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3bgp
From Proteopedia
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[[Image:3bgp.gif|left|200px]] | [[Image:3bgp.gif|left|200px]] | ||
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| - | | | + | {{STRUCTURE_3bgp| PDB=3bgp | SCENE= }} |
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'''Human Pim-1 complexed with a benzoisoxazole inhibitor VX1''' | '''Human Pim-1 complexed with a benzoisoxazole inhibitor VX1''' | ||
| + | |||
| + | ==Overview== | ||
| + | To supplement the hits from a high throughput screen, docking was performed against Pim-1 kinase. Glide docking was augmented with a filter to require traditional or aromatic CH..O hydrogen bonds to the kinase hinge. Four diverse actives, of 96 molecules assayed, had K(i) values between 0.091 and 4.5 microM. This gives a 14-fold enrichment over the earlier HTS run, and the two crystal structures solved confirmed the binding modes predicted by docking. | ||
==About this Structure== | ==About this Structure== | ||
3BGP is a [[Single protein]] 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=3BGP OCA]. | 3BGP is a [[Single protein]] 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=3BGP OCA]. | ||
| + | |||
| + | ==Reference== | ||
| + | Docking study yields four novel inhibitors of the protooncogene Pim-1 kinase., Pierce AC, Jacobs M, Stuver-Moody C, J Med Chem. 2008 Mar 27;51(6):1972-5. Epub 2008 Feb 22. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/18290603 18290603] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Non-specific serine/threonine protein kinase]] | [[Category: Non-specific serine/threonine protein kinase]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Jacobs, M D.]] | [[Category: Jacobs, M D.]] | ||
| - | [[Category: | + | [[Category: Alternative initiation]] |
| - | [[Category: | + | [[Category: Atp-binding]] |
| - | [[Category: | + | [[Category: Cytoplasm]] |
| - | [[Category: | + | [[Category: Kinase inhibitor phosphorylation]] |
| - | [[Category: | + | [[Category: Manganese]] |
| - | [[Category: | + | [[Category: Membrane]] |
| - | [[Category: | + | [[Category: Metal-binding]] |
| - | [[Category: | + | [[Category: Nucleotide-binding]] |
| - | [[Category: | + | [[Category: Nucleus]] |
| - | [[Category: | + | [[Category: Phosphoprotein]] |
| - | [[Category: | + | [[Category: Proto-oncogene]] |
| - | [[Category: | + | [[Category: Serine/threonine-protein kinase]] |
| - | [[Category: | + | [[Category: Transferase]] |
| - | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Apr 30 13:38:41 2008'' | |
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | |
Revision as of 10:38, 30 April 2008
Human Pim-1 complexed with a benzoisoxazole inhibitor VX1
Overview
To supplement the hits from a high throughput screen, docking was performed against Pim-1 kinase. Glide docking was augmented with a filter to require traditional or aromatic CH..O hydrogen bonds to the kinase hinge. Four diverse actives, of 96 molecules assayed, had K(i) values between 0.091 and 4.5 microM. This gives a 14-fold enrichment over the earlier HTS run, and the two crystal structures solved confirmed the binding modes predicted by docking.
About this Structure
3BGP is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Docking study yields four novel inhibitors of the protooncogene Pim-1 kinase., Pierce AC, Jacobs M, Stuver-Moody C, J Med Chem. 2008 Mar 27;51(6):1972-5. Epub 2008 Feb 22. PMID:18290603 Page seeded by OCA on Wed Apr 30 13:38:41 2008
Categories: Homo sapiens | Non-specific serine/threonine protein kinase | Single protein | Jacobs, M D. | Alternative initiation | Atp-binding | Cytoplasm | Kinase inhibitor phosphorylation | Manganese | Membrane | Metal-binding | Nucleotide-binding | Nucleus | Phosphoprotein | Proto-oncogene | Serine/threonine-protein kinase | Transferase
