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UniProtKB/TrEMBL - Old Release NotesN.B. From release 27, the UniProtKB/TrEMBL release notes are included in the UniProt release notes.
TrEMBL Release Notes
Release 13, May 2000
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) 702 58 60
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,
Kirill Degtyarenko, Wolfgang Fleischmann, Gill Fraser, Cathy Gedman,
Henning Hermjakob, Vivien Junker, Youla Karavidopoulou, Paul Kersey,
Fiona Lang, Minna Lehvaslaiho, Michele Magrane, Maria Jesus Martin,
Steffen Moeller, Nicoletta Mitaritonna, Virginie Mittard, Nicola Mulder,
Claire O'Donovan, John F. ORourke, Isabelle Phan, Sandrine Pilbout,
Lucia Rodriguez-Monge, Eleanor Whitfield and Allyson Williams
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) 2000 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 2000.
Nucl. Acids Res. 28:45-48(2000).
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 62 and contains 353'156 sequence entries, comprising 100'750'187 amino
acids. To minimise 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 26.4.2000 have been removed from TrEMBl release 13.
TrEMBL is split in two main sections: SP-TrEMBL and REM-TrEMBL:
SP-TrEMBL (Swiss-Prot TrEMBL) contains the entries (300'192) which should be
eventually incorporated into Swiss-Prot. Swiss-Prot accession numbers have
been assigned for all SP-TrEMBL entries.
SP-TrEMBL is organised in subsections:
arc.dat (Archaea): 11814 entries
fun.dat (Fungi): 8916 entries
hum.dat (Human): 13979 entries
inv.dat (Invertebrates): 45133 entries
mam.dat (Other Mammals): 5037 entries
mhc.dat (MHC proteins): 5265 entries
org.dat (Organelles): 25755 entries
phg.dat (Bacteriophages): 2667 entries
pln.dat (Plants): 28814 entries
pro.dat (Prokaryotes): 62455 entries
rod.dat (Rodents): 10377 entries
unc.dat (Unclassified): 31 entries
vrl.dat (Viruses): 72264 entries
vrt.dat (Other Vertebrates): 6788 entries
65'315 new entries have been integrated in SP-TrEMBL. The sequences of
1'204 SP-TrEMBL entries have been updated and the annotation has been
updated in 161'387 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 (53'861) that we do
not want to include in Swiss-Prot. REM-TrEMBL entries have no accession
numbers. This section is organised 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 specialised
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 specialised 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
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