نتایج جستجو برای: pantothenate kinase

تعداد نتایج: 227686  

Journal: :Journal of bacteriology 1992
W J Song S Jackowski

Pantothenate kinase catalyzes the rate-controlling step in coenzyme A (CoA) biosynthesis. The structural gene (coaA) located at 90 min of the Escherichia coli chromosome was cloned and sequenced. The coaA gene was transcribed in the opposite direction to the flanking genes birA and thrU and produced a single 1.1-kb transcript. Translation of the coaA gene produced two protein products (36.4 and...

2014
Dario Brunetti Sabrina Dusi Carla Giordano Costanza Lamperti Michela Morbin Valeria Fugnanesi Silvia Marchet Gigliola Fagiolari Ody Sibon Maurizio Moggio Giulia d’Amati Valeria Tiranti

Pantothenate kinase-associated neurodegeneration, caused by mutations in the PANK2 gene, is an autosomal recessive disorder characterized by dystonia, dysarthria, rigidity, pigmentary retinal degeneration and brain iron accumulation. PANK2 encodes the mitochondrial enzyme pantothenate kinase type 2, responsible for the phosphorylation of pantothenate or vitamin B5 in the biosynthesis of co-enzy...

2001
Kevin J. Saliba Kiaran Kirk

Pantothenate, the precursor of coenzyme A, is an essential nutrient for the intraerythrocytic stage of the malaria parasite Plasmodium falciparum. Pantothenate enters the malaria-infected erythrocyte via new permeation pathways induced by the parasite in the host cell membrane (Saliba, K. J., Horner, H. A., and Kirk, K. (1998) J. Biol. Chem. 273, 10190–10195). We show here that pantothenate is ...

Journal: :The Journal of biological chemistry 2001
K J Saliba K Kirk

Pantothenate, the precursor of coenzyme A, is an essential nutrient for the intraerythrocytic stage of the malaria parasite Plasmodium falciparum. Pantothenate enters the malaria-infected erythrocyte via new permeation pathways induced by the parasite in the host cell membrane (Saliba, K. J., Horner, H. A., and Kirk, K. (1998) J. Biol. Chem. 273, 10190-10195). We show here that pantothenate is ...

Journal: :Structure 2006
Bum Soo Hong Mi Kyung Yun Yong-Mei Zhang Shigeru Chohnan Charles O Rock Stephen W White Suzanne Jackowski Hee-Won Park Roberta Leonardi

Three distinct isoforms of pantothenate kinase (CoaA) in bacteria catalyze the first step in coenzyme A biosynthesis. The structures of the type II (Staphylococcus aureus, SaCoaA) and type III (Pseudomonas aeruginosa, PaCoaA) enzymes reveal that they assemble nearly identical subunits with actin-like folds into dimers that exhibit distinct biochemical properties. PaCoaA has a fully enclosed pan...

Journal: :PLoS pathogens 2018
Erick T Tjhin Christina Spry Alan L Sewell Annabelle Hoegl Leanne Barnard Anna E Sexton Ghizal Siddiqui Vanessa M Howieson Alexander G Maier Darren J Creek Erick Strauss Rodolfo Marquez Karine Auclair Kevin J Saliba

The malaria-causing blood stage of Plasmodium falciparum requires extracellular pantothenate for proliferation. The parasite converts pantothenate into coenzyme A (CoA) via five enzymes, the first being a pantothenate kinase (PfPanK). Multiple antiplasmodial pantothenate analogues, including pantothenol and CJ-15,801, kill the parasite by targeting CoA biosynthesis/utilisation. Their mechanism ...

2017
George P Paraskevas Christos Yapijakis Anastasia Bougea Vasilios Constantinides Mara Bourbouli Eleftherios Stamboulis Elisabeth Kapaki

Pantothenate-kinase-associated neurodegeneration is the most common autosomal recessive form of neurodegeneration with brain iron accumulation. Less than 100 mutations in PANK2 gene (20p13) are responsible for classic and atypical cases. We report here the first Greek case of atypical pantothenate-kinase-associated neurodegeneration, confirmed by molecular analysis that revealed two trans-actin...

2009
Sung-Hyouk Kim Young-Hee Sung Kee-Hyung Park Yeung-Bae Lee Hyeon-Mi Park Dong Jin Shin Gu-Hwan Kim

Pantothenate kinase-associated neurodegeneration (PKAN) is an autosomal recessive disorder that is characterized by mutations in the pantothenate kinase 2 gene (PANK2) and typical magnetic resonance imaging findings. We report a case of atypical PKAN presenting with generalized dystonia. Our patient had compound heterozygous mutations in the PANK2 gene, including mutation in exon 3 (p.D268G) an...

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