1c09

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
(New page: 200px<br /><applet load="1c09" size="450" color="white" frame="true" align="right" spinBox="true" caption="1c09, resolution 1.6&Aring;" /> '''RUBREDOXIN V44A CP'''...)
Current revision (23:22, 27 December 2023) (edit) (undo)
 
(16 intermediate revisions not shown.)
Line 1: Line 1:
-
[[Image:1c09.gif|left|200px]]<br /><applet load="1c09" size="450" color="white" frame="true" align="right" spinBox="true"
 
-
caption="1c09, resolution 1.6&Aring;" />
 
-
'''RUBREDOXIN V44A CP'''<br />
 
-
==Overview==
+
==RUBREDOXIN V44A CP==
-
Rubredoxins (Rds) may be separated into two classes based upon the, correlation of their reduction potentials with the identity of residue 44;, those with Ala44 have reduction potentials that are approximately 50 mV, higher than those with Val44. The smaller side chain volume occupied by, Ala44 relative to that occupied by Val44 has been proposed to explain the, increase in the reduction potential, based upon changes in the Gly43-Ala44, peptide bond orientation and the distance to the [Fe(SCys)(4)] center in, the Pyrococcus furiosus (Pf) Rd crystal structure compared to those of, Gly43-Val44 in the Clostridium pasteurianum (Cp) Rd crystal structure. As, an experimental test of this hypothesis, single-site Val44 &lt;--&gt; Ala44, exchange mutants, [V44A]Cp and [A44V]Pf Rds, have been cloned and, expressed. Reduction potentials of these residue 44 variants and pertinent, features of the X-ray crystal structure of [V44A]Cp Rd are reported., Relative to those of wild-type Cp and Pf Rds, the V44A mutation in Cp Rd, results in an 86 mV increase in midpoint reduction potential and the, [A44V] mutation in Pf Rd results in a 95 mV decrease in midpoint reduction, potential, respectively. In the crystal structure of [V44A]Cp Rd, the, peptide bond between residues 43 and 44 is approximately 0.3 A closer to, the Fe center and the hydrogen bond distance between the residue 44, peptide nitrogen and the Cys42 gamma-sulfur decreases by 0.32 A compared, to the analogous distances in the wild-type Cp Rd crystal structure. The, results described herein support the prediction that the identity of, residue 44 alone determines whether a Rd reduction potential of about -50, or 0 mV is observed.
+
<StructureSection load='1c09' size='340' side='right'caption='[[1c09]], [[Resolution|resolution]] 1.60&Aring;' scene=''>
 +
== Structural highlights ==
 +
<table><tr><td colspan='2'>[[1c09]] is a 3 chain structure with sequence from [https://en.wikipedia.org/wiki/Clostridium_pasteurianum Clostridium pasteurianum]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1C09 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1C09 FirstGlance]. <br>
 +
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.6&#8491;</td></tr>
 +
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=FE:FE+(III)+ION'>FE</scene></td></tr>
 +
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1c09 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1c09 OCA], [https://pdbe.org/1c09 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1c09 RCSB], [https://www.ebi.ac.uk/pdbsum/1c09 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1c09 ProSAT]</span></td></tr>
 +
</table>
 +
== Function ==
 +
[https://www.uniprot.org/uniprot/RUBR_CLOPA RUBR_CLOPA] Rubredoxin is a small nonheme, iron protein lacking acid-labile sulfide. Its single Fe, chelated to 4 Cys, functions as an electron acceptor and may also stabilize the conformation of the molecule.
 +
== Evolutionary Conservation ==
 +
[[Image:Consurf_key_small.gif|200px|right]]
 +
Check<jmol>
 +
<jmolCheckbox>
 +
<scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/c0/1c09_consurf.spt"</scriptWhenChecked>
 +
<scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
 +
<text>to colour the structure by Evolutionary Conservation</text>
 +
</jmolCheckbox>
 +
</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=1c09 ConSurf].
 +
<div style="clear:both"></div>
 +
<div style="background-color:#fffaf0;">
 +
== Publication Abstract from PubMed ==
 +
Rubredoxins (Rds) may be separated into two classes based upon the correlation of their reduction potentials with the identity of residue 44; those with Ala44 have reduction potentials that are approximately 50 mV higher than those with Val44. The smaller side chain volume occupied by Ala44 relative to that occupied by Val44 has been proposed to explain the increase in the reduction potential, based upon changes in the Gly43-Ala44 peptide bond orientation and the distance to the [Fe(SCys)(4)] center in the Pyrococcus furiosus (Pf) Rd crystal structure compared to those of Gly43-Val44 in the Clostridium pasteurianum (Cp) Rd crystal structure. As an experimental test of this hypothesis, single-site Val44 &lt;--&gt; Ala44 exchange mutants, [V44A]Cp and [A44V]Pf Rds, have been cloned and expressed. Reduction potentials of these residue 44 variants and pertinent features of the X-ray crystal structure of [V44A]Cp Rd are reported. Relative to those of wild-type Cp and Pf Rds, the V44A mutation in Cp Rd results in an 86 mV increase in midpoint reduction potential and the [A44V] mutation in Pf Rd results in a 95 mV decrease in midpoint reduction potential, respectively. In the crystal structure of [V44A]Cp Rd, the peptide bond between residues 43 and 44 is approximately 0.3 A closer to the Fe center and the hydrogen bond distance between the residue 44 peptide nitrogen and the Cys42 gamma-sulfur decreases by 0.32 A compared to the analogous distances in the wild-type Cp Rd crystal structure. The results described herein support the prediction that the identity of residue 44 alone determines whether a Rd reduction potential of about -50 or 0 mV is observed.
-
==About this Structure==
+
Modulation of the redox potential of the [Fe(SCys)(4)] site in rubredoxin by the orientation of a peptide dipole.,Eidsness MK, Burden AE, Richie KA, Kurtz DM Jr, Scott RA, Smith ET, Ichiye T, Beard B, Min T, Kang C Biochemistry. 1999 Nov 9;38(45):14803-9. PMID:10555962<ref>PMID:10555962</ref>
-
1C09 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Clostridium_pasteurianum Clostridium pasteurianum] with FE as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1C09 OCA].
+
-
==Reference==
+
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
-
Modulation of the redox potential of the [Fe(SCys)(4)] site in rubredoxin by the orientation of a peptide dipole., Eidsness MK, Burden AE, Richie KA, Kurtz DM Jr, Scott RA, Smith ET, Ichiye T, Beard B, Min T, Kang C, Biochemistry. 1999 Nov 9;38(45):14803-9. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=10555962 10555962]
+
</div>
-
[[Category: Clostridium pasteurianum]]
+
<div class="pdbe-citations 1c09" style="background-color:#fffaf0;"></div>
-
[[Category: Single protein]]
+
-
[[Category: Beard, B.]]
+
-
[[Category: Kang, C.]]
+
-
[[Category: Min, T.]]
+
-
[[Category: FE]]
+
-
[[Category: 3d-structure]]
+
-
[[Category: iron]]
+
-
[[Category: metal-binding]]
+
-
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 12:03:29 2007''
+
==See Also==
 +
*[[Rubredoxin 3D structures|Rubredoxin 3D structures]]
 +
*[[Rubredoxin PDB structures|Rubredoxin PDB structures]]
 +
== References ==
 +
<references/>
 +
__TOC__
 +
</StructureSection>
 +
[[Category: Clostridium pasteurianum]]
 +
[[Category: Large Structures]]
 +
[[Category: Beard B]]
 +
[[Category: Kang C]]
 +
[[Category: Min T]]

Current revision

RUBREDOXIN V44A CP

PDB ID 1c09

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools