5YSS
Crystal structure of aminocaproic acid cyclase in complex with NAD (+)
Summary for 5YSS
Entry DOI | 10.2210/pdb5yss/pdb |
Descriptor | 3-hydroxybutyrate dehydrogenase, NICOTINAMIDE-ADENINE-DINUCLEOTIDE (3 entities in total) |
Functional Keywords | cyclase, nad binding protein, complex, oxidoreductase |
Biological source | Citrobacter freundii |
Total number of polymer chains | 4 |
Total formula weight | 109329.55 |
Authors | Fu, Y.,Yeom, S.J.,Lee, S.G. (deposition date: 2017-11-15, release date: 2018-10-31, Last modification date: 2023-11-22) |
Primary citation | Yeom, S.J.,Kim, M.,Kwon, K.K.,Fu, Y.,Rha, E.,Park, S.H.,Lee, H.,Kim, H.,Lee, D.H.,Kim, D.M.,Lee, S.G. A synthetic microbial biosensor for high-throughput screening of lactam biocatalysts Nat Commun, 9:5053-5053, 2018 Cited by PubMed Abstract: Biocatalytic cyclization is highly desirable for efficient synthesis of biologically derived chemical substances, such as the commodity chemicals ε-caprolactam and δ-valerolactam. To identify biocatalysts in lactam biosynthesis, we develop a caprolactam-detecting genetic enzyme screening system (CL-GESS). The Alcaligenes faecalis regulatory protein NitR is adopted for the highly specific detection of lactam compounds against lactam biosynthetic intermediates. We further systematically optimize the genetic components of the CL-GESS to enhance sensitivity, achieving 10-fold improvement. Using this highly sensitive GESS, we screen marine metagenomes and find an enzyme that cyclizes ω-amino fatty acids to lactam. Moreover, we determine the X-ray crystal structure and catalytic residues based on mutational analysis of the cyclase. The cyclase is also used as a helper enzyme to sense intracellular ω-amino fatty acids. We expect this simple and accurate biosensor to have wide-ranging applications in rapid screening of new lactam-synthesizing enzymes and metabolic engineering for lactam bio-production. PubMed: 30498220DOI: 10.1038/s41467-018-07488-0 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.276 Å) |
Structure validation
Download full validation report