1fdh
From Proteopedia
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STRUCTURE OF HUMAN FOETAL DEOXYHAEMOGLOBIN
Disease
Known diseases associated with this structure: Aplasia of lacrimal and salivary glands OMIM:[602115], Erythremias, alpha- OMIM:[141800], Erythrocytosis OMIM:[141850], Heinz body anemia OMIM:[141850], Heinz body anemias, alpha- OMIM:[141800], Hemoglobin H disease OMIM:[141850], Hypochromic microcytic anemia OMIM:[141850], LADD syndrome OMIM:[602115], Methemoglobinemias, alpha- OMIM:[141800], Thalassemia, alpha- OMIM:[141850], Thalassemias, alpha- OMIM:[141800]
About this Structure
1FDH is a Protein complex structure of sequences from Homo sapiens with ACE and HEM as ligands. Full crystallographic information is available from OCA.
Reference
Structure of human foetal deoxyhaemoglobin., Frier JA, Perutz MF, J Mol Biol. 1977 May 5;112(1):97-112. PMID:881729
Page seeded by OCA on Mon Nov 12 16:51:55 2007