9G4T
Beta carbonic anhydrase CsoSCA from the Halothiobacillus neapolitanus alpha-carboxysome
Summary for 9G4T
| Entry DOI | 10.2210/pdb9g4t/pdb |
| EMDB information | 51067 |
| Descriptor | Immunoglobulin G-binding protein G,Carboxysome shell carbonic anhydrase, ZINC ION (2 entities in total) |
| Functional Keywords | carbonic anhydrase, carboxysome, rubisco, lyase |
| Biological source | Streptococcus sp. 'group G' More |
| Total number of polymer chains | 1 |
| Total formula weight | 68359.71 |
| Authors | Ng, P.C.,Marles-Wright, J.,Basle, A.,Liu, L. (deposition date: 2024-07-16, release date: 2025-07-30, Last modification date: 2025-11-26) |
| Primary citation | Ng, P.C.,Adegbite, O.,Li, T.,Basle, A.,Marles-Wright, J.,Liu, L.N. Structure and encapsulation of carbonic anhydrase within the alpha-carboxysome. Proc.Natl.Acad.Sci.USA, 122:e2523723122-e2523723122, 2025 Cited by PubMed Abstract: Carboxysomes in cyanobacteria and certain proteobacteria enable efficient CO fixation by encapsulating ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) and carbonic anhydrase (CA) within a semipermeable shell. Sequestered CA catalyze the rapid interconversion of CO and HCO, supplying elevated levels of CO to boost Rubisco carboxylation. Despite its essential role, the structure and encapsulation of CA within carboxysomes remain poorly understood. Here, we determined the molecular structure of α-carboxysomal CA from the model chemoautotrophic bacterium (CsoSCA). CsoSCA adopts a trimer-of-dimers oligomeric structure without the incorporation of a zinc ion at its symmetric center. Using synthetic minishells, we demonstrate that CsoSCA interacts with the CsoS1A shell hexamer and is incorporated into the minishells at the inner surface, independent of the CsoS2 linker protein. CsoSCA truncations suggest nonspecific interactions between CsoSCA and CsoS1A. We further show that CsoSCA bridges Rubisco and the shell facets. Our study offers insights into the assembly and encapsulation mechanisms of α-carboxysomes and provides the framework for reprogramming carboxysome structures for synthetic biology and biotechnological applications. PubMed: 41223214DOI: 10.1073/pnas.2523723122 PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (2.51 Å) |
Structure validation
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