4ZM4
Complex structure of PctV K276R mutant with PMP and 3-dehydroshkimate
Summary for 4ZM4
Entry DOI | 10.2210/pdb4zm4/pdb |
Related | 4ZM3 |
Descriptor | Aminotransferase, PYRIDOXAL-5'-PHOSPHATE, (3E,4R,5R)-4,5-dihydroxy-3-{[(Z)-{3-hydroxy-2-methyl-5-[(phosphonooxy)methyl]pyridin-4(1H)-ylidene}methyl]imino}cyclohex-1-ene-1-carboxylic acid, ... (4 entities in total) |
Functional Keywords | pyridoxal 5-phosphate, aminotransferase, transferase |
Biological source | Streptomyces pactum |
Total number of polymer chains | 6 |
Total formula weight | 288799.82 |
Authors | Hirayama, A.,Miyanaga, A.,Kudo, F.,Eguchi, T. (deposition date: 2015-05-02, release date: 2015-10-14, Last modification date: 2023-11-08) |
Primary citation | Hirayama, A.,Miyanaga, A.,Kudo, F.,Eguchi, T. Mechanism-Based Trapping of the Quinonoid Intermediate by Using the K276R Mutant of PLP-Dependent 3-Aminobenzoate Synthase PctV in the Biosynthesis of Pactamycin. Chembiochem, 16:2484-2490, 2015 Cited by PubMed Abstract: Mutational analysis of the pyridoxal 5'-phosphate (PLP)-dependent enzyme PctV was carried out to elucidate the multi-step reaction mechanism for the formation of 3-aminobenzoate (3-ABA) from 3-dehydroshikimate (3-DSA). Introduction of mutation K276R led to the accumulation of a quinonoid intermediate with an absorption maximum at 580 nm after the reaction of pyridoxamine 5'-phosphate (PMP) with 3-DSA. The chemical structure of this intermediate was supported by X-ray crystallographic analysis of the complex formed between the K276R mutant and the quinonoid intermediate. These results clearly show that a quinonoid intermediate is involved in the formation of 3-ABA. They also indicate that Lys276 (in the active site of PctV) plays multiple roles, including acid/base catalysis during the dehydration reaction of the quinonoid intermediate. PubMed: 26426567DOI: 10.1002/cbic.201500426 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.4 Å) |
Structure validation
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