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    Publisher: Academic Journals Inc., USA
   
  American Journal of Biochemistry and Molecular Biology is a peer-reviewed international journal dedicated to provide an active forum to the global scientific community for publishing and disseminating high quality research work in the field of biochemistry and molecular biology. Scope of the journal includes: General biochemistry, pathobiochemistry, molecular and cellular biology, molecular medicine, experimental methodologies and the diagnosis, therapy and monitoring of human disease, Host pathogen interaction, molecular detection of pathogen, current advancements in diagnostic techniques, structure, function, and regulation of biologically active molecules, cell signalling, cell cycle, gene structure and expression, gene editing, biochemical mechanisms, protein biosynthesis, protein folding and protein modelling.
  Editor-in-Chief:  Ashok K. Munjal
 
 
Agrimi, G., A. Russo, C.L. Pierri and F. Palmieri, 2012. The peroxisomal NAD+ carrier of Arabidopsis thaliana transports coenzyme A and its derivatives. J. Bioenergy Biomembr., 44: 333-340.
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Amoedo, N.D., G. Punzi, E. Obre, D. Lacombe, A. De Grassi, C.L. Pierri and R. Rossignol, 2016. AGC1/2, the mitochondrial aspartate-glutamate carriers. Biochim. Biophys. Acta Mol. Cell. Res., 1863: 2394-2412.
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Bossis, F., A. De Grassi, L.L. Palese and C.L. Pierri, 2014. Prediction of high-and low-affinity quinol-analogue-binding sites in the aa3 and bo3 terminal oxidases from Bacillus subtilis and Escherichia coli. Biochem. J., 461: 305-314.
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Carrozzo, R., A. Torraco, G. Fiermonte, D. Martinelli and M. Di Nottia et al., 2014. Riboflavin responsive mitochondrial myopathy is a new phenotype of dihydrolipoamide dehydrogenase deficiency. The chaperon-like effect of vitamin B2. Mitochondrion, 18: 49-57.
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Chaouch, A., V. Porcelli, D. Cox, S. Edvardson and P. Scarcia et al., 2014. Mutations in the mitochondrial citrate carrier SLC25A1 are associated with impaired neuromuscular transmission. J. Neuromuscular Dis., 1: 75-90.
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Cigliola, V., C. Populaire, C.L. Pierri, S. Deutsch and J.A. Haefliger et al., 2016. A variant of GJD2, encoding for connexin 36, alters the function of insulin producing β-cells. Plos One, Vol. 11. 10.1371/journal.pone.0150880.
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Curcio, R., L. Muto, C.L. Pierri, A. Montalto and G. Lauria et al., 2016. New insights about the structural rearrangements required for substrate translocation in the bovine mitochondrial oxoglutarate carrier. Biochim. Biophys. Acta Proteins Proteomics, 1864: 1473-1480.
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De Paola, D., E. Blanco, C.L. Pierri and G. Sonnante, 2012. Isolation and characterization of novel variants of BBI coding genes from the legume Lathyrus sativus. Plant Physiol. Biochem., 57: 45-53.
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Edvardson, S., V. Porcelli, C. Jalas, D. Soiferman and Y. Kellner et al., 2013. Agenesis of corpus callosum and optic nerve hypoplasia due to mutations in SLC25A1 encoding the mitochondrial citrate transporter. J. Med. Genet., 50: 240-245.
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Fiermonte, G., G. Parisi, D. Martinelli, F. De Leonardis and G. Torre et al., 2011. A new Caucasian case of neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD): A clinical, molecular and functional study. Mol. Genet. Metab., 104: 501-506.
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Gibellini, L., M. Pinti, F. Beretti, C.L. Pierri and A. Onofrio et al., 2014. Sirtuin 3 interacts with Lon protease and regulates its acetylation status. Mitochondrion, 18: 76-81.
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Lauria, G., G. Lauria, P. Sanchez, B.M.D. Rocca and C.L. Pierri et al., 2008. Structural-dynamical properties of the transmembrane segment VI of the mitochondrial oxoglutarate carrier studied by site directed spin-labeling. Mol. Membr. Biol., 25: 236-244.
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Lunetti, P., A.R. Cappello, R.M. Marsano, C.L. Pierri and C. Carrisi et al., 2013. Mitochondrial glutamate carriers from Drosophila melanogaster: Biochemical, evolutionary and modeling studies. Biochim. Biophys. Acta Bioenerg., 1827: 1245-1255.
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Marobbio, C.M., G. Giannuzzi, E. Paradies, C.L. Pierri and F. Palmieri, 2008. α-isopropylmalate, a leucine biosynthesis intermediate in yeast, is transported by the mitochondrial oxalacetate carrier. J. Biol. Chem., 283: 28445-28453.
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Marobbio, C.M., G. Punzi, C.L. Pierri, L. Palmieri, R. Calvello, M.A. Panaro and F. Palmieri, 2015. Pathogenic potential of SLC25A15 mutations assessed by transport assays and complementation of Saccharomyces cerevisiae ORT1 null mutant. Mol. Genet. Metab., 115: 27-32.
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Onofrio, A., G. Parisi, G. Punzi, S. Todisco and M.A. Di Noia et al., 2014. Distance-dependent hydrophobic-hydrophobic contacts in protein folding simulations. Phys. Chem. Chem. Phys., 16: 18907-18917.
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Palmieri, E.M., I. Spera, A. Menga, V. Infantino and V. Porcelli et al., 2015. Acetylation of human mitochondrial citrate carrier modulates mitochondrial citrate/malate exchange activity to sustain NADPH production during macrophage activation. Biochim. Biophys. Acta Bioenerg., 1847: 729-738.
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Palmieri, F. and C.L. Pierri, 2010. Mitochondrial metabolite transport. Essays Biochem., 47: 37-52.
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Palmieri, F. and C.L. Pierri, 2010. Structure and function of mitochondrial carriers: Role of the transmembrane helix P and G residues in the gating and transport mechanism. FEBS Lett., 584: 1931-1939.
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Palmieri, F., C.L. Pierri, A. De Grassi, A. Nunes-Nesi and A.R. Fernie, 2011. Evolution, structure and function of mitochondrial carriers: A review with new insights. Plant J., 66: 161-181.
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Pierri, C.L., A. De Grassi and A. Turi, 2008. Lattices for ab initio protein structure prediction. Proteins Struct. Funct. Bioinf., 73: 351-361.
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Pierri, C.L., F. Bossis, G. Punzi, A. De Grassi, M. Cetrone, G. Parisi and D. Tricarico, 2016. Molecular modeling of antibodies for the treatment of TNFα-related immunological diseases. Pharmacol. Res. Perspect., Vol. 4. 10.1002/prp2.197.
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Pierri, C.L., F. Palmieri and A. De Grassi, 2014. Single-nucleotide evolution quantifies the importance of each site along the structure of mitochondrial carriers. Cell. Mol. Life Sci., 71: 349-364.
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Pierri, C.L., G. Parisi and V. Porcelli, 2010. Computational approaches for protein function prediction: A combined strategy from multiple sequence alignment to molecular docking-based virtual screening. Biochim. Biophys. Acta Proteins Proteomics, 1804: 1695-1712.
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Pietropaolo, A., C.L. Pierri, F. Palmieri and M. Klingenberg, 2016. Dataset of the AAC2 conformations in the c-, intermediate- and m-states obtained from free-energy simulations. Data Brief, 7: 1355-1357.
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Pietropaolo, A., C.L. Pierri, F. Palmieri and M. Klingenberg, 2016. The switching mechanism of the mitochondrial ADP/ATP carrier explored by free-energy landscapes. Biochim. Biophys. Acta Bioenerg., 1857: 772-781.
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Regalado, A., C.L. Pierri, M. Bitetto, V.L. Laera and C. Pimentel et al., 2013. Characterization of mitochondrial dicarboxylate/tricarboxylate transporters from grape berries. Planta, 237: 693-703.
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Shteyer, E., S. Edvardson, S.L. Wynia-Smith, C.L. Pierri and T. Zangen et al., 2015. Truncating mutation in the nitric oxide synthase 1 gene is associated with infantile achalasia. Gastroenterology, 148: 533-536.
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Sonnante, G., R. D'Amore, E. Blanco, C.L. Pierri and M. De Palma et al., 2010. Novel hydroxycinnamoyl-coenzyme A quinate transferase genes from artichoke are involved in the synthesis of chlorogenic acid. Plant Physiol., 153: 1224-1238.
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Ta-Shma, A., C.L. Pierri, P. Stepensky, A. Shaag, S. Zenvirt, O. Elpeleg and A.J. Rein, 2013. Isolated truncus arteriosus associated with a mutation in the plexin-D1 gene. Am. J. Med. Genet. Part A, 161: 3115-3120.
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Tessa, A., G. Fiermonte, C. Dionisi-Vici, E. Paradies and M.R. Baumgartner et al., 2009. Identification of novel mutations in the SLC25A15 gene in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome: A clinical, molecular and functional study. Hum. Mutat., 30: 741-748.
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Todisco, S., M.A. Di Noia, A. Onofrio, G. Parisi and G. Punzi et al., 2016. Identification of new highly selective inhibitors of the human ADP/ATP carriers by molecular docking and in vitro transport assays. Biochem. Pharmacol., 100: 112-132.
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Vozza, A., F. De Leonardis, E. Paradies, A. De Grassi and C.L. Pierri et al., 2016. Biochemical characterization of a new mitochondrial transporter of dephosphocoenzyme A in Drosophila melanogaster. Biochim. Biophys. Acta Bioenerg., 1858: 137-146.
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Wibom, R., F.M. Lasorsa, V. Tohonen, M. Barbaro and F.H. Sterky et al., 2009. AGC1 deficiency associated with global cerebral hypomyelination. N. Engl. J. Med., 361: 489-495.
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