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6YS2

Crystal structure of FAP R451A in the dark at 100K

This is a non-PDB format compatible entry.
Summary for 6YS2
Entry DOI10.2210/pdb6ys2/pdb
DescriptorFatty acid Photodecarboxylase, STEARIC ACID, FLAVIN-ADENINE DINUCLEOTIDE, ... (4 entities in total)
Functional Keywordsgmc fold, biosynthetic protein
Biological sourceChlorella variabilis (Green alga)
Total number of polymer chains1
Total formula weight62354.95
Authors
Sorigue, D.,Gotthard, G.,Blangy, S.,Nurizzo, D.,Royant, A.,Beisson, F.,Arnoux, P. (deposition date: 2020-04-20, release date: 2021-04-21, Last modification date: 2024-01-24)
Primary citationSorigue, D.,Hadjidemetriou, K.,Blangy, S.,Gotthard, G.,Bonvalet, A.,Coquelle, N.,Samire, P.,Aleksandrov, A.,Antonucci, L.,Benachir, A.,Boutet, S.,Byrdin, M.,Cammarata, M.,Carbajo, S.,Cuine, S.,Doak, R.B.,Foucar, L.,Gorel, A.,Grunbein, M.,Hartmann, E.,Hienerwadel, R.,Hilpert, M.,Kloos, M.,Lane, T.J.,Legeret, B.,Legrand, P.,Li-Beisson, Y.,Moulin, S.L.Y.,Nurizzo, D.,Peltier, G.,Schiro, G.,Shoeman, R.L.,Sliwa, M.,Solinas, X.,Zhuang, B.,Barends, T.R.M.,Colletier, J.P.,Joffre, M.,Royant, A.,Berthomieu, C.,Weik, M.,Domratcheva, T.,Brettel, K.,Vos, M.H.,Schlichting, I.,Arnoux, P.,Muller, P.,Beisson, F.
Mechanism and dynamics of fatty acid photodecarboxylase.
Science, 372:-, 2021
Cited by
PubMed Abstract: Fatty acid photodecarboxylase (FAP) is a photoenzyme with potential green chemistry applications. By combining static, time-resolved, and cryotrapping spectroscopy and crystallography as well as computation, we characterized FAP reaction intermediates on time scales from subpicoseconds to milliseconds. High-resolution crystal structures from synchrotron and free electron laser x-ray sources highlighted an unusual bent shape of the oxidized flavin chromophore. We demonstrate that decarboxylation occurs directly upon reduction of the excited flavin by the fatty acid substrate. Along with flavin reoxidation by the alkyl radical intermediate, a major fraction of the cleaved carbon dioxide unexpectedly transformed in 100 nanoseconds, most likely into bicarbonate. This reaction is orders of magnitude faster than in solution. Two strictly conserved residues, R451 and C432, are essential for substrate stabilization and functional charge transfer.
PubMed: 33833098
DOI: 10.1126/science.abd5687
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.97 Å)
Structure validation

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