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Q9UKM0 (Q9UKM0_HUMAN) Unreviewed, UniProtKB/TrEMBL

Last modified July 9, 2014. Version 48. Feed History...

Clusters with 100%, 90%, 50% identity | Third-party data text xml rdf/xml gff fasta
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Names and origin

Protein names
EC=1.17.4.1 EMBL AAD53261.1
Gene names
Name:RR2M EMBL AAD53261.1
OrganismHomo sapiens (Human) EMBL AAD53261.1
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length33 AA.
Sequence statusFragment.
Protein existencePredicted

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Experimental info

Non-terminal residue331 EMBL AAD53261.1

Sequences

Sequence LengthMass (Da)Tools
Q9UKM0 [UniParc].

Last modified May 1, 2000. Version 1.
Checksum: 8CA99B6B0B62198B

FASTA333,616
        10         20         30 
MLSLRVPLAP ITDPQQLQLS PLKGLSLVDK ENT 

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References

[1]"Characterization of the promoter of the human ribonucleotide reductase R2 gene."
Park J.B., Levine M.
Biochem. Biophys. Res. Commun. 267:651-657(2000) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AF149206 Genomic DNA. Translation: AAD53261.1.
UniGeneHs.226390.

3D structure databases

ModBaseSearch...
MobiDBSearch...

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Gene expression databases

ArrayExpressQ9UKM0.
BgeeQ9UKM0.

Family and domain databases

ProtoNetSearch...

Entry information

Entry nameQ9UKM0_HUMAN
AccessionPrimary (citable) accession number: Q9UKM0
Entry history
Integrated into UniProtKB/TrEMBL: May 1, 2000
Last sequence update: May 1, 2000
Last modified: July 9, 2014
This is version 48 of the entry and version 1 of the sequence. [Complete history]
Entry statusUnreviewed (UniProtKB/TrEMBL)
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.