We are examining theoretical aspects of the structure, function, and evolution of proteins with emphasis upon protein sequences and upon those problems for which a computer is essential. We detect distant relationships and infer evolutionary trees of proteins and phylogenetic trees of species in which they occur, using sequence data. We organize all known sequences into the Superfamily List, a hierarchical tabulation with five levels of distinction based on sequence similarity. We plan to develop an improved computer model of the evolutionary process by incorporating additional data on point mutations, parameters for deletion-insertion events, and parameters to allow variable mutability at different positions in the chain. Groups of simulated sequences of known evolutionary distances will be constructed and used to test and improve the performance of our programs for detecting relationships and constructing trees. This grant also partially supports the Atlas of Protein Sequence and Structure Reference Data Center, which contains a complete, currently correct, continuing collection of protein sequence data and files of background information including evolutionary history, distant relationships, alignments, genetic relationships, and three-dimensional structures. The protein sequence data are made available to the scientific ccmmunity in several forms: published volumes of the Atlas of Protein Sequence and Structure and of the Protein Segment Dictionary, and computer-readable tapes of the sequence data. These are periodically updated. Data searches and other computer services using the up-to-date sequence data collection are performed at cost for other research workers upon request. In the 1980-81 grant year we obtained an administrative supplement to support partially the preparation of the information and the development of an efficient computer retrieval system for our Nuclic Acid Sequence Database.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA040474-26
Application #
3180492
Study Section
(SSS)
Project Start
1986-03-01
Project End
1991-02-28
Budget Start
1988-03-01
Budget End
1989-02-28
Support Year
26
Fiscal Year
1988
Total Cost
Indirect Cost
Name
National Biomedical Research Foundation
Department
Type
DUNS #
City
Washington
State
DC
Country
United States
Zip Code
20007
Ron, D; Zannini, M; Lewis, M et al. (1991) A region of proto-dbl essential for its transforming activity shows sequence similarity to a yeast cell cycle gene, CDC24, and the human breakpoint cluster gene, bcr. New Biol 3:372-9
Tsibris, J C; Hunt, L T; Ballejo, G et al. (1989) Selective inhibition of protein disulfide isomerase by estrogens. J Biol Chem 264:13967-70
Hunt, L T; Barker, W C (1989) Avidin-like domain in an epidermal growth factor homolog from a sea urchin. FASEB J 3:1760-4
Lewis, M T; Hunt, L T; Barker, W C (1989) Striking sequence similarity among sialic acid-binding lectin, pancreatic ribonucleases, and angiogenin: possible structural and functional relationships. Protein Seq Data Anal 2:101-5
Hunt, L T; Barker, W C (1988) Identification of a mouse homolog of the human laminin receptor. Nucleic Acids Res 16:5195
Marchalonis, J J; Schluter, S F; Hubbard, R A et al. (1988) Conservation of immunoglobulin variable and joining region structure and the design of universal anti-immunoglobulin antibodies reactive with antigen-binding T cell receptors. Int Rev Immunol 3:241-73
Hunt, L T; Barker, W C (1988) Relationship of promagainin to three other prohormones from the skin of Xenopus laevis: a different perspective. FEBS Lett 233:282-8
Elzanowski, A; Barker, W C; Hunt, L T et al. (1988) Cystatin domains in alpha-2-HS-glycoprotein and fetuin. FEBS Lett 227:167-70
Barker, W C; Hunt, L T; George, D G (1988) Identifying domains in protein sequences. Protein Seq Data Anal 1:363-73
Hunt, L T; Elzanowski, A; Barker, W C (1987) The homology of complement factor C8 gamma chain and alpha-1-microglobulin. Biochem Biophys Res Commun 149:282-8

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