Q5VWQ0 (RSBN1_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
April 3, 2013.
Version 67.
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: Round spermatid basic protein 1 | ||
| Gene names |
| ||
| 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 | 802 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at protein level |
General annotation (Comments)
| Subcellular location | Nucleus By similarity. |
| Post-translational modification | Phosphorylated by PKA By similarity. |
| Sequence similarities | Belongs to the round spermatid basic protein 1 family. |
| Sequence caution | The sequence AAH26155.1 differs from that shown. Reason: Erroneous initiation. The sequence BAA92075.1 differs from that shown. Reason: Erroneous initiation. The sequence BAB13974.1 differs from that shown. Reason: Erroneous initiation. The sequence CAH10493.1 differs from that shown. Reason: Erroneous initiation. Translation N-terminally extended. The sequence CAH10493.1 differs from that shown. Reason: Aberrant splicing. The sequence CAH72507.1 differs from that shown. Reason: Erroneous initiation. The sequence CAI19067.1 differs from that shown. Reason: Erroneous initiation. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Nucleus |
| Coding sequence diversity | Alternative splicing |
| PTM | Phosphoprotein |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Cellular_component | nucleus Inferred from electronic annotation. Source: UniProtKB-SubCell |
| Complete GO annotation... | |
Alternative products
| This entry describes 2 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q5VWQ0-1) 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 4 (identifier: Q5VWQ0-4) The sequence of this isoform differs from the canonical sequence as follows: 460-802: Missing. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 802 | 802 | Round spermatid basic protein 1 | PRO_0000299412 | |||||
Regions | |||||||||
| Motif | 252 – 263 | 12 | Nuclear localization signal Potential | ||||||
| Compositional bias | 103 – 165 | 63 | Pro-rich | ||||||
| Compositional bias | 114 – 117 | 4 | Poly-Arg | ||||||
| Compositional bias | 185 – 197 | 13 | His-rich | ||||||
| Compositional bias | 252 – 261 | 10 | Poly-Lys | ||||||
Amino acid modifications | |||||||||
| Modified residue | 81 | 1 | Phosphoserine Ref.5 | ||||||
Natural variations | |||||||||
| Alternative sequence | 460 – 802 | 343 | Missing in isoform 4. | VSP_027656 | |||||
Experimental info | |||||||||
| Sequence conflict | 39 – 40 | 2 | GP → SG in AAH26155. Ref.3 | ||||||
| Sequence conflict | 106 | 1 | E → G in BAF85241. Ref.1 | ||||||
| Sequence conflict | 120 | 1 | Q → R in BAA92075. Ref.1 | ||||||
Sequences
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References
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AK002082 mRNA. Translation: BAA92075.1. Different initiation. AK292552 mRNA. Translation: BAF85241.1. AK022166 mRNA. Translation: BAB13974.1. Different initiation. AL365321, AL137856 Genomic DNA. Translation: CAH72507.1. Different initiation. AL137856, AL365321 Genomic DNA. Translation: CAI19067.1. Different initiation. BC026155 mRNA. Translation: AAH26155.1. Different initiation. CR627402 mRNA. Translation: CAH10493.1. Sequence problems. |
| IPI | IPI00019999. IPI00855810. |
| RefSeq | NP_060834.2. NM_018364.3. |
| UniGene | Hs.486285. |
3D structure databases | |
| ProteinModelPortal | Q5VWQ0. |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | Q5VWQ0. 2 interactions. |
| STRING | 9606.ENSP00000261441. |
PTM databases | |
| PhosphoSite | Q5VWQ0. |
Polymorphism databases | |
| DMDM | 257050986. |
Proteomic databases | |
| PaxDb | Q5VWQ0. |
| PRIDE | Q5VWQ0. |
Protocols and materials databases | |
| DNASU | 54665. |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000261441; ENSP00000261441; ENSG00000081019. |
| GeneID | 54665. |
| KEGG | hsa:54665. |
| UCSC | uc001edq.3. human. |
Organism-specific databases | |
| CTD | 54665. |
| GeneCards | GC01M114304. |
| H-InvDB | HIX0000902. |
| HGNC | HGNC:25642. RSBN1. |
| HPA | HPA042124. |
| neXtProt | NX_Q5VWQ0. |
| PharmGKB | PA134869532. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG306264. |
| HOGENOM | HOG000043117. |
| HOVERGEN | HBG094904. |
| InParanoid | Q5VWQ0. |
| OMA | LKHKDKQ. |
| OrthoDB | EOG4HT8RZ. |
| PhylomeDB | Q5VWQ0. |
Gene expression databases | |
| Bgee | Q5VWQ0. |
| CleanEx | HS_RSBN1. |
| Genevestigator | Q5VWQ0. |
Family and domain databases | |
| InterPro | IPR026306. RSBN1. [Graphical view] |
| PANTHER | PTHR13354. PTHR13354. 1 hit. |
| ProtoNet | Search... |
Other | |
| GenomeRNAi | 54665. |
| NextBio | 57216. |
Entry information
| Entry name | RSBN1_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q5VWQ0 Secondary accession number(s): A8K937 Q9NUP6 | ||||||||
| 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 1 Human chromosome 1: entries, gene names and cross-references to MIM |
| SIMILARITY comments Index of protein domains and families |

Clusters with
