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1jdp

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(New page: 200px<br /> <applet load="1jdp" size="450" color="white" frame="true" align="right" spinBox="true" caption="1jdp, resolution 2.0&Aring;" /> '''Crystal Structure of...)
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[[Image:1jdp.gif|left|200px]]<br />
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[[Image:1jdp.gif|left|200px]]<br /><applet load="1jdp" size="350" color="white" frame="true" align="right" spinBox="true"
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<applet load="1jdp" size="450" color="white" frame="true" align="right" spinBox="true"
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caption="1jdp, resolution 2.0&Aring;" />
caption="1jdp, resolution 2.0&Aring;" />
'''Crystal Structure of Hormone/Receptor Complex'''<br />
'''Crystal Structure of Hormone/Receptor Complex'''<br />
==Overview==
==Overview==
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Natriuretic peptides (NPs) are vasoactive cyclic-peptide hormones, important in blood pressure regulation through interaction with, natriuretic cell-surface receptors. We report the hormone-binding, thermodynamics and crystal structures at 2.9 and 2.0 angstroms, respectively, of the extracellular domain of the unliganded human NP, receptor (NPR-C) and its complex with CNP, a 22-amino acid NP. A single, CNP molecule is bound in the interface of an NPR-C dimer, resulting in, asymmetric interactions between the hormone and the symmetrically related, receptors. Hormone binding induces a 20 angstrom closure between the, membrane-proximal domains of the dimer. In each monomer, the opening of an, interdomain cleft, which is tethered together by a linker peptide acting, as a molecular spring, is likely a conserved allosteric trigger for, intracellular signaling by the natriuretic receptor family.
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Natriuretic peptides (NPs) are vasoactive cyclic-peptide hormones important in blood pressure regulation through interaction with natriuretic cell-surface receptors. We report the hormone-binding thermodynamics and crystal structures at 2.9 and 2.0 angstroms, respectively, of the extracellular domain of the unliganded human NP receptor (NPR-C) and its complex with CNP, a 22-amino acid NP. A single CNP molecule is bound in the interface of an NPR-C dimer, resulting in asymmetric interactions between the hormone and the symmetrically related receptors. Hormone binding induces a 20 angstrom closure between the membrane-proximal domains of the dimer. In each monomer, the opening of an interdomain cleft, which is tethered together by a linker peptide acting as a molecular spring, is likely a conserved allosteric trigger for intracellular signaling by the natriuretic receptor family.
==Disease==
==Disease==
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==About this Structure==
==About this Structure==
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1JDP is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with NDG, NAG and CL as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1JDP OCA].
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1JDP is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=NDG:'>NDG</scene>, <scene name='pdbligand=NAG:'>NAG</scene> and <scene name='pdbligand=CL:'>CL</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1JDP OCA].
==Reference==
==Reference==
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: Chow, D.C.]]
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[[Category: Chow, D C.]]
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[[Category: Garcia, K.C.]]
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[[Category: Garcia, K C.]]
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[[Category: He, X.L.]]
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[[Category: He, X L.]]
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[[Category: Martick, M.M.]]
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[[Category: Martick, M M.]]
[[Category: CL]]
[[Category: CL]]
[[Category: NAG]]
[[Category: NAG]]
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[[Category: natriuretic peptide receptor]]
[[Category: natriuretic peptide receptor]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 17:39:50 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:21:27 2008''

Revision as of 11:21, 21 February 2008


1jdp, resolution 2.0Å

Drag the structure with the mouse to rotate

Crystal Structure of Hormone/Receptor Complex

Contents

Overview

Natriuretic peptides (NPs) are vasoactive cyclic-peptide hormones important in blood pressure regulation through interaction with natriuretic cell-surface receptors. We report the hormone-binding thermodynamics and crystal structures at 2.9 and 2.0 angstroms, respectively, of the extracellular domain of the unliganded human NP receptor (NPR-C) and its complex with CNP, a 22-amino acid NP. A single CNP molecule is bound in the interface of an NPR-C dimer, resulting in asymmetric interactions between the hormone and the symmetrically related receptors. Hormone binding induces a 20 angstrom closure between the membrane-proximal domains of the dimer. In each monomer, the opening of an interdomain cleft, which is tethered together by a linker peptide acting as a molecular spring, is likely a conserved allosteric trigger for intracellular signaling by the natriuretic receptor family.

Disease

Known diseases associated with this structure: Hypertension, salt-resistant (1) OMIM:[108962]

About this Structure

1JDP is a Protein complex structure of sequences from Homo sapiens with , and as ligands. Full crystallographic information is available from OCA.

Reference

Allosteric activation of a spring-loaded natriuretic peptide receptor dimer by hormone., He Xl, Chow Dc, Martick MM, Garcia KC, Science. 2001 Aug 31;293(5535):1657-62. PMID:11533490

Page seeded by OCA on Thu Feb 21 13:21:27 2008

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