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- PDB-4i9n: Crystal structure of rabbit LDHA in complex with AP28161 and AP28122 -
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Open data
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Basic information
Entry | Database: PDB / ID: 4i9n | ||||||
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Title | Crystal structure of rabbit LDHA in complex with AP28161 and AP28122 | ||||||
![]() | L-lactate dehydrogenase A chain | ||||||
![]() | OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR / cancer / fragment / inhibitor / OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR complex | ||||||
Function / homology | ![]() L-lactate dehydrogenase / lactate metabolic process / L-lactate dehydrogenase activity / pyruvate metabolic process / cytoplasm Similarity search - Function | ||||||
Biological species | ![]() ![]() | ||||||
Method | ![]() ![]() | ||||||
![]() | Zhou, T. / Kohlmann, A. / Stephan, Z.G. / Li, F. / Commodore, L. / Greenfield, M.T. / Shakespeare, W.C. / Zhu, X. / Dalgarno, D.C. | ||||||
![]() | ![]() Title: Fragment growing and linking lead to novel nanomolar lactate dehydrogenase inhibitors. Authors: Kohlmann, A. / Zech, S.G. / Li, F. / Zhou, T. / Squillace, R.M. / Commodore, L. / Greenfield, M.T. / Lu, X. / Miller, D.P. / Huang, W.S. / Qi, J. / Thomas, R.M. / Wang, Y. / Zhang, S. / ...Authors: Kohlmann, A. / Zech, S.G. / Li, F. / Zhou, T. / Squillace, R.M. / Commodore, L. / Greenfield, M.T. / Lu, X. / Miller, D.P. / Huang, W.S. / Qi, J. / Thomas, R.M. / Wang, Y. / Zhang, S. / Dodd, R. / Liu, S. / Xu, R. / Xu, Y. / Miret, J.J. / Rivera, V. / Clackson, T. / Shakespeare, W.C. / Zhu, X. / Dalgarno, D.C. | ||||||
History |
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Structure visualization
Structure viewer | Molecule: ![]() ![]() |
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Downloads & links
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Download
PDBx/mmCIF format | ![]() | 504.1 KB | Display | ![]() |
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PDB format | ![]() | 420.7 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Summary document | ![]() | 4.4 MB | Display | ![]() |
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Full document | ![]() | 4.5 MB | Display | |
Data in XML | ![]() | 103.1 KB | Display | |
Data in CIF | ![]() | 133.8 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 4i8xC ![]() 4i9hC ![]() 4i9uC ![]() 1i10S 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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2 | ![]()
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Unit cell |
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Components
#1: Protein | Mass: 36481.375 Da / Num. of mol.: 8 / Source method: isolated from a natural source / Source: (natural) ![]() ![]() #2: Chemical | ChemComp-1E6 / #3: Chemical | ChemComp-1E5 / #4: Water | ChemComp-HOH / | |
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-Experimental details
-Experiment
Experiment | Method: ![]() |
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Sample preparation
Crystal | Density Matthews: 2.79 Å3/Da / Density % sol: 55.88 % |
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Crystal grow | Temperature: 277 K / Method: vapor diffusion, hanging drop / pH: 8 Details: 0.1 M Tris, pH 8.0, 30% PEG550 MME, VAPOR DIFFUSION, HANGING DROP, temperature 277K |
-Data collection
Diffraction | Mean temperature: 100 K |
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Diffraction source | Source: ![]() |
Detector | Type: RIGAKU RAXIS IV++ / Detector: IMAGE PLATE / Date: Feb 8, 2010 |
Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 1.54 Å / Relative weight: 1 |
Reflection | Resolution: 2.35→50 Å / Num. all: 141773 / Num. obs: 133852 / % possible obs: 94.4 % / Observed criterion σ(F): 2 / Observed criterion σ(I): 2 |
Reflection shell | Highest resolution: 2.35 Å |
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Processing
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Refinement | Method to determine structure: ![]() Starting model: PDB ENTRY 1I10 Resolution: 2.35→50 Å / Occupancy max: 1 / Occupancy min: 0.5 / σ(F): 0 / Stereochemistry target values: Engh & Huber
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Displacement parameters | Biso max: 96.32 Å2 / Biso mean: 30.9829 Å2 / Biso min: 3.65 Å2
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Refinement step | Cycle: LAST / Resolution: 2.35→50 Å
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Refine LS restraints |
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Xplor file |
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