2KYQ
1H, 15N, 13C chemical shifts and structure of CKR-brazzein
Summary for 2KYQ
Entry DOI | 10.2210/pdb2kyq/pdb |
Related | 1BRZ 2KGQ |
NMR Information | BMRB: 16978 |
Descriptor | Defensin-like protein (1 entity in total) |
Functional Keywords | sweet-tasting protein, plant protein |
Biological source | Pentadiplandra brazzeana |
Cellular location | Secreted: P56552 |
Total number of polymer chains | 1 |
Total formula weight | 6408.24 |
Authors | Dittli, S.M.,Assadi-Porter, F.M.,Rao, H.,Tonelli, M. (deposition date: 2010-06-07, release date: 2011-05-18, Last modification date: 2011-11-30) |
Primary citation | Dittli, S.M.,Rao, H.,Tonelli, M.,Quijada, J.,Markley, J.L.,Max, M.,Assadi-Porter, F. Structural role of the terminal disulfide bond in the sweetness of brazzein. Chem Senses, 36:821-830, 2011 Cited by PubMed Abstract: Brazzein, a 54 residue sweet-tasting protein, is thought to participate in a multipoint binding interaction with the sweet taste receptor. Proposed sites for interaction with the receptor include 2 surface loops and the disulfide bond that connects the N- and C-termini. However, the importance of each site is not well understood. To characterize the structural role of the termini in the sweetness of brazzein, the position of the disulfide bond connecting the N- and C-termini was shifted by substituting K3-C4-K5 with C3-K4-R5. The apparent affinity and V(max) of the C3-K4-R5-brazzein (CKR-brazzein) variant were only modestly decreased compared with the wild-type (WT) brazzein. We determined a high-resolution structure of CKR-brazzein by nuclear magnetic resonance spectroscopy (backbone root mean square deviation of 0.39 Å). Comparing the structure of CKR-brazzein with that of WT-brazzein revealed that the terminal β-strands of the variant display extended β-structure and increased dynamics relative to WT-brazzein. These results support previous mutagenesis studies and further suggest that, whereas interactions involving the termini are necessary for full function of brazzein, the termini do not constitute the primary site of interaction between brazzein and the sweet taste receptor. PubMed: 21765060DOI: 10.1093/chemse/bjr057 PDB entries with the same primary citation |
Experimental method | SOLUTION NMR |
Structure validation
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