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3i3s

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[[Image:3i3s.png|left|200px]]
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{{STRUCTURE_3i3s| PDB=3i3s | SCENE= }}
{{STRUCTURE_3i3s| PDB=3i3s | SCENE= }}
===Crystal Structure of H-Ras with Thr50 replaced by Isoleucine===
===Crystal Structure of H-Ras with Thr50 replaced by Isoleucine===
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{{ABSTRACT_PUBMED_19966803}}
{{ABSTRACT_PUBMED_19966803}}
==About this Structure==
==About this Structure==
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[[3i3s]] is a 1 chain structure with sequence 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=3I3S OCA].
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[[3i3s]] is a 1 chain structure of [[GTPase HRas]] with sequence 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=3I3S OCA].
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==See Also==
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*[[GTPase HRas|GTPase HRas]]
==Reference==
==Reference==
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<ref group="xtra">PMID:19966803</ref><references group="xtra"/>
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<ref group="xtra">PMID:019966803</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Ahmadian, M R.]]
[[Category: Ahmadian, M R.]]
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[[Category: Merbitz-Zahradnik, T.]]
[[Category: Merbitz-Zahradnik, T.]]
[[Category: Wittinghofer, A.]]
[[Category: Wittinghofer, A.]]
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[[Category: Cell membrane]]
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[[Category: Disease mutation]]
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[[Category: Golgi apparatus]]
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[[Category: Gtp-binding]]
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[[Category: Gtpase]]
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[[Category: H-ra]]
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[[Category: Lipoprotein]]
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[[Category: Membrane]]
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[[Category: Methylation]]
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[[Category: Noonan syndrome]]
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[[Category: Nucleotide-binding]]
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[[Category: Palmitate]]
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[[Category: Prenylation]]
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[[Category: Proto-oncogene]]
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[[Category: S-nitrosylation]]
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[[Category: Signaling protein]]

Revision as of 11:19, 26 July 2012

Image:3i3s.png

Template:STRUCTURE 3i3s

Contents

Crystal Structure of H-Ras with Thr50 replaced by Isoleucine

Template:ABSTRACT PUBMED 19966803

About this Structure

3i3s is a 1 chain structure of GTPase HRas with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See Also

Reference

  • Cirstea IC, Kutsche K, Dvorsky R, Gremer L, Carta C, Horn D, Roberts AE, Lepri F, Merbitz-Zahradnik T, Konig R, Kratz CP, Pantaleoni F, Dentici ML, Joshi VA, Kucherlapati RS, Mazzanti L, Mundlos S, Patton MA, Silengo MC, Rossi C, Zampino G, Digilio C, Stuppia L, Seemanova E, Pennacchio LA, Gelb BD, Dallapiccola B, Wittinghofer A, Ahmadian MR, Tartaglia M, Zenker M. A restricted spectrum of NRAS mutations causes Noonan syndrome. Nat Genet. 2010 Jan;42(1):27-9. Epub 2009 Dec 6. PMID:19966803 doi:10.1038/ng.497

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