5t2k

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'''Unreleased structure'''
 
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The entry 5t2k is ON HOLD until Paper Publication
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==Geobacillus stearothermophilus HemQ with Manganese-Coproporphyrin III==
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<StructureSection load='5t2k' size='340' side='right'caption='[[5t2k]], [[Resolution|resolution]] 1.80&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5t2k]] is a 5 chain structure with sequence from [https://en.wikipedia.org/wiki/Geobacillus_stearothermophilus_10 Geobacillus stearothermophilus 10]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5T2K OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5T2K 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]] 1.8&#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=76R:[3,3,3,3-(3,8,13,17-TETRAMETHYLPORPHYRIN-2,7,12,18-TETRAYL-KAPPA~4~N~21~,N~22~,N~23~,N~24~)TETRA(PROPANOATO)(2-)]MANGANESE'>76R</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=5t2k FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5t2k OCA], [https://pdbe.org/5t2k PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5t2k RCSB], [https://www.ebi.ac.uk/pdbsum/5t2k PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5t2k ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/CHDC_GEOS3 CHDC_GEOS3] Involved in coproporphyrin-dependent heme b biosynthesis (PubMed:27936663). Catalyzes the decarboxylation of Fe-coproporphyrin III (coproheme) to heme b (protoheme IX), the last step of the pathway (PubMed:27936663). The reaction occurs in a stepwise manner with a three-propionate harderoheme intermediate (PubMed:27936663).<ref>PMID:27936663</ref>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Coproheme decarboxylase catalyzes two sequential oxidative decarboxylations with H2O2 as the oxidant, coproheme III as substrate and cofactor, and heme b as the product. Each reaction breaks a C-C bond and results in net loss of hydride, via steps that are not clear. Solution and solid-state structural characterization of the protein in complex with a substrate analog revealed a highly unconventional H2O2-activating distal environment with the reactive propionic acids (2 and 4) on the opposite side of the porphyrin plane. This suggested that, in contrast to direct C-H bond cleavage catalyzed by a high-valent iron intermediate, the coproheme oxidations must occur through mediating amino acid residues. A tyrosine that hydrogen bonds to propionate 2 in a position analogous to the substrate in ascorbate peroxidase is essential for both decarboxylations, while a lysine that salt bridges to propionate 4 is required solely for the second. A mechanism is proposed in which propionate 2 relays an oxidizing equivalent from a coproheme compound I intermediate to the reactive deprotonated tyro-sine, forming Tyrblacksquare, square, filled. This residue then abstracts a net hydrogen atom (Hblacksquare, square, filled) from propionate 2, followed by migration of the unpaired propionyl electron to the coproheme iron to yield the ferric harderoheme and CO2 products. A similar pathway is proposed for decarboxylation of propionate 4, but with a lysine residue as an essential proton shuttle. The proposed reaction suggests an extended relay of heme-mediated e-/H+ transfers and a novel route for the conversion of carboxylic acids to alkenes.
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Authors: Gauss, G.H., Celis, A.I., Dubois, J.L., Peters, J.W.
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A Structure-Based Mechanism for Oxidative Decarboxylation Reactions Mediated by Amino Acids and Heme Propionates in Coproheme Decarboxylase (HemQ).,Celis AI, Gauss GH, Streit BR, Shisler K, Moraski GC, Rodgers KR, Lukat-Rodgers GS, Peters JW, DuBois JL J Am Chem Soc. 2016 Dec 12. PMID:27936663<ref>PMID:27936663</ref>
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Description: Geobacillus stearothermophilus HemQ with Manganese-Coproporphyrin III
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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[[Category: Peters, J.W]]
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<div class="pdbe-citations 5t2k" style="background-color:#fffaf0;"></div>
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[[Category: Dubois, J.L]]
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== References ==
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[[Category: Celis, A.I]]
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<references/>
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[[Category: Gauss, G.H]]
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__TOC__
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</StructureSection>
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[[Category: Geobacillus stearothermophilus 10]]
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[[Category: Large Structures]]
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[[Category: Celis AI]]
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[[Category: Dubois JL]]
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[[Category: Gauss GH]]
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[[Category: Peters JW]]

Current revision

Geobacillus stearothermophilus HemQ with Manganese-Coproporphyrin III

PDB ID 5t2k

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