Evidence map›Paper›PMID 39179604›Full record

ArticleScientific reports2024

Novel druggable space in human KRAS G13D discovered using structural bioinformatics and a P-loop targeting monoclonal antibody.

Oscar Jungholm, Carolina Trkulja, Martin Moche, Sreesha P Srinivasa, Maria-Nefeli Christakopoulou, Max Davidson, Anna Reymer, Kent Jardemark, Rafaela Lenza Fogaça, Anaswara Ashok and 7 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Selenium Nanoparticles Selectively Target KRAS G13D to Inhibit Colorectal Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  3. Review
  4. Review
  5. 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

17 authors.

Oscar Jungholm *Department of Physiology and Pharmacology, Karolinska Institutet, 171 77, Stockholm, Sweden.
Carolina Trkulja *Oblique Therapeutics AB, 41346, Gothenburg, Sweden.
Martin Moche *Protein Science Facility, Karolinska Institutet, 171 77, Stockholm, Sweden.
Sreesha P SrinivasaOblique Therapeutics AB, 41346, Gothenburg, Sweden.
Maria-Nefeli ChristakopoulouDepartment of Physiology and Pharmacology, Karolinska Institutet, 171 77, Stockholm, Sweden.
Max DavidsonOblique Therapeutics AB, 41346, Gothenburg, Sweden.
Anna ReymerOblique Therapeutics AB, 41346, Gothenburg, Sweden.
Kent JardemarkDepartment of Physiology and Pharmacology, Karolinska Institutet, 171 77, Stockholm, Sweden.
Rafaela Lenza FogaçaOblique Therapeutics AB, 41346, Gothenburg, Sweden.
Anaswara AshokOblique Therapeutics AB, 41346, Gothenburg, Sweden.
Gavin JeffriesFluicell AB, Flöjelbergsgatan 8C, 431 37, Mölndal, Sweden.
Henry Ampah-KorsahProtein Science Facility, Karolinska Institutet, 171 77, Stockholm, Sweden.
Emilia StrandbackProtein Science Facility, Karolinska Institutet, 171 77, Stockholm, Sweden.
Juni AndréllProtein Science Facility, Karolinska Institutet, 171 77, Stockholm, Sweden.
Tomas NymanProtein Science Facility, Karolinska Institutet, 171 77, Stockholm, Sweden.
Ghada NouairiaDepartment of Medicine Huddinge, Karolinska Institutet, 171 77, Stockholm, Sweden.
Owe OrwarOblique Therapeutics AB, 41346, Gothenburg, Sweden. owe.orwar@ki.se.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

KRAS belongs to a family of small GTPases that act as binary switches upstream of several signalling cascades, controlling proliferation and survival of cells. Mutations in KRAS drive oncogenesis, especially in pancreatic, lung, and colorectal cancers (CRC). Although historic attempts at targeting mutant KRAS with small molecule inhibitors have proven challenging, there are recent successes with the G12C, and G12D mutations. However, clinically important RAS mutations such as G12V, G13D, Q61L, and A146T, remain elusive drug targets, and insights to their structural landscape is of critical importance to develop novel, and effective therapeutic concepts. We present a fully open, P-loop exposing conformer of KRAS G13D by X-ray crystallography at 1.4-2.4 Å resolution in Mg

Indexed as

Antibodies, MonoclonalProto-Oncogene Proteins p21(ras)Colorectal NeoplasmsComputational BiologyCrystallography, X-RayHumansModels, MolecularMutationAntibodies, MonoclonalKRAS protein, humanProto-Oncogene Proteins p21(ras)

Identifiers

PMID39179604
PMCPMC11344056

What Socratic holds

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LicenceCC BY
Read underepoch 390

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 Socratic graph.