3efw: Difference between revisions

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~~{{Seed}}~~

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

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

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==About this Structure==

~~3EFW~~ 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=3EFW OCA].

[[3efw]] is a 2 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=3EFW OCA].

==Reference==

Pyridyl-pyrimidine benzimidazole derivatives as potent, selective, and orally bioavailable inhibitors of Tie-2 kinase., Cee VJ, Cheng AC, Romero K, Bellon S, Mohr C, Whittington DA, Bak A, Bready J, Caenepeel S, Coxon A, Deak HL, Fretland J, Gu Y, Hodous BL, Huang X, Kim JL, Lin J, Long AM, Nguyen H, Olivieri PR, Patel VF, Wang L, Zhou Y, Hughes P, Geuns-Meyer S, Bioorg Med Chem Lett. 2008 Nov 20. PMID:~~[http://www.ncbi.nlm.nih.gov~~/~~pubmed~~/~~19062275 19062275]~~

[[Category: Homo sapiens]]

[[Category: Non-specific serine/threonine protein kinase]]

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[[Category: Nucleotide-binding]]

[[Category: Phosphoprotein]]

~~[[Category: Polymorphism]]~~

[[Category: Serine/threonine-protein kinase]]

[[Category: Stk6_human]]

[[Category: Transferase]]

[[Category: Transferase-inhibitor complex]]

~~''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Dec 24 11:31:51 2008''~~

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@@ Line 1: / Line 1: @@
-{{Seed}}
+[[Image:3efw.png|left|200px]]
-[[Image:3efw.jpg|left|200px]]
 <!--
@@ Line 20: / Line 19: @@
 ==About this Structure==
-EFW 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=3EFW OCA].
+[[3efw]] is a 2 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=3EFW OCA].
 ==Reference==
-Pyridyl-pyrimidine benzimidazole derivatives as potent, selective, and orally bioavailable inhibitors of Tie-2 kinase., Cee VJ, Cheng AC, Romero K, Bellon S, Mohr C, Whittington DA, Bak A, Bready J, Caenepeel S, Coxon A, Deak HL, Fretland J, Gu Y, Hodous BL, Huang X, Kim JL, Lin J, Long AM, Nguyen H, Olivieri PR, Patel VF, Wang L, Zhou Y, Hughes P, Geuns-Meyer S, Bioorg Med Chem Lett. 2008 Nov 20. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/19062275 19062275]
+<ref group="xtra">PMID:019062275</ref><references group="xtra"/>
 [[Category: Homo sapiens]]
 [[Category: Non-specific serine/threonine protein kinase]]
@@ Line 37: / Line 36: @@
 [[Category: Nucleotide-binding]]
 [[Category: Phosphoprotein]]
-[[Category: Polymorphism]]
 [[Category: Serine/threonine-protein kinase]]
 [[Category: Stk6_human]]
-[[Category: Transferase]]
+[[Category: Transferase-inhibitor complex]]
-''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Dec 24 11:31:51 2008''