3pb4
From Proteopedia
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===Crystal structure of the catalytic domain of human Golgi-resident glutaminyl cyclase at pH 6.0=== | ===Crystal structure of the catalytic domain of human Golgi-resident glutaminyl cyclase at pH 6.0=== | ||
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| + | The line below this paragraph, {{ABSTRACT_PUBMED_21288892}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 21288892 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_21288892}} | ||
==About this Structure== | ==About this Structure== | ||
[[3pb4]] 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=3PB4 OCA]. | [[3pb4]] 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=3PB4 OCA]. | ||
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| + | ==Reference== | ||
| + | <ref group="xtra">PMID:021288892</ref><references group="xtra"/> | ||
[[Category: Glutaminyl-peptide cyclotransferase]] | [[Category: Glutaminyl-peptide cyclotransferase]] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
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[[Category: Lo, Y C.]] | [[Category: Lo, Y C.]] | ||
[[Category: Wang, A H.J.]] | [[Category: Wang, A H.J.]] | ||
| + | [[Category: Alpha/beta protein]] | ||
| + | [[Category: Alpha/beta-mixed fold]] | ||
| + | [[Category: Glutaminyl cyclase]] | ||
| + | [[Category: Golgi membrane]] | ||
| + | [[Category: Transferase]] | ||
Revision as of 07:58, 3 August 2011
Crystal structure of the catalytic domain of human Golgi-resident glutaminyl cyclase at pH 6.0
Template:ABSTRACT PUBMED 21288892
About this Structure
3pb4 is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Huang KF, Liaw SS, Huang WL, Chia CY, Lo YC, Chen YL, Wang AH. Structures of human Golgi-resident glutaminyl cyclase and its complexes with inhibitors reveal a large loop movement upon inhibitor binding. J Biol Chem. 2011 Apr 8;286(14):12439-49. Epub 2011 Feb 1. PMID:21288892 doi:10.1074/jbc.M110.208595
