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[[Image:1e7n.jpg|left|200px]]


{{Structure
==The N-terminal domain of beta-B2-crystallin resembles the putative ancestral homodimer==
|PDB= 1e7n |SIZE=350|CAPTION= <scene name='initialview01'>1e7n</scene>, resolution 2.35&Aring;
<StructureSection load='1e7n' size='340' side='right'caption='[[1e7n]], [[Resolution|resolution]] 2.35&Aring;' scene=''>
|SITE=  
== Structural highlights ==
|LIGAND=  
<table><tr><td colspan='2'>[[1e7n]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1E7N OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1E7N FirstGlance]. <br>
|ACTIVITY=  
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.35&#8491;</td></tr>
|GENE=  
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1e7n FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1e7n OCA], [https://pdbe.org/1e7n PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1e7n RCSB], [https://www.ebi.ac.uk/pdbsum/1e7n PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1e7n ProSAT]</span></td></tr>
|DOMAIN=
</table>
|RELATEDENTRY=
== Function ==
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1e7n FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1e7n OCA], [http://www.ebi.ac.uk/pdbsum/1e7n PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1e7n RCSB]</span>
[https://www.uniprot.org/uniprot/CRBB2_MOUSE CRBB2_MOUSE] Crystallins are the dominant structural components of the vertebrate eye lens.
}}
== Evolutionary Conservation ==
[[Image:Consurf_key_small.gif|200px|right]]
Check<jmol>
  <jmolCheckbox>
    <scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/e7/1e7n_consurf.spt"</scriptWhenChecked>
    <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
    <text>to colour the structure by Evolutionary Conservation</text>
  </jmolCheckbox>
</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=1e7n ConSurf].
<div style="clear:both"></div>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
betagamma-crystallins from the eye lens are proteins consisting of two similar domains joined by a short linker. All three-dimensional structures of native proteins solved so far reveal similar pseudo-2-fold pairing of the domains reflecting their presumed ancient origin from a single-domain homodimer. However, studies of engineered single domains of members of the betagamma-crystallin superfamily have not revealed a prototype ancestral solution homodimer. Here we report the 2.35 A X-ray structure of the homodimer of the N-terminal domain of rat betaB2-crystallin (betaB2-N). The two identical domains pair in a symmetrical manner very similar to that observed in native betagamma-crystallins, where N and C-terminal domains (which share approximately 35% sequence identity) are related by a pseudo-2-fold axis. betaB2-N thus resembles the ancestral prototype of the betagamma-crystallin superfamily as it self-associates in solution to form a dimer with an essentially identical domain interface as that between the N and C domains in betagamma-crystallins, but without the benefit of a covalent linker. The structure provides further evidence for the role of two-domain pairing in stabilising the protomer fold. These results support the view that the betagamma-crystallin superfamily has evolved by a series of gene duplication and fusion events from a single-domain ancestor capable of forming homodimers.


'''THE N-TERMINAL DOMAIN OF BETA-B2-CRYSTALLIN RESEMBLES THE PUTATIVE ANCESTRAL HOMODIMER'''
The N-terminal domain of betaB2-crystallin resembles the putative ancestral homodimer.,Clout NJ, Basak A, Wieligmann K, Bateman OA, Jaenicke R, Slingsby C J Mol Biol. 2000 Dec 1;304(3):253-7. PMID:11090271<ref>PMID:11090271</ref>


From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 1e7n" style="background-color:#fffaf0;"></div>


==Overview==
==See Also==
betagamma-crystallins from the eye lens are proteins consisting of two similar domains joined by a short linker. All three-dimensional structures of native proteins solved so far reveal similar pseudo-2-fold pairing of the domains reflecting their presumed ancient origin from a single-domain homodimer. However, studies of engineered single domains of members of the betagamma-crystallin superfamily have not revealed a prototype ancestral solution homodimer. Here we report the 2.35 A X-ray structure of the homodimer of the N-terminal domain of rat betaB2-crystallin (betaB2-N). The two identical domains pair in a symmetrical manner very similar to that observed in native betagamma-crystallins, where N and C-terminal domains (which share approximately 35% sequence identity) are related by a pseudo-2-fold axis. betaB2-N thus resembles the ancestral prototype of the betagamma-crystallin superfamily as it self-associates in solution to form a dimer with an essentially identical domain interface as that between the N and C domains in betagamma-crystallins, but without the benefit of a covalent linker. The structure provides further evidence for the role of two-domain pairing in stabilising the protomer fold. These results support the view that the betagamma-crystallin superfamily has evolved by a series of gene duplication and fusion events from a single-domain ancestor capable of forming homodimers.
*[[Crystallin 3D structures|Crystallin 3D structures]]
 
== References ==
==About this Structure==
<references/>
1E7N is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1E7N OCA].
__TOC__
 
</StructureSection>
==Reference==
[[Category: Large Structures]]
The N-terminal domain of betaB2-crystallin resembles the putative ancestral homodimer., Clout NJ, Basak A, Wieligmann K, Bateman OA, Jaenicke R, Slingsby C, J Mol Biol. 2000 Dec 1;304(3):253-7. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/11090271 11090271]
[[Category: Mus musculus]]
[[Category: Mus musculus]]
[[Category: Single protein]]
[[Category: Basak A]]
[[Category: Basak, A.]]
[[Category: Bateman OA]]
[[Category: Bateman, O A.]]
[[Category: Clout NJ]]
[[Category: Clout, N J.]]
[[Category: Jaenicke R]]
[[Category: Jaenicke, R.]]
[[Category: Slingsby C]]
[[Category: Slingsby, C.]]
[[Category: Wieligmann K]]
[[Category: Wieligmann, K.]]
[[Category: 2-fold symmetry]]
[[Category: crystallin]]
[[Category: domain interaction]]
[[Category: eye lens]]
[[Category: protein structure]]
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 19:57:02 2008''

Latest revision as of 08:47, 9 May 2024

The N-terminal domain of beta-B2-crystallin resembles the putative ancestral homodimer

1e7n, resolution 2.35Å

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