Reviewed,
UniProtKB/Swiss-Prot Q86XK2 (FBX11_HUMAN)
Last modified
July 22, 2008.
Version 64.
History...
Clusters with 100%,
90%,
50% identity |
Documents (7) |
Third-party data |
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Names and origin
| Protein names | Recommended name: F-box only protein 11 Alternative name(s): Vitiligo-associated protein 1 Short name=VIT-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 | 927 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is not processed. |
| Protein existence | Evidence at protein level. |
General annotation (Comments)
| Function | Substrate recognition component of the a (SKP1-CUL1-F-box protein) E3 ubiquitin-protein ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Probably recognizes and binds to phosphorylated target proteins. Binds to and neddylates phosphorylated TP53/p53, inhibiting its transcriptional activity. SCF(FBXO11) does not seem to direct ubiquitination of TP53. |
| Pathway | |
| Subunit structure | Component of the probable SCF(FBXWO11) complex consisting of CUL1, RBX1, SKP1A and FBXO11. Interacts with TP53. |
| Subcellular location | |
| Tissue specificity | Isoform 5 is expressed in keratinocytes, fibroblasts and melanocytes. |
| Involvement in disease | FBXO11 is down-regulated in vitiligo [MIM:193200]. It is a skin disorder associated with progressive skin depigmentation. |
| Sequence similarities | Contains 1 F-box domain. Contains 19 PbH1 repeats. Contains 1 UBR-type zinc finger. |
| Sequence caution | The sequence AAF76888.1 differs from that shown. Reason: Miscellaneous discrepancy. Intron retention. The sequence AAN76518.1 differs from that shown. Reason: Frameshift at position 141. |
Ontologies
Keywords | |
|---|---|
| Biological process | Ubl conjugation pathway |
| Cellular component | Nucleus |
| Coding sequence diversity | Alternative splicing Polymorphism |
| Domain | Repeat Zinc-finger |
| Ligand | Metal-binding Zinc |
Gene Ontology (GO) | |
| Biological process | protein ubiquitination Ref.5 Non-traceable author statement. Source: UniProtKB ubiquitin-dependent protein catabolic process Ref.7Non-traceable author statement. Source: UniProtKB |
| Cellular component | cytoplasm Inferred from direct assay. Source: HGNC nucleusInferred from direct assay. Source: HGNC ubiquitin ligase complex Ref.5 Ref.7Non-traceable author statement. Source: UniProtKB |
| Molecular function | histone-arginine N-methyltransferase activity Inferred from direct assay. Source: HGNC peptidyl-arginine C-methyltransferase activityInferred from direct assay. Source: HGNC protein binding Ref.1Inferred from physical interaction. Source: IntAct ubiquitin-protein ligase activity Ref.5Non-traceable author statement. Source: UniProtKB |
| Complete GO annotation... | |
Alternative products
| This entry describes 5 isoforms produced by alternative splicing. [Align] [Select] | |||||
| Isoform 1 (identifier: Q86XK2-1) 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: Q86XK2-2) The sequence of this isoform differs from the canonical sequence as follows: 1-209: Missing. 744-770: LLEENDIFRNAQAGVLISTNSHPILRK → IVVNFALVKNPVFHYSSISLMINDIAN 771-927: Missing. | |||||
| Notes: No experimental confirmation available. | |||||
| Isoform 3 (identifier: Q86XK2-3) The sequence of this isoform differs from the canonical sequence as follows: 1-84: Missing. 670-927: Missing. | |||||
| Notes: No experimental confirmation available. | |||||
| Isoform 4 (identifier: Q86XK2-4) The sequence of this isoform differs from the canonical sequence as follows: 197-211: KRLYMEVFEYTRPMM → LGEVAHAYNPSTLGG 212-927: Missing. | |||||
| Isoform 5 (identifier: Q86XK2-5) The sequence of this isoform differs from the canonical sequence as follows: 885-885: R → RYVAHLLDILPNYFPPHFSNIWVSFCFR | |||||
| Notes: No experimental confirmation available. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | ||||
Molecule processing | ||||||||
|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 927 | 927 | F-box only protein 11 | |||||
Regions | ||||||||
| Domain | 153 – 199 | 47 | F-box | |||||
| Repeat | 395 – 417 | 23 | PbH1 1 | |||||
| Repeat | 418 – 440 | 23 | PbH1 2 | |||||
| Repeat | 441 – 463 | 23 | PbH1 3 | |||||
| Repeat | 464 – 486 | 23 | PbH1 4 | |||||
| Repeat | 487 – 509 | 23 | PbH1 5 | |||||
| Repeat | 510 – 532 | 23 | PbH1 6 | |||||
| Repeat | 533 – 555 | 23 | PbH1 7 | |||||
| Repeat | 556 – 578 | 23 | PbH1 8 | |||||
| Repeat | 579 – 601 | 23 | PbH1 9 | |||||
| Repeat | 602 – 624 | 23 | PbH1 10 | |||||
| Repeat | 625 – 647 | 23 | PbH1 11 | |||||
| Repeat | 648 – 670 | 23 | PbH1 12 | |||||
| Repeat | 671 – 693 | 23 | PbH1 13 | |||||
| Repeat | 694 – 716 | 23 | PbH1 14 | |||||
| Repeat | 717 – 739 | 23 | PbH1 15 | |||||
| Repeat | 740 – 762 | 23 | PbH1 16 | |||||
| Repeat | 763 – 785 | 23 | PbH1 17 | |||||
| Repeat | 786 – 808 | 23 | PbH1 18 | |||||
| Repeat | 809 – 830 | 22 | PbH1 19 | |||||
| Zinc finger | 833 – 904 | 72 | UBR-type | |||||
Natural variations | ||||||||
| Alternative sequence | 1 – 209 | 209 | Missing in isoform 2. | |||||
| Alternative sequence | 1 – 84 | 84 | Missing in isoform 3. | |||||
| Alternative sequence | 197 – 211 | 15 | KRLYM…TRPMM → LGEVAHAYNPSTLGG in isoform 4. | |||||
| Alternative sequence | 212 – 927 | 716 | Missing in isoform 4. | |||||
| Alternative sequence | 670 – 927 | 258 | Missing in isoform 3. | |||||
| Alternative sequence | 744 – 770 | 27 | LLEEN…PILRK → IVVNFALVKNPVFHYSSISL MINDIAN in isoform 2. | |||||
| Alternative sequence | 771 – 927 | 157 | Missing in isoform 2. | |||||
| Alternative sequence | 885 | 1 | R → RYVAHLLDILPNYFPPHFSN IWVSFCFR in isoform 5. | |||||
| Natural variant | 126 | 1 | T → S: dbSNP rs17036993. | |||||
Experimental info | ||||||||
| Sequence conflict | 239 | 1 | L → S in BAB14214. Ref.2 | |||||
| Sequence conflict | 577 | 1 | R → G in AAN76518. Ref.3 | |||||
| Sequence conflict | 632 | 1 | R → G in BAD97312. Ref.6 | |||||
| Sequence conflict | 903 | 1 | G → S in AAV87312. Ref.1 | |||||
| Sequence conflict | 903 | 1 | G → S in AAH43258. Ref.4 | |||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "FBXO11 promotes the neddylation of p53 and inhibits its transcriptional activity." Abida W.M., Nikolaev A., Zhao W., Zhang W., Gu W. J. Biol. Chem. 282:1797-1804(2007) [PubMed: 17098746] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1), FUNCTION, SUBCELLULAR LOCATION, INTERACTION WITH TP53, IDENTIFICATION IN A COMPLEX WITH SKP1A; CUL1 AND RBX1. |
| [2] | "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), NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 646-927 (ISOFORM 1). Tissue: Hepatoma and Teratocarcinoma. |
| [3] | "Isolation of full-length cDNA clones from human fetal brain cDNA library." Xie Y., Mao Y. Submitted (FEB-2001) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 3). Tissue: Fetal brain. |
| [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] OF 15-927 (ISOFORM 1). Tissue: Ovary and Testis. |
| [5] | "Identification of a family of human F-box proteins." Cenciarelli C., Chiaur D.S., Guardavaccaro D., Parks W., Vidal M., Pagano M. Curr. Biol. 9:1177-1179(1999) [PubMed: 10531035] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 16-212. |
| [6] | Totoki Y., Toyoda A., Takeda T., Sakaki Y., Tanaka A., Yokoyama S. Submitted (APR-2005) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 16-927 (ISOFORM 1). Tissue: Kidney. |
| [7] | "A family of mammalian F-box proteins." Winston J.T., Koepp D.M., Zhu C., Elledge S.J., Harper J.W. Curr. Biol. 9:1180-1182(1999) [PubMed: 10531037] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 20-927 (ISOFORM 4). |
| [8] | The German cDNA consortium Submitted (SEP-1999) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 720-927. Tissue: Brain. |
| [9] | "'VIT1', a novel gene associated with vitiligo." Le Poole I.C., Sarangarajan R., Zhao Y., Stennett L.S., Brown T.L., Sheth P., Miki T., Boissy R.E. Pigment Cell Res. 14:475-484(2001) [PubMed: 11775060] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 744-927 (ISOFORM 5), TISSUE SPECIFICITY, DISEASE. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| AY827075 mRNA. Translation: AAV87312.1. AK022735 mRNA. Translation: BAB14214.1. AK025477 mRNA. Translation: BAB15143.1. Different initiation. AF351618 mRNA. Translation: AAN76518.1. Sequence problems. BC012728 mRNA. Translation: AAH12728.2. BC043258 mRNA. Translation: AAH43258.2. AF174599 mRNA. Translation: AAF04520.1. AK223592 mRNA. Translation: BAD97312.1. Different initiation. AF176706 mRNA. Translation: AAF17611.1. AL117620 mRNA. Translation: CAB56019.1. AF264714 mRNA. Translation: AAF76888.1. Sequence problems. | |
| PIR | T17329. |
| RefSeq | NP_036299.1. NP_061163.2. NP_079409.3. |
| UniGene | Hs.352677 |
3D structure databases | |
| HSSP | HSSP built from PDB template 1FS1 based on UniProtKB Q13309. |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | Q86XK2. |
Genome annotation databases | |
| Ensembl | ENSG00000138081. Homo sapiens. [Contig view] |
| GeneID | 80204. |
| KEG | |

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