1A9P
BOVINE PURINE NUCLEOSIDE PHOSPHORYLASE COMPLEXED WITH 9-DEAZAINOSINE AND PHOSPHATE
Experimental procedure
Source type | ROTATING ANODE |
Source details | RIGAKU RUH2R |
Temperature [K] | 296 |
Detector technology | AREA DETECTOR |
Collection date | 1996-08 |
Detector | XUONG-HAMLIN MULTIWIRE |
Spacegroup name | P 21 3 |
Unit cell lengths | 94.200, 94.200, 94.200 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 8.000 - 2.400 |
R-factor | 0.19 * |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1pbn |
RMSD bond length | 0.007 |
RMSD bond angle | 1.200 * |
Data reduction software | SDMS |
Data scaling software | SDMS |
Phasing software | X-PLOR (3.8) |
Refinement software | X-PLOR (3.8) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 8.000 |
High resolution limit [Å] | 2.400 |
Number of reflections | 10457 |
Completeness [%] | 97.0 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Vapor diffusion, hanging drop * | PROTEIN WAS CRYSTALLIZED FROM 31-35% PEG-400 IN 100 MM HEPES OR TRIS BUFFER, PH 7.8-8.2; 100 MM MGCL2; 1% OCTYL-BETA- D-GLUCOPYRANOSIDE |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | reservoir | PEG400 | 31-35 (%) | |
2 | 1 | reservoir | HEPES | 100 (mM) | or Tris-HCl |
3 | 1 | reservoir | beta-D-glucopyranoside | 1 (%) |