Structure-Based Prototyping of Allosteric Inhibitors of Human Uridine/Cytidine Kinase 2 (UCK2).


Journal

Biochemistry
ISSN: 1520-4995
Titre abrégé: Biochemistry
Pays: United States
ID NLM: 0370623

Informations de publication

Date de publication:
01 11 2022
Historique:
pubmed: 4 10 2022
medline: 3 11 2022
entrez: 3 10 2022
Statut: ppublish

Résumé

Pyrimidine nucleotide biosynthesis in humans is a promising chemotherapeutic target for infectious diseases caused by RNA viruses. Because mammalian cells derive pyrimidine ribonucleotides through a combination of

Identifiants

pubmed: 36190114
doi: 10.1021/acs.biochem.2c00451
doi:

Substances chimiques

Pyrimidine Nucleotides 0
UCK2 protein, human EC 2.7.1.48
Uridine WHI7HQ7H85
Uridine Kinase EC 2.7.1.48

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2261-2266

Auteurs

Siavash Mashayekh (S)

Department of Chemistry, Stanford University, Stanford, California 94305, United States.

Lee M Stunkard (LM)

Department of Chemistry, Stanford University, Stanford, California 94305, United States.

Maryline Kienle (M)

Department of Chemistry, Stanford University, Stanford, California 94305, United States.

Irimpan I Mathews (II)

Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, Stanford University, Menlo Park, California 94025, United States.

Chaitan Khosla (C)

Department of Chemistry, Stanford University, Stanford, California 94305, United States.
Department of Chemical Engineering, Stanford University, Stanford, California 94305, United States.
Sarafan ChEM-H, Stanford University, Stanford, California 94305, United States.

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Classifications MeSH