1h0g: Difference between revisions

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[[Image:1h0g.png|left|200px]]


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==Complex of a chitinase with the natural product cyclopentapeptide argadin from Clonostachys==
The line below this paragraph, containing "STRUCTURE_1h0g", creates the "Structure Box" on the page.
<StructureSection load='1h0g' size='340' side='right'caption='[[1h0g]], [[Resolution|resolution]] 2.00&Aring;' scene=''>
You may change the PDB parameter (which sets the PDB file loaded into the applet)
== Structural highlights ==
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
<table><tr><td colspan='2'>[[1h0g]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Serratia_marcescens Serratia marcescens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1H0G OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1H0G FirstGlance]. <br>
or leave the SCENE parameter empty for the default display.
</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>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=0AR:N-[N-[(4S)-4-AZANYL-5-HYDROXY-5-OXO-PENTYL]CARBAMIMIDOYL]ETHANAMIDE'>0AR</scene>, <scene name='pdbligand=DPR:D-PROLINE'>DPR</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=HSE:L-HOMOSERINE'>HSE</scene>, <scene name='pdbligand=UN1:2-AMINOHEXANEDIOIC+ACID'>UN1</scene></td></tr>
{{STRUCTURE_1h0g|  PDB=1h0g  |  SCENE=  }}
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1h0g FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1h0g OCA], [https://pdbe.org/1h0g PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1h0g RCSB], [https://www.ebi.ac.uk/pdbsum/1h0g PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1h0g ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/CHIB_SERMA CHIB_SERMA]
== 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/h0/1h0g_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=1h0g ConSurf].
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== Publication Abstract from PubMed ==
Over the past years, family 18 chitinases have been validated as potential targets for the design of drugs against human pathogens that contain or interact with chitin during their normal life cycles. Thus far, only one potent chitinase inhibitor has been described in detail, the pseudotrisaccharide allosamidin. Recently, however, two potent natural-product cyclopentapeptide chitinase inhibitors, argifin and argadin, were reported. Here, we describe high-resolution crystal structures that reveal the details of the interactions of these cyclopeptides with a family 18 chitinase. The structures are examples of complexes of a carbohydrate-processing enzyme with high-affinity peptide-based inhibitors and show in detail how the peptide backbone and side chains mimic the interactions of the enzyme with chitooligosaccharides. Together with enzymological characterization, the structures explain why argadin shows an order of magnitude stronger inhibition than allosamidin, whereas argifin shows weaker inhibition. The peptides bind to the chitinase in remarkably different ways, which may explain the differences in inhibition constants. The two complexes provide a basis for structure-based design of potent chitinase inhibitors, accessible by standard peptide chemistry.


===COMPLEX OF A CHITINASE WITH THE NATURAL PRODUCT CYCLOPENTAPEPTIDE ARGADIN FROM CLONOSTACHYS===
High-resolution structures of a chitinase complexed with natural product cyclopentapeptide inhibitors: mimicry of carbohydrate substrate.,Houston DR, Shiomi K, Arai N, Omura S, Peter MG, Turberg A, Synstad B, Eijsink VG, van Aalten DM Proc Natl Acad Sci U S A. 2002 Jul 9;99(14):9127-32. Epub 2002 Jul 1. PMID:12093900<ref>PMID:12093900</ref>


From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 1h0g" style="background-color:#fffaf0;"></div>


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==See Also==
The line below this paragraph, {{ABSTRACT_PUBMED_12093900}}, adds the Publication Abstract to the page
*[[Chitinase 3D structures|Chitinase 3D structures]]
(as it appears on PubMed at http://www.pubmed.gov), where 12093900 is the PubMed ID number.
== References ==
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<references/>
{{ABSTRACT_PUBMED_12093900}}
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</StructureSection>
==About this Structure==
[[Category: Large Structures]]
1H0G is a 4 chains structure of sequences from [http://en.wikipedia.org/wiki/Serratia_marcescens Serratia marcescens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1H0G OCA].
 
==Reference==
<ref group="xtra">PMID:12093900</ref><references group="xtra"/>
[[Category: Hydrolase]]
[[Category: Serratia marcescens]]
[[Category: Serratia marcescens]]
[[Category: Aalten, D M.F Van.]]
[[Category: Aalten DMF]]
[[Category: Arai, N.]]
[[Category: Arai N]]
[[Category: Eijsink, V G.H.]]
[[Category: Eijsink VGH]]
[[Category: Houston, D R.]]
[[Category: Houston D]]
[[Category: Omura, S.]]
[[Category: Omura S]]
[[Category: Peter, M G.]]
[[Category: Peter MG]]
[[Category: Shiomi, K.]]
[[Category: Shiomi K]]
[[Category: Synstad, B.]]
[[Category: Synstad B]]
[[Category: Turberg, A.]]
[[Category: Turberg A]]
[[Category: Argadin]]
[[Category: Chitin degradation]]
[[Category: Hydrolase]]
[[Category: Inhibitor]]
 
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