4d9j: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
| Line 1: | Line 1: | ||
[[ | ==Structure of a 16 nm protein cage designed by fusing symmetric oligomeric domains== | ||
<StructureSection load='4d9j' size='340' side='right' caption='[[4d9j]], [[Resolution|resolution]] 3.92Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[4d9j]] is a 12 chain structure with sequence from [http://en.wikipedia.org/wiki/Atcc_10762 Atcc 10762]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4D9J OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4D9J FirstGlance]. <br> | |||
</td></tr><tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[3vdx|3vdx]]</td></tr> | |||
<tr><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">bpoA2, BROMOPEROXIDASE A2, M, M1 Matrix ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=1894 ATCC 10762])</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=4d9j FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4d9j OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4d9j RCSB], [http://www.ebi.ac.uk/pdbsum/4d9j PDBsum]</span></td></tr> | |||
<table> | |||
<div style="background-color:#fffaf0;"> | |||
== Publication Abstract from PubMed == | |||
Designing protein molecules that will assemble into various kinds of ordered materials represents an important challenge in nanotechnology. We report the crystal structure of a 12-subunit protein cage that self-assembles by design to form a tetrahedral structure roughly 16 nanometers in diameter. The strategy of fusing together oligomeric protein domains can be generalized to produce other kinds of cages or extended materials. | |||
Structure of a 16-nm cage designed by using protein oligomers.,Lai YT, Cascio D, Yeates TO Science. 2012 Jun 1;336(6085):1129. PMID:22654051<ref>PMID:22654051</ref> | |||
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |||
</div> | |||
== References == | |||
<references/> | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Atcc 10762]] | |||
== | |||
< | |||
[[Category: | |||
[[Category: Cascio, D.]] | [[Category: Cascio, D.]] | ||
[[Category: Lai, Y T.]] | [[Category: Lai, Y T.]] | ||
Revision as of 10:21, 5 June 2014
Structure of a 16 nm protein cage designed by fusing symmetric oligomeric domainsStructure of a 16 nm protein cage designed by fusing symmetric oligomeric domains
Structural highlights
Publication Abstract from PubMedDesigning protein molecules that will assemble into various kinds of ordered materials represents an important challenge in nanotechnology. We report the crystal structure of a 12-subunit protein cage that self-assembles by design to form a tetrahedral structure roughly 16 nanometers in diameter. The strategy of fusing together oligomeric protein domains can be generalized to produce other kinds of cages or extended materials. Structure of a 16-nm cage designed by using protein oligomers.,Lai YT, Cascio D, Yeates TO Science. 2012 Jun 1;336(6085):1129. PMID:22654051[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
|
| ||||||||||||||||||