Lista de

amino acid substitution
45
"Hidden Structural Codes in Protein Intrinsic Disorder" (2017) Borkosky, S.S.;Camporeale, G.;Chemes, L.B. (...)De Prat Gay, G. Biochemistry. 56(41):5560-5569
"Hidden Structural Codes in Protein Intrinsic Disorder" (2017) Borkosky, S.S.;Camporeale, G.;Chemes, L.B. (...)De Prat Gay, G. Biochemistry. 56(41):5560-5569
"Two novel DNA variants associated with glucose-6-phosphate dehydrogenase deficiency found in Argentine pediatric patients" (2016) Chaves, A.;Eberle, S.E.;Defelipe, L. (...)Feliú-Torres, A. Clinical Biochemistry. 49(10-11):808-810
"Binding of the substrate UDP-glucuronic acid induces conformational changes in the xanthan gum glucuronosyltransferase" (2016) Salinas, S.R.;Petruk, A.A.;Brukman, N.G. (...)Ielpi, L. Protein Engineering, Design and Selection. 29(6):197-207
"Anti-hemagglutinin antibody derived lead peptides for inhibitors of influenza virus binding" (2016) Memczak, H.;Lauster, D.;Kar, P. (...)Stöcklein, W.F.M. PLoS ONE. 11(7)
"More Cercospora species infect soybeans across the Americas than meets the eye" (2015) Soares, A.P.G.;Guillin, E.A.;Borges, L.L. (...)De Oliveira, L.O. PLoS ONE. 10(8)
"Enhancing antibacterial activity against Escherichia coli K-12 of peptide Ib-AMP4 with synthetic analogues" (2014) Flórez-Castillo, J.M.; Perullini, M.; Jobbágy, M.; De Jesús Cano Calle, H. International Journal of Peptide Research and Therapeutics. 20(3):365-369
"Hyperactivation of the human plasma membrane Ca2+ pump PMCA h4xb by mutation of Glu99 to Lys" (2014) Mazzitelli, L.R.; Adamo, H.P. Journal of Biological Chemistry. 289(15):10761-10768
"Tracking the molecular evolution of calcium permeability in a nicotinic acetylcholine receptor" (2014) Lipovsek, M.;Fierro, A.;Pérez, E.G. (...)Elgoyhen, A.B. Molecular Biology and Evolution. 31(12):3250-3265
"Molecular basis of thermal stability in truncated (2/2) hemoglobins" (2014) Bustamante, J.P.;Bonamore, A.;Nadra, A.D. (...)Boechi, L. Biochimica et Biophysica Acta - General Subjects. 1840(7):2281-2288
"Underlying Thermodynamics of pH-Dependent Allostery" (2014) Di Russo, N.V.; Martí, M.A.; Roitberg, A.E. Journal of Physical Chemistry B. 118(45):12818-12826
"Underlying Thermodynamics of pH-Dependent Allostery" (2014) Di Russo, N.V.; Martí, M.A.; Roitberg, A.E. Journal of Physical Chemistry B. 118(45):12818-12826
"Positive modulation of the α9α10 nicotinic cholinergic receptor by ascorbic acid" (2013) Boffi, J.C.;Wedemeyer, C.;Lipovsek, M. (...)Elgoyhen, A.B. British Journal of Pharmacology. 168(4):954-965
"Cellulose microfibril crystallinity is reduced by mutating C-terminal transmembrane region residues CESA1 A903V and CESA3 T942I of cellulose synthase" (2012) Harris, D.M.;Corbin, K.;Wang, T. (...)DeBolt, S. Proceedings of the National Academy of Sciences of the United States of America. 109(11):4098-4103
"The crystal structure of the MAP kinase LmaMPK10 from leishmania major reveals parasite-specific features and regulatory mechanisms" (2012) Horjales, S.;Schmidt-Arras, D.;Limardo, R.R. (...)Buschiazzo, A. Structure. 20(10):1649-1660
"Mutations in two putative phosphorylation motifs in the tomato pollen receptor kinase LePRK2 show antagonistic effects on pollen tube length" (2011) Salem, T.;Mazzella, A.;Barberini, M.L. (...)Muschietti, J. Journal of Biological Chemistry. 286(6):4882-4891
"Molecular basis for the substrate stereoselectivity in tryptophan dioxygenase" (2011) Capece, L.;Lewis-Ballester, A.;Marti, M.A. (...)Yeh, S.-R. Biochemistry. 50(50):10910-10918
"In vitro assembly of the feline immunodeficiency virus Gag polyprotein" (2010) Affranchino, J.L.; González, S.A. Virus Research. 150(1-2):153-157
"In vitro assembly of the feline immunodeficiency virus Gag polyprotein" (2010) Affranchino, J.L.; González, S.A. Virus Research. 150(1-2):153-157
"The effect of active-site isoleucine to alanine mutation on the DHFR catalyzed hydride-transfer" (2010) Stojković, V.;Perissinotti, L.L.;Lee, J. (...)Kohen, A. Chemical Communications. 46(47):8974-8976
"Genetic and biochemical studies in Argentinean patients with variegate porphyria" (2008) Rossetti, M.V.;Granata, B.X.;Giudice, J. (...)Batlle, A. BMC Medical Genetics. 9
"Diagnosis of familial amyloid polyneuropathy type I in Argentina " (2008) Pérez, G.;Romero, M.C.;Trigo, P. (...)Nesse, A. Medicina. 68(4):273-281
"Point mutations in the barley HvHAK1 potassium transporter lead to improved K+-nutrition and enhanced resistance to salt stress" (2008) Mangano, S.; Silberstein, S.; Santa-María, G.E. FEBS Letters. 582(28):3922-3928
"Point mutations in the barley HvHAK1 potassium transporter lead to improved K+-nutrition and enhanced resistance to salt stress" (2008) Mangano, S.; Silberstein, S.; Santa-María, G.E. FEBS Letters. 582(28):3922-3928
"Granulomatous nephritis associated with R334Q mutation in NOD2 [5]" (2007) Meiorin, S.M.;Espada, G.;Costa, C.E. (...)Rose, C.D. Journal of Rheumatology. 34(9):1945-1947
"Dynamical regulation of ligand migration by a gate-opening molecular switch in truncated hemoglobin-N from Mycobacterium tuberculosis" (2007) Bidon-Chanal, A.; Martí, M.A.; Estrin, D.A.; Luque, F.J. Journal of the American Chemical Society. 129(21):6782-6788
"Participation of epididymal cysteine-rich secretory proteins in sperm-egg fusion and their potential use for male fertility regulation" (2007) Cohen, D.J.;Da Ros, V.G.;Busso, D. (...)Cuasnicú, P.S. Asian Journal of Andrology. 9(4):528-532
"Evolutionary history of the Asr gene family" (2006) Frankel, N.; Carrari, F.; Hasson, E.; Iusem, N.D. Gene. 378(1-2):74-83
"Two distinct heme distal site states define Cerebratulus lacteus mini-hemoglobin oxygen affinity" (2006) Martí, M.A.;Bikiel, D.E.;Crespo, A. (...)Estrin, D.A. Proteins: Structure, Function and Genetics. 62(3):641-648
"Update on primary HIV-1 resistance in Argentina: Emergence of mutations conferring high-level resistance to nonnucleoside reverse transcriptase inhibitors in drug-naive patients" (2006) Petroni, A.;Deluchi, G.;Pryluka, D. (...)Benetucci, J.A. Journal of Acquired Immune Deficiency Syndromes. 42(4):506-510
"Associated thrombophilic defects in essential thrombocythaemia: Their relationship with clinical manifestations" (2004) Kornblihtt, L.I.;Heller, P.G.;Correa, G. (...)Molinas, F.C. Thrombosis Research. 112(3):131-135
"Comparative Molecular Population Genetics of the Xdh Locus in the Cactophilic Sibling Species Drosophila buzzatii and D. koepferae" (2004) Piccinali, R.; Aguadé, M.; Hasson, E. Molecular Biology and Evolution. 21(1):141-152
"Transpecific polymorphisms in an inversion linked esterase locus in drosophila buzzatii" (2003) Gómez, G.A.; Hasson, E. Molecular Biology and Evolution. 20(3):410-423
"Adaptive Evolution of the Water Stress-Induced Gene Asr2 in Lycopersicon Species Dwelling in Arid Habitats" (2003) Frankel, N.; Hasson, E.; Iusem, N.D.; Rossi, M.S. Molecular Biology and Evolution. 20(12):1955-1962
"Adaptive Evolution of the Water Stress-Induced Gene Asr2 in Lycopersicon Species Dwelling in Arid Habitats" (2003) Frankel, N.; Hasson, E.; Iusem, N.D.; Rossi, M.S. Molecular Biology and Evolution. 20(12):1955-1962
"Glutathione-like tripeptides as inhibitors of glutathionylspermidine synthetase. Part 1: Substitution of the glycine carboxylic acid group" (2002) Amssoms, K.;Oza, S.L.;Ravaschino, E. (...)Haemers, A. Bioorganic and Medicinal Chemistry Letters. 12(18):2553-2556
"Rapeseed chloroplast thioredoxin-m modulation of the affinity for target proteins" (2001) Duek, P.D.; Wolosiuk, R.A. Biochimica et Biophysica Acta - Protein Structure and Molecular Enzymology. 1546(2):299-311
"Identification of essential amino acids in the bacterial α-mannosyltransferase AceA" (2000) Abdian, P.L.;Lellouch, A.C.;Gautier, C. (...)Geremia, R.A. Journal of Biological Chemistry. 275(51):40568-40575
"Two new mutations (H106P and L178V) in the protoporphyrinogen oxidase gene in Argentinean patients with variegate porphyria." (2000) De Siervi, A.; Parera, V.E.; del C Batlle, A.M.; Rossetti, M.V. Human mutation. 16(6):532
"Two new mutations (H106P and L178V) in the protoporphyrinogen oxidase gene in Argentinean patients with variegate porphyria." (2000) De Siervi, A.; Parera, V.E.; del C Batlle, A.M.; Rossetti, M.V. Human mutation. 16(6):532