ArticleEukaryotic cell2011
Physiological and biochemical characterization of AnNitA, the Aspergillus nidulans high-affinity nitrite transporter.
Article in Eukaryotic cell, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
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Who cites it
7 citing papers in PubMed.
- The tumor suppressor folliculin inhibits lactate dehydrogenase A and regulates the Warburg effect.Nature structural & molecular biology · 2021Article
- Comparative genomics reveals high biological diversity and specific adaptations in the industrially and medically important fungal genus Aspergillus.Genome biology · 2017Article
- The C-terminal Six Amino Acids of the FNT Channel FocA Are Required for Formate Translocation But Not Homopentamer Integrity.Frontiers in microbiology · 2017Article
- High-affinity nitrate/nitrite transporters NrtA and NrtB of Aspergillus nidulans exhibit high specificity and different inhibitor sensitivity.Microbiology (Reading, England) · 2015Article
- Pyruvate formate-lyase interacts directly with the formate channel FocA to regulate formate translocation.Journal of molecular biology · 2014Article
- Ion selectivity and gating mechanisms of FNT channels.Current opinion in structural biology · 2013Review
- Pseudo-constitutivity of nitrate-responsive genes in nitrate reductase mutants.Fungal genetics and biology : FG & B · 2013Article
Corrections and comments
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Authors and funding
7 authors.
Funding
Abstract
High-affinity nitrite influx into mycelia of Aspergillus nidulans has been characterized by use of (13)NO(2)(-), giving average K(m) and V(max) values of 48 ± 8 μM and 228 ± 49 nmol mg(-1) dry weight (DW) h(-1), respectively. Kinetic analysis of a plot that included an additional large number of low-concentration fluxes gave an excellent monophasic fit (r(2) = 0.96), with no indication of sigmoidal kinetics. Two-dimensional (2D) and three-dimensional (3D) models of AnNitA are presented, and the possible roles of conserved asparagine residues N122 (transmembrane domain 3 ]Tm 3]), N173 (Tm 4), N214 (Tm 5), and N246 (Tm 6) are discussed.
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Registered trials
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