Reviewed,
UniProtKB/Swiss-Prot P56645 (PER3_HUMAN)
Last modified
July 22, 2008.
Version 71.
History...
Clusters with 100%,
90%,
50% identity |
Documents (6) |
Third-party data |
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Names and origin
| Protein names | Recommended name: Period circadian protein homolog 3 Alternative name(s): Circadian clock protein PERIOD 3 Short name=hPER3 Cell growth-inhibiting gene 13 protein | ||||
| Gene names |
| ||||
| 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 | 1201 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is not processed. |
| Protein existence | Evidence at transcript level. |
General annotation (Comments)
| Function | Component of the circadian clock mechanism which is essential for generating circadian rhythms. Function unknown. |
| Subunit structure | Homodimer. Component of the circadian core oscillator, which includes the CRY proteins, CLOCK or NPAS2, BMAL1 or BMAL2, CSNK1D and/or CSNK1E, TIMELESS and the PER proteins. Interacts directly with PER1, PER2, CRY1, CRY2, and TIMELESS. Interaction with CSNK1D or CSKN1E promotes nuclear location of PER proteins By similarity. |
| Subcellular location | CytoplasmBy similarity. NucleusBy similarity. Note= Mainly cytoplasmic. Translocates to the nucleus through binding PER1, PER2, CRY1 or CRY2, but not TIMELESS By similarity. |
| Post-translational modification | Phosphorylation appears to require association with PER1 and translocation to the nucleus By similarity. Ubiquitinated By similarity. |
| Sequence similarities | Contains 1 PAC (PAS-associated C-terminal) domain. Contains 2 PAS (PER-ARNT-SIM) domains. |
Ontologies
Keywords | |
|---|---|
| Biological process | Biological rhythms Transcription Transcription regulation |
| Cellular component | Cytoplasm Nucleus |
| Coding sequence diversity | Polymorphism |
| Domain | Repeat |
| PTM | Phosphoprotein Ubl conjugation |
Gene Ontology (GO) | |
| None. [Check GOA] | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | ||||
Molecule processing | ||||||||
|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 1201 | 1201 | Period circadian protein homolog 3 | |||||
Regions | ||||||||
| Domain | 121 – 188 | 68 | PAS 1 | |||||
| Domain | 262 – 328 | 67 | PAS 2 | |||||
| Domain | 337 – 380 | 44 | PAC | |||||
| Region | 502 – 731 | 230 | CSNK1E binding domain By similarity | |||||
| Region | 1123 – 1201 | 79 | CRY binding domain By similarity | |||||
| Motif | 400 – 412 | 13 | Nuclear export signal By similarity | |||||
| Motif | 729 – 745 | 17 | Nuclear localization signal By similarity | |||||
| Compositional bias | 567 – 570 | 4 | Poly-Ser | |||||
| Compositional bias | 750 – 753 | 4 | Poly-Ser | |||||
| Compositional bias | 769 – 895 | 127 | Pro-rich | |||||
| Compositional bias | 962 – 1081 | 120 | Ser-rich | |||||
Natural variations | ||||||||
| Natural variant | 639 | 1 | V → G Associated with delayed sleep phase syndrome (DSPS). dbSNP rs10462020. | |||||
| Natural variant | 827 | 1 | P → L: dbSNP rs228696. | |||||
| Natural variant | 856 | 1 | P → A: dbSNP rs228697. | |||||
| Natural variant | 1007 | 1 | A → T: dbSNP rs1776342. | |||||
| Natural variant | 1010 | 1 | T → I: dbSNP rs12033719. | |||||
| Natural variant | 1028 | 1 | M → T: dbSNP rs2640909. | |||||
| Natural variant | 1081 | 1 | S → C: dbSNP rs2640905. | |||||
| Natural variant | 1149 | 1 | H → R: dbSNP rs10462021. | |||||
Experimental info | ||||||||
| Sequence conflict | 199 | 1 | A → AA in BAB32925. Ref.1 | |||||
| Sequence conflict | 501 | 1 | E → ESANGGGE in BAB32925. Ref.1 | |||||
| Sequence conflict | 943 | 1 | Q → R in BAB32925. Ref.1 | |||||
| Sequence conflict | 954 | 1 | Y → YQ in BAB32925. Ref.1 | |||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "Homo sapiens mRNA for period (Drosophila) homolog 3 (hPer3), complete cds." Nagase T., Kikuno R., Ohara O. Submitted (AUG-2000) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [MRNA]. Tissue: Brain. |
| [2] | Rhodes S., Huckle E. Submitted (FEB-2000) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANT LEU-827. |
| [3] | "Identification of a growth inhibition gene." Kim J.W. Submitted (DEC-2003) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANT LEU-827. |
| [4] | "The DNA sequence and biological annotation of human chromosome 1." Gregory S.G., Barlow K.F., McLay K.E., Kaul R., Swarbreck D., Dunham A., Scott C.E., Howe K.L., Woodfine K., Spencer C.C.A., Jones M.C., Gillson C., Searle S., Zhou Y., Kokocinski F., McDonald L., Evans R., Phillips K. Bentley D.R.Nature 441:315-321(2006) [PubMed: 16710414] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA], VARIANT LEU-827. |
| [5] | "Association of structural polymorphisms in the human period3 gene with delayed sleep phase syndrome." Ebisawa T., Uchiyama M., Kajimura N., Mishima K., Kamei Y., Katoh M., Watanabe T., Sekimoto M., Shibui K., Kim K., Kudo Y., Ozeki Y., Sugishita M., Toyoshima R., Inoue Y., Yamada N., Nagase T., Ozaki N. Yamauchi T.EMBO Rep. 2:342-346(2001) [PubMed: 11306557] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 44-91 AND 724-882, VARIANTS GLY-639; ALA-856; THR-1028 AND ARG-1149. |
| [6] | "Circadian clock-related polymorphisms in seasonal affective disorder and their relevance to diurnal preference." Johansson C., Willeit M., Smedh C., Ekholm J., Paunio T., Kieseppa T., Lichtermann D., Praschak-Rieder N., Neumeister A., Nilsson L.G., Kasper S., Peltonen L., Adolfsson R., Schalling M., Partonen T. Neuropsychopharmacology 28:734-739(2003) [PubMed: 12655319] [Abstract] Cited for: VARIANT GLY-639. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| AB047686 mRNA. Translation: BAB32925.2. Different initiation. AL157954 mRNA. Translation: CAB76084.1. AY493418 mRNA. Translation: AAS72879.1. Z98884 Genomic DNA. Translation: CAI21436.1. AB047521 Genomic DNA. Translation: BAB63250.1. AB047530 Genomic DNA. Translation: BAB63251.1. AB047531 Genomic DNA. Translation: BAB63252.1. AB047532 Genomic DNA. Translation: BAB63253.1. AB047533 Genomic DNA. Translation: BAB63254.1. AB047534 Genomic DNA. Translation: BAB63255.1. | |
| RefSeq | NP_058515.1. |
| UniGene | Hs.533339 |
3D structure databases | |
| ModBase | Search... |
PTM databases | |
| PhosphoSite | P56645. |
Genome annotation databases | |
| Ensembl | ENSG00000049246. Homo sapiens. [Contig view] |
| GeneID | 8863. |
| KEGG | hsa:8863. |
Organism-specific databases | |
| HGNC | HGNC:8847. PER3. |
| MIM | 603427. gene. |
| PharmGKB | PA134911185. |
| GenAtlas | Search... |
| GeneCards | Search... |
Phylogenomic databases | |
| HOVERGEN | P56645. |
Gene expression databases | |
| ArrayExpress | P56645. |
| CleanEx | HS_PER3. |
| GermOnline | ENSG00000049246. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR001610. PAC. IPR000014. PAS. IPR000700. PAS-assoc_C. IPR013655. PAS_3. [Graphical view] |
| Pfam | PF08447. PAS_3. 1 hit. [Graphical view] |
| SMART | SM00086. PAC. 1 hit. SM00091. PAS. 2 hits. [Graphical view] |
| PROSITE | PS50113. PAC. False negative. PS50112. PAS. 1 hit. [Graphical view] |
| ProDom | P56645. [Graphical view] [Entries sharing at least one domain] |
| BLOCKS | Search... |
Other Resources | |
| LinkHub | P56645. |
| SOURCE | Search... |
| ProtoNet | Search... |
Entry information
| Entry name | PER3_HUMAN | ||||||||
| Accession | Primary (citable) accession number: P56645 Secondary accession number(s): Q5H8X4 Q9UGU8 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation project | HPI (Human Proteome Initiative) | ||||||||
Relevant documents
| Human chromosome 1 Human chromosome 1: 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 |
| UniProtKB secondary accession numbers Index of UniProtKB secondary accession numbers |
| SIMILARITY comments Index of protein domains and families |

Clusters with


