2K32
Truncated AcrA from Campylobacter jejuni for glycosylation studies
Summary for 2K32
| Entry DOI | 10.2210/pdb2k32/pdb |
| Related | 2K33 |
| NMR Information | BMRB: 15735 |
| Descriptor | A (1 entity in total) |
| Functional Keywords | nonglycosylated acra, membrane protein, transport protein |
| Biological source | Campylobacter jejuni |
| Total number of polymer chains | 1 |
| Total formula weight | 12748.24 |
| Authors | Slynko, V.,Schubert, M.,Numao, S.,Kowarik, M.,Aebi, M.,Allain, F. (deposition date: 2008-04-17, release date: 2009-02-03, Last modification date: 2024-05-08) |
| Primary citation | Slynko, V.,Schubert, M.,Numao, S.,Kowarik, M.,Aebi, M.,Allain, F.H. NMR structure determination of a segmentally labeled glycoprotein using in vitro glycosylation. J.Am.Chem.Soc., 131:1274-1281, 2009 Cited by PubMed Abstract: Although there is great interest in three-dimensional structures of glycoproteins and complex oligosaccharides, their structural determination have been hampered by inhomogeneous and incomplete glycosylation, poor expression, low tendency to crystallize, and severe chemical shift overlap. Using segmental labeling of the glycan and the protein component by in vitro glycosylation, we developed a novel method of NMR structural determination that overcomes some of these problems. Highly homogeneously glycosylated proteins in milligram amounts can be obtained. This allowed the determination of the structure of an N-linked glycoprotein from Campylobacter jejuni. The glycosylation acceptor site was found to be in a flexible loop. The presented methodology extends the observable NOE distance limit of oligosaccharides significantly over 4 A, resulting in a high number of distance restraints per glycosidic linkage. A well-defined glycan structure was obtained. PubMed: 19154179DOI: 10.1021/ja808682v PDB entries with the same primary citation |
| Experimental method | SOLUTION NMR |
Structure validation
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