Modes

Phaser runs in different modes, which perform Phaser's different functionalities. Modes can either be basic modes or modes that combine the functionality of basic modes.

Phaser Executable

The Phaser executable runs in different modes, which perform Phaser's different functionalities. The mode is selected with the MODE keyword.

Python Interface

Phaser can be compiled as a python library. The mode is selected by calling the appropriate run-job. Input to the run-job is via input-objects, which are passed to the run-job. Setter function on the input objects are equivalent to the keywords for input to the phaser executable. See Python Interface for details.

Modes

Automated Molecular Replacement

MODE MR_AUTO

Combines cell content analysis, anisotropy correction, translational NCS analysis, rotation function, [optional rotation refinement], translation function, packing, and refinement to automatically solve a structure by molecular replacement

Searches for multiple components by looping through the steps listed above

Two different search methods are available

FAST Uses amalgamation to combine placements from a single translation function

FULL' Heavily branched search without amalgamation

 ResultMR r = runMR_AUTO(i=InputMR_AUTO)

Rotation Function

MODE MR_ROT

Combines the anisotropy correction, translational NCS analysis, and EITHER likelihood-enhanced fast rotation function, by default rescored with the full rotation likelihood function OR a brute-force search of angles using the full likelihood rotation function

 ResultMR_RF r = runMR_FRF(i=InputMR_FRF)

Translation Function

MODE MR_TRA

Combines the anisotropy correction, translational NCS analysis, and EITHER likelihood-enhanced fast translation function, by default rescored by the full likelihood translation function OR a brute force search of positions using the full likelihood translation function to find the position of a previously oriented model

 ResultMR_TF r = runMR_FTF(i=InputMR_FTF)

Packing

MODE MR_PAK

Determines whether molecular replacement solutions pack in the unit cell using a C-alpha clash test

 ResultMR r = runMR_PAK(i=InputMR_PAK)

Refinement and Phasing

MODE MR_RNP

Combines the anisotropy correction, translational NCS analysis, and refinement against the likelihood function to optimize full or partial molecular replacement solutions and phase the data. At the end of refinement, the list of solutions is checked for duplicates, which are pruned

 ResultMR r = runMR_RNP(i=InputMR_RNP)

MODE GYRE

Combines the anisotropy correction, translational NCS analysis, and refinement against the likelihood function to optimize the rotations and relative translations (gyrations) between chains in an ensemble

 ResultGYRE r = runMR_GYRE(i=InputMR_RNP)

MODE GIMBLE

Combines the anisotropy correction, translational NCS analysis, and refinement against the likelihood function to optimize the rotations and translations between chains in an ensemble

 ResultMR r = runMR_GMBL(i=InputMR_RNP)

MODE PRUNE

Combines the anisotropy correction, translational NCS analysis, and occupancy refinement against the likelihood function to optimize the occupancies of residues. Occupancy refinement is performed for occupancies in sliding residue windows of a size determined by the expected LLG. The resides that decrease the LLG are pruned.

 ResultMR r = runMR_OCC(i=InputMR_OCC)

Anisotropy Correction

MODE ANO

Corrects the experimental data (amplitude and associated sigma) for anisotropy. First, the anisotropy is removed by scaling up data from weak directions and scaling down data from strong directions, preserving the overall equivalent isotropic B-factor. Then (as suggested by Strong et al. (2006), PNAS 103:8060-8065), the data are resharpened to restore the original falloff in the strong direction. The amount of resharpening can be controlled with the RESHARP keyword.

 ResultANO r = runANO(i=InputANO)

Translational NCS and Twin analysis

MODE NCS

Finds pseudo-translational NCS vectors and corrects the data for intensity variations due to the ptNCS using likelihood methods. The data are corrected for anisotropy first and analysed for twinning before and after data correction.

 ResultNCS r = runNCS(i=InputNCS)

Cell Content Analysis

MODE CCA

Determines the composition of the crystals using the "new" Matthews coefficients of Kantardjieff & Rupp (2003) ("Matthews coefficient probabilities: Improved estimates for unit cell contents of proteins, DNA and protein-nucleic acid complex crystals". Protein Science 12:1865-1871). The molecular weight of ONE complex or assembly to be packed into the asymmetric unit is given and the possible Z values (number of copies of the complex or assembly) that will fit in the asymmetric unit and the relative frequency of their corresponding VM values is reported.

 ResultCCA r = runCCA(i=InputCCA)

Expected log-likelihood-gain (eLLG) Analysis

MODE MR_ELLG

Determines the eLLG for any models defined as ensembles, reporting the eLLG at the full resolution of the data and the resolution predicted to reach the target LLG.

 ResultELLG r = runMR_ELLG(i=InputMR_ELLG)

Normal Mode Analysis/SCEDS

MODE NMA

Writes out coordinates of input structures that have been perturbed along normal modes, in a procedure similar to that described by Suhre & Sanejouand (Acta Cryst. D60, 796-799, 2004). Perturbed coordinates are output in RMS increments for use in MR trials. Each run of the program writes out a matrix FILEROOT.mat that contains the eigenvectors and eigenvalues of the atomic Hessian, and can be read into subsequent runs of the same job, to speed up the analysis.

 ResultNMA r = runNMAXYZ(i=InputNMA)

MODE SCEDS

Writes out domains generated by the SCEDS analysis of the coordinates perturbed along normal modes.

 ResultNMA r = runSCEDS(i=InputNMA)

Automated Experimental Phasing

MODE EP_AUTO

Combines anisotropy correction, translational NCS analysis, cell content analysis, and SAD phasing to automatically solve a structure by experimental phasing

 ResultEP r = runEP_AUTO(i=InputEP_AUTO)

Single Atom Molecular Replacement

MODE MR_ATOM

Combines automated molecular replacement with log-likelihood gradient completion to solve high resolution structures by single atom MR. The data are prepared with runMR_DAT and then the phasing is done withing the EP_AUTO mode.

 ResultEP r = runMR_ATOM(i=InputMR_ATOM)