1llf: Difference between revisions

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New page: left|200px<br /><applet load="1llf" size="450" color="white" frame="true" align="right" spinBox="true" caption="1llf, resolution 1.4Å" /> '''Cholesterol Esterase ...
 
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[[Image:1llf.gif|left|200px]]<br /><applet load="1llf" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1llf.gif|left|200px]]<br /><applet load="1llf" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1llf, resolution 1.4&Aring;" />
caption="1llf, resolution 1.4&Aring;" />
'''Cholesterol Esterase (Candida Cylindracea) Crystal Structure at 1.4A resolution'''<br />
'''Cholesterol Esterase (Candida Cylindracea) Crystal Structure at 1.4A resolution'''<br />


==Overview==
==Overview==
The three-dimensional structure of a Candida cylindracea cholesterol, esterase (ChE) homodimer (534 x 2 amino acids) in complex with a ligand of, proposed formula C(23)H(48)O(2) has been determined at 1.4 A resolution in, space group P1 using synchrotron low-temperature data. The structure, refined to R = 0.136 and R(free) = 0.169 and has revealed new, stereochemical details in addition to those detected for the apo- and, holo-forms at 1.9 and 2.0 A resolution, respectively [Ghosh et al. (1995), Structure, 3, 279-288]. The cholesterol esterase structure is a dimer with, four spatially separated interfacial contact areas and two, symmetry-related pairs of openings to an internal intradimer cavity., Hydrophobic active-site gorges in each subunit face each other across a, central interfacial cavity. The ChE subunits have carbohydrate chains, attached to their Asn314 and Asn351 residues, with two ordered, N-acetyl-D-glucosoamine moieties visible at each site. The side chains of, 14 residues have two alternative conformations with occupancy values of, 0.5 +/- 0.2. For each subunit the electron density in the enzyme, active-site gorge is well modeled by a C(23)-chain fatty acid.
The three-dimensional structure of a Candida cylindracea cholesterol esterase (ChE) homodimer (534 x 2 amino acids) in complex with a ligand of proposed formula C(23)H(48)O(2) has been determined at 1.4 A resolution in space group P1 using synchrotron low-temperature data. The structure refined to R = 0.136 and R(free) = 0.169 and has revealed new stereochemical details in addition to those detected for the apo- and holo-forms at 1.9 and 2.0 A resolution, respectively [Ghosh et al. (1995), Structure, 3, 279-288]. The cholesterol esterase structure is a dimer with four spatially separated interfacial contact areas and two symmetry-related pairs of openings to an internal intradimer cavity. Hydrophobic active-site gorges in each subunit face each other across a central interfacial cavity. The ChE subunits have carbohydrate chains attached to their Asn314 and Asn351 residues, with two ordered N-acetyl-D-glucosoamine moieties visible at each site. The side chains of 14 residues have two alternative conformations with occupancy values of 0.5 +/- 0.2. For each subunit the electron density in the enzyme active-site gorge is well modeled by a C(23)-chain fatty acid.


==About this Structure==
==About this Structure==
1LLF is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Candida_cylindracea Candida cylindracea] with F23 as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Triacylglycerol_lipase Triacylglycerol lipase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.1.3 3.1.1.3] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1LLF OCA].  
1LLF is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Candida_cylindracea Candida cylindracea] with <scene name='pdbligand=F23:'>F23</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Triacylglycerol_lipase Triacylglycerol lipase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.1.3 3.1.1.3] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1LLF OCA].  


==Reference==
==Reference==
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[[Category: sterol ester acylhydrolase]]
[[Category: sterol ester acylhydrolase]]


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