1y09: Difference between revisions

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==About this Structure==
==About this Structure==
1Y09 is a [[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=1Y09 OCA].  
1Y09 is a 4 chains 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=1Y09 OCA].  


==Reference==
==Reference==
Crystallographic evidence for a new ensemble of ligand-induced allosteric transitions in hemoglobin: the T-to-T(high) quaternary transitions., Kavanaugh JS, Rogers PH, Arnone A, Biochemistry. 2005 Apr 26;44(16):6101-21. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15835899 15835899]
<ref group="xtra">PMID:15835899</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Protein complex]]
[[Category: Arnone, A.]]
[[Category: Arnone, A.]]
[[Category: Kavanaugh, J S.]]
[[Category: Kavanaugh, J S.]]
Line 35: Line 34:
[[Category: Hemoglobin mutant]]
[[Category: Hemoglobin mutant]]


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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 13:25:53 2009''

Revision as of 11:25, 16 February 2009

File:1y09.png

Template:STRUCTURE 1y09

T-to-T(High) Quaternary Transitions in Human Hemoglobin: alphaN97A deoxy low-salt

Template:ABSTRACT PUBMED 15835899

Disease

Known disease associated with this structure: Erythremias, alpha- OMIM:[141800], Heinz body anemias, alpha- OMIM:[141800], Methemoglobinemias, alpha- OMIM:[141800], Thalassemias, alpha- OMIM:[141800]

About this Structure

1Y09 is a 4 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  1. Kavanaugh JS, Rogers PH, Arnone A. Crystallographic evidence for a new ensemble of ligand-induced allosteric transitions in hemoglobin: the T-to-T(high) quaternary transitions. Biochemistry. 2005 Apr 26;44(16):6101-21. PMID:15835899 doi:https://dx.doi.org/10.1021/bi047813a

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