1fdh: Difference between revisions
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[[Image:1fdh.gif|left|200px]] | [[Image:1fdh.gif|left|200px]] | ||
'''STRUCTURE OF HUMAN FOETAL DEOXYHAEMOGLOBIN''' | {{Structure | ||
|PDB= 1fdh |SIZE=350|CAPTION= <scene name='initialview01'>1fdh</scene>, resolution 2.5Å | |||
|SITE= | |||
|LIGAND= <scene name='pdbligand=ACE:ACETYL+GROUP'>ACE</scene> and <scene name='pdbligand=HEM:PROTOPORPHYRIN IX CONTAINING FE'>HEM</scene> | |||
|ACTIVITY= | |||
|GENE= | |||
}} | |||
'''STRUCTURE OF HUMAN FOETAL DEOXYHAEMOGLOBIN''' | |||
==Disease== | ==Disease== | ||
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==About this Structure== | ==About this Structure== | ||
1FDH is a [ | 1FDH 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=1FDH OCA]. | ||
==Reference== | ==Reference== | ||
Structure of human foetal deoxyhaemoglobin., Frier JA, Perutz MF, J Mol Biol. 1977 May 5;112(1):97-112. PMID:[http:// | Structure of human foetal deoxyhaemoglobin., Frier JA, Perutz MF, J Mol Biol. 1977 May 5;112(1):97-112. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/881729 881729] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Protein complex]] | [[Category: Protein complex]] | ||
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[[Category: oxygen transport]] | [[Category: oxygen transport]] | ||
''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 11:07:40 2008'' | ||
Revision as of 09:07, 20 March 2008
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| 1fdh, resolution 2.5Å | |||||||||||||
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| Ligands: | ACE and HEM | ||||||||||||
| 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
Page seeded by OCA on Thu Mar 20 11:07:40 2008
