3byo: Difference between revisions

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[[Image:3byo.~~jpg~~|left|200px]]

[[Image:3byo.png|left|200px]]

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==About this Structure==

3BYO is a 1 chain structure of 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=3BYO OCA].

3BYO 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=3BYO OCA].

==Reference==

Structure-based design of novel 2-amino-6-phenyl-pyrimido[5',4':5,6]pyrimido[1,2-a]benzimidazol-5(6H)-ones as potent and orally active inhibitors of lymphocyte specific kinase (Lck): synthesis, SAR, and in vivo anti-inflammatory activity., Martin MW, Newcomb J, Nunes JJ, Boucher C, Chai L, Epstein LF, Faust T, Flores S, Gallant P, Gore A, Gu Y, Hsieh F, Huang X, Kim JL, Middleton S, Morgenstern K, Oliveira-dos-Santos A, Patel VF, Powers D, Rose P, Tudor Y, Turci SM, Welcher AA, Zack D, Zhao H, Zhu L, Zhu X, Ghiron C, Ermann M, Johnston D, Saluste CG, J Med Chem. 2008 Mar 27;51(6):1637-48. Epub 2008 Feb 16. PMID:~~[http:~~//~~www.ncbi.nlm.nih.gov/pubmed/18278858 18278858]~~

[[Category: Homo sapiens]]

[[Category: Non-specific protein-tyrosine kinase]]

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[[Category: Tyrosine-protein kinase]]

''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed ~~Dec 31 10~~:15:~~16 2008~~''

''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Mar 3 14:02:00 2010''

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@@ Line 1: / Line 1: @@
 {{Seed}}
-[[Image:3byo.jpg|left|200px]]
+[[Image:3byo.png|left|200px]]
 <!--
@@ Line 23: / Line 23: @@
 ==About this Structure==
-BYO is a 1 chain structure of 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=3BYO OCA].
+BYO 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=3BYO OCA].
 ==Reference==
-Structure-based design of novel 2-amino-6-phenyl-pyrimido[5',4':5,6]pyrimido[1,2-a]benzimidazol-5(6H)-ones as potent and orally active inhibitors of lymphocyte specific kinase (Lck): synthesis, SAR, and in vivo anti-inflammatory activity., Martin MW, Newcomb J, Nunes JJ, Boucher C, Chai L, Epstein LF, Faust T, Flores S, Gallant P, Gore A, Gu Y, Hsieh F, Huang X, Kim JL, Middleton S, Morgenstern K, Oliveira-dos-Santos A, Patel VF, Powers D, Rose P, Tudor Y, Turci SM, Welcher AA, Zack D, Zhao H, Zhu L, Zhu X, Ghiron C, Ermann M, Johnston D, Saluste CG, J Med Chem. 2008 Mar 27;51(6):1637-48. Epub 2008 Feb 16. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/18278858 18278858]
+<ref group="xtra">PMID:18278858</ref><references group="xtra"/>
 [[Category: Homo sapiens]]
 [[Category: Non-specific protein-tyrosine kinase]]
@@ Line 50: / Line 50: @@
 [[Category: Tyrosine-protein kinase]]
-''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Dec 31 10:15:16 2008''
+''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Mar  3 14:02:00 2010''