Transport of vitamins, nucleosides, and related molecules (Homo sapiens)

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1, 17, 2933426, 483010, 23442, 815, 41461712, 13, 21, 27, 31...24, 29, 35, 43, 4538, 493328, 361819224416, 34207, 25, 40, 47171938, 491126, 48335, 9, 144232, 37, 39endoplasmic reticulum lumencytosollysosomal lumenGolgi lumenligands of SLC29A2SLCO2B1 substratesSLC35B4CMPLCFAsSLC35D1 hexamerTCCA UMPGDP-ManDIGXSLC28A2UDP-GlcASLC29A4GDP-FucGMPligands of SLC29A4ligands of SLC28A1LCNsligands of SLC28A1SLC35B4UMPGDP-FucAc-CoAnucleosidesSLC35D2UMPSLCO4C1UDP-sugarsGDP-MannucleosidesLCNs:lipidsPAPSUDP-sugarsUDP-GlcACDCA SLC29A2-likeproteinsSLCO2A1CMPPGT substratesUDP-Gal, UDP-GalNAcligands of SLC29A1Na+Na+UMPSLC27A1,4,6SLCO3A1-1GMPUMPALBSLC35C1SLCO1B1SLCO3A1 substratesNa+SLC35B2,3lipids UDP-xylSLC35D1 GCCA, TCCASLCO1A2albumin:bile saltand acid (OATP-A)complexSLC33A1SLC29A3PDZD11 SLC5A6:PDZD11UDP-XylT3,T4PAPSligands of SLC29A1Ac-CoAUDP-GlcNAcSLC28A3UDP-GlcNAcSLCO3A1 substratesligands of SLC29A4SLCO2B1 substratesUDP-GlcNAcGCCA vitamins transportedby SMVTCMP-Neu5AcSLC29A1-likeproteinsT3,T4UDP-Gal, UDP-GalNAcSLC5A6 GCCA ALBDIGXligands of SLC28A2ligands of SLC28A3ligands of SLC28A3UDP-GlcNAcALB ligands of SLC29A2ALB TCCA ligands of SLC28A2CMP-Neu5AcSLCO2B1vitamins transportedby SMVTNa+bile salts and acids(OATP-A)TCDCA Na+PGT substratesALB:(GCCA, TCCA)UMPUDP-GlcNAcSLC35A2Na+CCA SLCO1B3lipidsSLC35A1LCFAsSLC35A3SLC28A1Thyroid hormonetransporting SLCOs36223


Description

This pathway groups the processes mediated by SLC transporters, by which vitamins and cofactors, as well as nucleosides, nucleotides, nucleobases, and related molecules cross lipid bilayer membranes. Source:Reactome.

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Ontology Terms

 

Bibliography

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  1. Ishida N, Yoshioka S, Chiba Y, Takeuchi M, Kawakita M.; ''Molecular cloning and functional expression of the human Golgi UDP-N-acetylglucosamine transporter.''; PubMed Europe PMC Scholia
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  3. Perdomo G, Kim DH, Zhang T, Qu S, Thomas EA, Toledo FG, Slusher S, Fan Y, Kelley DE, Dong HH.; ''A role of apolipoprotein D in triglyceride metabolism.''; PubMed Europe PMC Scholia
  4. Anderson CM, Stahl A.; ''SLC27 fatty acid transport proteins.''; PubMed Europe PMC Scholia
  5. He L, Vasiliou K, Nebert DW.; ''Analysis and update of the human solute carrier (SLC) gene superfamily.''; PubMed Europe PMC Scholia
  6. Sharer JD, Shern JF, Van Valkenburgh H, Wallace DC, Kahn RA.; ''ARL2 and BART enter mitochondria and bind the adenine nucleotide transporter.''; PubMed Europe PMC Scholia
  7. Fiore C, Trézéguet V, Le Saux A, Roux P, Schwimmer C, Dianoux AC, Noel F, Lauquin GJ, Brandolin G, Vignais PV.; ''The mitochondrial ADP/ATP carrier: structural, physiological and pathological aspects.''; PubMed Europe PMC Scholia
  8. Segawa H, Kawakita M, Ishida N.; ''Human and Drosophila UDP-galactose transporters transport UDP-N-acetylgalactosamine in addition to UDP-galactose.''; PubMed Europe PMC Scholia
  9. Yang CY, Gu ZW, Blanco-Vaca F, Gaskell SJ, Yang M, Massey JB, Gotto AM, Pownall HJ.; ''Structure of human apolipoprotein D: locations of the intermolecular and intramolecular disulfide links.''; PubMed Europe PMC Scholia
  10. Engel K, Zhou M, Wang J.; ''Identification and characterization of a novel monoamine transporter in the human brain.''; PubMed Europe PMC Scholia
  11. Kanamori A, Nakayama J, Fukuda MN, Stallcup WB, Sasaki K, Fukuda M, Hirabayashi Y.; ''Expression cloning and characterization of a cDNA encoding a novel membrane protein required for the formation of O-acetylated ganglioside: a putative acetyl-CoA transporter.''; PubMed Europe PMC Scholia
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  13. Lin P, Li J, Liu Q, Mao F, Li J, Qiu R, Hu H, Song Y, Yang Y, Gao G, Yan C, Yang W, Shao C, Gong Y.; ''A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42).''; PubMed Europe PMC Scholia
  14. Grzyb J, Latowski D, Strzałka K.; ''Lipocalins - a family portrait.''; PubMed Europe PMC Scholia
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  16. Molho-Pessach V, Lerer I, Abeliovich D, Agha Z, Abu Libdeh A, Broshtilova V, Elpeleg O, Zlotogorski A.; ''The H syndrome is caused by mutations in the nucleoside transporter hENT3.''; PubMed Europe PMC Scholia
  17. Suda T, Kamiyama S, Suzuki M, Kikuchi N, Nakayama K, Narimatsu H, Jigami Y, Aoki T, Nishihara S.; ''Molecular cloning and characterization of a human multisubstrate specific nucleotide-sugar transporter homologous to Drosophila fringe connection.''; PubMed Europe PMC Scholia
  18. Gimeno RE, Ortegon AM, Patel S, Punreddy S, Ge P, Sun Y, Lodish HF, Stahl A.; ''Characterization of a heart-specific fatty acid transport protein.''; PubMed Europe PMC Scholia
  19. Fitscher BA, Riedel HD, Young KC, Stremmel W.; ''Tissue distribution and cDNA cloning of a human fatty acid transport protein (hsFATP4).''; PubMed Europe PMC Scholia
  20. Abe T, Kakyo M, Tokui T, Nakagomi R, Nishio T, Nakai D, Nomura H, Unno M, Suzuki M, Naitoh T, Matsuno S, Yawo H.; ''Identification of a novel gene family encoding human liver-specific organic anion transporter LST-1.''; PubMed Europe PMC Scholia
  21. Hsiang B, Zhu Y, Wang Z, Wu Y, Sasseville V, Yang WP, Kirchgessner TG.; ''A novel human hepatic organic anion transporting polypeptide (OATP2). Identification of a liver-specific human organic anion transporting polypeptide and identification of rat and human hydroxymethylglutaryl-CoA reductase inhibitor transporters.''; PubMed Europe PMC Scholia
  22. Newman LE, Zhou CJ, Mudigonda S, Mattheyses AL, Paradies E, Marobbio CM, Kahn RA.; ''The ARL2 GTPase is required for mitochondrial morphology, motility, and maintenance of ATP levels.''; PubMed Europe PMC Scholia
  23. Lu R, Kanai N, Bao Y, Schuster VL.; ''Cloning, in vitro expression, and tissue distribution of a human prostaglandin transporter cDNA(hPGT).''; PubMed Europe PMC Scholia
  24. Huber RD, Gao B, Sidler Pfändler MA, Zhang-Fu W, Leuthold S, Hagenbuch B, Folkers G, Meier PJ, Stieger B.; ''Characterization of two splice variants of human organic anion transporting polypeptide 3A1 isolated from human brain.''; PubMed Europe PMC Scholia
  25. Crawford CR, Patel DH, Naeve C, Belt JA.; ''Cloning of the human equilibrative, nitrobenzylmercaptopurine riboside (NBMPR)-insensitive nucleoside transporter ei by functional expression in a transport-deficient cell line.''; PubMed Europe PMC Scholia
  26. Ritzel MW, Yao SY, Huang MY, Elliott JF, Cass CE, Young JD.; ''Molecular cloning and functional expression of cDNAs encoding a human Na+-nucleoside cotransporter (hCNT1).''; PubMed Europe PMC Scholia
  27. Martinez-Duncker I, Dupré T, Piller V, Piller F, Candelier JJ, Trichet C, Tchernia G, Oriol R, Mollicone R.; ''Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporter.''; PubMed Europe PMC Scholia
  28. Ashikov A, Routier F, Fuhlrott J, Helmus Y, Wild M, Gerardy-Schahn R, Bakker H.; ''The human solute carrier gene SLC35B4 encodes a bifunctional nucleotide sugar transporter with specificity for UDP-xylose and UDP-N-acetylglucosamine.''; PubMed Europe PMC Scholia
  29. Kullak-Ublick GA, Hagenbuch B, Stieger B, Schteingart CD, Hofmann AF, Wolkoff AW, Meier PJ.; ''Molecular and functional characterization of an organic anion transporting polypeptide cloned from human liver.''; PubMed Europe PMC Scholia
  30. Pizzagalli F, Hagenbuch B, Stieger B, Klenk U, Folkers G, Meier PJ.; ''Identification of a novel human organic anion transporting polypeptide as a high affinity thyroxine transporter.''; PubMed Europe PMC Scholia
  31. Miura N, Ishida N, Hoshino M, Yamauchi M, Hara T, Ayusawa D, Kawakita M.; ''Human UDP-galactose translocator: molecular cloning of a complementary DNA that complements the genetic defect of a mutant cell line deficient in UDP-galactose translocator.''; PubMed Europe PMC Scholia
  32. Ishida N, Kuba T, Aoki K, Miyatake S, Kawakita M, Sanai Y.; ''Identification and characterization of human Golgi nucleotide sugar transporter SLC35D2, a novel member of the SLC35 nucleotide sugar transporter family.''; PubMed Europe PMC Scholia
  33. Handford M, Rodriguez-Furlán C, Orellana A.; ''Nucleotide-sugar transporters: structure, function and roles in vivo.''; PubMed Europe PMC Scholia
  34. Bailey LK, Campbell LJ, Evetts KA, Littlefield K, Rajendra E, Nietlispach D, Owen D, Mott HR.; ''The structure of binder of Arl2 (BART) reveals a novel G protein binding domain: implications for function.''; PubMed Europe PMC Scholia
  35. Tamai I, Nezu J, Uchino H, Sai Y, Oku A, Shimane M, Tsuji A.; ''Molecular identification and characterization of novel members of the human organic anion transporter (OATP) family.''; PubMed Europe PMC Scholia
  36. Barnes K, Dobrzynski H, Foppolo S, Beal PR, Ismat F, Scullion ER, Sun L, Tellez J, Ritzel MW, Claycomb WC, Cass CE, Young JD, Billeter-Clark R, Boyett MR, Baldwin SA.; ''Distribution and functional characterization of equilibrative nucleoside transporter-4, a novel cardiac adenosine transporter activated at acidic pH.''; PubMed Europe PMC Scholia
  37. Fujiwara K, Adachi H, Nishio T, Unno M, Tokui T, Okabe M, Onogawa T, Suzuki T, Asano N, Tanemoto M, Seki M, Shiiba K, Suzuki M, Kondo Y, Nunoki K, Shimosegawa T, Iinuma K, Ito S, Matsuno S, Abe T.; ''Identification of thyroid hormone transporters in humans: different molecules are involved in a tissue-specific manner.''; PubMed Europe PMC Scholia
  38. Griffiths M, Beaumont N, Yao SY, Sundaram M, Boumah CE, Davies A, Kwong FY, Coe I, Cass CE, Young JD, Baldwin SA.; ''Cloning of a human nucleoside transporter implicated in the cellular uptake of adenosine and chemotherapeutic drugs.''; PubMed Europe PMC Scholia
  39. Muraoka M, Kawakita M, Ishida N.; ''Molecular characterization of human UDP-glucuronic acid/UDP-N-acetylgalactosamine transporter, a novel nucleotide sugar transporter with dual substrate specificity.''; PubMed Europe PMC Scholia
  40. Prasad PD, Wang H, Huang W, Fei YJ, Leibach FH, Devoe LD, Ganapathy V.; ''Molecular and functional characterization of the intestinal Na+-dependent multivitamin transporter.''; PubMed Europe PMC Scholia
  41. Stahl A, Hirsch DJ, Gimeno RE, Punreddy S, Ge P, Watson N, Patel S, Kotler M, Raimondi A, Tartaglia LA, Lodish HF.; ''Identification of the major intestinal fatty acid transport protein.''; PubMed Europe PMC Scholia
  42. Kamiyama S, Sasaki N, Goda E, Ui-Tei K, Saigo K, Narimatsu H, Jigami Y, Kannagi R, Irimura T, Nishihara S.; ''Molecular cloning and characterization of a novel 3'-phosphoadenosine 5'-phosphosulfate transporter, PAPST2.''; PubMed Europe PMC Scholia
  43. Ozeran JD, Westley J, Schwartz NB.; ''Identification and partial purification of PAPS translocase.''; PubMed Europe PMC Scholia
  44. Kamiyama S, Suda T, Ueda R, Suzuki M, Okubo R, Kikuchi N, Chiba Y, Goto S, Toyoda H, Saigo K, Watanabe M, Narimatsu H, Jigami Y, Nishihara S.; ''Molecular cloning and identification of 3'-phosphoadenosine 5'-phosphosulfate transporter.''; PubMed Europe PMC Scholia
  45. Fischer J, Kleinau G, Müller A, Kühnen P, Zwanziger D, Kinne A, Rehders M, Moeller LC, Führer D, Grüters A, Krude H, Brix K, Biebermann H.; ''Modulation of monocarboxylate transporter 8 oligomerization by specific pathogenic mutations.''; PubMed Europe PMC Scholia
  46. Lübke T, Marquardt T, Etzioni A, Hartmann E, von Figura K, Körner C.; ''Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency.''; PubMed Europe PMC Scholia
  47. Klingenberg M.; ''Molecular aspects of the adenine nucleotide carrier from mitochondria.''; PubMed Europe PMC Scholia
  48. Visser WE, Philp NJ, van Dijk TB, Klootwijk W, Friesema EC, Jansen J, Beesley PW, Ianculescu AG, Visser TJ.; ''Evidence for a homodimeric structure of human monocarboxylate transporter 8.''; PubMed Europe PMC Scholia
  49. Kullak-Ublick GA, Ismair MG, Stieger B, Landmann L, Huber R, Pizzagalli F, Fattinger K, Meier PJ, Hagenbuch B.; ''Organic anion-transporting polypeptide B (OATP-B) and its functional comparison with three other OATPs of human liver.''; PubMed Europe PMC Scholia
  50. Ritzel MW, Ng AM, Yao SY, Graham K, Loewen SK, Smith KM, Ritzel RG, Mowles DA, Carpenter P, Chen XZ, Karpinski E, Hyde RJ, Baldwin SA, Cass CE, Young JD.; ''Molecular identification and characterization of novel human and mouse concentrative Na+-nucleoside cotransporter proteins (hCNT3 and mCNT3) broadly selective for purine and pyrimidine nucleosides (system cib).''; PubMed Europe PMC Scholia
  51. Duee ED, Vignais PV.; ''[Exchange between extra- and intramitochondrial adenine nucleotides].''; PubMed Europe PMC Scholia
  52. De Marcos Lousa C, Trézéguet V, Dianoux AC, Brandolin G, Lauquin GJ.; ''The human mitochondrial ADP/ATP carriers: kinetic properties and biogenesis of wild-type and mutant proteins in the yeast S. cerevisiae.''; PubMed Europe PMC Scholia
  53. Wang J, Su SF, Dresser MJ, Schaner ME, Washington CB, Giacomini KM.; ''Na(+)-dependent purine nucleoside transporter from human kidney: cloning and functional characterization.''; PubMed Europe PMC Scholia
  54. Li K, Warner CK, Hodge JA, Minoshima S, Kudoh J, Fukuyama R, Maekawa M, Shimizu Y, Shimizu N, Wallace DC.; ''A human muscle adenine nucleotide translocator gene has four exons, is located on chromosome 4, and is differentially expressed.''; PubMed Europe PMC Scholia
  55. Ishida N, Miura N, Yoshioka S, Kawakita M.; ''Molecular cloning and characterization of a novel isoform of the human UDP-galactose transporter, and of related complementary DNAs belonging to the nucleotide-sugar transporter gene family.''; PubMed Europe PMC Scholia
  56. Nabokina SM, Subramanian VS, Said HM.; ''Association of PDZ-containing protein PDZD11 with the human sodium-dependent multivitamin transporter.''; PubMed Europe PMC Scholia
  57. Zhang T, Li S, Zhang Y, Zhong C, Lai Z, Ding J.; ''Crystal structure of the ARL2-GTP-BART complex reveals a novel recognition and binding mode of small GTPase with effector.''; PubMed Europe PMC Scholia
  58. Hatch GM, Smith AJ, Xu FY, Hall AM, Bernlohr DA.; ''FATP1 channels exogenous FA into 1,2,3-triacyl-sn-glycerol and down-regulates sphingomyelin and cholesterol metabolism in growing 293 cells.''; PubMed Europe PMC Scholia
  59. Flower DR, North AC, Attwood TK.; ''Structure and sequence relationships in the lipocalins and related proteins.''; PubMed Europe PMC Scholia
  60. Hagenbuch B, Meier PJ.; ''Organic anion transporting polypeptides of the OATP/ SLC21 family: phylogenetic classification as OATP/ SLCO superfamily, new nomenclature and molecular/functional properties.''; PubMed Europe PMC Scholia
  61. Mikkaichi T, Suzuki T, Onogawa T, Tanemoto M, Mizutamari H, Okada M, Chaki T, Masuda S, Tokui T, Eto N, Abe M, Satoh F, Unno M, Hishinuma T, Inui K, Ito S, Goto J, Abe T.; ''Isolation and characterization of a digoxin transporter and its rat homologue expressed in the kidney.''; PubMed Europe PMC Scholia
  62. Wang H, Huang W, Fei YJ, Xia H, Yang-Feng TL, Leibach FH, Devoe LD, Ganapathy V, Prasad PD.; ''Human placental Na+-dependent multivitamin transporter. Cloning, functional expression, gene structure, and chromosomal localization.''; PubMed Europe PMC Scholia
  63. Pfaff E, Klingenberg M, Heldt HW.; ''Unspecific permeation and specific exchange of adenine nucleotides in liver mitochondria.''; PubMed Europe PMC Scholia
  64. Loewen SK, Ng AM, Yao SY, Cass CE, Baldwin SA, Young JD.; ''Identification of amino acid residues responsible for the pyrimidine and purine nucleoside specificities of human concentrative Na(+) nucleoside cotransporters hCNT1 and hCNT2.''; PubMed Europe PMC Scholia

History

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CompareRevisionActionTimeUserComment
114879view16:39, 25 January 2021ReactomeTeamReactome version 75
113325view11:39, 2 November 2020ReactomeTeamReactome version 74
112536view15:50, 9 October 2020ReactomeTeamReactome version 73
101449view11:32, 1 November 2018ReactomeTeamreactome version 66
100987view21:10, 31 October 2018ReactomeTeamreactome version 65
100523view19:44, 31 October 2018ReactomeTeamreactome version 64
100070view16:28, 31 October 2018ReactomeTeamreactome version 63
99621view15:00, 31 October 2018ReactomeTeamreactome version 62 (2nd attempt)
99228view12:44, 31 October 2018ReactomeTeamreactome version 62
94041view13:53, 16 August 2017ReactomeTeamreactome version 61
93665view11:30, 9 August 2017ReactomeTeamreactome version 61
86787view09:26, 11 July 2016ReactomeTeamreactome version 56
83207view10:22, 18 November 2015ReactomeTeamVersion54
81588view13:07, 21 August 2015ReactomeTeamVersion53
77048view08:34, 17 July 2014ReactomeTeamFixed remaining interactions
76753view12:11, 16 July 2014ReactomeTeamFixed remaining interactions
76078view10:14, 11 June 2014ReactomeTeamRe-fixing comment source
75788view11:31, 10 June 2014ReactomeTeamReactome 48 Update
75138view14:08, 8 May 2014AnweshaFixing comment source for displaying WikiPathways description
74785view08:52, 30 April 2014ReactomeTeamReactome46
45060view19:59, 6 October 2011KhanspersOntology Term : 'transport pathway' added !
42152view22:00, 4 March 2011MaintBotAutomatic update
39963view05:58, 21 January 2011MaintBotNew pathway

External references

DataNodes

View all...
NameTypeDatabase referenceComment
ALB ProteinP02768 (Uniprot-TrEMBL)
ALB:(GCCA, TCCA)ComplexR-HSA-194104 (Reactome)
ALBProteinP02768 (Uniprot-TrEMBL)
Ac-CoAMetaboliteCHEBI:15351 (ChEBI)
CCA MetaboliteCHEBI:16359 (ChEBI)
CDCA MetaboliteCHEBI:16755 (ChEBI)
CMP-Neu5AcMetaboliteCHEBI:16556 (ChEBI)
CMPMetaboliteCHEBI:17361 (ChEBI)
DIGXMetaboliteCHEBI:4551 (ChEBI)
GCCA MetaboliteCHEBI:17687 (ChEBI)
GCCA, TCCAR-ALL-194097 (Reactome)
GDP-FucMetaboliteCHEBI:17009 (ChEBI)
GDP-ManMetaboliteCHEBI:15820 (ChEBI)
GMPMetaboliteCHEBI:17345 (ChEBI)
LCFAsR-ALL-879544 (Reactome)
LCFAsR-ALL-879559 (Reactome)
LCNs:lipidsComplexR-HSA-5229291 (Reactome)
LCNsR-HSA-5229240 (Reactome)
Na+MetaboliteCHEBI:29101 (ChEBI)
PAPSMetaboliteCHEBI:17980 (ChEBI)
PDZD11 ProteinQ5EBL8 (Uniprot-TrEMBL)
PGT substratesR-ALL-879566 (Reactome)
PGT substratesR-ALL-879614 (Reactome)
SLC27A1,4,6R-HSA-879582 (Reactome)
SLC28A1ProteinO00337 (Uniprot-TrEMBL)
SLC28A2ProteinO43868 (Uniprot-TrEMBL)
SLC28A3ProteinQ9HAS3 (Uniprot-TrEMBL)
SLC29A1-like proteinsR-HSA-4127407 (Reactome) This CandidateSet contains sequences identified by William Pearson's analysis of Reactome catalyst entities. Catalyst entity sequences were used to identify analagous sequences that shared overall homology and active site homology. Sequences in this Candidate set were identified in an April 24, 2012 analysis.
SLC29A2-like proteinsR-HSA-3907272 (Reactome) This CandidateSet contains sequences identified by William Pearson's analysis of Reactome catalyst entities. Catalyst entity sequences were used to identify analagous sequences that shared overall homology and active site homology. Sequences in this Candidate set were identified in an April 24, 2012 analysis.
SLC29A3ProteinQ9BZD2 (Uniprot-TrEMBL)
SLC29A4ProteinQ7RTT9 (Uniprot-TrEMBL)
SLC33A1ProteinO00400 (Uniprot-TrEMBL)
SLC35A1ProteinP78382 (Uniprot-TrEMBL)
SLC35A2ProteinP78381 (Uniprot-TrEMBL)
SLC35A3ProteinQ9Y2D2 (Uniprot-TrEMBL)
SLC35B2,3R-HSA-3465611 (Reactome)
SLC35B4ProteinQ969S0 (Uniprot-TrEMBL)
SLC35C1ProteinQ96A29 (Uniprot-TrEMBL)
SLC35D1 ProteinQ9NTN3 (Uniprot-TrEMBL)
SLC35D1 hexamerComplexR-HSA-174388 (Reactome)
SLC35D2ProteinQ76EJ3 (Uniprot-TrEMBL)
SLC5A6 ProteinQ9Y289 (Uniprot-TrEMBL)
SLC5A6:PDZD11ComplexR-HSA-5359005 (Reactome)
SLCO1A2ProteinP46721 (Uniprot-TrEMBL)
SLCO1B1ProteinQ9Y6L6 (Uniprot-TrEMBL)
SLCO1B3ProteinQ9NPD5 (Uniprot-TrEMBL)
SLCO2A1ProteinQ92959 (Uniprot-TrEMBL)
SLCO2B1 substratesR-ALL-879553 (Reactome)
SLCO2B1 substratesR-ALL-879654 (Reactome)
SLCO2B1ProteinO94956 (Uniprot-TrEMBL)
SLCO3A1 substratesR-HSA-879529 (Reactome)
SLCO3A1 substratesR-HSA-879563 (Reactome)
SLCO3A1-1ProteinQ9UIG8-1 (Uniprot-TrEMBL)
SLCO4C1ProteinQ6ZQN7 (Uniprot-TrEMBL)
T3,T4R-ALL-879603 (Reactome)
T3,T4R-ALL-879628 (Reactome)
TCCA MetaboliteCHEBI:28865 (ChEBI)
TCDCA MetaboliteCHEBI:9407 (ChEBI)
Thyroid hormone transporting SLCOsR-HSA-879625 (Reactome)
UDP-Gal, UDP-GalNAcR-ALL-735691 (Reactome)
UDP-Gal, UDP-GalNAcR-ALL-735692 (Reactome)
UDP-GlcAMetaboliteCHEBI:17200 (ChEBI)
UDP-GlcNAcMetaboliteCHEBI:16264 (ChEBI)
UDP-XylMetaboliteCHEBI:16082 (ChEBI)
UDP-sugarsR-ALL-744229 (Reactome)
UDP-sugarsR-ALL-744234 (Reactome)
UDP-xylMetaboliteCHEBI:16082 (ChEBI)
UMPMetaboliteCHEBI:16695 (ChEBI)
albumin:bile salt

and acid (OATP-A)

complex		ComplexR-HSA-194110 (Reactome)
bile salts and acids (OATP-A)R-ALL-194131 (Reactome)
ligands of SLC28A1R-ALL-179738 (Reactome)
ligands of SLC28A1R-ALL-179739 (Reactome)
ligands of SLC28A2R-ALL-179740 (Reactome)
ligands of SLC28A2R-ALL-179741 (Reactome)
ligands of SLC28A3R-ALL-179737 (Reactome)
ligands of SLC28A3R-ALL-179743 (Reactome)
ligands of SLC29A1R-ALL-179745 (Reactome)
ligands of SLC29A1R-ALL-179746 (Reactome)
ligands of SLC29A2R-ALL-179742 (Reactome)
ligands of SLC29A2R-ALL-179747 (Reactome)
ligands of SLC29A4R-ALL-727737 (Reactome)
ligands of SLC29A4R-ALL-727774 (Reactome)
lipids MetaboliteCHEBI:18059 (ChEBI)
lipidsMetaboliteCHEBI:18059 (ChEBI)
nucleosidesR-ALL-727746 (Reactome)
nucleosidesR-ALL-727782 (Reactome)
vitamins transported by SMVTR-ALL-429605 (Reactome)
vitamins transported by SMVTR-ALL-429627 (Reactome)

Annotated Interactions

View all...
SourceTargetTypeDatabase referenceComment
ALB:(GCCA, TCCA)R-HSA-194079 (Reactome)
ALB:(GCCA, TCCA)R-HSA-194083 (Reactome)
ALBArrowR-HSA-194079 (Reactome)
ALBArrowR-HSA-194083 (Reactome)
ALBArrowR-HSA-194130 (Reactome)
Ac-CoAArrowR-HSA-727759 (Reactome)
Ac-CoAR-HSA-727759 (Reactome)
CMP-Neu5AcArrowR-HSA-727807 (Reactome)
CMP-Neu5AcR-HSA-727807 (Reactome)
CMPArrowR-HSA-727807 (Reactome)
CMPR-HSA-727807 (Reactome)
DIGXArrowR-HSA-879594 (Reactome)
DIGXR-HSA-879594 (Reactome)
GCCA, TCCAArrowR-HSA-194079 (Reactome)
GCCA, TCCAArrowR-HSA-194083 (Reactome)
GDP-FucArrowR-HSA-742345 (Reactome)
GDP-FucR-HSA-742345 (Reactome)
GDP-ManArrowR-HSA-744230 (Reactome)
GDP-ManR-HSA-744230 (Reactome)
GMPArrowR-HSA-744230 (Reactome)
GMPR-HSA-744230 (Reactome)
LCFAsArrowR-HSA-879585 (Reactome)
LCFAsR-HSA-879585 (Reactome)
LCNs:lipidsArrowR-HSA-5229283 (Reactome)
LCNsR-HSA-5229283 (Reactome)
Na+ArrowR-HSA-109530 (Reactome)
Na+ArrowR-HSA-109538 (Reactome)
Na+ArrowR-HSA-109539 (Reactome)
Na+ArrowR-HSA-429581 (Reactome)
Na+R-HSA-109530 (Reactome)
Na+R-HSA-109538 (Reactome)
Na+R-HSA-109539 (Reactome)
Na+R-HSA-429581 (Reactome)
PAPSArrowR-HSA-741449 (Reactome)
PAPSR-HSA-741449 (Reactome)
PGT substratesArrowR-HSA-879528 (Reactome)
PGT substratesR-HSA-879528 (Reactome)
R-HSA-109527 (Reactome) The plasma membrane-associated protein SLC29A2 mediates the reversible transport of one molecule of adenine, adenosine, cytidine, cytosine, guanine, guanosine, hypoxanthine, inosine, thymidine, thymine, uracil, or uridine from the extracellular space to the cytosol.
R-HSA-109529 (Reactome) The plasma membrane-associated protein SLC29A2 mediates the reversible transport of one molecule of adenine, adenosine, cytidine, cytosine, guanine, guanosine, hypoxanthine, inosine, thymidine, thymine, uracil, or uridine from the cytosol to the extracellular space.
R-HSA-109530 (Reactome) The plasma membrane-associated protein SLC28A1 mediates the transport of one molecule of 2'-deoxyadenosine, adenosine, cytidine, thymidine, or uridine, and one sodium ion, from the extracellular space to the cytosol.
R-HSA-109534 (Reactome) The plasma membrane-associated protein SLC29A1 mediates the reversible transport of one molecule of adenosine, cytosine, guanosine, inosine, thymidine, or uridine from the extracellular space to the cytosol.
R-HSA-109536 (Reactome) The plasma membrane-associated protein SLC29A1 mediates the reversible transport of one molecule of adenosine, guanosine, inosine, or uridine from the cytosol to the extracellular space.
R-HSA-109538 (Reactome) The plasma membrane-associated protein SLC28A3 mediates the transport of one molecule of adenosine, cytidine, guanosine, inosine, thymidine, or uridine, and two sodium ions, from the extracellular space to the cytosol.
R-HSA-109539 (Reactome) The plasma membrane-associated protein SLC28A2 mediates the transport of one molecule of adenosine, guanosine, inosine, or uridine, and one sodium ion, from the extracellular space to the cytosol.
R-HSA-174368 (Reactome) The UDP-glucuronic acid/UDP-N-acetylgalactosamine transporter (SLC35D1) in hexameric form transports both UDP-glucuronic acid (UDP-GlcA) and UDP-N-acetylgalactosamine (UDP-GalNAc) from the cytosol into the ER lumen across the ER membrane (Muraoka et al. 2001). These substrates participate in glucuronidation and/or chondroitin sulfate biosynthesis.
R-HSA-194079 (Reactome) A molecule of extracellular glycocholate or taurocholate is transported into the cytosol, mediated by OATP-8 (SLCO1B3) in the plasma membrane. Glycocholate and taurocholate exist in the blood as complexes with serum albumin, and their uptake by OATP-8 must involve disruption of these complexes, but the molecular mechanism coupling disruption and uptake is unknown. In the body, OATP-8 is expressed on the basolateral surfaces of hepatocytes and may play a role in the uptake of glycocholate and taurocholate by the liver under physiological conditions (Kullak-Ublick et al. 2004; Trauner and Boyer 2002).
R-HSA-194083 (Reactome) A molecule of extracellular glycocholate (GCCA) or taurocholate (TCCA) is transported into the cytosol, mediated by OATP-C (SLCO1B1) in the plasma membrane. GCCA and TCCA exist in the blood as complexes with serum albumin (ALB), and its uptake by OATP-C must involve disruption of this complex, but the molecular mechanism coupling disruption and uptake is unknown. In the body, OATP-C is expressed on the basolateral surfaces of hepatocytes and may play a role in the uptake of GCCA and TCCA by the liver under physiological conditions (Kullak-Ublick et al. 2004, Trauner & Boyer 2002).
R-HSA-194130 (Reactome) A molecule of extracellular bile salt (glyco- or taurocholate or taurochenodeoxycholate) or bile acid (cholate or chenodeoxycholate) is transported into the cytosol, mediated by OATP-A (SLCO1A2) in the plasma membrane. Bile salts and acids exist in the blood as complexes with serum albumin, and their uptake by OATP-A must involve disruption of this complex, but the molecular mechanism coupling release of a bile salt or acid from albumin to its uptake by OATP-A is unknown. In the body, OATP-A is expressed only at low levels on the basolateral surfaces of hepatocytes and may play only a minor role in the uptake of bile salts and acids by the liver (Kullak-Ublick et al. 2004; Trauner and Boyer 2002).
R-HSA-429581 (Reactome) Biotin (vitamin H or B7) is a water-soluble B-complex vitamin. Biotin is a cofactor in the metabolism of fatty acids and leucine, and it plays a role in gluconeogenesis. D-Pantothoate (vitamin B5), is a water-soluble vitamin needed to form coenzyme-A (CoA), and is critical in the metabolism and synthesis of carbohydrates, proteins, and fats. Lipoic acid is an organosulfur compound, the R-enantiomer of which is an essential cofactor for many enzyme complexes.

The human SLC5A6 encodes the Na+-dependent multivitamin transporter SMVT (Prasad PD et al, 1999; Wang H et al, 1999). SMVT co-transports these vitamins/cofactors into cells with Na+ ions electrogenically. PDZ domain-containing protein 11 (PDZD11 aka AIPP1) is a cytosolic protein with a single PDZ domain which can bind to the C-terminal class 1 PDZ binding motif of SMVT, resulting in a significant induction of vitamin uptake over that with SMVT alone (Nabokina et al. 2011).
R-HSA-5229283 (Reactome) Lipocalins (LCNs) are a family of extracellular proteins that are implicated in the transport of small hydrophobic molecules such as lipids, retinoids, steroids and bilins (Grzyb et al. 2006). The family members differ in amino acid sequence but they share a highly conserved beta-barrel structure comprised of an eight-stranded anti-parallel beta-sheet. This structure forms a ligand-binding pocket that is responsible for binding and transporting lipids and other small hydrophobic molecules (Flower et al. 1993). LCNs have been associated with many biological processes such as immune response, prostaglandin synthesis, retinoid binding and cancer cell interactions. Lipocalins 1, 9, 12, and 15 (LCN1, 9, 12 and 15) are all able to transport different types of hydrophobic molecules.

Apolipoprotein D (APOD) is a 29-kDa glycoprotein that is primarily associated with high density lipoproteins (HDLs) in human plasma (Drayna et al. 1986, Yang et al. 1994). It is an atypical apolipoprotein and, based on its primary structure, it is predicted to be a member of the lipocalin family. Lipocalins adopt a tertiary beta-barrel structure and transport small hydrophobic ligands. Although APOD can bind cholesterol, progesterone, pregnenolone, bilirubin and arachidonic acid, it is unclear if any, or all of these, represent its physiological ligands (Perdomo et al. 2010). APOD's role in lipid metabolism could have implication in atherosclerosis and ageing (Perdomo & Dong 2009).
R-HSA-727740 (Reactome) The human gene SLC29A4 encodes the equilibrative nucleoside transporter 4 (ENT4). It is ubiquitously expressed and mediates the reversible transport of the nucleoside adenosine at acidic pH (this transport is absent at pH 7.4) (Barnes K et al, 2006). ENT4 has also been shown to mediate the transport of biogenic amines such as serotonin, dopamine, norepinephrine and epinephrine. For this reason, ENT4 is also known as the plasma membrane monoamine transporter (PMAT) (Engel K et al, 2004).
R-HSA-727749 (Reactome) The human gene SLC29A3 encodes the equilibrative nucleoside transporter 3 (ENT3). It is abundant in many tissues, especially the placenta and is localized intracellularly on the lysosomal membrane. SLC29A3 mediates the reversible transport of nucleosides and the nucleobase adenine (Baldwin et al. 2005). Defects in SLC29A3 can cause histiocytosis-lymphadenopathy plus syndrome (HLAS; MIM:602782), an autosomal recessive disorder characterised by combined features from 2 or more of four histiocytic disorders (Molho-Pessach et al. 2008).
R-HSA-727759 (Reactome) The human gene SLC33A1 encodes acetyl-CoA transporter AT1 (Kanamori et al. 1997). Acetyl-CoA is transported to the lumen of the Golgi apparatus, where it serves as the substrate of acetyltransferases that O-acetylates sialyl residues of gangliosides and glycoproteins. Defects in SLC33A1 are the cause of spastic paraplegia autosomal dominant type 42 (SPG42) which is a neurodegenerative disorder (Lin et al. 2008).
R-HSA-727767 (Reactome) The human gene SLC29A3 encodes the equilibrative nucleoside transporter 3 (ENT3). It is abundant in many tissues, especially the placenta and is localized intracellularly on the lysosomal membrane. SLC29A3 mediates the reversible transport of nucleosides and the nucleobase adenine (Baldwin et al. 2005). Defects in SLC29A3 can cause histiocytosis-lymphadenopathy plus syndrome (HLAS; MIM:602782), an autosomal recessive disorder characterised by combined features from 2 or more of four histiocytic disorders (Molho-Pessach et al. 2008).
R-HSA-727768 (Reactome) The human gene SLC29A4 encodes the equilibrative nucleoside transporter 4 (ENT4). It is ubiquitously expressed and mediates the reversible transport of the nucleoside adenosine at acidic pH (this transport is absent at pH 7.4) (Barnes K et al, 2006). ENT4 has also been shown to mediate the transport of biogenic amines such as serotonin, dopamine, norepinephrine and epinephrine. For this reason, ENT4 is also known as the plasma membrane monoamine transporter (PMAT) (Engel K et al, 2004).
R-HSA-727807 (Reactome) The human gene SLC35A1 encodes the CMP-sialic acid transporter which mediates the antiport of CMP-sialic acid (CMP-Neu5Ac) into the Golgi lumen in exchange for CMP (Ishida et al. 1996). Defects in SLC35A1 are the cause of congenital disorder of glycosylation type 2F (CDG2F; MIM:603585). CDGs are a family of severe inherited diseases caused by a defect in protein N-glycosylation (Martinez-Duncker et al. 2005).
R-HSA-735702 (Reactome) The human gene SLC35A2 encodes the UDP-galactose transporter (Miura et al. 1996). It is located on the Golgi membrane and mediates the antiport of UDP-Gal into the Golgi lumen in exchange for UMP. This transporter is also known to transport UDP-N-acetylgalactosamine (UDP-GalNAc) by the same antiport mechanism (Segawa et al. 2002).
R-HSA-741449 (Reactome) The human gene SLC35B2 encodes the adenosine 3'-phospho 5'-phosphosulfate transporter 1 (PAPST1) (Ozeran et al. 1996, Kamiyama et al. 2003). In human tissues, PAPST1 is highly expressed in the placenta and pancreas and present at lower levels in the colon and heart. The human gene SLC35B3 encodes a human PAPS transporter gene that is closely related to PAPST1. Called PAPST2, it is predominantly expressed in the colon (Kamiyama et al. 2006).
R-HSA-741450 (Reactome) The human gene SLC35A3 encodes a UDP-GlcNAc transporter (Ishida et al. 1999). It is ubiquitously expressed and resides on the Golgi membrane where it transports UDP- N-acetylglucosamine (GlcNAc) into the Golgi lumen in exchange for UMP.
R-HSA-742345 (Reactome) The human gene SLC35C1 encodes the GDP-fucose transporter FUCT1. It resides on the Golgi membrane and mediates the transport of GDP-fucose into the Golgi lumen. Defects in SLC35C1 causes the congenital disorder of glycosylation type 2C, also known as leukocyte adhesion deficiency type II (LAD2) (Lubke et al. 2001).
R-HSA-742354 (Reactome) The human gene SLC35B4 encodes the bifunctional UDP-xylose and UDP-N-acetylglucosamine transporter YEA4. YEA4 resides on the Golgi membrane and mediates the influx of UDP-N-acetylglucosamine into the lumen (Ashikov A et al, 2005).
R-HSA-742373 (Reactome) The human gene SLC35B4 encodes the bifunctional UDP-xylose and UDP-N-acetylglucosamine transporter YEA4. YEA4 resides on the Golgi membrane and mediates the influx of UDP-xylose into the lumen (Ashikov A et al, 2005).
R-HSA-744230 (Reactome) The human gene SLC35D2 encodes the UDP-N-acetylglucosamine/UDP-glucose/GDP-mannose transporter (UGTREL8; homolog of Fringe connection protein 1, HFRC1). It resides on the Golgi membrane where it mediates the antiport of GDP-mannose into the Golgi lumen in exchange for GMP (Suda T et al, 2004; Ishida N et al, 2005).
R-HSA-744231 (Reactome) The human gene SLC35D2 encodes the UDP-N-acetylglucosamine/UDP-glucose/GDP-mannose transporter (UGTREL8; homolog of Fringe connection protein 1, HFRC1). It resides on the Golgi membrane where it mediates the transport of nucleotide sugars such as UDP-GlcNAc and UDP-glucose into the Golgi lumen in exchange for UMP (Suda et al. 2004, Ishida et al. 2005).
R-HSA-879528 (Reactome) The human gene SLCO2A1 encodes prostaglandin transporter PGT. It is ubiquitously expressed and can transport the protaglandins PGD2, PGE1, PGE2 and PGF2A (Lu et al. 1996).
R-HSA-879562 (Reactome) SLCO2B1 (formerly OATP-B) is abundantly expressed in human liver, where it is localized at the basolateral membrane of hepatocytes. It has a narrow substrate range, able to transport bromosulphophthalein (BSP), estrone-3-sulphate and dehydroepiandrosterone-sulphate (DHEAS) (Kullak-Ublick GA et al, 2001).
R-HSA-879575 (Reactome) Three organic anion transporting polypeptides (OATPs; now called solute carrier organic anion transporters, SLCOs) are able to mediate the transport of thryoid hormones, predominantly thyroxine (T4) and triiodothyronine (T3) (Fujiwara et al. 2001). SLCO1B1 (formerly OATP-C), which can also transport bile salts, is mainly expressed in the liver (Abe et al. 1999; Hsiang et al. 1999). SLCO4A1 (formerly OATP-E) is mainly expressed in peripheral tissue and has a broad substrate specificty (Tamai et al. 2000). SLCO1C1 (formerly OATP-F) is highly expressed in brain and is also a high affinity thyroid hormone transporter (Pizzagalli et al. 2002).
R-HSA-879584 (Reactome) The human gene SLCO3A1 encodes the organic anion transporting polypeptide D. Several variants are expressed but isoform 1 is ubiquitous and can transport a range of substrates including the prostaglandins E1 and E2, thyroxine and vasopressin (AVP) (Huber RD et al, 2007).
R-HSA-879585 (Reactome) The SLC27 gene family code for fatty acid transporter proteins (FATPs). Of the six FATPs characterized, only three have been shown to mediate the influx of long chain fatty acids (LCFAs) into cells; FATP1, 4 and 6. They have been shown to transport the prototypical LCFA oleic acid (OLEA) but are believed to be able to transport LCFAs with chain lengths longer than 10 carbons. FATP1 is highly expressed in adipose tissue and muscle (Hatch GM et al, 2002). FATP4 is the major intestinal LCFA transporter (Fitscher BA et al, 1998; Stahl A et al, 1999). FATP6 is localized to cardiac myocytes (Gimeno RE et al, 2003).
R-HSA-879594 (Reactome) Digoxin is a commonly prescribed drug for the treatment of heart failure. It is mainly eliminated from the body by the kidneys. Human SLCO4C1 (formerly OATP-H) is the first member of the organic anion transporting polypeptide (OATP) family expressed in human kidney. It is found on the baolateral membrane of the nephron and is thought to be the first step of the transport of digoxin into urine (Mikkaichi T et al, 2004).
SLC27A1,4,6mim-catalysisR-HSA-879585 (Reactome)
SLC28A1mim-catalysisR-HSA-109530 (Reactome)
SLC28A2mim-catalysisR-HSA-109539 (Reactome)
SLC28A3mim-catalysisR-HSA-109538 (Reactome)
SLC29A1-like proteinsmim-catalysisR-HSA-109534 (Reactome)
SLC29A1-like proteinsmim-catalysisR-HSA-109536 (Reactome)
SLC29A2-like proteinsmim-catalysisR-HSA-109527 (Reactome)
SLC29A2-like proteinsmim-catalysisR-HSA-109529 (Reactome)
SLC29A3mim-catalysisR-HSA-727749 (Reactome)
SLC29A3mim-catalysisR-HSA-727767 (Reactome)
SLC29A4mim-catalysisR-HSA-727740 (Reactome)
SLC29A4mim-catalysisR-HSA-727768 (Reactome)
SLC33A1mim-catalysisR-HSA-727759 (Reactome)
SLC35A1mim-catalysisR-HSA-727807 (Reactome)
SLC35A2mim-catalysisR-HSA-735702 (Reactome)
SLC35A3mim-catalysisR-HSA-741450 (Reactome)
SLC35B2,3mim-catalysisR-HSA-741449 (Reactome)
SLC35B4mim-catalysisR-HSA-742354 (Reactome)
SLC35B4mim-catalysisR-HSA-742373 (Reactome)
SLC35C1mim-catalysisR-HSA-742345 (Reactome)
SLC35D1 hexamermim-catalysisR-HSA-174368 (Reactome)
SLC35D2mim-catalysisR-HSA-744230 (Reactome)
SLC35D2mim-catalysisR-HSA-744231 (Reactome)
SLC5A6:PDZD11mim-catalysisR-HSA-429581 (Reactome)
SLCO1A2mim-catalysisR-HSA-194130 (Reactome)
SLCO1B1mim-catalysisR-HSA-194083 (Reactome)
SLCO1B3mim-catalysisR-HSA-194079 (Reactome)
SLCO2A1mim-catalysisR-HSA-879528 (Reactome)
SLCO2B1 substratesArrowR-HSA-879562 (Reactome)
SLCO2B1 substratesR-HSA-879562 (Reactome)
SLCO2B1mim-catalysisR-HSA-879562 (Reactome)
SLCO3A1 substratesArrowR-HSA-879584 (Reactome)
SLCO3A1 substratesR-HSA-879584 (Reactome)
SLCO3A1-1mim-catalysisR-HSA-879584 (Reactome)
SLCO4C1mim-catalysisR-HSA-879594 (Reactome)
T3,T4ArrowR-HSA-879575 (Reactome)
T3,T4R-HSA-879575 (Reactome)
Thyroid hormone transporting SLCOsmim-catalysisR-HSA-879575 (Reactome)
UDP-Gal, UDP-GalNAcArrowR-HSA-735702 (Reactome)
UDP-Gal, UDP-GalNAcR-HSA-735702 (Reactome)
UDP-GlcAArrowR-HSA-174368 (Reactome)
UDP-GlcAR-HSA-174368 (Reactome)
UDP-GlcNAcArrowR-HSA-174368 (Reactome)
UDP-GlcNAcArrowR-HSA-741450 (Reactome)
UDP-GlcNAcArrowR-HSA-742354 (Reactome)
UDP-GlcNAcR-HSA-174368 (Reactome)
UDP-GlcNAcR-HSA-741450 (Reactome)
UDP-GlcNAcR-HSA-742354 (Reactome)
UDP-XylR-HSA-742373 (Reactome)
UDP-sugarsArrowR-HSA-744231 (Reactome)
UDP-sugarsR-HSA-744231 (Reactome)
UDP-xylArrowR-HSA-742373 (Reactome)
UMPArrowR-HSA-735702 (Reactome)
UMPArrowR-HSA-741450 (Reactome)
UMPArrowR-HSA-744231 (Reactome)
UMPR-HSA-735702 (Reactome)
UMPR-HSA-741450 (Reactome)
UMPR-HSA-744231 (Reactome)
albumin:bile salt

and acid (OATP-A)

complex		R-HSA-194130 (Reactome)
bile salts and acids (OATP-A)ArrowR-HSA-194130 (Reactome)
ligands of SLC28A1ArrowR-HSA-109530 (Reactome)
ligands of SLC28A1R-HSA-109530 (Reactome)
ligands of SLC28A2ArrowR-HSA-109539 (Reactome)
ligands of SLC28A2R-HSA-109539 (Reactome)
ligands of SLC28A3ArrowR-HSA-109538 (Reactome)
ligands of SLC28A3R-HSA-109538 (Reactome)
ligands of SLC29A1ArrowR-HSA-109534 (Reactome)
ligands of SLC29A1ArrowR-HSA-109536 (Reactome)
ligands of SLC29A1R-HSA-109534 (Reactome)
ligands of SLC29A1R-HSA-109536 (Reactome)
ligands of SLC29A2ArrowR-HSA-109527 (Reactome)
ligands of SLC29A2ArrowR-HSA-109529 (Reactome)
ligands of SLC29A2R-HSA-109527 (Reactome)
ligands of SLC29A2R-HSA-109529 (Reactome)
ligands of SLC29A4ArrowR-HSA-727740 (Reactome)
ligands of SLC29A4ArrowR-HSA-727768 (Reactome)
ligands of SLC29A4R-HSA-727740 (Reactome)
ligands of SLC29A4R-HSA-727768 (Reactome)
lipidsR-HSA-5229283 (Reactome)
nucleosidesArrowR-HSA-727749 (Reactome)
nucleosidesArrowR-HSA-727767 (Reactome)
nucleosidesR-HSA-727749 (Reactome)
nucleosidesR-HSA-727767 (Reactome)
vitamins transported by SMVTArrowR-HSA-429581 (Reactome)
vitamins transported by SMVTR-HSA-429581 (Reactome)
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