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1yzi

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[[Image:1yzi.gif|left|200px]]<br />
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[[Image:1yzi.gif|left|200px]]<br /><applet load="1yzi" size="350" color="white" frame="true" align="right" spinBox="true"
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<applet load="1yzi" size="450" color="white" frame="true" align="right" spinBox="true"
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caption="1yzi, resolution 2.07&Aring;" />
caption="1yzi, resolution 2.07&Aring;" />
'''A novel quaternary structure of human carbonmonoxy hemoglobin'''<br />
'''A novel quaternary structure of human carbonmonoxy hemoglobin'''<br />
==Overview==
==Overview==
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The liganded hemoglobin (Hb) high-salt crystallization condition described, by Max Perutz has generated three different crystals of human adult, carbonmonoxy hemoglobin (COHbA). The first crystal is isomorphous with the, "classical" liganded or R Hb structure. The second crystal reveals a new, liganded Hb quaternary structure, RR2, that assumes an intermediate, conformation between the R form and another liganded Hb quaternary, structure, R2, which was discovered more than a decade ago. Like the R2, structure, the diagnostic R state hydrogen bond between beta2His97 and, alpha1Thr38 is missing in the RR2 structure. The third crystal adopts a, novel liganded Hb conformation, which we have termed R3, and it shows, substantial quaternary structural differences from the R, RR2, and R2, structures. The quaternary structure differences between T and R3 are as, large as those between T and R2; however, the T --&gt; R3 and T --&gt; R2, transitions are in different directions as defined by rigid-body screw, rotation. Moreover, R3 represents an end state. Compared to all known, liganded Hb structures, R3 shows remarkably reduced strain at the, alpha-heme, reduced steric contact between the beta-heme ligand and the, distal residues, smaller alpha- and beta-clefts, and reduced alpha1-alpha2, and beta1-beta2 iron-iron distances. Together, these unique structural, features in R3 should make it the most relaxed and/or greatly enhance its, affinity for oxygen compared to the other liganded Hbs. The current Hb, structure-function relationships that are now based on T --&gt; R, T --&gt;R --&gt;, R2, or T --&gt; R2 --&gt; R transitions may have to be reexamined to take into, account the RR2 and R3 liganded structures.
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The liganded hemoglobin (Hb) high-salt crystallization condition described by Max Perutz has generated three different crystals of human adult carbonmonoxy hemoglobin (COHbA). The first crystal is isomorphous with the "classical" liganded or R Hb structure. The second crystal reveals a new liganded Hb quaternary structure, RR2, that assumes an intermediate conformation between the R form and another liganded Hb quaternary structure, R2, which was discovered more than a decade ago. Like the R2 structure, the diagnostic R state hydrogen bond between beta2His97 and alpha1Thr38 is missing in the RR2 structure. The third crystal adopts a novel liganded Hb conformation, which we have termed R3, and it shows substantial quaternary structural differences from the R, RR2, and R2 structures. The quaternary structure differences between T and R3 are as large as those between T and R2; however, the T --&gt; R3 and T --&gt; R2 transitions are in different directions as defined by rigid-body screw rotation. Moreover, R3 represents an end state. Compared to all known liganded Hb structures, R3 shows remarkably reduced strain at the alpha-heme, reduced steric contact between the beta-heme ligand and the distal residues, smaller alpha- and beta-clefts, and reduced alpha1-alpha2 and beta1-beta2 iron-iron distances. Together, these unique structural features in R3 should make it the most relaxed and/or greatly enhance its affinity for oxygen compared to the other liganded Hbs. The current Hb structure-function relationships that are now based on T --&gt; R, T --&gt;R --&gt; R2, or T --&gt; R2 --&gt; R transitions may have to be reexamined to take into account the RR2 and R3 liganded structures.
==Disease==
==Disease==
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==About this Structure==
==About this Structure==
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1YZI 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 CMO, HEM and MBN as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1YZI OCA].
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1YZI 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 <scene name='pdbligand=CMO:'>CMO</scene>, <scene name='pdbligand=HEM:'>HEM</scene> and <scene name='pdbligand=MBN:'>MBN</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1YZI OCA].
==Reference==
==Reference==
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: Abraham, D.J.]]
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[[Category: Abraham, D J.]]
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[[Category: Safo, M.K.]]
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[[Category: Safo, M K.]]
[[Category: CMO]]
[[Category: CMO]]
[[Category: HEM]]
[[Category: HEM]]
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[[Category: tense]]
[[Category: tense]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 20:27:21 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:10:40 2008''

Revision as of 14:10, 21 February 2008


1yzi, resolution 2.07Å

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A novel quaternary structure of human carbonmonoxy hemoglobin

Contents

Overview

The liganded hemoglobin (Hb) high-salt crystallization condition described by Max Perutz has generated three different crystals of human adult carbonmonoxy hemoglobin (COHbA). The first crystal is isomorphous with the "classical" liganded or R Hb structure. The second crystal reveals a new liganded Hb quaternary structure, RR2, that assumes an intermediate conformation between the R form and another liganded Hb quaternary structure, R2, which was discovered more than a decade ago. Like the R2 structure, the diagnostic R state hydrogen bond between beta2His97 and alpha1Thr38 is missing in the RR2 structure. The third crystal adopts a novel liganded Hb conformation, which we have termed R3, and it shows substantial quaternary structural differences from the R, RR2, and R2 structures. The quaternary structure differences between T and R3 are as large as those between T and R2; however, the T --> R3 and T --> R2 transitions are in different directions as defined by rigid-body screw rotation. Moreover, R3 represents an end state. Compared to all known liganded Hb structures, R3 shows remarkably reduced strain at the alpha-heme, reduced steric contact between the beta-heme ligand and the distal residues, smaller alpha- and beta-clefts, and reduced alpha1-alpha2 and beta1-beta2 iron-iron distances. Together, these unique structural features in R3 should make it the most relaxed and/or greatly enhance its affinity for oxygen compared to the other liganded Hbs. The current Hb structure-function relationships that are now based on T --> R, T -->R --> R2, or T --> R2 --> R transitions may have to be reexamined to take into account the RR2 and R3 liganded structures.

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

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

Reference

The enigma of the liganded hemoglobin end state: a novel quaternary structure of human carbonmonoxy hemoglobin., Safo MK, Abraham DJ, Biochemistry. 2005 Jun 14;44(23):8347-59. PMID:15938624

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