Functional prediction: Identification of protein orthologs and paralogs
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[1] Y. Katsube,et al. Three-dimensional structure of a highly thermostable enzyme, 3-isopropylmalate dehydrogenase of Thermus thermophilus at 2.2 A resolution. , 1991, Journal of molecular biology.
[2] D. Strack,et al. Hydroxycinnamoyltransferases Involved in the Accumulation of Caffeic Acid Esters in Gametophytes and Sporophytes of Equisetum arvense , 1996, Plant physiology.
[3] J. Hurley,et al. Determinants of cofactor specificity in isocitrate dehydrogenase: structure of an engineered NADP+ --> NAD+ specificity-reversal mutant. , 1996, Biochemistry.
[4] H. Muirhead,et al. A specific, highly active malate dehydrogenase by redesign of a lactate dehydrogenase framework. , 1988, Science.
[5] R. Huber,et al. The complete genome of the hyperthermophilic bacterium Aquifex aeolicus , 1998, Nature.
[6] D E Koshland,et al. Structure of a bacterial enzyme regulated by phosphorylation, isocitrate dehydrogenase. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[7] L. McAlister-Henn,et al. Subunit structure, expression, and function of NAD(H)-specific isocitrate dehydrogenase in Saccharomyces cerevisiae , 1990, Journal of bacteriology.
[8] P. Serfozo,et al. Substrate determinants of the course of tartrate dehydrogenase-catalyzed reactions. , 1995, Biochemistry.
[9] D. Koshland,et al. Determinants of performance in the isocitrate dehydrogenase of Escherichia coli , 1996, Protein science : a publication of the Protein Society.
[10] L. Hall,et al. Molecular cloning and deduced amino acid sequences of the alpha- and beta- subunits of mammalian NAD(+)-isocitrate dehydrogenase. , 1995, The Biochemical journal.
[11] R. Jensen. Enzyme recruitment in evolution of new function. , 1976, Annual review of microbiology.
[12] P. Gadal,et al. Structure, functions and regulation of NAD and NADP dependent isocitrate dehydrogenases in higher plants and in other organisms , 1990 .
[13] G. Rutter,et al. The binding of Ca2+ ions to pig heart NAD+-isocitrate dehydrogenase and the 2-oxoglutarate dehydrogenase complex. , 1989, The Biochemical journal.
[14] Ridong Chen,et al. A general strategy for enzyme engineering. , 1999, Trends in biotechnology.
[15] D. Lipman,et al. A genomic perspective on protein families. , 1997, Science.
[16] Janet M. Thornton,et al. The future of bioinformatics , 1998 .
[17] A. Dean,et al. A highly active decarboxylating dehydrogenase with rationally inverted coenzyme specificity. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[18] D. Koshland,et al. Structure of isocitrate dehydrogenase with isocitrate, nicotinamide adenine dinucleotide phosphate, and calcium at 2.5-A resolution: a pseudo-Michaelis ternary complex. , 1993, Biochemistry.
[19] P. Gadal,et al. Do the mitochondria provide the 2-oxoglutarate needed for glutamate synthesis in higher plant chloroplasts? , 1990 .
[20] L. McAlister-Henn,et al. Kinetic analysis of NAD(+)-isocitrate dehydrogenase with altered isocitrate binding sites: contribution of IDH1 and IDH2 subunits to regulation and catalysis. , 1993, Biochemistry.
[21] Kay Hofmann,et al. Protein classification and functional assignment , 1998 .
[22] R. Colman,et al. Chemical characterization of distinct subunits of pig heart DPN-specific isocitrate dehydrogenase. , 1980, The Journal of biological chemistry.
[23] P C Babbitt,et al. A functionally diverse enzyme superfamily that abstracts the alpha protons of carboxylic acids , 1995, Science.
[24] A. Dean,et al. The role of glutamate 87 in the kinetic mechanism of Thermus thermophilus isopropylmalate dehydrogenase , 1995, Protein science : a publication of the Protein Society.
[25] A. Dean,et al. Structural constraints in protein engineering--the coenzyme specificity of Escherichia coli isocitrate dehydrogenase. , 1997, European journal of biochemistry.
[26] J. Hurley,et al. Second‐site suppression of regulatory phosphorylation in Escherichia coli isocitrate dehydrogenase , 1996, Protein science : a publication of the Protein Society.
[27] M. Hodges,et al. Molecular characterization of higher plant NAD-dependent isocitrate dehydrogenase: evidence for a heteromeric structure by the complementation of yeast mutants. , 1998, The Plant journal : for cell and molecular biology.
[28] Robert M. Stroud,et al. Catalytic mechanism of NADP(+)-dependent isocitrate dehydrogenase: implications from the structures of magnesium-isocitrate and NADP+ complexes. , 1991 .
[29] D E Koshland,et al. Mutagenesis and Laue structures of enzyme intermediates: isocitrate dehydrogenase. , 1995, Science.
[30] B. Beecher,et al. Tartrate dehydrogenase, a new member of the family of metal-dependent decarboxylating R-hydroxyacid dehydrogenases. , 1994, Archives of biochemistry and biophysics.
[31] A. Dean,et al. Redesigning secondary structure to invert coenzyme specificity in isopropylmalate dehydrogenase. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[32] Michael G. Rossmann,et al. Chemical and biological evolution of a nucleotide-binding protein , 1974, Nature.
[33] L. Hood,et al. Gene families: the taxonomy of protein paralogs and chimeras. , 1997, Science.
[34] J. Hurley,et al. Engineering secondary structure to invert coenzyme specificity in isopropylmalate dehydrogenase , 1997 .