Q9NPF8 (ADAP2_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
January 25, 2012.
Version 84.
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: Arf-GAP with dual PH domain-containing protein 2 Alternative name(s): Centaurin-alpha-2 Short name=Cnt-a2 | ||||
| Gene names |
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| 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 | 381 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Function | GTPase-activating protein for the ADP ribosylation factor family Potential. Binds phosphatidylinositol 3,4,5-trisphosphate (PtdInsP3) and inositol 1,3,4,5-tetrakisphosphate (InsP4). Possesses a stoichiometry of two binding sites for InsP4 with identical affinity. Ref.5 |
| Subcellular location | Cytoplasm. Cell membrane. Note: Constitutively associated with the plasma membrane. Excluded from the nucleus. Ref.5 |
| Tissue specificity | Highly expressed in placenta, spleen, kidney, skeletal muscle and adrenal gland. Weakly expressed in thyroid, liver, heart, lung, small intestine, peripheral blood leukocytes. Not detected in spinal cord, brain, stomach, trachea, colon, lymph node and bone marrow. Ref.5 |
| Sequence similarities | Contains 1 Arf-GAP domain. Contains 2 PH domains. |
Ontologies
Alternative products
| This entry describes 2 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q9NPF8-1) 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: Q9NPF8-2) The sequence of this isoform differs from the canonical sequence as follows: 269-269: Missing. | ||||||
| Note: May be due to a competing acceptor splice site. No experimental confirmation available. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 381 | 381 | Arf-GAP with dual PH domain-containing protein 2 | PRO_0000074206 | |||||
Regions | |||||||||
| Domain | 9 – 131 | 123 | Arf-GAP | ||||||
| Domain | 132 – 233 | 102 | PH 1 | ||||||
| Domain | 255 – 361 | 107 | PH 2 | ||||||
| Zinc finger | 25 – 48 | 24 | C4-type | ||||||
Natural variations | |||||||||
| Alternative sequence | 269 | 1 | Missing in isoform 2. | VSP_011180 | |||||
Experimental info | |||||||||
| Sequence conflict | 12 | 1 | L → P in CAC40651. Ref.3 | ||||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "Identification of centaurin-alpha2: a phosphatidylinositide-binding protein present in fat, heart and skeletal muscle." Whitley P., Gibbard A.M., Koumanov F., Oldfield S., Kilgour E.E., Prestwich G.D., Holman G.D. Eur. J. Cell Biol. 81:222-230(2002) [PubMed: 12018390] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1). |
| [2] | "A common set of at least 11 functional genes is lost in the majority of NF1 patients with gross deletions." Jenne D.E., Tinschert S., Stegmann E., Reimann H., Nuernberg P., Horn D., Naumann I., Buske A., Thiel G. Genomics 66:93-97(2000) [PubMed: 10843809] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1). |
| [3] | Bertsch U., Illies C., Mayr G.W. Submitted (MAY-1999) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1). |
| [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: 15489334] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2). Tissue: Leukocyte. |
| [5] | "Identification of gene structure and subcellular localization of human centaurin alpha 2, and p42IP4, a family of two highly homologous, Ins 1,3,4,5-P4-/PtdIns 3,4,5-P3-binding, adapter proteins." Hanck T., Stricker R., Sedehizade F., Reiser G. J. Neurochem. 88:326-336(2004) [PubMed: 14690521] [Abstract] Cited for: FUNCTION, TISSUE SPECIFICITY, SUBCELLULAR LOCATION. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AJ238994 mRNA. Translation: CAB88383.1. AJ272195 mRNA. Translation: CAB77266.1. AJ242782 mRNA. Translation: CAC40651.1. BC033758 mRNA. Translation: AAH33758.1. |
| IPI | IPI00020090. IPI00456640. |
| RefSeq | NP_060874.1. NM_018404.2. |
| UniGene | Hs.514063. |
3D structure databases | |
| ProteinModelPortal | Q9NPF8. |
| SMR | Q9NPF8. Positions 3-372. |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | Q9NPF8. 2 interactions. |
| MINT | MINT-1407535. |
| STRING | Q9NPF8. |
Polymorphism databases | |
| DMDM | 27923749. |
Proteomic databases | |
| PRIDE | Q9NPF8. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000330889; ENSP00000329468; ENSG00000184060. |
| GeneID | 55803. |
| KEGG | hsa:55803. |
| UCSC | uc002hfx.1. human. uc002hfy.1. human. |
Organism-specific databases | |
| CTD | 55803. |
| GeneCards | GC17P029248. |
| H-InvDB | HIX0013699. |
| HGNC | HGNC:16487. ADAP2. |
| MIM | 608635. gene. |
| neXtProt | NX_Q9NPF8. |
| PharmGKB | PA164714924. PA26405. |
| GenAtlas | Search... |
Phylogenomic databases | |
| GeneTree | ENSGT00530000062917. |
| HOVERGEN | HBG050888. |
| OrthoDB | EOG4P8FJB. |
| PhylomeDB | Q9NPF8. |
Gene expression databases | |
| ArrayExpress | Q9NPF8. |
| Bgee | Q9NPF8. |
| CleanEx | HS_ADAP2. |
| Genevestigator | Q9NPF8. |
| GermOnline | ENSG00000184060. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR001164. ArfGAP. IPR011993. PH_type. IPR001849. Pleckstrin_homology. [Graphical view] |
| Gene3D | G3DSA:2.30.29.30. PH_type. 2 hits. |
| Pfam | PF01412. ArfGap. 1 hit. PF00169. PH. 1 hit. [Graphical view] |
| PRINTS | PR00405. REVINTRACTNG. |
| SMART | SM00105. ArfGap. 1 hit. SM00233. PH. 2 hits. [Graphical view] |
| SUPFAM | SSF57863. ArfGAP. 1 hit. |
| PROSITE | PS50115. ARFGAP. 1 hit. PS50003. PH_DOMAIN. 2 hits. [Graphical view] |
| ProtoNet | Search... |
Other | |
| NextBio | 60951. |
| SOURCE | Search... |
Entry information
| Entry name | ADAP2_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q9NPF8 Secondary accession number(s): Q8N4Q6, Q96SD5 | ||||||||
| 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 17 Human chromosome 17: entries, gene names and cross-references to MIM |
| 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