1c6w

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Current revision (11:38, 22 November 2023) (edit) (undo)
 
(10 intermediate revisions not shown.)
Line 1: Line 1:
-
[[Image:1c6w.jpg|left|200px]]
 
-
{{Structure
+
==MAUROCALCIN FROM SCORPIO MAURUS==
-
|PDB= 1c6w |SIZE=350|CAPTION= <scene name='initialview01'>1c6w</scene>
+
<StructureSection load='1c6w' size='340' side='right'caption='[[1c6w]]' scene=''>
-
|SITE=
+
== Structural highlights ==
-
|LIGAND=
+
<table><tr><td colspan='2'>[[1c6w]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Scorpio_maurus Scorpio maurus]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1C6W OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1C6W FirstGlance]. <br>
-
|ACTIVITY=
+
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr>
-
|GENE=
+
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1c6w FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1c6w OCA], [https://pdbe.org/1c6w PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1c6w RCSB], [https://www.ebi.ac.uk/pdbsum/1c6w PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1c6w ProSAT]</span></td></tr>
-
|DOMAIN=
+
</table>
-
|RELATEDENTRY=
+
== Function ==
-
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1c6w FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1c6w OCA], [http://www.ebi.ac.uk/pdbsum/1c6w PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1c6w RCSB]</span>
+
[https://www.uniprot.org/uniprot/CAMAU_SCOPA CAMAU_SCOPA] This toxin stabilizes ryanodine receptor 1 (RyR1) opening in a long-lasting subconductance state (48%-60% of the full conductance state) (PubMed:10713267, PubMed:12869557, PubMed:27114612). Furthermore, it triggers calcium release from sarcoplasmic vesicles (6.6 nM are enough to induce a sharp release, and 60% of the total calcium is released after toxin (100 nM) addition) probably by acting as a cell-penetrating peptide (CPP) (PubMed:27114612). In addition, it has been shown to dose-dependently stimulate ryanodine binding to RyR1 (EC(50)=12.5-26.4 nM) (PubMed:12869557, PubMed:17291197, PubMed:17888395, PubMed:27114612). It also augments the bell-shaped calcium-[3H]ryanodine binding curve that is maximal at about 10 uM calcium concentration (PubMed:27114612). It binds a different site as ryanodine (PubMed:10713267). It acts synergistically with caffeine (By similarity). In vivo, intracerebroventricular injection into mice causes death (PubMed:10713267).[UniProtKB:A0A1L4BJ42][UniProtKB:B8QG00][UniProtKB:P59868]<ref>PMID:10713267</ref> <ref>PMID:12869557</ref> <ref>PMID:17291197</ref> <ref>PMID:17888395</ref> <ref>PMID:27114612</ref>
-
}}
+
<div style="background-color:#fffaf0;">
-
 
+
== Publication Abstract from PubMed ==
-
'''MAUROCALCIN FROM SCORPIO MAURUS'''
+
-
 
+
-
 
+
-
==Overview==
+
We determined the structure in solution by (1)H two-dimensional NMR of Maurocalcine from the venom of Scorpio maurus. This toxin has been demonstrated to be a potent effector of ryanodyne-sensitive calcium channel from skeletal muscles. This is the first description of a scorpion toxin which folds following the Inhibitor Cystine Knot fold (ICK) already described for numerous toxic and inhibitory peptides, as well as for various protease inhibitors. Its three dimensional structure consists of a compact disulfide-bonded core from which emerge loops and the N-terminus. A double-stranded antiparallel beta-sheet comprises residues 20-23 and 30-33. A third extended strand (residues 9-11) is perpendicular to the beta-sheet. Maurocalcine structure mimics the activating segment of the dihydropyridine receptor II-III loop and is therefore potentially useful for dihydropyridine receptor/ryanodine receptor interaction studies. Proteins 2000;40:436-442.
We determined the structure in solution by (1)H two-dimensional NMR of Maurocalcine from the venom of Scorpio maurus. This toxin has been demonstrated to be a potent effector of ryanodyne-sensitive calcium channel from skeletal muscles. This is the first description of a scorpion toxin which folds following the Inhibitor Cystine Knot fold (ICK) already described for numerous toxic and inhibitory peptides, as well as for various protease inhibitors. Its three dimensional structure consists of a compact disulfide-bonded core from which emerge loops and the N-terminus. A double-stranded antiparallel beta-sheet comprises residues 20-23 and 30-33. A third extended strand (residues 9-11) is perpendicular to the beta-sheet. Maurocalcine structure mimics the activating segment of the dihydropyridine receptor II-III loop and is therefore potentially useful for dihydropyridine receptor/ryanodine receptor interaction studies. Proteins 2000;40:436-442.
-
==About this Structure==
+
A new fold in the scorpion toxin family, associated with an activity on a ryanodine-sensitive calcium channel.,Mosbah A, Kharrat R, Fajloun Z, Renisio JG, Blanc E, Sabatier JM, El Ayeb M, Darbon H Proteins. 2000 Aug 15;40(3):436-42. PMID:10861934<ref>PMID:10861934</ref>
-
1C6W is a [[Protein complex]] structure of sequences from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1C6W OCA].
+
-
 
+
-
==Reference==
+
-
A new fold in the scorpion toxin family, associated with an activity on a ryanodine-sensitive calcium channel., Mosbah A, Kharrat R, Fajloun Z, Renisio JG, Blanc E, Sabatier JM, El Ayeb M, Darbon H, Proteins. 2000 Aug 15;40(3):436-42. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/10861934 10861934]
+
-
[[Category: Protein complex]]
+
-
[[Category: Ayeb, M.]]
+
-
[[Category: Blanc, E.]]
+
-
[[Category: Darbon, H.]]
+
-
[[Category: Fajloun, Z.]]
+
-
[[Category: Kharrat, R.]]
+
-
[[Category: Mosbah, A.]]
+
-
[[Category: Renisio, J G.]]
+
-
[[Category: Sabatier, J M.]]
+
-
[[Category: ryanodine receptor effector]]
+
-
[[Category: scorpion toxin]]
+
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 19:15:49 2008''
+
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
 +
</div>
 +
<div class="pdbe-citations 1c6w" style="background-color:#fffaf0;"></div>
 +
== References ==
 +
<references/>
 +
__TOC__
 +
</StructureSection>
 +
[[Category: Large Structures]]
 +
[[Category: Scorpio maurus]]
 +
[[Category: Ayeb M]]
 +
[[Category: Blanc E]]
 +
[[Category: Darbon H]]
 +
[[Category: Fajloun Z]]
 +
[[Category: Kharrat R]]
 +
[[Category: Mosbah A]]
 +
[[Category: Renisio J-G]]
 +
[[Category: Sabatier J-M]]

Current revision

MAUROCALCIN FROM SCORPIO MAURUS

PDB ID 1c6w

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "http://52.214.119.220/wiki/index.php/1c6w"
Personal tools