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B4DL95

- B4DL95_HUMAN

UniProt

B4DL95 - B4DL95_HUMAN

Protein
Submitted name:

cDNA FLJ54330, highly similar to Usher syndrome type-1G protein

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 27 (01 Oct 2014)
      Sequence version 1 (23 Sep 2008)
      Previous versions | rss
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    Names & Taxonomyi

    Protein namesi
    Submitted name:
    cDNA FLJ54330, highly similar to Usher syndrome type-1G proteinImported
    OrganismiHomo sapiens (Human)Imported
    Taxonomic identifieri9606 [NCBI]
    Taxonomic lineageiEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

    PTM / Processingi

    Proteomic databases

    PRIDEiB4DL95.

    Family & Domainsi

    Sequence similaritiesi

    Contains SAM (sterile alpha motif) domain.SAAS annotation

    Phylogenomic databases

    HOVERGENiHBG051882.

    Family and domain databases

    Gene3Di1.10.150.50. 1 hit.
    InterProiIPR001660. SAM.
    IPR013761. SAM/pointed.
    IPR021129. SAM_type1.
    [Graphical view]
    PfamiPF00536. SAM_1. 1 hit.
    [Graphical view]
    SMARTiSM00454. SAM. 1 hit.
    [Graphical view]
    SUPFAMiSSF47769. SSF47769. 1 hit.

    Sequencei

    Sequence statusi: Complete.

    B4DL95-1 [UniParc]FASTAAdd to Basket

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    MAAMKGHMEC VRYLDSIAAK QSSLNPKLVG KLKDKAFREA ERRIRECAKL    50
    QRRHHERMER RYRRELAERS DTLSFSSLTS STLSRRLQHL ALGSHLPYSQ 100
    ATLHGTARGK AKMQKKLERR KQGGEGTFKV SEDGRKSARS LSGLQLGSDV 150
    MFVRQGTYAN PKEWGRAPLR DMFLSDEDSV SRATLAAEPA HSEVSTDSGH 200
    DSLFTRPGLG TMVFRRNYLS SGLHGLGRED GGLDGVGAPR GRLQSSPSLD 250
    DDSLGSANSL QDRSCGEELP WDELDLGLDE DLEPETSPLE TFLASLHMED 300
    FAALLRQEKI DLEALMLCSD LDLRSISVPL GPRKKILGAV RRRRQAMERP 350
    PALEDTEL 358
    Length:358
    Mass (Da):39,912
    Last modified:September 23, 2008 - v1
    Checksum:iFB2E47C315AA67D9
    GO

    Sequence databases

    Select the link destinations:
    EMBL
    GenBank
    DDBJ
    Links Updated
    AK296899 mRNA. Translation: BAG59457.1.
    RefSeqiNP_001269418.1. NM_001282489.2.
    UniGeneiHs.376688.

    Genome annotation databases

    GeneIDi124590.

    Cross-referencesi

    Sequence databases

    Select the link destinations:
    EMBL
    GenBank
    DDBJ
    Links Updated
    AK296899 mRNA. Translation: BAG59457.1 .
    RefSeqi NP_001269418.1. NM_001282489.2.
    UniGenei Hs.376688.

    3D structure databases

    ModBasei Search...
    MobiDBi Search...

    Proteomic databases

    PRIDEi B4DL95.

    Protocols and materials databases

    Structural Biology Knowledgebase Search...

    Genome annotation databases

    GeneIDi 124590.

    Phylogenomic databases

    HOVERGENi HBG051882.

    Miscellaneous databases

    NextBioi 35472992.

    Family and domain databases

    Gene3Di 1.10.150.50. 1 hit.
    InterProi IPR001660. SAM.
    IPR013761. SAM/pointed.
    IPR021129. SAM_type1.
    [Graphical view ]
    Pfami PF00536. SAM_1. 1 hit.
    [Graphical view ]
    SMARTi SM00454. SAM. 1 hit.
    [Graphical view ]
    SUPFAMi SSF47769. SSF47769. 1 hit.
    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: TongueImported.

    Entry informationi

    Entry nameiB4DL95_HUMAN
    AccessioniPrimary (citable) accession number: B4DL95
    Entry historyi
    Integrated into UniProtKB/TrEMBL: September 23, 2008
    Last sequence update: September 23, 2008
    Last modified: October 1, 2014
    This is version 27 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.