Carbonic anhydrase inhibitors: X-ray crystallographic structure of the adduct of human isozyme II with EMATE, a dual inhibitor of carbonic anhydrases and steroid sulfatase

F Abbate, JY Winum, BVL Potter, A Casini, JL Montero, A Scozzafava, CT Supuran*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

145 Citations (Scopus)

Abstract

The X-ray crystal structure for the adduct of human carbonic anhydrase II (hCA II) with estrone-3-O-sulfamate (EMATE), an antiendocrine agent showing both CA and estrone sulfatase inhibitory properties, has been resolved at a resolution of 1.5 Angstrom. Its binding to the enzyme is similar to that of other sulfamates/sulfonamides, considering the interactions of the zinc anchoring group, but differs considerably when the steroidal scaffold of the inhibitor is analyzed. This part of the inhibitor interacts only within the hydrophobic half of the CA active site, interacting with residues Val 121, Phe 131, Val 135 and Pro 202, and leaving the hydrophilic half able to accommodate several water molecules not present in the uncomplexed enzyme. In addition, a very short bond of 1.78 Angstrom between the zinc ion and the coordinated nitrogen atom of the sulfamate moiety is observed, which may explain the high affinity of this inhibitor for hCA II (K-i of 10 nM). (C) 2003 Elsevier Ltd. All rights reserved.

Original languageEnglish
Pages (from-to)231-234
Number of pages4
JournalBioorganic & Medicinal Chemistry Letters
Volume14
Issue number1
DOIs
Publication statusPublished - 5-Jan-2004
Externally publishedYes

Keywords

  • ESTRONE SULFATASE
  • DRUG DESIGN
  • IX
  • SULFONAMIDES
  • EXPRESSION
  • ANTICANCER
  • HYPOXIA
  • PROTEIN
  • BINDING
  • DENSITY

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