Evidence map›Paper›PMID 30023565›Full record

ArticleACS omega2017

Small Molecules Targeting the Inactive Form of the Mnk1/2 Kinases.

Srinivasaraghavan Kannan, Mohan R Pradhan, Joseph Cherian, Thomas L Joseph, Zhi Ying Poh, Yang Hai Yan, Ho Melvyn, Liu Boping, Hill Jeffrey, Kassoum Nacro and 1 more

Open access · goldAbstract read
In one paragraph

Article in ACS omega, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

6 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. The MNK1/2-eIF4E Axis as a Potential Therapeutic Target in Melanoma.International journal of molecular sciences · 2020
    Review
  5. Article
  6. 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

11 authors at 1 institution in 1 country.

Srinivasaraghavan KannanBioinformatics Institute (ASTAR), 30 Biopolis Street, #07-01 Matrix, Singapore 138671, Singapore.
Mohan R PradhanBioinformatics Institute (ASTAR), 30 Biopolis Street, #07-01 Matrix, Singapore 138671, Singapore.
Joseph CherianExperimental Therapeutics Centre (ASTAR), 31 Biopolis Street, #03-01 Nanos, 138669, Singapore.
Thomas L JosephBioinformatics Institute (ASTAR), 30 Biopolis Street, #07-01 Matrix, Singapore 138671, Singapore.
Zhi Ying PohExperimental Therapeutics Centre (ASTAR), 31 Biopolis Street, #03-01 Nanos, 138669, Singapore.
Yang Hai YanExperimental Therapeutics Centre (ASTAR), 31 Biopolis Street, #03-01 Nanos, 138669, Singapore.
Ho MelvynExperimental Therapeutics Centre (ASTAR), 31 Biopolis Street, #03-01 Nanos, 138669, Singapore.
Liu BopingExperimental Therapeutics Centre (ASTAR), 31 Biopolis Street, #03-01 Nanos, 138669, Singapore.
Hill JeffreyExperimental Therapeutics Centre (ASTAR), 31 Biopolis Street, #03-01 Nanos, 138669, Singapore.
Kassoum NacroExperimental Therapeutics Centre (ASTAR), 31 Biopolis Street, #03-01 Nanos, 138669, Singapore.
Chandra S VermaBioinformatics Institute (ASTAR), 30 Biopolis Street, #07-01 Matrix, Singapore 138671, Singapore.
Agency for Science, Technology and Research · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overexpression of the eukaryotic initiation factor 4E (eIF4E) is linked to a variety of cancers. Both mitogen-activated protein kinases-interacting kinases 1 and 2 (Mnk1/2) activate the oncogene eIF4E through posttranslational modification (phosphorylating it at the conserved Ser209). Inhibition of Mnk prevents eIF4E phosphorylation, making the Mnk-eIF4E axis a potential therapeutic target for oncology. Recently, the design and synthesis of a series of novel potent compounds inhibiting the Mnk1/2 kinases were carried out in-house. Here, we describe computational models of the interactions between Mnk1/2 kinases and these inhibitors. Molecular modeling combined with free energy calculations show that these compounds bind to the inactive forms of the kinases. All compounds adopt similar conformations in the catalytic sites of both kinases, stabilized by hydrogen bonds with the hinge regions and with the catalytic Lys78 (Mnk1) and Lys113 (Mnk2). These hydrogen bond interactions clearly play a critical role in determining the conformational stability and potency of the compounds. We also find that van der Waals interactions with an allosteric pocket are key to their binding and potency. Two distinct hydration sites that appear to further stabilize the ligand binding/interactions were observed. Critically, the inclusion of explicit water molecules in the calculations results in improving the agreement between calculated and experimental binding free energies.

Identifiers

PMID30023565
PMCPMC6045392
OpenAlexW2769183497

What OpenQuestion holds

Textmetadata
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.