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New page: left|200px<br /> <applet load="2gfo" size="450" color="white" frame="true" align="right" spinBox="true" caption="2gfo, resolution 2.00Å" /> '''Structure of the Ca...
 
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[[Image:2gfo.gif|left|200px]]<br />
[[Image:2gfo.gif|left|200px]]<br /><applet load="2gfo" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="2gfo" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="2gfo, resolution 2.00&Aring;" />
caption="2gfo, resolution 2.00&Aring;" />
'''Structure of the Catalytic Domain of Human Ubiquitin Carboxyl-terminal Hydrolase 8'''<br />
'''Structure of the Catalytic Domain of Human Ubiquitin Carboxyl-terminal Hydrolase 8'''<br />


==Overview==
==Overview==
Ubiquitin-specific protease 8 (USP8) hydrolyzes mono and polyubiquitylated, targets such as epidermal growth factor receptors and is involved in, clathrin-mediated internalization. In 1182 residues, USP8 contains, multiple domains, including coiled-coil, rhodanese, and catalytic domains., We report the first high-resolution crystal structures of these domains, and discuss their implications for USP8 function. The amino-terminal, domain is a homodimer with a novel fold. It is composed of two five-helix, bundles, where the first helices are swapped, and carboxyl-terminal, helices are extended in an antiparallel fashion. The structure of the, rhodanese domain, determined in complex with the E3 ligase NRDP1, reveals, the canonical rhodanese fold but with a distorted primordial active site., The USP8 recognition domain of NRDP1 has a novel protein fold that, interacts with a conserved peptide loop of the rhodanese domain. A, consensus sequence of this loop is found in other NRDP1 targets, suggesting a common mode of interaction. The structure of the, carboxyl-terminal catalytic domain of USP8 exhibits the conserved, tripartite architecture but shows unique traits. Notably, the active site, including the ubiquitin binding pocket, is in a closed conformation, incompatible with substrate binding. The presence of a zinc ribbon, subdomain near the ubiquitin binding site further suggests a, polyubiquitin-specific binding site and a mechanism for substrate induced, conformational changes.
Ubiquitin-specific protease 8 (USP8) hydrolyzes mono and polyubiquitylated targets such as epidermal growth factor receptors and is involved in clathrin-mediated internalization. In 1182 residues, USP8 contains multiple domains, including coiled-coil, rhodanese, and catalytic domains. We report the first high-resolution crystal structures of these domains and discuss their implications for USP8 function. The amino-terminal domain is a homodimer with a novel fold. It is composed of two five-helix bundles, where the first helices are swapped, and carboxyl-terminal helices are extended in an antiparallel fashion. The structure of the rhodanese domain, determined in complex with the E3 ligase NRDP1, reveals the canonical rhodanese fold but with a distorted primordial active site. The USP8 recognition domain of NRDP1 has a novel protein fold that interacts with a conserved peptide loop of the rhodanese domain. A consensus sequence of this loop is found in other NRDP1 targets, suggesting a common mode of interaction. The structure of the carboxyl-terminal catalytic domain of USP8 exhibits the conserved tripartite architecture but shows unique traits. Notably, the active site, including the ubiquitin binding pocket, is in a closed conformation, incompatible with substrate binding. The presence of a zinc ribbon subdomain near the ubiquitin binding site further suggests a polyubiquitin-specific binding site and a mechanism for substrate induced conformational changes.


==About this Structure==
==About this Structure==
2GFO 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 ZN as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Ubiquitin_thiolesterase Ubiquitin thiolesterase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.2.15 3.1.2.15] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2GFO OCA].  
2GFO 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=ZN:'>ZN</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Ubiquitin_thiolesterase Ubiquitin thiolesterase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.2.15 3.1.2.15] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2GFO OCA].  


==Reference==
==Reference==
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[[Category: Ubiquitin thiolesterase]]
[[Category: Ubiquitin thiolesterase]]
[[Category: Arrowsmith, C.]]
[[Category: Arrowsmith, C.]]
[[Category: Avvakumov, G.V]]
[[Category: Avvakumov, G V]]
[[Category: Bochkarev, A.]]
[[Category: Bochkarev, A.]]
[[Category: Butler-Cole, C.]]
[[Category: Butler-Cole, C.]]
[[Category: Dhe-Paganon, S.]]
[[Category: Dhe-Paganon, S.]]
[[Category: Edwards, A.]]
[[Category: Edwards, A.]]
[[Category: Jr., P.J.Finerty.]]
[[Category: Jr., P J.Finerty.]]
[[Category: Newman, E.M.]]
[[Category: Newman, E M.]]
[[Category: SGC, Structural.Genomics.Consortium.]]
[[Category: SGC, Structural Genomics Consortium.]]
[[Category: Sundstrom, M.]]
[[Category: Sundstrom, M.]]
[[Category: Walker, J.R.]]
[[Category: Walker, J R.]]
[[Category: Weigelt, J.]]
[[Category: Weigelt, J.]]
[[Category: Xue, S.]]
[[Category: Xue, S.]]
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[[Category: zinc ribbon]]
[[Category: zinc ribbon]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 22:18:20 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 17:31:12 2008''