2XA3
crystal structure of the broadly neutralizing llama VHH D7 and its mode of HIV-1 gp120 interaction
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE BM14 |
Synchrotron site | ESRF |
Beamline | BM14 |
Temperature [K] | 100 |
Collection date | 2009-07-20 |
Detector | MARRESEARCH |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 37.370, 62.180, 62.740 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 24.027 - 1.500 |
R-factor | 0.167 |
Rwork | 0.166 |
R-free | 0.19350 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1hcv |
RMSD bond length | 0.006 |
RMSD bond angle | 1.065 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX ((PHENIX.REFINE)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 44.000 | |
High resolution limit [Å] | 1.500 | 1.500 |
Rmerge | 0.050 | 0.200 |
Number of reflections | 22695 | |
<I/σ(I)> | 23 | 6.5 |
Completeness [%] | 94.1 | 68.7 |
Redundancy | 3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 6 | 5 MG/ML OF D7 PROTEIN IN A SOLUTION OF 20MM HEPES PH 7, 0.1 M NACL MIXED WITH AN EQUAL VOLUME OF 100MM SODIUM CACODYLATE PH 6, 20 MM MAGNESIUM ACETATE, 1.7M AMMONIUM SULFATE AND 19 % GLYCEROL WELL CONDITION |