1k5s: Difference between revisions

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New page: left|200px<br /><applet load="1k5s" size="450" color="white" frame="true" align="right" spinBox="true" caption="1k5s, resolution 2.43Å" /> '''PENICILLIN ACYLASE, ...
 
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[[Image:1k5s.jpg|left|200px]]<br /><applet load="1k5s" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1k5s.jpg|left|200px]]<br /><applet load="1k5s" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1k5s, resolution 2.43&Aring;" />
caption="1k5s, resolution 2.43&Aring;" />
'''PENICILLIN ACYLASE, MUTANT COMPLEXED WITH PPA'''<br />
'''PENICILLIN ACYLASE, MUTANT COMPLEXED WITH PPA'''<br />


==Overview==
==Overview==
Penicillin acylase catalyses the condensation of Calpha-substituted, phenylacetic acids with beta-lactam nucleophiles, producing semi-synthetic, beta-lactam antibiotics. For efficient synthesis a low affinity for, phenylacetic acid and a high affinity for Calpha-substituted phenylacetic, acid derivatives is desirable. We made three active site mutants, alphaF146Y, betaF24A and alphaF146Y/betaF24A, which all had a 2- to, 10-fold higher affinity for Calpha-substituted compounds than wild-type, enzyme. In addition, betaF24A had a 20-fold reduced affinity for, phenylacetic acid. The molecular basis of the improved properties was, investigated by X-ray crystallography. These studies showed that the, higher affinity of alphaF146Y for (R)-alpha-methylphenylacetic acid can be, explained by van der Waals interactions between alphaY146:OH and the, Calpha-substituent. The betaF24A mutation causes an opening of the, phenylacetic acid binding site. Only (R)-alpha-methylphenylacetic acid, but not phenylacetic acid, induces a conformation with the ligand tightly, bound, explaining the weak binding of phenylacetic acid. A comparison of, the betaF24A structure with other open conformations of penicillin acylase, showed that betaF24 has a fixed position, whereas alphaF146 acts as a, flexible lid on the binding site and reorients its position to achieve, optimal substrate binding.
Penicillin acylase catalyses the condensation of Calpha-substituted phenylacetic acids with beta-lactam nucleophiles, producing semi-synthetic beta-lactam antibiotics. For efficient synthesis a low affinity for phenylacetic acid and a high affinity for Calpha-substituted phenylacetic acid derivatives is desirable. We made three active site mutants, alphaF146Y, betaF24A and alphaF146Y/betaF24A, which all had a 2- to 10-fold higher affinity for Calpha-substituted compounds than wild-type enzyme. In addition, betaF24A had a 20-fold reduced affinity for phenylacetic acid. The molecular basis of the improved properties was investigated by X-ray crystallography. These studies showed that the higher affinity of alphaF146Y for (R)-alpha-methylphenylacetic acid can be explained by van der Waals interactions between alphaY146:OH and the Calpha-substituent. The betaF24A mutation causes an opening of the phenylacetic acid binding site. Only (R)-alpha-methylphenylacetic acid, but not phenylacetic acid, induces a conformation with the ligand tightly bound, explaining the weak binding of phenylacetic acid. A comparison of the betaF24A structure with other open conformations of penicillin acylase showed that betaF24 has a fixed position, whereas alphaF146 acts as a flexible lid on the binding site and reorients its position to achieve optimal substrate binding.


==About this Structure==
==About this Structure==
1K5S is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with CA and GRO as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Penicillin_amidase Penicillin amidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.1.11 3.5.1.11] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1K5S OCA].  
1K5S is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with <scene name='pdbligand=CA:'>CA</scene> and <scene name='pdbligand=GRO:'>GRO</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Penicillin_amidase Penicillin amidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.1.11 3.5.1.11] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1K5S OCA].  


==Reference==
==Reference==
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[[Category: Penicillin amidase]]
[[Category: Penicillin amidase]]
[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Dijkstra, B.W.]]
[[Category: Dijkstra, B W.]]
[[Category: Hensgens, C.M.H.]]
[[Category: Hensgens, C M.H.]]
[[Category: Keizer, E.]]
[[Category: Keizer, E.]]
[[Category: Snijder, H.J.]]
[[Category: Snijder, H J.]]
[[Category: CA]]
[[Category: CA]]
[[Category: GRO]]
[[Category: GRO]]
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[[Category: ntn-hydrolase fold]]
[[Category: ntn-hydrolase fold]]


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