6a3f

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Current revision (09:17, 22 November 2023) (edit) (undo)
 
(One intermediate revision not shown.)
Line 1: Line 1:
==Levoglucosan dehydrogenase, apo form==
==Levoglucosan dehydrogenase, apo form==
-
<StructureSection load='6a3f' size='340' side='right' caption='[[6a3f]], [[Resolution|resolution]] 1.80&Aring;' scene=''>
+
<StructureSection load='6a3f' size='340' side='right'caption='[[6a3f]], [[Resolution|resolution]] 1.80&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
-
<table><tr><td colspan='2'>[[6a3f]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6A3F OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6A3F FirstGlance]. <br>
+
<table><tr><td colspan='2'>[[6a3f]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Pseudarthrobacter_phenanthrenivorans_Sphe3 Pseudarthrobacter phenanthrenivorans Sphe3]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6A3F OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6A3F FirstGlance]. <br>
-
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></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]] 1.8&#8491;</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=6a3f FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6a3f OCA], [http://pdbe.org/6a3f PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6a3f RCSB], [http://www.ebi.ac.uk/pdbsum/6a3f PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6a3f ProSAT]</span></td></tr>
+
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><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=6a3f FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6a3f OCA], [https://pdbe.org/6a3f PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6a3f RCSB], [https://www.ebi.ac.uk/pdbsum/6a3f PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6a3f ProSAT]</span></td></tr>
</table>
</table>
 +
== Function ==
 +
[https://www.uniprot.org/uniprot/F0M433_PSEPM F0M433_PSEPM]
<div style="background-color:#fffaf0;">
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
== Publication Abstract from PubMed ==
-
A levoglucosan (1,6-anhydro-beta-D-glucopyranose)-using bacterium, isolated from soil, was identified. It was shown to belong to the genus Arthrobacter and tentatively named Arthrobacter sp. I-552. A novel enzyme catalyzed the dehydrogenation of levoglucosan to form 1,6-anhydro-beta-D-ribo-hexopyranos-3-ulose (3-keto levoglucosan), using NAD+ as an electron acceptor, i.e. NAD+: 1,6-anhydro-beta-D-glucopyranose oxidoreductase (trivial name: levoglucosan dehydrogenase). This enzyme was purified and characterized. A possible reaction scheme for the glucose formation was proposed. This pathway for levoglucosan use is distinct from those in yeast and fungi.
+
Levoglucosan is the 1,6-anhydrosugar of D-glucose formed by pyrolysis of glucans and is found in the environment and industrial waste. Two types of microbial levoglucosan metabolic pathways are known. Although the eukaryotic pathway involving levoglucosan kinase has been well studied, the bacterial pathway involving levoglucosan dehydrogenase (LGDH) has not been well investigated. Here, we identified and cloned the lgdh gene from the bacterium Pseudarthrobacter phenanthrenivorans and characterized the recombinant protein. The enzyme exhibited high substrate specificity toward levoglucosan and NAD(+) for the oxidative reaction and was confirmed to be LGDH. LGDH also showed weak activities (~4%) toward L-sorbose and 1,5-anhydro-D-glucitol. The reverse (reductive) reaction using 3-keto levoglucosan and NADH exhibited significantly lower Km and higher kcat values than those of the forward reaction. The crystal structures of LGDH in the apo and complex forms with NADH, NADH + levoglucosan, and NADH + L-sorbose revealed that LGDH has a typical fold of Gfo/Idh/MocA family proteins, similar to those of scyllo-inositol dehydrogenase, aldose-aldose oxidoreductase, 1,5-anhydro-D-fructose reductase, and glucose-fructose oxidoreductase. The crystal structures also disclosed that the active site of LGDH is distinct from those of these enzymes. The LGDH active site extensively recognized the levoglucosan molecule with six hydrogen bonds, and the C3 atom of levoglucosan was closely located to the C4 atom of NADH nicotinamide. Our study is the first molecular characterization of LGDH, providing evidence for C3-specific oxidation, and representing a starting point for future biotechnological use of LGDH and levoglucosan-metabolizing bacteria.
-
Levoglucosan dehydrogenase involved in the assimilation of levoglucosan in Arthrobacter sp. I-552.,Nakahara K, Kitamura Y, Yamagishi Y, Shoun H, Yasui T Biosci Biotechnol Biochem. 1994 Dec;58(12):2193-6. doi: 10.1271/bbb.58.2193. PMID:7765713<ref>PMID:7765713</ref>
+
Identification, functional characterization, and crystal structure determination of bacterial levoglucosan dehydrogenase.,Sugiura M, Nakahara M, Yamada C, Arakawa T, Kitaoka M, Fushinobu S J Biol Chem. 2018 Sep 17. pii: RA118.004963. doi: 10.1074/jbc.RA118.004963. PMID:30224354<ref>PMID:30224354</ref>
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
Line 20: Line 23:
__TOC__
__TOC__
</StructureSection>
</StructureSection>
-
[[Category: Arakawa, T]]
+
[[Category: Large Structures]]
-
[[Category: Fushinobu, S]]
+
[[Category: Pseudarthrobacter phenanthrenivorans Sphe3]]
-
[[Category: Sugiura, M]]
+
[[Category: Arakawa T]]
-
[[Category: Yamada, C]]
+
[[Category: Fushinobu S]]
-
[[Category: Gfo/idh/moca family]]
+
[[Category: Sugiura M]]
-
[[Category: Nadh-dependent dehydrogenase]]
+
[[Category: Yamada C]]
-
[[Category: Oxidoreductase]]
+
-
[[Category: Rossmann fold]]
+

Current revision

Levoglucosan dehydrogenase, apo form

PDB ID 6a3f

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools