Identification and functional characterization of rat riboflavin transporter 2
S Yamamoto, K Inoue, K Ohta, R Fukatsu… - Journal of …, 2009 - academic.oup.com
We have newly identified rat riboflavin transporter 2 (rRFT2) and its human orthologue
(hRFT2), and carried out detailed functional characterization of rRFT2. The mRNA of rRFT2 …
(hRFT2), and carried out detailed functional characterization of rRFT2. The mRNA of rRFT2 …
Flavogenomics–a genomic and structural view of flavin‐dependent proteins
P Macheroux, B Kappes, SE Ealick - The FEBS journal, 2011 - Wiley Online Library
Riboflavin (vitamin B2) serves as the precursor for FMN and FAD in almost all organisms
that utilize the redox‐active isoalloxazine ring system as a coenzyme in enzymatic reactions …
that utilize the redox‐active isoalloxazine ring system as a coenzyme in enzymatic reactions …
[HTML][HTML] From cholesterogenesis to steroidogenesis: role of riboflavin and flavoenzymes in the biosynthesis of vitamin D
JT Pinto, AJL Cooper - Advances in nutrition, 2014 - Elsevier
Flavin-dependent monooxygenases and oxidoreductases are located at critical branch
points in the biosynthesis and metabolism of cholesterol and vitamin D. These flavoproteins …
points in the biosynthesis and metabolism of cholesterol and vitamin D. These flavoproteins …
FAD synthesis and degradation in the nucleus create a local flavin cofactor pool
TA Giancaspero, G Busco, C Panebianco… - Journal of Biological …, 2013 - ASBMB
Background: FAD synthase is known to catalyze the biosynthesis of FAD in cytosol and
mitochondria. Results: The existence of a nuclear FAD synthase and a FAD-hydrolyzing …
mitochondria. Results: The existence of a nuclear FAD synthase and a FAD-hydrolyzing …
Identification of the human mitochondrial FAD transporter and its potential role in multiple acyl-CoA dehydrogenase deficiency
AN Spaan, L IJlst, CWT van Roermund… - Molecular genetics and …, 2005 - Elsevier
Multiple acyl-CoA dehydrogenase deficiency (MADD) or glutaric aciduria type II (GAII) is
most often caused by mutations in the genes encoding the α-or β-subunit of electron transfer …
most often caused by mutations in the genes encoding the α-or β-subunit of electron transfer …
Impaired riboflavin transport due to missense mutations in SLC52A2 causes Brown-Vialetto-Van Laere syndrome
TB Haack, C Makowski, Y Yao, E Graf… - Journal of inherited …, 2012 - Springer
Abstract Brown-Vialetto-Van Laere syndrome (BVVLS [MIM 211530]) is a rare neurological
disorder characterized by infancy onset sensorineural deafness and ponto-bulbar palsy …
disorder characterized by infancy onset sensorineural deafness and ponto-bulbar palsy …
Clinical presentation and outcome of riboflavin transporter deficiency: mini review after five years of experience
B Jaeger, AM Bosch - Journal of inherited metabolic disease, 2016 - Springer
Introduction Riboflavin (vitamin B2) is absorbed in the small intestine by the human
riboflavin transporters RFVT1 and RFVT3. A third riboflavin transporter (RFVT2) is …
riboflavin transporters RFVT1 and RFVT3. A third riboflavin transporter (RFVT2) is …
Riboflavin uptake and FAD synthesis in Saccharomyces cerevisiae mitochondria: involvement of the Flx1p carrier in FAD export
V Bafunno, TA Giancaspero, C Brizio, D Bufano… - Journal of Biological …, 2004 - ASBMB
We have studied the functional steps by which Saccharomyces cerevisiae mitochondria can
synthesize FAD from cytosolic riboflavin (Rf). Riboflavin uptake into mitochondria took place …
synthesize FAD from cytosolic riboflavin (Rf). Riboflavin uptake into mitochondria took place …
The monocarboxylate transporter homolog Mch5p catalyzes riboflavin (vitamin B2) uptake in Saccharomyces cerevisiae
P Reihl, J Stolz - Journal of biological chemistry, 2005 - ASBMB
Riboflavin is a water-soluble vitamin (vitamin B 2) required for the production of the flavin
cofactors FMN and FAD. Mammals are unable to synthesize riboflavin and need a dietary …
cofactors FMN and FAD. Mammals are unable to synthesize riboflavin and need a dietary …
HepG2 cells develop signs of riboflavin deficiency within 4 days of culture in riboflavin-deficient medium
R Werner, KC Manthey, JB Griffin, J Zempleni - The Journal of nutritional …, 2005 - Elsevier
Flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD) are essential
coenzymes in redox reactions. For example, FAD is a coenzyme for both glutathione …
coenzymes in redox reactions. For example, FAD is a coenzyme for both glutathione …