1ton
From Proteopedia
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|PDB= 1ton |SIZE=350|CAPTION= <scene name='initialview01'>1ton</scene>, resolution 1.8Å | |PDB= 1ton |SIZE=350|CAPTION= <scene name='initialview01'>1ton</scene>, resolution 1.8Å | ||
|SITE= | |SITE= | ||
| - | |LIGAND= <scene name='pdbligand=ZN:ZINC ION'>ZN</scene> | + | |LIGAND= <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene> |
|ACTIVITY= | |ACTIVITY= | ||
|GENE= | |GENE= | ||
| + | |DOMAIN= | ||
| + | |RELATEDENTRY= | ||
| + | |RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1ton FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1ton OCA], [http://www.ebi.ac.uk/pdbsum/1ton PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1ton RCSB]</span> | ||
}} | }} | ||
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[[Category: Fujinaga, M.]] | [[Category: Fujinaga, M.]] | ||
[[Category: James, M N.G.]] | [[Category: James, M N.G.]] | ||
| - | [[Category: ZN]] | ||
[[Category: hydrolase(serine proteinase)]] | [[Category: hydrolase(serine proteinase)]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 23:58:59 2008'' |
Revision as of 20:59, 30 March 2008
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| , resolution 1.8Å | |||||||
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| Ligands: | |||||||
| Resources: | FirstGlance, OCA, PDBsum, RCSB | ||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||
RAT SUBMAXILLARY GLAND SERINE PROTEASE, TONIN. STRUCTURE SOLUTION AND REFINEMENT AT 1.8 ANGSTROMS RESOLUTION
Overview
Tonin is a mammalian serine protease that is capable of generating the vasoconstrictive agent, angiotensin II, directly from its precursor protein, angiotensinogen, a process that normally requires two enzymes, renin and angiotensin-converting enzyme. The X-ray crystallographic structure determination and refinement of tonin at 1.8 A resolution and the analysis of the resulting model are reported. The initial phases were obtained by the method of molecular replacement using as the search model the structure of bovine trypsin. The refined model of tonin consists of 227 amino acid residues out of the 235 in the complete molecule, 149 water molecules, and one zinc ion. The R-factor (R = sigma Fo - Fc/sigma Fo) is 0.196 for the 14,997 measured data between 8 and 1.8 A resolution with I greater than or equal to sigma (I). It is estimated that the overall root-mean-square error in the coordinates is about 0.3 A. The structure of tonin that has been determined is not in its active conformation, but one that has been perturbed by the binding of Zn2+ in the active site. Zn2+ was included in the buffer to aid the crystallization. Nevertheless, the structure of tonin that is described is for the most part similar to its native form as indicated by the close tertiary structural homology with kallikrein. The differences in the structures of the two enzymes are concentrated in several loop regions; these structural differences are probably responsible for the differences in their reactivities and specificities.
About this Structure
1TON is a Single protein structure of sequence from Rattus rattus. Full crystallographic information is available from OCA.
Reference
Rat submaxillary gland serine protease, tonin. Structure solution and refinement at 1.8 A resolution., Fujinaga M, James MN, J Mol Biol. 1987 May 20;195(2):373-96. PMID:2821276
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