1aim: Difference between revisions

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==CRUZAIN INHIBITED BY BENZOYL-TYROSINE-ALANINE-FLUOROMETHYLKETONE==
==CRUZAIN INHIBITED BY BENZOYL-TYROSINE-ALANINE-FLUOROMETHYLKETONE==
<StructureSection load='1aim' size='340' side='right' caption='[[1aim]], [[Resolution|resolution]] 2.00&Aring;' scene=''>
<StructureSection load='1aim' size='340' side='right' caption='[[1aim]], [[Resolution|resolution]] 2.00&Aring;' scene=''>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=ZYA:BENZOYL-TYROSINE-ALANINE-FLUORO-METHYL+KETONE'>ZYA</scene></td></tr>
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=ZYA:BENZOYL-TYROSINE-ALANINE-FLUORO-METHYL+KETONE'>ZYA</scene></td></tr>
<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">RTP ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=5693 TRYCR])</td></tr>
<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">RTP ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=5693 TRYCR])</td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1aim FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1aim OCA], [http://pdbe.org/1aim PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=1aim RCSB], [http://www.ebi.ac.uk/pdbsum/1aim PDBsum]</span></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1aim FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1aim OCA], [http://pdbe.org/1aim PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=1aim RCSB], [http://www.ebi.ac.uk/pdbsum/1aim PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=1aim ProSAT]</span></td></tr>
</table>
</table>
== Function ==
== Function ==
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</div>
</div>
<div class="pdbe-citations 1aim" style="background-color:#fffaf0;"></div>
<div class="pdbe-citations 1aim" style="background-color:#fffaf0;"></div>
==See Also==
*[[Cruzain|Cruzain]]
== References ==
== References ==
<references/>
<references/>

Revision as of 13:42, 15 November 2017

CRUZAIN INHIBITED BY BENZOYL-TYROSINE-ALANINE-FLUOROMETHYLKETONECRUZAIN INHIBITED BY BENZOYL-TYROSINE-ALANINE-FLUOROMETHYLKETONE

Structural highlights

1aim is a 1 chain structure with sequence from Trycr. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
Ligands:
Gene:RTP (TRYCR)
Resources:FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

Function

[CYSP_TRYCR] Hydrolyzes chromogenic peptides at the carboxyl Arg or Lys; requires at least one more amino acid, preferably Arg, Phe, Val or Leu, between the terminal Arg or Lys and the amino-blocking group. The cysteine protease may play an important role in the development and differentiation of the parasites at several stages of their life cycle.

Evolutionary Conservation

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

Publication Abstract from PubMed

The structure of cruzain, an essential protease from the parasite Trypanosoma cruzi, was determined by X-ray crystallography bound to two different covalent inhibitors. The cruzain S2 specificity pocket is able to productively bind both arginine and phenylalanine residues. The structures of cruzain bound to benzoyl-Arg-Ala-fluoromethyl ketone and benzoyl-Tyr-Ala-fluoromethyl ketone at 2.2 and 2.1 A, respectively, show a pH-dependent specificity switch. Glu 205 adjusts to restructure the S2 specificity pocket, conferring right binding to both hydrophobic and basic residues. Kinetic analysis of activated peptide substrates shows that substrates placing hydrophobic residues in the specificity pocket are cleaved at a broader pH range than hydrophilic substrates. These results demonstrate how cruzain binds both basic and hydrophobic residues and could be important for in vivo regulation of cruzain activity.

Structural determinants of specificity in the cysteine protease cruzain.,Gillmor SA, Craik CS, Fletterick RJ Protein Sci. 1997 Aug;6(8):1603-11. PMID:9260273[1]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

References

  1. Gillmor SA, Craik CS, Fletterick RJ. Structural determinants of specificity in the cysteine protease cruzain. Protein Sci. 1997 Aug;6(8):1603-11. PMID:9260273

1aim, resolution 2.00Å

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