1e6f

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
[[Image:1e6f.gif|left|200px]]
[[Image:1e6f.gif|left|200px]]
-
{{Structure
+
<!--
-
|PDB= 1e6f |SIZE=350|CAPTION= <scene name='initialview01'>1e6f</scene>, resolution 1.75&Aring;
+
The line below this paragraph, containing "STRUCTURE_1e6f", creates the "Structure Box" on the page.
-
|SITE=
+
You may change the PDB parameter (which sets the PDB file loaded into the applet)
-
|LIGAND=
+
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
-
|ACTIVITY=
+
or leave the SCENE parameter empty for the default display.
-
|GENE=
+
-->
-
|DOMAIN=
+
{{STRUCTURE_1e6f| PDB=1e6f | SCENE= }}
-
|RELATEDENTRY=
+
-
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1e6f FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1e6f OCA], [http://www.ebi.ac.uk/pdbsum/1e6f PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1e6f RCSB]</span>
+
-
}}
+
'''HUMAN MIR-RECEPTOR, REPEAT 11'''
'''HUMAN MIR-RECEPTOR, REPEAT 11'''
Line 33: Line 30:
[[Category: Schmidt, B.]]
[[Category: Schmidt, B.]]
[[Category: Uson, I.]]
[[Category: Uson, I.]]
-
[[Category: glycoprotein,]]
+
[[Category: Glycoprotein]]
-
[[Category: igf-ii receptor]]
+
[[Category: Igf-ii receptor]]
-
[[Category: mir-receptor]]
+
[[Category: Mir-receptor]]
-
[[Category: transport]]
+
[[Category: Transport]]
-
 
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 14:43:26 2008''
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 19:56:06 2008''
+

Revision as of 11:43, 2 May 2008

Template:STRUCTURE 1e6f

HUMAN MIR-RECEPTOR, REPEAT 11


Overview

Improved data quality now makes it feasible to exploit the weak anomalous signal derived only from the sulfurs inherent to the protein or in particular from halide ions incorporated by soaking. The latter technique requires the location of a high number of partially occupied halide sites. This number appears to be roughly proportional to the exposed protein surface. This paper explores the application of dual-space ab initio methods as implemented in the program SHELXD to the location of substructures of sulfur in SAD experiments, bromide in SAD and MAD experiments and iodide using SAD and SIRAS to determine the anomalous-atom substructure. Sets of atoms consistent with the Patterson function were generated as a starting point for the dual-space recycling procedure in SHELXD. The substructure is then expanded to the full structure by maximum-likelihood phasing with SHARP and density modification with the program DM. Success in the location of the substructures and subsequent phasing depends critically on the quality of the data and on the extent of the anomalous signal. This varies with each crystal and soak, but for the same crystal the significance of the anomalous signal was found to be highly sensitive to the redundancy of the intensity measurements, which in some cases made all the difference. This is illustrated by the determination of the previously unknown structure of repeat 11 of the human mannose-6-phosphate/insulin-like growth factor II receptor (Man6P/IGFII-receptor), with 310 amino acids in the asymmetric unit, which was phased by soaking the crystals in a cryoprotectant solution containing halide anions.

About this Structure

1E6F is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Locating the anomalous scatterer substructures in halide and sulfur phasing., Uson I, Schmidt B, von Bulow R, Grimme S, von Figura K, Dauter M, Rajashankar KR, Dauter Z, Sheldrick GM, Acta Crystallogr D Biol Crystallogr. 2003 Jan;59(Pt 1):57-66. Epub 2002, Dec 19. PMID:12499540 Page seeded by OCA on Fri May 2 14:43:26 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools