![]() ![]() ![]() | UniProt Knowledgebase Swiss-Prot Protein Knowledgebase TrEMBL Protein Database Forthcoming changes Release 15.15 of 02-Mar-2010 |
Also read about recent changes, and recent and forthcoming changes for the XML version of the UniProt Knowledgebase.
Table of contents
New feature key INTRAMEM
Change of release numbers
Change of release cycle
Change of the comment line (CC) topic INTERACTION
| New feature key INTRAMEM |
|---|
Not before: 23-Mar-2010
In addition to the feature keys TOPO_DOM (which describes the topology of regions for transmembrane proteins that span membrane compartments) and TRANSMEM (which describes the extent of the region spanning a membrane), we will introduce a new feature key INTRAMEM to describe the extent of a region located in a membrane without crossing it.
| Change of release numbers |
|---|
Not before: 23-Mar-2010
In the past, we have distinguished major and minor releases of the UniProt knowledgebase and this is reflected in the UniProtKB release number format: major releases are numbered x.0, minor releases are x.1, x.2, etc. We are going to abandon this distinction and therefore change the number format to YYYY_XX where YYYY is the calendar year and XX a 2-digit number that is incremented for each release of a given year, e.g. 2010_01, 2010_02, etc. We will archive previous releases on our ftp site for at least 2 years.
| Change of release cycle |
|---|
Not before: 23-Mar-2010
We are going to change our release cycle from 3 to 4 weeks.
| Change of the comment line (CC) topic INTERACTION |
|---|
Not before: 01-Aug-2010
The CC line topic INTERACTION conveys information about binary protein-protein interactions. A description of its current format is available in the UniProtKB User Manual. Currently, all interaction data is automatically derived from the IntAct database. In the future, we will start to add manually curated binary protein-protein interactions to this topic (these are currently described in the CC line topic SUBUNIT). In order to represent isoform- and chain-specific interactions (e.g. for viral polyproteins) and to add interactor-specific comments (e.g. PTMs and binding regions), we are going to modify the format of the INTERACTION lines. Each binary interaction will be represented by a block of 3 to 4 lines:
By
similarity) and, optionally, cross-reference(s) to other databases.
Protein1= line represents the protein of the currently displayed
entry, the Protein2= line the other interacting protein. If
Protein2 is from a different organism than Protein1, its organism is indicated
in an Organism= field.
Note: Variable values are represented in italics. Perl-style multipliers indicate whether a pattern (as delimited by parentheses) is optional (?), may occur 0 or more times (*), or 1 or more times (+). Alternative values are separated by a pipe symbol (|). Special characters are escaped by a backslash (\).
CC -!- INTERACTION: (CC Interact=status \(source|By similarity\)( \(Potential\))?;( Xref=xref;)? (CC Comment=free_text;)? CC Protein1=name [id(:ft_id)?];( Note=free_text;)? CC Protein2=name( [id(:ft_id)?])?;( Organism=tax_name [NCBI_TaxID:tax_id];)?( Note=free_text;)?)+Where:
Yes | No
Yes if there is experimental evidence that the two proteins
(or their orthologues) interact. An optional (Potential)
qualifier indicates that the physiological relevance of the interaction is
uncertain (e.g. the evidence results from a not further validated
yeast-two-hybrid experiment).No if there is experimental evidence that the two proteins do
not interact under the experimental conditions described in the cited
publication.PubMed or Ref).
IntAct database.
Name= or
OrderedLocusNames= or ORFNames=) or a dash '-'
if the gene name is unknown.
IsoId= field).
FTId= field).
Comment= contains additional information concerning the
interaction (like subcellular location).
Note= contains additional information concerning the interacting
protein (like PTM status, binding domains).
Examples:
CC -!- INTERACTION: CC Interact=Yes (PubMed:11533489); CC Comment=HDAC3 mediates the deacetylation of RELA; CC Protein1=RELA [Q04206]; CC Protein2=HDAC3 [O15379];
CC -!- INTERACTION: CC Interact=Yes (Ref.4); CC Comment=Heterodimers are called polygalacturonase-1 (PG1); CC Protein1=GP1 [Q40161]; CC Protein2=PG2 [P05117];
CC -!- INTERACTION: CC Interact=Yes (PubMed:11501947) (Potential); CC Protein1=ABI3 [Q9P2A4]; CC Protein2=ABI3BP [Q7Z7G0];
CC -!- INTERACTION: CC Interact=Yes (By similarity); CC Protein1=GABRG2 [Q5REA1]; CC Protein2=GABARAP;Isoform-specific interaction:
CC -!- INTERACTION: CC Interact=Yes (PubMed:10837489); CC Protein1=MCL1 [Q07820-1]; CC Protein2=BAK1 [Q16611]; CC Interact=Yes (PubMed:15901672, PubMed:17097560); Xref=IntAct:EBI-1003422,EBI-519866; CC Protein1=MCL1 [Q07820]; CC Protein2=BAK1 [Q16611];Negative isoform-specific interaction:
CC -!- INTERACTION: CC Interact=Yes (PubMed:11418237); Xref=IntAct:EBI-375446,EBI-389883; CC Protein1=ABI1 [Q8IZP0]; CC Protein2=NCK1 [P16333]; Note=SH3 1 domain; CC Interact=No (PubMed:12681507); CC Protein1=ABI1 [Q8IZP0-6]; CC Protein2=NCK1 [P16333]; CC Interact=Yes (By similarity); CC Protein1=ABI1 [Q8IZP0]; Note=N-terminus; CC Protein2=WASF1 [Q92558];Chain-specific host-virus interaction:
CC -!- INTERACTION: CC Interact=Yes (PubMed:11086025); CC Protein1=C1QR1 [Q9NPY3]; CC Protein2=Core protein p21 [P27958:PRO_0000037566)]; Organism=Hepatitis C virus genotype 1a (isolate H) [NCBI_TaxID=11108]; Note=See also other virus strains;Chain-specific virus-host interaction:
CC -!- INTERACTION: CC Interact=Yes (PubMed:11086025); CC Protein1=Core protein p21 [P27958:PRO_0000037566)]; CC Protein2=C1QR1 [Q9NPY3]; Organism=Homo sapiens [NCBI_TaxID=9606];Heterologous interaction between Bos taurus and Homo sapiens proteins:
CC -!- INTERACTION: CC Interact=Yes (PubMed:16470652); Xref=IntAct:EBI-907934,EBI-907894; CC Protein1=CNP [P06623]; CC Protein2=CABP1 [Q9NZU7]; Organism=Homo sapiens [NCBI_TaxID=9606];