2l9n
From Proteopedia
(Difference between revisions)
Line 1: | Line 1: | ||
- | + | [[Image:2l9n.jpg|left|200px]] | |
- | The | + | <!-- |
+ | The line below this paragraph, containing "STRUCTURE_2l9n", creates the "Structure Box" on the page. | ||
+ | You may change the PDB parameter (which sets the PDB file loaded into the applet) | ||
+ | or the SCENE parameter (which sets the initial scene displayed when the page is loaded), | ||
+ | or leave the SCENE parameter empty for the default display. | ||
+ | --> | ||
+ | {{STRUCTURE_2l9n| PDB=2l9n | SCENE= }} | ||
- | + | ===Structure of the human Shwachman-Bodian-Diamond syndrome (SBDS) protein=== | |
- | + | ||
+ | <!-- | ||
+ | The line below this paragraph, {{ABSTRACT_PUBMED_21536732}}, adds the Publication Abstract to the page | ||
+ | (as it appears on PubMed at http://www.pubmed.gov), where 21536732 is the PubMed ID number. | ||
+ | --> | ||
+ | {{ABSTRACT_PUBMED_21536732}} | ||
+ | |||
+ | ==About this Structure== | ||
+ | [[2l9n]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2L9N OCA]. | ||
+ | |||
+ | ==Reference== | ||
+ | <ref group="xtra">PMID:021536732</ref><references group="xtra"/> | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Freund, S M.V.]] | ||
+ | [[Category: Hilcenko, C.]] | ||
+ | [[Category: Warren, A J.]] |
Revision as of 04:37, 12 May 2011
Structure of the human Shwachman-Bodian-Diamond syndrome (SBDS) protein
Template:ABSTRACT PUBMED 21536732
About this Structure
2l9n is a 1 chain structure with sequence from Homo sapiens. Full experimental information is available from OCA.
Reference
- Finch AJ, Hilcenko C, Basse N, Drynan LF, Goyenechea B, Menne TF, Gonzalez Fernandez A, Simpson P, D'Santos CS, Arends MJ, Donadieu J, Bellanne-Chantelot C, Costanzo M, Boone C, McKenzie AN, Freund SM, Warren AJ. Uncoupling of GTP hydrolysis from eIF6 release on the ribosome causes Shwachman-Diamond syndrome. Genes Dev. 2011 May 1;25(9):917-29. PMID:21536732 doi:10.1101/gad.623011