1gzx: Difference between revisions
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[[Image:1gzx.gif|left|200px]]<br /> | [[Image:1gzx.gif|left|200px]]<br /><applet load="1gzx" size="450" color="white" frame="true" align="right" spinBox="true" | ||
<applet load="1gzx" size="450" color="white" frame="true" align="right" spinBox="true" | |||
caption="1gzx, resolution 2.1Å" /> | caption="1gzx, resolution 2.1Å" /> | ||
'''OXY T STATE HAEMOGLOBIN: OXYGEN BOUND AT ALL FOUR HAEMS'''<br /> | '''OXY T STATE HAEMOGLOBIN: OXYGEN BOUND AT ALL FOUR HAEMS'''<br /> | ||
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==About this Structure== | ==About this Structure== | ||
1GZX is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with HEM and OXY as [http://en.wikipedia.org/wiki/ligands ligands]. | 1GZX is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with HEM and OXY as [http://en.wikipedia.org/wiki/ligands ligands]. Known structural/functional Site: <scene name='pdbsite=HB1:O2 Binding Site For Chain D'>HB1</scene>. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1GZX OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: transport]] | [[Category: transport]] | ||
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on | ''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Dec 18 15:49:11 2007'' |
Revision as of 16:39, 18 December 2007
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OXY T STATE HAEMOGLOBIN: OXYGEN BOUND AT ALL FOUR HAEMS
OverviewOverview
The cooperative binding of oxygen by haemoglobin results from restraints, on ligand binding in the T state. The unfavourable interactions made by, the ligands at the haems destabilise the T state and favour the high, affinity R state. The T <==> R equilibrium leads, in the presence of a, ligand, to a rapid increase in the R state population and therefore, generates cooperative binding. There is now considerable understanding of, this phenomenon, but the interactions that reduce ligand affinity in the T, state have not yet been fully explored, owing to the difficulties in, preparing T state haemoglobin crystals in which all the subunits are, oxygenated. A protocol has been developed to oxygenate deoxy T state adult, human haemoglobin (HbA) crystals in air at 4 C at all four haems without, significant loss of crystalline order. The X-ray crystal structure, determined to 2.1 A spacing, shows significant changes in the alpha and, beta haem pockets as well as changes at the alpha(1)beta(2) interface in, the direction of the R quaternary structure. Most of the shifts and, deviations from deoxy T state HbA are similar to, but larger than, those, previously observed in the T state met and other partially liganded T, state forms. They provide clear evidence of haem-haem interaction in the T, state.
DiseaseDisease
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 StructureAbout this Structure
1GZX is a Protein complex structure of sequences from Homo sapiens with HEM and OXY as ligands. Known structural/functional Site: . Full crystallographic information is available from OCA.
ReferenceReference
Crystal structure of T state haemoglobin with oxygen bound at all four haems., Paoli M, Liddington R, Tame J, Wilkinson A, Dodson G, J Mol Biol. 1996 Mar 8;256(4):775-92. PMID:8642597
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