Q8N9V3 (WSDU1_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
May 29, 2013.
Version 87.
History...
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: WD repeat, SAM and U-box domain-containing protein 1 | ||||
| Gene names |
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| Organism | Homo sapiens (Human) [Reference proteome] | ||||
| Taxonomic identifier | 9606 [NCBI] | ||||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo![]() |
Protein attributes
| Sequence length | 476 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at protein level |
General annotation (Comments)
| Sequence similarities | Contains 1 SAM (sterile alpha motif) domain. Contains 1 U-box domain. Contains 7 WD repeats. |
Ontologies
| Keywords | |
|---|---|
| Coding sequence diversity | Alternative splicing Polymorphism |
| Domain | Repeat WD repeat |
| PTM | Phosphoprotein |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Cellular_component | ubiquitin ligase complex Inferred from electronic annotation. Source: InterPro |
| Molecular_function | ubiquitin-protein ligase activity Inferred from electronic annotation. Source: InterPro |
| Complete GO annotation... | |
Alternative products
| This entry describes 2 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q8N9V3-1) 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: Q8N9V3-2) The sequence of this isoform differs from the canonical sequence as follows: 226-317: Missing. | ||||||
| Note: No experimental confirmation available. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 476 | 476 | WD repeat, SAM and U-box domain-containing protein 1 | PRO_0000278608 | |||||
Regions | |||||||||
| Repeat | 10 – 47 | 38 | WD 1 | ||||||
| Repeat | 52 – 91 | 40 | WD 2 | ||||||
| Repeat | 95 – 134 | 40 | WD 3 | ||||||
| Repeat | 137 – 176 | 40 | WD 4 | ||||||
| Repeat | 178 – 228 | 51 | WD 5 | ||||||
| Repeat | 237 – 276 | 40 | WD 6 | ||||||
| Repeat | 279 – 318 | 40 | WD 7 | ||||||
| Domain | 332 – 396 | 65 | SAM | ||||||
| Domain | 403 – 476 | 74 | U-box | ||||||
Amino acid modifications | |||||||||
| Modified residue | 458 | 1 | Phosphothreonine Ref.4 | ||||||
Natural variations | |||||||||
| Alternative sequence | 226 – 317 | 92 | Missing in isoform 2. | VSP_023337 | |||||
| Natural variant | 215 | 1 | K → T. Corresponds to variant rs16843852 [ dbSNP | Ensembl ]. | VAR_030791 | |||||
| Natural variant | 223 | 1 | H → D. Ref.3 Corresponds to variant rs17852677 [ dbSNP | Ensembl ]. | VAR_030792 | |||||
| Natural variant | 320 | 1 | R → S. Ref.1 Corresponds to variant rs7591849 [ dbSNP | Ensembl ]. | VAR_030793 | |||||
Experimental info | |||||||||
| Sequence conflict | 173 | 1 | P → L in BAC04184. Ref.1 | ||||||
| Sequence conflict | 173 | 1 | P → L in AAH29520. Ref.3 | ||||||
Sequences
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References
| [1] | "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] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1), VARIANT SER-320. Tissue: Testis. |
| [2] | "Generation and annotation of the DNA sequences of human chromosomes 2 and 4." Hillier L.W., Graves T.A., Fulton R.S., Fulton L.A., Pepin K.H., Minx P., Wagner-McPherson C., Layman D., Wylie K., Sekhon M., Becker M.C., Fewell G.A., Delehaunty K.D., Miner T.L., Nash W.E., Kremitzki C., Oddy L., Du H. Wilson R.K.Nature 434:724-731(2005) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [3] | "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] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2), VARIANT ASP-223. Tissue: Brain. |
| [4] | "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] [Europe PMC] [Abstract] Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT THR-458, MASS SPECTROMETRY. Tissue: Cervix carcinoma. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AK093494 mRNA. Translation: BAC04184.1. AC008277 Genomic DNA. No translation available. AC009307 Genomic DNA. Translation: AAX93043.1. BC029520 mRNA. Translation: AAH29520.1. |
| IPI | IPI00167822. IPI00477952. |
| RefSeq | NP_001121684.1. NM_001128212.1. NP_689741.2. NM_152528.2. |
| UniGene | Hs.20848. |
3D structure databases | |
| ProteinModelPortal | Q8N9V3. |
| ModBase | Search... |
PTM databases | |
| PhosphoSite | Q8N9V3. |
Polymorphism databases | |
| DMDM | 229463016. |
Proteomic databases | |
| PaxDb | Q8N9V3. |
| PRIDE | Q8N9V3. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000358147; ENSP00000350866; ENSG00000196151. ENST00000359774; ENSP00000352820; ENSG00000196151. ENST00000392796; ENSP00000376545; ENSG00000196151. ENST00000409990; ENSP00000387078; ENSG00000196151. |
| GeneID | 151525. |
| KEGG | hsa:151525. |
| UCSC | uc010foo.3. human. |
Organism-specific databases | |
| CTD | 151525. |
| GeneCards | GC02M160092. |
| HGNC | HGNC:26697. WDSUB1. |
| HPA | HPA036840. |
| neXtProt | NX_Q8N9V3. |
| PharmGKB | PA128394761. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | COG2319. |
| HOGENOM | HOG000231980. |
| HOVERGEN | HBG080511. |
| InParanoid | Q8N9V3. |
| OMA | HCCCFSP. |
| OrthoDB | EOG4NCMCJ. |
| PhylomeDB | Q8N9V3. |
Enzyme and pathway databases | |
| SignaLink | Q8N9V3. |
Gene expression databases | |
| ArrayExpress | Q8N9V3. |
| Bgee | Q8N9V3. |
| CleanEx | HS_WDSUB1. |
| Genevestigator | Q8N9V3. |
Family and domain databases | |
| Gene3D | 1.10.150.50. 1 hit. 2.130.10.10. 2 hits. 3.30.40.10. 1 hit. |
| InterPro | IPR020472. G-protein_beta_WD-40_rep. IPR001660. SAM. IPR013761. SAM/pointed. IPR011510. SAM_2. IPR003613. Ubox_domain. IPR015943. WD40/YVTN_repeat-like_dom. IPR001680. WD40_repeat. IPR019775. WD40_repeat_CS. IPR017986. WD40_repeat_dom. IPR013083. Znf_RING/FYVE/PHD. [Graphical view] |
| Pfam | PF07647. SAM_2. 1 hit. PF04564. U-box. 1 hit. PF00400. WD40. 7 hits. [Graphical view] |
| PRINTS | PR00320. GPROTEINBRPT. |
| SMART | SM00454. SAM. 1 hit. SM00504. Ubox. 1 hit. SM00320. WD40. 7 hits. [Graphical view] |
| SUPFAM | SSF47769. SAM_homology. 1 hit. SSF50978. WD40_like. 1 hit. |
| PROSITE | PS50105. SAM_DOMAIN. 1 hit. PS00678. WD_REPEATS_1. 2 hits. PS50082. WD_REPEATS_2. 5 hits. PS50294. WD_REPEATS_REGION. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| GenomeRNAi | 151525. |
| NextBio | 86717. |
Entry information
| Entry name | WSDU1_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q8N9V3 Secondary accession number(s): Q53TI9, Q8N6N8 | ||||||||
| 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 2 Human chromosome 2: 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 |
| SIMILARITY comments Index of protein domains and families |

Clusters with
