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Q8WV74 (NUDT8_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 71. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (2) | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Nucleoside diphosphate-linked moiety X motif 8, mitochondrial

Short name=Nudix motif 8
EC=3.6.1.-
Gene names
Name:NUDT8
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length236 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is further processed into a mature form.
Protein existenceEvidence at transcript level

General annotation (Comments)

Function

Probably mediates the hydrolysis of some nucleoside diphosphate derivatives By similarity.

Cofactor

Magnesium or manganese By similarity.

Subcellular location

Mitochondrion By similarity.

Sequence similarities

Belongs to the Nudix hydrolase family.

Contains 1 nudix hydrolase domain.

Ontologies

Keywords
   Cellular componentMitochondrion
   Coding sequence diversityAlternative splicing
   DomainTransit peptide
   LigandMagnesium
Manganese
Metal-binding
   Molecular functionHydrolase
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Cellular componentmitochondrion

Inferred from electronic annotation. Source: UniProtKB-SubCell

   Molecular functionhydrolase activity

Inferred from electronic annotation. Source: UniProtKB-KW

metal ion binding

Inferred from electronic annotation. Source: UniProtKB-KW

Complete GO annotation...

Alternative products

This entry describes 2 isoforms produced by alternative splicing. [Align] [Select]
Isoform 1 (identifier: Q8WV74-1)

This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry.
Isoform 2 (identifier: Q8WV74-2)

The sequence of this isoform differs from the canonical sequence as follows:
     137-140: DEVF → SWGI
     141-236: Missing.
Note: No experimental confirmation available.

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Transit peptide1 – ?Mitochondrion Potential
Chain? – 236Nucleoside diphosphate-linked moiety X motif 8, mitochondrialPRO_0000019948

Regions

Domain25 – 172148Nudix hydrolase
Motif70 – 9122Nudix box

Sites

Metal binding851Magnesium or manganese By similarity
Metal binding891Magnesium or manganese By similarity

Natural variations

Alternative sequence137 – 1404DEVF → SWGI in isoform 2.
VSP_014282
Alternative sequence141 – 23696Missing in isoform 2.
VSP_014283

Sequences

Sequence LengthMass (Da)Tools
Isoform 1 [UniParc].

Last modified July 5, 2005. Version 2.
Checksum: 7DDD2A56010B4D9F

FASTA23625,370
        10         20         30         40         50         60 
MLPDCLSAEG ELRCRRLLAG ATARLRARPA SAAVLVPLCS VRGVPALLYT LRSSRLTGRH 

        70         80         90        100        110        120 
KGDVSFPGGK CDPADQDVVH TALRETREEL GLAVPEEHVW GLLRPVYDPQ KATVVPVLAG 

       130        140        150        160        170        180 
VGPLDPQSLR PNSEEVDEVF ALPLAHLLQT QNQGYTHFCR GGHFRYTLPV FLHGPHRVWG 

       190        200        210        220        230 
LTAVITEFAL QLLAPGTYQP RLAGLTCSGA EGLARPKQPL ASPCQASSTP GLNKGL 

« Hide

Isoform 2 [UniParc].

Checksum: CE854912E843E501
Show »

FASTA14015,052

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 [LARGE SCALE MRNA] (ISOFORM 1).
Tissue: Tongue.
[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] (ISOFORM 2).
Tissue: Placenta.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AK123561 mRNA. Translation: BAC85646.1.
BC018644 mRNA. Translation: AAH18644.1.
IPIIPI00291313.
IPI00607555.
RefSeqNP_001230679.1. NM_001243750.1.
NP_862826.1. NM_181843.2.
UniGeneHs.433329.

3D structure databases

ProteinModelPortalQ8WV74.
SMRQ8WV74. Positions 30-191.
ModBaseSearch...

Polymorphism databases

DMDM68565920.

Proteomic databases

PRIDEQ8WV74.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000376693; ENSP00000365883; ENSG00000167799.
GeneID254552.
KEGGhsa:254552.
UCSCuc001omn.1. human.
uc001omo.1. human.

Organism-specific databases

CTD254552.
GeneCardsGC11M067395.
HGNCHGNC:8055. NUDT8.
HPAHPA041252.
HPA041466.
neXtProtNX_Q8WV74.
PharmGKBPA31841.
GenAtlasSearch...

Phylogenomic databases

eggNOGprNOG10785.
GeneTreeENSGT00530000063767.
HOGENOMHBG729456.
HOVERGENHBG082068.
InParanoidQ8WV74.
OMAPAHETVT.
OrthoDBEOG49S67C.
PhylomeDBQ8WV74.

Gene expression databases

ArrayExpressQ8WV74.
BgeeQ8WV74.
CleanExHS_NUDT8.
GenevestigatorQ8WV74.

Family and domain databases

InterProIPR000086. NUDIX_hydrolase_dom.
IPR015797. NUDIX_hydrolase_dom-like.
[Graphical view]
Gene3DG3DSA:3.90.79.10. NUDIX_hydrolase. 1 hit.
KOK01529.
PfamPF00293. NUDIX. 1 hit.
[Graphical view]
SUPFAMSSF55811. NUDIX_hydrolase. 1 hit.
PROSITEPS51462. NUDIX. 1 hit.
PS00893. NUDIX_BOX. False negative.
[Graphical view]
ProtoNetSearch...

Other

NextBio92368.

Entry information

Entry nameNUDT8_HUMAN
AccessionPrimary (citable) accession number: Q8WV74
Secondary accession number(s): Q6ZW59
Entry history
Integrated into UniProtKB/Swiss-Prot: July 5, 2005
Last sequence update: July 5, 2005
Last modified: January 25, 2012
This is version 71 of the entry and version 2 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation programChordata Protein Annotation Program
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.

Relevant documents

Human chromosome 11

Human chromosome 11: entries, gene names and cross-references to MIM

SIMILARITY comments

Index of protein domains and families