Publications

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Solution NMR structures of IgG binding domains with artificially evolved high levels of sequence identity but different folds.
He Y, Yeh DC, Alexander P, Bryan PN, Orban J. 2005. Solution NMR structures of IgG binding domains with artificially evolved high levels of sequence identity but different folds. Biochemistry 44(43): 14055-61.
Directed evolution of highly homologous proteins with different folds by phage display: implications for the protein folding code.
Alexander PA, Rozak DA, Orban J, Bryan PN. 2005. Directed evolution of highly homologous proteins with different folds by phage display: implications for the protein folding code. Biochemistry 44(43): 14045-54.
S100A4, a mediator of metastasis.
Garrett SC, Varney KM, Weber DJ, Bresnick AR. 2006. S100A4, a mediator of metastasis. The Journal of biological chemistry 281(2): 677-80.
Refinement of the solution structure of rat olfactory marker protein (OMP).
Wright NT, Margolis JW, Margolis FL, Weber DJ. 2005. Refinement of the solution structure of rat olfactory marker protein (OMP). Journal of biomolecular NMR 33(1): 63-8.
Patterned assembly of genetically modified viral nanotemplates via nucleic acid hybridization.
Yi H, Nisar S, Lee SY, Powers MA, Bentley WE, Payne GF, Ghodssi R, Rubloff GW, Harris MT, Culver JN. 2005. Patterned assembly of genetically modified viral nanotemplates via nucleic acid hybridization. Nano letters 5(10): 1931-6.
Progress over the first decade of CASP experiments.
Kryshtafovych A, Venclovas C, Fidelis K, Moult J. 2005. Progress over the first decade of CASP experiments. Proteins 61 Suppl 7: 225-36.
Critical assessment of methods of protein structure prediction (CASP)--round 6.
Moult J, Fidelis K, Rost B, Hubbard T, Tramontano A. 2005. Critical assessment of methods of protein structure prediction (CASP)--round 6. Proteins 61 Suppl 7: 3-7.
Protein family clustering for structural genomics.
Yan Y, Moult J. 2005. Protein family clustering for structural genomics. Journal of molecular biology 353(3): 744-59.
The three-dimensional solution structure of Ca(2+)-bound S100A1 as determined by NMR spectroscopy.
Wright NT, Varney KM, Ellis KC, Markowitz J, Gitti RK, Zimmer DB, Weber DJ. 2005. The three-dimensional solution structure of Ca(2+)-bound S100A1 as determined by NMR spectroscopy. Journal of molecular biology 353(2): 410-26.
Loss of protein structure stability as a major causative factor in monogenic disease.
Yue P, Li Z, Moult J. 2005. Loss of protein structure stability as a major causative factor in monogenic disease. Journal of molecular biology 353(2): 459-73.
Lysosomal enzyme delivery by ICAM-1-targeted nanocarriers bypassing glycosylation- and clathrin-dependent endocytosis.
Muro S, Schuchman EH, Muzykantov VR. 2006. Lysosomal enzyme delivery by ICAM-1-targeted nanocarriers bypassing glycosylation- and clathrin-dependent endocytosis. Molecular therapy : the journal of the American Society of Gene Therapy 13(1): 135-41.
Interactions between the archaeal Cdc6 and MCM proteins modulate their biochemical properties.
Kasiviswanathan R, Shin JH, Kelman Z. 2005. Interactions between the archaeal Cdc6 and MCM proteins modulate their biochemical properties. Nucleic acids research 33(15): 4940-50.
Weak alignment NMR: a hawk-eyed view of biomolecular structure.
Bax A, Grishaev A. 2005. Weak alignment NMR: a hawk-eyed view of biomolecular structure. Current opinion in structural biology 15(5): 563-70.
Heterotrimeric G-protein alpha-subunit adopts a "preactivated" conformation when associated with betagamma-subunits.
Abdulaev NG, Ngo T, Zhang C, Dinh A, Brabazon DM, Ridge KD, Marino JP. 2005. Heterotrimeric G-protein alpha-subunit adopts a "preactivated" conformation when associated with betagamma-subunits. The Journal of biological chemistry 280(45): 38071-80.
Selective recognition of synthetic lysine and meso-diaminopimelic acid-type peptidoglycan fragments by human peptidoglycan recognition proteins I{alpha} and S.
Kumar S, Roychowdhury A, Ember B, Wang Q, Guan R, Mariuzza RA, Boons GJ. 2005. Selective recognition of synthetic lysine and meso-diaminopimelic acid-type peptidoglycan fragments by human peptidoglycan recognition proteins I{alpha} and S. The Journal of biological chemistry 280(44): 37005-12.