Q9BWW9 (APOL5_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
January 25, 2012.
Version 78.
History...
Names·Attributes·General annotation·Ontologies·Interactions·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Interactions·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Apolipoprotein L5 Alternative name(s): Apolipoprotein L-V Short name=ApoL-V | ||
| 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 | 433 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at protein level |
General annotation (Comments)
| Function | May affect the movement of lipids in the cytoplasm or allow the binding of lipids to organelles. |
| Subcellular location | Cytoplasm Probable. |
| Tissue specificity | Low level of expression; detected in uterus, testis, skeletal muscle and stomach. |
| Sequence similarities | Belongs to the apolipoprotein L family. |
Ontologies
| Keywords | |
|---|---|
| Biological process | Lipid transport Transport |
| Cellular component | Cytoplasm |
| Coding sequence diversity | Polymorphism |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Biological process | lipid metabolic process Non-traceable author statement Ref.1. Source: UniProtKB lipid transportInferred from electronic annotation. Source: UniProtKB-KW lipoprotein metabolic processInferred from electronic annotation. Source: InterPro |
| Cellular component | cytoplasm Inferred from electronic annotation. Source: UniProtKB-SubCell extracellular regionInferred from electronic annotation. Source: InterPro |
| Molecular function | high-density lipoprotein particle binding Non-traceable author statement Ref.1. Source: UniProtKB lipid bindingInferred from electronic annotation. Source: InterPro |
| Complete GO annotation... | |
Binary interactions
With | Entry | #Exp. | IntAct | Notes |
|---|---|---|---|---|
| ABL1 | P00519 | 1 | EBI-1753592,EBI-375543 | |
| CRK | P46108 | 1 | EBI-1753592,EBI-886 | |
| FYN | P06241 | 1 | EBI-1753592,EBI-515315 | |
| GRB2 | P62993 | 1 | EBI-1753592,EBI-401755 | |
| NCK1 | P16333 | 1 | EBI-1753592,EBI-389883 | |
| PIK3R1 | P27986 | 1 | EBI-1753592,EBI-79464 | |
| SRC | P12931 | 1 | EBI-1753592,EBI-621482 |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 433 | 433 | Apolipoprotein L5 | PRO_0000137603 | |||||
Natural variations | |||||||||
| Natural variant | 81 | 1 | E → K. Corresponds to variant rs5999985 [ dbSNP | Ensembl ]. | VAR_053012 | |||||
| Natural variant | 272 | 1 | T → M. Corresponds to variant rs2076671 [ dbSNP | Ensembl ]. | VAR_020355 | |||||
| Natural variant | 323 | 1 | T → M. Corresponds to variant rs2076672 [ dbSNP | Ensembl ]. | VAR_020356 | |||||
| Natural variant | 406 | 1 | S → C. Corresponds to variant rs2076673 [ dbSNP | Ensembl ]. | VAR_020357 | |||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "The human apolipoprotein L gene cluster: identification, classification, and sites of distribution." Page N.M., Butlin D.J., Lomthaisong K., Lowry P.J. Genomics 74:71-78(2001) [PubMed: 11374903] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA]. Tissue: Placenta. |
| [2] | "The DNA sequence of human chromosome 22." Dunham I., Hunt A.R., Collins J.E., Bruskiewich R., Beare D.M., Clamp M., Smink L.J., Ainscough R., Almeida J.P., Babbage A.K., Bagguley C., Bailey J., Barlow K.F., Bates K.N., Beasley O.P., Bird C.P., Blakey S.E., Bridgeman A.M. Wright H.Nature 402:489-495(1999) [PubMed: 10591208] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AY014878 mRNA. Translation: AAK07723.1. AL049748 Genomic DNA. No translation available. |
| IPI | IPI00032680. |
| RefSeq | NP_085145.1. NM_030642.1. |
| UniGene | Hs.326561. |
3D structure databases | |
| ProteinModelPortal | Q9BWW9. |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | Q9BWW9. 7 interactions. |
| MINT | MINT-7241622. |
| STRING | Q9BWW9. |
Polymorphism databases | |
| DMDM | 17433287. |
Proteomic databases | |
| PRIDE | Q9BWW9. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000249044; ENSP00000249044; ENSG00000128313. |
| GeneID | 80831. |
| KEGG | hsa:80831. |
| UCSC | uc003aof.1. human. |
Organism-specific databases | |
| CTD | 80831. |
| GeneCards | GC22P036113. |
| H-InvDB | HIX0203203. |
| HGNC | HGNC:14869. APOL5. |
| HPA | HPA040968. |
| MIM | 607255. gene. |
| neXtProt | NX_Q9BWW9. |
| PharmGKB | PA24908. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | prNOG09003. |
| GeneTree | ENSGT00510000046700. |
| InParanoid | Q9BWW9. |
| OMA | NSGFMAM. |
| OrthoDB | EOG49ZXPX. |
| PhylomeDB | Q9BWW9. |
Gene expression databases | |
| ArrayExpress | Q9BWW9. |
| Bgee | Q9BWW9. |
| CleanEx | HS_APOL5. |
| Genevestigator | Q9BWW9. |
| GermOnline | ENSG00000128313. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR008405. ApoL. [Graphical view] |
| KO | K14480. |
| PANTHER | PTHR14096. ApoL. 1 hit. |
| Pfam | PF05461. ApoL. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| NextBio | 71244. |
| SOURCE | Search... |
Entry information
| Entry name | APOL5_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q9BWW9 Secondary accession number(s): Q5TFL9, Q9UGW5 | ||||||||
| Entry history |
| ||||||||
| 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 22 Human chromosome 22: 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