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3hb5
From Proteopedia
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| + | {{STRUCTURE_3hb5| PDB=3hb5 | SCENE= }} | ||
| - | + | ===Binary and ternary crystal structures of a novel inhibitor of 17 beta-HSD type 1: a lead compound for breast cancer therapy=== | |
| - | Description: Binary and ternary crystal structures of a novel inhibitor of 17 beta-HSD type 1: a lead compound for breast cancer therapy | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | <!-- |
| + | The line below this paragraph, {{ABSTRACT_PUBMED_19929851}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 19929851 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_19929851}} | ||
| + | |||
| + | ==About this Structure== | ||
| + | 3HB5 is a 1 chain structure of 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=3HB5 OCA]. | ||
| + | |||
| + | ==Reference== | ||
| + | <ref group="xtra">PMID:19929851</ref><references group="xtra"/> | ||
| + | [[Category: Estradiol 17-beta-dehydrogenase]] | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Lin, S X.]] | ||
| + | [[Category: Mazumdar, M.]] | ||
| + | [[Category: 17beta-hsd1]] | ||
| + | [[Category: Cytoplasm]] | ||
| + | [[Category: Lipid synthesis]] | ||
| + | [[Category: Nadp]] | ||
| + | [[Category: Oxidoreductase]] | ||
| + | [[Category: Polymorphism]] | ||
| + | [[Category: Steroid biosynthesis]] | ||
| + | |||
| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Dec 16 13:01:15 2009'' | ||
Revision as of 11:01, 16 December 2009
Binary and ternary crystal structures of a novel inhibitor of 17 beta-HSD type 1: a lead compound for breast cancer therapy
Template:ABSTRACT PUBMED 19929851
About this Structure
3HB5 is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Mazumdar M, Fournier D, Zhu DW, Cadot C, Poirier D, Lin SX. Binary and ternary crystal structure analyses of a novel inhibitor with 17beta-HSD type 1: a lead compound for breast cancer therapy. Biochem J. 2009 Dec 10;424(3):357-66. PMID:19929851 doi:10.1042/BJ20091020
Page seeded by OCA on Wed Dec 16 13:01:15 2009
