7NDW
ThyX-FADH2 soaked with 20 mM Formaldehyde
7NDW の概要
エントリーDOI | 10.2210/pdb7ndw/pdb |
分子名称 | Flavin-dependent thymidylate synthase, [[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-bis(oxidanyl)oxolan-2-yl]methoxy-oxidanyl-phosphoryl] [(2R,3S,4S)-5-[5-methanoyl-7,8-dimethyl-2,4-bis(oxidanylidene)-1H-benzo[g]pteridin-10-yl]-2,3,4-tris(oxidanyl)pentyl] hydrogen phosphate, DI(HYDROXYETHYL)ETHER, ... (7 entities in total) |
機能のキーワード | flavin-dependent thymidylate synthase, methylenetetrahydrofolate, transferase |
由来する生物種 | Thermotoga maritima |
タンパク質・核酸の鎖数 | 4 |
化学式量合計 | 114442.98 |
構造登録者 | |
主引用文献 | Bou-Nader, C.,Stull, F.W.,Pecqueur, L.,Simon, P.,Guerineau, V.,Royant, A.,Fontecave, M.,Lombard, M.,Palfey, B.A.,Hamdane, D. An enzymatic activation of formaldehyde for nucleotide methylation. Nat Commun, 12:4542-4542, 2021 Cited by PubMed Abstract: Folate enzyme cofactors and their derivatives have the unique ability to provide a single carbon unit at different oxidation levels for the de novo synthesis of amino-acids, purines, or thymidylate, an essential DNA nucleotide. How these cofactors mediate methylene transfer is not fully settled yet, particularly with regard to how the methylene is transferred to the methylene acceptor. Here, we uncovered that the bacterial thymidylate synthase ThyX, which relies on both folate and flavin for activity, can also use a formaldehyde-shunt to directly synthesize thymidylate. Combining biochemical, spectroscopic and anaerobic crystallographic analyses, we showed that formaldehyde reacts with the reduced flavin coenzyme to form a carbinolamine intermediate used by ThyX for dUMP methylation. The crystallographic structure of this intermediate reveals how ThyX activates formaldehyde and uses it, with the assistance of active site residues, to methylate dUMP. Our results reveal that carbinolamine species promote methylene transfer and suggest that the use of a CHO-shunt may be relevant in several other important folate-dependent reactions. PubMed: 34315871DOI: 10.1038/s41467-021-24756-8 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2 Å) |
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