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Novel Quinazolinone Inhibitors of ALK2 Flip between Alternate Binding Modes: Structure-Activity Relationship, Structural Characterization, Kinase Profiling, and Cellular Proof of Concept.

  • Read more about Novel Quinazolinone Inhibitors of ALK2 Flip between Alternate Binding Modes: Structure-Activity Relationship, Structural Characterization, Kinase Profiling, and Cellular Proof of Concept.

Structural and atropisomeric factors governing the selectivity of pyrimido-benzodiazipinones as inhibitors of kinases and bromodomains.

  • Read more about Structural and atropisomeric factors governing the selectivity of pyrimido-benzodiazipinones as inhibitors of kinases and bromodomains.

Architecture of the native major royal jelly protein 1 oligomer.

  • Read more about Architecture of the native major royal jelly protein 1 oligomer.

The dual methyltransferase METTL13 targets N terminus and Lys55 of eEF1A and modulates codon-specific translation rates.

  • Read more about The dual methyltransferase METTL13 targets N terminus and Lys55 of eEF1A and modulates codon-specific translation rates.

BRAF/MAPK and GSK3 signaling converges to control MITF nuclear export.

  • Read more about BRAF/MAPK and GSK3 signaling converges to control MITF nuclear export.

Extending the Code of Sequence Readout by Gene Regulatory Proteins: The Role of Hoogsteen Base Pairing in p53-DNA Recognition.

  • Read more about Extending the Code of Sequence Readout by Gene Regulatory Proteins: The Role of Hoogsteen Base Pairing in p53-DNA Recognition.

Guaiacol as a drug candidate for treating adult polyglucosan body disease.

  • Read more about Guaiacol as a drug candidate for treating adult polyglucosan body disease.

Chemical Instability and Promiscuity of Arylmethylidenepyrazolinone-based MDMX Inhibitors.

  • Read more about Chemical Instability and Promiscuity of Arylmethylidenepyrazolinone-based MDMX Inhibitors.

Substrate binding allosterically relieves autoinhibition of the pseudokinase TRIB1.

  • Read more about Substrate binding allosterically relieves autoinhibition of the pseudokinase TRIB1.

Covalent inhibitors of EGFR family protein kinases induce degradation of human Tribbles 2 (TRIB2) pseudokinase in cancer cells.

  • Read more about Covalent inhibitors of EGFR family protein kinases induce degradation of human Tribbles 2 (TRIB2) pseudokinase in cancer cells.

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