This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.
Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.
2vya
From Proteopedia
CRYSTAL STRUCTURE OF FATTY ACID AMIDE HYDROLASE CONJUGATED WITH THE DRUG-LIKE INHIBITOR PF-750
Template:ABSTRACT PUBMED 18753625
About this Structure
2VYA is a Single protein structure of sequence from Rattus norvegicus. Full crystallographic information is available from OCA.
Reference
Structure-guided inhibitor design for human FAAH by interspecies active site conversion., Mileni M, Johnson DS, Wang Z, Everdeen DS, Liimatta M, Pabst B, Bhattacharya K, Nugent RA, Kamtekar S, Cravatt BF, Ahn K, Stevens RC, Proc Natl Acad Sci U S A. 2008 Sep 2;105(35):12820-4. Epub 2008 Aug 27. PMID:18753625
Page seeded by OCA on Wed Sep 17 13:10:51 2008
Categories: Amidase | Rattus norvegicus | Single protein | Ahn, K. | Bhattacharya, K. | Cravatt, B F. | Everdeen, D S. | Johnson, D S. | Kamtekar, S. | Liimatta, M. | Mileni, M. | Nugent, R A. | Pabst, B. | Stevens, R C. | Wang, Z. | Chimera | Covalent | Drug- like | Endoplasmic reticulum | Faah | Fatty acid amide hydrolyse | Golgi apparatus | Humanized | Hydrolase | Inhibitor | Membrane | Transmembrane
