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Yorodumi- PDB-1pkn: STRUCTURE OF RABBIT MUSCLE PYRUVATE KINASE COMPLEXED WITH MN2+, K... -
+Open data
-Basic information
Entry | Database: PDB / ID: 1pkn | |||||||||
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Title | STRUCTURE OF RABBIT MUSCLE PYRUVATE KINASE COMPLEXED WITH MN2+, K+, AND PYRUVATE | |||||||||
Components | PYRUVATE KINASE | |||||||||
Keywords | PHOSPHOTRANSFERASE | |||||||||
Function / homology | Function and homology information pyruvate kinase / pyruvate kinase activity / positive regulation of cytoplasmic translation / positive regulation of sprouting angiogenesis / potassium ion binding / rough endoplasmic reticulum / non-specific protein-tyrosine kinase / cellular response to insulin stimulus / protein tyrosine kinase activity / non-specific serine/threonine protein kinase ...pyruvate kinase / pyruvate kinase activity / positive regulation of cytoplasmic translation / positive regulation of sprouting angiogenesis / potassium ion binding / rough endoplasmic reticulum / non-specific protein-tyrosine kinase / cellular response to insulin stimulus / protein tyrosine kinase activity / non-specific serine/threonine protein kinase / mRNA binding / magnesium ion binding / ATP binding / nucleus Similarity search - Function | |||||||||
Biological species | Oryctolagus cuniculus (rabbit) | |||||||||
Method | X-RAY DIFFRACTION / Resolution: 2.9 Å | |||||||||
Authors | Larsen, T.M. / Laughlin, L.T. / Holden, H.M. / Rayment, I. / Reed, G.H. | |||||||||
Citation | Journal: Biochemistry / Year: 1994 Title: Structure of rabbit muscle pyruvate kinase complexed with Mn2+, K+, and pyruvate. Authors: Larsen, T.M. / Laughlin, L.T. / Holden, H.M. / Rayment, I. / Reed, G.H. | |||||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 1pkn.cif.gz | 108.1 KB | Display | PDBx/mmCIF format |
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PDB format | pdb1pkn.ent.gz | 81.3 KB | Display | PDB format |
PDBx/mmJSON format | 1pkn.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 1pkn_validation.pdf.gz | 391.6 KB | Display | wwPDB validaton report |
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Full document | 1pkn_full_validation.pdf.gz | 436.7 KB | Display | |
Data in XML | 1pkn_validation.xml.gz | 17.5 KB | Display | |
Data in CIF | 1pkn_validation.cif.gz | 24.9 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/pk/1pkn ftp://data.pdbj.org/pub/pdb/validation_reports/pk/1pkn | HTTPS FTP |
-Related structure data
Similar structure data |
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-Links
-Assembly
Deposited unit |
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1 |
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Unit cell |
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-Components
#1: Protein | Mass: 57797.547 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Oryctolagus cuniculus (rabbit) / References: UniProt: P11974, pyruvate kinase |
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#2: Chemical | ChemComp-K / |
#3: Chemical | ChemComp-MN / |
#4: Chemical | ChemComp-PYR / |
-Experimental details
-Experiment
Experiment | Method: X-RAY DIFFRACTION |
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-Sample preparation
Crystal grow | *PLUS pH: 6 / Method: batch method | ||||||||||||||||||||||||||||||||||||||||||||||||
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Components of the solutions | *PLUS
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-Data collection
Radiation | Scattering type: x-ray |
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Radiation wavelength | Relative weight: 1 |
Reflection | *PLUS Highest resolution: 2.7 Å / Lowest resolution: 100 Å / Num. obs: 104618 / % possible obs: 80 % / Num. measured all: 168794 / Rmerge(I) obs: 0.108 |
Reflection shell | *PLUS Highest resolution: 2.7 Å / Lowest resolution: 2.89 Å / % possible obs: 41 % / Num. unique obs: 9982 / Num. measured obs: 9442 / Rmerge(I) obs: 0.287 |
-Processing
Software | Name: TNT / Classification: refinement | ||||||||||||||||||||||||||||||
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Refinement | Resolution: 2.9→30 Å / Rfactor obs: 0.191 | ||||||||||||||||||||||||||||||
Refinement step | Cycle: LAST / Resolution: 2.9→30 Å
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Refine LS restraints |
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Software | *PLUS Name: TNT / Classification: refinement | ||||||||||||||||||||||||||||||
Refinement | *PLUS Rfactor obs: 0.191 | ||||||||||||||||||||||||||||||
Solvent computation | *PLUS | ||||||||||||||||||||||||||||||
Displacement parameters | *PLUS | ||||||||||||||||||||||||||||||
Refine LS restraints | *PLUS Type: t_angle_d / Dev ideal: 2.8 |