8ERW
Precisely patterned nanofibers made from extendable protein multiplexes
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ALS BEAMLINE 8.2.2 |
| Synchrotron site | ALS |
| Beamline | 8.2.2 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2016-04-05 |
| Detector | ADSC QUANTUM 315r |
| Wavelength(s) | 1.0000 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 55.318, 55.380, 145.134 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 43.990 - 2.880 |
| R-factor | 0.2641 |
| Rwork | 0.261 |
| R-free | 0.28640 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | Computational design model |
| Data reduction software | HKL-2000 (2.3.10) |
| Data scaling software | HKL-2000 (2.3.10) |
| Phasing software | PHASER (2.7.18) |
| Refinement software | PHENIX (1.19.1-4122-000) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 50.000 | 2.940 |
| High resolution limit [Å] | 2.880 | 2.880 |
| Rmeas | 0.125 | 0.776 |
| Rpim | 0.055 | 0.386 |
| Number of reflections | 10228 | 134 |
| <I/σ(I)> | 12.6 | 1.18 |
| Completeness [%] | 96.9 | 89.2 |
| Redundancy | 4.4 | 3.4 |
| CC(1/2) | 0.667 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 8.5 | 293.15 | 1:1 mixture of protein solution and crystallization solution consisting of 0.1M Tris-HCl pH 8.5, 25%(w/v) PEG 3000 |






