4V3O
Designed armadillo repeat protein with 5 internal repeats, 2nd generation C-cap and 3rd generation N-cap.
Summary for 4V3O
| Entry DOI | 10.2210/pdb4v3o/pdb |
| Related | 4V3Q 4V3R |
| Descriptor | YIII_M5_AII, CALCIUM ION, ACETATE ION, ... (4 entities in total) |
| Functional Keywords | de novo protein, rotein engineering, repeat protein, armadillo repeat |
| Biological source | SYNTHETIC CONSTRUCT |
| Total number of polymer chains | 4 |
| Total formula weight | 122732.02 |
| Authors | Reichen, C.,Madhurantakam, C.,Pluckthun, A.,Mittl, P. (deposition date: 2014-10-20, release date: 2016-01-13, Last modification date: 2024-01-10) |
| Primary citation | Reichen, C.,Madhurantakam, C.,Hansen, S.,Grutter, M.G.,Pluckthun, A.,Mittl, P.R.E. Structures of Designed Armadillo-Repeat Proteins Show Propagation of Inter-Repeat Interface Effects Acta Crystallogr.,Sect.D, 72:168-, 2016 Cited by PubMed Abstract: The armadillo repeat serves as a scaffold for the development of modular peptide-recognition modules. In order to develop such a system, three crystal structures of designed armadillo-repeat proteins with third-generation N-caps (YIII-type), four or five internal repeats (M-type) and second-generation C-caps (AII-type) were determined at 1.8 Å (His-YIIIM4AII), 2.0 Å (His-YIIIM5AII) and 1.95 Å (YIIIM5AII) resolution and compared with those of variants with third-generation C-caps. All constructs are full consensus designs in which the internal repeats have exactly the same sequence, and hence identical conformations of the internal repeats are expected. The N-cap and internal repeats M1 to M3 are indeed extremely similar, but the comparison reveals structural differences in internal repeats M4 and M5 and the C-cap. These differences are caused by long-range effects of the C-cap, contacting molecules in the crystal, and the intrinsic design of the repeat. Unfortunately, the rigid-body movement of the C-terminal part impairs the regular arrangement of internal repeats that forms the putative peptide-binding site. The second-generation C-cap improves the packing of buried residues and thereby the stability of the protein. These considerations are useful for future improvements of an armadillo-repeat-based peptide-recognition system. PubMed: 26894544DOI: 10.1107/S2059798315023116 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2 Å) |
Structure validation
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