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The Many Faces of Histidine Triad Nucleotide Binding Protein 1 (HINT1).

Maxwell DillenburgJacob SmithCarston R Wagner
Published in: ACS pharmacology & translational science (2023)
The histidine triad nucleotide binding protein 1 (HINT1) is a nucleoside phosphoramidase that has garnered interest due to its widespread expression and participation in a broad range of biological processes. Herein, we discuss the role of HINT1 as a regulator of several CNS functions, tumor suppressor, and mast cell activator via its interactions with multiple G-protein-coupled receptors and transcription factors. Importantly, altered HINT1 expression and mutation are connected to the progression of multiple disease states, including several neuropsychiatric disorders, peripheral neuropathy, and tumorigenesis. Additionally, due to its involvement in the activation of several clinically used phosphoramidate prodrugs, tremendous efforts have been made to better understand the interactions behind nucleoside binding and phosphoramidate hydrolysis by HINT1. We detail the substrate specificity and catalytic mechanism of HINT1 hydrolysis, while highlighting the structural biology behind these efforts. The aim of this review is to summarize the multitude of biological and pharmacological functions in which HINT1 participates while addressing the areas of need for future research.
Keyphrases
  • binding protein
  • poor prognosis
  • transcription factor
  • blood brain barrier
  • dna binding
  • long non coding rna
  • anaerobic digestion
  • nuclear factor
  • inflammatory response
  • toll like receptor