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| | ==Partial Structure of the C-terminal domain of the HPIV4B phosphoprotein, fused to MBP.== | | ==Partial Structure of the C-terminal domain of the HPIV4B phosphoprotein, fused to MBP.== |
| - | <StructureSection load='4kye' size='340' side='right' caption='[[4kye]], [[Resolution|resolution]] 2.60Å' scene=''> | + | <StructureSection load='4kye' size='340' side='right'caption='[[4kye]], [[Resolution|resolution]] 2.60Å' scene=''> |
| | == Structural highlights == | | == Structural highlights == |
| - | <table><tr><td colspan='2'>[[4kye]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Hpiv-4b Hpiv-4b]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4KYE OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4KYE FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[4kye]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Escherichia_coli_K-12 Escherichia coli K-12] and [https://en.wikipedia.org/wiki/Human_parainfluenza_virus_4b_(strain_68-333) Human parainfluenza virus 4b (strain 68-333)]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4KYE OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4KYE FirstGlance]. <br> |
| - | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=MAL:MALTOSE'>MAL</scene></td></tr> | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GLC:ALPHA-D-GLUCOSE'>GLC</scene>, <scene name='pdbligand=PRD_900001:alpha-maltose'>PRD_900001</scene></td></tr> |
| - | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4kyc|4kyc]], [[4kyd|4kyd]]</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=4kye FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4kye OCA], [https://pdbe.org/4kye PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4kye RCSB], [https://www.ebi.ac.uk/pdbsum/4kye PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4kye ProSAT]</span></td></tr> |
| - | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">b4034, JW3994, malE, P, P/V ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=11227 HPIV-4b])</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=4kye FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4kye OCA], [http://pdbe.org/4kye PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4kye RCSB], [http://www.ebi.ac.uk/pdbsum/4kye PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4kye ProSAT]</span></td></tr> | + | |
| | </table> | | </table> |
| | == Function == | | == Function == |
| - | [[http://www.uniprot.org/uniprot/MALE_ECOLI MALE_ECOLI]] Involved in the high-affinity maltose membrane transport system MalEFGK. Initial receptor for the active transport of and chemotaxis toward maltooligosaccharides. | + | [https://www.uniprot.org/uniprot/MALE_ECOLI MALE_ECOLI] Involved in the high-affinity maltose membrane transport system MalEFGK. Initial receptor for the active transport of and chemotaxis toward maltooligosaccharides.[https://www.uniprot.org/uniprot/PHOSP_PI4HB PHOSP_PI4HB] |
| | <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
| | == Publication Abstract from PubMed == | | == Publication Abstract from PubMed == |
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| | __TOC__ | | __TOC__ |
| | </StructureSection> | | </StructureSection> |
| - | [[Category: Hpiv-4b]] | + | [[Category: Escherichia coli K-12]] |
| - | [[Category: Bulloch, E M.M]] | + | [[Category: Large Structures]] |
| - | [[Category: Kingston, R L]] | + | [[Category: Bulloch EMM]] |
| - | [[Category: Yegambaram, K]] | + | [[Category: Kingston RL]] |
| - | [[Category: Helix bundle]] | + | [[Category: Yegambaram K]] |
| - | [[Category: Binding protein]]
| + | |
| - | [[Category: Viral nucleocapsid]]
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| - | [[Category: Viral protein]]
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| Structural highlights
Function
MALE_ECOLI Involved in the high-affinity maltose membrane transport system MalEFGK. Initial receptor for the active transport of and chemotaxis toward maltooligosaccharides.PHOSP_PI4HB
Publication Abstract from PubMed
Proteins are often classified in a binary fashion as either structured or disordered. However this approach has several deficits. Firstly, protein folding is always conditional on the physiochemical environment. A protein which is structured in some circumstances will be disordered in others. Secondly, it hides a fundamental asymmetry in behavior. While all structured proteins can be unfolded through a change in environment, not all disordered proteins have the capacity for folding. Failure to accommodate these complexities confuses the definition of both protein structural domains and intrinsically disordered regions. We illustrate these points with an experimental study of a family of small binding domains, drawn from the RNA polymerase of mumps virus and its closest relatives. Assessed at face value the domains fall on a structural continuum, with folded, partially folded, and near unstructured members. Yet the disorder present in the family is conditional, and these closely related polypeptides can access the same folded state under appropriate conditions. Any heuristic definition of the protein domain emphasizing conformational stability divides this domain family in two, in a way that makes no biological sense. Structural domains would be better defined by their ability to adopt a specific tertiary structure: a structure that may or may not be realized, dependent on the circumstances. This explicitly allows for the conditional nature of protein folding, and more clearly demarcates structural domains from intrinsically disordered regions that may function without folding.
Protein domain definition should allow for conditional disorder.,Yegambaram K, Bulloch EM, Kingston RL Protein Sci. 2013 Aug 20. doi: 10.1002/pro.2336. PMID:23963781[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Yegambaram K, Bulloch EM, Kingston RL. Protein domain definition should allow for conditional disorder. Protein Sci. 2013 Aug 20. doi: 10.1002/pro.2336. PMID:23963781 doi:10.1002/pro.2336
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