| filter.dccm {bio3d} | R Documentation |
Filter for Cross-correlation Matrices (Cij)
Description
This function builds various cij matrix for correlation network analysis
Usage
filter.dccm(x, cutoff.cij = NULL, cmap = NULL, xyz = NULL, fac = NULL,
cutoff.sims = NULL, collapse = TRUE, extra.filter = NULL, ...)
Arguments
x |
A matrix (nXn), a numeric array with 3 dimensions (nXnXm), a list with m cells each containing nXn matrix, or a list with ‘all.dccm’ component, containing atomic correlation values, where "n" is the number of residues and "m" the number of calculations. The matrix elements should be in between -1 and 1. See ‘dccm’ function in bio3d package for further details. |
cutoff.cij |
Threshold for each individual correlation value. If NULL, a guessed value will be used. See below for details. |
cmap |
logical or numerical matrix indicating the contact map.
If logical and TRUE, contact map will be calculated with input
|
xyz |
XYZ coordinates, or a ‘pdbs’ object obtained from
|
fac |
factor indicating distinct categories of input correlation matrices. |
cutoff.sims |
Threshold for the number of simulations with observed correlation
value above |
collapse |
logical, if TRUE the mean matrix will be returned. |
extra.filter |
Filter to apply in addition to the model chosen. |
... |
extra arguments passed to function |
Details
If cmap is TRUE or provided a numerical matrix, the function inspects a set of cross-correlation matrices, or DCCM, and decides edges for correlation network analysis based on:
1. min(abs(cij)) >= cutoff.cij, or
2. max(abs(cij)) >= cutoff.cij && residues contact each other
based on results from cmap.
Otherwise, the function filters DCCMs with cutoff.cij and
return the mean of correlations present in at least
cutoff.sims calculated matrices.
An internally guessed cuoff.cij is used if cutoff.cij=NULL is provided.
By default, the cutoff is determined by keeping 5% of all residue pairs connected.
Value
Returns a matrix of class "dccm" or a 3D array of filtered cross-correlations.
Author(s)
Xin-Qiu Yao, Guido Scarabelli & Barry Grant
References
Grant, B.J. et al. (2006) Bioinformatics 22, 2695–2696.
See Also
cna, dccm, dccm.nma, dccm.xyz,
cmap, plot.dccm
Examples
## Not run:
# Example of transducin
attach(transducin)
gaps.pos <- gap.inspect(pdbs$xyz)
modes <- nma.pdbs(pdbs, ncore=NULL)
dccms <- dccm.enma(modes, ncore=NULL)
cij <- filter.dccm(dccms, xyz=pdbs)
# Example protein kinase
# Select Protein Kinase PDB IDs
ids <- c("4b7t_A", "2exm_A", "1opj_A", "4jaj_A", "1a9u_A",
"1tki_A", "1csn_A", "1lp4_A")
# Download and split by chain ID
files <- get.pdb(ids, path = "raw_pdbs", split=TRUE)
# Alignment of structures
pdbs <- pdbaln(files) # Sequence identity
summary(c(seqidentity(pdbs)))
# NMA on all structures
modes <- nma.pdbs(pdbs, ncore=NULL)
# Calculate correlation matrices for each structure
cij <- dccm(modes)
# Set DCCM plot panel names for combined figure
dimnames(cij$all.dccm) = list(NULL, NULL, ids)
plot.dccm(cij$all.dccm)
# Filter to display only correlations present in all structures
cij.all <- filter.dccm(cij, cutoff.sims = 8, cutoff.cij = 0)
plot.dccm(cij.all, main = "Consensus Residue Cross Correlation")
detach(transducin)
## End(Not run)