1gzx

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==Overview==
==Overview==
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.
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.
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==Disease==
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Known diseases associated with this structure: Erythremias, alpha- OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141800 141800]], Erythremias, beta- OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141900 141900]], Erythrocytosis OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141850 141850]], HPFH, deletion type OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141900 141900]], Heinz body anemia OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141850 141850]], Heinz body anemias, alpha- OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141800 141800]], Heinz body anemias, beta- OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141900 141900]], Hemoglobin H disease OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141850 141850]], Hypochromic microcytic anemia OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141850 141850]], Methemoglobinemias, alpha- OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141800 141800]], Methemoglobinemias, beta- OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141900 141900]], Sickle cell anemia OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141900 141900]], Thalassemia, alpha- OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141850 141850]], Thalassemia-beta, dominant inclusion-body OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141900 141900]], Thalassemias, alpha- OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141800 141800]], Thalassemias, beta- OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141900 141900]]
==About this Structure==
==About this Structure==
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[[Category: transport]]
[[Category: transport]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 17:10:45 2007''

Revision as of 15:04, 12 November 2007


1gzx, resolution 2.1Å

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OXY T STATE HAEMOGLOBIN: OXYGEN BOUND AT ALL FOUR HAEMS

Contents

Overview

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.

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

1GZX is a Protein complex structure of sequences from Homo sapiens with HEM and OXY as ligands. Structure known Active Site: HB1. Full crystallographic information is available from OCA.

Reference

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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