3rsp

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==Overview==
==Overview==
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The peptide bonds preceding Pro 93 and Pro 114 of bovine pancreatic, ribonuclease A (RNase A) are in the cis conformation. The trans-to-cis, isomerization of these bonds had been indicted as the slow step during, protein folding. Here, site-directed mutagenesis was used to replace Pro, 93 or Pro 114 with a glycine residue, and the crystalline structure of the, P93G variant was determined by X-ray diffraction analysis to a resolution, of 1.7 A. This structure is essentially identical to that of the wild-type, protein, except for the 91-94 beta-turn containing the substitution. In, the wild-type protein, the beta-turn is of type VIa. In the P93G variant, this turn is of type II with the peptide bond preceding Gly 93 being, trans. The thermal stabilities of the P93G and P114G variants were, assessed by differential scanning calorimetry and thermal denaturation, experiments monitored by ultraviolet spectroscopy. The value of delta, deltaGm which reports on the stability lost in the variants, is 1.5-fold, greater for the P114G variant than for the P93G variant. The greater, stability of the P93G variant is likely due to the relatively facile, accommodation of residues 91-94 in a type II turn, which has a preference, for a glycine residue in its i + 2 position.
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The peptide bonds preceding Pro 93 and Pro 114 of bovine pancreatic ribonuclease A (RNase A) are in the cis conformation. The trans-to-cis isomerization of these bonds had been indicted as the slow step during protein folding. Here, site-directed mutagenesis was used to replace Pro 93 or Pro 114 with a glycine residue, and the crystalline structure of the P93G variant was determined by X-ray diffraction analysis to a resolution of 1.7 A. This structure is essentially identical to that of the wild-type protein, except for the 91-94 beta-turn containing the substitution. In the wild-type protein, the beta-turn is of type VIa. In the P93G variant, this turn is of type II with the peptide bond preceding Gly 93 being trans. The thermal stabilities of the P93G and P114G variants were assessed by differential scanning calorimetry and thermal denaturation experiments monitored by ultraviolet spectroscopy. The value of delta deltaGm which reports on the stability lost in the variants, is 1.5-fold greater for the P114G variant than for the P93G variant. The greater stability of the P93G variant is likely due to the relatively facile accommodation of residues 91-94 in a type II turn, which has a preference for a glycine residue in its i + 2 position.
==About this Structure==
==About this Structure==
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[[Category: Pancreatic ribonuclease]]
[[Category: Pancreatic ribonuclease]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Hargraves, S.R.]]
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[[Category: Hargraves, S R.]]
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[[Category: Klink, T.A.]]
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[[Category: Klink, T A.]]
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[[Category: Raines, R.T.]]
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[[Category: Raines, R T.]]
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[[Category: Schultz, L.W.]]
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[[Category: Schultz, L W.]]
[[Category: CL]]
[[Category: CL]]
[[Category: endonuclease]]
[[Category: endonuclease]]
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[[Category: x-ray diffraction]]
[[Category: x-ray diffraction]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Feb 3 10:52:32 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 19:11:14 2008''

Revision as of 17:11, 21 February 2008


3rsp, resolution 1.7Å

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STRUCTURE OF THE P93G VARIANT OF RIBONUCLEASE A

Overview

The peptide bonds preceding Pro 93 and Pro 114 of bovine pancreatic ribonuclease A (RNase A) are in the cis conformation. The trans-to-cis isomerization of these bonds had been indicted as the slow step during protein folding. Here, site-directed mutagenesis was used to replace Pro 93 or Pro 114 with a glycine residue, and the crystalline structure of the P93G variant was determined by X-ray diffraction analysis to a resolution of 1.7 A. This structure is essentially identical to that of the wild-type protein, except for the 91-94 beta-turn containing the substitution. In the wild-type protein, the beta-turn is of type VIa. In the P93G variant, this turn is of type II with the peptide bond preceding Gly 93 being trans. The thermal stabilities of the P93G and P114G variants were assessed by differential scanning calorimetry and thermal denaturation experiments monitored by ultraviolet spectroscopy. The value of delta deltaGm which reports on the stability lost in the variants, is 1.5-fold greater for the P114G variant than for the P93G variant. The greater stability of the P93G variant is likely due to the relatively facile accommodation of residues 91-94 in a type II turn, which has a preference for a glycine residue in its i + 2 position.

About this Structure

3RSP is a Single protein structure of sequence from Bos taurus with as ligand. Active as Pancreatic ribonuclease, with EC number 3.1.27.5 Known structural/functional Sites: , , and . Full crystallographic information is available from OCA.

Reference

Structure and stability of the P93G variant of ribonuclease A., Schultz LW, Hargraves SR, Klink TA, Raines RT, Protein Sci. 1998 Jul;7(7):1620-5. PMID:9684895

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