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

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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]

C11orf1 is located on chromosome 11 and is neighbored by:

  • FDXACB1-201
  • ALG9-201
  • ALG9-202
  • AP001781.5-201

Protein

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Structure

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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

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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

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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

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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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Further reading

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