.com/SBRG/GEMPro/tree/master/GEMPro_recon/).

conclusionsTranslating genome-scale, protein-related information to structured data in the format of a GEM provides a direct mapping of gene to gene-product to protein structure to biochemical reaction to network states to phenotypic function. Integration of molecular-level details of individual proteins, such as their physical, chemical, and structural properties, further expands the description of biochemical network-level properties, and can ultimately influence how to model and predict whole cell phenotypes as well as perform comparative systems biology approaches to study differences between organisms. GEM-PRO offers insight into the physical embodiment of an organism's genotype, and its use in this comparative framework enables exploration of adaptive strategies for these organisms, opening the door to many new lines of research. With these provided tools, tutorials, and background, the reader will be in a position to run GEM-PRO for their own purposes.

Indexed as

ProteomicsEscherichia coliEscherichia coli ProteinsModels, BiologicalModels, MolecularProtein ConformationSequence Homology, Amino AcidSystems BiologyTemperatureThermotoga maritimaEscherichia coli Proteins

Identifiers

PMID26969117
PMCPMC4787049

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.