Skip Header

Contribute Send feedback
Read comments (?) or add your own

Q9BVV7 (TIM21_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 74. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (4) | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Mitochondrial import inner membrane translocase subunit Tim21
Alternative name(s):
TIM21-like protein, mitochondrial
Gene names
Name:TIMM21
ORF Names:C18orf55, HSPC154, TIM21
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length248 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is further processed into a mature form.
Protein existenceEvidence 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 processProtein transport
Translocation
Transport
   Cellular componentMembrane
Mitochondrion
   Coding sequence diversityPolymorphism
   DomainTransit peptide
Transmembrane
Transmembrane helix
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Biological processprotein transport

Inferred from electronic annotation. Source: UniProtKB-KW

   Cellular componentintegral to membrane

Inferred from electronic annotation. Source: UniProtKB-KW

mitochondrial membrane

Inferred from electronic annotation. Source: UniProtKB-SubCell

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Transit peptide1 – 1818Mitochondrion Potential
Chain19 – 248230Mitochondrial import inner membrane translocase subunit Tim21
PRO_0000043228

Regions

Transmembrane108 – 12821Helical; Potential

Natural variations

Natural variant791G → S.
Corresponds to variant rs3737512 [ dbSNP | Ensembl ].
VAR_052306

Experimental info

Sequence conflict341C → Y in AAF29118. Ref.1

Sequences

Sequence LengthMass (Da)Tools
Q9BVV7 [UniParc].

Last modified June 1, 2001. Version 1.
Checksum: 7BA2694A9DCD9024

FASTA24828,202
        10         20         30         40         50         60 
MICTFLRAVQ YTEKLHRSSA KRLLLPYIVL NKACLKTEPS LRCGLQYQKK TLRPRCILGV 

        70         80         90        100        110        120 
TQKTIWTQGP SPRKAKEDGS KQVSVHRSQR GGTAVPTSQK VKEAGRDFTY LIVVLFGISI 

       130        140        150        160        170        180 
TGGLFYTIFK ELFSSSSPSK IYGRALEKCR SHPEVIGVFG ESVKGYGEVT RRGRRQHVRF 

       190        200        210        220        230        240 
TEYVKDGLKH TCVKFYIEGS EPGKQGTVYA QVKENPGSGE YDFRYIFVEI ESYPRRTIII 


EDNRSQDD 

« Hide

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. expand/collapse author list , Gu J., Chen S.-J., 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.
IPIIPI00306439.
RefSeqNP_054896.2. NM_014177.2.
UniGeneHs.532835.

3D structure databases

ProteinModelPortalQ9BVV7.
ModBaseSearch...

PTM databases

PhosphoSiteQ9BVV7.

Polymorphism databases

DMDM73918912.

Proteomic databases

PRIDEQ9BVV7.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000169551; ENSP00000169551; ENSG00000075336.
GeneID29090.
KEGGhsa:29090.
UCSCuc010dqr.1. human.

Organism-specific databases

CTD29090.
GeneCardsGC18P071815.
H-InvDBHIX0014521.
HGNCHGNC:25010. TIMM21.
HPAHPA010587.
neXtProtNX_Q9BVV7.
GenAtlasSearch...

Phylogenomic databases

eggNOGprNOG08000.
GeneTreeENSGT00390000011552.
HOGENOMHBG281361.
HOVERGENHBG084542.
InParanoidQ9BVV7.
OMAMRVKFYI.
OrthoDBEOG4X6C99.
PhylomeDBQ9BVV7.

Gene expression databases

ArrayExpressQ9BVV7.
BgeeQ9BVV7.
CleanExHS_C18orf55.
GenevestigatorQ9BVV7.
GermOnlineENSG00000075336. Homo sapiens.

Family and domain databases

InterProIPR013261. Tim21.
[Graphical view]
PfamPF08294. TIM21. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

NextBio52098.

Entry information

Entry nameTIM21_HUMAN
AccessionPrimary (citable) accession number: Q9BVV7
Secondary accession number(s): Q9P010
Entry history
Integrated into UniProtKB/Swiss-Prot: August 30, 2005
Last sequence update: June 1, 2001
Last modified: January 25, 2012
This is version 74 of the entry and version 1 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation programChordata Protein Annotation Program
DisclaimerAny 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