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 (%) | 






