2oi2: Difference between revisions

Revision as of 19:18, 21 February 2008

Streptococcus pneumoniae Mevalonate Kinase in Complex with Diphosphomevalonate

OverviewOverview

Streptococcus pneumoniae, a ubiquitous gram-positive pathogen with an alarming, steadily evolving resistance to frontline antimicrobials, poses a severe global health threat both in the community and in the clinic. The recent discovery that diphosphomevalonate (DPM), an essential intermediate in the isoprenoid biosynthetic pathway, potently and allosterically inhibits S. pneumoniae mevalonate kinase (SpMK) without affecting the human isozyme established a new target and lead compound for antimicrobial design. Here we present the crystal structure of the first S. pneumoniae mevalonate kinase, at a resolution of 2.5 A and in complex with DPM.Mg(2+) in the active-site cleft. Structural comparison of SpMK with other members of the GHMP kinase family reveals that DPM functions as a partial bisubstrate analog (mevalonate linked to the pyrophosphoryl moiety of ATP) in that it elicits a ternary-complexlike form of the enzyme, except for localized disordering in a region that would otherwise interact with the missing portion of the nucleotide. Features of the SpMK-binding pockets are discussed in the context of established mechanistic findings and inherited human diseases linked to MK deficiency.

About this StructureAbout this Structure

2OI2 is a Single protein structure of sequence from Streptococcus pneumoniae with and as ligands. Active as Mevalonate kinase, with EC number 2.7.1.36 Full crystallographic information is available from OCA.

ReferenceReference

Crystal structure of the Streptococcus pneumoniae mevalonate kinase in complex with diphosphomevalonate., Andreassi JL 2nd, Bilder PW, Vetting MW, Roderick SL, Leyh TS, Protein Sci. 2007 May;16(5):983-9. Epub 2007 Mar 30. PMID:17400916

Page seeded by OCA on Thu Feb 21 18:18:44 2008

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OCA

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 ==Overview==
-Streptococcus pneumoniae, a ubiquitous gram-positive pathogen with an, alarming, steadily evolving resistance to frontline antimicrobials, poses, a severe global health threat both in the community and in the clinic. The, recent discovery that diphosphomevalonate (DPM), an essential intermediate, in the isoprenoid biosynthetic pathway, potently and allosterically, inhibits S. pneumoniae mevalonate kinase (SpMK) without affecting the, human isozyme established a new target and lead compound for antimicrobial, design. Here we present the crystal structure of the first S. pneumoniae, mevalonate kinase, at a resolution of 2.5 A and in complex with DPM.Mg(2+), in the active-site cleft. Structural comparison of SpMK with other members, of the GHMP kinase family reveals that DPM functions as a partial, bisubstrate analog (mevalonate linked to the pyrophosphoryl moiety of ATP), in that it elicits a ternary-complexlike form of the enzyme, except for, localized disordering in a region that would otherwise interact with the, missing portion of the nucleotide. Features of the SpMK-binding pockets, are discussed in the context of established mechanistic findings and, inherited human diseases linked to MK deficiency.
+Streptococcus pneumoniae, a ubiquitous gram-positive pathogen with an alarming, steadily evolving resistance to frontline antimicrobials, poses a severe global health threat both in the community and in the clinic. The recent discovery that diphosphomevalonate (DPM), an essential intermediate in the isoprenoid biosynthetic pathway, potently and allosterically inhibits S. pneumoniae mevalonate kinase (SpMK) without affecting the human isozyme established a new target and lead compound for antimicrobial design. Here we present the crystal structure of the first S. pneumoniae mevalonate kinase, at a resolution of 2.5 A and in complex with DPM.Mg(2+) in the active-site cleft. Structural comparison of SpMK with other members of the GHMP kinase family reveals that DPM functions as a partial bisubstrate analog (mevalonate linked to the pyrophosphoryl moiety of ATP) in that it elicits a ternary-complexlike form of the enzyme, except for localized disordering in a region that would otherwise interact with the missing portion of the nucleotide. Features of the SpMK-binding pockets are discussed in the context of established mechanistic findings and inherited human diseases linked to MK deficiency.
 ==About this Structure==
@@ Line 14: / Line 14: @@
 [[Category: Single protein]]
 [[Category: Streptococcus pneumoniae]]
-[[Category: Andreassi, J.L.]]
+[[Category: Andreassi, J L.]]
-[[Category: Bilder, P.W.]]
+[[Category: Bilder, P W.]]
-[[Category: Leyh, T.S.]]
+[[Category: Leyh, T S.]]
-[[Category: Roderick, S.L.]]
+[[Category: Roderick, S L.]]
-[[Category: Vetting, M.W.]]
+[[Category: Vetting, M W.]]
 [[Category: DP6]]
 [[Category: MG]]
 [[Category: enzyme-inhibitor complex]]
-''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 23 15:28:22 2008''
+''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 18:18:44 2008''