1aj2: Difference between revisions

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New page: left|200px<br /><applet load="1aj2" size="450" color="white" frame="true" align="right" spinBox="true" caption="1aj2, resolution 2.00Å" /> '''CRYSTAL STRUCTURE OF...
 
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[[Image:1aj2.gif|left|200px]]<br /><applet load="1aj2" size="450" color="white" frame="true" align="right" spinBox="true"
caption="1aj2, resolution 2.00&Aring;" />
'''CRYSTAL STRUCTURE OF A BINARY COMPLEX OF E. COLI DIHYDROPTEROATE SYNTHASE'''<br />


==Overview==
==CRYSTAL STRUCTURE OF A BINARY COMPLEX OF E. COLI DIHYDROPTEROATE SYNTHASE==
Sulfonamides were amongst the first clinically useful antibacterial agents, to be discovered. The identification of sulfanilamide as the active, component of the dye Prontosil rubrum led to the synthesis of clinically, useful analogues. Today sulfamethoxazole (in combination with, trimethoprim), is used to treat urinary tract infections caused by, bacteria such as Escherichia coli and is also a first-line treatment for, pneumonia caused by the fungus Pneumocystis carinii, a common condition in, AIDS patients. The site of action is the de novo folate biosynthesis, enzyme dihydropteroate synthase (DHPS) where sulfonamides act as analogues, of one of the substrates, para-aminobenzoic acid (pABA). We report here, the crystal structure of E.coli DHPS at 2.0 A resolution refined to an, R-factor of 0.185. The single domain of 282 residues forms an, eight-stranded alpha/beta-barrel. The 7,8-dihydropterin pyrophosphate, (DHPPP) substrate binds in a deep cleft in the barrel, whilst, sulfanilamide binds closer to the surface. The DHPPP ligand site is highly, conserved amongst prokaryotic and eukaryotic DHPSs.
<StructureSection load='1aj2' size='340' side='right'caption='[[1aj2]], [[Resolution|resolution]] 2.00&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[1aj2]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1AJ2 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1AJ2 FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=2PH:[7,8-DIHYDRO-PTERIN-6-YL+METHANYL]-PHOSPHONOPHOSPHATE'>2PH</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1aj2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1aj2 OCA], [https://pdbe.org/1aj2 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1aj2 RCSB], [https://www.ebi.ac.uk/pdbsum/1aj2 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1aj2 ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/DHPS_ECOLI DHPS_ECOLI] DHPS catalyzes the formation of the immediate precursor of folic acid. It is implicated in resistance to sulfonamide.<ref>PMID:368012</ref>
== Evolutionary Conservation ==
[[Image:Consurf_key_small.gif|200px|right]]
Check<jmol>
  <jmolCheckbox>
    <scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/aj/1aj2_consurf.spt"</scriptWhenChecked>
    <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
    <text>to colour the structure by Evolutionary Conservation</text>
  </jmolCheckbox>
</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=1aj2 ConSurf].
<div style="clear:both"></div>


==About this Structure==
==See Also==
1AJ2 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with SO4 and 2PH as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Dihydropteroate_synthase Dihydropteroate synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.5.1.15 2.5.1.15] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1AJ2 OCA].
*[[Dihydropteroate synthase 3D structures|Dihydropteroate synthase 3D structures]]
 
== References ==
==Reference==
<references/>
Crystal structure of the anti-bacterial sulfonamide drug target dihydropteroate synthase., Achari A, Somers DO, Champness JN, Bryant PK, Rosemond J, Stammers DK, Nat Struct Biol. 1997 Jun;4(6):490-7. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=9187658 9187658]
__TOC__
[[Category: Dihydropteroate synthase]]
</StructureSection>
[[Category: Escherichia coli]]
[[Category: Escherichia coli]]
[[Category: Single protein]]
[[Category: Large Structures]]
[[Category: Achari, A.]]
[[Category: Achari A]]
[[Category: Bryant, P.K.]]
[[Category: Bryant PK]]
[[Category: Champness, J.N.]]
[[Category: Champness JN]]
[[Category: Rosemond, J.]]
[[Category: Rosemond J]]
[[Category: Somers, D.O.]]
[[Category: Somers DO]]
[[Category: Stammers, D.K.]]
[[Category: Stammers DK]]
[[Category: 2PH]]
[[Category: SO4]]
[[Category: antibiotic]]
[[Category: biosynthesis]]
[[Category: folate]]
[[Category: resistance]]
[[Category: synthase]]
[[Category: transferase]]
 
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 10:53:40 2007''

Latest revision as of 09:31, 7 February 2024

CRYSTAL STRUCTURE OF A BINARY COMPLEX OF E. COLI DIHYDROPTEROATE SYNTHASECRYSTAL STRUCTURE OF A BINARY COMPLEX OF E. COLI DIHYDROPTEROATE SYNTHASE

Structural highlights

1aj2 is a 1 chain structure with sequence from Escherichia coli. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
Method:X-ray diffraction, Resolution 2Å
Ligands:,
Resources:FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

Function

DHPS_ECOLI DHPS catalyzes the formation of the immediate precursor of folic acid. It is implicated in resistance to sulfonamide.[1]

Evolutionary Conservation

Check, as determined by ConSurfDB. You may read the explanation of the method and the full data available from ConSurf.

See Also

References

  1. ↑ Swedberg G, Castensson S, Skold O. Characterization of mutationally altered dihydropteroate synthase and its ability to form a sulfonamide-containing dihydrofolate analog. J Bacteriol. 1979 Jan;137(1):129-36. PMID:368012

1aj2, resolution 2.00Å

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