This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.


Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.


6yc8

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
(New page: '''Unreleased structure''' The entry 6yc8 is ON HOLD Authors: Di Pisa, F. Description: Crystal structure of KRED1-Pglu enzyme Category: Unreleased Structures [[Category: Di Pisa, F...)
Current revision (13:23, 24 January 2024) (edit) (undo)
 
(3 intermediate revisions not shown.)
Line 1: Line 1:
-
'''Unreleased structure'''
 
-
The entry 6yc8 is ON HOLD
+
==Crystal structure of KRED1-Pglu enzyme==
 +
<StructureSection load='6yc8' size='340' side='right'caption='[[6yc8]], [[Resolution|resolution]] 1.77&Aring;' scene=''>
 +
== Structural highlights ==
 +
<table><tr><td colspan='2'>[[6yc8]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Ogataea_glucozyma Ogataea glucozyma]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6YC8 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6YC8 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]] 1.77&#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=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=EPE:4-(2-HYDROXYETHYL)-1-PIPERAZINE+ETHANESULFONIC+ACID'>EPE</scene>, <scene name='pdbligand=NAP:NADP+NICOTINAMIDE-ADENINE-DINUCLEOTIDE+PHOSPHATE'>NAP</scene>, <scene name='pdbligand=PEG:DI(HYDROXYETHYL)ETHER'>PEG</scene>, <scene name='pdbligand=PGE:TRIETHYLENE+GLYCOL'>PGE</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=6yc8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6yc8 OCA], [https://pdbe.org/6yc8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6yc8 RCSB], [https://www.ebi.ac.uk/pdbsum/6yc8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6yc8 ProSAT]</span></td></tr>
 +
</table>
 +
== Function ==
 +
[https://www.uniprot.org/uniprot/A0A0H4SN47_9ASCO A0A0H4SN47_9ASCO]
 +
<div style="background-color:#fffaf0;">
 +
== Publication Abstract from PubMed ==
 +
Benzil reductases are dehydrogenases preferentially active on aromatic 1,2-diketones, but the reasons for this peculiar substrate recognition have not yet been clarified. The benzil reductase (KRED1-Pglu) from the non-conventional yeast Pichia glucozyma showed excellent activity and stereoselectivity in the monoreduction of space-demanding aromatic 1,2-dicarbonyls, making this enzyme attractive as biocatalyst in organic chemistry. Structural insights into the stereoselective monoreduction of 1,2-diketones catalyzed by KRED1-Pglu were investigated starting from its 1.77 A resolution crystal structure, followed by QM and classical calculations; this study allowed for the identification and characterization of the KRED1-Pglu reactive site. Once identified the recognition elements involved in the stereoselective desymmetrization of bulky 1,2-dicarbonyls mediated by KRED1-Pglu, a mechanism was proposed together with an in silico prediction of substrates reactivity.
-
Authors: Di Pisa, F.
+
Structural insights into the desymmetrization of bulky 1,2-dicarbonyls through enzymatic monoreduction.,Rabuffetti M, Cannazza P, Contente ML, Pinto A, Romano D, Hoyos P, Alcantara AR, Eberini I, Laurenzi T, Gourlay L, Di Pisa F, Molinari F Bioorg Chem. 2021 Jan 11;108:104644. doi: 10.1016/j.bioorg.2021.104644. PMID:33486371<ref>PMID:33486371</ref>
-
Description: Crystal structure of KRED1-Pglu enzyme
+
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
-
[[Category: Unreleased Structures]]
+
</div>
-
[[Category: Di Pisa, F]]
+
<div class="pdbe-citations 6yc8" style="background-color:#fffaf0;"></div>
 +
== References ==
 +
<references/>
 +
__TOC__
 +
</StructureSection>
 +
[[Category: Large Structures]]
 +
[[Category: Ogataea glucozyma]]
 +
[[Category: Di Pisa F]]

Current revision

Crystal structure of KRED1-Pglu enzyme

PDB ID 6yc8

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools