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B4DFZ1

- B4DFZ1_HUMAN

UniProt

B4DFZ1 - B4DFZ1_HUMAN

Protein
Submitted name:

cDNA FLJ54613, highly similar to Mucolipin-1

Gene
N/A
Organism
Homo sapiens (Human)
Status
Unreviewed - Annotation score: 1 out of 5- Experimental evidence at transcript leveli
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    • History
      Entry version 29 (01 Oct 2014)
      Sequence version 1 (23 Sep 2008)
      Previous versions | rss
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    Functioni

    GO - Molecular functioni

    1. NAADP-sensitive calcium-release channel activity Source: Ensembl

    GO - Biological processi

    1. release of sequestered calcium ion into cytosol Source: Ensembl

    Names & Taxonomyi

    Protein namesi
    Submitted name:
    cDNA FLJ54613, highly similar to Mucolipin-1Imported
    OrganismiHomo sapiens (Human)Imported
    Taxonomic identifieri9606 [NCBI]
    Taxonomic lineageiEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

    Subcellular locationi

    GO - Cellular componenti

    1. lysosomal membrane Source: UniProtKB

    Expressioni

    Gene expression databases

    ArrayExpressiB4DFZ1.
    BgeeiB4DFZ1.

    Family & Domainsi

    Phylogenomic databases

    HOVERGENiHBG052430.

    Family and domain databases

    InterProiIPR013122. PKD1_2_channel.
    [Graphical view]
    PfamiPF08016. PKD_channel. 1 hit.
    [Graphical view]

    Sequencei

    Sequence statusi: Complete.

    B4DFZ1-1 [UniParc]FASTAAdd to Basket

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    MSPCDKFRAK GRKPCKLMLQ VVKILVVTVQ LILFGLSNQL AVTFREENTI    50
    AFRHLFLLGY SDGADDTFAA YTREQLYQAI FHAVDQYLAL PDVSLGRYAY 100
    VRGGGDPWTN GSGLALCQRY YHRGHVDPAN DTFDIDPMVV TDCIQVDPPE 150
    RPPPPPSDDL TLLESSSSYK NLTLKFHKLV NVTIHFRLKT INLQSLINNE 200
    IPDCYTFSVL ITFDNKAHSG RIPISLETQA HIQECKHPSV FQHGDNSFRL 250
    LFDVVVILTC SLSFLLCARS LLRGFLLQNE FVGFMWRQRG RVISLWERLE 300
    FVNGWYILLV TSDVLTISGT IMKIGIEAKN LASYDVCSIL LGTSTLLVWV 350
    GVIRYLTFFH NYNILIATLR VALPSVMRFC CCVAVIYLGY CFCGWIVLGP 400
    YHVKFRSLSM VSECLFSLIN GDDMFVTFAA MQAQQGRSSL VWLFSQLYLY 450
    SFISLFIYMV LSLFIALITG AYDTIKHPGG AGAEESELQA YIAQCQDSPT 500
    SGKFRRGSGS ACSLLCCCGR DPSEEHSLLV N 531
    Length:531
    Mass (Da):59,685
    Last modified:September 23, 2008 - v1
    Checksum:i5A15B061C5306641
    GO

    Sequence databases

    Select the link destinations:
    EMBL
    GenBank
    DDBJ
    Links Updated
    AK294330 mRNA. Translation: BAG57602.1.
    UniGeneiHs.631858.

    Cross-referencesi

    Sequence databases

    Select the link destinations:
    EMBL
    GenBank
    DDBJ
    Links Updated
    AK294330 mRNA. Translation: BAG57602.1 .
    UniGenei Hs.631858.

    3D structure databases

    ModBasei Search...
    MobiDBi Search...

    Protocols and materials databases

    Structural Biology Knowledgebase Search...

    Phylogenomic databases

    HOVERGENi HBG052430.

    Miscellaneous databases

    NextBioi 35471618.

    Gene expression databases

    ArrayExpressi B4DFZ1.
    Bgeei B4DFZ1.

    Family and domain databases

    InterProi IPR013122. PKD1_2_channel.
    [Graphical view ]
    Pfami PF08016. PKD_channel. 1 hit.
    [Graphical view ]
    ProtoNeti Search...

    Publicationsi

    1. "NEDO human cDNA sequencing project focused on splicing variants."
      Wakamatsu A., Yamamoto J., Kimura K., Ishii S., Watanabe K., Sugiyama A., Murakawa K., Kaida T., Tsuchiya K., Fukuzumi Y., Kumagai A., Oishi Y., Yamamoto S., Ono Y., Komori Y., Yamazaki M., Kisu Y., Nishikawa T.
      , Sugano S., Nomura N., Isogai T.
      Submitted (OCT-2007) to the EMBL/GenBank/DDBJ databases
      Cited for: NUCLEOTIDE SEQUENCE.
      Tissue: AmygdalaImported.

    Entry informationi

    Entry nameiB4DFZ1_HUMAN
    AccessioniPrimary (citable) accession number: B4DFZ1
    Entry historyi
    Integrated into UniProtKB/TrEMBL: September 23, 2008
    Last sequence update: September 23, 2008
    Last modified: October 1, 2014
    This is version 29 of the entry and version 1 of the sequence. [Complete history]
    Entry statusiUnreviewed (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.