1utr: Difference between revisions

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New page: left|200px<br /><applet load="1utr" size="450" color="white" frame="true" align="right" spinBox="true" caption="1utr" /> '''UTEROGLOBIN-PCB COMPLEX (REDUCED FORM)'''<br...
 
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[[Image:1utr.jpg|left|200px]]<br /><applet load="1utr" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1utr.jpg|left|200px]]<br /><applet load="1utr" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1utr" />
caption="1utr" />
'''UTEROGLOBIN-PCB COMPLEX (REDUCED FORM)'''<br />
'''UTEROGLOBIN-PCB COMPLEX (REDUCED FORM)'''<br />


==Overview==
==Overview==
Metabolites of polychlorinated biphenyls (PCBs) bind with high affinity to, uteroglobin, a small homodimeric protein that also binds progesterone. We, present the solution structure of the reduced form of rat uteroglobin in, complex with a PCB methylsulphone, (MeSO2)2-TCB. The structure reveals the, molecular basis for the accumulation of (MeSO2)2-TCB by uteroglobin. The, structure also shows how ligand binding and release might be controlled by, reduction/oxidation of two intermolecular disulphide bonds. Breakage of, these bonds induces a local unfolding of the N- and C-termini and a, separation of helices creating a channel into the binding site. These, effects make the ligand binding cavity readily accessible to entry of the, ligand.
Metabolites of polychlorinated biphenyls (PCBs) bind with high affinity to uteroglobin, a small homodimeric protein that also binds progesterone. We present the solution structure of the reduced form of rat uteroglobin in complex with a PCB methylsulphone, (MeSO2)2-TCB. The structure reveals the molecular basis for the accumulation of (MeSO2)2-TCB by uteroglobin. The structure also shows how ligand binding and release might be controlled by reduction/oxidation of two intermolecular disulphide bonds. Breakage of these bonds induces a local unfolding of the N- and C-termini and a separation of helices creating a channel into the binding site. These effects make the ligand binding cavity readily accessible to entry of the ligand.


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


==Reference==
==Reference==
Line 13: Line 13:
[[Category: Rattus norvegicus]]
[[Category: Rattus norvegicus]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Barnes, H.J.]]
[[Category: Barnes, H J.]]
[[Category: Gustafsson, J.A.]]
[[Category: Gustafsson, J A.]]
[[Category: Hard, T.]]
[[Category: Hard, T.]]
[[Category: Larsson, C.]]
[[Category: Larsson, C.]]
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[[Category: uteroglobin]]
[[Category: uteroglobin]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 04:19:22 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:28:16 2008''