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6MBV

Carbonic Anhydrase II in complex with Nicotinic Acid

Summary for 6MBV
Entry DOI10.2210/pdb6mbv/pdb
DescriptorCarbonic anhydrase 2, ZINC ION, NICOTINIC ACID, ... (5 entities in total)
Functional Keywordscarbonic anhydrase ii, carboxylic acid, nicotinic acid, lyase
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight29213.25
Authors
Lomelino, C.L.,McKenna, R. (deposition date: 2018-08-30, release date: 2019-03-13, Last modification date: 2023-10-11)
Primary citationLomelino, C.L.,McKenna, R.
Carbonic anhydrase II in complex with carboxylic acid-based inhibitors.
Acta Crystallogr F Struct Biol Commun, 75:166-170, 2019
Cited by
PubMed Abstract: Carbonic anhydrases (CAs) are molecular targets in various diseases. While many sulfonamide-based drugs are in clinical use, CA inhibitor design is moving towards the incorporation of alternative zinc-binding groups, such as carboxylic acids, to promote CA isoform-specific inhibition. Here, X-ray crystal structures of CA II in complex with nicotinic acid and ferulic acid determined to 1.70 and 1.50 Å resolution, respectively, are reported. Furthermore, the structures of these two compounds are superimposed with previously determined structures to compare the mechanisms of inhibition and the properties of carboxylic acid-based CA inhibitors. This study examines an important class of alternative, non-sulfonamide-based CA inhibitors and provides insight to facilitate the structure-guided design of CA isoform-specific inhibitors.
PubMed: 30839290
DOI: 10.1107/S2053230X18018344
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.695 Å)
Structure validation

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