1qoi

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(New page: 200px<br /> <applet load="1qoi" size="450" color="white" frame="true" align="right" spinBox="true" caption="1qoi, resolution 2.00&Aring;" /> '''U4/U6 SNRNP-SPECIFI...)
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'''U4/U6 SNRNP-SPECIFIC CYCLOPHILIN SNUCYP-20'''<br />
'''U4/U6 SNRNP-SPECIFIC CYCLOPHILIN SNUCYP-20'''<br />
==Overview==
==Overview==
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The cyclophilin SnuCyp-20 is a specific component of the human U4/U6 small, nuclear ribonucleoprotein particle involved in the nuclear splicing of, pre-mRNA. It stably associates with the U4/U6-60kD and -90kD proteins, the, human orthologues of the Saccharomyces cerevisiae Prp4 and Prp3 splicing, factors. We have determined the crystal structure of SnuCyp-20 at 2.0-A, resolution by molecular replacement. The structure of SnuCyp-20 closely, resembles that of human cyclophilin A (hCypA). In particular, the, catalytic centers of SnuCyp-20 and hCypA superimpose perfectly, which is, reflected by the observed peptidyl-prolyl-cis/trans-isomerase activity of, SnuCyp-20. The surface properties of both proteins, however, differ, significantly. Apart from seven additional amino-terminal residues, the, insertion of five amino acids in the loop alpha1-beta3 and of one amino, acid in the loop alpha2-beta8 changes the conformations of both loops. The, enlarged loop alpha1-beta3 is involved in the formation of a wide cleft, with predominantly hydrophobic character. We propose that this enlarged, loop is required for the interaction with the U4/U6-60kD protein.
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The cyclophilin SnuCyp-20 is a specific component of the human U4/U6 small nuclear ribonucleoprotein particle involved in the nuclear splicing of pre-mRNA. It stably associates with the U4/U6-60kD and -90kD proteins, the human orthologues of the Saccharomyces cerevisiae Prp4 and Prp3 splicing factors. We have determined the crystal structure of SnuCyp-20 at 2.0-A resolution by molecular replacement. The structure of SnuCyp-20 closely resembles that of human cyclophilin A (hCypA). In particular, the catalytic centers of SnuCyp-20 and hCypA superimpose perfectly, which is reflected by the observed peptidyl-prolyl-cis/trans-isomerase activity of SnuCyp-20. The surface properties of both proteins, however, differ significantly. Apart from seven additional amino-terminal residues, the insertion of five amino acids in the loop alpha1-beta3 and of one amino acid in the loop alpha2-beta8 changes the conformations of both loops. The enlarged loop alpha1-beta3 is involved in the formation of a wide cleft with predominantly hydrophobic character. We propose that this enlarged loop is required for the interaction with the U4/U6-60kD protein.
==Disease==
==Disease==
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==About this Structure==
==About this Structure==
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1QOI is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1QOI OCA].
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1QOI is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1QOI OCA].
==Reference==
==Reference==
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[[Category: spliceosomal]]
[[Category: spliceosomal]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 18:55:10 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:41:56 2008''

Revision as of 12:42, 21 February 2008


1qoi, resolution 2.00Å

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U4/U6 SNRNP-SPECIFIC CYCLOPHILIN SNUCYP-20

Contents

Overview

The cyclophilin SnuCyp-20 is a specific component of the human U4/U6 small nuclear ribonucleoprotein particle involved in the nuclear splicing of pre-mRNA. It stably associates with the U4/U6-60kD and -90kD proteins, the human orthologues of the Saccharomyces cerevisiae Prp4 and Prp3 splicing factors. We have determined the crystal structure of SnuCyp-20 at 2.0-A resolution by molecular replacement. The structure of SnuCyp-20 closely resembles that of human cyclophilin A (hCypA). In particular, the catalytic centers of SnuCyp-20 and hCypA superimpose perfectly, which is reflected by the observed peptidyl-prolyl-cis/trans-isomerase activity of SnuCyp-20. The surface properties of both proteins, however, differ significantly. Apart from seven additional amino-terminal residues, the insertion of five amino acids in the loop alpha1-beta3 and of one amino acid in the loop alpha2-beta8 changes the conformations of both loops. The enlarged loop alpha1-beta3 is involved in the formation of a wide cleft with predominantly hydrophobic character. We propose that this enlarged loop is required for the interaction with the U4/U6-60kD protein.

Disease

Known diseases associated with this structure: Cardiomyopathy, dilated OMIM:[605906], Cardiomyopathy, dilated, with left ventricular noncompaction OMIM:[605906], Myopathy, myofibrillar, ZASP-related OMIM:[605906]

About this Structure

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

Reference

Crystal structure of the human U4/U6 small nuclear ribonucleoprotein particle-specific SnuCyp-20, a nuclear cyclophilin., Reidt U, Reuter K, Achsel T, Ingelfinger D, Luhrmann R, Ficner R, J Biol Chem. 2000 Mar 17;275(11):7439-42. PMID:10713041

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