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Journal Abstract Search

272 related items for PubMed ID: 12079353

  • 21. Understanding how noncatalytic carbohydrate binding modules can display specificity for xyloglucan.
    Luís AS, Venditto I, Temple MJ, Rogowski A, Baslé A, Xue J, Knox JP, Prates JA, Ferreira LM, Fontes CM, Najmudin S, Gilbert HJ.
    J Biol Chem; 2013 Feb 15; 288(7):4799-809. PubMed ID: 23229556
    [Abstract] [Full Text] [Related]

  • 22. Molecular determinants of ligand specificity in family 11 carbohydrate binding modules: an NMR, X-ray crystallography and computational chemistry approach.
    Viegas A, Brás NF, Cerqueira NM, Fernandes PA, Prates JA, Fontes CM, Bruix M, Romão MJ, Carvalho AL, Ramos MJ, Macedo AL, Cabrita EJ.
    FEBS J; 2008 May 15; 275(10):2524-35. PubMed ID: 18422658
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  • 27. Carbohydrate-binding domains: multiplicity of biological roles.
    Guillén D, Sánchez S, Rodríguez-Sanoja R.
    Appl Microbiol Biotechnol; 2010 Feb 15; 85(5):1241-9. PubMed ID: 19908036
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  • 29. The overall architecture and receptor binding of pneumococcal carbohydrate-antigen-hydrolyzing enzymes.
    Higgins MA, Ficko-Blean E, Meloncelli PJ, Lowary TL, Boraston AB.
    J Mol Biol; 2011 Sep 02; 411(5):1017-36. PubMed ID: 21767550
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  • 30. Family 6 carbohydrate binding modules recognize the non-reducing end of beta-1,3-linked glucans by presenting a unique ligand binding surface.
    van Bueren AL, Morland C, Gilbert HJ, Boraston AB.
    J Biol Chem; 2005 Jan 07; 280(1):530-7. PubMed ID: 15501830
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  • 32. Cello-oligomer-binding dynamics and directionality in family 4 carbohydrate-binding modules.
    Kognole AA, Payne CM.
    Glycobiology; 2015 Oct 07; 25(10):1100-11. PubMed ID: 26153106
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  • 33. Analysis of nasturtium TmNXG1 complexes by crystallography and molecular dynamics provides detailed insight into substrate recognition by family GH16 xyloglucan endo-transglycosylases and endo-hydrolases.
    Mark P, Baumann MJ, Eklöf JM, Gullfot F, Michel G, Kallas AM, Teeri TT, Brumer H, Czjzek M.
    Proteins; 2009 Jun 07; 75(4):820-36. PubMed ID: 19004021
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  • 35. Structural basis for enantiomer binding and separation of a common beta-blocker: crystal structure of cellobiohydrolase Cel7A with bound (S)-propranolol at 1.9 A resolution.
    Ståhlberg J, Henriksson H, Divne C, Isaksson R, Pettersson G, Johansson G, Jones TA.
    J Mol Biol; 2001 Jan 05; 305(1):79-93. PubMed ID: 11114249
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  • 36. X-ray crystal structures of Phanerochaete chrysosporium Laminarinase 16A in complex with products from lichenin and laminarin hydrolysis.
    Vasur J, Kawai R, Andersson E, Igarashi K, Sandgren M, Samejima M, Ståhlberg J.
    FEBS J; 2009 Jul 05; 276(14):3858-69. PubMed ID: 19769746
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  • 37. Structures of mutants of cellulase Cel48F of Clostridium cellulolyticum in complex with long hemithiocellooligosaccharides give rise to a new view of the substrate pathway during processive action.
    Parsiegla G, Reverbel C, Tardif C, Driguez H, Haser R.
    J Mol Biol; 2008 Jan 11; 375(2):499-510. PubMed ID: 18035374
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  • 38. The structure and characterization of a modular endo-beta-1,4-mannanase from Cellulomonas fimi.
    Le Nours J, Anderson L, Stoll D, Stålbrand H, Lo Leggio L.
    Biochemistry; 2005 Sep 27; 44(38):12700-8. PubMed ID: 16171384
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  • 39. Re-engineering specificity in 1,3-1, 4-β-glucanase to accept branched xyloglucan substrates.
    Addington T, Calisto B, Alfonso-Prieto M, Rovira C, Fita I, Planas A.
    Proteins; 2011 Feb 27; 79(2):365-75. PubMed ID: 21069723
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