3ceh: Difference between revisions
From Proteopedia
Jump to navigationJump to search
No edit summary |
No edit summary |
||
| Line 23: | Line 23: | ||
==About this Structure== | ==About this Structure== | ||
3CEH is a | 3CEH is a 2 chains structure of 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=3CEH OCA]. | ||
==Reference== | ==Reference== | ||
<ref group="xtra">PMID:18373353</ref><references group="xtra"/> | |||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Phosphorylase]] | [[Category: Phosphorylase]] | ||
[[Category: Anderka, O.]] | [[Category: Anderka, O.]] | ||
[[Category: Defossa, E.]] | [[Category: Defossa, E.]] | ||
| Line 53: | Line 52: | ||
[[Category: Transferase]] | [[Category: Transferase]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 09:55:22 2009'' | ||
Revision as of 07:55, 17 February 2009
Human liver glycogen phosphorylase (tense state) in complex with the allosteric inhibitor AVE5688
Template:ABSTRACT PUBMED 18373353
Disease
Known disease associated with this structure: Glycogen storage disease VI OMIM:[232700]
About this Structure
3CEH is a 2 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Anderka O, Loenze P, Klabunde T, Dreyer MK, Defossa E, Wendt KU, Schmoll D. Thermodynamic characterization of allosteric glycogen phosphorylase inhibitors. Biochemistry. 2008 Apr 22;47(16):4683-91. Epub 2008 Mar 29. PMID:18373353 doi:10.1021/bi702397d
Page seeded by OCA on Tue Feb 17 09:55:22 2009
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- Homo sapiens
- Phosphorylase
- Anderka, O.
- Defossa, E.
- Dreyer, M K.
- Klabunde, T.
- Loenze, P.
- Schmoll, D.
- Wendt, K U.
- Acetylation
- Allosteric enzyme
- Allosteric inhibitor
- Carbohydrate metabolism
- Disease mutation
- Glycogen metabolism
- Glycogen storage disease
- Glycosyltransferase
- Nucleotide-binding
- Phosphoprotein
- Polymorphism
- Protein ligand complex
- Pyridoxal phosphate
- Tense state
- Transferase