Detail Information for IndEnz0002007553
IED ID IndEnz0002007553
Enzyme Type ID protease007553
Protein Name ATP-binding cassette sub-family C member 2
EC 7.6.2.-
EC 7.6.2.2
EC 7.6.2.3
Canalicular multidrug resistance protein
Canalicular multispecific organic anion transporter 1
Multidrug resistance-associated protein 2
Gene Name Abcc2 Cmoat Cmrp Mrp2
Organism Rattus norvegicus (Rat)
Taxonomic Lineage cellular organisms Eukaryota Opisthokonta Metazoa Eumetazoa Bilateria Deuterostomia Chordata Craniata Vertebrata Gnathostomata (jawed vertebrates) Teleostomi Euteleostomi Sarcopterygii Dipnotetrapodomorpha Tetrapoda Amniota Mammalia Theria Eutheria Boreoeutheria Euarchontoglires Glires (Rodents and rabbits) Rodentia Myomorpha (mice and others) Muroidea Muridae Murinae Rattus Rattus norvegicus (Rat)
Enzyme Sequence MDKFCNSTFWDLSLLESPEADLPLCFEQTVLVWIPLGFLWLLAPWQLYSVYRSRTKRSSITKFYLAKQVFVVFLLILAAIDLSLALTEDTGQATVPPVRYTNPILYLCTWLLVLAVQHSRQWCVRKNSWFLSLFWILSVLCGVFQFQTLIRALLKDSKSNMAYSYLFFVSYGFQIVLLILTAFSGPSDSTQTPSVTASFLSSITFSWYDRTVLKGYKHPLTLEDVWDIDEGFKTRSVTSKFEAAMTKDLQKARQAFQRRLQKSQRKPEATLHGLNKKQSQSQDVLVLEEAKKKSEKTTKDYPKSWLIKSLFKTFHVVILKSFILKLIHDLLVFLNPQLLKLLIGFVKSSNSYVWFGYICAILMFAVTLIQSFCLQSYFQHCFVLGMCVRTTVMSSIYKKALTLSNLARKQYTIGETVNLMSVDSQKLMDATNYMQLVWSSVIQITLSIFFLWRELGPSILAGVGVMVLLIPVNGVLATKIRNIQVQNMKNKDKRLKIMNEILSGIKILKYFAWEPSFQEQVQGIRKKELKNLLRFGQLQSLLIFILQITPILVSVVTFSVYVLVDSANVLNAEKAFTSITLFNILRFPLSMLPMVTSSILQASVSVDRLERYLGGDDLDTSAIRRVSNFDKAVKFSEASFTWDPDLEATIQDVNLDIKPGQLVAVVGTVGSGKSSLVSAMLGEMENVHGHITIQGSTAYVPQQSWIQNGTIKDNILFGSEYNEKKYQQVLKACALLPDLEILPGGDMAEIGEKGINLSGGQKQRVSLARAAYQDADIYILDDPLSAVDAHVGKHIFNKVVGPNGLLAGKTRIFVTHGIHFLPQVDEIVVLGKGTILEKGSYRDLLDKKGVFARNWKTFMKHSGPEGEATVNNDSEAEDDDDGLIPTMEEIPEDAASLAMRRENSLRRTLSRSSRSSSRRGKSLKNSLKIKNVNVLKEKEKEVEGQKLIKKEFVETGKVKFSIYLKYLQAVGWWSILFIILFYGLNNVAFIGSNLWLSAWTSDSDNLNGTNNSSSHRDMRIGVFGALGLAQGICLLISTLWSIYACRNASKALHGQLLTNILRAPMRFFDTTPTGRIVNRFSGDISTVDDLLPQTLRSWMMCFFGIAGTLVMICMATPVFAIIIIPLSILYISVQVFYVATSRQLRRLDSVTKSPIYSHFSETVTGLPIIRAFEHQQRFLAWNEKQIDINQKCVFSWITSNRWLAIRLELVGNLVVFCSALLLVIYRKTLTGDVVGFVLSNALNITQTLNWLVRMTSEAETNIVAVERISEYINVENEAPWVTDKRPPADWPRHGEIQFNNYQVRYRPELDLVLKGITCNIKSGEKVGVVGRTGAGKSSLTNCLFRILESAGGQIIIDGIDVASIGLHDLRERLTIIPQDPILFSGSLRMNLDPFNKYSDEEVWRALELAHLRSFVSGLQLGLLSEVTEGGDNLSIGQRQLLCLGRAVLRKSKILVLDEATAAVDLETDSLIQTTIRKEFSQCTVITIAHRLHTIMDSDKIMVLDNGKIVEYGSPEELLSNRGSFYLMAKEAGIENVNHTEL
Enzyme Length 1541
Uniprot Accession Number Q63120
Absorption
Active Site
Activity Regulation
Binding Site
Calcium Binding
catalytic Activity CATALYTIC ACTIVITY: Reaction=an S-substituted glutathione(in) + ATP + H2O = ADP + an S-substituted glutathione(out) + H(+) + phosphate; Xref=Rhea:RHEA:19121, ChEBI:CHEBI:15377, ChEBI:CHEBI:15378, ChEBI:CHEBI:30616, ChEBI:CHEBI:43474, ChEBI:CHEBI:90779, ChEBI:CHEBI:456216; EC=7.6.2.3; Evidence={ECO:0000269|PubMed:10220572, ECO:0000269|PubMed:8662992};PhysiologicalDirection=left-to-right; Xref=Rhea:RHEA:19122; Evidence={ECO:0000305|PubMed:10220572, ECO:0000305|PubMed:8662992}; CATALYTIC ACTIVITY: Reaction=ATP + H2O + taurolithocholate 3-sulfate(in) = ADP + H(+) + phosphate + taurolithocholate 3-sulfate(out); Xref=Rhea:RHEA:50084, ChEBI:CHEBI:15377, ChEBI:CHEBI:15378, ChEBI:CHEBI:30616, ChEBI:CHEBI:43474, ChEBI:CHEBI:58301, ChEBI:CHEBI:456216; Evidence={ECO:0000269|PubMed:11248200};PhysiologicalDirection=left-to-right; Xref=Rhea:RHEA:50085; Evidence={ECO:0000269|PubMed:11248200}; CATALYTIC ACTIVITY: Reaction=ATP + H(2)O + xenobiotic(Side 1) = ADP + phosphate + xenobiotic(Side 2).; EC=7.6.2.2; Evidence={ECO:0000269|PubMed:10220572}; CATALYTIC ACTIVITY: Reaction=17beta-estradiol 17-O-(beta-D-glucuronate)(in) + ATP + H2O = 17beta-estradiol 17-O-(beta-D-glucuronate)(out) + ADP + H(+) + phosphate; Xref=Rhea:RHEA:60128, ChEBI:CHEBI:15377, ChEBI:CHEBI:15378, ChEBI:CHEBI:30616, ChEBI:CHEBI:43474, ChEBI:CHEBI:82961, ChEBI:CHEBI:456216; Evidence={ECO:0000269|PubMed:10220572};PhysiologicalDirection=left-to-right; Xref=Rhea:RHEA:60129; Evidence={ECO:0000269|PubMed:10220572}; CATALYTIC ACTIVITY: Reaction=ATP + H2O + leukotriene C4(in) = ADP + H(+) + leukotriene C4(out) + phosphate; Xref=Rhea:RHEA:38963, ChEBI:CHEBI:15377, ChEBI:CHEBI:15378, ChEBI:CHEBI:30616, ChEBI:CHEBI:43474, ChEBI:CHEBI:57973, ChEBI:CHEBI:456216; Evidence={ECO:0000269|PubMed:10220572, ECO:0000269|PubMed:8662992};PhysiologicalDirection=left-to-right; Xref=Rhea:RHEA:38964; Evidence={ECO:0000305|PubMed:10220572}; CATALYTIC ACTIVITY: Reaction=ATP + bilirubin-glucuronoside(in) + H2O = ADP + bilirubin-glucuronoside(out) + H(+) + phosphate; Xref=Rhea:RHEA:66180, ChEBI:CHEBI:15377, ChEBI:CHEBI:15378, ChEBI:CHEBI:30616, ChEBI:CHEBI:43474, ChEBI:CHEBI:57767, ChEBI:CHEBI:456216; Evidence={ECO:0000269|PubMed:10421658};PhysiologicalDirection=left-to-right; Xref=Rhea:RHEA:66181; Evidence={ECO:0000305|PubMed:10421658}; CATALYTIC ACTIVITY: Reaction=ATP + bilirubin-bisglucuronoside(in) + H2O = ADP + bilirubin-bisglucuronoside(out) + H(+) + phosphate; Xref=Rhea:RHEA:66192, ChEBI:CHEBI:15377, ChEBI:CHEBI:15378, ChEBI:CHEBI:30616, ChEBI:CHEBI:43474, ChEBI:CHEBI:58471, ChEBI:CHEBI:456216; Evidence={ECO:0000305|PubMed:10421658};
DNA Binding
EC Number 7.6.2.-; 7.6.2.2; 7.6.2.3
Enzyme Function FUNCTION: ATP-dependent transporter of the ATP-binding cassette (ABC) family that binds and hydrolyzes ATP to enable active transport of various substrates including many drugs, toxicants and endogenous compound across cell membranes. Transports a wide variety of conjugated organic anions such as sulfate-, glucuronide- and glutathione (GSH)-conjugates of endo- and xenobiotics substrates (PubMed:8662992, PubMed:10421658, PubMed:10220572, PubMed:11248200). Mediates hepatobiliary excretion of mono- and bis-glucuronidated bilirubin molecules and therefore play an important role in bilirubin detoxification (PubMed:10421658). Mediates also hepatobiliary excretion of others glucuronide conjugates such as 17beta-estradiol 17-glucosiduronic acid and leukotriene C4 (PubMed:10220572, PubMed:8662992). Transports sulfated bile salt such as taurolithocholate sulfate (PubMed:11248200). Transport various anticancer drugs, such as anthracycline, vinca alkaloid and methotrexate and HIV-drugs such as protease inhibitors (By similarity). {ECO:0000250|UniProtKB:Q92887, ECO:0000269|PubMed:10220572, ECO:0000269|PubMed:10421658, ECO:0000269|PubMed:11248200, ECO:0000269|PubMed:8662992}.
Temperature Dependency
PH Dependency
Pathway
nucleotide Binding NP_BIND 667..674; /note=ATP 1; /evidence=ECO:0000255|PROSITE-ProRule:PRU00434; NP_BIND 1330..1337; /note=ATP 2; /evidence=ECO:0000255|PROSITE-ProRule:PRU00434
Features Chain (1); Domain (4); Glycosylation (4); Modified residue (6); Nucleotide binding (2); Region (2); Sequence conflict (1); Topological domain (18); Transmembrane (17)
Keywords ATP-binding;Cell membrane;Glycoprotein;Lipid transport;Membrane;Nucleotide-binding;Phosphoprotein;Reference proteome;Repeat;Translocase;Transmembrane;Transmembrane helix;Transport
Interact With
Induction
Subcellular Location SUBCELLULAR LOCATION: Apical cell membrane {ECO:0000269|PubMed:10220572, ECO:0000269|PubMed:8662992}; Multi-pass membrane protein {ECO:0000255}. Note=Localized to the canalicular membrane of hepatocytes. {ECO:0000269|PubMed:8662992}.
Modified Residue MOD_RES 279; /note=Phosphoserine; /evidence=ECO:0007744|PubMed:22673903; MOD_RES 281; /note=Phosphoserine; /evidence=ECO:0007744|PubMed:22673903; MOD_RES 874; /note=Phosphoserine; /evidence=ECO:0007744|PubMed:22673903; MOD_RES 922; /note=Phosphoserine; /evidence=ECO:0000250|UniProtKB:Q92887; MOD_RES 926; /note=Phosphoserine; /evidence=ECO:0000250|UniProtKB:Q92887; MOD_RES 1434; /note=Phosphoserine; /evidence=ECO:0000250|UniProtKB:Q92887
Post Translational Modification
Signal Peptide
Structure 3D
Cross Reference PDB -
Mapped Pubmed ID 11557524; 11897625; 12085350; 12538788; 12623073; 12663688; 12702498; 12883478; 13678533; 14636316; 14724430; 15057744; 15057914; 15319330; 15374814; 15504935; 15770136; 15816878; 15917434; 16037978; 16139386; 16483613; 16504477; 16537972; 16572733; 16584400; 16737587; 16757538; 16785030; 16857726; 16899240; 16925582; 16946557; 17009103; 17038627; 17135344; 17234897; 17437408; 17463180; 17467962; 17615179; 17664251; 17683490; 17724374; 17959626; 17963604; 18088505; 18159133; 18175959; 18378562; 18538350; 18638490; 18662814; 18687803; 18700187; 19010343; 19027009; 19063911; 19074644; 19156843; 19211616; 19214140; 19255943; 19299525; 19339379; 19356064; 19525466; 19541926; 19656454; 19703566; 19935650; 19944137; 20404332; 20487213; 20676911; 20702406; 20738239; 20868650; 21131269; 21134393; 21198435; 21660137; 21881227; 22057277; 22330094; 22361279; 22446938; 22472606; 22576625; 22579010; 22613706; 22711747; 22812007; 22925079; 22992436; 23041646; 23059061; 23096566; 23125159; 23442774; 23562342; 23569176; 25152023; 25200138; 25539456; 25547484; 25813982; 26053941; 26244301; 26254357; 26646631; 27090119; 27237619; 27780379; 28298215; 28842383; 29052767; 30068870; 32476256; 34303734;
Motif
Gene Encoded By
Mass 173,384
Kinetics BIOPHYSICOCHEMICAL PROPERTIES: Kinetic parameters: KM=3.9 uM for taurolithocholate 3-sulfate {ECO:0000269|PubMed:11248200}; KM=6.9 uM for 17beta-estradiol 17-O-(beta-D-glucuronate) {ECO:0000269|PubMed:10220572}; KM=1.1 uM for leukotriene C4 {ECO:0000269|PubMed:10220572}; KM=0.8 uM for bilirubin-glucuronoside {ECO:0000269|PubMed:10421658}; KM=0.5 uM for bilirubin-bisglucuronoside {ECO:0000269|PubMed:10421658}; Vmax=1486 pmol/min/mg enzyme for taurolithocholate 3-sulfate {ECO:0000269|PubMed:11248200}; Vmax=152 pmol/min/mg enzyme for bilirubin-glucuronoside transport {ECO:0000269|PubMed:10421658}; Vmax=264 pmol/min/mg enzyme bilirubin-bisglucuronoside transport {ECO:0000269|PubMed:10421658};
Metal Binding
Rhea ID RHEA:19121; RHEA:19122; RHEA:50084; RHEA:50085; RHEA:60128; RHEA:60129; RHEA:38963; RHEA:38964; RHEA:66180; RHEA:66181; RHEA:66192
Cross Reference Brenda 7.6.2.3;