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New page: left|200px<br /><applet load="1byu" size="450" color="white" frame="true" align="right" spinBox="true" caption="1byu, resolution 2.15Å" /> '''CANINE GDP-RAN'''<br...
 
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[[Image:1byu.gif|left|200px]]<br /><applet load="1byu" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1byu.gif|left|200px]]<br /><applet load="1byu" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1byu, resolution 2.15&Aring;" />
caption="1byu, resolution 2.15&Aring;" />
'''CANINE GDP-RAN'''<br />
'''CANINE GDP-RAN'''<br />


==Overview==
==Overview==
We report the 2.3 A resolution X-ray crystal structure of the GDP-bound, form of the RanQ69L mutant that is used extensively in studies of, nucleocytoplasmic transport and cell-cycle progression. When the structure, of GDP-RanQ69L from monoclinic crystals with P21 symmetry was compared, with the structure of wild-type Ran obtained from monoclinic crystals, the, Q69L mutant showed a large conformational change in residues 68-74, which, are in the switch II region of the molecule which changes conformation in, response to nucleotide state and which forms the major interaction, interface with nuclear transport factor 2 (NTF2, sometimes called p10)., This conformational change alters the positions of key residues such as, Lys71, Phe72 and Arg76 that are crucial for the interaction of GDP-Ran, with NTF2 and indeed, solution binding studies were unable to detect any, interaction between NTF2 and GDP-RanQ69L under conditions where GDP-Ran, bound effectively. This interaction between NTF2 and GDP-Ran is required, for efficient nuclear protein import and may function between the docking, and translocation steps of the pathway.
We report the 2.3 A resolution X-ray crystal structure of the GDP-bound form of the RanQ69L mutant that is used extensively in studies of nucleocytoplasmic transport and cell-cycle progression. When the structure of GDP-RanQ69L from monoclinic crystals with P21 symmetry was compared with the structure of wild-type Ran obtained from monoclinic crystals, the Q69L mutant showed a large conformational change in residues 68-74, which are in the switch II region of the molecule which changes conformation in response to nucleotide state and which forms the major interaction interface with nuclear transport factor 2 (NTF2, sometimes called p10). This conformational change alters the positions of key residues such as Lys71, Phe72 and Arg76 that are crucial for the interaction of GDP-Ran with NTF2 and indeed, solution binding studies were unable to detect any interaction between NTF2 and GDP-RanQ69L under conditions where GDP-Ran bound effectively. This interaction between NTF2 and GDP-Ran is required for efficient nuclear protein import and may function between the docking and translocation steps of the pathway.


==About this Structure==
==About this Structure==
1BYU is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Canis_lupus_familiaris Canis lupus familiaris] with MG and GDP as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1BYU OCA].  
1BYU is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Canis_lupus_familiaris Canis lupus familiaris] with <scene name='pdbligand=MG:'>MG</scene> and <scene name='pdbligand=GDP:'>GDP</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1BYU OCA].  


==Reference==
==Reference==
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[[Category: Canis lupus familiaris]]
[[Category: Canis lupus familiaris]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Kent, H.M.]]
[[Category: Kent, H M.]]
[[Category: Mccoy, A.J.]]
[[Category: Mccoy, A J.]]
[[Category: Stewart, M.]]
[[Category: Stewart, M.]]
[[Category: GDP]]
[[Category: GDP]]
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[[Category: nuclear transport]]
[[Category: nuclear transport]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 12:02:03 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:00:37 2008''