1fdh

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Image:1fdh.gif


PDB ID 1fdh

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, resolution 2.5Å
Ligands: and
Coordinates: save as pdb, mmCIF, xml



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. 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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