|
|
Line 3: |
Line 3: |
| <StructureSection load='4uz8' size='340' side='right'caption='[[4uz8]], [[Resolution|resolution]] 2.30Å' scene=''> | | <StructureSection load='4uz8' size='340' side='right'caption='[[4uz8]], [[Resolution|resolution]] 2.30Å' scene=''> |
| == Structural highlights == | | == Structural highlights == |
- | <table><tr><td colspan='2'>[[4uz8]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/"bacillus_alcalophilus_subsp._halodurans"_boyer_et_al._1973 "bacillus alcalophilus subsp. halodurans" boyer et al. 1973]. 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> | + | <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> |
- | </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='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> |
- | <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>
| + | <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> |
- | <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>
| + | |
- | <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://pdbe.org/4uz8 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4uz8 RCSB], [http://www.ebi.ac.uk/pdbsum/4uz8 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4uz8 ProSAT]</span></td></tr> | + | |
| </table> | | </table> |
| + | == Function == |
| + | [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 == |
Line 20: |
Line 20: |
| | | |
| ==See Also== | | ==See Also== |
- | *[[Glucanase|Glucanase]] | + | *[[Glucanase 3D structures|Glucanase 3D structures]] |
| == References == | | == References == |
| <references/> | | <references/> |
| __TOC__ | | __TOC__ |
| </StructureSection> | | </StructureSection> |
- | [[Category: Bacillus alcalophilus subsp. halodurans boyer et al. 1973]] | + | [[Category: Alkalihalobacillus halodurans]] |
| [[Category: Large Structures]] | | [[Category: Large Structures]] |
- | [[Category: Ferreira, L M.A]] | + | [[Category: Ferreira LMA]] |
- | [[Category: Fontes, C M.G A]] | + | [[Category: Fontes CMGA]] |
- | [[Category: Najmudin, S]] | + | [[Category: Najmudin S]] |
- | [[Category: Sakka, K]] | + | [[Category: Sakka K]] |
- | [[Category: Santos, H]] | + | [[Category: Santos H]] |
- | [[Category: Venditto, I]] | + | [[Category: Venditto I]] |
- | [[Category: Bacillus haloduran]]
| + | |
- | [[Category: Carbohydrate binding protein]]
| + | |
- | [[Category: Carbohydrate-binding module family 46]]
| + | |
- | [[Category: Cbm46]]
| + | |
- | [[Category: Cel5b]]
| + | |
- | [[Category: Semet derivative]]
| + | |
- | [[Category: Sugar binding protein]]
| + | |
| Structural highlights
Function
Q9KF82_HALH5
Publication Abstract from PubMed
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.
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[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
See Also
References
- ↑ Venditto I, Najmudin S, Luis AS, Ferreira LM, Sakka K, Knox JP, Gilbert HJ, Fontes CM. Family 46 Carbohydrate-Binding Modules contribute to the enzymatic hydrolysis of xyloglucan and beta-1,3-1,4-glucans through distinct mechanisms. J Biol Chem. 2015 Feb 23. pii: jbc.M115.637827. PMID:25713075 doi:http://dx.doi.org/10.1074/jbc.M115.637827
|