2wfa
From Proteopedia
(Difference between revisions)
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<StructureSection load='2wfa' size='340' side='right' caption='[[2wfa]], [[Resolution|resolution]] 1.65Å' scene=''> | <StructureSection load='2wfa' size='340' side='right' caption='[[2wfa]], [[Resolution|resolution]] 1.65Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>[[2wfa]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Lactococcus_lactis Lactococcus lactis]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2WFA OCA]. <br> | + | <table><tr><td colspan='2'>[[2wfa]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Lactococcus_lactis Lactococcus lactis]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2WFA OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2WFA FirstGlance]. <br> |
- | </td></tr><tr><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=BEF:BERYLLIUM+TRIFLUORIDE+ION'>BEF</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>< | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=BEF:BERYLLIUM+TRIFLUORIDE+ION'>BEF</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene></td></tr> |
- | <tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1z4o|1z4o]], [[2wf5|2wf5]], [[1o03|1o03]], [[1zol|1zol]], [[1z4n|1z4n]], [[1lvh|1lvh]], [[1o08|1o08]], [[2wf6|2wf6]], [[2wf8|2wf8]], [[2wf7|2wf7]], [[2wf9|2wf9]]</td></tr> | + | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1z4o|1z4o]], [[2wf5|2wf5]], [[1o03|1o03]], [[1zol|1zol]], [[1z4n|1z4n]], [[1lvh|1lvh]], [[1o08|1o08]], [[2wf6|2wf6]], [[2wf8|2wf8]], [[2wf7|2wf7]], [[2wf9|2wf9]]</td></tr> |
- | <tr><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/ | + | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Beta-phosphoglucomutase Beta-phosphoglucomutase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=5.4.2.6 5.4.2.6] </span></td></tr> |
- | <tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2wfa FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2wfa OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2wfa RCSB], [http://www.ebi.ac.uk/pdbsum/2wfa PDBsum]</span></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=2wfa FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2wfa OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2wfa RCSB], [http://www.ebi.ac.uk/pdbsum/2wfa PDBsum]</span></td></tr> |
- | <table> | + | </table> |
+ | == Function == | ||
+ | [[http://www.uniprot.org/uniprot/PGMB_LACLA PGMB_LACLA]] Catalyzes the interconversion of D-glucose 1-phosphate (G1P) and D-glucose 6-phosphate (G6P), forming beta-D-glucose 1,6-(bis)phosphate (beta-G16P) as an intermediate. The beta-phosphoglucomutase (Beta-PGM) acts on the beta-C(1) anomer of G1P. Glucose or lactose are used in preference to maltose, which is only utilized after glucose or lactose has been exhausted. It plays a key role in the regulation of the flow of carbohydrate intermediates in glycolysis and the formation of the sugar nucleotide UDP-glucose.<ref>PMID:9084169</ref> <ref>PMID:15005616</ref> | ||
== Evolutionary Conservation == | == Evolutionary Conservation == | ||
[[Image:Consurf_key_small.gif|200px|right]] | [[Image:Consurf_key_small.gif|200px|right]] | ||
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Near attack conformers dominate beta-phosphoglucomutase complexes where geometry and charge distribution reflect those of substrate.,Griffin JL, Bowler MW, Baxter NJ, Leigh KN, Dannatt HR, Hounslow AM, Blackburn GM, Webster CE, Cliff MJ, Waltho JP Proc Natl Acad Sci U S A. 2012 May 1;109(18):6910-5. Epub 2012 Apr 13. PMID:22505741<ref>PMID:22505741</ref> | Near attack conformers dominate beta-phosphoglucomutase complexes where geometry and charge distribution reflect those of substrate.,Griffin JL, Bowler MW, Baxter NJ, Leigh KN, Dannatt HR, Hounslow AM, Blackburn GM, Webster CE, Cliff MJ, Waltho JP Proc Natl Acad Sci U S A. 2012 May 1;109(18):6910-5. Epub 2012 Apr 13. PMID:22505741<ref>PMID:22505741</ref> | ||
- | From | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> |
</div> | </div> | ||
+ | |||
+ | ==See Also== | ||
+ | *[[Beta-phosphoglucomutase|Beta-phosphoglucomutase]] | ||
== References == | == References == | ||
<references/> | <references/> | ||
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[[Category: Beta-phosphoglucomutase]] | [[Category: Beta-phosphoglucomutase]] | ||
[[Category: Lactococcus lactis]] | [[Category: Lactococcus lactis]] | ||
- | [[Category: Alizadeh, T | + | [[Category: Alizadeh, T]] |
- | [[Category: Baxter, N J | + | [[Category: Baxter, N J]] |
- | [[Category: Bermel, W | + | [[Category: Bermel, W]] |
- | [[Category: Blackburn, G M | + | [[Category: Blackburn, G M]] |
- | [[Category: Bowler, M W | + | [[Category: Bowler, M W]] |
- | [[Category: Cliff, M J | + | [[Category: Cliff, M J]] |
- | [[Category: Hollfelder, F | + | [[Category: Hollfelder, F]] |
- | [[Category: Hounslow, A M | + | [[Category: Hounslow, A M]] |
- | [[Category: Pollard, S | + | [[Category: Pollard, S]] |
- | [[Category: Waltho, J P | + | [[Category: Waltho, J P]] |
- | [[Category: Webster, C E | + | [[Category: Webster, C E]] |
- | [[Category: Williams, N H | + | [[Category: Williams, N H]] |
[[Category: Haloacid dehalogenase superfamily]] | [[Category: Haloacid dehalogenase superfamily]] | ||
[[Category: Isomerase]] | [[Category: Isomerase]] | ||
[[Category: Phosphotransferase]] | [[Category: Phosphotransferase]] | ||
[[Category: Transition state analogue]] | [[Category: Transition state analogue]] |
Revision as of 02:07, 25 December 2014
Structure of Beta-Phosphoglucomutase inhibited with Beryllium trifluoride, in an open conformation.
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Categories: Beta-phosphoglucomutase | Lactococcus lactis | Alizadeh, T | Baxter, N J | Bermel, W | Blackburn, G M | Bowler, M W | Cliff, M J | Hollfelder, F | Hounslow, A M | Pollard, S | Waltho, J P | Webster, C E | Williams, N H | Haloacid dehalogenase superfamily | Isomerase | Phosphotransferase | Transition state analogue