2qtw: Difference between revisions
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[[Image:2qtw. | {{Seed}} | ||
[[Image:2qtw.png|left|200px]] | |||
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{{STRUCTURE_2qtw| PDB=2qtw | SCENE= }} | {{STRUCTURE_2qtw| PDB=2qtw | SCENE= }} | ||
===The Crystal Structure of PCSK9 at 1.9 Angstroms Resolution Reveals structural homology to Resistin within the C-terminal domain=== | |||
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{{ABSTRACT_PUBMED_17804797}} | |||
==About this Structure== | ==About this Structure== | ||
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[[Category: Steroid metabolism]] | [[Category: Steroid metabolism]] | ||
[[Category: Zymogen]] | [[Category: Zymogen]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | |||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jul 29 02:26:58 2008'' |
Revision as of 02:26, 29 July 2008
The Crystal Structure of PCSK9 at 1.9 Angstroms Resolution Reveals structural homology to Resistin within the C-terminal domainThe Crystal Structure of PCSK9 at 1.9 Angstroms Resolution Reveals structural homology to Resistin within the C-terminal domain
Template:ABSTRACT PUBMED 17804797
About this StructureAbout this Structure
2QTW is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
ReferenceReference
The self-inhibited structure of full-length PCSK9 at 1.9 A reveals structural homology with resistin within the C-terminal domain., Hampton EN, Knuth MW, Li J, Harris JL, Lesley SA, Spraggon G, Proc Natl Acad Sci U S A. 2007 Sep 11;104(37):14604-9. Epub 2007 Sep 5. PMID:17804797
Page seeded by OCA on Tue Jul 29 02:26:58 2008
Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)
OCACategories:
- Pages with broken file links
- Homo sapiens
- Protein complex
- Hampton, E N.
- Harris, J L.
- Knuth, M W.
- Lesley, S A.
- Li, J.
- Spraggon, G.
- Alternative splicing
- Autocatalytic cleavage
- Calcium
- Cholesterol metabolism
- Coronary heart disease
- Disease mutation
- Glycoprotein
- Hydrolase
- Hypercholesterolemia
- Lipid metabolism
- Low density lipoprotein receptor
- Phosphorylation
- Polymorphism
- Pro-protein convertase
- Protease
- Secreted
- Serine protease
- Steroid metabolism
- Zymogen