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Paper · 42929068

Sequence space exploration in SHP2: mechanistic insights from disease-associated mutations.

van Vlimmeren AE and 3 others. Biochem J, 2026.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Sequence space exploration in SHP2: mechanistic insights from disease-associated mutations. Papers, record 42929068. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/42929068

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title
Sequence space exploration in SHP2: mechanistic insights from disease-associated mutations.
Journal
Biochem J
Year
2026
Publication types
Journal Article, Review
Revised in PubMed
2026-11-02

Source PubMed

Authors4

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

Source PubMed

Topics6

NLM's MeSH indexing of the paper, its major topics first.

MeSH termMajor
Protein Tyrosine Phosphatase, Non-Receptor Type 11Major topic
MutationMajor topic
Humans
Signal Transduction
Animals
Protein Conformation

Source PubMed

Grants3

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

Grant, as the record writes itAgencyCountryNIH projectStated bySource
R35 GM138014NIGMS NIH HHSUnited StatesR35GM138014PubMedNIH RePORTER
RSG-23-1038049-01-TBEAmerican Cancer Society (ACS)PubMedPubMed
R35GM138014HHS | NIH | National Institute of General Medical Sciences (NIGMS)R35GM138014PubMedNIH RePORTER

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References147

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

OrderPMIDTitleJournalYearIn PapersSource
132,248,557Autosomal dominant hyper IgE syndrome from a single centre in Chongqing, China (2009-2018).Scand J Immunol2020https://conductscience.org/library/papers/32248557PubMed
241,867,803Cancer-Causing Mutations Alter the Interplay Between Loop Dynamics and Catalysis in the Protein Tyrosine Phosphatases SHP-1 and SHP-2.bioRxiv2026https://conductscience.org/library/papers/41867803PubMed
316,474,405Germline KRAS mutations cause Noonan syndrome.Nat Genet2006https://conductscience.org/library/papers/16474405PubMed
441,225,768The pathogenic E139D mutation stabilizes a non-canonical active state of the multi-domain phosphatase SHP2.Protein Sci2025https://conductscience.org/library/papers/41225768PubMed
524,825,865Integrated genomic sequencing reveals mutational landscape of T-cell prolymphocytic leukemia.Blood2014https://conductscience.org/library/papers/24825865PubMed
640,638,710Scalable emulation of protein equilibrium ensembles with generative deep learning.Science2025https://conductscience.org/library/papers/40638710PubMed
726,889,708The Role of Protein Loops and Linkers in Conformational Dynamics and Allostery.Chem Rev2016https://conductscience.org/library/papers/26889708PubMed
823,584,145Protein tyrosine phosphatase SHP2/PTPN11 mistargeting as a consequence of SH2-domain point mutations associated with Noonan Syndrome and leukemia.J Proteomics2013https://conductscience.org/library/papers/23584145PubMed
917,157,040SHP-2 phosphatase negatively regulates the TRIF adaptor protein-dependent type I interferon and proinflammatory cytokine production.Immunity2006https://conductscience.org/library/papers/17157040PubMed
1035,231,400Receptor tyrosine kinases regulate signal transduction through a liquid-liquid phase separated state.Mol Cell2022https://conductscience.org/library/papers/35231400PubMed

Cited by0

The papers in our copy of PubMed whose reference list names this one, newest first.

None in this release.

Genes0

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

None in this release.

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed
2026-11-06
PubMed
iCite
2026-11-05
iCite
PMC's ID file
2026-11-05
PMC's ID file
NIH RePORTER's grant and paper links
2026-11-01
NIH RePORTER's grant and paper links
Trials
2026-11-12
Gene search
2026-11-11
Pipelines
2026-09-18

Sources 11

  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • HGNCCC0
  • iCiteCC BY 4.0
  • NCBI GenePublic domain (US government)
  • NIH RePORTER's grant and paper linksPublic domain
  • Open TargetsCC0 1.0
  • PMC's ID filePublic domain (US government)
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • HGNCCC0: https://www.genenames.org/about/license/
  • iCiteCC BY 4.0
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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