Comparative structural modeling and inference of conserved protein classes in Drosophila seminal fluid

• DOI: 10.1073/pnas.0405579101
• Publication Date: 2004-09-03T00:23:54Z
• Authors: Jacob L. Mueller; Daniel R. Ripoll; Charles F. Aquadro; Mariana F. Wolfner
• Keywords: Male; Models, Molecular; 0303 health sciences; Binding Sites; Molecular Sequence Data; Seminal Plasma Proteins; Lipase; 03 medical and health sciences; Drosophila melanogaster; Ribonucleases; Semen; Lectins; Endopeptidases; Animals; Drosophila Proteins; Intercellular Signaling Peptides and Proteins; Amino Acid Sequence; Peptides; Sequence Alignment; Conserved Sequence

The constituents of seminal fluid are a complex mixture of proteins and other molecules, most of whose functions have yet to be determined and many of which are rapidly evolving. As a step in elucidating the roles of these proteins and exposing potential functional similarities hidden by their rapid evolution, we performed comparative structural modeling on 28 of 52 predicted seminal proteins produced in the Drosophila melanogaster male accessory gland. Each model was characterized by defining residues likely to be important for structure and function. Comparisons of known protein structures with predicted accessory gland proteins (Acps) revealed similarities undetectable by primary sequence alignments. The structures predict that Acps fall into several categories: regulators of proteolysis, lipid modifiers, immunity/protection, sperm-binding proteins, and peptide hormones. The comparative structural modeling approach indicates that major functional classes of mammalian and Drosophila seminal fluid proteins are conserved, despite differences in reproductive strategies. This is particularly striking in the face of the rapid protein sequence evolution that characterizes many reproductive proteins, including Drosophila and mammalian seminal proteins.