2ihw: Difference between revisions

New page: left|200px<br /><applet load="2ihw" size="450" color="white" frame="true" align="right" spinBox="true" caption="2ihw, resolution 2.700Å" /> '''Crystal structure o...
 
No edit summary
Line 1: Line 1:
[[Image:2ihw.jpg|left|200px]]<br /><applet load="2ihw" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:2ihw.jpg|left|200px]]<br /><applet load="2ihw" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="2ihw, resolution 2.700&Aring;" />
caption="2ihw, resolution 2.700&Aring;" />
'''Crystal structure of a cubic core of the dihydrolipoamide acyltransferase (E2b) component in the branched-chain alpha-ketoacid dehydrogenase complex (BCKDC), apo form'''<br />
'''Crystal structure of a cubic core of the dihydrolipoamide acyltransferase (E2b) component in the branched-chain alpha-ketoacid dehydrogenase complex (BCKDC), apo form'''<br />


==Overview==
==Overview==
The dihydrolipoamide acyltransferase (E2b) component of the branched-chain, alpha-ketoacid dehydrogenase complex forms a cubic scaffold that catalyzes, acyltransfer from S-acyldihydrolipoamide to CoA to produce acyl-CoA. We, have determined the first crystal structures of a mammalian (bovine) E2b, core domain with and without a bound CoA or acyl-CoA. These structures, reveal both hydrophobic and the previously unreported ionic interactions, between two-fold-related trimers that build up the cubic core. The, entrance of the dihydrolipoamide-binding site in a 30-A long active-site, channel is closed in the apo and acyl-CoA-bound structures. CoA binding to, one entrance of the channel promotes a conformational change in the, channel, resulting in the opening of the opposite dihydrolipoamide gate., Binding experiments show that the affinity of the E2b core for, dihydrolipoamide is markedly increased in the presence of CoA. The result, buttresses the model that CoA binding is responsible for the opening of, the dihydrolipoamide gate. We suggest that this gating mechanism, synchronizes the binding of the two substrates to the active-site channel, which serves as a feed-forward switch to coordinate the E2b-catalyzed, acyltransfer reaction.
The dihydrolipoamide acyltransferase (E2b) component of the branched-chain alpha-ketoacid dehydrogenase complex forms a cubic scaffold that catalyzes acyltransfer from S-acyldihydrolipoamide to CoA to produce acyl-CoA. We have determined the first crystal structures of a mammalian (bovine) E2b core domain with and without a bound CoA or acyl-CoA. These structures reveal both hydrophobic and the previously unreported ionic interactions between two-fold-related trimers that build up the cubic core. The entrance of the dihydrolipoamide-binding site in a 30-A long active-site channel is closed in the apo and acyl-CoA-bound structures. CoA binding to one entrance of the channel promotes a conformational change in the channel, resulting in the opening of the opposite dihydrolipoamide gate. Binding experiments show that the affinity of the E2b core for dihydrolipoamide is markedly increased in the presence of CoA. The result buttresses the model that CoA binding is responsible for the opening of the dihydrolipoamide gate. We suggest that this gating mechanism synchronizes the binding of the two substrates to the active-site channel, which serves as a feed-forward switch to coordinate the E2b-catalyzed acyltransfer reaction.


==About this Structure==
==About this Structure==
2IHW is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus] with ACT and CL as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Dihydrolipoyllysine-residue_(2-methylpropanoyl)transferase Dihydrolipoyllysine-residue (2-methylpropanoyl)transferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.1.168 2.3.1.168] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2IHW OCA].  
2IHW is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus] with <scene name='pdbligand=ACT:'>ACT</scene> and <scene name='pdbligand=CL:'>CL</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Dihydrolipoyllysine-residue_(2-methylpropanoyl)transferase Dihydrolipoyllysine-residue (2-methylpropanoyl)transferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.1.168 2.3.1.168] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2IHW OCA].  


==Reference==
==Reference==
Line 14: Line 14:
[[Category: Dihydrolipoyllysine-residue (2-methylpropanoyl)transferase]]
[[Category: Dihydrolipoyllysine-residue (2-methylpropanoyl)transferase]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Brautigam, C.A.]]
[[Category: Brautigam, C A.]]
[[Category: Chuang, D.T.]]
[[Category: Chuang, D T.]]
[[Category: Chuang, J.L.]]
[[Category: Chuang, J L.]]
[[Category: Custorio, M.]]
[[Category: Custorio, M.]]
[[Category: Kato, M.]]
[[Category: Kato, M.]]
[[Category: Wynn, R.M.]]
[[Category: Wynn, R M.]]
[[Category: ACT]]
[[Category: ACT]]
[[Category: CL]]
[[Category: CL]]
Line 26: Line 26:
[[Category: homo trimer]]
[[Category: homo trimer]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 12:19:42 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 17:52:52 2008''

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA