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New page: left|200px<br /><applet load="1pek" size="450" color="white" frame="true" align="right" spinBox="true" caption="1pek, resolution 2.2Å" /> '''STRUCTURE OF THE COMP...
 
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[[Image:1pek.jpg|left|200px]]<br /><applet load="1pek" size="450" color="white" frame="true" align="right" spinBox="true"
caption="1pek, resolution 2.2&Aring;" />
'''STRUCTURE OF THE COMPLEX OF PROTEINASE K WITH A SUBSTRATE-ANALOGUE HEXA-PEPTIDE INHIBITOR AT 2.2 ANGSTROMS RESOLUTION'''<br />


==Overview==
==STRUCTURE OF THE COMPLEX OF PROTEINASE K WITH A SUBSTRATE-ANALOGUE HEXA-PEPTIDE INHIBITOR AT 2.2 ANGSTROMS RESOLUTION==
The crystal structure of a transition state/product complex formed by the, interaction between proteinase K and the substrate analogue, N-Ac-L-Pro-L-Ala-L-Pro-L-Phe-D-Ala-L-Ala-NH2 has been determined at a, resolution of 2.2 A and refined to an R-factor of 0.165 for 12,725, reflections. The inhibitor forms a stable complex through a series of, hydrogen bonds with protein atoms and water molecules. The inhibitor is, hydrolyzed between Phe 4I and D-Ala5I (I indicates inhibitor). The two, fragments are separated by a distance of 3.07 A between the carbonyl, carbon and the main chain nitrogen. Both fragments remain bound to the, protein. The N-terminal fragment occupies subsites S5 to S1, whereas the, C-terminal part is bound in S1' and S2', the first time that electron, density for a substrate analogue has been observed in the P1' and P2', sites of a subtilisin-like enzyme. The flexible segments of the substrate, recognition sites Gly100-Tyr104 and Ser132-Gly136 move appreciably to, accommodate the inhibitor. Biochemical results indicate an inhibition by, this specifically designed peptide of 95%.
<StructureSection load='1pek' size='340' side='right'caption='[[1pek]], [[Resolution|resolution]] 2.20&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[1pek]] is a 3 chain structure with sequence from [https://en.wikipedia.org/wiki/Parengyodontium_album Parengyodontium album]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1PEK OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1PEK 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]] 2.2&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=DAL:D-ALANINE'>DAL</scene>, <scene name='pdbligand=NH2:AMINO+GROUP'>NH2</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=1pek FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1pek OCA], [https://pdbe.org/1pek PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1pek RCSB], [https://www.ebi.ac.uk/pdbsum/1pek PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1pek ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/PRTK_PARAQ PRTK_PARAQ] Hydrolyzes keratin at aromatic and hydrophobic residues.
== 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/pe/1pek_consurf.spt"</scriptWhenChecked>
    <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview03.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=1pek ConSurf].
<div style="clear:both"></div>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
The crystal structure of a transition state/product complex formed by the interaction between proteinase K and the substrate analogue N-Ac-L-Pro-L-Ala-L-Pro-L-Phe-D-Ala-L-Ala-NH2 has been determined at a resolution of 2.2 A and refined to an R-factor of 0.165 for 12,725 reflections. The inhibitor forms a stable complex through a series of hydrogen bonds with protein atoms and water molecules. The inhibitor is hydrolyzed between Phe 4I and D-Ala5I (I indicates inhibitor). The two fragments are separated by a distance of 3.07 A between the carbonyl carbon and the main chain nitrogen. Both fragments remain bound to the protein. The N-terminal fragment occupies subsites S5 to S1, whereas the C-terminal part is bound in S1' and S2', the first time that electron density for a substrate analogue has been observed in the P1' and P2' sites of a subtilisin-like enzyme. The flexible segments of the substrate recognition sites Gly100-Tyr104 and Ser132-Gly136 move appreciably to accommodate the inhibitor. Biochemical results indicate an inhibition by this specifically designed peptide of 95%.


==About this Structure==
Structure of the complex of proteinase K with a substrate analogue hexapeptide inhibitor at 2.2-A resolution.,Betzel C, Singh TP, Visanji M, Peters K, Fittkau S, Saenger W, Wilson KS J Biol Chem. 1993 Jul 25;268(21):15854-8. PMID:8340410<ref>PMID:8340410</ref>
1PEK is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/ ]. Active as [http://en.wikipedia.org/wiki/Peptidase_K Peptidase K], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.64 3.4.21.64] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1PEK OCA].


==Reference==
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
Structure of the complex of proteinase K with a substrate analogue hexapeptide inhibitor at 2.2-A resolution., Betzel C, Singh TP, Visanji M, Peters K, Fittkau S, Saenger W, Wilson KS, J Biol Chem. 1993 Jul 25;268(21):15854-8. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=8340410 8340410]
</div>
[[Category: Peptidase K]]
<div class="pdbe-citations 1pek" style="background-color:#fffaf0;"></div>
[[Category: Single protein]]
[[Category: Betzel, C.]]
[[Category: Fittkau, S.]]
[[Category: Peters, K.]]
[[Category: Saenger, W.]]
[[Category: Singh, T.P.]]
[[Category: Visanji, M.]]
[[Category: Wilson, K.S.]]
[[Category: hydrolase]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 23:44:32 2007''
==See Also==
*[[Proteinase 3D structures|Proteinase 3D structures]]
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Large Structures]]
[[Category: Parengyodontium album]]
[[Category: Betzel C]]
[[Category: Fittkau S]]
[[Category: Peters K]]
[[Category: Saenger W]]
[[Category: Singh TP]]
[[Category: Visanji M]]
[[Category: Wilson KS]]

Latest revision as of 07:12, 30 October 2024

STRUCTURE OF THE COMPLEX OF PROTEINASE K WITH A SUBSTRATE-ANALOGUE HEXA-PEPTIDE INHIBITOR AT 2.2 ANGSTROMS RESOLUTION

1pek, resolution 2.20Å

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