3oy1
From Proteopedia
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- | + | [[Image:3oy1.jpg|left|200px]] | |
- | The | + | <!-- |
+ | The line below this paragraph, containing "STRUCTURE_3oy1", 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_3oy1| PDB=3oy1 | SCENE= }} | ||
- | + | ===Highly Selective c-Jun N-Terminal Kinase (JNK) 2 and 3 Inhibitors with In Vitro CNS-like Pharmacokinetic Properties=== | |
- | + | ||
+ | <!-- | ||
+ | The line below this paragraph, {{ABSTRACT_PUBMED_21112785}}, adds the Publication Abstract to the page | ||
+ | (as it appears on PubMed at http://www.pubmed.gov), where 21112785 is the PubMed ID number. | ||
+ | --> | ||
+ | {{ABSTRACT_PUBMED_21112785}} | ||
+ | |||
+ | ==About this Structure== | ||
+ | [[3oy1]] 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=3OY1 OCA]. | ||
+ | |||
+ | ==Reference== | ||
+ | <ref group="xtra">PMID:021112785</ref><references group="xtra"/> | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Mitogen-activated protein kinase]] | ||
+ | [[Category: Bowers, S.]] | ||
+ | [[Category: Galemmo, R A.]] | ||
+ | [[Category: Hom, R K.]] | ||
+ | [[Category: Konradi, A W.]] | ||
+ | [[Category: Neitz, J.]] | ||
+ | [[Category: Pan, H.]] | ||
+ | [[Category: Probst, G D.]] | ||
+ | [[Category: Quincy, D.]] | ||
+ | [[Category: Sealy, J M.]] | ||
+ | [[Category: Sham, H L.]] | ||
+ | [[Category: Truong, A.]] | ||
+ | [[Category: Yao, N.]] | ||
+ | [[Category: Cn]] | ||
+ | [[Category: Kinase inhibitor]] | ||
+ | [[Category: Selectivity]] | ||
+ | [[Category: Transferase]] | ||
+ | [[Category: Transherase-transferase inhibitor complex]] |
Revision as of 06:18, 17 August 2011
Highly Selective c-Jun N-Terminal Kinase (JNK) 2 and 3 Inhibitors with In Vitro CNS-like Pharmacokinetic Properties
Template:ABSTRACT PUBMED 21112785
About this Structure
3oy1 is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Probst GD, Bowers S, Sealy JM, Truong AP, Hom RK, Galemmo RA Jr, Konradi AW, Sham HL, Quincy DA, Pan H, Yao N, Lin M, Toth G, Artis DR, Zmolek W, Wong K, Qin A, Lorentzen C, Nakamura DF, Quinn KP, Sauer JM, Powell K, Ruslim L, Wright S, Chereau D, Ren Z, Anderson JP, Bard F, Yednock TA, Griswold-Prenner I. Highly selective c-Jun N-terminal kinase (JNK) 2 and 3 inhibitors with in vitro CNS-like pharmacokinetic properties prevent neurodegeneration. Bioorg Med Chem Lett. 2011 Jan 1;21(1):315-9. Epub 2010 Nov 5. PMID:21112785 doi:10.1016/j.bmcl.2010.11.010
Categories: Homo sapiens | Mitogen-activated protein kinase | Bowers, S. | Galemmo, R A. | Hom, R K. | Konradi, A W. | Neitz, J. | Pan, H. | Probst, G D. | Quincy, D. | Sealy, J M. | Sham, H L. | Truong, A. | Yao, N. | Cn | Kinase inhibitor | Selectivity | Transferase | Transherase-transferase inhibitor complex