2b7u

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[[Image:2b7u.gif|left|200px]]
[[Image:2b7u.gif|left|200px]]
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{{Structure
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|PDB= 2b7u |SIZE=350|CAPTION= <scene name='initialview01'>2b7u</scene>, resolution 1.60&Aring;
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The line below this paragraph, containing "STRUCTURE_2b7u", creates the "Structure Box" on the page.
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|SITE=
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=MES:2-(N-MORPHOLINO)-ETHANESULFONIC+ACID'>MES</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/rRNA_N-glycosylase rRNA N-glycosylase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.2.22 3.2.2.22] </span>
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or leave the SCENE parameter empty for the default display.
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|GENE=
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|DOMAIN=
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{{STRUCTURE_2b7u| PDB=2b7u | SCENE= }}
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|RELATEDENTRY=[[1nio|1NIO]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2b7u FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2b7u OCA], [http://www.ebi.ac.uk/pdbsum/2b7u PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2b7u RCSB]</span>
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}}
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'''Ribosome inactivating protein type 1 from Charybdis maritima AGG'''
'''Ribosome inactivating protein type 1 from Charybdis maritima AGG'''
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==About this Structure==
==About this Structure==
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2B7U is a [[Protein complex]] structure of sequences from [http://en.wikipedia.org/wiki/Charybdis_maritima Charybdis maritima]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2B7U OCA].
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Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2B7U OCA].
==Reference==
==Reference==
Isolation, characterization, sequencing and crystal structure of charybdin, a type 1 ribosome-inactivating protein from Charybdis maritima agg., Touloupakis E, Gessmann R, Kavelaki K, Christofakis E, Petratos K, Ghanotakis DF, FEBS J. 2006 Jun;273(12):2684-92. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/16817896 16817896]
Isolation, characterization, sequencing and crystal structure of charybdin, a type 1 ribosome-inactivating protein from Charybdis maritima agg., Touloupakis E, Gessmann R, Kavelaki K, Christofakis E, Petratos K, Ghanotakis DF, FEBS J. 2006 Jun;273(12):2684-92. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/16817896 16817896]
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[[Category: Charybdis maritima]]
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[[Category: RRNA N-glycosylase]]
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[[Category: Protein complex]]
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[[Category: rRNA N-glycosylase]]
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[[Category: Gessmann, R.]]
[[Category: Gessmann, R.]]
[[Category: Petratos, K.]]
[[Category: Petratos, K.]]
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[[Category: ribosome inactivating protein]]
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[[Category: Ribosome inactivating protein]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 19:57:52 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 02:02:38 2008''
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Revision as of 16:57, 3 May 2008

Template:STRUCTURE 2b7u

Ribosome inactivating protein type 1 from Charybdis maritima AGG


Overview

A novel, type 1 ribosome-inactivating protein designated charybdin was isolated from bulbs of Charybdis maritima agg. The protein, consisting of a single polypeptide chain with a molecular mass of 29 kDa, inhibited translation in rabbit reticulocytes with an IC50 of 27.2 nm. Plant genomic DNA extracted from the bulb was amplified by PCR between primers based on the N-terminal and C-terminal sequence of the protein from dissolved crystals. The complete mature protein sequence was derived by partial DNA sequencing and terminal protein sequencing, and was confirmed by high-resolution crystal structure analysis. The protein contains Val at position 79 instead of the conserved Tyr residue of the ribosome-inactivating proteins known to date. To our knowledge, this is the first observation of a natural substitution of a catalytic residue at the active site of a natural ribosome-inactivating protein. This substitution in the active site may be responsible for the relatively low in vitro translation inhibitory effect compared with other ribosome-inactivating proteins. Single crystals were grown in the cold room from PEG6000 solutions. Diffraction data collected to 1.6 A resolution were used to determine the protein structure by the molecular replacement method. The fold of the protein comprises two structural domains: an alpha + beta N-terminal domain (residues 4-190) and a mainly alpha-helical C-terminal domain (residues 191-257). The active site is located in the interface between the two domains and comprises residues Val79, Tyr117, Glu167 and Arg170.

About this Structure

Full crystallographic information is available from OCA.

Reference

Isolation, characterization, sequencing and crystal structure of charybdin, a type 1 ribosome-inactivating protein from Charybdis maritima agg., Touloupakis E, Gessmann R, Kavelaki K, Christofakis E, Petratos K, Ghanotakis DF, FEBS J. 2006 Jun;273(12):2684-92. PMID:16817896 Page seeded by OCA on Sat May 3 19:57:52 2008

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