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Diversity and complexity of flavodiiron NO/O2 reductases

期刊

FEMS MICROBIOLOGY LETTERS
卷 365, 期 3, 页码 -

出版社

OXFORD UNIV PRESS
DOI: 10.1093/femsle/fnx267

关键词

flavodiiron; oxygen; nitric oxide; rubredoxin; oxidative stress; nitrosative stress

资金

  1. Portuguese Fundacao para a Ciencia e Tecnologia (FCT) [PTDC/BBB-BQB/3135/2014]
  2. MOSTMICRO Research Unit - FCT [LISBOA-01-0145-FEDER-007660]
  3. FEDER
  4. Fundação para a Ciência e a Tecnologia [PTDC/BBB-BQB/3135/2014] Funding Source: FCT

向作者/读者索取更多资源

Flavodiiron proteins (FDPs) are a family of enzymes endowed with nitric oxide (NO) or oxygen reductase activities, forming the innocuous nitrous oxide (N2O) or water molecules, respectively. FDPs are widespread in the three life kingdoms, and have a modular nature, being each monomer minimally constituted by a metallo-beta-lactamase-like domain containing a catalytic diiron centre, followed by a flavodoxin one, with a flavin mononucleotide. Since their discovery, additional domains have been found in FDPs, attached to the C-terminus, and containing either extra metal (iron) centers or extra flavin binding modules. Following an extensive analysis of genomic databases, we identified novel domain compositions, and proposed a new classification of FDPs in eight classes based on the nature and number of extra

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