2vya
From Proteopedia
(New page: '''Unreleased structure''' The entry 2vya is ON HOLD Authors: Mileni, M., Johnson, D.S., Wang, Z., Everdeen, D.S., Liimatta, M., Pabst, B., Bhattacharya, K., Nugent, R.A., Kamtekar, S.,...) |
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+ | [[Image:2vya.jpg|left|200px]] | ||
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+ | {{STRUCTURE_2vya| PDB=2vya | SCENE= }} | ||
- | + | ===CRYSTAL STRUCTURE OF FATTY ACID AMIDE HYDROLASE CONJUGATED WITH THE DRUG-LIKE INHIBITOR PF-750=== | |
- | Description: Crystal Structure of fatty acid amide hydrolase conjugated with the drug-like inhibitor PF-750 | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | <!-- |
+ | The line below this paragraph, {{ABSTRACT_PUBMED_18753625}}, adds the Publication Abstract to the page | ||
+ | (as it appears on PubMed at http://www.pubmed.gov), where 18753625 is the PubMed ID number. | ||
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+ | {{ABSTRACT_PUBMED_18753625}} | ||
+ | |||
+ | ==About this Structure== | ||
+ | 2VYA is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Rattus_norvegicus Rattus norvegicus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2VYA 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:[http://www.ncbi.nlm.nih.gov/pubmed/18753625 18753625] | ||
+ | [[Category: Amidase]] | ||
+ | [[Category: Rattus norvegicus]] | ||
+ | [[Category: Single protein]] | ||
+ | [[Category: Ahn, K.]] | ||
+ | [[Category: Bhattacharya, K.]] | ||
+ | [[Category: Cravatt, B F.]] | ||
+ | [[Category: Everdeen, D S.]] | ||
+ | [[Category: Johnson, D S.]] | ||
+ | [[Category: Kamtekar, S.]] | ||
+ | [[Category: Liimatta, M.]] | ||
+ | [[Category: Mileni, M.]] | ||
+ | [[Category: Nugent, R A.]] | ||
+ | [[Category: Pabst, B.]] | ||
+ | [[Category: Stevens, R C.]] | ||
+ | [[Category: Wang, Z.]] | ||
+ | [[Category: Chimera]] | ||
+ | [[Category: Covalent]] | ||
+ | [[Category: Drug- like]] | ||
+ | [[Category: Endoplasmic reticulum]] | ||
+ | [[Category: Faah]] | ||
+ | [[Category: Fatty acid amide hydrolyse]] | ||
+ | [[Category: Golgi apparatus]] | ||
+ | [[Category: Humanized]] | ||
+ | [[Category: Hydrolase]] | ||
+ | [[Category: Inhibitor]] | ||
+ | [[Category: Membrane]] | ||
+ | [[Category: Transmembrane]] | ||
+ | |||
+ | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Sep 10 10:47:25 2008'' |
Revision as of 07:47, 10 September 2008
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 10 10:47:25 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