Literature DB >> 22607884

Structure, function and applications of carbonic anhydrase isozymes.

Md Imtaiyaz Hassan1, Bushra Shajee, Abdul Waheed, Faizan Ahmad, William S Sly.   

Abstract

The carbonic anhydrases enzymes (CAs, EC 4.2.1.1) are zinc containing metalloproteins, which efficiently catalyse the reversible conversion of carbon dioxide to bicarbonate and release proton. These enzymes are essentially important for biological system and play several important physiological and patho-physiological functions. There are 16 different alpha-carbonic anhydrase isoforms studied, differing widely in their cellular localization and biophysical properties. The catalytic domains of all CAs possess a conserved tertiary structure fold, with predominately β-strands. We performed an extensive analysis of all 16 mammalian CAs for its structure and function in order to establish a structure-function relationship. CAs have been a potential therapeutic target for many diseases. Sulfonamides are considered as a strong and specific inhibitor of CA, and are being used as diuretics, anti-glaucoma, anti-epileptic, anti-ulcer agents. Currently CA inhibitors are widely used as a drug for the treatment of neurological disorders, anti-glaucoma drugs, anti-cancer, or anti-obesity agents. Here we tried to emphasize how CAs can be used for drug discovery, design and screening. Furthermore, we discussed the role of CA in carbon capture, carbon sensor and metabolon. We hope this review provide many useful information on structure, function, mechanism, and applications of CAs in various discipline.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22607884     DOI: 10.1016/j.bmc.2012.04.044

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  46 in total

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Journal:  World J Gastroenterol       Date:  2015-01-14       Impact factor: 5.742

2.  Intracellular and extracellular carbonic anhydrases cooperate non-enzymatically to enhance activity of monocarboxylate transporters.

Authors:  Michael Klier; Fabian T Andes; Joachim W Deitmer; Holger M Becker
Journal:  J Biol Chem       Date:  2013-12-12       Impact factor: 5.157

3.  GPI-anchored carbonic anhydrase IV displays both intra- and extracellular activity in cRNA-injected oocytes and in mouse neurons.

Authors:  Hans-Peter Schneider; Marco D Alt; Michael Klier; Alena Spiess; Fabian T Andes; Abdul Waheed; William S Sly; Holger M Becker; Joachim W Deitmer
Journal:  Proc Natl Acad Sci U S A       Date:  2013-01-07       Impact factor: 11.205

Review 4.  Is carbonic anhydrase IX a validated target for molecular imaging of cancer and hypoxia?

Authors:  Jianbo Li; Guojian Zhang; Xuemei Wang; Xiao-Feng Li
Journal:  Future Oncol       Date:  2015       Impact factor: 3.404

5.  Towards New Drug Targets? Function Prediction of Putative Proteins of Neisseria meningitidis MC58 and Their Virulence Characterization.

Authors:  Mohd Shahbaaz; Krishna Bisetty; Faizan Ahmad; Md Imtaiyaz Hassan
Journal:  OMICS       Date:  2015-06-15

6.  Transgenic expression of carbonic anhydrase III in cardiac muscle demonstrates a mechanism to tolerate acidosis.

Authors:  Han-Zhong Feng; J-P Jin
Journal:  Am J Physiol Cell Physiol       Date:  2019-08-07       Impact factor: 4.249

Review 7.  Carbonic anhydrase XII functions in health and disease.

Authors:  Abdul Waheed; William S Sly
Journal:  Gene       Date:  2017-04-19       Impact factor: 3.688

8.  Evidence from simultaneous intracellular- and surface-pH transients that carbonic anhydrase II enhances CO2 fluxes across Xenopus oocyte plasma membranes.

Authors:  Raif Musa-Aziz; Rossana Occhipinti; Walter F Boron
Journal:  Am J Physiol Cell Physiol       Date:  2014-06-25       Impact factor: 4.249

9.  Immunocytochemical localization of carbonic anhydrase in the pseudobranch tissue of the rainbow trout Oncorhynchus mykiss.

Authors:  S M Rahim; A G Mazlan; K D Simon; J P Delaunoy; P Laurent
Journal:  J Zhejiang Univ Sci B       Date:  2014-02       Impact factor: 3.066

10.  Tuning the Dual Inhibition of Carbonic Anhydrase and Cyclooxygenase by Dihydrothiazole Benzensulfonamides.

Authors:  Rita Meleddu; Simona Distinto; Filippo Cottiglia; Rossella Angius; Marco Gaspari; Domenico Taverna; Claudia Melis; Andrea Angeli; Giulia Bianco; Serenella Deplano; Benedetta Fois; Sonia Del Prete; Clemente Capasso; Stefano Alcaro; Francesco Ortuso; Matilde Yanez; Claudiu T Supuran; Elias Maccioni
Journal:  ACS Med Chem Lett       Date:  2018-09-17       Impact factor: 4.345

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