Q96P15 (SPB11_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
May 1, 2013.
Version 83.
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: Serpin B11 | ||
| 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 | 392 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Function | Has no serine protease inhibitory activity, probably due to mutations in the scaffold impairing conformational change. Ref.1 |
| Subcellular location | Cytoplasm By similarity. |
| Tissue specificity | Detected in a restricted number of tissues, including lung, placenta, prostate, and tonsil. Ref.1 |
| Polymorphism | According to some authors, 4 of the identified SERPIN11 transcripts contained coding sequences that could be distinguished by different combinations of single nucleotide polymorphisms (designated SERPINB11a, SERPINB11b, SERPINB11c, and SERPINB11d), and one contained a nonsense mutation introducing a premature stop codon in position 90 identified in the official genome sequence (SERPINB11f) (Ref.1). The sequence displayed here corresponds to SERPINB11a. |
| Sequence similarities | Belongs to the serpin family. Ov-serpin subfamily. |
| Caution | Mutations in the scaffold leading to either a stop codon instead of a Glu at position 90, an Arg instead of the well conserved Trp at position 188, or a Pro instead of Ser at position 303 lead to the loss of inhibitory activity. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Cytoplasm |
| Coding sequence diversity | Alternative splicing Polymorphism |
| Molecular function | Protease inhibitor Serine protease inhibitor |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Biological_process | regulation of proteolysis Inferred from Biological aspect of Ancestor. Source: RefGenome |
| Cellular_component | cytoplasm Inferred from electronic annotation. Source: UniProtKB-SubCell |
| Molecular_function | serine-type endopeptidase inhibitor activity Inferred from Biological aspect of Ancestor. Source: RefGenome |
| Complete GO annotation... | |
Alternative products
| This entry describes 3 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q96P15-1) Also known as: SERPINB11a; 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: Q96P15-2) Also known as: SERPINB11e; The sequence of this isoform differs from the canonical sequence as follows: 120-206: Missing. | ||||||
| Isoform 3 (identifier: Q96P15-3) Also known as: SERPINB11g; The sequence of this isoform differs from the canonical sequence as follows: 57-258: Missing. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 392 | 392 | Serpin B11 | PRO_0000094117 | |||||
Regions | |||||||||
| Region | 341 – 365 | 25 | RCL By similarity | ||||||
Sites | |||||||||
| Site | 357 – 358 | 2 | Reactive bond By similarity | ||||||
Natural variations | |||||||||
| Alternative sequence | 57 – 258 | 202 | Missing in isoform 3. | VSP_040670 | |||||
| Alternative sequence | 120 – 206 | 87 | Missing in isoform 2. | VSP_040671 | |||||
| Natural variant | 51 | 1 | A → E. Ref.1 Ref.3 Corresponds to variant rs1395268 [ dbSNP | Ensembl ]. | VAR_060331 | |||||
| Natural variant | 148 | 1 | M → T in allele B and allele D. Ref.1 Corresponds to variant rs17071550 [ dbSNP | Ensembl ]. | VAR_012472 | |||||
| Natural variant | 181 | 1 | I → A in allele D; requires 2 nucleotide substitutions. Ref.1 | VAR_064572 | |||||
| Natural variant | 181 | 1 | I → T in allele B and allele C. Ref.1 Ref.2 Ref.4 | VAR_012473 | |||||
| Natural variant | 188 | 1 | R → W in allele D. Ref.1 Corresponds to variant rs1506419 [ dbSNP | Ensembl ]. | VAR_060332 | |||||
| Natural variant | 293 | 1 | I → T. Ref.1 Corresponds to variant rs1395266 [ dbSNP | Ensembl ]. | VAR_060333 | |||||
| Natural variant | 303 | 1 | P → S. Ref.1 Corresponds to variant rs1395267 [ dbSNP | Ensembl ]. | VAR_060334 | |||||
| Natural variant | 354 | 1 | I → T. Corresponds to variant rs34811964 [ dbSNP | Ensembl ]. | VAR_057177 | |||||
Experimental info | |||||||||
| Sequence conflict | 12 | 1 | C → R in AAV73921. Ref.1 | ||||||
| Sequence conflict | 43 | 1 | L → P in AAV73923. Ref.1 | ||||||
| Sequence conflict | 91 | 1 | F → S in AAV73920. Ref.1 | ||||||
| Sequence conflict | 267 | 1 | T → A in AAV73920. Ref.1 | ||||||
| Sequence conflict | 356 | 1 | V → A in AAV73921. Ref.1 | ||||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "SERPINB11 is a new noninhibitory intracellular serpin. Common single nucleotide polymorphisms in the scaffold impair conformational change." Askew D.J., Cataltepe S., Kumar V., Edwards C., Pace S.M., Howarth R.N., Pak S.C., Askew Y.S., Bromme D., Luke C.J., Whisstock J.C., Silverman G.A. J. Biol. Chem. 282:24948-24960(2007) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA], FUNCTION, TISSUE SPECIFICITY, VARIANTS GLU-51; THR-148; ALA-181; THR-181; TRP-188; THR-293 AND SER-303. |
| [2] | "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], VARIANT THR-181. Tissue: Trachea. |
| [3] | "DNA sequence and analysis of human chromosome 18." Nusbaum C., Zody M.C., Borowsky M.L., Kamal M., Kodira C.D., Taylor T.D., Whittaker C.A., Chang J.L., Cuomo C.A., Dewar K., FitzGerald M.G., Yang X., Abouelleil A., Allen N.R., Anderson S., Bloom T., Bugalter B., Butler J. Lander E.S.Nature 437:551-555(2005) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA], VARIANT GLU-51. |
| [4] | "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], VARIANT THR-181. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AF419953 mRNA. Translation: AAL16056.1. AF419954 mRNA. Translation: AAL16057.1. AF419955 mRNA. Translation: AAL16058.1. AY792323 mRNA. Translation: AAV73920.1. AY792324 mRNA. Translation: AAV73921.1. AY792325 mRNA. Translation: AAV73922.1. AY792326 mRNA. Translation: AAV73923.1. AK292775 mRNA. Translation: BAF85464.1. AC069356 Genomic DNA. No translation available. BC069596 mRNA. Translation: AAH69596.1. |
| IPI | IPI00289606. IPI00979204. IPI00982372. |
| RefSeq | NP_536723.2. NM_080475.2. |
| UniGene | Hs.350958. |
3D structure databases | |
| ProteinModelPortal | Q96P15. |
| ModBase | Search... |
Protein family/group databases | |
| MEROPS | I04.956. |
PTM databases | |
| PhosphoSite | Q96P15. |
Polymorphism databases | |
| DMDM | 20140144. |
Proteomic databases | |
| PaxDb | Q96P15. |
| PRIDE | Q96P15. |
Protocols and materials databases | |
| DNASU | 89778. |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000382749; ENSP00000421854; ENSG00000206072. |
| GeneID | 89778. |
| KEGG | hsa:89778. |
Organism-specific databases | |
| CTD | 89778. |
| GeneCards | GC18P061350. |
| H-InvDB | HIX0039713. |
| HGNC | HGNC:14221. SERPINB11. |
| neXtProt | NX_Q96P15. |
| PharmGKB | PA37860. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | COG4826. |
| HOVERGEN | HBG005957. |
| KO | K13966. |
Gene expression databases | |
| ArrayExpress | Q96P15. |
| Bgee | Q96P15. |
| Genevestigator | Q96P15. |
Family and domain databases | |
| InterPro | IPR023795. Protease_inhib_I4_serpin_CS. IPR023796. Serpin_dom. IPR000215. Serpin_fam. [Graphical view] |
| PANTHER | PTHR11461. PTHR11461. 1 hit. |
| Pfam | PF00079. Serpin. 1 hit. [Graphical view] |
| SMART | SM00093. SERPIN. 1 hit. [Graphical view] |
| SUPFAM | SSF56574. Prot_inh_serpin. 1 hit. |
| PROSITE | PS00284. SERPIN. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| ChiTaRS | SERPINB11. human. |
| GenomeRNAi | 89778. |
| NextBio | 76259. |
Entry information
| Entry name | SPB11_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q96P15 Secondary accession number(s): A8K9R0 Q96P14 | ||||||||
| 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 18 Human chromosome 18: 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
