PaperBLAST
PaperBLAST Hits for EX31_RS24375 (84 a.a., MDRNDEVIQT...)
Show query sequence
>EX31_RS24375
MDRNDEVIQTHPLVGWDISTVDSYDAMMIRLHYLSSKDQTPEDAQVDRTLWLTTDVARQL
INILEAGIEKIESNEYEYSDHRKH
Running BLASTp...
Found 10 similar proteins in the literature:
G4234_05420 biofilm formation regulator BssS from Serratia marcescens
87% identity, 100% coverage
NJ56_16600 biofilm formation regulator BssS from Yersinia ruckeri
86% identity, 100% coverage
CH1034_180150 biofilm formation regulator BssS from Klebsiella pneumoniae
67% identity, 100% coverage
SGP1_RS09085 biofilm formation regulator BssS from Sodalis glossinidius str. 'morsitans'
74% identity, 100% coverage
KPK_3485 hypothetical protein from Klebsiella pneumoniae 342
67% identity, 100% coverage
STM1161 putative cytoplasmic protein from Salmonella enterica subsp. enterica serovar Typhimurium str. LT2
STM1161.S biofilm formation regulatory protein BssS from Salmonella typhimurium LT2
SC1109 putative cytoplasmic protein from Salmonella enterica subsp. enterica serovar Choleraesuis str. SC-B67
67% identity, 100% coverage
EAE_16280 biofilm formation regulator BssS from Klebsiella aerogenes KCTC 2190
64% identity, 100% coverage
YceP / b1060 regulator of biofilm formation from Escherichia coli K-12 substr. MG1655 (see 7 papers)
BSSS_ECOLI / P0AB33 Biofilm regulator BssS from Escherichia coli (strain K12) (see 2 papers)
c1327 biofilm formation regulatory protein BssS from Escherichia coli CFT073
NP_415578 regulator of biofilm formation from Escherichia coli str. K-12 substr. MG1655
b1060 orf, hypothetical protein from Escherichia coli str. K-12 substr. MG1655
64% identity, 100% coverage
- function: Represses biofilm formation in M9C glu and LB glu media but not in M9C and LB media. Seems to act as a global regulator of several genes involved in catabolite repression and stress response and regulation of the uptake and export of signaling pathways. Could be involved the regulation of indole as well as uptake and export of AI-2 through a cAMP-dependent pathway.
disruption phenotype: Cells show increased biofilm formation when glucose is present in the medium. In a continuous-flow system with M9C medium supplemented with glucose, the biofilm had a 240-fold greater biomass, a 2800 fold-greater average thickness and a 16-fold increased surface coverage than the wild-type. - 21st Congress of the European Hematology Association Copenhagen, Denmark, June 9–12, 2016
, Haematologica 2016 - 46th Annual Meeting February 23-27, 2002, Moscone Convention Center, San Francisco, California : Wednesday, February 27, 2002, Part 3
, Biophysical journal 2002 - YliH (BssR) and YceP (BssS) regulate Escherichia coli K-12 biofilm formation by influencing cell signaling.
Domka, Applied and environmental microbiology 2006 - GeneRIF: YceP (BssS) regulates biofilm formation through signal secretion together with YliH [BssS]
- Escherichia coli toxin/antitoxin pair MqsR/MqsA regulate toxin CspD
Kim, Environmental microbiology 2010 - “...repressor bssR b0836 3.3 1.3 1.2 Repressor of biofilm formation by indole transport regulation bssS b1060 1.2 3.0 2.5 Repressor of biofilm formation by indole transport regulation; global regulator, e.g. of AI-2 transport and motility genes mqsA b3021 3.5 3.7 2.5 Antitoxin part in MqsR-MqsA TA...”
- Sxy induces a CRP-S regulon in Escherichia coli
Sinha, Journal of bacteriology 2009 - “...E. COLI 5185 TABLE 1--Continued Gene Designation Induction (fold) b1060 b1322 b2592 b2614 b0014 b2699 b0966 b3686 b3687 b3635 b4140 b0631 bssS ycjF clpB grpE...”
- YcfR (BhsA) influences Escherichia coli biofilm formation through stress response and surface hydrophobicity
Zhang, Journal of bacteriology 2007 - “...b3512 b3506 b0019 b3509 b3510 b3511 b4376 b1283 b1060 b3494 b0014 b1646 b0814 b0966 Glutamate decarboxylase A subunit, acid resistance protein Glutamate...”
- YliH (BssR) and YceP (BssS) regulate Escherichia coli K-12 biofilm formation by influencing cell signaling
Domka, Applied and environmental microbiology 2006 - “...Here, it is shown that deletion of yceP (b1060) and yliH (b0836) increases biofilm formation in continuous-flow chambers with minimal glucose medium by...”
- Gene expression in Escherichia coli biofilms
Ren, Applied microbiology and biotechnology 2004 (PubMed)- “...genes of unknown function (ybaJ, ychM, yefM, ygfA, b1060, b1112, b2377, b3022, b1373, b1601, and b0836). The DNA microarray results were corroborated with RNA...”
- “...Anthranilate synthase component I 37 21 17 8 35 4 7 8 b1601 ygfA b1060 b1373 b0836 ychM yefM 5 5 4 3 3 2 2 6 8 5 1.3 3 3 3 b1601 b2912 b1060 b1373 b0836 b1206...”
- Global RNA half-life analysis in Escherichia coli reveals positional patterns of transcript degradation
Selinger, Genome research 2003 - “...b0553 b2398 b3494 b3556 b3685 b0726 b1205 b3362 b0162 b1060 b2080 b2377 b3361 b4132 b4396 yjfN IldD cpxP(2) cspG cpxP(1) nmpC yfeC uspB cspA yidE sucA ychH...”
- Combined, functional genomic-biochemical approach to intermediary metabolism: interaction of acivicin, a glutamine amidotransferase inhibitor, with Escherichia coli K-12
Smulski, Journal of bacteriology 2001 - “...b0806 b0836 b0865 b0897 b0964 b0966 b1003 b1045 b1050 b1060 b1103 b1104 b1105 b1107 b1108 b1111 b1112 b1128 b1145 b1168 b1178 b1195 b1205 b1256 b1257 b1273...”
- DNA microarray-mediated transcriptional profiling of the Escherichia coli response to hydrogen peroxide
Zheng, Journal of bacteriology 2001 - “...b4326 b2414 b4322 b2365 b4217 b2616 b4062 b2366 b3924 b1166 b2012 b2654 b0389 b1060 b3049 b1426 b3707 30 29 25 23 22 20 20 19 18 18 17 17 17 16 16 15 15 15 phoH...”
- More
B2G73_RS09175 biofilm formation regulator BssS from Citrobacter werkmanii
64% identity, 100% coverage
BHW77_11525 biofilm formation regulator BssS from Escherichia coli
ECs_1438 biofilm regulator from Escherichia coli O157:H7 str. Sakai
ECs1438 biofilm formation regulatory protein BssS from Escherichia coli O157:H7 str. Sakai
S1144 biofilm formation regulatory protein BssS from Shigella flexneri 2a str. 2457T
Z1697 orf, hypothetical protein from Escherichia coli O157:H7 EDL933
64% identity, 100% coverage
- Genomewide transcriptional response of Escherichia coli O157:H7 to norepinephrine
Sharma, BMC genomics 2022 - “...cyclase +2.87 3.86E-08 BHW77_21465 bolA transcriptional regulator +3.22 2.57E-05 BHW77_19190 bssR transcriptional regulator +2.76 1.25E-04 BHW77_11525 bssS transcriptional regulator +7.75 4.94E-08 BHW77_17570 flhC transcriptional regulator 1.62 2.44E-02 BHW77_16255 sodC superoxide dismutase + 2.81 3.37E-04 a Gene group/gene designations were selected from RAST Server [ 109 ]...”
- Pre-Harvest Survival and Post-Harvest Chlorine Tolerance of Enterohemorrhagic Escherichia coli on Lettuce
Tyagi, Toxins 2019 - “...1.7 ECs_1154 cbpM chaperone modulatory protein CbpM 1.8 1.8 ECs_1387 ybdM transcriptional regulator 2.1 1.7 ECs_1438 bssS transcriptional regulator biofilm 2.5 1.6 ECs_1683 ycgB SpoVR family stationary phase protein 1.7 1.6 ECs_1883 pspC envelope stress response membrane protein PspC 4.0 2.5 ECs_1885 pspE thiosulfate sulfurtransferase PspE...”
- Pre-Harvest Survival and Post-Harvest Chlorine Tolerance of Enterohemorrhagic Escherichia coli on Lettuce
Tyagi, Toxins 2019 - “...2.1 ECs1388 pchD Putative transcriptional regulator 3.7 3.9 ECs1417 csgD Transcriptional regulator CsgD 4.5 3.3 ECs1438 bssS biofilm regulator 3.4 4.2 ECs1490 bhsA multiple stress resistance protein (YcfR) 3.5 4.2 ECs1926 zntB Zinc transport protein ZntB 1.8 1.8 ECs2062 ybfL type IV secretion protein Rhs 3.9...”
- Gene expression induced in Escherichia coli O157:H7 upon exposure to model apple juice
Bergholz, Applied and environmental microbiology 2009 - “...ECs1243 ECs1246 ECs1293 ECs1318 ECs1342 ECs1350 ECs1397 ECs1438 ECs1441 ECs1488 ECs1490 ECs1576 ECs1588 ECs1593 ECs1612 ECs1654 ECs1655 ECs1691 ECs1760 ECs1763...”
- Global transcriptional response of Escherichia coli O157:H7 to growth transitions in glucose minimal medium
Bergholz, BMC microbiology 2007 - “...terE -2.90 1 ECs0507 ybaY 3.19 2 ECs1423 - 2.34 2 ECs0509 ybaA 2.56 2 ECs1438 yceP 4.78 2 ECs0518 aefA 2.12 2 ECs1466 yceD -2.86 1 ECs1467 rpmF -2.36 1 ECs2307 ydgG -2.69 1 ECs1500 potC -2.14 1 ECs2308 pntB -2.80 1 ECs1603 purB -3.58...”
- Addendum
, Open forum infectious diseases 2019 - Comparison of strand-specific transcriptomes of enterohemorrhagic Escherichia coli O157:H7 EDL933 (EHEC) under eleven different environmental conditions including radish sprouts and cattle feces
Landstorfer, BMC genomics 2014 - “...(168) 3.3 (472) 0.5 (18) 0.5 (11) 3.8 (440) 0.3 (23) 5.6 (1336) 7.5 (0) Z1697 biofilm formation regulatory protein BssS 1 (113) 2.4 (386) 2.5 (116) 6.7 (10874) 4.4 (2326) 1.5 (89) 3.7 (512) 1.5 (219) 3.0 (556) 6.1 (4555) 4.7 (530) Z2243 nitrite extrusion...”
- “...5 ). An additional indicator for adhesion to radish sprouts is the up-regulation of bssS (Z1697, Table 5 ), a regulatory gene for biofilm formation [ 92 ]. The increased transcription level of curli-related genes together with bssS corroborates the hypothesis of Fink et al ....”
- Transcriptional responses of Escherichia coli K-12 and O157:H7 associated with lettuce leaves
Fink, Applied and environmental microbiology 2012 - “...Symbol Description Day 1 Day 3 Biofilm Z1027 Z1697 ybiM yceP (bssS) Hypothetical protein Hypothetical protein 31.30 7.90 68.30 7.90 Cell envelope Z2775 Z1037...”
For advice on how to use these tools together, see
Interactive tools for functional annotation of bacterial genomes.
The PaperBLAST database links 793,807 different protein sequences to 1,259,118 scientific articles. Searches against EuropePMC were last performed on March 13 2025.
PaperBLAST builds a database of protein sequences that are linked
to scientific articles. These links come from automated text searches
against the articles in EuropePMC
and from manually-curated information from GeneRIF, UniProtKB/Swiss-Prot,
BRENDA,
CAZy (as made available by dbCAN),
BioLiP,
CharProtDB,
MetaCyc,
EcoCyc,
TCDB,
REBASE,
the Fitness Browser,
and a subset of the European Nucleotide Archive with the /experiment tag.
Given this database and a protein sequence query,
PaperBLAST uses protein-protein BLAST
to find similar sequences with E < 0.001.
To build the database, we query EuropePMC with locus tags, with RefSeq protein
identifiers, and with UniProt
accessions. We obtain the locus tags from RefSeq or from MicrobesOnline. We use
queries of the form "locus_tag AND genus_name" to try to ensure that
the paper is actually discussing that gene. Because EuropePMC indexes
most recent biomedical papers, even if they are not open access, some
of the links may be to papers that you cannot read or that our
computers cannot read. We query each of these identifiers that
appears in the open access part of EuropePMC, as well as every locus
tag that appears in the 500 most-referenced genomes, so that a gene
may appear in the PaperBLAST results even though none of the papers
that mention it are open access. We also incorporate text-mined links
from EuropePMC that link open access articles to UniProt or RefSeq
identifiers. (This yields some additional links because EuropePMC
uses different heuristics for their text mining than we do.)
For every article that mentions a locus tag, a RefSeq protein
identifier, or a UniProt accession, we try to select one or two
snippets of text that refer to the protein. If we cannot get access to
the full text, we try to select a snippet from the abstract, but
unfortunately, unique identifiers such as locus tags are rarely
provided in abstracts.
PaperBLAST also incorporates manually-curated protein functions:
- Proteins from NCBI's RefSeq are included if a
GeneRIF
entry links the gene to an article in
PubMed®.
GeneRIF also provides a short summary of the article's claim about the
protein, which is shown instead of a snippet.
- Proteins from Swiss-Prot (the curated part of UniProt)
are included if the curators
identified experimental evidence for the protein's function (evidence
code ECO:0000269). For these proteins, the fields of the Swiss-Prot entry that
describe the protein's function are shown (with bold headings).
- Proteins from BRENDA,
a curated database of enzymes, are included if they are linked to a paper in PubMed
and their full sequence is known.
- Every protein from the non-redundant subset of
BioLiP,
a database
of ligand-binding sites and catalytic residues in protein structures, is included. Since BioLiP itself
does not include descriptions of the proteins, those are taken from the
Protein Data Bank.
Descriptions from PDB rely on the original submitter of the
structure and cannot be updated by others, so they may be less reliable.
(For SitesBLAST and Sites on a Tree, we use a larger subset of BioLiP so that every
ligand is represented among a group of structures with similar sequences, but for
PaperBLAST, we use the non-redundant set provided by BioLiP.)
- Every protein from EcoCyc, a curated
database of the proteins in Escherichia coli K-12, is included, regardless
of whether they are characterized or not.
- Proteins from the MetaCyc metabolic pathway database
are included if they are linked to a paper in PubMed and their full sequence is known.
- Proteins from the Transport Classification Database (TCDB)
are included if they have known substrate(s), have reference(s),
and are not described as uncharacterized or putative.
(Some of the references are not visible on the PaperBLAST web site.)
- Every protein from CharProtDB,
a database of experimentally characterized protein annotations, is included.
- Proteins from the CAZy database of carbohydrate-active enzymes
are included if they are associated with an Enzyme Classification number.
Even though CAZy does not provide links from individual protein sequences to papers,
these should all be experimentally-characterized proteins.
- Proteins from the REBASE database
of restriction enzymes are included if they have known specificity.
- Every protein with an evidence-based reannotation (based on mutant phenotypes)
in the Fitness Browser is included.
- Sequence-specific transcription factors (including sigma factors and DNA-binding response regulators)
with experimentally-determined DNA binding sites from the
PRODORIC database of gene regulation in prokaryotes.
- Putative transcription factors from RegPrecise
that have manually-curated predictions for their binding sites. These predictions are based on
conserved putative regulatory sites across genomes that contain similar transcription factors,
so PaperBLAST clusters the TFs at 70% identity and retains just one member of each cluster.
- Coding sequence (CDS) features from the
European Nucleotide Archive (ENA)
are included if the /experiment tag is set (implying that there is experimental evidence for the annotation),
the nucleotide entry links to paper(s) in PubMed,
and the nucleotide entry is from the STD data class
(implying that these are targeted annotated sequences, not from shotgun sequencing).
Also, to filter out genes whose transcription or translation was detected, but whose function
was not studied, nucleotide entries or papers with more than 25 such proteins are excluded.
Descriptions from ENA rely on the original submitter of the
sequence and cannot be updated by others, so they may be less reliable.
Except for GeneRIF and ENA,
the curated entries include a short curated
description of the protein's function.
For entries from BioLiP, the protein's function may not be known beyond binding to the ligand.
Many of these entries also link to articles in PubMed.
For more information see the
PaperBLAST paper (mSystems 2017)
or the code.
You can download PaperBLAST's database here.
Changes to PaperBLAST since the paper was written:
- November 2023: incorporated PRODORIC and RegPrecise. Many PRODORIC entries were not linked to a protein sequence (no UniProt identifier), so we added this information.
- February 2023: BioLiP changed their download format. PaperBLAST now includes their non-redundant subset. SitesBLAST and Sites on a Tree use a larger non-redundant subset that ensures that every ligand is represented within each cluster. This should ensure that every binding site is represented.
- June 2022: incorporated some coding sequences from ENA with the /experiment tag.
- March 2022: incorporated BioLiP.
- April 2020: incorporated TCDB.
- April 2019: EuropePMC now returns table entries in their search results. This has expanded PaperBLAST's database, but most of the new entries are of low relevance, and the resulting snippets are often just lists of locus tags with annotations.
- February 2018: the alignment page reports the conservation of the hit's functional sites (if available from from Swiss-Prot or UniProt)
- January 2018: incorporated BRENDA.
- December 2017: incorporated MetaCyc, CharProtDB, CAZy, REBASE, and the reannotations from the Fitness Browser.
- September 2017: EuropePMC no longer returns some table entries in their search results. This has shrunk PaperBLAST's database, but has also reduced the number of low-relevance hits.
Many of these changes are described in Interactive tools for functional annotation of bacterial genomes.
PaperBLAST cannot provide snippets for many of the papers that are
published in non-open-access journals. This limitation applies even if
the paper is marked as "free" on the publisher's web site and is
available in PubmedCentral or EuropePMC. If a journal that you publish
in is marked as "secret," please consider publishing elsewhere.
Many important articles are missing from PaperBLAST, either because
the article's full text is not in EuropePMC (as for many older
articles), or because the paper does not mention a protein identifier such as a locus tag, or because of PaperBLAST's heuristics. If you notice an
article that characterizes a protein's function but is missing from
PaperBLAST, please notify the curators at UniProt
or add an entry to GeneRIF.
Entries in either of these databases will eventually be incorporated
into PaperBLAST. Note that to add an entry to UniProt, you will need
to find the UniProt identifier for the protein. If the protein is not
already in UniProt, you can ask them to create an entry. To add an
entry to GeneRIF, you will need an NCBI Gene identifier, but
unfortunately many prokaryotic proteins in RefSeq do not have
corresponding Gene identifers.
References
PaperBLAST: Text-mining papers for information about homologs.
M. N. Price and A. P. Arkin (2017). mSystems, 10.1128/mSystems.00039-17.
Europe PMC in 2017.
M. Levchenko et al (2017). Nucleic Acids Research, 10.1093/nar/gkx1005.
Gene indexing: characterization and analysis of NLM's GeneRIFs.
J. A. Mitchell et al (2003). AMIA Annu Symp Proc 2003:460-464.
UniProt: the universal protein knowledgebase.
The UniProt Consortium (2016). Nucleic Acids Research, 10.1093/nar/gkw1099.
BRENDA in 2017: new perspectives and new tools in BRENDA.
S. Placzek et al (2017). Nucleic Acids Research, 10.1093/nar/gkw952.
The EcoCyc database: reflecting new knowledge about Escherichia coli K-12.
I. M. Keeseler et al (2016). Nucleic Acids Research, 10.1093/nar/gkw1003.
The MetaCyc database of metabolic pathways and enzymes.
R. Caspi et al (2018). Nucleic Acids Research, 10.1093/nar/gkx935.
CharProtDB: a database of experimentally characterized protein annotations.
R. Madupu et al (2012). Nucleic Acids Research, 10.1093/nar/gkr1133.
The carbohydrate-active enzymes database (CAZy) in 2013.
V. Lombard et al (2014). Nucleic Acids Research, 10.1093/nar/gkt1178.
The Transporter Classification Database (TCDB): recent advances
M. H. Saier, Jr. et al (2016). Nucleic Acids Research, 10.1093/nar/gkv1103.
REBASE - a database for DNA restriction and modification: enzymes, genes and genomes.
R. J. Roberts et al (2015). Nucleic Acids Research, 10.1093/nar/gku1046.
Deep annotation of protein function across diverse bacteria from mutant phenotypes.
M. N. Price et al (2016). bioRxiv, 10.1101/072470.
by Morgan Price,
Arkin group
Lawrence Berkeley National Laboratory