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Q59EE3 (Q59EE3_HUMAN) Unreviewed, UniProtKB/TrEMBL

Last modified January 22, 2014. Version 18. 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 length180 AA.
Sequence statusFragment.
Protein existenceEvidence at transcript level

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Experimental info

Non-terminal residue11 EMBL BAD93105.1

Sequences

Sequence LengthMass (Da)Tools
Q59EE3 [UniParc].

Last modified April 26, 2005. Version 1.
Checksum: 0CF02B89D8978BCB

FASTA18020,196
        10         20         30         40         50         60 
DPVDPVASQT ALLKINQAEL AAFNDAVTLC LLVCLYCQMV RSMSTDSCLS SDPRALCTED 

        70         80         90        100        110        120 
AYLHLFTSHF LWSHTYLQSH ILSEHILSFI SPSPTSAPLP LFSHPREWPQ QEFAQLSEVV 

       130        140        150        160        170        180 
PFLPRLLDYA SATPGFFPFL NCGKSILTSQ SLHPFLLWNA HPLDLYLADS FSSFRFQLSS 

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References

[1]"Homo sapiens protein coding cDNA."
Totoki Y., Toyoda A., Takeda T., Sakaki Y., Tanaka A., Yokoyama S., Ohara O., Nagase T., Kikuno R.F.
Submitted (MAR-2005) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE.
Tissue: Aorta endothelial cell EMBL BAD93105.1.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AB209868 mRNA. Translation: BAD93105.1.
UniGeneHs.480042.

3D structure databases

ModBaseSearch...
MobiDBSearch...

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Family and domain databases

ProtoNetSearch...

Entry information

Entry nameQ59EE3_HUMAN
AccessionPrimary (citable) accession number: Q59EE3
Entry history
Integrated into UniProtKB/TrEMBL: April 26, 2005
Last sequence update: April 26, 2005
Last modified: January 22, 2014
This is version 18 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.