O60296 (TRAK2_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
April 3, 2013.
Version 105.
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: Trafficking kinesin-binding protein 2 Alternative name(s): Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 3 protein | ||||
| 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 | 914 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at protein level |
General annotation (Comments)
| Function | May regulate endosome-to-lysosome trafficking of membrane cargo, including EGFR By similarity. |
| Subunit structure | Interacts with GABA-A receptor and O-GlcNAc transferase. Interacts with HGS By similarity. Interacts with RHOT1/Miro-1 and RHOT2/Miro-2. Ref.5 |
| Subcellular location | Cytoplasm By similarity. Early endosome By similarity. Mitochondrion By similarity. Note: Colocalizes with MGARP at the mitochondria. Translocates from the cytoplasm to the mitochondria in a MGARP-dependent manner By similarity. |
| Tissue specificity | Widely expressed, with highest expression in heart. |
| Post-translational modification | O-glycosylated By similarity. |
| Sequence similarities | Contains 1 HAP1 N-terminal domain. |
Ontologies
| Keywords | |
|---|---|
| Biological process | Transport |
| Cellular component | Cytoplasm Endosome Mitochondrion |
| Coding sequence diversity | Polymorphism |
| Domain | Coiled coil |
| PTM | Glycoprotein |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Biological_process | protein O-linked glycosylation Inferred from electronic annotation. Source: Compara protein targetingInferred from electronic annotation. Source: Compara regulation of transcription from RNA polymerase II promoterInferred from electronic annotation. Source: Compara |
| Cellular_component | early endosome Inferred from electronic annotation. Source: UniProtKB-SubCell mitochondrionInferred from sequence or structural similarity. Source: UniProtKB nucleusInferred from electronic annotation. Source: Compara plasma membraneInferred from sequence or structural similarity PubMed 12034717. Source: UniProtKB |
| Molecular_function | GABA receptor binding Non-traceable author statement PubMed 15644324. Source: HGNC |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 914 | 914 | Trafficking kinesin-binding protein 2 | PRO_0000064538 | |||||
Regions | |||||||||
| Domain | 48 – 353 | 306 | HAP1 N-terminal | ||||||
| Region | 359 – 509 | 151 | Interaction with HGS By similarity | ||||||
| Coiled coil | 134 – 354 | 221 | Potential | ||||||
Natural variations | |||||||||
| Natural variant | 142 | 1 | V → I. Ref.1 Ref.2 Corresponds to variant rs13022344 [ dbSNP | Ensembl ]. | VAR_014201 | |||||
| Natural variant | 528 | 1 | T → I. Ref.1 Corresponds to variant rs2244438 [ dbSNP | Ensembl ]. | VAR_014434 | |||||
| Natural variant | 863 | 1 | I → N. Ref.4 Corresponds to variant rs34594680 [ dbSNP | Ensembl ]. | VAR_051458 | |||||
Experimental info | |||||||||
| Sequence conflict | 301 – 311 | 11 | HVIEKEELKLH → VGLFIHSTDIC Ref.2 | ||||||
| Sequence conflict | 312 – 914 | 603 | Missing Ref.2 | ||||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "Cloning and characterization of three novel genes, ALS2CR1, ALS2CR2, and ALS2CR3, in the juvenile amyotrophic lateral sclerosis (ALS2) critical region at chromosome 2q33-q34: candidate genes for ALS2." Hadano S., Yanagisawa Y., Skaug J., Fichter K., Nasir J., Martindale D., Koop B.F., Scherer S.W., Nicholson D.W., Rouleau G.A., Ikeda J.-E., Hayden M.R. Genomics 71:200-213(2001) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA], VARIANTS ILE-142 AND ILE-528. |
| [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 ILE-142. Tissue: Cerebellum. |
| [3] | "Prediction of the coding sequences of unidentified human genes. IX. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro." Nagase T., Ishikawa K., Miyajima N., Tanaka A., Kotani H., Nomura N., Ohara O. DNA Res. 5:31-39(1998) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 446-914. Tissue: Brain. |
| [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] OF 798-914, VARIANT ASN-863. Tissue: Skin. |
| [5] | "The atypical Rho GTPases Miro-1 and Miro-2 have essential roles in mitochondrial trafficking." Fransson S., Ruusala A., Aspenstroem P. Biochem. Biophys. Res. Commun. 344:500-510(2006) [PubMed] [Europe PMC] [Abstract] Cited for: INTERACTION WITH RHOT1 AND RHOT2. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AB038964 Genomic DNA. Translation: BAB32550.1. AB038951 mRNA. Translation: BAB32501.1. AK054763 mRNA. Translation: BAB70803.1. AB011121 mRNA. Translation: BAA25475.1. BC017999 mRNA. Translation: AAH17999.1. |
| IPI | IPI00297257. |
| RefSeq | NP_055864.2. NM_015049.2. |
| UniGene | Hs.152774. |
3D structure databases | |
| ProteinModelPortal | O60296. |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | O60296. 1 interaction. |
| STRING | 9606.ENSP00000328875. |
PTM databases | |
| PhosphoSite | O60296. |
Proteomic databases | |
| PaxDb | O60296. |
| PRIDE | O60296. |
Protocols and materials databases | |
| DNASU | 66008. |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000332624; ENSP00000328875; ENSG00000115993. |
| GeneID | 66008. |
| KEGG | hsa:66008. |
| UCSC | uc002uyb.4. human. |
Organism-specific databases | |
| CTD | 66008. |
| GeneCards | GC02M202241. |
| H-InvDB | HIX0002738. |
| HGNC | HGNC:13206. TRAK2. |
| HPA | HPA015827. |
| MIM | 607334. gene. |
| neXtProt | NX_O60296. |
| PharmGKB | PA24744. |
| HUGE | Search... |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG246318. |
| HOGENOM | HOG000143414. |
| HOVERGEN | HBG069248. |
| InParanoid | O60296. |
| KO | K15374. |
| OMA | EETFRYM. |
| OrthoDB | EOG48KR9V. |
| PhylomeDB | O60296. |
Gene expression databases | |
| ArrayExpress | O60296. |
| Bgee | O60296. |
| CleanEx | HS_TRAK2. |
| Genevestigator | O60296. |
| GermOnline | ENSG00000115993. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR006933. HAP1_N. IPR022154. Traffickng_kinesin-bd_prot_dom. [Graphical view] |
| Pfam | PF04849. HAP1_N. 1 hit. PF12448. Milton. 2 hits. [Graphical view] |
| ProtoNet | Search... |
Other | |
| ChiTaRS | TRAK2. human. |
| GenomeRNAi | 66008. |
| NextBio | 67530. |
| SOURCE | Search... |
Entry information
| Entry name | TRAK2_HUMAN | ||||||||
| Accession | Primary (citable) accession number: O60296 Secondary accession number(s): Q8WVH7 Q9C0K6 | ||||||||
| 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 2 Human chromosome 2: 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
