2ves

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[[Image:2ves.jpg|left|200px]]
[[Image:2ves.jpg|left|200px]]
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{{Structure
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<!--
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|PDB= 2ves |SIZE=350|CAPTION= <scene name='initialview01'>2ves</scene>, resolution 1.90&Aring;
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The line below this paragraph, containing "STRUCTURE_2ves", creates the "Structure Box" on the page.
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|SITE= <scene name='pdbsite=AC1:Zn+Binding+Site+For+Chain+A'>AC1</scene>, <scene name='pdbsite=AC2:Zn+Binding+Site+For+Chain+B'>AC2</scene>, <scene name='pdbsite=AC3:Zn+Binding+Site+For+Chain+C'>AC3</scene>, <scene name='pdbsite=AC4:Gvr+Binding+Site+For+Chain+A'>AC4</scene>, <scene name='pdbsite=AC5:Gvr+Binding+Site+For+Chain+B'>AC5</scene>, <scene name='pdbsite=AC6:Gvr+Binding+Site+For+Chain+C'>AC6</scene>, <scene name='pdbsite=AC7:Zn+Binding+Site+For+Chain+A'>AC7</scene>, <scene name='pdbsite=AC8:Zn+Binding+Site+For+Chain+B'>AC8</scene>, <scene name='pdbsite=AC9:Zn+Binding+Site+For+Chain+C'>AC9</scene>, <scene name='pdbsite=BC1:Zn+Binding+Site+For+Chain+C'>BC1</scene>, <scene name='pdbsite=BC2:So4+Binding+Site+For+Chain+B'>BC2</scene> and <scene name='pdbsite=BC3:So4+Binding+Site+For+Chain+C'>BC3</scene>
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=GVR:(2R)-N-HYDROXY-3-NAPHTHALEN-2-YL-2-[(NAPHTHALEN-2-YLSULFONYL)AMINO]PROPANAMIDE'>GVR</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY=
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|GENE=
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-->
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|DOMAIN=
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{{STRUCTURE_2ves| PDB=2ves | SCENE= }}
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|RELATEDENTRY=
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2ves FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ves OCA], [http://www.ebi.ac.uk/pdbsum/2ves PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2ves RCSB]</span>
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}}
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'''CRYSTAL STRUCTURE OF LPXC FROM PSEUDOMONAS AERUGINOSA COMPLEXED WITH THE POTENT BB-78485 INHIBITOR'''
'''CRYSTAL STRUCTURE OF LPXC FROM PSEUDOMONAS AERUGINOSA COMPLEXED WITH THE POTENT BB-78485 INHIBITOR'''
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[[Category: Knafels, J.]]
[[Category: Knafels, J.]]
[[Category: Mochalkin, I.]]
[[Category: Mochalkin, I.]]
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[[Category: antibiotic]]
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[[Category: Antibiotic]]
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[[Category: bb-78485]]
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[[Category: Bb-78485]]
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[[Category: deacetylase]]
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[[Category: Deacetylase]]
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[[Category: gram-negative bacteria]]
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[[Category: Gram-negative bacteria]]
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[[Category: hydrolase]]
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[[Category: Hydrolase]]
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[[Category: hydroxamic acid]]
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[[Category: Hydroxamic acid]]
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[[Category: lipid a biosynthesis]]
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[[Category: Lipid a biosynthesis]]
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[[Category: lipid synthesis]]
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[[Category: Lipid synthesis]]
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[[Category: lipopolysaccharide]]
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[[Category: Lipopolysaccharide]]
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[[Category: lpxc]]
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[[Category: Lpxc]]
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[[Category: metalloprotease]]
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[[Category: Metalloprotease]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 18:40:59 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 05:11:22 2008''
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Revision as of 15:41, 4 May 2008

Template:STRUCTURE 2ves

CRYSTAL STRUCTURE OF LPXC FROM PSEUDOMONAS AERUGINOSA COMPLEXED WITH THE POTENT BB-78485 INHIBITOR


Overview

The cell wall in Gram-negative bacteria is surrounded by an outer membrane comprised of charged lipopolysaccharide (LPS) molecules that prevent entry of hydrophobic agents into the cell and protect the bacterium from many antibiotics. The hydrophobic anchor of LPS is lipid A, the biosynthesis of which is essential for bacterial growth and viability. UDP-3-O-(R-3-hydroxymyristoyl)-N-acetylglucosamine deacetylase (LpxC) is an essential zinc-dependant enzyme that catalyzes the conversion of UDP-3-O-(R-3-hydroxymyristoyl)-N-acetylglucosamine to UDP-3-O-(R-3-hydroxymyristoyl)glucosamine and acetate in the biosynthesis of lipid A, and for this reason, LpxC is an attractive target for antibacterial drug discovery. Here we disclose a 1.9 A resolution crystal structure of LpxC from Pseudomonas aeruginosa (paLpxC) in a complex with the potent BB-78485 inhibitor. To our knowledge, this is the first crystal structure of LpxC with a small-molecule inhibitor that shows antibacterial activity against a wide range of Gram-negative pathogens. Accordingly, this structure can provide important information for lead optimization and rational design of the effective small-molecule LpxC inhibitors for successful treatment of Gram-negative infections.

About this Structure

2VES is a Single protein structure of sequence from Pseudomonas aeruginosa. Full crystallographic information is available from OCA.

Reference

Crystal structure of LpxC from Pseudomonas aeruginosa complexed with the potent BB-78485 inhibitor., Mochalkin I, Knafels JD, Lightle S, Protein Sci. 2008 Mar;17(3):450-7. PMID:18287278 Page seeded by OCA on Sun May 4 18:40:59 2008

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