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Ribonucleotide reductase metallocofactor: assembly, maintenance and inhibition 被引量:3
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作者 Caiguo ZHANG Guoqi LIU Mingxia HUANG 《Frontiers in Biology》 CAS CSCD 2014年第2期104-113,共10页
Ribonucleotide rcductase (RNR) supplies cellular deoxyribonucleotidc triphosphates (dNTP) pools by converting ribonucleotides to the corresponding deoxy forms using radical-based chemistry. Eukaryotic RNR comprise... Ribonucleotide rcductase (RNR) supplies cellular deoxyribonucleotidc triphosphates (dNTP) pools by converting ribonucleotides to the corresponding deoxy forms using radical-based chemistry. Eukaryotic RNR comprises a and β subunits: u contains the catalytic and ailosteric sites; β houses a diferric-tyrosyl radical cofactor (FeⅢ2-Y· ) that is required to initiates nucleotide reduction in α. Cells have evolved multi-layered mechanisms to regulate RNR level and activity in order to maintain the adequate sizes and ratios of their dNTP pools to ensure high- fidelity DNA replication and repair. The central role of RNR in nucleotide metabolism also makes it a proven target of chemotherapeutics. In this review, we discuss recent progress in understanding the function and regulation of eukaryofic RNRs, with a focus on studies revealing the cellular machineries involved in RNR metaUocofactor biosynthesis and its implication in RNR-targeting therapeutics. 展开更多
关键词 ribonucleotide reductase (RNR) diferric-tyrosyl radical (FeⅢ2-Y·) iron homeostasis
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