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1miu

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(New page: 200px<br /> <applet load="1miu" size="450" color="white" frame="true" align="right" spinBox="true" caption="1miu, resolution 3.1&Aring;" /> '''Structure of a BRCA2...)
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[[Image:1miu.gif|left|200px]]<br /><applet load="1miu" size="350" color="white" frame="true" align="right" spinBox="true"
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<applet load="1miu" size="450" color="white" frame="true" align="right" spinBox="true"
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caption="1miu, resolution 3.1&Aring;" />
caption="1miu, resolution 3.1&Aring;" />
'''Structure of a BRCA2-DSS1 complex'''<br />
'''Structure of a BRCA2-DSS1 complex'''<br />
==Overview==
==Overview==
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Mutations in the BRCA2 (breast cancer susceptibility gene 2) tumor, suppressor lead to chromosomal instability due to defects in the repair of, double-strand DNA breaks (DSBs) by homologous recombination, but BRCA2's, role in this process has been unclear. Here, we present the 3.1 angstrom, crystal structure of a approximately 90-kilodalton BRCA2 domain bound to, DSS1, which reveals three oligonucleotide-binding (OB) folds and a, helix-turn-helix (HTH) motif. We also (i) demonstrate that this BRCA2, domain binds single-stranded DNA, (ii) present its 3.5 angstrom structure, bound to oligo(dT)9, (iii) provide data that implicate the HTH motif in, dsDNA binding, and (iv) show that BRCA2 stimulates RAD51-mediated, recombination in vitro. These findings establish that BRCA2 functions, directly in homologous recombination and provide a structural and, biochemical basis for understanding the loss of recombination-mediated DSB, repair in BRCA2-associated cancers.
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Mutations in the BRCA2 (breast cancer susceptibility gene 2) tumor suppressor lead to chromosomal instability due to defects in the repair of double-strand DNA breaks (DSBs) by homologous recombination, but BRCA2's role in this process has been unclear. Here, we present the 3.1 angstrom crystal structure of a approximately 90-kilodalton BRCA2 domain bound to DSS1, which reveals three oligonucleotide-binding (OB) folds and a helix-turn-helix (HTH) motif. We also (i) demonstrate that this BRCA2 domain binds single-stranded DNA, (ii) present its 3.5 angstrom structure bound to oligo(dT)9, (iii) provide data that implicate the HTH motif in dsDNA binding, and (iv) show that BRCA2 stimulates RAD51-mediated recombination in vitro. These findings establish that BRCA2 functions directly in homologous recombination and provide a structural and biochemical basis for understanding the loss of recombination-mediated DSB repair in BRCA2-associated cancers.
==Disease==
==Disease==
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==About this Structure==
==About this Structure==
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1MIU is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus] with HG as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1MIU OCA].
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1MIU is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus] with <scene name='pdbligand=HG:'>HG</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1MIU OCA].
==Reference==
==Reference==
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[[Category: Mus musculus]]
[[Category: Mus musculus]]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: Chen, P.L.]]
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[[Category: Chen, P L.]]
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[[Category: Jeffrey, P.D.]]
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[[Category: Jeffrey, P D.]]
[[Category: Kinnucan, E.]]
[[Category: Kinnucan, E.]]
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[[Category: Lee, W.H.]]
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[[Category: Lee, W H.]]
[[Category: Miller, J.]]
[[Category: Miller, J.]]
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[[Category: Pavletich, N.P.]]
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[[Category: Pavletich, N P.]]
[[Category: Sun, Y.]]
[[Category: Sun, Y.]]
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[[Category: Thoma, N.H.]]
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[[Category: Thoma, N H.]]
[[Category: Yang, H.]]
[[Category: Yang, H.]]
[[Category: Zheng, N.]]
[[Category: Zheng, N.]]
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[[Category: tumor suppressor]]
[[Category: tumor suppressor]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 18:11:54 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:55:36 2008''

Revision as of 11:55, 21 February 2008


1miu, resolution 3.1Å

Drag the structure with the mouse to rotate

Structure of a BRCA2-DSS1 complex

Contents

Overview

Mutations in the BRCA2 (breast cancer susceptibility gene 2) tumor suppressor lead to chromosomal instability due to defects in the repair of double-strand DNA breaks (DSBs) by homologous recombination, but BRCA2's role in this process has been unclear. Here, we present the 3.1 angstrom crystal structure of a approximately 90-kilodalton BRCA2 domain bound to DSS1, which reveals three oligonucleotide-binding (OB) folds and a helix-turn-helix (HTH) motif. We also (i) demonstrate that this BRCA2 domain binds single-stranded DNA, (ii) present its 3.5 angstrom structure bound to oligo(dT)9, (iii) provide data that implicate the HTH motif in dsDNA binding, and (iv) show that BRCA2 stimulates RAD51-mediated recombination in vitro. These findings establish that BRCA2 functions directly in homologous recombination and provide a structural and biochemical basis for understanding the loss of recombination-mediated DSB repair in BRCA2-associated cancers.

Disease

Known disease associated with this structure: Split hand/foot malformation, type 1 OMIM:[183600]

About this Structure

1MIU is a Protein complex structure of sequences from Homo sapiens and Mus musculus with as ligand. Full crystallographic information is available from OCA.

Reference

BRCA2 function in DNA binding and recombination from a BRCA2-DSS1-ssDNA structure., Yang H, Jeffrey PD, Miller J, Kinnucan E, Sun Y, Thoma NH, Zheng N, Chen PL, Lee WH, Pavletich NP, Science. 2002 Sep 13;297(5588):1837-48. PMID:12228710

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