Evidence map›Paper›PMID 38033723›Full record

ArticleRSC chemical biology2023

Covalent targeting of non-cysteine residues in PI4KIIIβ.

Brett Cosgrove, Emma K Grant, Sophie Bertrand, Kenneth D Down, Don O Somers, John P Evans, Nicholas C O Tomkinson, Michael D Barker

Abstract read
In one paragraph

Article in RSC chemical biology, 2023. 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
–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

2 citing papers in PubMed.

  1. Article
  2. Review
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

8 authors.

Brett CosgroveMedicinal Chemistry, GlaxoSmithKline Medicines Research Centre Stevenage SG1 2NY UK.ORCID https://orcid.org/0000-0002-3949-500X
Emma K GrantMedicinal Chemistry, GlaxoSmithKline Medicines Research Centre Stevenage SG1 2NY UK.
Sophie BertrandMedicinal Chemistry, GlaxoSmithKline Medicines Research Centre Stevenage SG1 2NY UK.
Kenneth D DownMedicinal Chemistry, GlaxoSmithKline Medicines Research Centre Stevenage SG1 2NY UK.
Don O SomersStructural and Biophysical Science, GlaxoSmithKline Medicines Research Centre Stevenage SG1 2NY UK.
John P EvansScreening, Profiling and Mechanistic Biology, GlaxoSmithKline Medicines Research Centre Stevenage SG1 2NY UK.
Nicholas C O TomkinsonDepartment of Pure and Applied Chemistry, University of Strathclyde Glasgow G1 1XL UK Nicholas.Tomkinson@strath.ac.uk.ORCID https://orcid.org/0000-0002-5509-0133
Michael D BarkerMedicinal Chemistry, GlaxoSmithKline Medicines Research Centre Stevenage SG1 2NY UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The synthesis and characterisation of fluorosulfate covalent inhibitors of the lipid kinase PI4KIIIβ is described. The conserved lysine residue located within the ATP binding site was targeted, and optimised compounds based upon reversible inhibitors with good activity and physicochemical profile showed strong reversible interactions and slow onset times for the covalent inhibition, resulting in an excellent selectivity profile for the lipid kinase target. X-Ray crystallography demonstrated a distal tyrosine residue could also be targeted using a fluorosulfate strategy. Combination of this knowledge showed that a dual covalent inhibitor could be developed which reveals potential in addressing the challenges associated with drug resistant mutations.

Identifiers

PMID38033723
PMCPMC10685791

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Registered trials

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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.