Evidence map›Paper›PMID 24695729›Full record

ReviewThe Journal of biological chemistry2014

Protein splicing: how inteins escape from precursor proteins.

Kenneth V Mills, Margaret A Johnson, Francine B Perler

Open access · hybridAbstract readReview
In one paragraph

Review in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers.

0numbers the graph read from it
0cells of the map it votes in
86citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

86 citing papers in PubMed, 145 citations in OpenAlex.

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  20. Conditional protein splicing of thebioRxiv : the preprint server for biology · 2024
    Article

26 more citing papers are in PubMed but not listed here.

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 at 1 institution in 1 country.

Kenneth V MillsFrom the Department of Chemistry, College of the Holy Cross, Worcester, Massachusetts 01610.
Margaret A Johnsonthe Department of Chemistry, University of Alabama at Birmingham, Birmingham, Alabama 35294, and.
Francine B PerlerNew England Biolabs, Inc., Ipswich, Massachusetts 01938 perler@neb.com.
New England Biolabs (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inteins are nature's escape artists; they facilitate their excision from flanking polypeptides (exteins) concomitant with extein ligation to produce a mature host protein. Splicing requires sequential nucleophilic displacement reactions catalyzed by strategies similar to proteases and asparagine lyases. Inteins require precise reaction coordination rather than rapid turnover or tight substrate binding because they are single turnover enzymes with covalently linked substrates. This has allowed inteins to explore alternative mechanisms with different steps or to use different methods for activation and coordination of the steps. Pressing issues include understanding the underlying details of catalysis and how the splicing steps are controlled.

Indexed as

Models, GeneticAmino AcidsExteinsInteinsMolecular StructureProtein PrecursorsProteinsProtein SplicingAmino AcidsProtein PrecursorsProteinsAsparagine CyclizationBacterial Intein-like DomainEnzyme KineticsEnzyme MechanismsHedgehogInteinPost-translational ModificationProtein MotifsProtein SplicingThioester

Identifiers

PMID24695729
PMCPMC4031507
OpenAlexW1971093707

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.