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7COJ

Crystal structure of the b-carbonic anhydrase CafA of the fungal pathogen Aspergillus fumigatus

Summary for 7COJ
Entry DOI10.2210/pdb7coj/pdb
DescriptorCarbonic anhydrase, ZINC ION, 5-ACETAMIDO-1,3,4-THIADIAZOLE-2-SULFONAMIDE, ... (4 entities in total)
Functional Keywordsb-class carbonic anhydrase, cafa, zinc metalloenzyme, aspergillus fumigatus, lyase
Biological sourceNeosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100)
Total number of polymer chains4
Total formula weight124620.68
Authors
Jin, M.S.,Kim, S.,Yeon, J.,Sung, J. (deposition date: 2020-08-04, release date: 2020-10-14, Last modification date: 2023-11-29)
Primary citationKim, S.,Yeon, J.,Sung, J.,Jin, M.S.
Crystal Structure of beta-Carbonic Anhydrase CafA from the Fungal Pathogen Aspergillus fumigatus .
Mol.Cells, 43:831-840, 2020
Cited by
PubMed Abstract: The β-class of carbonic anhydrases (β-CAs) are zinc metalloenzymes widely distributed in the fungal kingdom that play essential roles in growth, survival, differentiation, and virulence by catalyzing the reversible interconversion of carbon dioxide (CO) and bicarbonate (HCO). Herein, we report the biochemical and crystallographic characterization of the β-CA CafA from the fungal pathogen , the main causative agent of invasive aspergillosis. CafA exhibited apparent CO hydration activity in neutral to weak alkaline conditions, but little activity at acidic pH. The high-resolution crystal structure of CafA revealed a tetramer comprising a dimer of dimers, in which the catalytic zinc ion is tetrahedrally coordinated by three conserved residues (C119, H175, C178) and an acetate anion presumably acquired from the crystallization solution, indicating a freely accessible ″open″ conformation. Furthermore, knowledge of the structure of CafA in complex with the potent inhibitor acetazolamide, together with its functional intolerance of nitrate (NO) ions, could be exploited to develop new antifungal agents for the treatment of invasive aspergillosis.
PubMed: 32975213
DOI: 10.14348/molcells.2020.0168
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2 Å)
Structure validation

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数据于2024-10-30公开中

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