7WSB
The ternary complex structure of FtmOx1 with a-ketoglutarate and 13-oxo-fumitremorgin B
Summary for 7WSB
Entry DOI | 10.2210/pdb7wsb/pdb |
Descriptor | Verruculogen synthase, COBALT (II) ION, 13-Oxofumitremorgin B, ... (7 entities in total) |
Functional Keywords | dioxygenase, non-heme, iron dependent, oxidoreductase |
Biological source | Aspergillus fumigatus Af293 |
Total number of polymer chains | 6 |
Total formula weight | 219542.80 |
Authors | Wang, J.,Wang, X.Y.,Wang, Y.Y.,Yan, W.P. (deposition date: 2022-01-28, release date: 2022-07-06, Last modification date: 2023-11-29) |
Primary citation | Zhu, G.,Yan, W.,Wang, X.,Cheng, R.,Naowarojna, N.,Wang, K.,Wang, J.,Song, H.,Wang, Y.,Liu, H.,Xia, X.,Costello, C.E.,Liu, X.,Zhang, L.,Liu, P. Dissecting the Mechanism of the Nonheme Iron Endoperoxidase FtmOx1 Using Substrate Analogues. Jacs Au, 2:1686-1698, 2022 Cited by PubMed Abstract: FtmOx1 is a nonheme iron (NHFe) endoperoxidase, catalyzing three disparate reactions, endoperoxidation, alcohol dehydrogenation, and dealkylation, under in vitro conditions; the diversity complicates its mechanistic studies. In this study, we use two substrate analogues to simplify the FtmOx1-catalyzed reaction to either a dealkylation or an alcohol dehydrogenation reaction for structure-function relationship analysis to address two key FtmOx1 mechanistic questions: (1) Y224 flipping in the proposed COX-like model vs α-ketoglutarate (αKG) rotation proposed in the CarC-like mechanistic model and (2) the involvement of a Y224 radical (COX-like model) or a Y68 radical (CarC-like model) in FtmOx1-catalysis. When 13-oxo-fumitremorgin B () is used as the substrate, FtmOx1-catalysis changes from the endoperoxidation to a hydroxylation reaction and leads to dealkylation. In addition, consistent with the dealkylation side-reaction in the COX-like model prediction, the X-ray structure of the FtmOx1•Co•αKG• ternary complex reveals a flip of Y224 to an alternative conformation relative to the FtmOx1•Fe•αKG binary complex. Verruculogen () was used as a second substrate analogue to study the alcohol dehydrogenation reaction to examine the involvement of the Y224 radical or Y68 radical in FtmOx1-catalysis, and again, the results from the verruculogen reaction are more consistent with the COX-like model. PubMed: 35911443DOI: 10.1021/jacsau.2c00248 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.87 Å) |
Structure validation
Download full validation report