3s7l
From Proteopedia
(Difference between revisions)
m (Protected "3s7l" [edit=sysop:move=sysop]) |
|||
Line 1: | Line 1: | ||
- | + | [[Image:3s7l.jpg|left|200px]] | |
- | The | + | <!-- |
+ | The line below this paragraph, containing "STRUCTURE_3s7l", creates the "Structure Box" on the page. | ||
+ | You may change the PDB parameter (which sets the PDB file loaded into the applet) | ||
+ | or the SCENE parameter (which sets the initial scene displayed when the page is loaded), | ||
+ | or leave the SCENE parameter empty for the default display. | ||
+ | --> | ||
+ | {{STRUCTURE_3s7l| PDB=3s7l | SCENE= }} | ||
- | + | ===Pyrazolyl and Thienyl Aminohydantoins as Potent BACE1 Inhibitors=== | |
- | + | ||
+ | <!-- | ||
+ | The line below this paragraph, {{ABSTRACT_PUBMED_21835615}}, adds the Publication Abstract to the page | ||
+ | (as it appears on PubMed at http://www.pubmed.gov), where 21835615 is the PubMed ID number. | ||
+ | --> | ||
+ | {{ABSTRACT_PUBMED_21835615}} | ||
+ | |||
+ | ==About this Structure== | ||
+ | [[3s7l]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3S7L OCA]. | ||
+ | |||
+ | ==Reference== | ||
+ | <ref group="xtra">PMID:021835615</ref><references group="xtra"/> | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Memapsin 2]] | ||
+ | [[Category: Chopra, R.]] | ||
+ | [[Category: Olland, A.]] | ||
+ | [[Category: Svenson, K.]] | ||
+ | [[Category: Aspartyl protease]] | ||
+ | [[Category: Disulfide bond]] | ||
+ | [[Category: Hydrolase-hydrolase inhibitor complex]] | ||
+ | [[Category: Protease]] |
Revision as of 06:48, 31 August 2011
Pyrazolyl and Thienyl Aminohydantoins as Potent BACE1 Inhibitors
Template:ABSTRACT PUBMED 21835615
About this Structure
3s7l is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Malamas MS, Erdei J, Gunawan I, Barnes K, Hui Y, Johnson M, Robichaud A, Zhou P, Yan Y, Solvibile W, Turner J, Fan KY, Chopra R, Bard J, Pangalos MN. New pyrazolyl and thienyl aminohydantoins as potent BACE1 inhibitors: Exploring the S2' region. Bioorg Med Chem Lett. 2011 Sep 15;21(18):5164-70. Epub 2011 Jul 23. PMID:21835615 doi:10.1016/j.bmcl.2011.07.057