2vtr: Difference between revisions
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{{Seed}} | {{Seed}} | ||
[[Image:2vtr. | [[Image:2vtr.png|left|200px]] | ||
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==About this Structure== | ==About this Structure== | ||
2VTR is a | 2VTR 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=2VTR OCA]. | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Berdini, V.]] | [[Category: Berdini, V.]] | ||
[[Category: Boulstridge, J A.]] | [[Category: Boulstridge, J A.]] | ||
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[[Category: Transferase]] | [[Category: Transferase]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 19:57:12 2009'' | ||
Revision as of 20:57, 17 February 2009
IDENTIFICATION OF N-(4-PIPERIDINYL)-4-(2,6-DICHLOROBENZOYLAMINO)-1H-PYRAZOLE-3-CARBOXAMIDE (AT7519), A NOVEL CYCLIN DEPENDENT KINASE INHIBITOR USING FRAGMENT-BASED X-RAY CRYSTALLOGRAPHY AND STRUCTURE BASED DRUG DESIGN.IDENTIFICATION OF N-(4-PIPERIDINYL)-4-(2,6-DICHLOROBENZOYLAMINO)-1H-PYRAZOLE-3-CARBOXAMIDE (AT7519), A NOVEL CYCLIN DEPENDENT KINASE INHIBITOR USING FRAGMENT-BASED X-RAY CRYSTALLOGRAPHY AND STRUCTURE BASED DRUG DESIGN.
About this StructureAbout this Structure
2VTR is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Page seeded by OCA on Tue Feb 17 19:57:12 2009
Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)
OCACategories:
- Pages with broken file links
- Homo sapiens
- Berdini, V.
- Boulstridge, J A.
- Brien, M A.O.
- Carr, M G.
- Cross, D M.
- Danillon, D.
- Davis, D J.
- Devine, L A.
- Early, T R.
- Feltell, R E.
- Lewis, E J.
- Mcmenamin, R L.
- Navarro, E F.
- Reilly, M O.
- Reule, M.
- Saxty, G.
- Seavers, L C.A.
- Smith, D M.
- Squires, M S.
- Trewartha, G.
- Walker, M T.
- Woodhead, A J.
- Woolford, A J.A.
- Wyatt, P G.
- Atp-binding
- Cell cycle
- Cell division
- Fragment screening
- Kinase
- Mitosis
- Nucleotide-binding
- Phosphoprotein
- Phosphorylation
- Polymorphism
- Protein kinase
- Serine/threonine protein kinase
- Serine/threonine-protein kinase
- Structure based drug design
- Transferase