1BXQ

ACID PROTEINASE (PENICILLOPEPSIN) COMPLEX WITH PHOSPHONATE INHIBITOR.

1BXQ の概要

• エントリーDOI: 10.2210/pdb1bxq/pdb
• 分子名称: PROTEIN (PENICILLOPEPSIN), alpha-D-mannopyranose, SULFATE ION, ... (7 entities in total)
• 機能のキーワード: hydrolase, phosphonate inhibitors
• 由来する生物種: Penicillium janthinellum
• 細胞内の位置: Secreted : P00798
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 34983.25

構造登録者

Parrish, J.C.,Khan, A.R.,Fraser, M.E.,Smith, W.W.,Bartlett, P.A.,James, M.N.G. (登録日: 1998-10-07, 公開日: 1998-10-14, 最終更新日: 2024-10-30)

主引用文献

Khan, A.R.,Parrish, J.C.,Fraser, M.E.,Smith, W.W.,Bartlett, P.A.,James, M.N.
Lowering the entropic barrier for binding conformationally flexible inhibitors to enzymes.
Biochemistry, 37:16839-16845, 1998

PubMed Abstract: The design of inhibitors with enhanced potency against proteolytic enzymes has many applications for the treatment of human diseases. In addition to the optimization of chemical interactions between the enzyme and inhibitor, the binding affinity can be increased by constraining the inhibitor to the conformation that is recognized by the enzyme, thus lowering the entropic barrier to complex formation. We have structurally characterized the complexes of a macrocyclic pentapeptide inhibitor and its acyclic analogue with penicillopepsin, an aspartic proteinase, to study the effect of conformational constraint on the binding affinity. The phosphonate-based macrocycle PPi4 (Ki = 0.10 nM) is covalently linked at the P2-Asn and P1'-Phe side chains [nomenclature of Schechter and Berger, Biochim. Biophys. Res. Commun. (1967) 27, 157-162] via an amide bond, relative to the acyclic compound PPi3 (Ki = 42 nM). Comparisons of the high-resolution crystal structures of PPi4-penicillopepsin (0.95 A) and PPi3-penicillopepsin (1.45 A) reveal that the conformations of the inhibitors and their interactions with the enzyme are similar. The 420-fold increase in the binding affinity of PPi4 is attributed to a reduction in its conformational flexibility, thus providing the first rigorous measure of the entropic contribution to the binding energy in a protein-ligand complex and stressing the advantages of the design strategy.

PubMed: 9836576
DOI: 10.1021/bi9821364

実験手法

X-RAY DIFFRACTION (1.41 Å)