This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.


Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.


1xrz

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
[[Image:1xrz.jpg|left|200px]]<br /><applet load="1xrz" size="350" color="white" frame="true" align="right" spinBox="true"
+
[[Image:1xrz.jpg|left|200px]]
-
caption="1xrz" />
+
 
-
'''NMR Structure of a Zinc Finger with Cyclohexanylalanine Substituted for the Central Aromatic Residue'''<br />
+
{{Structure
 +
|PDB= 1xrz |SIZE=350|CAPTION= <scene name='initialview01'>1xrz</scene>
 +
|SITE=
 +
|LIGAND= <scene name='pdbligand=ZN:ZINC ION'>ZN</scene>
 +
|ACTIVITY=
 +
|GENE=
 +
}}
 +
 
 +
'''NMR Structure of a Zinc Finger with Cyclohexanylalanine Substituted for the Central Aromatic Residue'''
 +
 
==Overview==
==Overview==
Line 10: Line 19:
==About this Structure==
==About this Structure==
-
1XRZ is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/ ] with <scene name='pdbligand=ZN:'>ZN</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1XRZ OCA].
+
1XRZ is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1XRZ OCA].
==Reference==
==Reference==
-
Solvation and the hidden thermodynamics of a zinc finger probed by nonstandard repair of a protein crevice., Lachenmann MJ, Ladbury JE, Qian X, Huang K, Singh R, Weiss MA, Protein Sci. 2004 Dec;13(12):3115-26. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=15557258 15557258]
+
Solvation and the hidden thermodynamics of a zinc finger probed by nonstandard repair of a protein crevice., Lachenmann MJ, Ladbury JE, Qian X, Huang K, Singh R, Weiss MA, Protein Sci. 2004 Dec;13(12):3115-26. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15557258 15557258]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Huang, K.]]
[[Category: Huang, K.]]
Line 25: Line 34:
[[Category: zinc finger]]
[[Category: zinc finger]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:58:02 2008''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 15:13:49 2008''

Revision as of 13:13, 20 March 2008


PDB ID 1xrz

Drag the structure with the mouse to rotate
Ligands:
Coordinates: save as pdb, mmCIF, xml



NMR Structure of a Zinc Finger with Cyclohexanylalanine Substituted for the Central Aromatic Residue


Contents

Overview

The classical Zn finger contains a phenylalanine at the crux of its three architectural elements: a beta-hairpin, an alpha-helix, and a Zn(2+)-binding site. Surprisingly, phenylalanine is not required for high-affinity Zn2+ binding, but instead contributes to the specification of a precise DNA-binding surface. Substitution of phenylalanine by leucine leads to a floppy but native-like structure whose Zn affinity is maintained by marked entropy-enthalpy compensation (DeltaDeltaH -8.3 kcal/mol and -TDeltaDeltaS 7.7 kcal/mol). Phenylalanine and leucine differ in shape, size, and aromaticity. To distinguish which features correlate with dynamic stability, we have investigated a nonstandard finger containing cyclohexanylalanine at this site. The structure of the nonstandard finger is similar to that of the native domain. The cyclohexanyl ring assumes a chair conformation, and conformational fluctuations characteristic of the leucine variant are damped. Although the nonstandard finger exhibits a lower affinity for Zn2+ than does the native domain (DeltaDeltaG -1.2 kcal/mol), leucine-associated perturbations in enthalpy and entropy are almost completely attenuated (DeltaDeltaH -0.7 kcal/mol and -TDeltaDeltaS -0.5 kcal/mol). Strikingly, global changes in entropy (as inferred from calorimetry) are in each case opposite in sign from changes in configurational entropy (as inferred from NMR). This seeming paradox suggests that enthalpy-entropy compensation is dominated by solvent reorganization rather than nominal molecular properties. Together, these results demonstrate that dynamic and thermodynamic perturbations correlate with formation or repair of a solvated packing defect rather than type of physical interaction (aromatic or aliphatic) within the core.

Disease

Known disease associated with this structure: Spastic paraplegia 33 OMIM:[610243]

About this Structure

1XRZ is a Single protein structure of sequence from [1]. Full crystallographic information is available from OCA.

Reference

Solvation and the hidden thermodynamics of a zinc finger probed by nonstandard repair of a protein crevice., Lachenmann MJ, Ladbury JE, Qian X, Huang K, Singh R, Weiss MA, Protein Sci. 2004 Dec;13(12):3115-26. PMID:15557258

Page seeded by OCA on Thu Mar 20 15:13:49 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools