1kd2

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Image:1kd2.jpg


PDB ID 1kd2

Drag the structure with the mouse to rotate
, resolution 1.87Å
Ligands:
Coordinates: save as pdb, mmCIF, xml



Crystal Structure of Human Deoxyhemoglobin in Absence of Any Anions


Disease

Known diseases associated with this structure: Erythremias, alpha- OMIM:[141800], Erythremias, beta- OMIM:[141900], Erythrocytosis OMIM:[141850], HPFH, deletion type OMIM:[141900], Heinz body anemia OMIM:[141850], Heinz body anemias, alpha- OMIM:[141800], Heinz body anemias, beta- OMIM:[141900], Hemoglobin H disease OMIM:[141850], Hypochromic microcytic anemia OMIM:[141850], Methemoglobinemias, alpha- OMIM:[141800], Methemoglobinemias, beta- OMIM:[141900], Sickle cell anemia OMIM:[141900], Thalassemia, alpha- OMIM:[141850], Thalassemia-beta, dominant inclusion-body OMIM:[141900], Thalassemias, alpha- OMIM:[141800], Thalassemias, beta- OMIM:[141900]

About this Structure

1KD2 is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

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