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Q1ET61 (Q1ET61_HUMAN) Unreviewed, UniProtKB/TrEMBL

Last modified November 16, 2011. Version 55. 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

Phenol sulfotransferase 1A5*1B EMBL BAE94933.1

Sulfotransferase family, cytosolic, 1A, phenol-preferring, member 3 EMBL AAI32915.1

cDNA FLJ16185 fis, clone BRTHA2005864, highly similar to Monoamine-sulfating phenol sulfotransferase (EC 2.8.2.1) EMBL BAG53679.1
Gene names
Name:ST1A5 EMBL BAE94933.1
Synonyms:SULT1A3 EMBL AAI32915.1
OrganismHomo sapiens (Human) EMBL BAE94933.1
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length295 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

Ontologies

Keywords
   Molecular functionTransferase EMBL BAE94933.1
Gene Ontology (GO)
   Molecular functionsulfotransferase activity

Inferred from electronic annotation. Source: InterPro

Complete GO annotation...

Sequences

Sequence LengthMass (Da)Tools
Q1ET61 [UniParc].

Last modified July 11, 2006. Version 1.
Checksum: ECDDEC03DBE30D46

FASTA29534,196
        10         20         30         40         50         60 
MELIQDTSRP PLEYVKGVPL IKYFAEALGP LQSFQARPDD LLINTYPKSG TTWVSQILDM 

        70         80         90        100        110        120 
IYQGGDLEKC NRAPIYVRVP FLEVNDPGEP SGLETLKDTP PPRLIKSHLP LALLPQTLLD 

       130        140        150        160        170        180 
QKVKVVYVAR NPKDVAVSYY HFHRMEKAHP EPGTWDSFLE KFMAGEVSYG SWYQHVQEWW 

       190        200        210        220        230        240 
ELSRTHPVLY LFYEDMKENP KREIQKILEF VGRSLPEETM DFMVQHTSFK EMKKNPMTNY 

       250        260        270        280        290 
TTVPQELMDH SISPFMRKGM AGDWKTTFTV AQNERFDADY AEKMAGCSLS FRSEL 

« Hide

References

« Hide 'large scale' references
[1]"Complete sequencing and characterization of 21,243 full-length human cDNAs."
Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S. expand/collapse author list , Yamamoto J., Saito K., Kawai Y., Isono Y., Nakamura Y., Nagahari K., Murakami K., Yasuda T., Iwayanagi T., Wagatsuma M., Shiratori A., Sudo H., Hosoiri T., Kaku Y., Kodaira H., Kondo H., Sugawara M., Takahashi M., Kanda K., Yokoi T., Furuya T., Kikkawa E., Omura Y., Abe K., Kamihara K., Katsuta N., Sato K., Tanikawa M., Yamazaki M., Ninomiya K., Ishibashi T., Yamashita H., Murakawa K., Fujimori K., Tanai H., Kimata M., Watanabe M., Hiraoka S., Chiba Y., Ishida S., Ono Y., Takiguchi S., Watanabe S., Yosida M., Hotuta T., Kusano J., Kanehori K., Takahashi-Fujii A., Hara H., Tanase T.O., Nomura Y., Togiya S., Komai F., Hara R., Takeuchi K., Arita M., Imose N., Musashino K., Yuuki H., Oshima A., Sasaki N., Aotsuka S., Yoshikawa Y., Matsunawa H., Ichihara T., Shiohata N., Sano S., Moriya S., Momiyama H., Satoh N., Takami S., Terashima Y., Suzuki O., Nakagawa S., Senoh A., Mizoguchi H., Goto Y., Shimizu F., Wakebe H., Hishigaki H., Watanabe T., Sugiyama A., Takemoto M., Kawakami B., Yamazaki M., Watanabe K., Kumagai A., Itakura S., Fukuzumi Y., Fujimori Y., Komiyama M., Tashiro H., Tanigami A., Fujiwara T., Ono T., Yamada K., Fujii Y., Ozaki K., Hirao M., Ohmori Y., Kawabata A., Hikiji T., Kobatake N., Inagaki H., Ikema Y., Okamoto S., Okitani R., Kawakami T., Noguchi S., Itoh T., Shigeta K., Senba T., Matsumura K., Nakajima Y., Mizuno T., Morinaga M., Sasaki M., Togashi T., Oyama M., Hata H., Watanabe M., Komatsu T., Mizushima-Sugano J., Satoh T., Shirai Y., Takahashi Y., Nakagawa K., Okumura K., Nagase T., Nomura N., Kikuchi H., Masuho Y., Yamashita R., Nakai K., Yada T., Nakamura Y., Ohara O., Isogai T., Sugano S.
Nat. Genet. 36:40-45(2004) [PubMed: 14702039] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE.
Tissue: Thalamus EMBL BAG53679.1.
[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: Brain EMBL AAI32915.1.
[3]"Isolation of seven variants of catecholamine sulfotransferase cDNAs from human kidney."
Terazawa R., Shimada M., Nagata K., Yamazoe Y.
Submitted (MAY-2003) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE.
Tissue: Kidney EMBL BAE94933.1.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
BC132914 mRNA. Translation: AAI32915.1.
BC132920 mRNA. Translation: AAI32921.1.
BC144354 mRNA. Translation: AAI44355.1.
BC144355 mRNA. Translation: AAI44356.1.
BC171772 mRNA. Translation: AAI71772.1.
AB111093 mRNA. Translation: BAE94927.1.
AB111099 mRNA. Translation: BAE94933.1.
AK122707 mRNA. Translation: BAG53679.1.
IPIIPI00030730.
RefSeqNP_001017390.1. NM_001017390.2.
NP_808220.1. NM_177552.3.
UniGeneHs.460558.
Hs.728806.

3D structure databases

ProteinModelPortalQ1ET61.
SMRQ1ET61. Positions 9-295.
ModBaseSearch...

Protein-protein interaction databases

STRINGQ1ET61.

Proteomic databases

PRIDEQ1ET61.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

GeneID445329.
6818.
KEGGhsa:445329.
hsa:6818.

Organism-specific databases

CTD445329.
6818.

Phylogenomic databases

HOVERGENHBG001195.
PhylomeDBQ1ET61.

Gene expression databases

ArrayExpressQ1ET61.
BgeeQ1ET61.

Family and domain databases

InterProIPR000863. Sulfotransferase_dom.
[Graphical view]
KOK01014.
PfamPF00685. Sulfotransfer_1. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

NextBio111370.

Entry information

Entry nameQ1ET61_HUMAN
AccessionPrimary (citable) accession number: Q1ET61
Entry history
Integrated into UniProtKB/TrEMBL: July 11, 2006
Last sequence update: July 11, 2006
Last modified: November 16, 2011
This is version 55 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.