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Reviewed, UniProtKB/Swiss-Prot Q03403 (TFF2_HUMAN)

Last modified June 16, 2009. Version 75. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (5) | Third-party data | Customize display text xml rdf/xml gff fasta
Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Sequence annotation (Features) · Sequences · References · Web resources · Cross-references · Entry information · Relevant documents

Names and origin

Protein namesRecommended name:
    Trefoil factor 2
Alternative name(s):
    Spasmolytic polypeptide
      Short name=SP
    Spasmolysin
Gene names
Name: TFF2
Synonyms: SML1
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length129 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is further processed into a mature form.
Protein existenceEvidence at protein level.

General annotation (Comments)

Function

Inhibits gastrointestinal motility and gastric acid secretion. Could function as a structural component of gastric mucus, possibly by stabilizing glycoproteins in the mucus gel through interactions with carbohydrate side chains By similarity.

Subcellular location

Secreted.

Tissue specificity

Stomach.

Sequence similarities

Contains 2 P-type (trefoil) domains.

Ontologies

Keywords
   Cellular componentSecreted
   Coding sequence diversityPolymorphism
   DomainRepeat
Signal
   PTMDisulfide bond
Gene Ontology (GO)
   Biological processdigestion

Traceable author statement. Source: ProtInc

   Cellular componentextracellular region

Inferred from electronic annotation. Source: UniProtKB-SubCell

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Signal peptide1 – 2323 Potential
Chain24 – 129106Trefoil factor 2
PRO_0000023460

Regions

Domain29 – 7345P-type 1
Domain79 – 12244P-type 2

Amino acid modifications

Disulfide bond29 ↔ 127 By similarity
Disulfide bond31 ↔ 58 By similarity
Disulfide bond42 ↔ 57 By similarity
Disulfide bond52 ↔ 69 By similarity
Disulfide bond81 ↔ 107 By similarity
Disulfide bond91 ↔ 106 By similarity
Disulfide bond101 ↔ 118 By similarity

Natural variations

Natural variant31R → W: dbSNP rs7277409.
VAR_053564

Experimental info

Sequence conflict1 – 1919MGRRD…LGLCA → RHGTARRPAPGSAPRPGAMC Ref.1
Sequence conflict1221K → N in CAA35995. Ref.1

Sequences

Sequence LengthMass (Da)Tools
Q03403-1 [UniParc].

Last modified November 1, 1997. Version 2.
Checksum: 6A296A11AD9CCC5D

FASTA12914,284
        10         20         30         40         50         60 
MGRRDAQLLA ALLVLGLCAL AGSEKPSPCQ CSRLSPHNRT NCGFPGITSD QCFDNGCCFD 

        70         80         90        100        110        120 
SSVTGVPWCF HPLPKQESDQ CVMEVSDRRN CGYPGISPEE CASRKCCFSN FIFEVPWCFF 


PKSVEDCHY 

« Hide

References

« Hide 'large scale' references
[1]"hSP, the domain-duplicated homolog of pS2 protein, is co-expressed with pS2 in stomach but not in breast carcinoma."
Tomasetto C., Rio M.C., Gautier C., Wolf C., Hareuveni M., Chambon P., Lathe R.
EMBO J. 9:407-414(1990) [PubMed: 2303034] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA / MRNA].
Tissue: Stomach.
[2]"The three human trefoil genes TFF1, TFF2, and TFF3 are located within a region of 55 kb on chromosome 21q22.3."
Seib T., Blin N., Hilgert K., Seifert M., Theisinger B., Engel M., Dooley S., Zang K.D., Welter C.
Genomics 40:200-202(1997) [PubMed: 9070946] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA].
[3]"Refined localization of autosomal recessive nonsyndromic deafness DFNB10 locus using 34 novel microsatellite markers, genomic structure, and exclusion of six known genes in the region."
Berry A., Scott H.S., Kudoh J., Talior I., Korostishevsky M., Wattenhofer M., Guipponi M., Barras C., Rossier C., Shibuya K., Wang J., Kawasaki K., Asakawa S., Minoshima S., Shimizu N., Antonarakis S.E., Bonne-Tamir B.
Genomics 68:22-29(2000) [PubMed: 10950923] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA].
[4]"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res. 14:2121-2127(2004) [PubMed: 15489334] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
Tissue: Colon.
+Additional computationally mapped references.

Cross-references

Sequence databases

X51698 mRNA. Translation: CAA35995.1.
U47292 expand/collapse EMBL AC list , U47289, U47290, U47291 Genomic DNA. Translation: AAB05397.1.
AB038162 Genomic DNA. Translation: BAB13730.1.
BC032820 mRNA. Translation: AAH32820.1.
IPIIPI00010675.
PIRS12371.
RefSeqNP_005414.1.
UniGeneHs.2979

3D structure databases

HSSPHSSP built from PDB template 1PCP based on UniProtKB P01359.
SMRQ03403. Positions 24-129.
ModBaseSearch...

Proteomic databases

PeptideAtlasQ03403.
PRIDEQ03403.

Genome annotation databases

EnsemblENSG00000160181. Homo sapiens. [Contig view]
GeneID7032.
KEGGhsa:7032.

Organism-specific databases

GeneCardsGC21M042639.
HGNCHGNC:11756. TFF2.
MIM182590. gene.
PharmGKBPA36471.
GenAtlasSearch...

Phylogenomic databases

HOGENOMQ03403.
HOVERGENQ03403.
OMAQ03403. FPGITSD.

Gene expression databases

ArrayExpressQ03403.
BgeeQ03403.
CleanExHS_TFF2.
GermOnlineENSG00000160181. Homo sapiens.

Family and domain databases

InterProIPR000519. P_trefoil.
IPR017994. P_trefoil_chordata.
IPR017957. P_trefoil_CS.
[Graphical view]
PfamPF00088. Trefoil. 2 hits.
[Graphical view]
PRINTSPR00680. PTREFOIL.
SMARTSM00018. PD. 2 hits.
[Graphical view]
PROSITEPS00025. P_TREFOIL_1. 2 hits.
PS51448. P_TREFOIL_2. 2 hits.
[Graphical view]
ProtoNetSearch...

Other Resources

NextBio27473.
SOURCESearch...

Entry information

Entry nameTFF2_HUMAN
AccessionPrimary (citable) accession number: Q03403
Secondary accession number(s): Q15854
Entry history
Integrated into UniProtKB/Swiss-Prot: October 1, 1994
Last sequence update: November 1, 1997
Last modified: June 16, 2009
This is version 75 of the entry and version 2 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation projectHPI (Human Proteome Initiative)

Relevant documents

Human chromosome 21

Human chromosome 21: entries, gene names and cross-references to MIM

Human entries with polymorphisms or disease mutations

List of human entries with polymorphisms or disease mutations

Human polymorphisms and disease mutations

Index of human polymorphisms and disease mutations

MIM cross-references

Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot

SIMILARITY comments

Index of protein domains and families

Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Sequence annotation (Features) · Sequences · References · Web resources · Cross-references · Entry information · Relevant documents