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Open data
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Basic information
Entry | Database: PDB / ID: 2pd5 | ||||||
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Title | Human aldose reductase mutant V47I complexed with zopolrestat | ||||||
![]() | Aldose reductase | ||||||
![]() | OXIDOREDUCTASE / TIM barrel / V47I mutant | ||||||
Function / homology | ![]() glyceraldehyde oxidoreductase activity / Fructose biosynthesis / fructose biosynthetic process / L-glucuronate reductase activity / aldose reductase / D/L-glyceraldehyde reductase / glycerol dehydrogenase (NADP+) activity / C21-steroid hormone biosynthetic process / NADP-retinol dehydrogenase / Pregnenolone biosynthesis ...glyceraldehyde oxidoreductase activity / Fructose biosynthesis / fructose biosynthetic process / L-glucuronate reductase activity / aldose reductase / D/L-glyceraldehyde reductase / glycerol dehydrogenase (NADP+) activity / C21-steroid hormone biosynthetic process / NADP-retinol dehydrogenase / Pregnenolone biosynthesis / allyl-alcohol dehydrogenase / allyl-alcohol dehydrogenase activity / L-ascorbic acid biosynthetic process / prostaglandin H2 endoperoxidase reductase activity / metanephric collecting duct development / regulation of urine volume / all-trans-retinol dehydrogenase (NADP+) activity / daunorubicin metabolic process / doxorubicin metabolic process / retinal dehydrogenase activity / aldose reductase (NADPH) activity / epithelial cell maturation / retinoid metabolic process / cellular hyperosmotic salinity response / renal water homeostasis / carbohydrate metabolic process / electron transfer activity / negative regulation of apoptotic process / mitochondrion / extracellular space / extracellular exosome / nucleoplasm / cytosol Similarity search - Function | ||||||
Biological species | ![]() | ||||||
Method | ![]() ![]() | ||||||
![]() | Steuber, H. / Heine, A. / Klebe, G. | ||||||
![]() | ![]() Title: Merging the binding sites of aldose and aldehyde reductase for detection of inhibitor selectivity-determining features. Authors: Steuber, H. / Heine, A. / Podjarny, A. / Klebe, G. | ||||||
History |
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Structure visualization
Structure viewer | Molecule: ![]() ![]() |
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Downloads & links
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Download
PDBx/mmCIF format | ![]() | 87.8 KB | Display | ![]() |
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PDB format | ![]() | 63.5 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Summary document | ![]() | 971.6 KB | Display | ![]() |
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Full document | ![]() | 978.3 KB | Display | |
Data in XML | ![]() | 18 KB | Display | |
Data in CIF | ![]() | 26.6 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 2pd9C ![]() 2pdbC ![]() 2pdcC ![]() 2pdfC ![]() 2pdgC ![]() 2pdhC ![]() 2pdiC ![]() 2pdjC ![]() 2pdkC ![]() 2pdlC ![]() 2pdmC ![]() 2pdnC ![]() 2pdpC ![]() 2pdqC ![]() 2pduC ![]() 2pdwC ![]() 2pdxC ![]() 2pdyC ![]() 1el3S C: citing same article ( S: Starting model for refinement |
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Similar structure data |
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Links
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Assembly
Deposited unit | ![]()
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1 |
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Unit cell |
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Details | The asymmetric unit contains one biological monomer. |
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Components
#1: Protein | Mass: 35912.367 Da / Num. of mol.: 1 / Mutation: V47I Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() ![]() |
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#2: Chemical | ChemComp-NAP / |
#3: Chemical | ChemComp-ZST / |
#4: Water | ChemComp-HOH / |
-Experimental details
-Experiment
Experiment | Method: ![]() |
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Sample preparation
Crystal | Density Matthews: 2.2 Å3/Da / Density % sol: 44.87 % |
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Crystal grow | Temperature: 293 K / Method: vapor diffusion, hanging drop / pH: 5 Details: 20 % PEG 6000 in 120 mM ammonium citrate, pH 5.0, VAPOR DIFFUSION, HANGING DROP, temperature 293K |
-Data collection
Diffraction | Mean temperature: 100 K |
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Diffraction source | Source: ![]() |
Detector | Type: RIGAKU RAXIS IV / Detector: IMAGE PLATE / Date: Oct 4, 2005 / Details: mirrors |
Radiation | Monochromator: graphite / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 1.5418 Å / Relative weight: 1 |
Reflection | Resolution: 1.6→50 Å / Num. all: 37079 / Num. obs: 37079 / % possible obs: 90 % / Redundancy: 2.2 % / Rmerge(I) obs: 0.032 / Rsym value: 3.2 / Net I/σ(I): 26.7 |
Reflection shell | Resolution: 1.6→1.63 Å / Redundancy: 2.2 % / Rmerge(I) obs: 0.115 / Mean I/σ(I) obs: 10.6 / Num. unique all: 1257 / Rsym value: 11.5 / % possible all: 59.6 |
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Processing
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Refinement | Method to determine structure: ![]() Starting model: 1el3 Resolution: 1.6→30 Å / Num. parameters: 11744 / Num. restraintsaints: 10909 / Cross valid method: FREE R / σ(F): 0 / σ(I): 0 / Stereochemistry target values: ENGH AND HUBER Details: ANISOTROPIC SCALING APPLIED BY THE METHOD OF PARKIN, MOEZZI & HOPE, J.APPL.CRYST.28(1995)53-56
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Refine analyze | Num. disordered residues: 9 / Occupancy sum hydrogen: 2528 / Occupancy sum non hydrogen: 2898 | |||||||||||||||||||||||||||||||||
Refinement step | Cycle: LAST / Resolution: 1.6→30 Å
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Refine LS restraints |
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