1y3g: Difference between revisions

From Proteopedia
Jump to navigationJump to search
OCA (talk | contribs)
New page: left|200px<br /><applet load="1y3g" size="450" color="white" frame="true" align="right" spinBox="true" caption="1y3g, resolution 2.10Å" /> '''Crystal Structure of...
 
OCA (talk | contribs)
No edit summary
Line 1: Line 1:
[[Image:1y3g.gif|left|200px]]<br /><applet load="1y3g" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1y3g.gif|left|200px]]<br /><applet load="1y3g" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1y3g, resolution 2.10&Aring;" />
caption="1y3g, resolution 2.10&Aring;" />
'''Crystal Structure of a Silanediol Protease Inhibitor Bound to Thermolysin'''<br />
'''Crystal Structure of a Silanediol Protease Inhibitor Bound to Thermolysin'''<br />


==Overview==
==Overview==
Dialkylsilanediols have been found to be an effective functional group for, the design of active-site-directed protease inhibitors, including aspartic, (HIV protease) and metallo (ACE and thermolysin) proteases. The use of, silanediols is predicated on its resemblance to the hydrated carbonyl, transition-state structure of amide hydrolysis. This concept has been, tested by replacing the presumed tetrahedral carbon of a thermolysin, substrate with a silanediol group, resulting in an inhibitor with an, inhibition constant K(i) = 40 nM. The structure of the silanediol bound to, the active site of thermolysin was found to have a conformation very, similar to that of a corresponding phosphonamidate inhibitor (K(i) = 10, nM). In both cases, a single oxygen is within bonding distance to the, active-site zinc ion, mimicking the presumed tetrahedral transition state., There are binding differences that appear to be related to the presence or, absence of protons on the oxygens attached to the silicon or phosphorus., This is the first crystal structure of an organosilane bound to the active, site of a protease.
Dialkylsilanediols have been found to be an effective functional group for the design of active-site-directed protease inhibitors, including aspartic (HIV protease) and metallo (ACE and thermolysin) proteases. The use of silanediols is predicated on its resemblance to the hydrated carbonyl transition-state structure of amide hydrolysis. This concept has been tested by replacing the presumed tetrahedral carbon of a thermolysin substrate with a silanediol group, resulting in an inhibitor with an inhibition constant K(i) = 40 nM. The structure of the silanediol bound to the active site of thermolysin was found to have a conformation very similar to that of a corresponding phosphonamidate inhibitor (K(i) = 10 nM). In both cases, a single oxygen is within bonding distance to the active-site zinc ion, mimicking the presumed tetrahedral transition state. There are binding differences that appear to be related to the presence or absence of protons on the oxygens attached to the silicon or phosphorus. This is the first crystal structure of an organosilane bound to the active site of a protease.


==About this Structure==
==About this Structure==
1Y3G is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bacillus_thermoproteolyticus Bacillus thermoproteolyticus] with CA, ZN, DMS and 3PL as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Thermolysin Thermolysin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.24.27 3.4.24.27] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1Y3G OCA].  
1Y3G is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bacillus_thermoproteolyticus Bacillus thermoproteolyticus] with <scene name='pdbligand=CA:'>CA</scene>, <scene name='pdbligand=ZN:'>ZN</scene>, <scene name='pdbligand=DMS:'>DMS</scene> and <scene name='pdbligand=3PL:'>3PL</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Thermolysin Thermolysin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.24.27 3.4.24.27] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1Y3G OCA].  


==Reference==
==Reference==
Line 14: Line 14:
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Thermolysin]]
[[Category: Thermolysin]]
[[Category: Juers, D.H.]]
[[Category: Juers, D H.]]
[[Category: Kim, J.]]
[[Category: Kim, J.]]
[[Category: Matthews, B.W.]]
[[Category: Matthews, B W.]]
[[Category: Sieburth, S.M.]]
[[Category: Sieburth, S M.]]
[[Category: 3PL]]
[[Category: 3PL]]
[[Category: CA]]
[[Category: CA]]
Line 25: Line 25:
[[Category: thermolysin]]
[[Category: thermolysin]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 06:32:31 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:01:25 2008''