\name{PFAMCAZY}
\alias{PFAMCAZY}
\alias{PFAMDE}
\alias{PFAMID}
\alias{PFAMHOMSTRAD}
\alias{PFAMINTERPRO}
\alias{PFAMLOAD}
\alias{PFAMMEROPS}
\alias{PFAMMIM}
\alias{PFAMPRINTS}
\alias{PFAMPROSITE}
\alias{PFAMPROSITEPROFILE}
\alias{PFAMRM}
\alias{PFAMSMART}
\alias{PFAMTC}
\alias{PFAMTP}
\alias{PFAMURL}
\title{Mappings from a PFAM Accession number to another kind of ID}
\description{
This is an R object that always contains mappings from a PFAM ID to the
other ID type named by the object
}
\details{
For each of the aliases listed above, there is a mapping object that
corresponds which will map you from the appropriate PFAM accession
number to the ID type that is in the environments name. So for
example PFAMCAZY will map from PFAM IDs to CAZY IDs while
PFAMDE will map from PFAM IDs to Descriptions.
CAZY: The CAZy database ()
describes the families of structurally-related catalytic and
carbohydrate-binding modules (or functional domains) of enzymes
that degrade, modify, or create glycosidic bonds.
DE: Definition for all the Accession number in the database.
ID: Associated Identification for all the Accession number in the
database.
HOMSTRAD: HOMSTRAD (HOMologous STRucture Alignment Database, ) is a curated database
of structure-based alignments for homologous protein families.
Reference: Mizuguchi K, Deane CM, Blundell TL, Overington JP.
(1998) HOMSTRAD: a database of protein structure alignments for
homologous families. Protein Science 7:2469-2471.
INTERPRO: Associated INTERPRO ID for all the Accession number in the
database.
LOAD: LOAD ID for all the Accession number in the database.
MEROPS: The MEROPS database () is
an information resource for peptidases (also termed proteases,
proteinases and proteolytic enzymes) and the proteins that inhibit
them. Reference: Rawlings, N.D., Tolle, D.P. & Barrett, A.J. (2004)
MEROPS: the peptidase database. Nucleic Acids Res. 32 Database
issue, D160-D164
MIM: MIM (a.k.a. OMIM, ) is a
catalog of human genes and genetic disorders authored and edited by
Dr. Victor A. McKusick and his colleagues at Johns Hopkins and
elsewhere. Reference: MIM: McKusick, V.A.: Mendelian
Inheritance in Man. A Catalog of Human Genes and Genetic
Disorders. Baltimore: Johns Hopkins University Press, 1998 (12th
edition). Online Mendelian Inheritance in Man, OMIM
(TM). McKusick-Nathans Institute for Genetic Medicine, Johns
Hopkins University (Baltimore, MD) and National Center for
Biotechnology Information, National Library of Medicine (Bethesda,
MD), 2000
PRINTS: PRINTS ()
is a compendium of protein fingerprints.
PROSITEPROFILE: A list of associated PROSITE PROFILE ID.
RM: Reference Medline ()
SMART: SMART (a Simple Modular Architecture Research Tool, ) allows the identification and
annotation of genetically mobile domains and the analysis of domain
architectures. Reference: (1) Schultz et al. (1998)
Proc. Natl. Acad. Sci. USA 95, 5857-5864. (2) Letunic et al. (2004)
Nucleic Acids Res 32, D142-D144
TC: Trusted cutoff for all the Accession number in the database.
TP: A list of associated Type field for the given Accession.
URL: A list of associated URL for all the Accession number in the
database.
}
\references{\url{http://www.sanger.ac.uk/Software/Pfam/} and
\url{ftp://ftp.sanger.ac.uk/pub/databases/Pfam/current_release/userman.txt}}
\examples{
#To map from PFAM to CAZYs:
x <- PFAMCAZY
# Get the PFAM identifiers that are mapped to a CAZY
mapped_keys <- mappedkeys(x)
# Convert to a list
xx <- as.list(x[mapped_keys])
if(length(xx) > 0) {
# Get the CAZY for the first five PFAM IDs
xx[1:5]
# Get the first one
xx[[1]]
}
#Or to use the DE mapping:
x <- PFAMDE
# Get the PFAM identifiers that are mapped to a DE
mapped_keys <- mappedkeys(x)
# Convert to a list
xx <- as.list(x[mapped_keys])
if(length(xx) > 0) {
# Get the DE for the first five PFAM IDs
xx[1:5]
# Get the first one
xx[[1]]
}
#etc.
}
\keyword{datasets}