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| Hargrove TY, Wawrzak Z, Fisher PM, et al. (2018) Binding of a physiological substrate causes large-scale conformational reorganization in cytochrome P450 51. The Journal of Biological Chemistry |
| Wang C, Pallan PS, Zhang W, et al. (2017) Functional Analysis of Human Cytochrome P450 21A2 Variants Involved in Congenital Adrenal Hyperplasia. The Journal of Biological Chemistry |
| Hargrove TY, Friggeri L, Wawrzak Z, et al. (2016) Human sterol 14α-demethylase (CYP51) as a target for anticancer chemotherapy: Towards structure-aided drug design. Journal of Lipid Research |
| Guengerich FP, Waterman MR, Egli M. (2016) Recent Structural Insights into Cytochrome P450 Function. Trends in Pharmacological Sciences |
| Goldstone JV, Sundaramoorthy M, Zhao B, et al. (2015) Genetic and structural analyses of cytochrome P450 hydroxylases in sex hormone biosynthesis: Sequential origin and subsequent coevolution. Molecular Phylogenetics and Evolution |
| Pallan PS, Lei L, Wang C, et al. (2015) Research Resource: Correlating Human Cytochrome P450 21A2 Crystal Structure and Phenotypes of Mutations in Congenital Adrenal Hyperplasia. Molecular Endocrinology (Baltimore, Md.). 29: 1375-84 |
| Lepesheva GI, Hargrove TY, Rachakonda G, et al. (2015) VFV as a New Effective CYP51 Structure-Derived Drug Candidate for Chagas Disease and Visceral Leishmaniasis. The Journal of Infectious Diseases. 212: 1439-48 |
| Pallan PS, Wang C, Lei L, et al. (2015) Human Cytochrome P450 21A2, the Major Steroid 21-Hydroxylase: STRUCTURE OF THE ENZYME·PROGESTERONE SUBSTRATE COMPLEX AND RATE-LIMITING C-H BOND CLEAVAGE. The Journal of Biological Chemistry. 290: 13128-43 |
| Pallan PS, Nagy LD, Lei L, et al. (2015) Structural and kinetic basis of steroid 17α,20-lyase activity in teleost fish cytochrome P450 17A1 and its absence in cytochrome P450 17A2. The Journal of Biological Chemistry. 290: 3248-68 |
| Friggeri L, Hargrove TY, Rachakonda G, et al. (2014) Structural basis for rational design of inhibitors targeting Trypanosoma cruzi sterol 14α-demethylase: two regions of the enzyme molecule potentiate its inhibition. Journal of Medicinal Chemistry. 57: 6704-17 |