✦ LIBER ✦

Crystal structure of carbonic anhydrase from Neisseria gonorrhoeae and its complex with the inhibitor acetazolamide

✍ Scribed by Shenghua Huang; Yafeng Xue; Elisabeth Sauer-Eriksson; Laura Chirica; Sven Lindskog; Bengt-Harald Jonsson

Book ID: 115628760
Publisher: Elsevier Science
Year: 1998
Tongue: English
Weight: 379 KB
Volume: 283
Category: Article
ISSN: 0022-2836
DOI: 10.1006/jmbi.1998.2077

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A zinc complex of the carbonic anhydrase

A zinc complex of the carbonic anhydrase inhibitor acetazolamide (aaaH): crystal structure of (aaa)2Zn(NH3)2

✍ Hartmann, Uwe.; Vahrenkamp, Heinrich. 📂 Article 📅 1991 🏛 American Chemical Society 🌐 English ⚖ 274 KB

Crystal Structure of the Complex between

Crystal Structure of the Complex between Human Carbonic Anhydrase II and the Aromatic Inhibitor 1,2,4-Triazole

✍ Stefano Mangani; Anders Liljas 📂 Article 📅 1993 🏛 Elsevier Science 🌐 English ⚖ 329 KB

A ternary complex of carbonic anhydrase:

A ternary complex of carbonic anhydrase: X-ray crystallographic structure of the adduct of human carbonic anhydrase II with the activator phenylalanine and the inhibitor azide

✍ Fabrizio Briganti; Valeria Iaconi; Stefano Mangani; Pierluigi Orioli; Andrea Sco 📂 Article 📅 1998 🏛 Elsevier Science 🌐 English ⚖ 746 KB

Ultrahigh Resolution Crystal Structures

Ultrahigh Resolution Crystal Structures of Human Carbonic Anhydrases I and II Complexed with “Two-Prong” Inhibitors Reveal the Molecular Basis of High Affinity

✍ Jude, Kevin M.; Banerjee, Abir L.; Haldar, Manas K.; Manokaran, Sumathra; Roy, B 📂 Article 📅 2006 🏛 American Chemical Society 🌐 English ⚖ 644 KB

Crystal structures of isomaltase from Sa

Crystal structures of isomaltase from Saccharomyces cerevisiae and in complex with its competitive inhibitor maltose

✍ Keizo Yamamoto; Hideo Miyake; Masami Kusunoki; Shigeyoshi Osaki 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 632 KB

Carbonic anhydrase inhibitors. The X-ray

Carbonic anhydrase inhibitors. The X-ray crystal structure of human isoform II in adduct with an adamantyl analogue of acetazolamide resides in a less utilized binding pocket than most hydrophobic inhibitors

✍ Balendu Sankara Avvaru; Jason M. Wagner; Alfonso Maresca; Andrea Scozzafava; Art 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 916 KB

We investigated the inhibitory activity of several 1,3,4-thiadiazole-sulfonamides against all catalytically active CA (EC 4.2.1.1), CA I-XV. The tail derivatizing the 5-position in the 1,3,4-thiadiazole-2-sulfonamide scaffold was observed to be critical as an inhibitory determinant of these compound