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Q9UKK4 (Q9UKK4_HUMAN) Unreviewed, UniProtKB/TrEMBL

Last modified July 9, 2014. Version 59. 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 attributes

Sequence length56 AA.
Sequence statusFragment.
Protein existencePredicted

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Experimental info

Non-terminal residue11 EMBL AAD47248.1
Non-terminal residue561 EMBL AAD47248.1

Sequences

Sequence LengthMass (Da)Tools
Q9UKK4 [UniParc].

Last modified May 1, 2000. Version 1.
Checksum: A7AF3AA24B1730BF

FASTA565,976
        10         20         30         40         50 
IAREAEAAIY HLQLFEELRR LAPITSDPTE ATAVGAVEAS FKCCSGAIIV LTKSGR 

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References

[1]"Polymorphism in the inter-subunit contact domain region of the pyruvate kinase M2 gene in a normal cell line."
Bamezai R.N.K., Anitha M., Saha A.
Submitted (JUN-1999) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AF157692 Genomic DNA. Translation: AAD47248.1.
UniGeneHs.534770.

3D structure databases

ProteinModelPortalQ9UKK4.
ModBaseSearch...
MobiDBSearch...

Proteomic databases

PRIDEQ9UKK4.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Gene expression databases

ArrayExpressQ9UKK4.
BgeeQ9UKK4.

Family and domain databases

Gene3D3.40.1380.20. 1 hit.
InterProIPR001697. Pyr_Knase.
IPR015794. Pyrv_Knase_a/b.
IPR015795. Pyrv_Knase_C.
[Graphical view]
PANTHERPTHR11817. PTHR11817. 1 hit.
SUPFAMSSF52935. SSF52935. 1 hit.
ProtoNetSearch...

Entry information

Entry nameQ9UKK4_HUMAN
AccessionPrimary (citable) accession number: Q9UKK4
Entry history
Integrated into UniProtKB/TrEMBL: May 1, 2000
Last sequence update: May 1, 2000
Last modified: July 9, 2014
This is version 59 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.