Evidence map›Paper›PMID 28824574›Full record

ArticleFrontiers in microbiology2017

Functional Characterization of Four Putative δ

Giuseppe Forlani, Boguslaw Nocek, Srinivas Chakravarthy, Andrzej Joachimiak

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.2field-weighted citation impact, top 50% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. The Substrate Versatility of ΔMolecules (Basel, Switzerland) · 2026
    Article
  2. Article
  3. Article
  4. Functional Characterization ofMicroorganisms · 2022
    Article
  5. Article
  6. Review
  7. L-Proline Synthesis Mutants ofFrontiers in microbiology · 2022
    Article
  8. Peculiar substrate specificity of δMolecular biology reports · 2021
    Article
  9. Enzymology and Regulation of δFrontiers in plant science · 2021
    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

4 authors at 3 institutions in 2 countries.

Giuseppe ForlaniDepartment of Life Science and Biotechnology, University of FerraraFerrara, Italy.
Boguslaw NocekCenter for Structural Genomics of Infectious Diseases, University of ChicagoChicago, IL, United States.
Srinivas ChakravarthyArgonne National Laboratory, BioCAT, Center for Synchrotron Radiation Research and InstrumentationArgonne, IL, United States.
Andrzej JoachimiakCenter for Structural Genomics of Infectious Diseases, University of ChicagoChicago, IL, United States.
University of Chicago · USArgonne National Laboratory · USUniversity of Ferrara · IT

Funding

Time resolved SAXS studies on the RP2/Arl3 complex pp.484-485P41GM103622 · NIGMS · ILLINOIS INSTITUTE OF TECHNOLOGY · PI IRVING, THOMAS C · 2012 to 2020
$11.9M
Advanced Pixel Array Detector for Time-Resolved SAXS and Fiber DiffractionS10OD018090 · OD · ILLINOIS INSTITUTE OF TECHNOLOGY · PI IRVING, THOMAS C · 2014 to 2014
$529k
NIAID NIH HHS HHSN272200700058CNIAID NIH HHS HHSN272201200026CNIGMS NIH HHS P41 GM103622NIH HHS S10 OD018090
6 · The paper itself

Abstract

In most living organisms, the amino acid proline is synthesized starting from both glutamate and ornithine. In prokaryotes, in the absence of an ornithine cyclodeaminase that has been identified to date only in a small number of soil and plant bacteria, these pathways share the last step, the reduction of δ

Indexed as

Bacillus subtilisisoenzyme propertiesoligomeric structureP5C reductaseproduct inhibitionproline synthesissubstrate ambiguity

Identifiers

PMID28824574
PMCPMC5539093
OpenAlexW2741917966

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.