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- PDB-6abp: SUGAR-BINDING AND CRYSTALLOGRAPHIC STUDIES OF AN ARABINOSE-BINDIN... -
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Open data
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Basic information
Entry | Database: PDB / ID: 6abp | |||||||||
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Title | SUGAR-BINDING AND CRYSTALLOGRAPHIC STUDIES OF AN ARABINOSE-BINDING PROTEIN MUTANT (MET108LEU) WHICH EXHIBITS ENHANCED AFFINITY AND ALTERED SPECIFICITY | |||||||||
![]() | L-ARABINOSE-BINDING PROTEIN | |||||||||
![]() | BINDING PROTEINS | |||||||||
Function / homology | ![]() L-arabinose transmembrane transport / ABC-type monosaccharide transporter activity / monosaccharide binding / ATP-binding cassette (ABC) transporter complex, substrate-binding subunit-containing / outer membrane-bounded periplasmic space / carbohydrate binding / membrane Similarity search - Function | |||||||||
Biological species | ![]() ![]() | |||||||||
Method | ![]() | |||||||||
![]() | Vermersch, P.S. / Tesmer, J.J.G. / Quiocho, F.A. | |||||||||
![]() | ![]() Title: Sugar-binding and crystallographic studies of an arabinose-binding protein mutant (Met108Leu) that exhibits enhanced affinity and altered specificity. Authors: Vermersch, P.S. / Lemon, D.D. / Tesmer, J.J. / Quiocho, F.A. #1: ![]() Title: Substrate Specificity and Affinity of a Protein Modulated by Bound Water Molecules Authors: Quiocho, F.A. / Wilson, D.K. / Vyas, N.K. #2: ![]() Title: Novel Stereospecificity of the L-Arabinose-Binding Protein Authors: Quiocho, F.A. / Vyas, N.K. #3: ![]() Title: Hinge-Bending in L-Arabinose-Binding Protein. The "Venus'S-Flytrap" Model Authors: Mao, B. / Pear, M.R. / Mccammon, J.A. / Quiocho, F.A. #4: ![]() Title: Structure of the L-Arabinose-Binding Protein from Escherichia Coli at 2.4 Angstroms Resolution Authors: Gilliland, G.L. / Quiocho, F.A. #5: ![]() Title: L-Arabinose-Binding Protein-Sugar Complex at 2.4 Angstroms Resolution. Stereochemistry and Evidence for a Structural Change Authors: Newcomer, M.E. / Gilliand, G.L. / Quiocho, F.A. #6: ![]() Title: The Radius of Gyration of L-Arabinose-Binding Protein Decreases Upon Binding of Ligand Authors: Newcomer, M.E. / Lewis, B.A. / Quiocho, F.A. #7: ![]() Title: The Thiol Group of the L-Arabinose-Binding Protein. Chromophoric Labeling and Chemical Identification of the Sugar-Binding Site Authors: Miller /III, D.M. / Newcomer, M.E. / Quiocho, F.A. #8: ![]() Title: Location of the Sugar-Binding Site of L-Arabinose-Binding Protein. Sugar Derivative Syntheses, Sugar Binding Specificity, and Difference Fourier Analyses Authors: Newcomer, M.E. / Miller /III, D.M. / Quiocho, F.A. #9: ![]() Title: The 2.8-Angstroms Resolution Structure of the L-Arabinose-Binding Protein from Escherichia Coli Authors: Quiocho, F.A. / Gilliland, G.L. / Phillips Jr., G.N. #10: ![]() Title: Structure of L-Arabinose-Binding Protein from Escherichia Coli at 5 Angstroms Resolution and Preliminary Results at 3.5 Angstroms Authors: Phillips Jr., G.N. / Mahajan, V.K. / Siu, A.K.Q. / Quiocho, F.A. | |||||||||
History |
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Structure visualization
Structure viewer | Molecule: ![]() ![]() |
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Downloads & links
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Download
PDBx/mmCIF format | ![]() | 75.4 KB | Display | ![]() |
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PDB format | ![]() | 56 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Arichive directory | ![]() ![]() | HTTPS FTP |
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-Related structure data
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Links
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Assembly
Deposited unit | ![]()
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Unit cell |
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Components
#1: Protein | Mass: 33232.957 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() |
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#2: Sugar | ChemComp-ARA / |
#3: Sugar | ChemComp-ARB / |
#4: Water | ChemComp-HOH / |
-Experimental details
-Experiment
Experiment | Method: ![]() |
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Sample preparation
Crystal | Density Matthews: 2.35 Å3/Da / Density % sol: 47.66 % | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Crystal grow | *PLUS Temperature: 4 ℃ / pH: 5 / Method: vapor diffusion, hanging drop / Details: referred to J.Biol.Chem. 265.16592-16603 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Components of the solutions | *PLUS
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-Data collection
Reflection | *PLUS Highest resolution: 1.67 Å / Lowest resolution: 8 Å / Num. obs: 35212 / % possible obs: 95 % / Num. measured all: 121531 / Rmerge F obs: 0.0417 |
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Processing
Software | Name: PROLSQ / Classification: refinement | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Refinement | Resolution: 1.67→8 Å /
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Refinement step | Cycle: LAST / Resolution: 1.67→8 Å
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Refine LS restraints |
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Refinement | *PLUS Highest resolution: 1.67 Å / Lowest resolution: 8 Å / Num. reflection obs: 31106 / Rfactor obs: 0.16 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Solvent computation | *PLUS | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Displacement parameters | *PLUS | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Refine LS restraints | *PLUS
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