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1u7t
From Proteopedia
(Difference between revisions)
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[[Image:1u7t.png|left|200px]] | [[Image:1u7t.png|left|200px]] | ||
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{{STRUCTURE_1u7t| PDB=1u7t | SCENE= }} | {{STRUCTURE_1u7t| PDB=1u7t | SCENE= }} | ||
===Crystal Structure of ABAD/HSD10 with a Bound Inhibitor=== | ===Crystal Structure of ABAD/HSD10 with a Bound Inhibitor=== | ||
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==About this Structure== | ==About this Structure== | ||
| - | + | [[1u7t]] is a 4 chain structure of [[Alcohol dehydrogenase]] 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=1U7T OCA]. | |
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| + | ==See Also== | ||
| + | *[[Alcohol dehydrogenase|Alcohol dehydrogenase]] | ||
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:015342248</ref><references group="xtra"/> |
[[Category: 3-hydroxyacyl-CoA dehydrogenase]] | [[Category: 3-hydroxyacyl-CoA dehydrogenase]] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
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[[Category: Showalter, R E.]] | [[Category: Showalter, R E.]] | ||
[[Category: Villafranca, J E.]] | [[Category: Villafranca, J E.]] | ||
| + | [[Category: Oxidoreductase]] | ||
[[Category: Protein-inhibitor complex]] | [[Category: Protein-inhibitor complex]] | ||
[[Category: Rossmann fold]] | [[Category: Rossmann fold]] | ||
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| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 12:53:01 2009'' | ||
Revision as of 12:33, 25 July 2012
Contents |
Crystal Structure of ABAD/HSD10 with a Bound Inhibitor
Template:ABSTRACT PUBMED 15342248
About this Structure
1u7t is a 4 chain structure of Alcohol dehydrogenase with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Kissinger CR, Rejto PA, Pelletier LA, Thomson JA, Showalter RE, Abreo MA, Agree CS, Margosiak S, Meng JJ, Aust RM, Vanderpool D, Li B, Tempczyk-Russell A, Villafranca JE. Crystal structure of human ABAD/HSD10 with a bound inhibitor: implications for design of Alzheimer's disease therapeutics. J Mol Biol. 2004 Sep 17;342(3):943-52. PMID:15342248 doi:10.1016/j.jmb.2004.07.071
