Mechanistically diverse enzyme superfamilies represent sets of divergent proteins whose substrates, products and even overall functions can be substantially different. Divergent evolution of such broadly varied chemical reactions can be described by the chemistry-constrained model of enzyme evolution, in which nature re-engineers the ancestral scaffold for a variety of functions by conserving a fundamental chemical capability such as a partial reaction, while evolving variations in substrate binding, and therefore overall chemistry. This renewal proposal has three aims, which extend the progress achieved in the previous grant. 1) Investigate additional mechanistically diverse enzyme superfamilies to determine how the delivery of catalysis is constrained by the common catalytic module in each. We will also detail for each how new catalysts have arisen to perform a variety of functions. We expect the results to reveal general principles of enzyme design utilized in nature and identify specific rules applicable for functional inference and mechanistic understanding for each of the superfamilies investigated. These rules will be used to predict molecular function/functional properties of superfamily sequences. This information will be made available to the scientific community via our """"""""Structure-Function Linkage Database (SFLD)"""""""" to aid others in inference of function and to guide protein engineering/design for applications to human health. 2) Identify sequence/structural differences that discriminate subgroups/families in characterized superfamilies to achieve more precision in functional inference than can be obtained by prediction of the superfamily-common functions alone. Because members of mechanistically diverse superfamilies show high levels of misannotation in public databases, we will also use this information to identify and correct misannotated sequences in these superfamilies to the extent possible. 3) Investigate superfamilies that utilize complex co-factors to learn how such superfamilies differ from the relatively more """"""""simple"""""""" types of superfamilies we have previously studied. These studies will focus first on superfamilies that use FAD cofactors.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
3R01GM060595-09S1
Application #
7849996
Study Section
Special Emphasis Panel (ZRG1-BCMB-Q (02))
Program Officer
Jones, Warren
Project Start
2000-03-01
Project End
2011-06-30
Budget Start
2008-08-01
Budget End
2011-06-30
Support Year
9
Fiscal Year
2009
Total Cost
$216,611
Indirect Cost
Name
University of California San Francisco
Department
Pharmacology
Type
Schools of Pharmacy
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Holliday, Gemma L; Akiva, Eyal; Meng, Elaine C et al. (2018) Atlas of the Radical SAM Superfamily: Divergent Evolution of Function Using a ""Plug and Play"" Domain. Methods Enzymol 606:1-71
Davidson, Rebecca; Baas, Bert-Jan; Akiva, Eyal et al. (2018) A global view of structure-function relationships in the tautomerase superfamily. J Biol Chem 293:2342-2357
LeVieux, Jake A; Baas, Bert-Jan; Kaoud, Tamer S et al. (2017) Kinetic and structural characterization of a cis-3-Chloroacrylic acid dehalogenase homologue in Pseudomonas sp. UW4: A potential step between subgroups in the tautomerase superfamily. Arch Biochem Biophys 636:50-56
Knutson, Stacy T; Westwood, Brian M; Leuthaeuser, Janelle B et al. (2017) An approach to functionally relevant clustering of the protein universe: Active site profile-based clustering of protein structures and sequences. Protein Sci 26:677-699
Finn, Robert D; Attwood, Teresa K; Babbitt, Patricia C et al. (2017) InterPro in 2017-beyond protein family and domain annotations. Nucleic Acids Res 45:D190-D199
Holliday, Gemma L; Davidson, Rebecca; Akiva, Eyal et al. (2017) Evaluating Functional Annotations of Enzymes Using the Gene Ontology. Methods Mol Biol 1446:111-132
Harper, Angela F; Leuthaeuser, Janelle B; Babbitt, Patricia C et al. (2017) An Atlas of Peroxiredoxins Created Using an Active Site Profile-Based Approach to Functionally Relevant Clustering of Proteins. PLoS Comput Biol 13:e1005284
Holliday, Gemma L; Brown, Shoshana D; Akiva, Eyal et al. (2017) Biocuration in the structure-function linkage database: the anatomy of a superfamily. Database (Oxford) 2017:
Holliday, Gemma L; Brown, Shoshana D; Akiva, Eyal et al. (2017) Biocuration in the structure-function linkage database: the anatomy of a superfamily. Database (Oxford) 2017:
Akiva, Eyal; Copp, Janine N; Tokuriki, Nobuhiko et al. (2017) Evolutionary and molecular foundations of multiple contemporary functions of the nitroreductase superfamily. Proc Natl Acad Sci U S A 114:E9549-E9558

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