The European Molecular Biology Laboratory (EMBL) is a molecular biology research institution supported by 22 member states. EMBL was created in 1974 and operates from five sites, performing basic research in molecular biology and molecular medicine. A key function of EMBL is the EMBL Nucleotide Sequence Database, maintained at the European Bioinformatics Institute, which incorporates and distributes nucleotide sequences from public sources as part of an international collaboration.

1. EMBL
 The European Molecular Biology Laboratory (EMBL) is a molecular biology research
institution supported by 22 member states, four prospect and two associate member states.
 EMBL was created in 1974 and is an intergovernmental organisation funded by public
research money from its member states.
 The Laboratory operates from five sites: the main laboratory in Heidelberg, and outstations
in Hinxton (the European Bioinformatics Institute (EBI), in England), Grenoble (France),
Hamburg (Germany), and Monterotondo (near Rome).
 EMBL groups and laboratories perform basic research in molecular biology and molecular
medicine as well as training for scientists, students and visitors.
 Israel is the only Asian state that has full membership.
 The EMBL Nucleotide Sequence Database (http:// www.ebi.ac.uk/embl/), maintained at
the European Bioinformatics Institute (EBI),
 It is used to incorporate and distributes nucleotide sequences from public sources.
 The database is a part of an international collaboration with DDBJ (Japan) and GenBank
(USA).
 Data are exchanged between the collaborating databases on a daily basis.
 The web-based tool, Webin, is the preferred system for individual submission of
nucleotide sequences, including Third Party Annotation (TPA) and alignment data.
 Automatic submission procedures are used for submission of data from large-scale genome
sequencing
 The latest data collection can be accessed via FTP, email and WWW interfaces.
 The EBI's Sequence Retrieval System (SRS) integrates and links the main nucleotide and
protein databases as well as many other specialist molecular biology databases.
 For sequence similarity searching, a variety of tools (e.g. FASTA and BLAST) are
available that allow external users to compare their own sequences against the data in the
EMBL Nucleotide Sequence Database and other databases.
 All available resources can be accessed via the EBI home page at http://www.ebi.ac.uk.

2. EMBL format
ID LISOD standard; DNA; PRO; 756 BP.
XX
AC X64011; S78972;
XX
SV X64011.1
XX
DT 28-APR-1992 (Rel. 31, Created)
DT 30-JUN-1993 (Rel. 36, Last updated, Version 6)
XX
DE L.ivanovii sod gene for superoxide dismutase
XX
KW sod gene; superoxide dismutase.
XX
OS Listeria ivanovii
OC Bacteria; Firmicutes; Bacillus/Clostridium group;
OC Bacillus/Staphylococcus group; Listeria.
XX
RN [1]
RX MEDLINE; 92140371.
RA Haas A., Goebel W.;
RT "Cloning of a superoxide dismutase gene from Listeria ivanovii by
RT functional complementation in Escherichia coli and characterization of
the
RT gene product.";

3. RL Mol. Gen. Genet. 231:313-322(1992).
XX
RN [2]
RP 1-756
RA Kreft J.;
RT ;
RL Submitted (21-APR-1992) to the EMBL/GenBank/DDBJ databases.
RL J. Kreft, Institut f. Mikrobiologie, Universitaet Wuerzburg, Biozentrum
Am
RL Hubland, 8700 Wuerzburg, FRG
XX
DR SWISS-PROT; P28763; SODM_LISIV.
XX
FH Key Location/Qualifiers
FH
FT source 1..756
FT /db_xref="taxon:1638"
FT /organism="Listeria ivanovii"
FT /strain="ATCC 19119"
FT RBS 95..100
FT /gene="sod"
FT terminator 723..746
FT /gene="sod"
FT CDS 109..717
FT /db_xref="SWISS-PROT:P28763"
FT /transl_table=11
FT /gene="sod"
FT /EC_number="1.15.1.1"
FT /product="superoxide dismutase"
FT /protein_id="CAA45406.1"
FT /translation="MTYELPKLPYTYDALEPNFDKETMEIHYTKHHNIYVTKLNEA
VSG
FT HAELASKPGEELVANLDSVPEEIRGAVRNHGGGHANHTLFWSSLSPNGGGAPTGNL
KAA
FT IESEFGTFDEFKEKFNAAAAARFGSGWAWLVVNNGKLEIVSTANQDSPLSEGKTPV
LGL
FT DVWEHAYYLKFQNRRPEYIDTFWNVINWDERNKRFDAAK"
XX
SQ Sequence 756 BP; 247 A; 136 C; 151 G; 222 T; 0 other;
cgttatttaa ggtgttacat agttctatgg aaatagggtc tatacctttc
gccttacaat 60
gtaatttctt ttcacataaa taataaacaa tccgaggagg aatttttaat
gacttacgaa 120
ttaccaaaat taccttatac ttatgatgct ttggagccga attttgataa
agaaacaatg 180
gaaattcact atacaaagca ccacaatatt tatgtaacaa aactaaatga
agcagtctca 240
ggacacgcag aacttgcaag taaacctggg gaagaattag ttgctaatct
agatagcgtt 300
cctgaagaaa ttcgtggcgc agtacgtaac cacggtggtg gacatgctaa
ccatacttta 360
ttctggtcta gtcttagccc aaatggtggt ggtgctccaa ctggtaactt
aaaagcagca 420
atcgaaagcg aattcggcac atttgatgaa ttcaaagaaa aattcaatgc
ggcagctgcg 480
gctcgttttg gttcaggatg ggcatggcta gtagtgaaca atggtaaact
agaaattgtt 540

4. tccactgcta accaagattc tccacttagc gaaggtaaaa ctccagttct
tggcttagat 600
gtttgggaac atgcttatta tcttaaattc caaaaccgtc gtcctgaata
cattgacaca 660
ttttggaatg taattaactg ggatgaacga aataaacgct ttgacgcagc
aaaataatta 720
tcgaaaggct cacttaggtg ggtcttttta
tttcta 756
//
ID - Identification.
AC - Accession number(s).
DT - Date.
DE - Description.
GN - Gene name(s).
OS - Organism species.
OG - Organelle.
OC - Organism classification.
RN - Reference number.
RP - Reference position.
RC - Reference comments.
RX - Reference cross-references.
RA - Reference authors.
RL - Reference location.
CC - Comments or notes.
DR - Database cross-references.
KW - Keywords.
FT - Feature table data.
SQ - Sequence header.
- (blanks) sequence data.
// - Termination line.

5. Some entries do not contain all of the line types, and some line types occur many times in a single
entry. Each entry must begin with an identification line (ID) and end with a terminator line (//).