Homotrimeric, β-Stranded Viral Adhesins and Tail Proteins
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[1] S. Venyaminov,et al. Expression and Properties of Bacteriophage T4 Gene Product 11 , 2001, Biochemistry (Moscow).
[2] W. Rabsch,et al. A comparative study on the frequency of prophages among natural isolates of Salmonella and Escherichia coli with emphasis on generalized transducers , 2004, Antonie van Leeuwenhoek.
[3] G. Lemay,et al. Computational Sequence Analysis of Mammalian Reovirus Proteins , 2004, Virus Genes.
[4] I. Riede. Receptor specificity of the short tail fibres (gp12) of T-even type Escherichia coli phages , 2004, Molecular and General Genetics MGG.
[5] P. Pring-Åkerblom,et al. Adenovirus Type 37 Uses Sialic Acid as a Cellular Receptor on Chang C Cells , 2002, Journal of Virology.
[6] J. Sodroski,et al. Highly Stable Trimers Formed by Human Immunodeficiency Virus Type 1 Envelope Glycoproteins Fused with the Trimeric Motif of T4 Bacteriophage Fibritin , 2002, Journal of Virology.
[7] J. King,et al. The interdigitated β‐helix domain of the P22 tailspike protein acts as a molecular clamp in trimer stabilization , 2002, Protein science : a publication of the Protein Society.
[8] P. Bork,et al. CASH – a β-helix domain widespread among carbohydrate-binding proteins , 2002 .
[9] Fumio Arisaka,et al. Structure of the cell-puncturing device of bacteriophage T4 , 2002, Nature.
[10] Thilo Stehle,et al. Crystal structure of reovirus attachment protein σ1 reveals evolutionary relationship to adenovirus fiber , 2002, The EMBO journal.
[11] P. Bork,et al. CASH--a beta-helix domain widespread among carbohydrate-binding proteins. , 2002, TIBS -Trends in Biochemical Sciences. Regular ed.
[12] B. Berger,et al. betawrap: Successful prediction of parallel β-helices from primary sequence reveals an association with many microbial pathogens , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[13] S. Miller,et al. Crystal structure of a heat and protease-stable part of the bacteriophage T4 short tail fibre. , 2001, Journal of molecular biology.
[14] R. Pickersgill,et al. The architecture of parallel β-helices and related folds , 2001 .
[15] M. Chilosi,et al. Heparan Sulfate Glycosaminoglycans Are Receptors Sufficient To Mediate the Initial Binding of Adenovirus Types 2 and 5 , 2001, Journal of Virology.
[16] G. Schoehn,et al. Identification and Crystallisation of a Heat- and Protease-Stable Fragment of the Bacteriophage T4 Short Tail Fibre , 2001, Biological chemistry.
[17] R. Kammerer,et al. Stabilization of short collagen-like triple helices by protein engineering. , 2001, Journal of molecular biology.
[18] Asma Nusrat,et al. Junction Adhesion Molecule Is a Receptor for Reovirus , 2001, Cell.
[19] R. Pickersgill,et al. The architecture of parallel beta-helices and related folds. , 2001, Progress in biophysics and molecular biology.
[20] M. Rossmann,et al. Structure of bacteriophage T4 gene product 11, the interface between the baseplate and short tail fibers. , 2000, Journal of molecular biology.
[21] I. Molineux,et al. Role of the Gp16 lytic transglycosylase motif in bacteriophage T7 virions at the initiation of infection , 2000, Molecular microbiology.
[22] D. Bamford,et al. Bacteriophage PRD1 DNA entry uses a viral membrane‐associated transglycosylase activity , 2000, Molecular microbiology.
[23] M. Hofnung,et al. The C-Terminal Portion of the Tail Fiber Protein of Bacteriophage Lambda Is Responsible for Binding to LamB, Its Receptor at the Surface of Escherichia coli K-12 , 2000, Journal of bacteriology.
[24] M. Bewley,et al. Structural analysis of the mechanism of adenovirus binding to its human cellular receptor, CAR. , 1999, Science.
[25] Anna Mitraki,et al. A triple β-spiral in the adenovirus fibre shaft reveals a new structural motif for a fibrous protein , 1999, Nature.
[26] M. Rossmann,et al. The structure of bacteriophage T4 gene product 9: the trigger for tail contraction. , 1999, Structure.
[27] S. Miller,et al. Folding of coliphage T4 short tail fiber in vitro. Analysing the role of a bacteriophage-encoded chaperone. , 1999, European journal of biochemistry.
[28] R. Ruigrok,et al. Unfolding studies of human adenovirus type 2 fibre trimers. Evidence for a stable domain. , 1999, European journal of biochemistry.
[29] P. Stewart,et al. Role of αv Integrins in Adenovirus Cell Entry and Gene Delivery , 1999, Microbiology and Molecular Biology Reviews.
[30] J. King,et al. There's a right way and a wrong way: in vivo and in vitro folding, misfolding and subunit assembly of the P22 tailspike. , 1999, Structure.
[31] S. Kanamaru,et al. The C-Terminal Fragment of the Precursor Tail Lysozyme of Bacteriophage T4 Stays as a Structural Component of the Baseplate after Cleavage , 1999, Journal of bacteriology.
[32] R. Lamb,et al. Structural basis for paramyxovirus-mediated membrane fusion. , 1999, Molecular cell.
[33] H. Schmieger. Molecular Survey of the Salmonella Phage Typing System of Anderson , 1999, Journal of bacteriology.
[34] G. Lemay,et al. A glycosyl hydrolase activity of mammalian reovirus sigma1 protein can contribute to viral infection through a mucus layer. , 1999, Journal of molecular biology.
[35] A. Steven,et al. Engineering trimeric fibrous proteins based on bacteriophage T4 adhesins. , 1998, Protein engineering.
[36] M G Rossmann,et al. Structure of bacteriophage T4 fibritin: a segmented coiled coil and the role of the C-terminal domain. , 1997, Structure.
[37] Deborah Fass,et al. Core Structure of gp41 from the HIV Envelope Glycoprotein , 1997, Cell.
[38] S. Steinbacher,et al. Phage P22 tailspike protein: crystal structure of the head-binding domain at 2.3 Å, fully refined structure of the endorhamnosidase at 1.56 Å resolution, and the molecular basis of O-antigen recognition and cleavage1 , 1997, Journal of Molecular Biology.
[39] S. Steinbacher,et al. Interaction of Salmonella Phage P22 with Its O-Antigen Receptor Studied by X-Ray Crystallography , 1997, Biological chemistry.
[40] T. Dermody,et al. Mutations in type 3 reovirus that determine binding to sialic acid are contained in the fibrous tail domain of viral attachment protein sigma1 , 1997, Journal of virology.
[41] J. Bergelson,et al. Isolation of a Common Receptor for Coxsackie B Viruses and Adenoviruses 2 and 5 , 1997, Science.
[42] S. Steinbacher,et al. Crystal structure of phage P22 tailspike protein complexed with Salmonella sp. O-antigen receptors. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[43] J. Conway,et al. Stoichiometry and domainal organization of the long tail-fiber of bacteriophage T4: a hinged viral adhesin. , 1996, Journal of molecular biology.
[44] M. Coffey,et al. Co‐translational trimerization of the reovirus cell attachment protein. , 1996, The EMBO journal.
[45] P. C. Lee,et al. C-terminal Trimerization, but Not N-terminal Trimerization, of the Reovirus Cell Attachment Protein Is a Posttranslational and Hsp70/ATP-dependent Process (*) , 1996, Journal of Biological Chemistry.
[46] M. Nibert,et al. Infectious subvirion particles of reovirus type 3 Dearing exhibit a loss in infectivity and contain a cleaved sigma 1 protein , 1995, Journal of virology.
[47] S Cusack,et al. Adenovirus fiber. , 1995, Current topics in microbiology and immunology.
[48] S. Steinbacher,et al. Crystal structure of P22 tailspike protein: interdigitated subunits in a thermostable trimer. , 1994, Science.
[49] P. Kitts,et al. Cell-binding domain of adenovirus serotype 2 fiber , 1994, Journal of virology.
[50] J. Drake,et al. Molecular Biology of Bacteriophage T4 , 1994 .
[51] S. Miller,et al. Folding and assembly of phage P22 tailspike endorhamnosidase lacking the N-terminal, head-binding domain. , 1993, European journal of biochemistry.
[52] M. Yoder,et al. New domain motif: the structure of pectate lyase C, a secreted plant virulence factor. , 1993, Science.
[53] B L Trus,et al. The short tail-fiber of bacteriophage T4: molecular structure and a mechanism for its conformational transition. , 1993, Virology.
[54] C. Sander,et al. New triple-helical model for the shaft of the adenovirus fibre. , 1992, Journal of molecular biology.
[55] S. Broder,et al. From the National Institutes of Health. , 1992, JAMA.
[56] J. King,et al. Thermal unfolding pathway for the thermostable P22 tailspike endorhamnosidase. , 1991, Biochemistry.
[57] R. Ruigrok,et al. Structure of adenovirus fibre. II. Morphology of single fibres. , 1990, Journal of molecular biology.
[58] B L Trus,et al. Molecular structure of the cell-attachment protein of reovirus: correlation of computer-processed electron micrographs with sequence-based predictions , 1990, Journal of virology.
[59] M. Nibert,et al. Proteolytic digestion of reovirus in the intestinal lumens of neonatal mice , 1989, Journal of virology.
[60] M. Nibert,et al. Sigma 1 protein of mammalian reoviruses extends from the surfaces of viral particles , 1988, Journal of virology.
[61] P. Boulanger,et al. Crystallization, enzymatic cleavage, and the polarity of the adenovirus type 2 fiber. , 1987, Virology.
[62] F. Arisaka,et al. Isolation and characterization of the bacteriophage T4 tail-associated lysozyme , 1985, Journal of virology.
[63] I. Ørskov,et al. Summary of a Workshop on the Clone Concept in the Epidemiology, Taxonomy, and Evolution of the Enterobacteriaceae and other Bacteria , 1983 .
[64] N M Green,et al. Evidence for a repeating cross‐beta sheet structure in the adenovirus fibre. , 1983, The EMBO journal.
[65] I. Katsura. Tail Assembly and Injection , 1983 .
[66] I. Orskov,et al. From the national institutes of health. Summary of a workshop on the clone concept in the epidemiology, taxonomy, and evolution of the enterobacteriaceae and other bacteria. , 1983, The Journal of infectious diseases.
[67] I. Wilson,et al. Structure of the haemagglutinin membrane glycoprotein of influenza virus at 3 Å resolution , 1981, Nature.
[68] W. McClain,et al. Baseplate protein of bacteriophage T4 with both structural and lytic functions , 1980, Journal of virology.
[69] R. Crowther. Mutants of bacteriophage T4 that produce infective fibreless particles. , 1980, Journal of Molecular Biology.
[70] J. Blok,et al. Effect of calcium ions on the infection of Bacillus subtilis by bacteriophage SF 6. , 1979, The Journal of general virology.
[71] W. Wood,et al. Attachment of tail fibers in bacteriophage T4 assembly: role of the phage whiskers. , 1979, Journal of molecular biology.
[72] R A Crowther,et al. Molecular reorganization in the hexagon to star transition of the baseplate of bacteriophage T4. , 1977, Journal of molecular biology.
[73] M. J. Harvey,et al. The potential of Ultrogel®, an agarose‐polyacrylamide copolymer, as a matrix for affinity chromatography , 1976, FEBS letters.
[74] S. Iwashita,et al. Enzymic and molecular properties of base-plate parts of bacteriophage P22. , 1976, European journal of biochemistry.
[75] J. King,et al. Bacteriophage T4 tail assembly: structural proteins and their genetic identification. , 1973, Journal of molecular biology.
[76] J. King,et al. Polypeptides of the tail fibres of bacteriophage T4. , 1971, Journal of molecular biology.
[77] L. Simon. The infection of Escherichia coli by T2 and T4 bacteriophages as seen in the electron microscope. 3. Membrane-associated intracellular bacteriophages. , 1969, Virology.
[78] L. Simon,et al. The infection of Escherichia coli by T2 and T4 bacteriophages as seen in the electron microscope. I. Attachment and penetration. , 1967, Virology.