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Open data
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Basic information
Entry | Database: PDB / ID: 1gbj | |||||||||
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Title | ALPHA-LYTIC PROTEASE WITH MET 190 REPLACED BY ALA | |||||||||
![]() | ALPHA-LYTIC PROTEASE | |||||||||
![]() | HYDROLASE (SERINE PROTEINASE) / ACTIVE-SITE MUTATION | |||||||||
Function / homology | ![]() alpha-lytic endopeptidase / serine-type endopeptidase activity / proteolysis / extracellular region Similarity search - Function | |||||||||
Biological species | ![]() | |||||||||
Method | ![]() | |||||||||
![]() | Mace, J.E. / Agard, D.A. | |||||||||
![]() | ![]() Title: Kinetic and structural characterization of mutations of glycine 216 in alpha-lytic protease: a new target for engineering substrate specificity. Authors: Mace, J.E. / Agard, D.A. #1: ![]() Title: Structural Basis for Broad Specificity in Alpha-Lytic Protease Authors: Bone, R. / Fujushige, A. / Kettner, C.A. / Agard, D.A. #2: ![]() Title: Structural Plasticity Broadens the Specificity of an Engineered Protease Authors: Bone, R. / Silen, J.L. / Agard, D.A. #3: ![]() Title: Structural Analysis of Specificity: Alpha-Lytic Protease Complexes with Analogues of Reaction Intermediates Authors: Bone, R. / Frank, D. / Kettner, D. / Agard, D.A. #4: ![]() Title: Serine Protease Mechanism: Structure of an Inhibitory Complex of Alpha-Lytic Protease and a Tightly Bound Peptide Boronic Acid Authors: Bone, R. / Shenvi, A.B. / Kettner, C.A. / Agard, D.A. #5: ![]() Title: Refined Structure of Alpha-Lytic Protease at 1.7 Angstroms Resolution. Analysis of Hydrogen Bonding and Solvent Structure Authors: Fujinaga, M. / Delbaere, L.T.J. / Brayer, G.D. / James, M.N.G. #6: ![]() Title: Molecular Structure of the Alpha-Lytic Protease from Myxobacter 495 at 2.8 Angstroms Resolution Authors: Brayer, G.D. / Delbaere, L.T.J. / James, M.N.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 | ![]() | 48 KB | Display | ![]() |
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PDB format | ![]() | 36.5 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Summary document | ![]() | 415.9 KB | Display | ![]() |
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Full document | ![]() | 417.1 KB | Display | |
Data in XML | ![]() | 11.2 KB | Display | |
Data in CIF | ![]() | 15.8 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 1gbaC ![]() 1gbbC ![]() 1gbcC ![]() 1gbdC ![]() 1gbeC ![]() 1gbfC ![]() 1gbhC ![]() 1gbiC ![]() 1gbkC ![]() 1gblC ![]() 1gbmC C: citing same article ( |
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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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Atom site foot note | 1: CIS PROLINE - PRO A 95 |
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Components
#1: Protein | Mass: 19815.014 Da / Num. of mol.: 1 / Mutation: M190A Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() ![]() | ||
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#2: Chemical | #3: Water | ChemComp-HOH / | |
-Experimental details
-Experiment
Experiment | Method: ![]() |
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Sample preparation
Crystal | Density Matthews: 2.56 Å3/Da / Density % sol: 51.95 % | ||||||||||||||||||
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Crystal | *PLUS Density % sol: 48.2 % | ||||||||||||||||||
Crystal grow | *PLUS Temperature: 4 ℃ / pH: 8 / Method: vapor diffusion, hanging drop | ||||||||||||||||||
Components of the solutions | *PLUS
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-Data collection
Diffraction source | Wavelength: 1.5418 |
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Detector | Type: RIGAKU / Detector: IMAGE PLATE / Date: Oct 26, 1990 |
Radiation | Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 1.5418 Å / Relative weight: 1 |
Reflection | Resolution: 2→17.5 Å / Num. obs: 13873 / % possible obs: 98 % |
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Processing
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Refinement | Resolution: 2→17.5 Å / σ(F): 2 /
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Refinement step | Cycle: LAST / Resolution: 2→17.5 Å
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Refine LS restraints |
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Software | *PLUS Name: ![]() | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Refinement | *PLUS | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Solvent computation | *PLUS | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Displacement parameters | *PLUS | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Refine LS restraints | *PLUS
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