1cb6: Difference between revisions

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New page: left|200px<br /> <applet load="1cb6" size="450" color="white" frame="true" align="right" spinBox="true" caption="1cb6, resolution 2.0Å" /> '''STRUCTURE OF HUMAN A...
 
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[[Image:1cb6.gif|left|200px]]<br />
[[Image:1cb6.gif|left|200px]]<br /><applet load="1cb6" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1cb6" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1cb6, resolution 2.0&Aring;" />
caption="1cb6, resolution 2.0&Aring;" />
'''STRUCTURE OF HUMAN APOLACTOFERRIN AT 2.0 A RESOLUTION.'''<br />
'''STRUCTURE OF HUMAN APOLACTOFERRIN AT 2.0 A RESOLUTION.'''<br />


==Overview==
==Overview==
The three-dimensional structure of a form of human apolactoferrin, in, which one lobe (the N-lobe) has an open conformation and the other lobe, (the C-lobe) is closed, has been refined at 2.0 A resolution. The, refinement, by restrained least-squares methods, used synchrotron, radiation X-ray diffraction data combined with a lower resolution, diffractometer data set. The final refined model (5346 protein atoms from, residues 1-691, two Cl- ions and 363 water molecules) gives a, crystallographic R factor of 0.201 (Rfree = 0. 286) for all 51305, reflections in the resolution range 10.0-2.0 A. The conformational change, in the N-lobe, which opens up the binding cleft, involves a 54 degrees, rotation of the N2 domain relative to the N1 domain. This also results in, a small reorientation of the two lobes relative to one another with a, further approximately 730 A2 of surface area being buried as the N2 domain, contacts the C-lobe and the inter-lobe helix. These new contacts also, involve the C-terminal helix and provide a mechanism through which the, conformational and iron-binding status of the N-lobe can be signalled to, the C-lobe. Surface-area calculations indicate a fine balance between open, and closed forms of lactoferrin, which both have essentially the same, solvent-accessible surface. Chloride ions are bound in the anion-binding, sites of both lobes, emphasizing the functional significance of these, sites. The closed configuration of the C-lobe, attributed in part to weak, stabilization by crystal packing interactions, has important implications, for lactoferrin dynamics. It shows that a stable closed structure, essentially identical to that of the iron-bound form, can be formed in the, absence of iron binding.
The three-dimensional structure of a form of human apolactoferrin, in which one lobe (the N-lobe) has an open conformation and the other lobe (the C-lobe) is closed, has been refined at 2.0 A resolution. The refinement, by restrained least-squares methods, used synchrotron radiation X-ray diffraction data combined with a lower resolution diffractometer data set. The final refined model (5346 protein atoms from residues 1-691, two Cl- ions and 363 water molecules) gives a crystallographic R factor of 0.201 (Rfree = 0. 286) for all 51305 reflections in the resolution range 10.0-2.0 A. The conformational change in the N-lobe, which opens up the binding cleft, involves a 54 degrees rotation of the N2 domain relative to the N1 domain. This also results in a small reorientation of the two lobes relative to one another with a further approximately 730 A2 of surface area being buried as the N2 domain contacts the C-lobe and the inter-lobe helix. These new contacts also involve the C-terminal helix and provide a mechanism through which the conformational and iron-binding status of the N-lobe can be signalled to the C-lobe. Surface-area calculations indicate a fine balance between open and closed forms of lactoferrin, which both have essentially the same solvent-accessible surface. Chloride ions are bound in the anion-binding sites of both lobes, emphasizing the functional significance of these sites. The closed configuration of the C-lobe, attributed in part to weak stabilization by crystal packing interactions, has important implications for lactoferrin dynamics. It shows that a stable closed structure, essentially identical to that of the iron-bound form, can be formed in the absence of iron binding.


==Disease==
==Disease==
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==About this Structure==
==About this Structure==
1CB6 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with CL as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1CB6 OCA].  
1CB6 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=CL:'>CL</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1CB6 OCA].  


==Reference==
==Reference==
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Anderson, B.F.]]
[[Category: Anderson, B F.]]
[[Category: Baker, E.N.]]
[[Category: Baker, E N.]]
[[Category: Jameson, G.B.]]
[[Category: Jameson, G B.]]
[[Category: Norris, G.E.]]
[[Category: Norris, G E.]]
[[Category: Thomas, D.H.]]
[[Category: Thomas, D H.]]
[[Category: CL]]
[[Category: CL]]
[[Category: apolactoferrin]]
[[Category: apolactoferrin]]
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[[Category: iron transport]]
[[Category: iron transport]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 16:19:50 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:04:18 2008''