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4V3O

Designed armadillo repeat protein with 5 internal repeats, 2nd generation C-cap and 3rd generation N-cap.

Summary for 4V3O
Entry DOI10.2210/pdb4v3o/pdb
Related4V3Q 4V3R
DescriptorYIII_M5_AII, CALCIUM ION, ACETATE ION, ... (4 entities in total)
Functional Keywordsde novo protein, rotein engineering, repeat protein, armadillo repeat
Biological sourceSYNTHETIC CONSTRUCT
Total number of polymer chains4
Total formula weight122732.02
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 citationReichen, 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: 26894544
DOI: 10.1107/S2059798315023116
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2 Å)
Structure validation

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