4uz8

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==The SeMet structure of the family 46 carbohydrate-binding module (CBM46) of endo-beta-1,4-glucanase B (Cel5B) from Bacillus halodurans==
==The SeMet structure of the family 46 carbohydrate-binding module (CBM46) of endo-beta-1,4-glucanase B (Cel5B) from Bacillus halodurans==
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<StructureSection load='4uz8' size='340' side='right' caption='[[4uz8]], [[Resolution|resolution]] 2.30&Aring;' scene=''>
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<StructureSection load='4uz8' size='340' side='right'caption='[[4uz8]], [[Resolution|resolution]] 2.30&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>[[4uz8]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4UZ8 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4UZ8 FirstGlance]. <br>
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<table><tr><td colspan='2'>[[4uz8]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Alkalihalobacillus_halodurans Alkalihalobacillus halodurans]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4UZ8 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4UZ8 FirstGlance]. <br>
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</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>
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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]] 2.3&#8491;</td></tr>
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<tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=MSE:SELENOMETHIONINE'>MSE</scene></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=MSE:SELENOMETHIONINE'>MSE</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
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<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4uyp|4uyp]], [[4uyq|4uyq]], [[4uzn|4uzn]], [[4uzp|4uzp]]</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=4uz8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4uz8 OCA], [https://pdbe.org/4uz8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4uz8 RCSB], [https://www.ebi.ac.uk/pdbsum/4uz8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4uz8 ProSAT]</span></td></tr>
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<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=4uz8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4uz8 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4uz8 RCSB], [http://www.ebi.ac.uk/pdbsum/4uz8 PDBsum]</span></td></tr>
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</table>
</table>
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== Function ==
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[https://www.uniprot.org/uniprot/Q9KF82_HALH5 Q9KF82_HALH5]
<div style="background-color:#fffaf0;">
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
== Publication Abstract from PubMed ==
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Plant cell-wall polysaccharides offer an abundant energy source utilized by many microorganisms, thus playing a central role in carbon recycling. Aerobic microorganisms secrete carbohydrate-active enzymes (CAZymes) that catabolize this composite structure, comprising cellulose, hemicellulose and lignin, into simple compounds such as glucose. Carbohydrate-binding modules (CBMs) enhance the efficacy of associated CAZYmes. They are organized into families based on primary-sequence homology. CBM family 46 contains more than 40 different members, but has yet to be fully characterized. Here, a recombinant derivative of the C-terminal family 46 CBM module (BhCBM46) of Bacillus halodurans endo-beta-1,4-glucanase B (CelB) was overexpressed in Escherichia coli and purified by immobilized metal-ion affinity chromatography. Preliminary structural characterization was carried out on BhCBM46 crystallized in different conditions. The crystals of BhCBM46 belonged to the tetragonal space group I4(1)22. Data were collected for the native form and a selenomethionine derivative to 2.46 and 2.3 A resolution, respectively. The BhCBM46 structure was determined by a single-wavelength anomalous dispersion experiment using AutoSol from the PHENIX suite.
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Structural carbohydrates comprise an extraordinary source of energy that remains poorly utilized by the biofuel sector as enzymes have restricted access to their substrates within the intricacy of plant cell walls. Carbohydrate Active enZYmes (CAZYmes) that target recalcitrant polysaccharides are modular enzymes containing non-catalytic Carbohydrate Binding Modules (CBMs) that direct enzymes to their cognate substrate, thus potentiating catalysis. In general, CBMs are functionally and structurally autonomous from their associated catalytic domains from which they are separated through flexible linker sequences. Here we show that a C-terminal CBM46 derived from BhCel5B, a Bacillus halodurans endoglucanase, does not interact with beta-glucans independently but, uniquely, acts co-operatively with the catalytic domain of the enzyme in substrate recognition. The structure of BhCBM46 revealed a beta-sandwich fold that abuts onto the region of the substrate binding cleft upstream of the active site. BhCBM46 as a discrete entity is unable to bind to beta-glucans. Removal of BhCBM46 from BhCel5B, however, abrogates binding to beta-1,3-1,4-glucans while substantially decreasing the affinity for decorated beta-1,4-glucan homopolymers such as xyloglucan. The CBM46 was shown to contribute to xyloglucan hydrolysis only in the context of intact plant cell walls, but potentiates enzymatic activity against purified beta-1,3-1,4-glucans in solution or within the cell wall. This report reveals the mechanism by which a CBM can promote enzyme activity through direct interaction with the substrate or by targeting regions of the plant cell wall where the target glucan is abundant.
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Overproduction, purification, crystallization and preliminary X-ray characterization of the family 46 carbohydrate-binding module (CBM46) of endo-beta-1,4-glucanase B (CelB) from Bacillus halodurans.,Venditto I, Santos H, Ferreira LM, Sakka K, Fontes CM, Najmudin S Acta Crystallogr F Struct Biol Commun. 2014 Jun;70(Pt 6):754-7. doi:, 10.1107/S2053230X14008395. Epub 2014 May 10. PMID:24915086<ref>PMID:24915086</ref>
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Family 46 Carbohydrate-Binding Modules contribute to the enzymatic hydrolysis of xyloglucan and beta-1,3-1,4-glucans through distinct mechanisms.,Venditto I, Najmudin S, Luis AS, Ferreira LM, Sakka K, Knox JP, Gilbert HJ, Fontes CM J Biol Chem. 2015 Feb 23. pii: jbc.M115.637827. PMID:25713075<ref>PMID:25713075</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>
</div>
</div>
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<div class="pdbe-citations 4uz8" style="background-color:#fffaf0;"></div>
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==See Also==
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*[[Glucanase 3D structures|Glucanase 3D structures]]
== References ==
== References ==
<references/>
<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
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[[Category: Ferreira, L M.A]]
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[[Category: Alkalihalobacillus halodurans]]
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[[Category: Fontes, C M.G A]]
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[[Category: Large Structures]]
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[[Category: Najmudin, S]]
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[[Category: Ferreira LMA]]
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[[Category: Sakka, K]]
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[[Category: Fontes CMGA]]
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[[Category: Santos, H]]
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[[Category: Najmudin S]]
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[[Category: Venditto, I]]
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[[Category: Sakka K]]
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[[Category: Bacillus haloduran]]
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[[Category: Santos H]]
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[[Category: Carbohydrate binding protein]]
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[[Category: Venditto I]]
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[[Category: Carbohydrate-binding module family 46]]
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[[Category: Cbm46]]
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[[Category: Cel5b]]
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[[Category: Semet derivative]]
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[[Category: Sugar binding protein]]
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Current revision

The SeMet structure of the family 46 carbohydrate-binding module (CBM46) of endo-beta-1,4-glucanase B (Cel5B) from Bacillus halodurans

PDB ID 4uz8

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