We apologize for Proteopedia being slow to respond. For the past two years, a new implementation of Proteopedia has been being built. Soon, it will replace this 18-year old system. All existing content will be moved to the new system at a date that will be announced here.

1yl2

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
(New page: 200px<br /><applet load="1yl2" size="450" color="white" frame="true" align="right" spinBox="true" caption="1yl2" /> '''Conkunitzin-S1 is the first member of a new ...)
Line 1: Line 1:
-
[[Image:1yl2.jpg|left|200px]]<br /><applet load="1yl2" size="450" color="white" frame="true" align="right" spinBox="true"
+
[[Image:1yl2.jpg|left|200px]]<br /><applet load="1yl2" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1yl2" />
caption="1yl2" />
'''Conkunitzin-S1 is the first member of a new Kunitz-type neurotoxin family- Structural and functional characterization'''<br />
'''Conkunitzin-S1 is the first member of a new Kunitz-type neurotoxin family- Structural and functional characterization'''<br />
==Overview==
==Overview==
-
Conkunitzin-S1 (Conk-S1) is a 60-residue neurotoxin from the venom of the, cone snail Conus striatus that interacts with voltage-gated potassium, channels. Conk-S1 shares sequence homology with Kunitz-type proteins but, contains only two out of the three highly conserved cysteine bridges, which are typically found in these small, basic protein modules. In this, study the three-dimensional structure of Conk-S1 has been solved by, multidimensional NMR spectroscopy. The solution structure of recombinant, Conk-S1 shows that a Kunitz fold is present, even though one of the highly, conserved disulfide cross-links is missing. Introduction of a third, homologous disulfide bond into Conk-S1 results in a functional toxin with, similar affinity for Shaker potassium channels. The affinity of Conk-S1, can be enhanced by a pore mutation within the Shaker channel pore, indicating an interaction of Conk-S1 with the vestibule of potassium, channels.
+
Conkunitzin-S1 (Conk-S1) is a 60-residue neurotoxin from the venom of the cone snail Conus striatus that interacts with voltage-gated potassium channels. Conk-S1 shares sequence homology with Kunitz-type proteins but contains only two out of the three highly conserved cysteine bridges, which are typically found in these small, basic protein modules. In this study the three-dimensional structure of Conk-S1 has been solved by multidimensional NMR spectroscopy. The solution structure of recombinant Conk-S1 shows that a Kunitz fold is present, even though one of the highly conserved disulfide cross-links is missing. Introduction of a third, homologous disulfide bond into Conk-S1 results in a functional toxin with similar affinity for Shaker potassium channels. The affinity of Conk-S1 can be enhanced by a pore mutation within the Shaker channel pore indicating an interaction of Conk-S1 with the vestibule of potassium channels.
==About this Structure==
==About this Structure==
-
1YL2 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Conus_striatus Conus striatus]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1YL2 OCA].
+
1YL2 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Conus_striatus Conus striatus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1YL2 OCA].
==Reference==
==Reference==
Line 18: Line 18:
[[Category: Graf, R.]]
[[Category: Graf, R.]]
[[Category: Korukottu, J.]]
[[Category: Korukottu, J.]]
-
[[Category: Olivera, B.M.]]
+
[[Category: Olivera, B M.]]
[[Category: Terlau, H.]]
[[Category: Terlau, H.]]
[[Category: Vijayan, V.]]
[[Category: Vijayan, V.]]
Line 24: Line 24:
[[Category: neurotoxin; kunitz-domain; potassium channel blocker]]
[[Category: neurotoxin; kunitz-domain; potassium channel blocker]]
-
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 06:52:50 2007''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:06:28 2008''

Revision as of 14:06, 21 February 2008


1yl2

Drag the structure with the mouse to rotate

Conkunitzin-S1 is the first member of a new Kunitz-type neurotoxin family- Structural and functional characterization

Overview

Conkunitzin-S1 (Conk-S1) is a 60-residue neurotoxin from the venom of the cone snail Conus striatus that interacts with voltage-gated potassium channels. Conk-S1 shares sequence homology with Kunitz-type proteins but contains only two out of the three highly conserved cysteine bridges, which are typically found in these small, basic protein modules. In this study the three-dimensional structure of Conk-S1 has been solved by multidimensional NMR spectroscopy. The solution structure of recombinant Conk-S1 shows that a Kunitz fold is present, even though one of the highly conserved disulfide cross-links is missing. Introduction of a third, homologous disulfide bond into Conk-S1 results in a functional toxin with similar affinity for Shaker potassium channels. The affinity of Conk-S1 can be enhanced by a pore mutation within the Shaker channel pore indicating an interaction of Conk-S1 with the vestibule of potassium channels.

About this Structure

1YL2 is a Protein complex structure of sequences from Conus striatus. Full crystallographic information is available from OCA.

Reference

Conkunitzin-S1 is the first member of a new Kunitz-type neurotoxin family. Structural and functional characterization., Bayrhuber M, Vijayan V, Ferber M, Graf R, Korukottu J, Imperial J, Garrett JE, Olivera BM, Terlau H, Zweckstetter M, Becker S, J Biol Chem. 2005 Jun 24;280(25):23766-70. Epub 2005 Apr 15. PMID:15833744

Page seeded by OCA on Thu Feb 21 16:06:28 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools