4Q39
PylD in complex with pyrrolysine and NADH
Summary for 4Q39
Entry DOI | 10.2210/pdb4q39/pdb |
Related | 3T7V 4FFP 4J4H 4Q3A 4Q3B 4Q3C 4Q3D 4Q3E |
Descriptor | PYLD, pyrrolysine synthase, 1,4-DIHYDRONICOTINAMIDE ADENINE DINUCLEOTIDE, SODIUM ION, ... (9 entities in total) |
Functional Keywords | rossmann fold, dehydrogenase, pyrrolysine, oxidoreductase |
Biological source | Methanosarcina barkeri |
Total number of polymer chains | 2 |
Total formula weight | 58278.19 |
Authors | Quitterer, F.,Beck, P.,Bacher, A.,Groll, M. (deposition date: 2014-04-11, release date: 2014-04-23, Last modification date: 2024-10-30) |
Primary citation | Quitterer, F.,Beck, P.,Bacher, A.,Groll, M. The Formation of Pyrroline and Tetrahydropyridine Rings in Amino Acids Catalyzed by Pyrrolysine Synthase (PylD). Angew.Chem.Int.Ed.Engl., 53:8150-8153, 2014 Cited by PubMed Abstract: The dehydrogenase PylD catalyzes the ultimate step of the pyrrolysine pathway by converting the isopeptide L-lysine-Nε-3R-methyl-D-ornithine to the 22nd proteinogenic amino acid. In this study, we demonstrate how PylD can be harnessed to oxidize various isopeptides to novel amino acids by combining chemical synthesis with enzyme kinetics and X-ray crystallography. The data enable a detailed description of the PylD reaction trajectory for the biosynthesis of pyrroline and tetrahydropyridine rings as constituents of pyrrolysine analogues. PubMed: 24916332DOI: 10.1002/anie.201402595 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.2 Å) |
Structure validation
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