TrEMBL release 12.0
Published November 1, 1999
TrEMBL Release Notes
Release 12, November 1999
EMBL Outstation
European Bioinformatics Institute (EBI)
Wellcome Trust Genome Campus
Hinxton
Cambridge CB10 1SD
United Kingdom
Telephone: (+44 1223) 494 444
Fax: (+44 1223) 494 468
Electronic mail address: DATALIB@EBI.AC.UK
WWW server: http://www.ebi.ac.uk/
Amos Bairoch
Swiss Institute of Bioinformatics (SIB)
Centre Medical Universitaire
1, rue Michel Servet
1211 Geneva 4
Switzerland
Telephone: (+41 22) 784 40 82
Fax: (+41 22) 702 55 02
Electronic mail address: BAIROCH@CMU.UNIGE.CH
WWW server: http://www.expasy.ch/
Acknowledgements
TrEMBL has been prepared by:
o Rolf Apweiler, Kirsty Bates, Margaret Biswas, Sergio Contrino,
Wolfgang Fleischmann, Gill Fraser, Cathy Gedman, Henning Hermjakob,
Vivien Junker, Youla Karavidopoulou, Fiona Lang, Minna Lehvaslaiho,
Michele Magrane, Maria Jesus Martin, Steffen Moeller, Nicoletta
Mitaritonna, Virginie Mittard, Nicola Mulder, Claire O'Donovan,
Isabelle Phan, Sandrine Pilbout, Lucia Rodriguez-Monge and Eleanor
Whitfield at the EMBL Outstation - European Bioinformatics Institute
(EBI) in Hinxton, UK;
o Amos Bairoch and Alain Gateau at the Swiss Institute of Bioinformatics
in Geneva, Switzerland.
Copyright Notice
TrEMBL copyright (c) 1999 EMBL-EBI
This manual and the database it accompanies may be copied and
redistributed freely, without advance permission, provided
that this copyright statement is reproduced with each copy.
Citation
If you want to cite TrEMBL in a publication please use the
following reference:
Bairoch A, and Apweiler R.
The SWISS-PROT protein sequence data bank and its supplement
TrEMBL in 1999.
Nucleic Acids Res. 27:49-54(1999).
1. Introduction
TrEMBL is a computer-annotated protein sequence database supplementing the
SWISS-PROT Protein Sequence Data Bank. TrEMBL contains the translations of
all coding sequences (CDS) present in the EMBL Nucleotide Sequence Database
not yet integrated in SWISS-PROT. TrEMBL can be considered as a preliminary
section of SWISS-PROT. For all TrEMBL entries which should finally be
upgraded to the standard SWISS-PROT quality, SWISS-PROT accession numbers
have been assigned.
2. Why a supplement to SWISS-PROT?
The ongoing gene sequencing and mapping projects have dramatically
increased the number of protein sequences to be incorporated into SWISS-PROT.
We do not want to dilute the quality standards of SWISS-PROT by incorporating
sequences without proper sequence analysis and annotation, but we do want to
make the sequences available as fast as possible. TrEMBL achieves this second
goal, and is a major step in the process of speeding up subsequent
upgrading of annotation to the standard SWISS-PROT quality.
To address the problem of redundancy, the translations of all coding
sequences (CDS) in the EMBL Nucleotide Sequence Database already included
in SWISS-PROT have been removed from TrEMBL.
3. The Release
This TrEMBL release was created from the EMBL Nucleotide Sequence Database
release 60 and contains 276'472 sequence entries, comprising 75'524'740 amino
acids. To minimize redundancy, the translations of all coding sequences (CDS)
in the EMBL Nucleotide Sequence Database already included in SWISS-PROT release
38 and updates up to 18.10.1999 have been removed from TrEMBl release 12.
TrEMBL is split in two main sections: SP-TrEMBL and REM-TrEMBL:
SP-TrEMBL (SWISS-PROT TrEMBL) contains the entries (225'878) which should be
eventually incorporated into SWISS-PROT. SWISS-PROT accession numbers have
been assigned for all SP-TrEMBL entries.
SP-TrEMBL is organized in subsections:
arc.dat (Archaea): 10017 entries
fun.dat (Fungi): 7130 entries
hum.dat (Human): 9417 entries
inv.dat (Invertebrates): 26516 entries
mam.dat (Other Mammals): 3498 entries
mhc.dat (MHC proteins): 4563 entries
org.dat (Organelles): 18368 entries
phg.dat (Bacteriophages): 2201 entries
pln.dat (Plants): 18993 entries
pro.dat (Prokaryotes): 51151 entries
rod.dat (Rodents): 7992 entries
unc.dat (Unclassified): 129 entries
vrl.dat (Viruses): 61006 entries
vrt.dat (Other Vertebrates): 4897 entries
28'141 new entries have been integrated in SP-TrEMBL. The sequences of
522 SP-TrEMBL entries have been updated and the annotation has been updated in
56'201 entries.
In the document deleteac.txt, you will find a list of all accession numbers
which were previously present in TrEMBL, but which have now been deleted from
the database.
REM-TrEMBL (REMaining TrEMBL) contains the entries (50'594) that we do
not want to include in SWISS-PROT. REM-TrEMBL entries have no accession
numbers. This section is organized in six subsections:
1) Immunoglobulins and T-cell receptors (Immuno.dat)
Most REM-TrEMBL entries are immunoglobulins and T-cell receptors. We
stopped entering immunoglobulins and T-cell receptors into SWISS-PROT,
because we only want to keep the germ line gene derived translations
of these proteins in SWISS-PROT and not all known somatic recombinated
variations of these proteins. We would like to create a specialized
database dealing with these sequences as a further supplement to
SWISS-PROT and keep only a representative cross-section of these
proteins in SWISS-PROT.
2) Synthetic sequences (Synth.dat)
Another category of data, which will not be included in SWISS-PROT are
synthetic sequences. Again, we do not want to leave these entries in
TrEMBL. Ideally one should build a specialized database for artificial
sequences as a further supplement to SWISS-PROT.
3) Patent application sequences (Patent.dat)
A third subsection consists of coding sequences captured from patent
applications. A thorough survey of these entries have shown that
apart from a rather small minority (which in most cases have already
been integrated in SWISS-PROT), most of these sequences contain either
erroneous data or concern artificially generated sequences outside the
scope of SWISS-PROT.
4) Small fragments (Smalls.dat)
Another subsection consists of fragments with less than eight amino
acids.
5) CDS not coding for real proteins (Pseudo.dat)
This subsection consists of CDS translations where we have strong
evidence to believe that these CDS are not coding for real proteins.
6) Truncated proteins (Truncated.dat)
The last subsection consists of truncated proteins which result from
events like mutations introducing a stop codon leading to the truncation
of the protein product.
4. Format Differences Between SWISS-PROT and TrEMBL
The format and conventions used by TrEMBL follow as closely as possible
that of SWISS-PROT. Hence, it is not necessary to produce an additional
user manual and extensive release notes for TrEMBL. The information given
in the SWISS-PROT release notes and user manual are in general valid for
TrEMBL. The differences are mentioned below.
The general structure of an entry is identical in SWISS-PROT and TrEMBL.
The data class used in TrEMBL (in the ID line) is always 'PRELIMINARY',
whereas in SWISS-PROT it is always 'STANDARD'.
Differences in line types present in SWISS-PROT and TrEMBL:
The ID line (IDentification):
The entry name used in SP-TrEMBL is the same as the Accession Number of the
entry. The entry name used in REM-TrEMBL is the stable part of the protein_id
tagged to the corresponding CDS in the EMBL Nucleotide Sequence Database.
'protein_id' stands for the "Protein Identification" number. It is a number
that you will find in the feature table of the EMBL nucleotide sequence
entries in a qualifier called "/protein_id" which is tagged to every CDS.
Example:
FT CDS 339..1514
FT /codon_start=1
FT /db_xref="PID:g1256015"
FT /product="dystrobrevin-epsilon"
FT /protein_id="AAC50431.1"
The protein_id is defined as follows in the The DDBJ/EMBL/GenBank Feature Table
Definition documentation
Qualifier /protein_id
Definition Protein Identifier, issued by International collaborators.
This qualifier consists of a stable ID portion (3+5 format
with 3 position letters and 5 numbers) plus a version
number after the decimal point.
Value format <identifier>
Example /protein_id="AAA12345.1"
Comment When the protein sequence encoded by the CDS changes, only
the version number of the /protein_id value is incremented.
The stable part of the /protein_id remains unchanged and
as a result will permanently be associated with a given
protein. This qualifier is valid only on CDS features
which translate into a valid protein.
The DT line (DaTe)
The format of the DT lines that serve to indicate when an entry was
created and updated are identical to that defined in SWISS-PROT; but the
DT lines in TrEMBL refer to the TrEMBL release. The difference is
shown in the example below.
DT lines in a SWISS-PROT entry:
DT 01-JAN-1988 (Rel. 06, Created)
DT 01-JUL-1989 (Rel. 11, Last sequence update)
DT 01-AUG-1992 (Rel. 23, Last annotation update)
DT lines in a TrEMBL entry:
DT 01-NOV-1996 (TrEMBLrel. 01, Created)
DT 01-NOV-1996 (TrEMBLrel. 01, Last sequence update)
DT 01-FEB-1997 (TrEMBLrel. 02, Last annotation update)
5. Weekly updates of TrEMBL and non-redundant data sets
Weekly cumulative updates of TrEMBL are available by anonymous FTP and
from the EBI SRS server.
We also produce every week a complete non-redundant protein sequence
collection by providing three compressed files (these are in the directory
/pub/databases/sp_tr_nrdb on the EBI FTP server and in databases/sp_tr_nrdb
on the ExPASy server): sprot.dat.Z, trembl.dat.Z and trembl_new.dat.Z.
This set of non-redundant files is especially important for two types of
users:
(i) Managers of similarity search services. They can now provide what is
currently the most comprehensive and non-redundant data set of protein
sequences.
(ii) Anybody wanting to update their full copy of SWISS-PROT + TrEMBL to
their own schedule without having to wait for full releases of SWISS-PROT
or of TrEMBL.
6. Access/Data Distribution
FTP server: ftp.ebi.ac.uk/pub/databases/trembl
SRS server: http://srs.ebi.ac.uk/
TrEMBL is also available on the SWISS-PROT CD-ROM.
SWISS-PROT + TrEMBL is searchable on the following servers at the EBI:
FASTA3 (http://www2.ebi.ac.uk/fasta3/)
BLAST2 (http://www2.ebi.ac.uk/blast2/)
Bic_sw (http://www2.ebi.ac.uk/bic_sw/)
Scanps (http://www2.ebi.ac.uk/scanps/)
SSearch (http://www2.ebi.ac.uk/ssearch3/)
7. Description of changes made to TrEMBL since release 11.
7.1 Addition of new subsection of REM-TrEMBL.
In this release we have created a new subsection called truncated.dat.
7.2 Changes concerning cross-references (DR line)
We have added cross-references from TrEMBL to:
a) the PRINTS database available at ftp.seqnet.dl.ac.uk (see: Attwood, T.K.,
Beck, M.E., Bleasby, A.J. and Parry-Smith, D.J. (1994) PRINTS - A database of
protein motif fingerprints. Nucleic Acids Res. 24:182-188(1994)).
b) the HSSP: Homology derived Secondary Structure of Proteins database
available at http://www.sander.ebi.ac.uk/hssp/ (see: Sander C. & Schneider R.
(1991) Database of homology-derived protein structures. Proteins, Structure,
Function & Genetics, 9:56-68).
A list of all crossreferences in TrEMBL to other databases is provided below:
AARHUS/GHENT-2DPAGE;
EMBL
FLYBASE
GCRDB
HSSP
MENDEL
MGD
MIM
PDB
PFAM
PIR
PRINTS
PROSITE
SGD
SUBTILIST
TIGR
TRANSFAC
WORMPEP
ZFIN