Evidence map›Paper›PMID 35960875›Full record

ArticleJournal of the American Chemical Society2022

A Chemical Proteomic Map of Heme-Protein Interactions.

Rick A Homan, Appaso M Jadhav, Louis P Conway, Christopher G Parker

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Chemical Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.0field-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

16 citing papers in PubMed, 35 citations in OpenAlex.

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  9. Proteomic strategies to interrogate the Fe-S proteome.Biochimica et biophysica acta. Molecular cell research · 2024
    Review
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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 1 institution in 1 country.

Rick A HomanDepartment of Chemistry, The Scripps Research Institute, La Jolla, California 92037, United States.
Appaso M JadhavDepartment of Chemistry, The Scripps Research Institute, La Jolla, California 92037, United States.
Louis P ConwayDepartment of Chemistry, The Scripps Research Institute, La Jolla, California 92037, United States.
Christopher G ParkerDepartment of Chemistry, The Scripps Research Institute, La Jolla, California 92037, United States.ORCID 0000-0001-8509-9289
Scripps Research Institute · US

Funding

Scripps Translational Science InstituteUL1TR002550 · NCATS · SCRIPPS RESEARCH INSTITUTE, THE · PI TOPOL, ERIC JEFFREY · 2018 to 2022
$28.9M
Scripps Clinical and Translational Science HubUM1TR004407 · NCATS · SCRIPPS RESEARCH INSTITUTE, THE · PI Eric Jeffrey Topol · 2023 to 2026
$24.2M
Chemoproteomic-Enabled Strategy to Study SLC Transporter Roles in InflammationR01AI156268 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI PARKER, CHRISTOPHER G · 2021 to 2025
$3.3M
Mindfulness Meditation: Regulating Eating and ObesityU01AT002550 · NCCIH · INDIANA STATE UNIVERSITY · PI KRISTELLER, JEAN L · 2004 to 2007
$1.3M
NRSA Training CoreTL1TR002551 · NCATS · SCRIPPS RESEARCH INSTITUTE, THE · PI TEYTON, LUC · 2018 to 2022
$1.2M
NCATS NIH HHS TL1 TR002551NCATS NIH HHS UL1 TR002550NCATS NIH HHS UM1 TR004407NCCIH NIH HHS U01 AT002550NIAID NIH HHS R01 AI156268
6 · The paper itself

Abstract

Heme is an essential cofactor for many human proteins as well as the primary transporter of oxygen in blood. Recent studies have also established heme as a signaling molecule, imparting its effects through binding with protein partners rather than through reactivity of its metal center. However, the comprehensive annotation of such heme-binding proteins in the human proteome remains incomplete. Here, we describe a strategy which utilizes a heme-based photoaffinity probe integrated with quantitative proteomics to map heme-protein interactions across the proteome. In these studies, we identified 350+ unique heme-protein interactions, the vast majority of which were heretofore unknown and consist of targets from diverse functional classes, including transporters, receptors, enzymes, transcription factors, and chaperones. Among these proteins is the immune-related interleukin receptor-associated kinase 1 (IRAK1), where we provide preliminary evidence that heme agonizes its catalytic activity. Our findings should improve the current understanding of heme's regulation as well as its signaling functions and facilitate new insights of its roles in human disease.

Indexed as

HemeProteomicsCarrier ProteinsHumansProtein BindingProteomeSignal TransductionTranscription FactorsCarrier ProteinsHemeProteomeTranscription Factors

Identifiers

PMID35960875
PMCPMC9811995
OpenAlexW4290879854

What OpenQuestion holds

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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.