1coh

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(New page: 200px<br /> <applet load="1coh" size="450" color="white" frame="true" align="right" spinBox="true" caption="1coh, resolution 2.9&Aring;" /> '''STRUCTURE OF HAEMOGL...)
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==Overview==
==Overview==
We report the X-ray crystal structure of two analogues of human, haemoglobin in the deoxy quaternary (T) state with ligand bound, exclusively at the alpha haems. These models were prepared from symmetric, mixed-metal hybrid haemoglobin molecules. The structures of alpha Fe(II), beta Co(II), its carbonmonoxy derivative alpha Fe(II)CO beta Co(II), and, alpha Fe(II)O2 beta Ni(II) are compared with native deoxy haemoglobin by, difference Fourier syntheses at 2.8, 2.9 and 3.5 A resolution, respectively, and the refined alpha Fe(II)CO beta Co(II) structure is, analysed. In both the native deoxy and liganded T molecules, the mean, plane of the alpha-subunit haem is parallel with the axis of the F helix, but this plane is tilted with respect to the helix axis in the, oxy-quaternary R state. The side-chains of LeuFG3 and ValFG5 sterically, restrict haem tilting in the T state. We propose that strain energy, develops at the contact between the haem and these residues in the, liganded T-state haemoglobin, and that the strain is, in part, responsible, for the low affinity of the T-state alpha haem.
We report the X-ray crystal structure of two analogues of human, haemoglobin in the deoxy quaternary (T) state with ligand bound, exclusively at the alpha haems. These models were prepared from symmetric, mixed-metal hybrid haemoglobin molecules. The structures of alpha Fe(II), beta Co(II), its carbonmonoxy derivative alpha Fe(II)CO beta Co(II), and, alpha Fe(II)O2 beta Ni(II) are compared with native deoxy haemoglobin by, difference Fourier syntheses at 2.8, 2.9 and 3.5 A resolution, respectively, and the refined alpha Fe(II)CO beta Co(II) structure is, analysed. In both the native deoxy and liganded T molecules, the mean, plane of the alpha-subunit haem is parallel with the axis of the F helix, but this plane is tilted with respect to the helix axis in the, oxy-quaternary R state. The side-chains of LeuFG3 and ValFG5 sterically, restrict haem tilting in the T state. We propose that strain energy, develops at the contact between the haem and these residues in the, liganded T-state haemoglobin, and that the strain is, in part, responsible, for the low affinity of the T-state alpha haem.
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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: oxygen transport]]
[[Category: oxygen transport]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Thu Nov 8 12:59:30 2007''
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 16:24:14 2007''

Revision as of 14:17, 12 November 2007


1coh, resolution 2.9Å

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STRUCTURE OF HAEMOGLOBIN IN THE DEOXY QUATERNARY STATE WITH LIGAND BOUND AT THE ALPHA HAEMS

Contents

Overview

We report the X-ray crystal structure of two analogues of human, haemoglobin in the deoxy quaternary (T) state with ligand bound, exclusively at the alpha haems. These models were prepared from symmetric, mixed-metal hybrid haemoglobin molecules. The structures of alpha Fe(II), beta Co(II), its carbonmonoxy derivative alpha Fe(II)CO beta Co(II), and, alpha Fe(II)O2 beta Ni(II) are compared with native deoxy haemoglobin by, difference Fourier syntheses at 2.8, 2.9 and 3.5 A resolution, respectively, and the refined alpha Fe(II)CO beta Co(II) structure is, analysed. In both the native deoxy and liganded T molecules, the mean, plane of the alpha-subunit haem is parallel with the axis of the F helix, but this plane is tilted with respect to the helix axis in the, oxy-quaternary R state. The side-chains of LeuFG3 and ValFG5 sterically, restrict haem tilting in the T state. We propose that strain energy, develops at the contact between the haem and these residues in the, liganded T-state haemoglobin, and that the strain is, in part, responsible, for the low affinity of the T-state alpha haem.

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

1COH is a Protein complex structure of sequences from Homo sapiens with HEM, CMO and COH as ligands. Full crystallographic information is available from OCA.

Reference

Structure of haemoglobin in the deoxy quaternary state with ligand bound at the alpha haems., Luisi B, Shibayama N, J Mol Biol. 1989 Apr 20;206(4):723-36. PMID:2738915

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