HADDOCK2.4 manual - Diffusion Anisotropy Restraints
Diffusion anisotropy data (relaxation data) can provide useful information on the orientation of the molecules to be docked (comparable to RDCs). They can be introduced in HADDOCK as direct restraints (DANI statement in CNS).
For this, the tensor components need first to be determined. In the case of complexes, this can be easily done by using the known structures of the single domains. The software Tensor2 (Dosset, Marion and Blackledge (2000). J. Biomol. NMR 16, 23-28) can be used for this purpose.
You need for this to generate a Tensor2 input file containing your relaxation data.
A csh script called uname -pana_pdb_tensor2.csh is provided in the haddock/DANItools directory that will calculate from the experimental relaxation data the tensor parameters for all PDB files present in the current directory by best-fitting the data to the corresponding 3D structures.
Usage:
$HADDOCK/DANItools/ana_pdb_tensor2.csh tensor2.inp
Note that you have to define the fitting options in the tensor2 GUI manually. Tensor2 writes its output for each structure to a file called resaniso.0; each of these are moved to a subdirectory with directory name equal to the corresponding pdb file.
The script extracts the tensor parameters Dx, Dy and Dz and the chi2-value of the fit; these can be combined with the following command:
paste D?_all.tmp chi2_all.tmp | awk '{print $1,$8,$16,$24,$27*100/100}' | sort -n +4 > tensor2_fit.lis
The components from the structure giving the best fit to the experimental data can be used to calculate the tensor parameters that are needed in run.cns with the script calc_tens.csh (provided in the haddock/DANItools directory).
Usage:
$HADDOCK/DANItools/calc_tens.csh dx dy dz
Where dx, dy and dz are the values from the file tensor2_fit.lis. The output of calc_tens.csh can be used directly in run.cns as dan1_tc, dan1_anis and dan1_r, the rotational correlation time, anisotropy and rhombicity of the rotational diffusion tensor, respectively. Alternatively, average values could be used; these can be calculated with:
cat tensor2_fit.lis | awk '{print $2}' | $HADDOCKTOOLS/average.perl cat tensor2_fit.lis | awk '{print $3}' | $HADDOCKTOOLS/average.perl cat tensor2_fit.lis | awk '{print $4}' | $HADDOCKTOOLS/average.perl
Check the values in tensor2_fit.lis to make sure they match (e.g. same sign) before averaging them. Also make sure that an anisotropic model is in accordance with your data.
Use of relaxation data as restraints for docking
The proper format for DANI restraints is the following:
assi ( resid 999 and name OO ) ( resid 999 and name Z ) ( resid 999 and name X ) ( resid 999 and name Y ) ( resid 20 and name N and segid A ) ( resid 20 and name HN and segid A ) 8.705 0.200
The restraints use the R2/R1 value; one should filter out residues where chemical exchange or mobility influences these values. Given a file containing residue_number R2/R1value and Segid a DANI restraint file in CNS format can be generated with the gawk script generate_dani provided in the HADDOCK/DANItools directory:
$HADDOCK/DANItools/generate_dani dani_data_file
The error on the R2/R1 values is set by default to 0.2. This can be overruled by giving the error value as argument:
$HADDOCK/DANItools/generate_dani ERR=0.5 dani_data_file
The 2.4 version of HADDOCK supports up to 5 different DANI restraints sets. Each can have a separate tensor. The tensor residue number should be in the range 999-995. You can edit and modify the generate_dani script to change the tensor number. To use DANI restraints in HADDOCK, use DANI in run.cns in the diffusion anisotropy section and define the proper tensor parameters that are output by the calc_tens.csh script. The DANI restraints are first used in the rigid body energy minimization step using as force constant the value defined for the hot phase.
The DANI restraints should be defined by the DANIX_FILE parameter in the run.param
file used to setup a run, with X being the number of the restraint set. An example entry in run.param
would be:
DANI1_FILE=./dani.tbl
Example taken from the protein-protein-dani
example provided with HADDOCK2.4.