2rb8

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[[Image:2rb8.jpg|left|200px]]
[[Image:2rb8.jpg|left|200px]]
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{{Structure
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|PDB= 2rb8 |SIZE=350|CAPTION= <scene name='initialview01'>2rb8</scene>, resolution 1.45&Aring;
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The line below this paragraph, containing "STRUCTURE_2rb8", creates the "Structure Box" on the page.
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|GENE= TNC, HXB ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
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{{STRUCTURE_2rb8| PDB=2rb8 | SCENE= }}
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2rb8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2rb8 OCA], [http://www.ebi.ac.uk/pdbsum/2rb8 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2rb8 RCSB]</span>
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'''High resolution design of a protein loop'''
'''High resolution design of a protein loop'''
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[[Category: Kuhlman, B.]]
[[Category: Kuhlman, B.]]
[[Category: Wang, H.]]
[[Category: Wang, H.]]
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[[Category: alternative splicing]]
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[[Category: Alternative splicing]]
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[[Category: beta sheet,loop design]]
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[[Category: Beta sheet,loop design]]
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[[Category: cell adhesion]]
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[[Category: coiled coil]]
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[[Category: Coiled coil]]
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[[Category: extracellular matrix]]
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[[Category: Extracellular matrix]]
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[[Category: Glycoprotein]]
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[[Category: Phosphorylation]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 16:35:18 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 04:58:31 2008''
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Revision as of 13:35, 4 May 2008

Template:STRUCTURE 2rb8

High resolution design of a protein loop


Overview

Despite having irregular structure, protein loops often adopt specific conformations that are critical to protein function. Most studies in de novo protein design have focused on creating proteins with regular elements of secondary structure connected by very short loops or turns. To design longer protein loops that adopt specific conformations, we have developed a protocol within the Rosetta molecular modeling program that iterates between optimizing the sequence and conformation of a loop in search of low-energy sequence-structure pairs. We have tested the procedure by designing 10-residue loops for the connection between the second and third strand in the beta-sandwich protein tenascin. Three low-energy designs from 7,200 flexible backbone trajectories were selected for experimental characterization. All three designs, called LoopA, LoopB, and LoopC, adopt stable folded structures. High-resolution crystal structures of LoopA and LoopB have been solved. LoopB adopts a structure very similar to the design model (0.46 A rmsd), and all but one of the side chains are modeled in the correct rotamers. LoopA crystallized at low pH in a structure that differs dramatically from our design model. It forms a strand-swapped dimer mediated by hydrogen bonds to protonated glutamic acids. Gel filtration indicates that the protein is not a dimer at neutral pH. These results suggest that the high-resolution design of protein loops is possible; however, they also highlight how small changes in protein energetics can dramatically perturb the low free energy structure of a protein.

About this Structure

2RB8 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

High-resolution design of a protein loop., Hu X, Wang H, Ke H, Kuhlman B, Proc Natl Acad Sci U S A. 2007 Nov 6;104(45):17668-73. Epub 2007 Oct 30. PMID:17971437 Page seeded by OCA on Sun May 4 16:35:18 2008

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