Structural studies of duck δ2 crystallin mutants provide insight into the role of Thr161 and the 280s loop in catalysis
| Autor: | P. Lynne Howell, Yuri D. Lobsanov, Penelope W. Codding, Liliana M. Sampaleanu, May Tsai, Cathy Horvatin, G. David Smith |
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| Rok vydání: | 2004 |
| Předmět: |
Models
Molecular Protein Folding Protein Conformation Stereochemistry Molecular Sequence Data delta-Crystallins Crystallography X-Ray Biochemistry Argininosuccinic Acid Avian Proteins Protein structure Crystallin Animals Protein Isoforms Amino Acid Sequence Binding site Threonine Molecular Biology Binding Sites Molecular Structure biology Chemistry Active site Cell Biology Lyase Argininosuccinate lyase Ducks Mutation Mutagenesis Site-Directed biology.protein Protein folding Crystallization Protein Binding Research Article |
| Zdroj: | Biochemical Journal. 384:437-447 |
| ISSN: | 1470-8728 0264-6021 |
| DOI: | 10.1042/bj20040656 |
| Popis: | Delta crystallin, a taxon-specific crystallin present in avian eye lenses, is homologous to the urea cycle enzyme ASL (argininosuccinate lyase). Although there are two delta crystallin isoforms in duck lenses, ddeltac1 (duck delta1 crystallin) and ddeltac2 (duck delta2 crystallin), only ddeltac2 is catalytically active. Previous structural studies have suggested that residues Ser283 and His162 in the multi-subunit active site of ddeltac2/ASL are the putative catalytic acid/base, while the highly conserved, positively charged Lys289 is thought to help stabilize the carbanion intermediate. The strict conservation of a small hydroxy-containing residue (Thr or Ser) at position 161 adjacent to the putative catalytic base, as well as its proximity to the substrate in the S283A ddeltac2 enzyme-substrate complex, prompted us to investigate further the role this residue. Structures of the active T161S and inactive T161D ddeltac2 mutants, as well as T161D complexed with argininosuccinate, have been determined to 2.0 A resolution. The structures suggest that a hydroxy group is required at position 161 to help correctly position the side chain of Lys289 and the fumarate moiety of the substrate. Threonine is probably favoured over serine, because the interaction of its methyl group with Leu206 would restrict its conformational flexibility. Residues larger than Thr or Ser interfere with substrate binding, supporting previous suggestions that correct positioning of the substrate's fumarate moiety is essential for catalysis to occur. The presence of the 280s loop (i.e. a loop formed by residues 270-290) in the 'open' conformation suggests that loop closure, thought to be essential for sequestration of the substrate, may be triggered by the formation of the carbanion or aci-carboxylate intermediates, whose charge distribution more closely mimics that of the sulphate ion found in the active-site region of the inactive ddeltac1. The 280s loop in ddeltac1 is in the closed conformation. |
| Databáze: | OpenAIRE |
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