3l58
From Proteopedia
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| + | {{STRUCTURE_3l58| PDB=3l58 | SCENE= }} | ||
| - | + | ===Structure of BACE Bound to SCH589432=== | |
| - | Description: Structure of BACE Bound to SCH589432 | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | <!-- |
| + | The line below this paragraph, {{ABSTRACT_PUBMED_20043696}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 20043696 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_20043696}} | ||
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| + | ==About this Structure== | ||
| + | 3L58 is a 2 chains structure with sequences 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=3L58 OCA]. | ||
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| + | ==Reference== | ||
| + | <ref group="xtra">PMID:20043696</ref><references group="xtra"/> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Memapsin 2]] | ||
| + | [[Category: Strickland, C.]] | ||
| + | [[Category: Zhu, Z.]] | ||
| + | [[Category: Alternative splicing]] | ||
| + | [[Category: Alzheimer]] | ||
| + | [[Category: Aspartyl protease]] | ||
| + | [[Category: Bace1]] | ||
| + | [[Category: Disulfide bond]] | ||
| + | [[Category: Endoplasmic reticulum]] | ||
| + | [[Category: Endosome]] | ||
| + | [[Category: Glycoprotein]] | ||
| + | [[Category: Golgi apparatus]] | ||
| + | [[Category: Hydrolase]] | ||
| + | [[Category: Membrane]] | ||
| + | [[Category: Polymorphism]] | ||
| + | [[Category: Protease]] | ||
| + | [[Category: Transmembrane]] | ||
| + | [[Category: Zymogen]] | ||
| + | |||
| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Feb 17 10:28:24 2010'' | ||
Revision as of 08:28, 17 February 2010
Structure of BACE Bound to SCH589432
Template:ABSTRACT PUBMED 20043696
About this Structure
3L58 is a 2 chains structure with sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Zhu Z, Sun ZY, Ye Y, Voigt J, Strickland C, Smith EM, Cumming J, Wang L, Wong J, Wang YS, Wyss DF, Chen X, Kuvelkar R, Kennedy ME, Favreau L, Parker E, McKittrick BA, Stamford A, Czarniecki M, Greenlee W, Hunter JC. Discovery of Cyclic Acylguanidines as Highly Potent and Selective beta-Site Amyloid Cleaving Enzyme (BACE) Inhibitors: Part I-Inhibitor Design and Validation ( parallel) (1). J Med Chem. 2010 Feb 11;53(3):951-65. PMID:20043696 doi:10.1021/jm901408p
Page seeded by OCA on Wed Feb 17 10:28:24 2010
