1erq: Difference between revisions

New page: left|200px<br /><applet load="1erq" size="450" color="white" frame="true" align="right" spinBox="true" caption="1erq, resolution 1.90Å" /> '''X-RAY CRYSTAL STRUCT...
 
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[[Image:1erq.jpg|left|200px]]<br /><applet load="1erq" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1erq.jpg|left|200px]]<br /><applet load="1erq" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1erq, resolution 1.90&Aring;" />
caption="1erq, resolution 1.90&Aring;" />
'''X-RAY CRYSTAL STRUCTURE OF TEM-1 BETA LACTAMASE IN COMPLEX WITH A DESIGNED BORONIC ACID INHIBITOR (1R)-1-ACETAMIDO-2-(3-CARBOXY-2-HYDROXYPHENYL)ETHYL BORONIC ACID'''<br />
'''X-RAY CRYSTAL STRUCTURE OF TEM-1 BETA LACTAMASE IN COMPLEX WITH A DESIGNED BORONIC ACID INHIBITOR (1R)-1-ACETAMIDO-2-(3-CARBOXY-2-HYDROXYPHENYL)ETHYL BORONIC ACID'''<br />


==Overview==
==Overview==
Transition state analogue boronic acid inhibitors mimicking the structures, and interactions of good penicillin substrates for the TEM-1, beta-lactamase of Escherchia coli were designed using graphic analyses, based on the enzyme's 1.7 A crystallographic structure. The synthesis of, two of these transition state analogues, (1R)-1-phenylacetamido-2-(3-carboxyphenyl)ethylboronic acid (1) and, (1R)-1-acetamido-2-(3-carboxy-2-hydroxyphenyl)ethylboronic acid (2), is, reported. Kinetic measurements show that, as designed, compounds 1 and 2, are highly effective deacylation transition state analogue inhibitors of, TEM-1 beta-lactamase, with inhibition constants of 5.9 and 13 nM, respectively. These values identify them as among the most potent, competitive inhibitors yet reported for a beta-lactamase. The best, inhibitor of the current series was, (1R)-1-phenylacetamido-2-(3-carboxyphenyl)ethylboronic acid (1, K(I) = 5.9, nM), which resembles most closely the best known substrate of TEM-1, benzylpenicillin (penicillin G). The high-resolution crystallographic, structures of these two inhibitors covalently bound to TEM-1 are also, described. In addition to verifying the design features, these two, structures show interesting and unanticipated changes in the active site, area, including strong hydrogen bond formation, water displacement, and, rearrangement of side chains. The structures provide new insights into the, further design of this potent class of beta-lactamase inhibitors.
Transition state analogue boronic acid inhibitors mimicking the structures and interactions of good penicillin substrates for the TEM-1 beta-lactamase of Escherchia coli were designed using graphic analyses based on the enzyme's 1.7 A crystallographic structure. The synthesis of two of these transition state analogues, (1R)-1-phenylacetamido-2-(3-carboxyphenyl)ethylboronic acid (1) and (1R)-1-acetamido-2-(3-carboxy-2-hydroxyphenyl)ethylboronic acid (2), is reported. Kinetic measurements show that, as designed, compounds 1 and 2 are highly effective deacylation transition state analogue inhibitors of TEM-1 beta-lactamase, with inhibition constants of 5.9 and 13 nM, respectively. These values identify them as among the most potent competitive inhibitors yet reported for a beta-lactamase. The best inhibitor of the current series was (1R)-1-phenylacetamido-2-(3-carboxyphenyl)ethylboronic acid (1, K(I) = 5.9 nM), which resembles most closely the best known substrate of TEM-1, benzylpenicillin (penicillin G). The high-resolution crystallographic structures of these two inhibitors covalently bound to TEM-1 are also described. In addition to verifying the design features, these two structures show interesting and unanticipated changes in the active site area, including strong hydrogen bond formation, water displacement, and rearrangement of side chains. The structures provide new insights into the further design of this potent class of beta-lactamase inhibitors.


==About this Structure==
==About this Structure==
1ERQ is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with BJH as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Beta-lactamase Beta-lactamase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.2.6 3.5.2.6] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1ERQ OCA].  
1ERQ is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with <scene name='pdbligand=BJH:'>BJH</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Beta-lactamase Beta-lactamase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.2.6 3.5.2.6] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1ERQ OCA].  


==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Gold, M.]]
[[Category: Gold, M.]]
[[Category: Jones, J.B.]]
[[Category: Jones, J B.]]
[[Category: Kindler, A.M.]]
[[Category: Kindler, A M.]]
[[Category: Martin, R.]]
[[Category: Martin, R.]]
[[Category: Ness, S.]]
[[Category: Ness, S.]]
[[Category: Paetzel, M.]]
[[Category: Paetzel, M.]]
[[Category: Strynadka, N.C.J.]]
[[Category: Strynadka, N C.J.]]
[[Category: BJH]]
[[Category: BJH]]
[[Category: beta-lactamase]]
[[Category: beta-lactamase]]
Line 26: Line 26:
[[Category: structure-based design]]
[[Category: structure-based design]]


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