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1oh0

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[[Image:1oh0.gif|left|200px]]<br />
 
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<applet load="1oh0" size="450" color="white" frame="true" align="right" spinBox="true"
 
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caption="1oh0, resolution 1.1&Aring;" />
 
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'''CRYSTAL STRUCTURE OF KETOSTEROID ISOMERASE COMPLEXED WITH EQUILENIN'''<br />
 
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==Overview==
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==CRYSTAL STRUCTURE OF KETOSTEROID ISOMERASE COMPLEXED WITH EQUILENIN==
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Bacterial Delta5-3-ketosteroid isomerase (KSI) catalyzes a stereospecific, isomerization of steroid substrates at an extremely fast rate, overcoming, a large disparity of pKa values between a catalytic residue and its, target. The crystal structures of KSI from Pseudomonas putida and of the, enzyme in complex with equilenin, an analogue of the reaction, intermediate, have been determined at 1.9 and 2.5 A resolution, respectively. The structures reveal that the side chains of Tyr14 and, Asp99 (a newly identified catalytic residue) form hydrogen bonds directly, with the oxyanion of the bound inhibitor in a completely apolar milieu of, the active site. No water molecule is found at the active site, and the, access of bulk solvent is blocked by a layer of apolar residues. Asp99 is, surrounded by six apolar residues, and consequently, its pKa appears to be, elevated as high as 9.5 to be consistent with early studies. No, interaction was found between the bound inhibitor and the residue 101, (phenylalanine in Pseudomonas testosteroni and methionine in P. putida, KSI) which was suggested to contribute significantly to the rate, enhancement based on mutational analysis. This observation excludes the, residue 101 as a potential catalytic residue and requires that the rate, enhancement should be explained solely by Tyr14 and Asp99. Kinetic, analyses of Y14F and D99L mutant enzymes demonstrate that Tyr14, contributes much more significantly to the rate enhancement than Asp99., Previous studies and the structural analysis strongly suggest that the, low-barrier hydrogen bond of Tyr14 (&gt;7.1 kcal/mol), along with a moderate, strength hydrogen bond of Asp99 ( approximately 4 kcal/mol), accounts for, the required energy of 11 kcal/mol for the transition-state stabilization.
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<StructureSection load='1oh0' size='340' side='right'caption='[[1oh0]], [[Resolution|resolution]] 1.10&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[1oh0]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Pseudomonas_putida Pseudomonas putida]. This structure supersedes the now removed PDB entry [http://oca.weizmann.ac.il/oca-bin/send-pdb?obs=1&id=4tsu 4tsu]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1OH0 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1OH0 FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.1&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=BME:BETA-MERCAPTOETHANOL'>BME</scene>, <scene name='pdbligand=EQU:EQUILENIN'>EQU</scene></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1oh0 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1oh0 OCA], [https://pdbe.org/1oh0 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1oh0 RCSB], [https://www.ebi.ac.uk/pdbsum/1oh0 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1oh0 ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/SDIS_PSEPU SDIS_PSEPU]
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== Evolutionary Conservation ==
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[[Image:Consurf_key_small.gif|200px|right]]
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Check<jmol>
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<jmolCheckbox>
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<scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/oh/1oh0_consurf.spt"</scriptWhenChecked>
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<scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
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<text>to colour the structure by Evolutionary Conservation</text>
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</jmolCheckbox>
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</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=1oh0 ConSurf].
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<div style="clear:both"></div>
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==About this Structure==
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==See Also==
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1OH0 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Pseudomonas_putida Pseudomonas putida] with EQU and BME as [http://en.wikipedia.org/wiki/ligands ligands]. This structure superseeds the now removed PDB entry 4TSU. Active as [http://en.wikipedia.org/wiki/Steroid_Delta-isomerase Steroid Delta-isomerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=5.3.3.1 5.3.3.1] Structure known Active Site: AC1. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1OH0 OCA].
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*[[Ketosteroid Isomerase|Ketosteroid Isomerase]]
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__TOC__
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==Reference==
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</StructureSection>
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High-resolution crystal structures of delta5-3-ketosteroid isomerase with and without a reaction intermediate analogue., Kim SW, Cha SS, Cho HS, Kim JS, Ha NC, Cho MJ, Joo S, Kim KK, Choi KY, Oh BH, Biochemistry. 1997 Nov 18;36(46):14030-6. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=9369474 9369474]
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[[Category: Large Structures]]
[[Category: Pseudomonas putida]]
[[Category: Pseudomonas putida]]
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[[Category: Single protein]]
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[[Category: Byun M]]
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[[Category: Steroid Delta-isomerase]]
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[[Category: Cha S-S]]
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[[Category: Byun, M.]]
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[[Category: Kim K-H]]
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[[Category: Cha, S.S.]]
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[[Category: Oh B-H]]
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[[Category: Kim, K.H.]]
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[[Category: Oh, B.H.]]
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[[Category: BME]]
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[[Category: EQU]]
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[[Category: equilenin]]
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[[Category: isomerase]]
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[[Category: ketosteroid isomerase]]
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[[Category: ksi]]
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[[Category: lbhb]]
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[[Category: pi]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 5 15:14:31 2007''
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Current revision

CRYSTAL STRUCTURE OF KETOSTEROID ISOMERASE COMPLEXED WITH EQUILENIN

PDB ID 1oh0

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