3ud5
From Proteopedia
(Difference between revisions)
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- | + | [[Image:3ud5.jpg|left|200px]] | |
- | The | + | <!-- |
+ | The line below this paragraph, containing "STRUCTURE_3ud5", creates the "Structure Box" on the page. | ||
+ | You may change the PDB parameter (which sets the PDB file loaded into the applet) | ||
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+ | {{STRUCTURE_3ud5| PDB=3ud5 | SCENE= }} | ||
- | + | ===Crystal structure of E. coli HPPK in complex with bisubstrate analogue inhibitor J1A=== | |
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+ | <!-- | ||
+ | The line below this paragraph, {{ABSTRACT_PUBMED_22169600}}, adds the Publication Abstract to the page | ||
+ | (as it appears on PubMed at http://www.pubmed.gov), where 22169600 is the PubMed ID number. | ||
+ | --> | ||
+ | {{ABSTRACT_PUBMED_22169600}} | ||
+ | |||
+ | ==About this Structure== | ||
+ | [[3ud5]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3UD5 OCA]. | ||
+ | |||
+ | ==Reference== | ||
+ | <ref group="xtra">PMID:022169600</ref><ref group="xtra">PMID:011311059</ref><references group="xtra"/> | ||
+ | [[Category: 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase]] | ||
+ | [[Category: Escherichia coli]] | ||
+ | [[Category: Ji, X.]] | ||
+ | [[Category: Shaw, G.]] | ||
+ | [[Category: Shi, G.]] | ||
+ | [[Category: Alpha beta]] | ||
+ | [[Category: Atp binding]] | ||
+ | [[Category: Kinase]] | ||
+ | [[Category: Pyrophosphoryl transfer]] | ||
+ | [[Category: Transferase-transferase inhibitor complex]] |
Revision as of 06:03, 4 January 2012
Crystal structure of E. coli HPPK in complex with bisubstrate analogue inhibitor J1A
Template:ABSTRACT PUBMED 22169600
About this Structure
3ud5 is a 1 chain structure with sequence from Escherichia coli. Full crystallographic information is available from OCA.
Reference
- Shi G, Shaw G, Liang YH, Subburaman P, Li Y, Wu Y, Yan H, Ji X. Bisubstrate analogue inhibitors of 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase: New design with improved properties. Bioorg Med Chem. 2012 Jan 1;20(1):47-57. Epub 2011 Nov 23. PMID:22169600 doi:10.1016/j.bmc.2011.11.032
- Shi G, Blaszczyk J, Ji X, Yan H. Bisubstrate analogue inhibitors of 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase: synthesis and biochemical and crystallographic studies. J Med Chem. 2001 Apr 26;44(9):1364-71. PMID:11311059