1z2b: Difference between revisions

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[[Image:1z2b.gif|left|200px]]<br /><applet load="1z2b" size="350" color="white" frame="true" align="right" spinBox="true"
[[Image:1z2b.gif|left|200px]]
caption="1z2b, resolution 4.10&Aring;" />
 
'''Tubulin-colchicine-vinblastine: stathmin-like domain complex'''<br />
{{Structure
|PDB= 1z2b |SIZE=350|CAPTION= <scene name='initialview01'>1z2b</scene>, resolution 4.10&Aring;
|SITE=
|LIGAND= <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=GTP:GUANOSINE-5'-TRIPHOSPHATE'>GTP</scene>, <scene name='pdbligand=GDP:GUANOSINE-5'-DIPHOSPHATE'>GDP</scene>, <scene name='pdbligand=CN2:2-MERCAPTO-N-[1,2,3,10-TETRAMETHOXY-9-OXO-5,6,7,9-TETRAHYDRO-BENZO[A]HEPTALEN-7-YL]ACETAMIDE'>CN2</scene> and <scene name='pdbligand=VLB:(2ALPHA,2'BETA,3BETA,4ALPHA,5BETA)-VINCALEUKOBLASTINE'>VLB</scene>
|ACTIVITY=
|GENE= Stmn4 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=10116 Rattus norvegicus])
}}
 
'''Tubulin-colchicine-vinblastine: stathmin-like domain complex'''
 


==Overview==
==Overview==
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==About this Structure==
==About this Structure==
1Z2B is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus] and [http://en.wikipedia.org/wiki/Rattus_norvegicus Rattus norvegicus] with <scene name='pdbligand=MG:'>MG</scene>, <scene name='pdbligand=GTP:'>GTP</scene>, <scene name='pdbligand=GDP:'>GDP</scene>, <scene name='pdbligand=CN2:'>CN2</scene> and <scene name='pdbligand=VLB:'>VLB</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1Z2B OCA].  
1Z2B is a [[Protein complex]] structure of sequences from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus] and [http://en.wikipedia.org/wiki/Rattus_norvegicus Rattus norvegicus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1Z2B OCA].  


==Reference==
==Reference==
Structural basis for the regulation of tubulin by vinblastine., Gigant B, Wang C, Ravelli RB, Roussi F, Steinmetz MO, Curmi PA, Sobel A, Knossow M, Nature. 2005 May 26;435(7041):519-22. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=15917812 15917812]
Structural basis for the regulation of tubulin by vinblastine., Gigant B, Wang C, Ravelli RB, Roussi F, Steinmetz MO, Curmi PA, Sobel A, Knossow M, Nature. 2005 May 26;435(7041):519-22. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15917812 15917812]
[[Category: Bos taurus]]
[[Category: Bos taurus]]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: vinblastine]]
[[Category: vinblastine]]


''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:11:25 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 15:30:24 2008''

Revision as of 13:30, 20 March 2008

File:1z2b.gif


Drag the structure with the mouse to rotate
1z2b, resolution 4.10Å
Ligands: MG, GTP, GDP, CN2 and VLB
Gene: Stmn4 (Rattus norvegicus)
Coordinates: save as pdb, mmCIF, xml



Tubulin-colchicine-vinblastine: stathmin-like domain complex


Overview

Vinblastine is one of several tubulin-targeting Vinca alkaloids that have been responsible for many chemotherapeutic successes since their introduction in the clinic as antitumour drugs. In contrast with the two other classes of small tubulin-binding molecules (Taxol and colchicine), the binding site of vinblastine is largely unknown and the molecular mechanism of this drug has remained elusive. Here we report the X-ray structure of vinblastine bound to tubulin in a complex with the RB3 protein stathmin-like domain (RB3-SLD). Vinblastine introduces a wedge at the interface of two tubulin molecules and thus interferes with tubulin assembly. Together with electron microscopical and biochemical data, the structure explains vinblastine-induced tubulin self-association into spiral aggregates at the expense of microtubule growth. It also shows that vinblastine and the amino-terminal part of RB3-SLD binding sites share a hydrophobic groove on the alpha-tubulin surface that is located at an intermolecular contact in microtubules. This is an attractive target for drugs designed to perturb microtubule dynamics by interfacial interference, for which tubulin seems ideally suited because of its propensity to self-associate.

About this Structure

1Z2B is a Protein complex structure of sequences from Bos taurus and Rattus norvegicus. Full crystallographic information is available from OCA.

Reference

Structural basis for the regulation of tubulin by vinblastine., Gigant B, Wang C, Ravelli RB, Roussi F, Steinmetz MO, Curmi PA, Sobel A, Knossow M, Nature. 2005 May 26;435(7041):519-22. PMID:15917812

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