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Mutational and structural analyses of the ribonucleotide reductase inhibitor Sml1 define its Rnr1 interaction domain whose inactivation allows suppression of mec1 and rad53 lethality.
Umeå University, Faculty of Medicine, Medical Biochemistry and Biophsyics.ORCID iD: 0000-0003-1708-8259
Umeå University, Faculty of Medicine, Medical Biochemistry and Biophsyics.
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2000 (English)In: Mol Cell Biol, ISSN 0270-7306, Vol. 20, no 23, 9076-83 p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2000. Vol. 20, no 23, 9076-83 p.
Keyword [en]
Cell Cycle Proteins, Chromosomes; Fungal, DNA Mutational Analysis, Enzyme Inhibitors, Fungal Proteins/*genetics, Humans, Mutation; Missense, Protein Binding, Protein Kinases/*genetics, Protein Structure; Secondary, Protein Structure; Tertiary, Protein-Serine-Threonine Kinases, Ribonucleotide Reductases/*antagonists & inhibitors, Saccharomyces cerevisiae Proteins, Solutions, Species Specificity, Suppression; Genetic, Two-Hybrid System Techniques
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URN: urn:nbn:se:umu:diva-10301PubMedID: 11074005OAI: oai:DiVA.org:umu-10301DiVA: diva2:149972
Available from: 2008-08-11 Created: 2008-08-11 Last updated: 2014-06-12Bibliographically approved

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Chabes, AndreiDomkin, VladimirSchleucher, JurgenThelander, Lars

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