1WLC
Congerin II Y16S/T88I double mutant
Summary for 1WLC
| Entry DOI | 10.2210/pdb1wlc/pdb |
| Related | 1IS3 1WLD |
| Descriptor | Congerin II, 2-(N-MORPHOLINO)-ETHANESULFONIC ACID (3 entities in total) |
| Functional Keywords | galectin, beta-sandwich, thermostability, double-mutant, sugar binding protein |
| Biological source | Conger myriaster (whitespotted conger) |
| Total number of polymer chains | 1 |
| Total formula weight | 15485.31 |
| Authors | Shionyu-Mitsuyama, C.,Ito, Y.,Konno, A.,Miwa, Y.,Ogawa, T.,Muramoto, K.,Shirai, T. (deposition date: 2004-06-22, release date: 2005-06-07, Last modification date: 2024-05-29) |
| Primary citation | Shionyu-Mitsuyama, C.,Ito, Y.,Konno, A.,Miwa, Y.,Ogawa, T.,Muramoto, K.,Shirai, T. In vitro evolutionary thermostabilization of congerin II: a limited reproduction of natural protein evolution by artificial selection pressure J.Mol.Biol., 347:385-397, 2005 Cited by PubMed Abstract: The thermostability of the conger eel galectin, congerin II, was improved by in vitro evolutionary protein engineering. Two rounds of random PCR mutagenesis and selection experiments increased the congerin II thermostability to a level comparative to its naturally thermostable isoform, congerin I. The crystal structures of the most thermostable double mutant, Y16S/T88I, and the related single mutants, Y16S and T88I, were determined at 2.0 angstroms, 1.8 angstroms, and 1.6 angstroms resolution, respectively. The exclusion of two interior water molecules by the Thr88Ile mutation, and the relief of adjacent conformational stress by the Tyr16Ser mutation were the major contributions to the thermostability. These features in the congerin II mutants are similar to those observed in congerin I. The natural evolution of congerin genes, with the K(A)/K(S) ratio of 2.6, was accelerated under natural selection pressures. The thermostabilizing selection pressure artificially applied to congerin II mimicked the implied natural pressure on congerin I. The results showed that the artificial pressure made congerin II partially reproduce the natural evolution of congerin I. PubMed: 15740748DOI: 10.1016/j.jmb.2005.01.027 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2 Å) |
Structure validation
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