1iyc

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
(New page: 200px<br /><applet load="1iyc" size="450" color="white" frame="true" align="right" spinBox="true" caption="1iyc" /> '''Solution structure of antifungal peptide, sc...)
Line 1: Line 1:
-
[[Image:1iyc.jpg|left|200px]]<br /><applet load="1iyc" size="450" color="white" frame="true" align="right" spinBox="true"
+
[[Image:1iyc.jpg|left|200px]]<br /><applet load="1iyc" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1iyc" />
caption="1iyc" />
'''Solution structure of antifungal peptide, scarabaecin'''<br />
'''Solution structure of antifungal peptide, scarabaecin'''<br />
==Overview==
==Overview==
-
Scarabaecin isolated from hemolymph of the coconut rhinoceros beetle, Oryctes rhinoceros is a 36-residue polypeptide that has antifungal, activity. The solution structure of scarabaecin has been determined from, twodimensional 1H NMR spectroscopic data and hybrid distance, geometry-simulated annealing protocol calculation. Based on 492, interproton and 10 hydrogen-bonding distance restraints and 36 dihedral, angle restraints, we obtained 20 structures. The average backbone, root-mean-square deviation for residues 4-35 is 0.728 +/- 0.217 A from the, mean structure. The solution structure consists of a two-stranded, antiparallel beta-sheet connected by a type-I beta-turn after a short, helical turn. All secondary structures and a conserved disulfide bond are, located in the C-terminal half of the peptide, residues 18-36. Overall, folding is stabilized by a combination of a disulfide bond, seven hydrogen, bonds, and numerous hydrophobic interactions. The structural motif of the, C-terminal half shares a significant tertiary structural similarity with, chitin-binding domains of plant and invertebrate chitin-binding proteins, even though scarabaecin has no overall sequence similarity to other, peptide/polypeptides including chitin-binding proteins. The length of its, primary structure, the number of disulfide bonds, and the pattern of, conserved functional residues binding to chitin in scarabaecin differ from, those of chitin-binding proteins in other invertebrates and plants, suggesting that scarabaecin does not share a common ancestor with them., These results are thought to provide further strong experimental evidence, to the hypothesis that chitin-binding proteins of invertebrates and plants, are correlated by a convergent evolution process.
+
Scarabaecin isolated from hemolymph of the coconut rhinoceros beetle Oryctes rhinoceros is a 36-residue polypeptide that has antifungal activity. The solution structure of scarabaecin has been determined from twodimensional 1H NMR spectroscopic data and hybrid distance geometry-simulated annealing protocol calculation. Based on 492 interproton and 10 hydrogen-bonding distance restraints and 36 dihedral angle restraints, we obtained 20 structures. The average backbone root-mean-square deviation for residues 4-35 is 0.728 +/- 0.217 A from the mean structure. The solution structure consists of a two-stranded antiparallel beta-sheet connected by a type-I beta-turn after a short helical turn. All secondary structures and a conserved disulfide bond are located in the C-terminal half of the peptide, residues 18-36. Overall folding is stabilized by a combination of a disulfide bond, seven hydrogen bonds, and numerous hydrophobic interactions. The structural motif of the C-terminal half shares a significant tertiary structural similarity with chitin-binding domains of plant and invertebrate chitin-binding proteins, even though scarabaecin has no overall sequence similarity to other peptide/polypeptides including chitin-binding proteins. The length of its primary structure, the number of disulfide bonds, and the pattern of conserved functional residues binding to chitin in scarabaecin differ from those of chitin-binding proteins in other invertebrates and plants, suggesting that scarabaecin does not share a common ancestor with them. These results are thought to provide further strong experimental evidence to the hypothesis that chitin-binding proteins of invertebrates and plants are correlated by a convergent evolution process.
==About this Structure==
==About this Structure==
-
1IYC is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1IYC OCA].
+
1IYC is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1IYC OCA].
==Reference==
==Reference==
Line 22: Line 22:
[[Category: nmr]]
[[Category: nmr]]
-
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 17:46:13 2007''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:16:57 2008''

Revision as of 11:16, 21 February 2008


1iyc

Drag the structure with the mouse to rotate

Solution structure of antifungal peptide, scarabaecin

Overview

Scarabaecin isolated from hemolymph of the coconut rhinoceros beetle Oryctes rhinoceros is a 36-residue polypeptide that has antifungal activity. The solution structure of scarabaecin has been determined from twodimensional 1H NMR spectroscopic data and hybrid distance geometry-simulated annealing protocol calculation. Based on 492 interproton and 10 hydrogen-bonding distance restraints and 36 dihedral angle restraints, we obtained 20 structures. The average backbone root-mean-square deviation for residues 4-35 is 0.728 +/- 0.217 A from the mean structure. The solution structure consists of a two-stranded antiparallel beta-sheet connected by a type-I beta-turn after a short helical turn. All secondary structures and a conserved disulfide bond are located in the C-terminal half of the peptide, residues 18-36. Overall folding is stabilized by a combination of a disulfide bond, seven hydrogen bonds, and numerous hydrophobic interactions. The structural motif of the C-terminal half shares a significant tertiary structural similarity with chitin-binding domains of plant and invertebrate chitin-binding proteins, even though scarabaecin has no overall sequence similarity to other peptide/polypeptides including chitin-binding proteins. The length of its primary structure, the number of disulfide bonds, and the pattern of conserved functional residues binding to chitin in scarabaecin differ from those of chitin-binding proteins in other invertebrates and plants, suggesting that scarabaecin does not share a common ancestor with them. These results are thought to provide further strong experimental evidence to the hypothesis that chitin-binding proteins of invertebrates and plants are correlated by a convergent evolution process.

About this Structure

1IYC is a Single protein structure of sequence from [1]. Full crystallographic information is available from OCA.

Reference

Structural basis for new pattern of conserved amino acid residues related to chitin-binding in the antifungal peptide from the coconut rhinoceros beetle Oryctes rhinoceros., Hemmi H, Ishibashi J, Tomie T, Yamakawa M, J Biol Chem. 2003 Jun 20;278(25):22820-7. Epub 2003 Apr 3. PMID:12676931

Page seeded by OCA on Thu Feb 21 13:16:57 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools