1nqp: Difference between revisions

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[[Image:1nqp.jpg|left|200px]]
[[Image:1nqp.jpg|left|200px]]


{{Structure
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{{STRUCTURE_1nqp| PDB=1nqp  | SCENE= }}  
|RELATEDENTRY=[[1bbb|1BBB]]
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1nqp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1nqp OCA], [http://www.ebi.ac.uk/pdbsum/1nqp PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1nqp RCSB]</span>
}}


'''Crystal structure of Human hemoglobin E at 1.73 A resolution'''
'''Crystal structure of Human hemoglobin E at 1.73 A resolution'''
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[[Category: Dutta, P.]]
[[Category: Dutta, P.]]
[[Category: Sen, U.]]
[[Category: Sen, U.]]
[[Category: hemoglobin e oxygen transport beta thalassemia]]
[[Category: Hemoglobin e oxygen transport beta thalassemia]]
 
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Revision as of 02:52, 3 May 2008

File:1nqp.jpg

Template:STRUCTURE 1nqp

Crystal structure of Human hemoglobin E at 1.73 A resolution


OverviewOverview

Hemoglobin A(2) (alpha(2)delta(2)), a minor (2-3%) component of circulating red blood cells, acts as an anti-sickling agent and its elevated concentration in beta-thalassemia is a useful clinical diagnostic. In beta-thalassemia major, where there is a failure of beta-chain production, HbA(2) acts as the predominant oxygen delivery mechanism. Hemoglobin E, is another common abnormal hemoglobin, caused by splice site mutation in exon 1 of beta globin gene, when combines with beta-thalassemia, causes severe microcytic anemia. The purification, crystallization, and preliminary structural studies of HbA(2) and HbE are reported here. HbA(2) and HbE are purified by cation exchange column chromatography in presence of KCN from the blood samples of individuals suffering from beta-thalassemia minor and E beta-thalassemia. X-ray diffraction data of HbA(2) and HbE were collected upto 2.1 and 1.73 A, respectively. HbA(2) crystallized in space group P2(1) with unit cell parameters a=54.33 A, b=83.73 A, c=62.87 A, and beta=99.80 degrees whereas HbE crystallized in space group P2(1)2(1)2(1) with unit cell parameters a=60.89 A, b=95.81 A, and c=99.08 A. Asymmetric unit in each case contains one Hb tetramer in R(2) state.

About this StructureAbout this Structure

1NQP is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

ReferenceReference

Crystallization and preliminary X-ray structural studies of hemoglobin A2 and hemoglobin E, isolated from the blood samples of beta-thalassemic patients., Dasgupta J, Sen U, Choudhury D, Datta P, Chakrabarti A, Chakrabarty SB, Chakrabarty A, Dattagupta JK, Biochem Biophys Res Commun. 2003 Apr 4;303(2):619-23. PMID:12659864 Page seeded by OCA on Sat May 3 02:52:08 2008

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