1yg5: Difference between revisions
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==Disease== | ==Disease== | ||
Known disease associated with this structure: Erythremias, beta- OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141900 141900]], | Known disease associated with this structure: Erythremias, beta- OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141900 141900]], Heinz body anemias, beta- OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141900 141900]], Hereditary persistence of fetal hemoglobin OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141900 141900]], Methemoglobinemias, beta- OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141900 141900]], Sickle cell anemia OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141900 141900]], Thalassemia-beta, dominant inclusion-body OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141900 141900]], Thalassemias, beta- OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141900 141900]] | ||
==About this Structure== | ==About this Structure== | ||
1YG5 is a | 1YG5 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=1YG5 OCA]. | ||
==Reference== | ==Reference== | ||
<ref group="xtra">PMID:15835899</ref><references group="xtra"/> | |||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Arnone, A.]] | [[Category: Arnone, A.]] | ||
[[Category: Kavanaugh, J S.]] | [[Category: Kavanaugh, J S.]] | ||
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[[Category: Hemoglobin mutant]] | [[Category: Hemoglobin mutant]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 21:43:48 2009'' |