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.

2fqc

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
[[Image:2fqc.gif|left|200px]]
+
{{Seed}}
 +
[[Image:2fqc.png|left|200px]]
<!--
<!--
Line 9: Line 10:
{{STRUCTURE_2fqc| PDB=2fqc | SCENE= }}
{{STRUCTURE_2fqc| PDB=2fqc | SCENE= }}
-
'''Solution structure of conotoxin pl14a'''
+
===Solution structure of conotoxin pl14a===
-
==Overview==
+
<!--
-
Using assay-directed fractionation of the venom from the vermivorous cone snail Conus planorbis, we isolated a new conotoxin, designated pl14a, with potent activity at both nicotinic acetylcholine receptors and a voltage-gated potassium channel subtype. pl14a contains 25 amino acid residues with an amidated C-terminus, an elongated N-terminal tail (six residues), and two disulfide bonds (1-3, 2-4 connectivity) in a novel framework distinct from other conotoxins. The peptide was chemically synthesized, and its three-dimensional structure was demonstrated to be well-defined, with an alpha-helix and two 3(10)-helices present. Analysis of a cDNA clone encoding the prepropeptide precursor of pl14a revealed a novel signal sequence, indicating that pl14a belongs to a new gene superfamily, the J-conotoxin superfamily. Five additional peptides in the J-superfamily were identified. Intracranial injection of pl14a in mice elicited excitatory symptoms that included shaking, rapid circling, barrel rolling, and seizures. Using the oocyte heterologous expression system, pl14a was shown to inhibit both a K+ channel subtype (Kv1.6, IC50 = 1.59 microM) and neuronal (IC50 = 8.7 microM for alpha3beta4) and neuromuscular (IC50 = 0.54 microM for alpha1beta1 epsilondelta) subtypes of the nicotinic acetylcholine receptor (nAChR). Similarities in sequence and structure are apparent between the middle loop of pl14a and the second loop of a number of alpha-conotoxins. This is the first conotoxin shown to affect the activity of both voltage-gated and ligand-gated ion channels.
+
The line below this paragraph, {{ABSTRACT_PUBMED_16819832}}, adds the Publication Abstract to the page
 +
(as it appears on PubMed at http://www.pubmed.gov), where 16819832 is the PubMed ID number.
 +
-->
 +
{{ABSTRACT_PUBMED_16819832}}
==About this Structure==
==About this Structure==
-
Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2FQC OCA].
+
Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2FQC OCA].
==Reference==
==Reference==
Line 24: Line 28:
[[Category: Alpha-helix]]
[[Category: Alpha-helix]]
[[Category: Disulfide bond]]
[[Category: Disulfide bond]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 04:11:52 2008''
+
 
 +
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jul 29 13:39:18 2008''

Revision as of 10:39, 29 July 2008

Image:2fqc.png

Template:STRUCTURE 2fqc

Solution structure of conotoxin pl14a

Template:ABSTRACT PUBMED 16819832

About this Structure

Full experimental information is available from OCA.

Reference

A novel conotoxin inhibitor of Kv1.6 channel and nAChR subtypes defines a new superfamily of conotoxins., Imperial JS, Bansal PS, Alewood PF, Daly NL, Craik DJ, Sporning A, Terlau H, Lopez-Vera E, Bandyopadhyay PK, Olivera BM, Biochemistry. 2006 Jul 11;45(27):8331-40. PMID:16819832

Page seeded by OCA on Tue Jul 29 13:39:18 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "http://52.214.119.220/wiki/index.php/2fqc"
Personal tools