1py2: Difference between revisions

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[[Image:1py2.jpg|left|200px]]
[[Image:1py2.jpg|left|200px]]


{{Structure
<!--
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The line below this paragraph, containing "STRUCTURE_1py2", creates the "Structure Box" on the page.
|SITE=
You may change the PDB parameter (which sets the PDB file loaded into the applet)
|LIGAND= <scene name='pdbligand=FRH:5-[2,3-DICHLORO-4-(5-{1-[2-(2-GUANIDINO-4-METHYL-PENTANOYLAMINO)-ACETYL]-PIPERIDIN-4-YL}-1-METHYL-1H-PYRAZOL-3-YL)-PHENOXYMETHYL]-FURAN-2-CARBOXYLIC+ACID'>FRH</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene>
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|ACTIVITY=
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|GENE= IL2 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
-->
|DOMAIN=
{{STRUCTURE_1py2| PDB=1py2  | SCENE= }}  
|RELATEDENTRY=
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1py2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1py2 OCA], [http://www.ebi.ac.uk/pdbsum/1py2 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1py2 RCSB]</span>
}}


'''Structure of a 60 nM Small Molecule Bound to a Hot Spot on IL-2'''
'''Structure of a 60 nM Small Molecule Bound to a Hot Spot on IL-2'''
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[[Category: Thanos, C D.]]
[[Category: Thanos, C D.]]
[[Category: Wells, J A.]]
[[Category: Wells, J A.]]
[[Category: hot spot]]
[[Category: Hot spot]]
[[Category: il-2]]
[[Category: Il-2]]
[[Category: interleukin 2]]
[[Category: Interleukin 2]]
[[Category: molecular recognition]]
[[Category: Molecular recognition]]
[[Category: small molecule]]
[[Category: Small molecule]]
 
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Revision as of 05:37, 3 May 2008

File:1py2.jpg

Template:STRUCTURE 1py2

Structure of a 60 nM Small Molecule Bound to a Hot Spot on IL-2


OverviewOverview

The complexes between IL-2 and two similar small molecules, one a lead compound and the other a potent, affinity-optimized compound, were determined by X-ray crystallography. The lead compound (IC50 = 6 muM) bound to a hot spot on IL-2 in a groove that is not apparent in either the unliganded protein or a complex between IL-2 and a weakly bound drug fragment. The affinity-optimized compound (IC50 = 0.06 muM), which has an added aromatic acid fragment, bound in the same groove as the lead compound. In addition, a novel binding site was formed for the aromatic acid which is unseen in the complex with the lead compound. Thus, the hot spot on IL-2 is highly dynamic, with the protein changing form at multiple sites to maximize packing for each compound. Binding-site rigidity is often thought to play a role in high-affinity interactions. However, in this case, specific contacts between the small molecule and the protein are made despite the adaptivity of the hot spot. Given the change in morphology that was observed in IL-2, it is unlikely that a potent inhibitor could have been found by rational design. Therefore, fragment assembly methods offer the stochastic advantage of finding fragments in flexible protein regions where structural changes are unpredictable.

DiseaseDisease

Known disease associated with this structure: Severe combined immunodeficiency due to IL2 deficiency OMIM:[147680]

About this StructureAbout this Structure

1PY2 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

ReferenceReference

Potent small-molecule binding to a dynamic hot spot on IL-2., Thanos CD, Randal M, Wells JA, J Am Chem Soc. 2003 Dec 17;125(50):15280-1. PMID:14664558 Page seeded by OCA on Sat May 3 05:37:56 2008

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