| Year |
Citation |
Score |
| 2015 |
Gregg KJ, Suits MD, Deng L, Vocadlo DJ, Boraston AB. Structural analysis of a family 101 glycoside hydrolase in complex with carbohydrates reveals insights into its mechanism. The Journal of Biological Chemistry. PMID 26304114 DOI: 10.1074/Jbc.M115.680470 |
0.636 |
|
| 2013 |
Deng L, Tsybina P, Gregg KJ, Mosi R, Zandberg WF, Boraston AB, Vocadlo DJ. Synthesis of 4-methylumbelliferyl α-d-mannopyranosyl-(1→6)-β-d-mannopyranoside and development of a coupled fluorescent assay for GH125 exo-α-1,6-mannosidases. Bioorganic & Medicinal Chemistry. 21: 4839-45. PMID 23816041 DOI: 10.1016/J.Bmc.2013.05.062 |
0.598 |
|
| 2011 |
Gregg KJ, Zandberg WF, Hehemann JH, Whitworth GE, Deng L, Vocadlo DJ, Boraston AB. Analysis of a new family of widely distributed metal-independent alpha-mannosidases provides unique insight into the processing of N-linked glycans. The Journal of Biological Chemistry. 286: 15586-96. PMID 21388958 DOI: 10.1074/Jbc.M111.223172 |
0.634 |
|
| 2009 |
Gregg KJ, Boraston AB. Cloning, recombinant production, crystallization and preliminary X-ray diffraction analysis of a family 101 glycoside hydrolase from Streptococcus pneumoniae. Acta Crystallographica. Section F, Structural Biology and Crystallization Communications. 65: 133-5. PMID 19194003 DOI: 10.1107/S1744309108042474 |
0.638 |
|
| 2009 |
Ficko-Blean E, Gregg KJ, Adams JJ, Hehemann JH, Czjzek M, Smith SP, Boraston AB. Portrait of an enzyme, a complete structural analysis of a multimodular {beta}-N-acetylglucosaminidase from Clostridium perfringens. The Journal of Biological Chemistry. 284: 9876-84. PMID 19193644 DOI: 10.1074/Jbc.M808954200 |
0.656 |
|
| 2009 |
van Bueren AL, Ghinet MG, Gregg K, Fleury A, Brzezinski R, Boraston AB. The structural basis of substrate recognition in an exo-beta-D-glucosaminidase involved in chitosan hydrolysis. Journal of Molecular Biology. 385: 131-9. PMID 18976664 DOI: 10.1016/J.Jmb.2008.10.031 |
0.636 |
|
| 2008 |
Adams JJ, Gregg K, Bayer EA, Boraston AB, Smith SP. Structural basis of Clostridium perfringens toxin complex formation. Proceedings of the National Academy of Sciences of the United States of America. 105: 12194-9. PMID 18716000 DOI: 10.1073/Pnas.0803154105 |
0.628 |
|
| 2008 |
Gregg KJ, Finn R, Abbott DW, Boraston AB. Divergent modes of glycan recognition by a new family of carbohydrate-binding modules. The Journal of Biological Chemistry. 283: 12604-13. PMID 18292090 DOI: 10.1074/Jbc.M709865200 |
0.663 |
|
| 2008 |
Chitayat S, Gregg K, Adams JJ, Ficko-Blean E, Bayer EA, Boraston AB, Smith SP. Three-dimensional structure of a putative non-cellulosomal cohesin module from a Clostridium perfringens family 84 glycoside hydrolase. Journal of Molecular Biology. 375: 20-8. PMID 17999932 DOI: 10.1016/J.Jmb.2007.10.031 |
0.672 |
|
| 2007 |
Chitayat S, Ficko-Blean E, Adams JJ, Gregg K, Boraston AB, Smith SP. NMR assignment of backbone and side chain resonances for a putative protein-protein interaction module from a family 84 glycoside hydrolase of Clostridium perfringens. Biomolecular Nmr Assignments. 1: 7-9. PMID 19636812 DOI: 10.1007/S12104-007-9001-8 |
0.608 |
|
| 2007 |
Chitayat S, Ficko-Blean E, Adams J, Gregg K, Boraston A, Smith S. 1H, 13C, 15N sequence-specific backbone and sidechain resonance assignmentsfor a putative protein-protein interaction module from a family 84 glycosidehydrolase of Clostridium perfringens Journal of Back and Musculoskeletal Rehabilitation. DOI: 10.13018/Bmr7270 |
0.584 |
|
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