Q15652 (JHD2C_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
January 25, 2012.
Version 88.
History...
Names·Attributes·General annotation·Ontologies·Interactions·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Interactions·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Probable JmjC domain-containing histone demethylation protein 2C EC=1.14.11.- Alternative name(s): Jumonji domain-containing protein 1C Thyroid receptor-interacting protein 8 Short name=TR-interacting protein 8 Short name=TRIP-8 | ||||
| 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 | 2540 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at protein level |
General annotation (Comments)
| Function | Probable histone demethylase that specifically demethylates 'Lys-9' of histone H3, thereby playing a central role in histone code. Demethylation of Lys residue generates formaldehyde and succinate. May be involved in hormone-dependent transcriptional activation, by participating in recruitment to androgen-receptor target genes By similarity. |
| Cofactor | Binds 1 Fe2+ ion per subunit By similarity. |
| Subunit structure | Interacts specifically with the ligand-binding domain of the thyroid receptor (TR). Requires the presence of thyroid hormone for its interaction. Ref.5 |
| Subcellular location | Nucleus By similarity. |
| Domain | Leu-Xaa-Xaa-Leu-Leu (LXXLL) motifs are known to mediate the association with nuclear receptors By similarity. |
| Post-translational modification | Phosphorylated upon DNA damage, probably by ATM or ATR. Ref.7 Ref.8 |
| Sequence similarities | Belongs to the JHDM2 histone demethylase family. Contains 1 JmjC domain. |
| Sequence caution | The sequence AAC41741.1 differs from that shown. Reason: Frameshift at position 2171. The sequence CAD97921.1 differs from that shown. Reason: Frameshift at position 1697. The sequence CAI10947.1 differs from that shown. Reason: Erroneous gene model prediction. |
Ontologies
Binary interactions
With | Entry | #Exp. | IntAct | Notes |
|---|---|---|---|---|
| AR | P10275 | 2 | EBI-1224969,EBI-608057 |
Alternative products
| This entry describes 2 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q15652-1) 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: Q15652-2) The sequence of this isoform differs from the canonical sequence as follows: 1-219: Missing. 1692-1699: TGIPRSVL → SCHLVKTE 1700-2540: Missing. | ||||||
| Note: No experimental confirmation available. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 2540 | 2540 | Probable JmjC domain-containing histone demethylation protein 2C | PRO_0000084284 | |||||
Regions | |||||||||
| Domain | 2274 – 2498 | 225 | JmjC | ||||||
| Zinc finger | 1846 – 1871 | 26 | C6-type Potential | ||||||
| Motif | 2066 – 2070 | 5 | LXXLL motif | ||||||
Sites | |||||||||
| Metal binding | 2336 | 1 | Iron; catalytic By similarity | ||||||
| Metal binding | 2338 | 1 | Iron; catalytic By similarity | ||||||
| Metal binding | 2466 | 1 | Iron; catalytic By similarity | ||||||
Amino acid modifications | |||||||||
| Modified residue | 317 | 1 | Phosphoserine By similarity | ||||||
| Modified residue | 373 | 1 | Phosphoserine Ref.8 | ||||||
| Modified residue | 376 | 1 | Phosphoserine Ref.8 | ||||||
| Modified residue | 379 | 1 | Phosphoserine Ref.8 | ||||||
| Modified residue | 430 | 1 | Phosphoserine Ref.7 | ||||||
| Modified residue | 552 | 1 | N6-acetyllysine Ref.9 | ||||||
| Modified residue | 638 | 1 | Phosphoserine Ref.8 | ||||||
| Modified residue | 641 | 1 | Phosphoserine Ref.8 | ||||||
Natural variations | |||||||||
| Alternative sequence | 1 – 219 | 219 | Missing in isoform 2. | VSP_018303 | |||||
| Alternative sequence | 1692 – 1699 | 8 | TGIPRSVL → SCHLVKTE in isoform 2. | VSP_018304 | |||||
| Alternative sequence | 1700 – 2540 | 841 | Missing in isoform 2. | VSP_018305 | |||||
| Natural variant | 272 | 1 | A → T. Corresponds to variant rs34798625 [ dbSNP | Ensembl ]. | VAR_049654 | |||||
| Natural variant | 394 | 1 | E → D. Corresponds to variant rs35380596 [ dbSNP | Ensembl ]. | VAR_049655 | |||||
| Natural variant | 464 | 1 | S → T. Ref.1 Corresponds to variant rs10761725 [ dbSNP | Ensembl ]. | VAR_049656 | |||||
| Natural variant | 591 | 1 | M → V. Corresponds to variant rs41274072 [ dbSNP | Ensembl ]. | VAR_061277 | |||||
| Natural variant | 1393 | 1 | N → Y. Corresponds to variant rs9703886 [ dbSNP | Ensembl ]. | VAR_049657 | |||||
| Natural variant | 2400 | 1 | D → E. Corresponds to variant rs34491125 [ dbSNP | Ensembl ]. | VAR_049658 | |||||
| Natural variant | 2535 | 1 | E → D. Ref.1 Corresponds to variant rs1935 [ dbSNP | Ensembl ]. | VAR_049659 | |||||
Experimental info | |||||||||
| Sequence conflict | 488 | 1 | T → A in CAD97921. Ref.1 | ||||||
| Sequence conflict | 779 | 1 | T → A in CAD97921. Ref.1 | ||||||
| Sequence conflict | 783 | 1 | T → P in CAD97921. Ref.1 | ||||||
| Sequence conflict | 2093 | 1 | S → A in AAC41741. Ref.5 | ||||||
| Sequence conflict | 2148 | 1 | Missing in BAA92618. Ref.4 | ||||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "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., Bloecker H., Heubner D., Hoerlein A., Michel G., Wedler H., Koehrer K., Ottenwaelder B., Poustka A., Wiemann S., Schupp I. BMC Genomics 8:399-399(2007) [PubMed: 17974005] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2), NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 379-2540, VARIANTS THR-464 AND ASP-2535. Tissue: Amygdala and Cervix. |
| [2] | "The DNA sequence and comparative analysis of human chromosome 10." Deloukas P., Earthrowl M.E., Grafham D.V., Rubenfield M., French L., Steward C.A., Sims S.K., Jones M.C., Searle S., Scott C., Howe K., Hunt S.E., Andrews T.D., Gilbert J.G.R., Swarbreck D., Ashurst J.L., Taylor A., Battles J. Rogers J.Nature 429:375-381(2004) [PubMed: 15164054] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [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] OF 1-427. Tissue: Embryo. |
| [4] | "Prediction of the coding sequences of unidentified human genes. XVI. The complete sequences of 150 new cDNA clones from brain which code for large proteins in vitro." Nagase T., Kikuno R., Ishikawa K., Hirosawa M., Ohara O. DNA Res. 7:65-73(2000) [PubMed: 10718198] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 1275-2540. Tissue: Brain. |
| [5] | "Two classes of proteins dependent on either the presence or absence of thyroid hormone for interaction with the thyroid hormone receptor." Lee J.W., Choi H.-S., Gyuris J., Brent R., Moore D.D. Mol. Endocrinol. 9:243-254(1995) [PubMed: 7776974] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 2030-2212, INTERACTION WITH THYROID RECEPTOR. |
| [6] | "Identification and characterization of TRIP8 gene in silico." Katoh M., Katoh M. Int. J. Mol. Med. 12:817-821(2003) [PubMed: 14533015] [Abstract] Cited for: IDENTIFICATION OF THE GENE. |
| [7] | "ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage." Matsuoka S., Ballif B.A., Smogorzewska A., McDonald E.R. III, Hurov K.E., Luo J., Bakalarski C.E., Zhao Z., Solimini N., Lerenthal Y., Shiloh Y., Gygi S.P., Elledge S.J. Science 316:1160-1166(2007) [PubMed: 17525332] [Abstract] Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-430, MASS SPECTROMETRY. Tissue: Embryonic kidney. |
| [8] | "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-373; SER-376; SER-379; SER-638 AND SER-641, MASS SPECTROMETRY. Tissue: Cervix carcinoma. |
| [9] | "Lysine acetylation targets protein complexes and co-regulates major cellular functions." Choudhary C., Kumar C., Gnad F., Nielsen M.L., Rehman M., Walther T., Olsen J.V., Mann M. Science 325:834-840(2009) [PubMed: 19608861] [Abstract] Cited for: ACETYLATION [LARGE SCALE ANALYSIS] AT LYS-552, MASS SPECTROMETRY. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | BX537954 mRNA. Translation: CAD97921.1. Frameshift. AL713895 Genomic DNA. Translation: CAI10947.1. Sequence problems. AL713895, AL590502 Genomic DNA. Translation: CAI10948.1. AL713895, AL607128, AC022022 Genomic DNA. Translation: CAI10950.1. AL607128, AL713895, AC022022 Genomic DNA. Translation: CAI14188.1. AK027280 mRNA. No translation available. AL831917 mRNA. Translation: CAD38578.1. AB037801 mRNA. Translation: BAA92618.1. L40411 mRNA. Translation: AAC41741.1. Frameshift. |
| IPI | IPI00384202. IPI00902772. |
| RefSeq | NP_004232.2. NM_004241.2. NP_116165.1. NM_032776.1. |
| UniGene | Hs.413416. |
3D structure databases | |
| ProteinModelPortal | Q15652. |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | Q15652. 1 interaction. |
| STRING | Q15652. |
PTM databases | |
| PhosphoSite | Q15652. |
Polymorphism databases | |
| DMDM | 85541650. |
Proteomic databases | |
| PRIDE | Q15652. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000399262; ENSP00000382204; ENSG00000171988. |
| GeneID | 221037. |
| KEGG | hsa:221037. |
| NMPDR | fig|9606.3.peg.4012. |
| UCSC | uc001jml.1. human. uc001jmn.1. human. |
Organism-specific databases | |
| CTD | 221037. |
| GeneCards | GC10M064926. |
| HGNC | HGNC:12313. JMJD1C. |
| MIM | 604503. gene. |
| neXtProt | NX_Q15652. |
| HUGE | Search... |
| GenAtlas | Search... |
Phylogenomic databases | |
| GeneTree | ENSGT00530000063039. |
| HOVERGEN | HBG079631. |
| InParanoid | Q15652. |
| OMA | MKHSVPQ. |
| OrthoDB | EOG447FS9. |
| PhylomeDB | Q15652. |
Enzyme and pathway databases | |
| Reactome | REACT_604. Hemostasis. |
Gene expression databases | |
| ArrayExpress | Q15652. |
| Bgee | Q15652. |
| CleanEx | HS_JMJD1C. |
| Genevestigator | Q15652. |
| GermOnline | ENSG00000171988. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR013129. TF_JmjC. IPR003347. TF_JmjC_AAH. [Graphical view] |
| KO | K11449. |
| Pfam | PF02373. JmjC. 1 hit. [Graphical view] |
| SMART | SM00558. JmjC. 1 hit. [Graphical view] |
| PROSITE | PS51184. JMJC. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| NextBio | 91161. |
| SOURCE | Search... |
Entry information
| Entry name | JHD2C_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q15652 Secondary accession number(s): Q5SQZ8 Q9P2G7 | ||||||||
| 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 10 Human chromosome 10: 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