2HPT
Crystal Structure of E. coli PepN (Aminopeptidase N)in complex with Bestatin
2HPT の概要
| エントリーDOI | 10.2210/pdb2hpt/pdb |
| 関連するPDBエントリー | 2HPO |
| 分子名称 | Aminopeptidase N, ZINC ION, 2-(3-AMINO-2-HYDROXY-4-PHENYL-BUTYRYLAMINO)-4-METHYL-PENTANOIC ACID, ... (5 entities in total) |
| 機能のキーワード | bestatin complex, compartmentalized active site, hydrolase |
| 由来する生物種 | Escherichia coli K12 |
| 細胞内の位置 | Cell inner membrane; Peripheral membrane protein; Cytoplasmic side: P04825 |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 102091.26 |
| 構造登録者 | |
| 主引用文献 | Addlagatta, A.,Gay, L.,Matthews, B.W. Structure of aminopeptidase N from Escherichia coli suggests a compartmentalized, gated active site. Proc.Natl.Acad.Sci.Usa, 103:13339-13344, 2006 Cited by PubMed Abstract: Aminopeptidase N from Escherichia coli is a major metalloprotease that participates in the controlled hydrolysis of peptides in the proteolytic pathway. Determination of the 870-aa structure reveals that it has four domains similar to the tricorn-interacting factor F3. The thermolysin-like active site is enclosed within a large cavity with a volume of 2,200 A(3), which is inaccessible to substrates except for a small opening of approximately 8-10 A. The substrate-based inhibitor bestatin binds to the protein with minimal changes, suggesting that this is the active form of the enzyme. The previously described structure of F3 had three distinct conformations that were described as "closed," "intermediate," and "open." The structure of aminopeptidase N from E. coli, however, is substantially more closed than any of these. Taken together, the results suggest that these proteases, which are involved in intracellular peptide degradation, prevent inadvertent hydrolysis of inappropriate substrates by enclosing the active site within a large cavity. There is also some evidence that the open form of the enzyme, which admits substrates, remains inactive until it adopts the closed form. PubMed: 16938892DOI: 10.1073/pnas.0606167103 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.3 Å) |
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