Evidence map›Paper›PMID 28745017›Full record

ArticleChembiochem : a European journal of chemical biology2017

Activation of Engineered Protein Tyrosine Phosphatases with the Biarsenical Compound AsCy3-EDT

Wai Cheung Chan, Gregory S Knowlton, Anthony C Bishop

Abstract read
In one paragraph

Article in Chembiochem : a European journal of chemical biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

3 authors at 1 institution in 1 country.

Wai Cheung ChanAmherst College, Department of Chemistry, Amherst, MA, 01002, USA.
Gregory S KnowltonAmherst College, Department of Chemistry, Amherst, MA, 01002, USA.
Anthony C BishopAmherst College, Department of Chemistry, Amherst, MA, 01002, USA.ORCID 0000-0001-8394-280X
Amherst College · US

Funding

Target-specific inhibition and activation of protein tyrosine phosphatasesR15GM071388 · NIGMS · AMHERST COLLEGE · PI BISHOP, ANTHONY C · 2005 to 2021
$1.6M
NIGMS NIH HHS R15 GM071388
6 · The paper itself

Abstract

Methods for activating signaling enzymes hold significant potential for the study of cellular signal transduction. Here we present a strategy for engineering chemically activatable protein tyrosine phosphatases (actPTPs). To generate actPTP1B, we introduced three cysteine point mutations in the enzyme's WPD loop. Biarsenical compounds were screened for the capability to bind actPTP1B's WPD loop and increase its phosphatase activity. We identified AsCy3-EDT

Indexed as

Protein EngineeringArsenicalsDose-Response Relationship, DrugModels, MolecularMolecular StructureProtein Tyrosine PhosphatasesTime FactorsArsenicalsAsCy3 compoundProtein Tyrosine PhosphatasesAsCy3enzyme activationenzymesprotein engineeringprotein tyrosine phosphatases

Identifiers

PMID28745017
PMCPMC5923034
OpenAlexW2737713068

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.