Evidence map›Paper›PMID 33103835›Full record

ArticleChembiochem : a European journal of chemical biology2021

Structural Insights into the Interaction of Heme with Protein Tyrosine Kinase JAK2*.

Benjamin Franz Schmalohr, Al-Hassan M Mustafa, Oliver H Krämer, Diana Imhof

Open access · hybridAbstract read
In one paragraph

Article in Chembiochem : a European journal of chemical biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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  4. Structural Insights into the Interaction of Heme with Protein Tyrosine Kinase JAK2*.Chembiochem : a European journal of chemical biology · 2021
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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

4 authors at 2 institutions in 1 country.

Benjamin Franz SchmalohrPharmaceutical Biochemistry and Bioanalytics, Pharmaceutical Institute, University of Bonn, An der Immenburg 4, 53121, Bonn, Germany.ORCID 0000-0001-6710-5251
Al-Hassan M MustafaUniversity Medical Center Mainz, Institute of Toxicology, Obere Zahlbacher Straße 67, 55131, Mainz, Germany.
Oliver H KrämerUniversity Medical Center Mainz, Institute of Toxicology, Obere Zahlbacher Straße 67, 55131, Mainz, Germany.ORCID 0000-0003-3973-045X
Diana ImhofPharmaceutical Biochemistry and Bioanalytics, Pharmaceutical Institute, University of Bonn, An der Immenburg 4, 53121, Bonn, Germany.ORCID 0000-0003-4163-7334
Johannes Gutenberg University Mainz · DEUniversity of Bonn · DE

Funding

German Academic Exchange Service
6 · The paper itself

Abstract

Janus kinase 2 (JAK2) is the most important signal-transducing tyrosine kinase in erythropoietic precursor cells. Its malfunction drives several myeloproliferative disorders. Heme is a small metal-ion-carrying molecule that is incorporated into hemoglobin in erythroid precursor cells to transport oxygen. In addition, heme is a signaling molecule and regulator of various biochemical processes. Here, we show that heme exposure leads to hyperphosphorylation of JAK2 in a myeloid cancer cell line. Two peptides identified in JAK2 are heme-regulatory motifs and show low-micromolar affinities for heme. These peptides map to the kinase domain of JAK2, which is essential for downstream signaling. We suggest these motifs to be the interaction sites of heme with JAK2, which drive the heme-induced hyperphosphorylation. The results presented herein could facilitate the development of heme-related pharmacological tools to combat myeloproliferative disorders.

Indexed as

HemeHumansJanus Kinase 2Leukemia, MyeloidPhosphorylationProtein ConformationSignal TransductionTumor Cells, CulturedTyrosineHemeJAK2 protein, humanJanus Kinase 2Tyrosinehemeheme-regulatory motif (HRM)kinasespeptide-protein complexesphosphorylation

Identifiers

PMID33103835
PMCPMC7984354
OpenAlexW3094622130

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.