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1nki

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(New page: 200px<br /><applet load="1nki" size="450" color="white" frame="true" align="right" spinBox="true" caption="1nki, resolution 0.95&Aring;" /> '''CRYSTAL STRUCURE OF ...)
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'''CRYSTAL STRUCURE OF THE FOSFOMYCIN RESISTANCE PROTEIN A (FOSA) CONTAINING BOUND PHOSPHONOFORMATE'''<br />
'''CRYSTAL STRUCURE OF THE FOSFOMYCIN RESISTANCE PROTEIN A (FOSA) CONTAINING BOUND PHOSPHONOFORMATE'''<br />
==Overview==
==Overview==
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Fosfomycin [(1R,2S)-epoxypropylphosphonic acid] is a simple phosphonate, found to have antibacterial activity against both Gram-positive and, Gram-negative microorganisms. Early resistance to the clinical use of the, antibiotic was linked to a plasmid-encoded resistance protein, FosA, that, catalyzes the addition of glutathione to the oxirane ring, rendering the, antibiotic inactive. Subsequent studies led to the discovery of a, genomically encoded homologue in the pathogen Pseudomonas aeruginosa. The, proteins are Mn(II)-dependent enzymes where the metal is proposed to act, as a Lewis acid stabilizing the negative charge that develops on the, oxirane oxygen in the transition state. Several simple phosphonates, including the antiviral compound phosphonoformate (K(i) = 0.4 +/- 0.1, microM, K(d) approximately 0.2 microM), are shown to be inhibitors of, FosA. The crystal structure of FosA from P. aeruginosa with, phosphonoformate bound in the active site has been determined at 0.95 A, resolution and reveals that the inhibitor forms a five-coordinate complex, with the Mn(II) center with a geometry similar to that proposed for the, transition state of the reaction. Binding studies show that, phosphonoformate has a near-diffusion-controlled on rate (k(on), approximately 10(7)-10(8) M(-1) s(-1)) and an off rate (k(off) = 5 s(-1)), that is slower than that for fosfomycin (k(off) = 30 s(-1)). Taken, together, these data suggest that the FosA-catalyzed reaction has a very, early transition state and phosphonoformate acts as a minimal transition, state analogue inhibitor.
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Fosfomycin [(1R,2S)-epoxypropylphosphonic acid] is a simple phosphonate found to have antibacterial activity against both Gram-positive and Gram-negative microorganisms. Early resistance to the clinical use of the antibiotic was linked to a plasmid-encoded resistance protein, FosA, that catalyzes the addition of glutathione to the oxirane ring, rendering the antibiotic inactive. Subsequent studies led to the discovery of a genomically encoded homologue in the pathogen Pseudomonas aeruginosa. The proteins are Mn(II)-dependent enzymes where the metal is proposed to act as a Lewis acid stabilizing the negative charge that develops on the oxirane oxygen in the transition state. Several simple phosphonates, including the antiviral compound phosphonoformate (K(i) = 0.4 +/- 0.1 microM, K(d) approximately 0.2 microM), are shown to be inhibitors of FosA. The crystal structure of FosA from P. aeruginosa with phosphonoformate bound in the active site has been determined at 0.95 A resolution and reveals that the inhibitor forms a five-coordinate complex with the Mn(II) center with a geometry similar to that proposed for the transition state of the reaction. Binding studies show that phosphonoformate has a near-diffusion-controlled on rate (k(on) approximately 10(7)-10(8) M(-1) s(-1)) and an off rate (k(off) = 5 s(-1)) that is slower than that for fosfomycin (k(off) = 30 s(-1)). Taken together, these data suggest that the FosA-catalyzed reaction has a very early transition state and phosphonoformate acts as a minimal transition state analogue inhibitor.
==About this Structure==
==About this Structure==
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1NKI is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Pseudomonas_aeruginosa_pao1 Pseudomonas aeruginosa pao1] with K, MN and PPF as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Glutathione_transferase Glutathione transferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.5.1.18 2.5.1.18] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1NKI OCA].
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1NKI is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Pseudomonas_aeruginosa_pao1 Pseudomonas aeruginosa pao1] with <scene name='pdbligand=K:'>K</scene>, <scene name='pdbligand=MN:'>MN</scene> and <scene name='pdbligand=PPF:'>PPF</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Glutathione_transferase Glutathione transferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.5.1.18 2.5.1.18] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1NKI OCA].
==Reference==
==Reference==
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[[Category: Pseudomonas aeruginosa pao1]]
[[Category: Pseudomonas aeruginosa pao1]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Armstrong, R.N.]]
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[[Category: Armstrong, R N.]]
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[[Category: Newcomer, M.E.]]
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[[Category: Newcomer, M E.]]
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[[Category: Pharris, R.E.]]
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[[Category: Pharris, R E.]]
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[[Category: Rife, C.L.]]
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[[Category: Rife, C L.]]
[[Category: K]]
[[Category: K]]
[[Category: MN]]
[[Category: MN]]
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[[Category: potassium binding loop]]
[[Category: potassium binding loop]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:07:01 2008''

Revision as of 12:07, 21 February 2008


1nki, resolution 0.95Å

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CRYSTAL STRUCURE OF THE FOSFOMYCIN RESISTANCE PROTEIN A (FOSA) CONTAINING BOUND PHOSPHONOFORMATE

Overview

Fosfomycin [(1R,2S)-epoxypropylphosphonic acid] is a simple phosphonate found to have antibacterial activity against both Gram-positive and Gram-negative microorganisms. Early resistance to the clinical use of the antibiotic was linked to a plasmid-encoded resistance protein, FosA, that catalyzes the addition of glutathione to the oxirane ring, rendering the antibiotic inactive. Subsequent studies led to the discovery of a genomically encoded homologue in the pathogen Pseudomonas aeruginosa. The proteins are Mn(II)-dependent enzymes where the metal is proposed to act as a Lewis acid stabilizing the negative charge that develops on the oxirane oxygen in the transition state. Several simple phosphonates, including the antiviral compound phosphonoformate (K(i) = 0.4 +/- 0.1 microM, K(d) approximately 0.2 microM), are shown to be inhibitors of FosA. The crystal structure of FosA from P. aeruginosa with phosphonoformate bound in the active site has been determined at 0.95 A resolution and reveals that the inhibitor forms a five-coordinate complex with the Mn(II) center with a geometry similar to that proposed for the transition state of the reaction. Binding studies show that phosphonoformate has a near-diffusion-controlled on rate (k(on) approximately 10(7)-10(8) M(-1) s(-1)) and an off rate (k(off) = 5 s(-1)) that is slower than that for fosfomycin (k(off) = 30 s(-1)). Taken together, these data suggest that the FosA-catalyzed reaction has a very early transition state and phosphonoformate acts as a minimal transition state analogue inhibitor.

About this Structure

1NKI is a Single protein structure of sequence from Pseudomonas aeruginosa pao1 with , and as ligands. Active as Glutathione transferase, with EC number 2.5.1.18 Full crystallographic information is available from OCA.

Reference

Phosphonoformate: a minimal transition state analogue inhibitor of the fosfomycin resistance protein, FosA., Rigsby RE, Rife CL, Fillgrove KL, Newcomer ME, Armstrong RN, Biochemistry. 2004 Nov 2;43(43):13666-73. PMID:15504029

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