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UniProtKB/Swiss-Prot entry Q6TEK4


[Entry info] [Name and origin] [References] [Comments] [Cross-references] [Keywords] [Features] [Sequence] [Tools]

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Entry information
Entry name VKOR1_RAT
Primary accession number Q6TEK4
Secondary accession numbers None
Integrated into Swiss-Prot on April 12, 2005
Sequence was last modified on July 5, 2004 (Sequence version 1)
Annotations were last modified on    September 2, 2008 (Entry version 30)
Name and origin of the protein
Protein name Vitamin K epoxide reductase complex subunit 1
Synonyms EC 1.1.4.1
Vitamin K1 2,3-epoxide reductase subunit 1
Gene name
Name: Vkorc1
From
Rattus norvegicus (Rat) [TaxID: 10116] 
Taxonomy Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Sciurognathi; Muroidea; Muridae; Murinae; Rattus.
Protein existence 1: Evidence at protein level;
References
[1]
NUCLEOTIDE SEQUENCE [MRNA].
STRAIN=Sprague-Dawley;
TISSUE=Liver;
DOI=10.1038/nature02214; PubMed=14765194 [NCBI, ExPASy, EBI, Israel, Japan]
Rost S., Fregin A., Ivaskevicius V., Conzelmann E., Hoertnagel K., Pelz H.-J., Lappegard K., Seifried E., Scharrer I., Tuddenham E.G.D., Mueller C.R., Strom T.M., Oldenburg J.;
"Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2.";
Nature 427:537-541(2004).
[2]
MUTAGENESIS OF CYS-132 AND CYS-135.
DOI=10.1074/jbc.M413982200; PubMed=15640149 [NCBI, ExPASy, EBI, Israel, Japan]
Wajih N., Sane D.C., Hutson S.M., Wallin R.;
"Engineering of a recombinant vitamin K-dependent (gamma)-carboxylation system with enhanced (gamma)-carboxyglutamic acid forming capacity: evidence for a functional CxxC redox center in the system.";
J. Biol. Chem. 280:10540-10547(2005).
Comments
  • FUNCTION: Involved in vitamin K metabolism. Catalytic subunit of the vitamin K epoxide reductase (VKOR) complex which reduces inactive vitamin K 2,3-epoxide to active vitamin K.
  • CATALYTIC ACTIVITY: 2-methyl-3-phytyl-1,4-naphthoquinone + oxidized dithiothreitol = 2,3-epoxy-2,3-dihydro-2-methyl-3-phytyl-1,4-naphthoquinone + 1,4-dithiothreitol.
  • SUBCELLULAR LOCATION: Endoplasmic reticulum membrane; Multi-pass membrane protein (By similarity).
  • MISCELLANEOUS: The location of two cysteine active-site residues within a proposed transmembrane is consistent both with the known hydrophobic environment of the thiol redox site of the enzyme and with the lipophilicity of vitamin K and warfarin.
  • SIMILARITY: Belongs to the VKOR family.
Copyright
Copyrighted by the UniProt Consortium, see http://www.uniprot.org/terms. Distributed under the Creative Commons Attribution-NoDerivs License.
Cross-references
Sequence databases
EMBL
AY423047; AAR82917.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
RefSeq NP_976080.1; -.
UniGene Rn.97942
3D structure databases
ModBase Q6TEK4.
Organism-specific databases
RGD 1303107; Vkorc1.
Gene expression databases
ArrayExpress Q6TEK4; -.
GermOnline ENSRNOG00000019399; Rattus norvegicus.
Ontologies
GO
GO:0005789; Cellular component: endoplasmic reticulum membrane (inferred from electronic annotation from UniProtKB-SubCell).
QuickGo view.
Family and domain databases
InterPro IPR012932; VKOR.
Graphical view of domain structure.
Pfam PF07884; VKOR; 1.
Pfam graphical view of domain structure.
SMART SM00756; VKc; 1.
SMART graphical view of domain structure.
BLOCKS Q6TEK4.
Genome annotation databases
Ensembl ENSRNOG00000019399; Rattus norvegicus. [Contig view]
GeneID 309004; -.
KEGG rno:309004; -.
NMPDR fig|10116.3.peg.3056; -.
Phylogenomic databases
HOVERGEN Q6TEK4; -.
Other
ProtoNet Q6TEK4.
UniRef View cluster of proteins with at least 50% / 90% / 100% identity.
Keywords
Endoplasmic reticulum; Membrane; Oxidoreductase; Redox-active center; Transmembrane.
Features
SEVIEWER logo Feature table viewer FT aligner logo Feature aligner
KeyFrom   To Length Description FTId
CHAIN   1   161  161     Vitamin K epoxide reductase complex subunit 1. PRO_0000191670
TOPO_DOM   1    10  10     Lumenal (Potential). 
TRANSMEM   11    31  21     Potential. 
TOPO_DOM   32    80  49     Cytoplasmic (Potential). 
TRANSMEM   81    97  17     Potential. 
TOPO_DOM   98   100  3     Lumenal (Potential). 
TRANSMEM   101   123  23     Potential. 
TOPO_DOM   124   126  3     Cytoplasmic (Potential). 
TRANSMEM   127   149  23     Potential. 
TOPO_DOM   150   161  12     Lumenal (Potential). 
DISULFID   132   135        Redox-active (Potential). 
MUTAGEN   132   132        C->S: No increased VKOR activity when overexpressed together with GGCX. 
MUTAGEN   135   135        C->S: No increased VKOR activity when overexpressed together with GGCX. 
Sequence information
Length: 161 AA [This is the length of the unprocessed precursor] Molecular weight: 17783 Da [This is the MW of the unprocessed precursor] CRC64: BBCE9897B00807DD [This is a checksum on the sequence]
        10         20         30         40         50         60 
MGTTWRSPGR LRLALCLAGL ALSLYALHVK AARARNEDYR ALCDVGTAIS CSRVFSSRWG 

        70         80         90        100        110        120 
RGFGLVEHVL GADSILNQSN SIFGCMFYTI QLLLGCLRGR WASILLILSS LVSVAGSLYL 

       130        140        150        160 
AWILFFVLYD FCIVCITTYA INAGLMLLSF QKVPEHKVKK P 

Q6TEK4 in FASTA format

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