Evidence map›Paper›PMID 36385940›Full record

ArticleACS medicinal chemistry letters2022

Covalent Modification of the JH2 Domain of Janus Kinase 2.

Sean P Henry, Maria-Elena Liosi, Joseph A Ippolito, Fabian Menges, Ana S Newton, Joseph Schlessinger, William L Jorgensen

Abstract read
In one paragraph

Article in ACS medicinal chemistry letters, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Chemical neighborhood exploration for substrate discovery in biocatalysis.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Review
  3. 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

7 authors.

Sean P HenryDepartment of Chemistry, Yale University, New Haven, Connecticut 06520-8107, United States.
Maria-Elena LiosiDepartment of Chemistry, Yale University, New Haven, Connecticut 06520-8107, United States.
Joseph A IppolitoDepartment of Chemistry, Yale University, New Haven, Connecticut 06520-8107, United States.
Fabian MengesDepartment of Chemistry, Yale University, New Haven, Connecticut 06520-8107, United States.ORCID https://orcid.org/0000-0002-5859-9197
Ana S NewtonDepartment of Chemistry, Yale University, New Haven, Connecticut 06520-8107, United States.ORCID https://orcid.org/0000-0002-0196-0869
Joseph SchlessingerDepartment of Pharmacology, Yale University School of Medicine, New Haven, Connecticut 06520-8066, United States.ORCID https://orcid.org/0000-0002-5085-5969
William L JorgensenDepartment of Chemistry, Yale University, New Haven, Connecticut 06520-8107, United States.ORCID https://orcid.org/0000-0002-3993-9520

Funding

POTENTIAL FUNCTIONS FOR WATER PROTEIN INTERACTIONSR01GM032136 · NIGMS · YALE UNIVERSITY · PI JORGENSEN, WILLIAM L. · 1985 to 2023
$8.2M
NIGMS NIH HHS R01 GM032136
6 · The paper itself

Abstract

Probe molecules that covalently modify the JAK2 pseudokinase domain (JH2) are reported. Selective targeting of JH2 domains over the kinase (JH1) domains is a necessary feature for ligands intended to evaluate JH2 domains as therapeutic targets. The JH2 domains of three Janus kinases (JAK1, JAK2, and TYK2) possess a cysteine residue in the catalytic loop that does not occur in their JH1 domains. Starting from a non-selective kinase binding molecule, computer-aided design directed attachment of substituents terminating in acrylamide warheads to modify Cys675 of JAK2 JH2. Successful covalent attachment was demonstrated first through observation of enhanced binding with increasing incubation time in fluorescence polarization experiments. Covalent binding also increased selectivity to as much as ca. 30-fold for binding the JAK2 JH2 domain over the JH1 domain after a 20-h incubation. Covalency was confirmed through HPLC electrospray quadrupole time-of-flight HRMS experiments, which revealed the expected mass shifts.

Identifiers

PMID36385940
PMCPMC9661697

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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.