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2vwy
From Proteopedia
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| - | == | + | ==ephB4 kinase domain inhibitor complex== |
<StructureSection load='2vwy' size='340' side='right' caption='[[2vwy]], [[Resolution|resolution]] 1.65Å' scene=''> | <StructureSection load='2vwy' size='340' side='right' caption='[[2vwy]], [[Resolution|resolution]] 1.65Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[2vwy]] is a 1 chain structure | + | <table><tr><td colspan='2'>[[2vwy]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2VWY OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2VWY FirstGlance]. <br> |
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=7X5:N-(5-CHLORO-1,3-BENZODIOXOL-4-YL)-N-(3-METHYLSULFONYLPHENYL)PYRIMIDINE-2,4-DIAMINE'>7X5</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene></td></tr> | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=7X5:N-(5-CHLORO-1,3-BENZODIOXOL-4-YL)-N-(3-METHYLSULFONYLPHENYL)PYRIMIDINE-2,4-DIAMINE'>7X5</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene></td></tr> | ||
<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[2vwz|2vwz]], [[2bba|2bba]], [[2vwu|2vwu]], [[2vwv|2vwv]], [[2vww|2vww]], [[2vwx|2vwx]], [[2vx0|2vx0]], [[2vx1|2vx1]]</td></tr> | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[2vwz|2vwz]], [[2bba|2bba]], [[2vwu|2vwu]], [[2vwv|2vwv]], [[2vww|2vww]], [[2vwx|2vwx]], [[2vx0|2vx0]], [[2vx1|2vx1]]</td></tr> | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| - | [[Category: Human]] | ||
[[Category: Receptor protein-tyrosine kinase]] | [[Category: Receptor protein-tyrosine kinase]] | ||
[[Category: Barratt, D]] | [[Category: Barratt, D]] | ||
| Line 44: | Line 43: | ||
[[Category: Kettle, J G]] | [[Category: Kettle, J G]] | ||
[[Category: Leach, A G]] | [[Category: Leach, A G]] | ||
| - | [[Category: | + | [[Category: McCall, E J]] |
[[Category: Read, J]] | [[Category: Read, J]] | ||
[[Category: Valentine, A L]] | [[Category: Valentine, A L]] | ||
| Line 54: | Line 53: | ||
[[Category: Nucleotide-binding]] | [[Category: Nucleotide-binding]] | ||
[[Category: Phosphoprotein]] | [[Category: Phosphoprotein]] | ||
| + | [[Category: Polymorphism]] | ||
[[Category: Receptor]] | [[Category: Receptor]] | ||
[[Category: Receptor tyrosine kinase]] | [[Category: Receptor tyrosine kinase]] | ||
Revision as of 11:01, 3 August 2017
ephB4 kinase domain inhibitor complex
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Categories: Receptor protein-tyrosine kinase | Barratt, D | Brassington, C A | Green, I | Kettle, J G | Leach, A G | McCall, E J | Read, J | Valentine, A L | Atp-binding | Glycoprotein | Kinase | Membrane | Mutant | Nucleotide-binding | Phosphoprotein | Polymorphism | Receptor | Receptor tyrosine kinase | Transferase | Transmembrane | Tyrosine-protein kinase | Unphosphorylated

