2a2k

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[[Image:2a2k.gif|left|200px]]<br /><applet load="2a2k" size="350" color="white" frame="true" align="right" spinBox="true"
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[[Image:2a2k.gif|left|200px]]
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caption="2a2k, resolution 1.52&Aring;" />
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'''Crystal Structure of an active site mutant, C473S, of Cdc25B Phosphatase Catalytic Domain'''<br />
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{{Structure
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|PDB= 2a2k |SIZE=350|CAPTION= <scene name='initialview01'>2a2k</scene>, resolution 1.52&Aring;
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|SITE=
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|LIGAND= <scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene> and <scene name='pdbligand=SO4:SULFATE ION'>SO4</scene>
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|ACTIVITY= [http://en.wikipedia.org/wiki/Protein-tyrosine-phosphatase Protein-tyrosine-phosphatase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.3.48 3.1.3.48]
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|GENE= CDC25B, CDC25HU2 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
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}}
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'''Crystal Structure of an active site mutant, C473S, of Cdc25B Phosphatase Catalytic Domain'''
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==Overview==
==Overview==
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==About this Structure==
==About this Structure==
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2A2K is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=CL:'>CL</scene> and <scene name='pdbligand=SO4:'>SO4</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Protein-tyrosine-phosphatase Protein-tyrosine-phosphatase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.3.48 3.1.3.48] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2A2K OCA].
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2A2K 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=2A2K OCA].
==Reference==
==Reference==
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Experimental validation of the docking orientation of Cdc25 with its Cdk2-CycA protein substrate., Sohn J, Parks JM, Buhrman G, Brown P, Kristjansdottir K, Safi A, Edelsbrunner H, Yang W, Rudolph J, Biochemistry. 2005 Dec 20;44(50):16563-73. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=16342947 16342947]
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Experimental validation of the docking orientation of Cdc25 with its Cdk2-CycA protein substrate., Sohn J, Parks JM, Buhrman G, Brown P, Kristjansdottir K, Safi A, Edelsbrunner H, Yang W, Rudolph J, Biochemistry. 2005 Dec 20;44(50):16563-73. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/16342947 16342947]
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Protein-tyrosine-phosphatase]]
[[Category: Protein-tyrosine-phosphatase]]
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[[Category: substrate trapping]]
[[Category: substrate trapping]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:22:58 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 15:44:37 2008''

Revision as of 13:44, 20 March 2008


PDB ID 2a2k

Drag the structure with the mouse to rotate
, resolution 1.52Å
Ligands: and
Gene: CDC25B, CDC25HU2 (Homo sapiens)
Activity: Protein-tyrosine-phosphatase, with EC number 3.1.3.48
Coordinates: save as pdb, mmCIF, xml



Crystal Structure of an active site mutant, C473S, of Cdc25B Phosphatase Catalytic Domain


Overview

Cdc25 phosphatases are key activators of the eukaryotic cell cycle and compelling anticancer targets because their overexpression has been associated with numerous cancers. However, drug discovery targeting these phosphatases has been hampered by the lack of structural information about how Cdc25s interact with their native protein substrates, the cyclin-dependent kinases. Herein, we predict a docked orientation for Cdc25B with its Cdk2-pTpY-CycA protein substrate by a rigid-body docking method and refine the docked models with full-scale molecular dynamics simulations and minimization. We validate the stable ensemble structure experimentally by a variety of in vitro and in vivo techniques. Specifically, we compare our model with a crystal structure of the substrate-trapping mutant of Cdc25B. We identify and validate in vivo a novel hot-spot residue on Cdc25B (Arg492) that plays a central role in protein substrate recognition. We identify a hot-spot residue on the substrate Cdk2 (Asp206) and confirm its interaction with hot-spot residues on Cdc25 using hot-spot swapping and double mutant cycles to derive interaction energies. Our experimentally validated model is consistent with previous studies of Cdk2 and its interaction partners and initiates the opportunity for drug discovery of inhibitors that target the remote binding sites of this protein-protein interaction.

About this Structure

2A2K is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Experimental validation of the docking orientation of Cdc25 with its Cdk2-CycA protein substrate., Sohn J, Parks JM, Buhrman G, Brown P, Kristjansdottir K, Safi A, Edelsbrunner H, Yang W, Rudolph J, Biochemistry. 2005 Dec 20;44(50):16563-73. PMID:16342947

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