1fdh | pdb_00001fdh

STRUCTURE OF HUMAN FOETAL DEOXYHAEMOGLOBIN

File:1fdh.gif

spinqualitylabelsall models 1fdh, resolution 2.5Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D

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

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