2A5V

Crystal structure of M. tuberculosis beta carbonic anhydrase, Rv3588c, tetrameric form

Summary for 2A5V

• Entry DOI: 10.2210/pdb2a5v/pdb
• Related: 1ym3
• Descriptor: CARBONIC ANHYDRASE (CARBONATE DEHYDRATASE) (CARBONIC DEHYDRATASE), THIOCYANATE ION, ZINC ION, ... (4 entities in total)
• Functional Keywords: tetramer, carboxylate shift, open, lyase
• Biological source: Mycobacterium tuberculosis
• Total number of polymer chains: 4
• Total formula weight: 91237.67

Authors

Covarrubias, A.S.,Bergfors, T.,Jones, T.A.,Hogbom, M. (deposition date: 2005-07-01, release date: 2005-09-20, Last modification date: 2023-08-23)

Primary citation

Covarrubias, A.S.,Bergfors, T.,Jones, T.A.,Hogbom, M.
Structural Mechanics of the pH-dependent Activity of beta-Carbonic Anhydrase from Mycobacterium tuberculosis
J.Biol.Chem., 281:4993-4999, 2006

PubMed Abstract: Carbonic anhydrases catalyze the reversible hydration of carbon dioxide to form bicarbonate, a reaction required for many functions, including carbon assimilation and pH homeostasis. Carbonic anhydrases are divided into at least three classes and are believed to share a zinc-hydroxide mechanism for carbon dioxide hydration. beta-carbonic anhydrases are broadly spread among the domains of life, and existing structures from different organisms show two distinct active site setups, one with three protein coordinations to the zinc (accessible) and the other with four (blocked). The latter is believed to be inconsistent with the zinc-hydroxide mechanism. The Mycobacterium tuberculosis Rv3588c gene, shown to be required for in vivo growth of the pathogen, encodes a beta-carbonic anhydrase with a steep pH dependence of its activity, being active at pH 8.4 but not at pH 7.5. We have recently solved the structure of this protein, which was a dimeric protein with a blocked active site. Here we present the structure of the thiocyanate complexed protein in a different crystal form. The protein now forms distinct tetramers and shows large structural changes, including a carboxylate shift yielding the accessible active site. This structure demonstrated for the first time that a beta-carbonic anhydrase can switch between the two states. A pH-dependent dimer to tetramer equilibrium was also demonstrated by dynamic light scattering measurements. The data presented here, therefore, suggest a carboxylate shift on/off switch for the enzyme, which may, in turn, be controlled by a dimer-to-tetramer equilibrium.

PubMed: 16321983
DOI: 10.1074/jbc.M510756200

Experimental method

X-RAY DIFFRACTION (2.2 Å)