1U9P
Permuted single-chain Arc
Summary for 1U9P
Entry DOI | 10.2210/pdb1u9p/pdb |
Descriptor | pArc (2 entities in total) |
Functional Keywords | arc, parc, unknown function |
Biological source | Escherichia coli |
Total number of polymer chains | 1 |
Total formula weight | 13760.58 |
Authors | Tabtiang, R.K.,Cezairliyan, B.O.,Grant, R.A.,Cochrane, J.C.,Sauer, R.T. (deposition date: 2004-08-10, release date: 2005-02-15, Last modification date: 2024-02-14) |
Primary citation | Tabtiang, R.K.,Cezairliyan, B.O.,Grant, R.A.,Cochrane, J.C.,Sauer, R.T. Consolidating critical binding determinants by noncyclic rearrangement of protein secondary structure Proc.Natl.Acad.Sci.Usa, 102:2305-2309, 2005 Cited by PubMed Abstract: We designed a single-chain variant of the Arc repressor homodimer in which the beta strands that contact operator DNA are connected by a hairpin turn and the alpha helices that form the tetrahelical scaffold of the dimer are attached by a short linker. The designed protein represents a noncyclic permutation of secondary structural elements in another single-chain Arc molecule (Arc-L1-Arc), in which the two subunits are fused by a single linker. The permuted protein binds operator DNA with nanomolar affinity, refolds on the sub-millisecond time scale, and is as stable as Arc-L1-Arc. The crystal structure of the permuted protein reveals an essentially wild-type fold, demonstrating that crucial folding information is not encoded in the wild-type order of secondary structure. Noncyclic rearrangement of secondary structure may allow grouping of critical active-site residues in other proteins and could be a useful tool for protein design and minimization. PubMed: 15689399DOI: 10.1073/pnas.0409562102 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.9 Å) |
Structure validation
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