1kd2
From Proteopedia
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| - | [[Image:1kd2.jpg|left|200px]] | + | [[Image:1kd2.jpg|left|200px]] |
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| - | '''Crystal Structure of Human Deoxyhemoglobin in Absence of Any Anions''' | + | {{Structure |
| + | |PDB= 1kd2 |SIZE=350|CAPTION= <scene name='initialview01'>1kd2</scene>, resolution 1.87Å | ||
| + | |SITE= | ||
| + | |LIGAND= <scene name='pdbligand=HEM:PROTOPORPHYRIN IX CONTAINING FE'>HEM</scene> | ||
| + | |ACTIVITY= | ||
| + | |GENE= | ||
| + | }} | ||
| + | |||
| + | '''Crystal Structure of Human Deoxyhemoglobin in Absence of Any Anions''' | ||
| + | |||
==Disease== | ==Disease== | ||
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==About this Structure== | ==About this Structure== | ||
| - | 1KD2 is a [ | + | 1KD2 is a [[Protein complex]] 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=1KD2 OCA]. |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Protein complex]] | [[Category: Protein complex]] | ||
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[[Category: Seixas, F A.V.]] | [[Category: Seixas, F A.V.]] | ||
[[Category: HEM]] | [[Category: HEM]] | ||
| - | [[Category: allosteric anion binding | + | [[Category: allosteric anion binding site]] |
| - | [[Category: chloride binding | + | [[Category: chloride binding site]] |
[[Category: high o2 affinity t state]] | [[Category: high o2 affinity t state]] | ||
[[Category: human deoxy hemoglobin]] | [[Category: human deoxy hemoglobin]] | ||
[[Category: hydration]] | [[Category: hydration]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 12:15:43 2008'' |
Revision as of 10:15, 20 March 2008
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| , resolution 1.87Å | |||||||
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| 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.
Page seeded by OCA on Thu Mar 20 12:15:43 2008
