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1a7f

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[[Image:1a7f.png|left|200px]]
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{{STRUCTURE_1a7f| PDB=1a7f | SCENE= }}
{{STRUCTURE_1a7f| PDB=1a7f | SCENE= }}
===INSULIN MUTANT B16 GLU, B24 GLY, DES-B30, NMR, 20 STRUCTURES===
===INSULIN MUTANT B16 GLU, B24 GLY, DES-B30, NMR, 20 STRUCTURES===
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{{ABSTRACT_PUBMED_9636695}}
{{ABSTRACT_PUBMED_9636695}}
==About this Structure==
==About this Structure==
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1A7F is a [[Protein complex]] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1A7F OCA].
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[[1a7f]] is a 2 chain structure of [[Molecular Playground/Insulin]] with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1A7F OCA].
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==See Also==
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*[[Molecular Playground/Insulin|Molecular Playground/Insulin]]
==Reference==
==Reference==
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A structural switch in a mutant insulin exposes key residues for receptor binding., Ludvigsen S, Olsen HB, Kaarsholm NC, J Mol Biol. 1998 May 29;279(1):1-7. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/9636695 9636695]
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<ref group="xtra">PMID:009636695</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Protein complex]]
 
[[Category: Kaarsholm, N C.]]
[[Category: Kaarsholm, N C.]]
[[Category: Ludvigsen, S.]]
[[Category: Ludvigsen, S.]]
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[[Category: Monomer]]
[[Category: Monomer]]
[[Category: Neutral ph]]
[[Category: Neutral ph]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jun 30 16:18:24 2008''
 

Revision as of 21:16, 25 July 2012

Template:STRUCTURE 1a7f

Contents

INSULIN MUTANT B16 GLU, B24 GLY, DES-B30, NMR, 20 STRUCTURES

Template:ABSTRACT PUBMED 9636695

About this Structure

1a7f is a 2 chain structure of Molecular Playground/Insulin with sequence from Homo sapiens. Full experimental information is available from OCA.

See Also

Reference

  • Ludvigsen S, Olsen HB, Kaarsholm NC. A structural switch in a mutant insulin exposes key residues for receptor binding. J Mol Biol. 1998 May 29;279(1):1-7. PMID:9636695 doi:S0022-2836(98)91801-0

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