Q9BVV7 (TIM21_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
January 25, 2012.
Version 74.
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: Mitochondrial import inner membrane translocase subunit Tim21 Alternative name(s): TIM21-like protein, mitochondrial | ||||
| 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 | 248 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is further processed into a mature form. |
| Protein existence | Evidence at protein level |
General annotation (Comments)
| Function | May participate in the translocation of transit peptide-containing proteins across the mitochondrial inner membrane By similarity. |
| Subcellular location | Mitochondrion membrane; Single-pass membrane protein Potential. |
| Sequence similarities | Belongs to the TIM21 family. |
Ontologies
| Keywords | |
|---|---|
| Biological process | Protein transport Translocation Transport |
| Cellular component | Membrane Mitochondrion |
| Coding sequence diversity | Polymorphism |
| Domain | Transit peptide Transmembrane Transmembrane helix |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Biological process | protein transport Inferred from electronic annotation. Source: UniProtKB-KW |
| Cellular component | integral to membrane Inferred from electronic annotation. Source: UniProtKB-KW mitochondrial membraneInferred from electronic annotation. Source: UniProtKB-SubCell |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Transit peptide | 1 – 18 | 18 | Mitochondrion Potential | ||||||
| Chain | 19 – 248 | 230 | Mitochondrial import inner membrane translocase subunit Tim21 | PRO_0000043228 | |||||
Regions | |||||||||
| Transmembrane | 108 – 128 | 21 | Helical; Potential | ||||||
Natural variations | |||||||||
| Natural variant | 79 | 1 | G → S. Corresponds to variant rs3737512 [ dbSNP | Ensembl ]. | VAR_052306 | |||||
Experimental info | |||||||||
| Sequence conflict | 34 | 1 | C → Y in AAF29118. Ref.1 | ||||||
Sequences
| ||||||||||||||||||
References
| [1] | "Cloning and functional analysis of cDNAs with open reading frames for 300 previously undefined genes expressed in CD34+ hematopoietic stem/progenitor cells." Zhang Q.-H., Ye M., Wu X.-Y., Ren S.-X., Zhao M., Zhao C.-J., Fu G., Shen Y., Fan H.-Y., Lu G., Zhong M., Xu X.-R., Han Z.-G., Zhang J.-W., Tao J., Huang Q.-H., Zhou J., Hu G.-X. Chen Z.Genome Res. 10:1546-1560(2000) [PubMed: 11042152] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]. Tissue: Umbilical cord blood. |
| [2] | "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]. Tissue: Cervix carcinoma. |
| [3] | "Initial characterization of the human central proteome." Burkard T.R., Planyavsky M., Kaupe I., Breitwieser F.P., Buerckstuemmer T., Bennett K.L., Superti-Furga G., Colinge J. BMC Syst. Biol. 5:17-17(2011) [PubMed: 21269460] [Abstract] Cited for: IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS]. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AF161503 mRNA. Translation: AAF29118.1. BC000892 mRNA. Translation: AAH00892.1. |
| IPI | IPI00306439. |
| RefSeq | NP_054896.2. NM_014177.2. |
| UniGene | Hs.532835. |
3D structure databases | |
| ProteinModelPortal | Q9BVV7. |
| ModBase | Search... |
PTM databases | |
| PhosphoSite | Q9BVV7. |
Polymorphism databases | |
| DMDM | 73918912. |
Proteomic databases | |
| PRIDE | Q9BVV7. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000169551; ENSP00000169551; ENSG00000075336. |
| GeneID | 29090. |
| KEGG | hsa:29090. |
| UCSC | uc010dqr.1. human. |
Organism-specific databases | |
| CTD | 29090. |
| GeneCards | GC18P071815. |
| H-InvDB | HIX0014521. |
| HGNC | HGNC:25010. TIMM21. |
| HPA | HPA010587. |
| neXtProt | NX_Q9BVV7. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | prNOG08000. |
| GeneTree | ENSGT00390000011552. |
| HOGENOM | HBG281361. |
| HOVERGEN | HBG084542. |
| InParanoid | Q9BVV7. |
| OMA | MRVKFYI. |
| OrthoDB | EOG4X6C99. |
| PhylomeDB | Q9BVV7. |
Gene expression databases | |
| ArrayExpress | Q9BVV7. |
| Bgee | Q9BVV7. |
| CleanEx | HS_C18orf55. |
| Genevestigator | Q9BVV7. |
| GermOnline | ENSG00000075336. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR013261. Tim21. [Graphical view] |
| Pfam | PF08294. TIM21. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| NextBio | 52098. |
Entry information
| Entry name | TIM21_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q9BVV7 Secondary accession number(s): Q9P010 | ||||||||
| 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 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