6M53
Crystal structure of 2, 3-dihydroxybenzoic acid decarboxylase from Fusarium oxysporum
Summary for 6M53
Entry DOI | 10.2210/pdb6m53/pdb |
Descriptor | 2,3-dihydroxybenzoate decarboxylase, ZINC ION, GLYCEROL, ... (4 entities in total) |
Functional Keywords | 2, 3-dihydroxybenzoic acid decarboxylase, biosynthetic protein |
Biological source | Fusarium oxysporum (Fusarium vascular wilt) |
Total number of polymer chains | 4 |
Total formula weight | 157699.47 |
Authors | Song, M.K.,Feng, J.H.,Liu, W.D.,Wu, Q.Q.,Zhu, D.M. (deposition date: 2020-03-09, release date: 2020-07-15, Last modification date: 2023-11-29) |
Primary citation | Song, M.,Zhang, X.,Liu, W.,Feng, J.,Cui, Y.,Yao, P.,Wang, M.,Guo, R.T.,Wu, Q.,Zhu, D. 2,3-Dihydroxybenzoic Acid Decarboxylase from Fusarium oxysporum: Crystal Structures and Substrate Recognition Mechanism. Chembiochem, 21:2950-2956, 2020 Cited by PubMed Abstract: A 2,3-dihydroxybenzoic acid decarboxylase from Fusarium oxysporum (2,3-DHBD_Fo) has a relatively high catalytic efficiency for the decarboxylation of 2,3-dihydroxybenzoic acid (DHBA) and carboxylation of catechol, thus it has a different substrate spectrum from other benzoic acid decarboxylases. We have determined the structures of 2,3-DHBD_Fo in its apo form and complexes with catechol or 2,5-dihydroxybenzoic acid at 1.55, 1.97, and 2.45 Å resolution, respectively. The crystal structures of 2,3-DHBD_Fo show that the enzyme exists as a homotetramer, and each active center has a Zn ion coordinated by E8, H167, D291 and three water molecules. This is different from 2,6-DHBD from Rhizobium sporomusa, in which the Zn ion is also coordinated with H10. Surprisingly, mutation of A10 of 2,3-DHBD_Fo to His resulted in almost complete loss of the enzyme activity. Enzyme-substrate docking and site-directed mutation studies indicate that residue R233 interacts with the 3-hydroxy group of 2,3-DHBA, and plays an important role in substrate recognition for this enzyme, thus revealing the molecular basis 2,3-dihydroxybenzoic acid decarboxylase. PubMed: 32421914DOI: 10.1002/cbic.202000244 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.55 Å) |
Structure validation
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