1vwt: Difference between revisions

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[[Image:1vwt.gif|left|200px]]<br />
[[Image:1vwt.gif|left|200px]]<br /><applet load="1vwt" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1vwt" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1vwt, resolution 1.9&Aring;" />
caption="1vwt, resolution 1.9&Aring;" />
'''T STATE HUMAN HEMOGLOBIN [ALPHA V96W], ALPHA AQUOMET, BETA DEOXY'''<br />
'''T STATE HUMAN HEMOGLOBIN [ALPHA V96W], ALPHA AQUOMET, BETA DEOXY'''<br />


==Overview==
==Overview==
One of the most promising approaches for the development of a synthetic, blood substitute has been the engineering of novel mutants of human, hemoglobin (Hb) A which maintain cooperativity, but possess lowered oxygen, affinity. We describe here two crystal structures of one such potential, blood substitute, recombinant (r) Hb(alpha 96Val--&gt;Trp), refined to 1.9 A, resolution in an alpha-aquomet, beta-deoxy T-state, and to 2.5 A, resolution in a carbonmonoxy R-state. On the basis of molecular dynamics, simulations, a particular conformation had been predicted for the, engineered Trp residue, and the lowered oxygen affinity had been, attributed to a stabilization of the deoxy T-state interface by alpha, 96Trp-beta 99Asp hydrogen bonds. Difference Fourier maps of the T-state, structure clearly show that alpha 96Trp is in a conformation different, from that predicted by the simulation, with its indole side chain directed, away from the interface and into the central cavity. In this conformation, the indole nitrogen makes novel water-mediated hydrogen bonds across the, T-state interface with beta 101Glu. We propose that these water-mediated, hydrogen bonds are the structural basis for the lowered oxygen affinity of, rHb(alpha 96Val--&gt;Trp), and discuss the implications of these findings for, future molecular dynamics studies and the design of Hb mutants.
One of the most promising approaches for the development of a synthetic blood substitute has been the engineering of novel mutants of human hemoglobin (Hb) A which maintain cooperativity, but possess lowered oxygen affinity. We describe here two crystal structures of one such potential blood substitute, recombinant (r) Hb(alpha 96Val--&gt;Trp), refined to 1.9 A resolution in an alpha-aquomet, beta-deoxy T-state, and to 2.5 A resolution in a carbonmonoxy R-state. On the basis of molecular dynamics simulations, a particular conformation had been predicted for the engineered Trp residue, and the lowered oxygen affinity had been attributed to a stabilization of the deoxy T-state interface by alpha 96Trp-beta 99Asp hydrogen bonds. Difference Fourier maps of the T-state structure clearly show that alpha 96Trp is in a conformation different from that predicted by the simulation, with its indole side chain directed away from the interface and into the central cavity. In this conformation, the indole nitrogen makes novel water-mediated hydrogen bonds across the T-state interface with beta 101Glu. We propose that these water-mediated hydrogen bonds are the structural basis for the lowered oxygen affinity of rHb(alpha 96Val--&gt;Trp), and discuss the implications of these findings for future molecular dynamics studies and the design of Hb mutants.


==Disease==
==Disease==
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==About this Structure==
==About this Structure==
1VWT 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 SO4 and HEM as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1VWT OCA].  
1VWT 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=SO4:'>SO4</scene> and <scene name='pdbligand=HEM:'>HEM</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1VWT OCA].  


==Reference==
==Reference==
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Almo, S.C.]]
[[Category: Almo, S C.]]
[[Category: Ho, C.]]
[[Category: Ho, C.]]
[[Category: Ho, N.T.]]
[[Category: Ho, N T.]]
[[Category: Puius, Y.A.]]
[[Category: Puius, Y A.]]
[[Category: Zou, M.]]
[[Category: Zou, M.]]
[[Category: HEM]]
[[Category: HEM]]
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[[Category: oxygen transport]]
[[Category: oxygen transport]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 19:44:55 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:38:30 2008''