P78524 (ST5_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
January 25, 2012.
Version 71.
History...
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Suppression of tumorigenicity 5 protein Alternative name(s): DENN domain-containing protein 2B HeLa tumor suppression 1 | ||||
| Gene names |
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| Organism | Homo sapiens (Human) | ||||
| Taxonomic identifier | 9606 [NCBI] | ||||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo |
Protein attributes
| Sequence length | 1137 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at protein level |
General annotation (Comments)
| Function | May be involved in cytoskeletal organization and tumorgenicity. Isoform 1 seems to be involved in a signaling transduction pathway leading to activation of MAPK1/ERK2. Isoform 3 may block ERK2 activation stimulated by ABL1. Isoform 3 may alter cell morphology and cell growth. Ref.8 Ref.9 |
| Subunit structure | |
| Tissue specificity | Widely expressed with the exception of peripheral blood lymphocytes. Isoform 1 is expressed in several epithelial and fibroblast (including tumorigenic) but absent in lymphoid cell lines (at protein level). Isoform 3 is expressed in primary cell or weakly tumorigenic but not in tumorigenic cell lines (at protein level). Ref.9 |
| Sequence similarities | Contains 1 dDENN domain. Contains 1 DENN domain. Contains 1 uDENN domain. |
| Sequence caution | The sequence AAC50925.1 differs from that shown. Reason: Frameshift at positions 159 and 169. |
Ontologies
| Keywords | |
|---|---|
| Coding sequence diversity | Alternative promoter usage Alternative splicing Polymorphism |
| PTM | Phosphoprotein |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Biological process | positive regulation of ERK1 and ERK2 cascade Inferred from direct assay Ref.8. Source: MGI |
| Complete GO annotation... | |
Alternative products
| This entry describes 3 isoforms produced by alternative promoter usage and alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: P78524-1) Also known as: p126; This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry. | ||||||
| Note: Produced by alternative promoter usage. | ||||||
| Isoform 2 (identifier: P78524-2) Also known as: p82; The sequence of this isoform differs from the canonical sequence as follows: 28-447: Missing. | ||||||
| Note: Produced by alternative splicing of isoform 1. | ||||||
| Isoform 3 (identifier: P78524-3) Also known as: p70; The sequence of this isoform differs from the canonical sequence as follows: 1-528: Missing. | ||||||
| Note: Produced by alternative promoter usage. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 1137 | 1137 | Suppression of tumorigenicity 5 protein | PRO_0000247448 | |||||
Regions | |||||||||
| Domain | 709 – 784 | 76 | UDENN | ||||||
| Domain | 791 – 975 | 185 | DENN | ||||||
| Domain | 1022 – 1089 | 68 | dDENN | ||||||
| Region | 401 – 447 | 47 | Interaction with ABL1 | ||||||
| Compositional bias | 33 – 93 | 61 | Pro-rich | ||||||
| Compositional bias | 350 – 434 | 85 | Pro-rich | ||||||
Amino acid modifications | |||||||||
| Modified residue | 622 | 1 | Phosphoserine Ref.11 | ||||||
| Modified residue | 1011 | 1 | Phosphoserine Ref.10 | ||||||
| Modified residue | 1013 | 1 | Phosphoserine Ref.10 | ||||||
| Modified residue | 1015 | 1 | Phosphoserine Ref.10 | ||||||
Natural variations | |||||||||
| Alternative sequence | 1 – 528 | 528 | Missing in isoform 3. | VSP_019987 | |||||
| Alternative sequence | 28 – 447 | 420 | Missing in isoform 2. | VSP_019988 | |||||
| Natural variant | 316 | 1 | K → N. Ref.6 Corresponds to variant rs3794153 [ dbSNP | Ensembl ]. | VAR_027101 | |||||
| Natural variant | 399 | 1 | D → E. Ref.1 Ref.2 Corresponds to variant rs3812762 [ dbSNP | Ensembl ]. | VAR_027102 | |||||
| Natural variant | 620 | 1 | I → T. Ref.6 Corresponds to variant rs17853683 [ dbSNP | Ensembl ]. | VAR_027103 | |||||
| Natural variant | 657 | 1 | S → F. Corresponds to variant rs11042047 [ dbSNP | Ensembl ]. | VAR_030642 | |||||
| Natural variant | 774 | 1 | S → G. Ref.6 Corresponds to variant rs17853682 [ dbSNP | Ensembl ]. | VAR_027104 | |||||
Experimental info | |||||||||
| Sequence conflict | 113 | 1 | A → T in AAC50925. Ref.1 | ||||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "Differential expression of the human ST5 gene in HeLa-fibroblast hybrid cell lines mediated by YY1: evidence that YY1 plays a part in tumor suppression." Lichy J.H., Majidi M., Elbaum J., Tsai M.M. Nucleic Acids Res. 24:4700-4708(1996) [PubMed: 8972856] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORMS 1; 2 AND 3), VARIANT GLU-399. |
| [2] | "Comparative genomic sequencing reveals a strikingly similar architecture of a conserved syntenic region on human chromosome 11p15.3 (including gene ST5) and mouse chromosome 7." Amid C., Bahr A., Mujica A., Sampson N., Bikar S.E., Winterpacht A., Zabel B., Hankeln T., Schmidt E.R. Cytogenet. Cell Genet. 93:284-290(2001) [PubMed: 11528127] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA], VARIANT GLU-399. |
| [3] | "Complete sequencing and characterization of 21,243 full-length human cDNAs." Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S. Sugano S.Nat. Genet. 36:40-45(2004) [PubMed: 14702039] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 2 AND 3). Tissue: Brain and Spleen. |
| [4] | "Human chromosome 11 DNA sequence and analysis including novel gene identification." Taylor T.D., Noguchi H., Totoki Y., Toyoda A., Kuroki Y., Dewar K., Lloyd C., Itoh T., Takeda T., Kim D.-W., She X., Barlow K.F., Bloom T., Bruford E., Chang J.L., Cuomo C.A., Eichler E., FitzGerald M.G. Sakaki Y.Nature 440:497-500(2006) [PubMed: 16554811] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [5] | Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M., Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R., Flanigan M.J., Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V., Hannenhalli S., Turner R. Venter J.C.Submitted (SEP-2005) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [6] | "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] (ISOFORM 1), VARIANTS ASN-316; THR-620 AND GLY-774. Tissue: Testis. |
| [7] | "Identification of a human chromosome 11 gene which is differentially regulated in tumorigenic and nontumorigenic somatic cell hybrids of HeLa cells." Lichy J.H., Modi W.S., Seuanez H.N., Howley P.M. Cell Growth Differ. 3:541-548(1992) [PubMed: 1390339] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 493-1137. |
| [8] | "Activation of extracellular signal-regulated kinase 2 by a novel Abl-binding protein, ST5." Majidi M., Hubbs A.E., Lichy J.H. J. Biol. Chem. 273:16608-16614(1998) [PubMed: 9632734] [Abstract] Cited for: FUNCTION, INTERACTION WITH ABL1. |
| [9] | "Expression of an isoform of the novel signal transduction protein ST5 is linked to cell morphology." Hubbs A.E., Majidi M., Lichy J.H. Oncogene 18:2519-2525(1999) [PubMed: 10229203] [Abstract] Cited for: FUNCTION, TISSUE SPECIFICITY. |
| [10] | "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks." Olsen J.V., Blagoev B., Gnad F., Macek B., Kumar C., Mortensen P., Mann M. Cell 127:635-648(2006) [PubMed: 17081983] [Abstract] Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-1011; SER-1013 AND SER-1015, MASS SPECTROMETRY. Tissue: Cervix carcinoma. |
| [11] | "A quantitative atlas of mitotic phosphorylation." Dephoure N., Zhou C., Villen J., Beausoleil S.A., Bakalarski C.E., Elledge S.J., Gygi S.P. Proc. Natl. Acad. Sci. U.S.A. 105:10762-10767(2008) [PubMed: 18669648] [Abstract] Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-622, MASS SPECTROMETRY. Tissue: Cervix carcinoma. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | U15131 mRNA. Translation: AAC50925.1. Frameshift. U15779 mRNA. Translation: AAB97097.1. U15780 mRNA. Translation: AAC50926.1. AJ400879 Genomic DNA. Translation: CAC35387.1. AK127763 mRNA. Translation: BAG54568.1. AK312758 mRNA. Translation: BAG35624.1. AC026894 Genomic DNA. No translation available. AC091053 Genomic DNA. No translation available. CH471064 Genomic DNA. Translation: EAW68618.1. BC036655 mRNA. Translation: AAH36655.1. S45936 mRNA. Translation: AAB23647.1. |
| IPI | IPI00162743. IPI00298518. IPI00783821. |
| PIR | A49013. |
| RefSeq | NP_005409.3. NM_005418.3. NP_631896.1. NM_139157.2. NP_998783.1. NM_213618.1. |
| UniGene | Hs.117715. |
3D structure databases | |
| ProteinModelPortal | P78524. |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | P78524. 3 interactions. |
| MINT | MINT-1184327. |
| STRING | P78524. |
PTM databases | |
| PhosphoSite | P78524. |
Polymorphism databases | |
| DMDM | 110816432. |
Proteomic databases | |
| PRIDE | P78524. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000313726; ENSP00000319678; ENSG00000166444. ENST00000357665; ENSP00000350294; ENSG00000166444. ENST00000396665; ENSP00000379900; ENSG00000166444. |
| GeneID | 6764. |
| KEGG | hsa:6764. |
| UCSC | uc001mgt.1. human. |
Organism-specific databases | |
| CTD | 6764. |
| GeneCards | GC11M008671. |
| HGNC | HGNC:11350. ST5. |
| MIM | 140750. gene. |
| neXtProt | NX_P78524. |
| PharmGKB | PA36172. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | prNOG15669. |
| HOVERGEN | HBG079980. |
| InParanoid | P78524. |
| OMA | ACRYPSH. |
| OrthoDB | EOG4CRKZC. |
| PhylomeDB | P78524. |
Gene expression databases | |
| ArrayExpress | P78524. |
| Bgee | P78524. |
| CleanEx | HS_ST5. |
| Genevestigator | P78524. |
| GermOnline | ENSG00000166444. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR005112. dDENN. IPR001194. DENN. IPR005113. uDENN. [Graphical view] |
| Pfam | PF03455. dDENN. 1 hit. PF02141. DENN. 1 hit. PF03456. uDENN. 1 hit. [Graphical view] |
| SMART | SM00801. dDENN. 1 hit. SM00799. DENN. 1 hit. SM00800. uDENN. 1 hit. [Graphical view] |
| PROSITE | PS50947. DDENN. 1 hit. PS50211. DENN. 1 hit. PS50946. UDENN. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| NextBio | 26398. |
| SOURCE | Search... |
Entry information
| Entry name | ST5_HUMAN | ||||||||
| Accession | Primary (citable) accession number: P78524 Secondary accession number(s): B2R6X7 Q9BQQ6 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation program | Chordata Protein Annotation Program | ||||||||
| Disclaimer | Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care. | ||||||||
Relevant documents
| Human chromosome 11 Human chromosome 11: 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 |

Clusters with