C11orf1
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Chromosome 11 open reading frame one, also known as C11orf1, is a protein-coding gene.[1] It has been found by yeast two hybrid screen to bind to SETDB1 a histone protein methyltransferase enzyme. SETDB1 has been implicated in Huntington's disease, a neurodegenerative disorder.[2]
C11orf1 is a nuclear protein with unknown function but has been shown to show preferential expression in some disease states in microarray data.[3][4]
Species distribution
[edit | edit source]C11orf1 shows conservation through mammals and orthologs can be found in sea squirts and sea anemone. The below table shows some orthologs found using BLAST.[5]
| Species | Organism Common Name | NCBI Accession | Sequence identity | Expected value | Length (AAs) | Gene Common Name |
|---|---|---|---|---|---|---|
| Homo sapiens | Human | CAG33659 | 100% | 8e−86 | 150 | C11orf1 |
| Bos taurus | Bovine | NP_001033266.1 | 85% | 1e−70 | 149 | UPF0686 protein C11orf1 homolog |
| Canis lupus familiaris | Dog | XP_536577.1 | 88% | 3e−68 | 485 | PREDICTED: hypothetical protein XP_536577 [Canis familiaris] |
| Mus musculus | Mouse | NP_075972.2 | 78% | 4e−65 | 466 | hypothetical protein LOC68721 [Mus musculus] |
| Ciona intestinalis | Sea Squirt | XP_002127073.1 | 49% | 3e−23 | 156 | PREDICTED: similar to predicted protein [Ciona intestinalis] |
Gene
[edit | edit source]C11orf1 is located on chromosome 11 and is neighbored by:
- FDXACB1-201
- ALG9-201
- ALG9-202
- AP001781.5-201
Protein
[edit | edit source]Structure
[edit | edit source]This protein is part of the UPF0686 superfamily. This family is characterized by the presence of a domain of unknown function (DUF)1143 shared by the family.[6] This family DUF1143 has a domain that includes almost all 149 of the 150 amino acids in the human ortholog. C11orf1 has six splicesomal variants and one unspliced variant.
Predicted properties
[edit | edit source]The following properties of C11orf1 were predicted using bioinformatic analysis:
- Molecular Weight: 17.76 KDal[7]
- Isoelectric point: 7.28[8]
- Post-translational modification: twelve possible post-translational modifications are predicted:
- Two O-(N-acetylaminogalactosyl)-L-threonine Glycosylations at position 138 and 142 on the protein sequence[9]
- Two O-phospho-L-serine Phosphorylation sites at 112 and 141.[9]
- Four O-phospho-L-threonine Phosphorylation sites at 59, 99, 113, and 138.[9]
- Four O4'-phospho-L-tyrosine Phosphorylation sites at 64, 101, 105 and 143.[9]
Tissue distribution
[edit | edit source]C11orf1 appears to be ubiquitously expressed at low levels but particularly high expression in the parathyroid. Expression data indicate expression in most tissues.[10] This gene has also been found in one experiment to be under expressed in Huntington's disease patients while SETDB1 is over-expressed.[3]
Binding partners
[edit | edit source]The human protein SET domain bifurcated 1, was found to be a binding partner for C11orf1 by Yeast Two Hybrid.[11]
References
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External links
[edit | edit source]- Human C11orf1 genome location and C11orf1 gene details page in the UCSC Genome Browser.
Further reading
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