1ipf
From Proteopedia
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|PDB= 1ipf |SIZE=350|CAPTION= <scene name='initialview01'>1ipf</scene>, resolution 2.50Å | |PDB= 1ipf |SIZE=350|CAPTION= <scene name='initialview01'>1ipf</scene>, resolution 2.50Å | ||
|SITE= | |SITE= | ||
| - | |LIGAND= <scene name='pdbligand=NDP:NADPH+DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE+PHOSPHATE'>NDP</scene> | + | |LIGAND= <scene name='pdbligand=NDP:NADPH+DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE+PHOSPHATE'>NDP</scene>, <scene name='pdbligand=TNE:8-METHYL-8-AZABICYCLO[3,2,1]OCTAN-3-ONE'>TNE</scene> |
| - | |ACTIVITY= [http://en.wikipedia.org/wiki/Tropinone_reductase_II Tropinone reductase II], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.1.1.236 1.1.1.236] | + | |ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Tropinone_reductase_II Tropinone reductase II], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.1.1.236 1.1.1.236] </span> |
|GENE= | |GENE= | ||
| + | |DOMAIN= | ||
| + | |RELATEDENTRY=[[1ipe|1IPE]] | ||
| + | |RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1ipf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1ipf OCA], [http://www.ebi.ac.uk/pdbsum/1ipf PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1ipf RCSB]</span> | ||
}} | }} | ||
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[[Category: Yamada, Y.]] | [[Category: Yamada, Y.]] | ||
[[Category: Yamashita, A.]] | [[Category: Yamashita, A.]] | ||
| - | [[Category: NDP]] | ||
| - | [[Category: TNE]] | ||
[[Category: laue diffraction]] | [[Category: laue diffraction]] | ||
[[Category: oxidoreductase]] | [[Category: oxidoreductase]] | ||
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[[Category: tropinone]] | [[Category: tropinone]] | ||
| - | ''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 21:22:51 2008'' |
Revision as of 18:22, 30 March 2008
| |||||||
| , resolution 2.50Å | |||||||
|---|---|---|---|---|---|---|---|
| Ligands: | , | ||||||
| Activity: | Tropinone reductase II, with EC number 1.1.1.236 | ||||||
| Related: | 1IPE
| ||||||
| Resources: | FirstGlance, OCA, PDBsum, RCSB | ||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||
TROPINONE REDUCTASE-II COMPLEXED WITH NADPH AND TROPINONE
Overview
To understand the catalytic mechanism of an enzyme, it is crucial to determine the crystallographic structures corresponding to the individual reaction steps. Here, we report two crystal structures of enzyme-substrate complexes prior to reaction initiation: tropinone reductase-II (TR-II)-NADPH and TR-II-NADPH-tropinone complexes, determined from the identical crystals. A combination of two kinetic crystallographic techniques, a continuous flow of the substrates and Laue diffraction measurements, enabled us to capture the transit structures prior to the reaction proceeding. A structure comparison of the enzyme-substrate complex elucidated in this study with the enzyme-product complex in our previous study indicates that one of the substrates, tropinone, is rotated relative to the product so as to make the spatial organization in the active site favorable for the reaction to proceed. Side chains of the residues in the active site also alter their conformations to keep the complementarity of the space for the substrate or the product and to assist the rotational movement.
About this Structure
1IPF is a Single protein structure of sequence from Datura stramonium. Full crystallographic information is available from OCA.
Reference
Capturing enzyme structure prior to reaction initiation: tropinone reductase-II-substrate complexes., Yamashita A, Endo M, Higashi T, Nakatsu T, Yamada Y, Oda J, Kato H, Biochemistry. 2003 May 20;42(19):5566-73. PMID:12741812
Page seeded by OCA on Sun Mar 30 21:22:51 2008
Categories: Datura stramonium | Single protein | Tropinone reductase II | Endo, M. | Higashi, T. | Kato, H. | Nakatsu, T. | Oda, J. | RSGI, RIKEN Structural Genomics/Proteomics Initiative. | Yamada, Y. | Yamashita, A. | Laue diffraction | Oxidoreductase | Reduction of tropinone to pseudotropine | Riken structural genomics/proteomics initiative | Rsgi | Short-chain dehydrogenase | Structural genomic | Tropane alkaloid biosynthesis | Tropinone
