1ccq: Difference between revisions

New page: left|200px<br /><applet load="1ccq" size="450" color="white" frame="true" align="right" spinBox="true" caption="1ccq" /> '''NMR STRUCTURE WITH TIGHTLY BOUND WATER MOLEC...
 
No edit summary
Line 1: Line 1:
[[Image:1ccq.gif|left|200px]]<br /><applet load="1ccq" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1ccq.gif|left|200px]]<br /><applet load="1ccq" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1ccq" />
caption="1ccq" />
'''NMR STRUCTURE WITH TIGHTLY BOUND WATER MOLECULES OF CYTOTOXIN II (CARDIOTOXIN) FROM NAJA NAJA OXIANA IN AQUEOUS SOLUTION (MINOR FORM).'''<br />
'''NMR STRUCTURE WITH TIGHTLY BOUND WATER MOLECULES OF CYTOTOXIN II (CARDIOTOXIN) FROM NAJA NAJA OXIANA IN AQUEOUS SOLUTION (MINOR FORM).'''<br />


==Overview==
==Overview==
1H-NMR spectroscopy data, such as NOE intraprotein and (bound, water)/protein contacts, 3J coupling constants and deuterium exchange, rates were used to determine the in-solution spatial structure of, cytotoxin II from Naja naja oxiana snake venom (CTII). Exploiting, information from two 1H-NMR spectral components, shown to be due to, cis/trans isomerization of the Val7-Pro8 peptide bond, spatial structures, of CTII minor and major forms (1 : 6) were calculated using the torsion, angle dynamics algorithm of the DYANA program and then energy refined, using the FANTOM program. Each form, major and minor, is represented by 20, resulting conformers, demonstrating mean backbone rmsd values of 0.51 and, 0.71 A, respectively. Two forms of CTII preserve the structural skeleton, as three large loops, including two beta-sheets with bend regions, and, demonstrate structural differences at loop I, where cis/trans, isomerization occurs. The CTII side-chain distribution constitutes, hydrophilic and hydrophobic belts around the protein, alternating in the, trend of the three main loops. Because of the Omega-shaped backbone, formed in participation with two bound water molecules, the tip of loop II, bridges the tips of loops I and III. This ensures the continuity of the, largest hydrophobic belt, formed with the residues of these tips., Comparison revealed pronounced differences in the spatial organization of, the tips of the three main loops between CTII and previous structures of, homologous cytotoxins (cardiotoxins) in solution.
1H-NMR spectroscopy data, such as NOE intraprotein and (bound water)/protein contacts, 3J coupling constants and deuterium exchange rates were used to determine the in-solution spatial structure of cytotoxin II from Naja naja oxiana snake venom (CTII). Exploiting information from two 1H-NMR spectral components, shown to be due to cis/trans isomerization of the Val7-Pro8 peptide bond, spatial structures of CTII minor and major forms (1 : 6) were calculated using the torsion angle dynamics algorithm of the DYANA program and then energy refined using the FANTOM program. Each form, major and minor, is represented by 20 resulting conformers, demonstrating mean backbone rmsd values of 0.51 and 0.71 A, respectively. Two forms of CTII preserve the structural skeleton as three large loops, including two beta-sheets with bend regions, and demonstrate structural differences at loop I, where cis/trans isomerization occurs. The CTII side-chain distribution constitutes hydrophilic and hydrophobic belts around the protein, alternating in the trend of the three main loops. Because of the Omega-shaped backbone, formed in participation with two bound water molecules, the tip of loop II bridges the tips of loops I and III. This ensures the continuity of the largest hydrophobic belt, formed with the residues of these tips. Comparison revealed pronounced differences in the spatial organization of the tips of the three main loops between CTII and previous structures of homologous cytotoxins (cardiotoxins) in solution.


==About this Structure==
==About this Structure==
1CCQ is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Naja_oxiana Naja oxiana]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1CCQ OCA].  
1CCQ is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Naja_oxiana Naja oxiana]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1CCQ OCA].  


==Reference==
==Reference==
Line 13: Line 13:
[[Category: Naja oxiana]]
[[Category: Naja oxiana]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Arseniev, A.S.]]
[[Category: Arseniev, A S.]]
[[Category: Bocharov, E.V.]]
[[Category: Bocharov, E V.]]
[[Category: Dementieva, D.V.]]
[[Category: Dementieva, D V.]]
[[Category: bound water]]
[[Category: bound water]]
[[Category: cis/trans isomerization]]
[[Category: cis/trans isomerization]]
Line 21: Line 21:
[[Category: membrane perturbation]]
[[Category: membrane perturbation]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 12:21:12 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:04:44 2008''

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA