1m4u

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(New page: 200px<br /> <applet load="1m4u" size="450" color="white" frame="true" align="right" spinBox="true" caption="1m4u, resolution 2.42&Aring;" /> '''Crystal structure o...)
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<applet load="1m4u" size="450" color="white" frame="true" align="right" spinBox="true"
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caption="1m4u, resolution 2.42&Aring;" />
caption="1m4u, resolution 2.42&Aring;" />
'''Crystal structure of Bone Morphogenetic Protein-7 (BMP-7) in complex with the secreted antagonist Noggin'''<br />
'''Crystal structure of Bone Morphogenetic Protein-7 (BMP-7) in complex with the secreted antagonist Noggin'''<br />
==Overview==
==Overview==
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The interplay between bone morphogenetic proteins (BMPs) and their, antagonists governs developmental and cellular processes as diverse as, establishment of the embryonic dorsal-ventral axis, induction of neural, tissue, formation of joints in the skeletal system and neurogenesis in the, adult brain. So far, the three-dimensional structures of BMP antagonists, and the structural basis for inactivation have remained unknown. Here we, report the crystal structure of the antagonist Noggin bound to BMP-7, which shows that Noggin inhibits BMP signalling by blocking the molecular, interfaces of the binding epitopes for both type I and type II receptors., The BMP-7-binding affinity of site-specific variants of Noggin is, correlated with alterations in bone formation and apoptosis in chick limb, development, showing that Noggin functions by sequestering its ligand in, an inactive complex. The scaffold of Noggin contains a cystine (the, oxidized form of cysteine) knot topology similar to that of BMPs; thus, ligand and antagonist seem to have evolved from a common ancestral gene.
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The interplay between bone morphogenetic proteins (BMPs) and their antagonists governs developmental and cellular processes as diverse as establishment of the embryonic dorsal-ventral axis, induction of neural tissue, formation of joints in the skeletal system and neurogenesis in the adult brain. So far, the three-dimensional structures of BMP antagonists and the structural basis for inactivation have remained unknown. Here we report the crystal structure of the antagonist Noggin bound to BMP-7, which shows that Noggin inhibits BMP signalling by blocking the molecular interfaces of the binding epitopes for both type I and type II receptors. The BMP-7-binding affinity of site-specific variants of Noggin is correlated with alterations in bone formation and apoptosis in chick limb development, showing that Noggin functions by sequestering its ligand in an inactive complex. The scaffold of Noggin contains a cystine (the oxidized form of cysteine) knot topology similar to that of BMPs; thus, ligand and antagonist seem to have evolved from a common ancestral gene.
==Disease==
==Disease==
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==About this Structure==
==About this Structure==
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1M4U is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1M4U OCA].
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1M4U is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1M4U OCA].
==Reference==
==Reference==
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[[Category: Affolter, M.]]
[[Category: Affolter, M.]]
[[Category: Choe, S.]]
[[Category: Choe, S.]]
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[[Category: Economides, A.N.]]
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[[Category: Economides, A N.]]
[[Category: Greenwald, J.]]
[[Category: Greenwald, J.]]
[[Category: Groppe, J.]]
[[Category: Groppe, J.]]
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[[Category: Izpisua-Belmonte, J.C.]]
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[[Category: Izpisua-Belmonte, J C.]]
[[Category: Kwiatkowski, W.]]
[[Category: Kwiatkowski, W.]]
[[Category: Rodriguez-Leon, J.]]
[[Category: Rodriguez-Leon, J.]]
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[[Category: Vale, W.W.]]
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[[Category: Vale, W W.]]
[[Category: Wiater, E.]]
[[Category: Wiater, E.]]
[[Category: bmp antagonist]]
[[Category: bmp antagonist]]
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[[Category: noggin]]
[[Category: noggin]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 18:07:27 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:51:30 2008''

Revision as of 11:51, 21 February 2008


1m4u, resolution 2.42Å

Drag the structure with the mouse to rotate

Crystal structure of Bone Morphogenetic Protein-7 (BMP-7) in complex with the secreted antagonist Noggin

Contents

Overview

The interplay between bone morphogenetic proteins (BMPs) and their antagonists governs developmental and cellular processes as diverse as establishment of the embryonic dorsal-ventral axis, induction of neural tissue, formation of joints in the skeletal system and neurogenesis in the adult brain. So far, the three-dimensional structures of BMP antagonists and the structural basis for inactivation have remained unknown. Here we report the crystal structure of the antagonist Noggin bound to BMP-7, which shows that Noggin inhibits BMP signalling by blocking the molecular interfaces of the binding epitopes for both type I and type II receptors. The BMP-7-binding affinity of site-specific variants of Noggin is correlated with alterations in bone formation and apoptosis in chick limb development, showing that Noggin functions by sequestering its ligand in an inactive complex. The scaffold of Noggin contains a cystine (the oxidized form of cysteine) knot topology similar to that of BMPs; thus, ligand and antagonist seem to have evolved from a common ancestral gene.

Disease

Known diseases associated with this structure: Stapes ankylosis syndrome without symphalangism OMIM:[602991], Symphalangism, proximal OMIM:[602991], Synostoses syndrome, multiple, 1 OMIM:[602991], Tarsal-carpal coalition syndrome OMIM:[602991]

About this Structure

1M4U is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Structural basis of BMP signalling inhibition by the cystine knot protein Noggin., Groppe J, Greenwald J, Wiater E, Rodriguez-Leon J, Economides AN, Kwiatkowski W, Affolter M, Vale WW, Belmonte JC, Choe S, Nature. 2002 Dec 12;420(6916):636-42. PMID:12478285

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