1k5s: Difference between revisions
From Proteopedia
Jump to navigationJump to search
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, ... |
No edit summary |
||
| Line 1: | Line 1: | ||
[[Image:1k5s.jpg|left|200px]]<br /><applet load="1k5s" size=" | [[Image:1k5s.jpg|left|200px]]<br /><applet load="1k5s" size="350" color="white" frame="true" align="right" spinBox="true" | ||
caption="1k5s, resolution 2.43Å" /> | caption="1k5s, resolution 2.43Å" /> | ||
'''PENICILLIN ACYLASE, MUTANT COMPLEXED WITH PPA'''<br /> | '''PENICILLIN ACYLASE, MUTANT COMPLEXED WITH PPA'''<br /> | ||
==Overview== | ==Overview== | ||
Penicillin acylase catalyses the condensation of Calpha-substituted | 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:// | 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== | ||
| Line 14: | Line 14: | ||
[[Category: Penicillin amidase]] | [[Category: Penicillin amidase]] | ||
[[Category: Protein complex]] | [[Category: Protein complex]] | ||
[[Category: Dijkstra, B | [[Category: Dijkstra, B W.]] | ||
[[Category: Hensgens, C | [[Category: Hensgens, C M.H.]] | ||
[[Category: Keizer, E.]] | [[Category: Keizer, E.]] | ||
[[Category: Snijder, H | [[Category: Snijder, H J.]] | ||
[[Category: CA]] | [[Category: CA]] | ||
[[Category: GRO]] | [[Category: GRO]] | ||
| Line 24: | Line 24: | ||
[[Category: ntn-hydrolase fold]] | [[Category: ntn-hydrolase fold]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:30:28 2008'' | ||