Evidence map›Paper›PMID 28663786›Full record

ReviewF1000Research2017

The advantage of channeling nucleotides for very processive functions.

Diana Zala, Uwe Schlattner, Thomas Desvignes, Julien Bobe, Aurélien Roux, Philippe Chavrier, Mathieu Boissan

Abstract readReview
In one paragraph

Review in F1000Research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing 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

38 citing papers in PubMed.

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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

7 authors.

Diana Zala *ESPCI - Paris, PSL Research University, Paris, F-75005, France.ORCID https://orcid.org/0000-0002-0052-8011
Uwe SchlattnerLaboratory of Fundamental and Applied Bioenergetics (LBFA), and SFR Environmental and Systems Biology (BEeSy), U1055, University Grenoble Alpes, Grenoble, 38058, France.ORCID https://orcid.org/0000-0003-1159-5911
Thomas DesvignesInstitute of Neuroscience, University of Oregon, Eugene, OR, 97401, USA.ORCID https://orcid.org/0000-0001-5126-8785
Julien BobeINRA, UR1037 LPGP, Campus de Beaulieu, Rennes, F-35000, France.ORCID https://orcid.org/0000-0002-9355-8227
Aurélien RouxDepartment of Biochemistry, University of Geneva, Geneva, CH-1211, Switzerland.
Philippe ChavrierInstitut Curie, Paris, F-75248, France.ORCID https://orcid.org/0000-0002-7351-733X
Mathieu Boissan *Sorbonne Universités, UPMC Univ Paris 06, INSERM, UMRS938, Saint-Antoine Research Center, Paris, F-75012, France.ORCID https://orcid.org/0000-0001-6494-5722

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nucleoside triphosphate (NTP)s, like ATP (adenosine 5'-triphosphate) and GTP (guanosine 5'-triphosphate), have long been considered sufficiently concentrated and diffusible to fuel all cellular ATPases (adenosine triphosphatases) and GTPases (guanosine triphosphatases) in an energetically healthy cell without becoming limiting for function. However, increasing evidence for the importance of local ATP and GTP pools, synthesised in close proximity to ATP- or GTP-consuming reactions, has fundamentally challenged our view of energy metabolism. It has become evident that cellular energy metabolism occurs in many specialised 'microcompartments', where energy in the form of NTPs is transferred preferentially from NTP-generating modules directly to NTP-consuming modules. Such energy channeling occurs when diffusion through the cytosol is limited, where these modules are physically close and, in particular, if the NTP-consuming reaction has a very high turnover,

Indexed as

ATPbioenergeticscreatine kinasedynaminGlycolysisGTPnucleoside diphosphate kinaseoxidative phosphorylation

Identifiers

PMID28663786
PMCPMC5473427

What OpenQuestion holds

Textmetadata
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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.