Q8N729 (NPW_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
April 3, 2013.
Version 70.
History...
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Neuropeptide W Alternative name(s): Preproprotein L8 Short name=hPPL8 Cleaved into the following 2 chains:
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| 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 | 165 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is further processed into a mature form. |
| Protein existence | Evidence at protein level |
General annotation (Comments)
| Function | Plays a regulatory role in the organization of neuroendocrine signals accessing the anterior pituitary gland. Stimulates water drinking and food intake. May play a role in the hypothalamic response to stress By similarity. NPW23 activates GPR7 and GPR8 more efficiently than NPW30. |
| Subcellular location | |
| Tissue specificity | Detected at high levels in the substantia nigra, fetal kidney and trachea; at lower levels in testis, uterus, ovary and placenta. Not detectable in many regions of the central nervous system. Also detected at high levels in lymphoblastic leukemia and colorectal adenocarcinoma. |
| Sequence similarities | Belongs to the neuropeptide B/W family. |
| Sequence caution | The sequence BAC07172.1 differs from that shown. Reason: Erroneous initiation. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Secreted |
| Coding sequence diversity | Polymorphism |
| Domain | Signal |
| Molecular function | Neuropeptide |
| PTM | Cleavage on pair of basic residues |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Biological_process | G-protein coupled receptor signaling pathway Inferred from direct assay Ref.2. Source: HGNC feeding behaviorInferred from direct assay PubMed 12959997. Source: HGNC neuropeptide signaling pathwayInferred from electronic annotation. Source: UniProtKB-KW |
| Cellular_component | extracellular region Traceable author statement. Source: Reactome |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Signal peptide | 1 – 32 | 32 | Potential | ||||||
| Peptide | 33 – 62 | 30 | Neuropeptide W-30 | PRO_0000019843 | |||||
| Peptide | 33 – 55 | 23 | Neuropeptide W-23 | PRO_0000019844 | |||||
| Propeptide | 65 – 165 | 101 | Potential | PRO_0000019845 | |||||
Natural variations | |||||||||
| Natural variant | 149 | 1 | D → A. Corresponds to variant rs2286472 [ dbSNP | Ensembl ]. | VAR_050292 | |||||
Sequences
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References
| [1] | "Identification of neuropeptide W as the endogenous ligand for orphan G-protein-coupled receptors GPR7 and GPR8." Shimomura Y., Harada M., Goto M., Sugo T., Matsumoto Y., Abe M., Watanabe T., Asami T., Kitada C., Mori M., Onda H., Fujino M. J. Biol. Chem. 277:35826-35832(2002) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA], CHARACTERIZATION, SYNTHESIS OF NPW23 AND NPW30. |
| [2] | "Identification of natural ligands for the orphan G protein-coupled receptors GPR7 and GPR8." Brezillon S., Lannoy V., Franssen J.-D., Le Poul E., Dupriez V., Lucchetti J., Detheux M., Parmentier M. J. Biol. Chem. 278:776-783(2003) [PubMed] [Europe PMC] [Abstract] Cited for: CHARACTERIZATION. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AB084276 mRNA. Translation: BAC07172.1. Different initiation. |
| IPI | IPI00853190. |
| RefSeq | NP_001092926.2. NM_001099456.2. |
| UniGene | Hs.233533. |
3D structure databases | |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | 9606.ENSP00000330070. |
PTM databases | |
| PhosphoSite | Q8N729. |
Proteomic databases | |
| PaxDb | Q8N729. |
| PRIDE | Q8N729. |
Protocols and materials databases | |
| DNASU | 283869. |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000329610; ENSP00000330070; ENSG00000183971. |
| GeneID | 283869. |
| KEGG | hsa:283869. |
| UCSC | uc002coh.4. human. |
Organism-specific databases | |
| CTD | 283869. |
| GeneCards | GC16P002059. |
| H-InvDB | HIX0038533. |
| HGNC | HGNC:30509. NPW. |
| MIM | 607997. gene. |
| neXtProt | NX_Q8N729. |
| PharmGKB | PA142671248. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG42832. |
| HOGENOM | HOG000113846. |
| InParanoid | Q8N729. |
| OrthoDB | EOG4X6C9W. |
Enzyme and pathway databases | |
| Reactome | REACT_111102. Signal Transduction. |
Gene expression databases | |
| ArrayExpress | Q8N729. |
| Bgee | Q8N729. |
| CleanEx | HS_NPW. |
| Genevestigator | Q8N729. |
| GermOnline | ENSG00000183971. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR013297. Neuropept_BW_pre. IPR013299. Neuropept_W_pre. [Graphical view] |
| PRINTS | PR01888. NROPEPTIDEBW. PR01890. PPNRPEPTIDEW. |
| ProDom | PD601995. Neuropept_W_pre. 1 hit. [Graphical view] [Entries sharing at least one domain] |
| ProtoNet | Search... |
Other | |
| NextBio | 94311. |
| SOURCE | Search... |
Entry information
| Entry name | NPW_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q8N729 | ||||||||
| 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 16 Human chromosome 16: 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
