1u1x

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|PDB= 1u1x |SIZE=350|CAPTION= <scene name='initialview01'>1u1x</scene>, resolution 1.88&Aring;
|PDB= 1u1x |SIZE=350|CAPTION= <scene name='initialview01'>1u1x</scene>, resolution 1.88&Aring;
|SITE=
|SITE=
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|LIGAND= <scene name='pdbligand=HHA:(2S,3S)-TRANS-2,3-DIHYDRO-3-HYDROXYANTHRANILIC ACID'>HHA</scene>
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|LIGAND= <scene name='pdbligand=HHA:(2S,3S)-TRANS-2,3-DIHYDRO-3-HYDROXYANTHRANILIC+ACID'>HHA</scene>
|ACTIVITY=
|ACTIVITY=
|GENE= phzF ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=294 Pseudomonas fluorescens])
|GENE= phzF ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=294 Pseudomonas fluorescens])
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|DOMAIN=
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|RELATEDENTRY=[[1bwz|1bwz]], [[1sdj|1sdj]], [[1s7j|1s7j]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1u1x FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1u1x OCA], [http://www.ebi.ac.uk/pdbsum/1u1x PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1u1x RCSB]</span>
}}
}}
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[[Category: Thomashow, L S.]]
[[Category: Thomashow, L S.]]
[[Category: Tong, L.]]
[[Category: Tong, L.]]
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[[Category: HHA]]
 
[[Category: acid/base catalysis]]
[[Category: acid/base catalysis]]
[[Category: closed form]]
[[Category: closed form]]
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[[Category: substrate complex]]
[[Category: substrate complex]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 14:26:14 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 00:04:16 2008''

Revision as of 21:04, 30 March 2008


PDB ID 1u1x

Drag the structure with the mouse to rotate
, resolution 1.88Å
Ligands:
Gene: phzF (Pseudomonas fluorescens)
Related: 1bwz, 1sdj, 1s7j


Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



Structure and function of phenazine-biosynthesis protein PhzF from Pseudomonas fluorescens 2-79


Overview

Phenazines produced by Pseudomonas and Streptomyces spp. are heterocyclic nitrogen-containing metabolites with antibiotic, antitumor, and antiparasitic activity. The antibiotic properties of pyocyanin, produced by Pseudomonas aeruginosa, were recognized in the 1890s, although this blue phenazine is now known to be a virulence factor in human disease. Despite their biological significance, the biosynthesis of phenazines is not fully understood. Here we present structural and functional studies of PhzF, an enzyme essential for phenazine synthesis in Pseudomonas spp. PhzF shares topology with diaminopimelate epimerase DapF but lacks the same catalytic residues. The structure of PhzF in complex with its substrate, trans-2,3-dihydro-3-hydroxyanthranilic acid, suggests that it is an isomerase using the conserved glutamate E45 to abstract a proton from C3 of the substrate. The proton is returned to C1 of the substrate after rearrangement of the double-bond system, yielding an enol that converts to the corresponding ketone. PhzF is a dimer that may be bifunctional, providing a shielded cavity for ketone dimerization via double Schiff-base formation to produce the phenazine scaffold. Our proposed mechanism is supported by mass and NMR spectroscopy. The results are discussed in the context of related structures and protein sequences of unknown biochemical function.

About this Structure

1U1X is a Single protein structure of sequence from Pseudomonas fluorescens. Full crystallographic information is available from OCA.

Reference

Structure and function of the phenazine biosynthetic protein PhzF from Pseudomonas fluorescens., Blankenfeldt W, Kuzin AP, Skarina T, Korniyenko Y, Tong L, Bayer P, Janning P, Thomashow LS, Mavrodi DV, Proc Natl Acad Sci U S A. 2004 Nov 23;101(47):16431-6. Epub 2004 Nov 15. PMID:15545603

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