4cla: Difference between revisions

New page: left|200px<br /><applet load="4cla" size="450" color="white" frame="true" align="right" spinBox="true" caption="4cla, resolution 2.0Å" /> '''ALTERNATIVE BINDING M...
 
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'''ALTERNATIVE BINDING MODES FOR CHLORAMPHENICOL AND 1-SUBSTITUTED CHLORAMPHENICOL ANALOGUES REVEALED BY SITE-DIRECTED MUTAGENESIS AND X-RAY CRYSTALLOGRAPHY OF CHLORAMPHENICOL ACETYLTRANSFERASE'''<br />
'''ALTERNATIVE BINDING MODES FOR CHLORAMPHENICOL AND 1-SUBSTITUTED CHLORAMPHENICOL ANALOGUES REVEALED BY SITE-DIRECTED MUTAGENESIS AND X-RAY CRYSTALLOGRAPHY OF CHLORAMPHENICOL ACETYLTRANSFERASE'''<br />


==Overview==
==Overview==
Leucine-160 of chloramphenicol acetyltransferase (CAT) has been replaced, by site-directed mutagenesis to investigate enzyme-ligand interactions at, the 1-hydroxyl substituent of the substrate chloramphenicol. The, consequences of the substitution of Leu-160 by glutamine and by, phenylalanine were deduced from the steady-state kinetic parameters for, acetyl transfer from acetyl-CoA to the 3-hydroxyl of chloramphenicol and, its analogues 1-deoxychloramphenicol and 1-acetylchloramphenicol. The, acetyl group of the latter, which is a substrate both in vivo and in, vitro, could potentially bind in a similar position to the 1-hydroxyl of, chloramphenicol, in close proximity to the side chain of Leu-160. In the, case of Gln-160 CAT, large increases in Km for the three acetyl acceptors, were accompanied by small decreases in kcat and in apparent affinity for, acetyl-CoA. Such results are consistent with the introduction of the, relatively hydrophilic amide in place of the delta-methyl groups of, Leu-160. The kinetic properties of Phe-160 CAT were unexpected in that Km, for each of the three acetyl acceptors was unchanged or reduced, compared, to the equivalent parameters for the wild-type enzyme, whereas kcat fell, significantly (44-83-fold) in each case. The ratios of specificity, constants (kcat/Km) for the acetylation of chloramphenicol compared with, the alternative acyl acceptors were similar for wild-type and mutant, enzymes. As the residue substitutions for Leu-160 do not result in, enhanced discrimination against the binding and acetylation of, 1-acetylchloramphenicol, it appears unlikely that the 1-acetyl group binds, to the CAT active site in the same position as that occupied by the, 1-hydroxyl of chloramphenicol.(ABSTRACT TRUNCATED AT 250 WORDS)
Leucine-160 of chloramphenicol acetyltransferase (CAT) has been replaced by site-directed mutagenesis to investigate enzyme-ligand interactions at the 1-hydroxyl substituent of the substrate chloramphenicol. The consequences of the substitution of Leu-160 by glutamine and by phenylalanine were deduced from the steady-state kinetic parameters for acetyl transfer from acetyl-CoA to the 3-hydroxyl of chloramphenicol and its analogues 1-deoxychloramphenicol and 1-acetylchloramphenicol. The acetyl group of the latter, which is a substrate both in vivo and in vitro, could potentially bind in a similar position to the 1-hydroxyl of chloramphenicol, in close proximity to the side chain of Leu-160. In the case of Gln-160 CAT, large increases in Km for the three acetyl acceptors were accompanied by small decreases in kcat and in apparent affinity for acetyl-CoA. Such results are consistent with the introduction of the relatively hydrophilic amide in place of the delta-methyl groups of Leu-160. The kinetic properties of Phe-160 CAT were unexpected in that Km for each of the three acetyl acceptors was unchanged or reduced, compared to the equivalent parameters for the wild-type enzyme, whereas kcat fell significantly (44-83-fold) in each case. The ratios of specificity constants (kcat/Km) for the acetylation of chloramphenicol compared with the alternative acyl acceptors were similar for wild-type and mutant enzymes. As the residue substitutions for Leu-160 do not result in enhanced discrimination against the binding and acetylation of 1-acetylchloramphenicol, it appears unlikely that the 1-acetyl group binds to the CAT active site in the same position as that occupied by the 1-hydroxyl of chloramphenicol.(ABSTRACT TRUNCATED AT 250 WORDS)


==About this Structure==
==About this Structure==
4CLA 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 CO and CLM as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Chloramphenicol_O-acetyltransferase Chloramphenicol O-acetyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.1.28 2.3.1.28] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=4CLA OCA].  
4CLA 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=CO:'>CO</scene> and <scene name='pdbligand=CLM:'>CLM</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Chloramphenicol_O-acetyltransferase Chloramphenicol O-acetyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.1.28 2.3.1.28] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4CLA OCA].  


==Reference==
==Reference==
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[[Category: Escherichia coli]]
[[Category: Escherichia coli]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Leslie, A.G.W.]]
[[Category: Leslie, A G.W.]]
[[Category: CLM]]
[[Category: CLM]]
[[Category: CO]]
[[Category: CO]]
[[Category: transferase (acyltransferase)]]
[[Category: transferase (acyltransferase)]]


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