7oqr

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Current revision (12:54, 1 February 2024) (edit) (undo)
 
(One intermediate revision not shown.)
Line 1: Line 1:
==Crystal structure of Trypanosoma cruzi peroxidase==
==Crystal structure of Trypanosoma cruzi peroxidase==
-
<StructureSection load='7oqr' size='340' side='right'caption='[[7oqr]]' scene=''>
+
<StructureSection load='7oqr' size='340' side='right'caption='[[7oqr]], [[Resolution|resolution]] 1.76&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
-
<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7OQR OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7OQR FirstGlance]. <br>
+
<table><tr><td colspan='2'>[[7oqr]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Trypanosoma_cruzi Trypanosoma cruzi]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7OQR OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7OQR FirstGlance]. <br>
-
</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=7oqr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7oqr OCA], [https://pdbe.org/7oqr PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7oqr RCSB], [https://www.ebi.ac.uk/pdbsum/7oqr PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7oqr ProSAT]</span></td></tr>
+
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.76&#8491;</td></tr>
 +
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ACT:ACETATE+ION'>ACT</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=HEM:PROTOPORPHYRIN+IX+CONTAINING+FE'>HEM</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand=OXY:OXYGEN+MOLECULE'>OXY</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=7oqr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7oqr OCA], [https://pdbe.org/7oqr PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7oqr RCSB], [https://www.ebi.ac.uk/pdbsum/7oqr PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7oqr ProSAT]</span></td></tr>
</table>
</table>
 +
== Function ==
 +
[https://www.uniprot.org/uniprot/Q8I1N3_TRYCR Q8I1N3_TRYCR]
 +
<div style="background-color:#fffaf0;">
 +
== Publication Abstract from PubMed ==
 +
The protozoan parasite Trypanosoma cruzi is the causative agent of American trypanosomiasis, otherwise known as Chagas disease. To survive in the host, the T. cruzi parasite needs antioxidant defense systems. One of these is a hybrid heme peroxidase, the T. cruzi ascorbate peroxidase-cytochrome c peroxidase enzyme (TcAPx-CcP). TcAPx-CcP has high sequence identity to members of the class I peroxidase family, notably ascorbate peroxidase (APX) and cytochrome c peroxidase (CcP), as well as a mitochondrial peroxidase from Leishmania major (LmP). The aim of this work was to solve the structure and examine the reactivity of the TcAPx-CcP enzyme. Low temperature electron paramagnetic resonance spectra support the formation of an exchange-coupled [Fe(IV)=O Trp(233)(*+)] compound I radical species, analogous to that used in CcP and LmP. We demonstrate that TcAPx-CcP is similar in overall structure to APX and CcP, but there are differences in the substrate-binding regions. Furthermore, the electron transfer pathway from cytochrome c to the heme in CcP and LmP is preserved in the TcAPx-CcP structure. Integration of steady state kinetic experiments, molecular dynamic simulations, and bioinformatic analyses indicates that TcAPx-CcP preferentially oxidizes cytochrome c but is still competent for oxidization of ascorbate. The results reveal that TcAPx-CcP is a credible cytochrome c peroxidase, which can also bind and use ascorbate in host cells, where concentrations are in the millimolar range. Thus, kinetically and functionally TcAPx-CcP can be considered a hybrid peroxidase.
 +
 +
Crystal structure of Trypanosoma cruzi heme peroxidase and characterization of its substrate specificity and compound I intermediate.,Freeman SL, Skafar V, Kwon H, Fielding AJ, Moody PCE, Martinez A, Issoglio FM, Inchausti L, Smircich P, Zeida A, Piacenza L, Radi R, Raven EL J Biol Chem. 2022 Aug;298(8):102204. doi: 10.1016/j.jbc.2022.102204. Epub 2022 , Jun 27. PMID:35772495<ref>PMID:35772495</ref>
 +
 +
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
 +
</div>
 +
<div class="pdbe-citations 7oqr" style="background-color:#fffaf0;"></div>
 +
 +
==See Also==
 +
*[[Ascorbate peroxidase 3D structures|Ascorbate peroxidase 3D structures]]
 +
== References ==
 +
<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Large Structures]]
[[Category: Large Structures]]
 +
[[Category: Trypanosoma cruzi]]
[[Category: Fielding AJ]]
[[Category: Fielding AJ]]
[[Category: Freeman SL]]
[[Category: Freeman SL]]

Current revision

Crystal structure of Trypanosoma cruzi peroxidase

PDB ID 7oqr

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools