Reviewed,
UniProtKB/Swiss-Prot Q9NZI7 (UBIP1_HUMAN)
Last modified
June 16, 2009.
Version 56.
History...
Clusters with 100%,
90%,
50% identity |
Documents (5) |
Third-party data |
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Names and origin
| Protein names | Recommended name: Upstream-binding protein 1 Alternative name(s): LBP-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 | 540 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is not processed. |
| Protein existence | Evidence at transcript level. |
General annotation (Comments)
| Function | Functions as a transcriptional activator in a promoter context-dependent manner. Modulates the placental expression of CYP11A1. Involved in regulation of the alpha-globin gene in erythroid cells. Activation of the alpha-globin promoter in erythroid cells is via synergistic interaction with TFCP2 By similarity. Involved in regulation of the alpha-globin gene in erythroid cells. Activation of the alpha-globin promoter in erythroid cells is via synergistic interaction with TFCP2 By similarity. Binds strongly to sequences around the HIV-1 initiation site and weakly over the TATA-box. Represses HIV-1 transcription by inhibiting the binding of TFIID to the TATA-box. |
| Subunit structure | Interacts with TFCP2. Interacts with PIAS1, and is probably part of a complex containing TFCP2, UBP1 and PIAS1 By similarity. |
| Subcellular location | |
| Tissue specificity | Expressed in adrenal tissue, JEG-3, NCI-H295A, HepG2 and HeLa cell lines. Ref.2 |
| Induction | Induced by HIV-1 infection of lymphocytes. Ref.6 |
| Sequence similarities | Belongs to the grh/CP2 family. CP2 subfamily. |
Ontologies
| Keywords | |
|---|---|
| Biological process | Transcription Transcription regulation |
| Cellular component | Nucleus |
| Coding sequence diversity | Alternative splicing Polymorphism |
| Ligand | DNA-binding |
| Gene Ontology (GO) | |
| Biological process | negative regulation of transcription Ref.1 Traceable author statement. Source: UniProtKB regulation of transcription from RNA polymerase II promoter Ref.1Traceable author statement. Source: ProtInc transcriptionInferred from electronic annotation. Source: UniProtKB-KW viral genome replication Ref.1Traceable author statement. Source: ProtInc |
| Cellular component | nucleus Ref.1 Traceable author statement. Source: UniProtKB |
| Molecular function | specific transcriptional repressor activity Ref.1 Traceable author statement. Source: UniProtKB transcription corepressor activity Ref.1Traceable author statement. Source: ProtInc transcription factor activity Ref.1Traceable author statement. Source: ProtInc |
| Complete GO annotation... | |
Alternative products
| This entry describes 2 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q9NZI7-1) Also known as: LBP-1b; 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. | ||||||
| Isoform 2 (identifier: Q9NZI7-4) Also known as: LBP-1a; The sequence of this isoform differs from the canonical sequence as follows: 274-309: Missing. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 540 | 540 | Upstream-binding protein 1 | PRO_0000229026 | |||||
Natural variations | |||||||||
| Alternative sequence | 274 – 309 | 36 | Missing in isoform 2. | VSP_017730 | |||||
| Natural variant | 109 | 1 | N → S: dbSNP rs3736563. Ref.1 | VAR_049294 | |||||
| Natural variant | 212 | 1 | T → A: dbSNP rs17854430. Ref.4 | VAR_025730 | |||||
Experimental info | |||||||||
| Sequence conflict | 93 – 94 | 2 | EI → D in BAB14501. Ref.3 | ||||||
| Sequence conflict | 273 | 1 | E → EE Ref.1 | ||||||
| Sequence conflict | 291 – 297 | 7 | SSKRTLP → VQQADFA Ref.1 | ||||||
| Sequence conflict | 418 | 1 | Y → V Ref.1 | ||||||
| Sequence conflict | 424 | 1 | R → RR in CAH18658. Ref.5 | ||||||
| Sequence conflict | 503 | 1 | G → GH Ref.1 | ||||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "Characterization of a family of related cellular transcription factors which can modulate human immunodeficiency virus type 1 transcription in vitro." Yoon J.-B., Li G., Roeder R.G. Mol. Cell. Biol. 14:1776-1785(1994) [PubMed: 8114710] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORMS 1 AND 2), FUNCTION, SUBCELLULAR LOCATION, VARIANT SER-109. |
| [2] | "Cloning of factors related to HIV-inducible LBP proteins that regulate steroidogenic factor-1-independent human placental transcription of the cholesterol side-chain cleavage enzyme, P450scc." Huang N., Miller W.L. J. Biol. Chem. 275:2852-2858(2000) [PubMed: 10644752] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1), FUNCTION, TISSUE SPECIFICITY. Tissue: Placenta. |
| [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] (ISOFORM 2). |
| [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] (ISOFORM 1), VARIANT ALA-212. Tissue: Brain. |
| [5] | "The full-ORF clone resource of the German cDNA consortium." Bechtel S., Rosenfelder H., Duda A., Schmidt C.P., Ernst U., Wellenreuther R., Mehrle A., Schuster C., Bahr A., Blocker H., Heubner D., Hoerlein A., Michel G., Wedler H., Kohrer K., Ottenwalder B., Poustka A., Wiemann S., Schupp I. BMC Genomics 8:399-399(2007) [PubMed: 17974005] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 394-540. Tissue: Amygdala. |
| [6] | "Repression of HIV-1 transcription by a cellular protein." Kato H., Horikoshi M., Roeder R.G. Science 251:1476-1479(1991) [PubMed: 2006421] [Abstract] Cited for: FUNCTION, INDUCTION. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| AF198487 mRNA. Translation: AAF32274.1. AK023274 mRNA. Translation: BAB14501.1. BC047235 mRNA. Translation: AAH47235.1. CR749798 mRNA. Translation: CAH18658.1. | |
| IPI | IPI00005018. IPI00294870. |
| PIR | A56205. B56205. |
| RefSeq | NP_001121632.1. NP_001121633.1. NP_055332.3. |
| UniGene | Hs.714881 |
3D structure databases | |
| ModBase | Search... |
PTM databases | |
| PhosphoSite | Q9NZI7. |
Proteomic databases | |
| PRIDE | Q9NZI7. |
Genome annotation databases | |
| Ensembl | ENSG00000153560. Homo sapiens. [Contig view] |
| GeneID | 7342. |
| KEGG | hsa:7342. |
Organism-specific databases | |
| GeneCards | GC03M033404. |
| H-InvDB | HIX0003156. |
| HGNC | HGNC:12507. UBP1. |
| MIM | 609784. gene. |
| PharmGKB | PA28420. |
| GenAtlas | Search... |
Phylogenomic databases | |
| HOGENOM | Q9NZI7. |
| HOVERGEN | Q9NZI7. |
| OMA | Q9NZI7. SPWPDTP. |
Gene expression databases | |
| Bgee | Q9NZI7. |
| CleanEx | HS_UBP1. |
| GermOnline | ENSG00000153560. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR007604. CP2. [Graphical view] |
| Pfam | PF04516. CP2. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other Resources | |
| NextBio | 28742. |
| SOURCE | Search... |
Entry information
| Entry name | UBIP1_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q9NZI7 Secondary accession number(s): Q68CT0 Q9UD78 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation project | HPI (Human Proteome Initiative) | ||||||||
Relevant documents
| Human chromosome 3 Human chromosome 3: 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


