2e19

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caption="2e19" />
caption="2e19" />
'''Solution structure of the homeobox domain from human NIL-2-A zinc finger protein, transcription factor 8'''<br />
'''Solution structure of the homeobox domain from human NIL-2-A zinc finger protein, transcription factor 8'''<br />
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==Disease==
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Known disease associated with this structure: Corneal dystrophy, posterior polymorphous, 3 OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=189909 189909]]
==About this Structure==
==About this Structure==
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[[Category: Koshiba, S.]]
[[Category: Koshiba, S.]]
[[Category: Ohnishi, S.]]
[[Category: Ohnishi, S.]]
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[[Category: RSGI, RIKEN.Structural.Genomics/Proteomics.Initiative.]]
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[[Category: RSGI, RIKEN Structural Genomics/Proteomics Initiative.]]
[[Category: Tochio, N.]]
[[Category: Tochio, N.]]
[[Category: Watanabe, S.]]
[[Category: Watanabe, S.]]
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[[Category: transcription factor]]
[[Category: transcription factor]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 23 15:34:09 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 17:04:53 2008''

Revision as of 15:05, 21 February 2008


2e19

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Solution structure of the homeobox domain from human NIL-2-A zinc finger protein, transcription factor 8

Disease

Known disease associated with this structure: Corneal dystrophy, posterior polymorphous, 3 OMIM:[189909]

About this Structure

2E19 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Page seeded by OCA on Thu Feb 21 17:04:53 2008

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