1.A.56 The Copper Transporter (Ctr) Family

Copper (Cu+) transporters of the Ctr family are sequence diverse eukaryotic proteins that function by a channel mechanism.  Bioinformatic analyses of sequenced Ctr proteins (Dumay et al., 2006) revealed multiple paralogues in single organisms, and these may be either closely or distantly related to each other. Protein phylogeny generally correlates with organismal source and protein size with proteins of each cluster being derived from a specific eukaryotic kingdom and exhibiting characteristic domain arrangements. Some homologues exhibit repeats of the basic 3 TMS unit. Regions of conserved hydrophobicity and amphipathicity suggest functional roles, particularly for putative TMSs 2 and 3 which possess a nearly fully conserved M X3 M motif in putative TMS2. This motif may comprise the transmembrane Cu+ binding site in oligomeric channels that take up Cu+ by a passive, membrane potential-dependent mechanism (Dumay et al., 2006). De Feo et al. (2010) have presented a mechanistic model in which copper transport occurs along the center of the trimer.

Six proteins, one from Arabidopsis thaliana (CopT1, 169 amino acyl residues), one from humans (hCTR1, 190 residues), three from Saccharomyces cerevisiae (Ctr1p, 406 residues; Ctr2p, 189 residues; and Ctr3p, 241 residues) and one from Candida albicans (Ctr1p, 251 residues) have been cloned, sequenced and expressed in mutant S. cerevisiae (Dancis et al., 1994a,b; Marvin et al., 2004). They have multiple homologues in Schizosaccharomyces pombe, C. elegans, and Drosophilia melanogaster. A few of these proteins exhibit 2 or 2 1/2 repeat units of about 124 residues each.

The Ctr6 (148 aa) protein of Schizosaccharomyces pombe is an integral membrane protein, the synthesis of which is induced by copper limitation (Bellemare et al., 2002). It can trimerize and harbors a putative copper-binding M-XC-XM-XM motif in its N-terminus that is essential for function. The physiological function of Ctr6 is to mobilize stored copper from the vacuole to the cytosol (Bellemare et al., 2002). The Ctr1 homologue of S. cerevisiae transports Cu+ and the platinium anticancer drug, cisplatin. A Ctr1 allele defective in copper transport enhanced cellular cisplatin accumulation. N-terminal methionine-rich motifs were reported to be dispensable for copper transport but critical for cisplatin uptake (Sinani et al., 2007). The Ctr1 multimeric complex may thus use distinct mechanisms for copper and cisplatin transport.

The H. sapiens, A. thaliana, S. cerevisiae and T. parva proteins have 3 putative transmembrane α-helical spanners and display N-terminal hydrophilic sequences homologous to the methionine and histidine-rich copper binding domains of various copper binding proteins. Human CTR1 has its N-terminus extracellular and its C-terminus intracellular (Eisses and Kaplan, 2002). It transports copper, which induces internalization and degradation, presumably as a copper protective mechanism. The chemotherapeutic drug, cisplatin (cis-diamminedichloroplatinum [DDP]), stabilizes formation of a homotrimeric complex of human Ctr1 (Guo et al., 2004). It is not clear that all of these proteins are localized to the plasma membrane, but the majority of the evidence implicates them in Cu+ uptake.

The homotrimeric Ctr1 of humans appears to bind Cu+ in the channel, altering transport rates. The hydrophilic N- and C-termini are non-essential for transport but play a role in delivering Cu+ to the transport pathway. A model suggests that a Cu+ binding site, close to the intracellular exit site, undergoes a conformational change that is rate limiting for transport (Eisses and Kaplan, 2005). Complexation with Cu+ induces a change in the secondary structure of the Cys/Trp motif, which results in the peptide embedding in the lipid bilayer (Okada et al. 2018).

Cu+ is taken up via an energy (ATP) independent process, and the trimeric complex probably uses a channel-type mechanism (Nose et al., 2006). For example, human high affinity (~3 μM) Ctr1, a homotrimer, takes up Cu+ across the plasma membrane by an energy-independent mechanism that is stimulated by extracellular acidic pH and high K+ concentrations (Lee et al., 2002). The mouse Ctr1 transporter is essential for copper homeostasis and embryonic development (Andrews, 2001; Kuo et al., 2001; Lee et al., 2001). The Arabidopsis CopT1 protein plays a role in root elongation and pollen development, revealing a role for copper acquisition in these processes (Sancenón et al., 2004).

In S. pombe, two proteins, Ctr4 and Ctr5, together comprise a heteromeric Cu+ uptake transporter. Both proteins exhibit regions of strong sequence similarity with Ctr3 of S. cerevisiae. They exhibit 2 and 3 putative TMSs, respectively, and are coregulated by copper and the Cuf1 transcription factor. They have been shown to physically interact to yield the transporter (Zhou and Thiele, 2001). The fact that Ctr proteins have only 3 TMS per polypeptide chain argues for a channel-type mechanism (Nose et al., 2006).

Distantly related to the proteins described above, two proteins, Ctr1p of Saccharomyces cerevisiae and Ctr1p of Candida albicans were initally characterized as high affinity Cu+ uptake permeases. Ctr1p of S. cerevisiae possesses N-terminal repeats rich in serine and methionine that might be involved in copper binding. This Ctr1p includes a repeated M-XXM motif that occurs 11 times. The shorter C. albicans homologue has an MXM motif that occurs 6 times, and an MXMXM motif that occurs twice. Two or three putative transmembrane α-helical spanners in the S. cerevisiae homologue (residues 153-173 and either 251-271 or 241-261 and 262-281) and a C-terminal region that is O-glycosylated characterize the protein. The C. albicans protein also has these 3 TMSs. Ctr1p of S. cerevisiae is probably present in the membrane as an oligomer. The synthesis of Ctr1p is induced by copper deficiency and repressed by copper excess. The protein transports Cu+, but not Cu2+ or any other metal ion. The N-terminal repeat sequences noted above are found in a number of proteins including putative DNA binding proteins.

Wu et al., 2009 have provided evidence that in response to excess copper, yeast Ctr1-mediated copper transport is rapidly blocked in a C terminus-dependent mechanism associated with direct binding of copper. They suggest that conformational changes in the cytosolic tail of yeast Ctr1 allows copper sensing within this domain and leads to the inhibition of Ctr1-mediated copper transport. This regulatory mechanism may allow yeast cells to maintain homeostatic levels of copper.

Electron crystallography with human Ctr1 revealed the 6 Å resolution structure (Aller and Unger, 2006; De Feo et al., 2007). It is trimeric with 9 TMSs, three per subunit. It has radial symmetry like other ion channels such as K+ and gap junction channels. A region of low density at the center of the trimer suggests that the pore is along the center of the 3-fold axis of the trimer (De Feo et al., 2007).

De Feo et al., 2009 reported an additional structure of the human CTR1 protein, solved by electron crystallography to an in plane resolution of 7 A. Trimeric hCTR1 forms a pore that stretches across the membrane bilayer at the interface between the subunits. The second transmembrane helix is probably the key element lining the pore. How functionally important residues on this helix participate in Cu(I)-coordination during transport was suggested. Aligned with and sealing both ends of the pore, extracellular and intracellular domains appear to provide additional metal binding sites. Consistent with the existence of distinct metal binding sites, hCTR1 stably binds 2 Cu(I)-ions through 3-coordinate Cu-S bonds. In a minireview, Kaplan and Lutsenko (2009) have discussed the molecular mechanisms by which copper enters and exits animal cells.

Yang et al. (2012) determined the 3-d structure and oligomerization of the transmembrane domains (TMDs) of hCtr1 using solution-state NMR spectroscopy. TMS1 forms an α-helical structure from Gly67 to Glu84 and is dimerized by close packing of its C-terminal helix; TMS2 forms an α-helical structure from Leu134 to Thr155 and is self-associated as a trimer by the hydrophobic contact of TMS2 monomers; TMS3 adopts a discontinuous helix structure, known as 'α-helix-coiled segment-α-helix', and is dimerized by the interaction between the N-terminal helices. The motif GxxxG in TMS3 is partially unstructured as a linker between helices. The flexible linker of TMS3 may serve as a gating adapter to mediate a pore on and off switch. The differences in the structure and aggregation of the TMS peptides may be related to their different roles in channel formation and transport function (Yang et al., 2012).

The trimeric hCtr1 transports copper and silver with TMS 2 lining the central pore, and the MXXXM motif in the C-terminal end of TMD2 being important for metal binding and function. A trimer of the isolated hCtr1-TMD2 forms in SDS micelles which binds Ag+ in a stoichiometry of 3:2 for peptide:Ag+ (Dong et al. 2015).  The N-terminal, extracellular regions of eukaryotic high affinity copper transport (Ctr) proteins vary in composition of the Cu+ binding amino acids: methionine, histidine, and cysteine. To examine why certain amino acids are exploited over others in Ctrs from different organisms, the relative Cu+ binding affinities and the dependence of binding on pH were examined for 3 peptides of the sequence MG(2)XG(2)MK, where X is either Met, His, or Cys. Cu+ affinity was examined (Rubino et al., 20102011). The relative affinities of the peptides with Cu+ proved to be Cys > His > Met at pH 7.4 but Cys > Met > His at pH 4.5. Ligand geometry and metric parameters were determined with X-ray absorption spectroscopy.

A comprehensive phylogeny and a molecular structure analysis of the Ctr (COPT) family in plants and animals has been presented with an emphasis on the copper transporters in Populus trichocarpa (PtCOPT). Structural analyses of PtCOPTs showed that most have 3 TMSs, with an exception of PtCOPT4 (2 TMSs). Tandem and segmental duplications probably contributed to the expansion and evolution, and promoter analyses showed that the function of PtCOPTs is related to Cu and Fe transport. The genes are expressed at high levels in roots and leaves. Quantitative real-time RT-PCR (qRT-PCR) analysis revealed that the expression of PtCOPT genes were induced not only in limited and excessive Cu, Fe, zinc (Zn) and manganese (Mn) stress, but also in lead (Pb), and cadmium (Cd) stress (Zhang et al. 2015).

The generalized transport reaction catalyzed by proteins of the Ctr family is:

Cu+ (out) → Cu+ (in)



This family belongs to the .

 

References:

Aller, S.G. and V.M. Unger. (2006). Projection structure of the human copper transporter CTR1 at 6 Å resolution reveals a compact trimer with a novel channel-like architecture. Proc. Natl. Acad. Sci. USA 103: 3627-3632.

Andrés-Colás, N., A. Perea-García, S. Puig, and L. Peñarrubia. (2010). Deregulated copper transport affects Arabidopsis development especially in the absence of environmental cycles. Plant Physiol. 153: 170-184.

Andrews, N.C. (2001). Mining copper transport genes. Proc. Natl. Acad. Sci. USA 98: 6543-6545.

Barhoom, S., M. Kupiec, X. Zhao, J.R. Xu, and A. Sharon. (2008). Functional characterization of CgCTR2, a putative vacuole copper transporter that is involved in germination and pathogenicity in Colletotrichum gloeosporioides. Eukaryot. Cell. 7: 1098-1108.

Barresi, V., A. Trovato-Salinaro, G. Spampinato, N. Musso, S. Castorina, E. Rizzarelli, and D.F. Condorelli. (2016). Transcriptome analysis of copper homeostasis genes reveals coordinated upregulation of SLC31A1,SCO1, and COX11 in colorectal cancer. FEBS Open Bio 6: 794-806.

Beaudoin J., Thiele DJ., Labbe S. and Puig S. (2011). Dissection of the relative contribution of the Schizosaccharomyces pombe Ctr4 and Ctr5 proteins to the copper transport and cell surface delivery functions. Microbiology. 157(Pt 4):1021-31.

Beaudoin, J., S. Ekici, F. Daldal, S. Ait-Mohand, B. Guérin, and S. Labbé. (2013). Copper transport and regulation in Schizosaccharomyces pombe. Biochem Soc Trans 41: 1679-1686.

Bellemare, D.R., L. Shaner, K.A. Morano, J. Beaudoin, R. Langlois, and S. Labbé. (2002). Ctr6, a vacuolar membrane copper transporter in Schizosaccharomyces pombe. J. Biol. Chem. 277: 46676-46686.

Bertinato, J., E. Swist, L.J. Plouffe, S.P. Brooks, and M.R. L'abbé. (2008). Ctr2 is partially localized to the plasma membrane and stimulates copper uptake in COS-7 cells. Biochem. J. 409(3): 731-740.

Bertinato, J., N. Hidiroglou, R. Peace, K.A. Cockell, K.D. Trick, P. Jee, A. Giroux, R. Madère, G. Bonacci, M. Iskandar, S. Hayward, N. Giles, and M.R. L'Abbé. (2007). Sparing effects of selenium and ascorbic acid on vitamin C and E in guinea pig tissues. Nutr J 6: 7.

Bossak, K., S.C. Drew, E. Stefaniak, D. Płonka, A. Bonna, and W. Bal. (2018). The Cu(II) affinity of the N-terminus of human copper transporter CTR1: Comparison of human and mouse sequences. J Inorg Biochem. [Epub: Ahead of Print]

Choveaux, D.L., J.M. Przyborski, and J.D. Goldring. (2012). A Plasmodium falciparum copper-binding membrane protein with copper transport motifs. Malar J 11: 397.

Dancis, A., D. Haile, D.S. Yuan, and R.D. Klausner. (1994a). The Saccharomyces cerevisiae copper transport protein (Ctrlp). Biochemical characterization, regulation by copper, and physiologic role in copper uptake. J. Biol. Chem. 269: 25660-25667.

Dancis, A., D.S. Yuan, D. Haile, C. Askwith, D. Eide, C. Moehle, J. Kaplan, and R.D. Klausner. (1994b). Molecular characterization of a copper transport protein in S. cerevisiae: An unexpected role for copper in iron transport. Cell 76: 393-402.

De Feo, C.J., S. Mootien, and V.M. Unger. (2010). Tryptophan scanning analysis of the membrane domain of CTR-copper transporters. J. Membr. Biol. 234: 113-123.

De Feo, C.J., S.G. Aller, and V.M. Unger. (2007). A structural perspective on copper uptake in eukaryotes. Biometals 20: 705-716.

De Feo, C.J., S.G. Aller, G.S. Siluvai, N.J. Blackburn, and V.M. Unger. (2009). Three-dimensional structure of the human copper transporter hCTR1. Proc. Natl. Acad. Sci. USA 106: 4237-4242.

Dong Z., Wang Y., Wang C., Xu H., Guan L., Li Z. and Li F. (2015). Self-Assembly of the Second Transmembrane Domain of hCtr1 in Micelles and Interaction with Silver Ion. J Phys Chem B. 119(26):8302-12.

Du X., Wang X., Li H. and Sun H. (2012). Comparison between copper and cisplatin transport mediated by human copper transporter 1 (hCTR1). Metallomics. 4(7):679-85.

Dumay, Q.C., A.J. Debut, N.M. Mansour, and M.H. Saier, Jr. (2006). The copper transporter (Ctr) family of Cu+ uptake systems. J. Mol. Microbiol. Biotechnol. 11: 10-19.

Eide, D. and M. L. Guerinot. (1997). Metal ion uptake in eukaryotes. ASM News 63: 199-205.

Eisses, J.F. and J.H. Kaplan. (2002). Molecular characterization of hCTR1, the human copper uptake protein. J. Biol. Chem. 277: 29162-29171.

Eisses, J.F. and Kaplan, J.H. (2005). The mechanism of copper uptake mediated by human CTR1: a mutational analysis. J. Biol. Chem. 280: 37159-37168.

Garcia-Molina, A., N. Andrés-Colás, A. Perea-García, S. Del Valle-Tascón, L. Peñarrubia, and S. Puig. (2011). The intracellular Arabidopsis COPT5 transport protein is required for photosynthetic electron transport under severe copper deficiency. Plant J. 65: 848-860.

Guo, Y., K. Smith, and M.J. Petris. (2004). Cisplatin stabilizes a multimeric complex of the human Ctr1 copper transporter. Requirement for the extracellular methionine-rich clusters. J. Biol. Chem. 279: 46393-46399.

Harris, E.D. (2000). Cellular copper transport and metabolism. Annu. Rev. Nutr. 20: 291-310.

Ilyechova, E.Y., E. Bonaldi, I.A. Orlov, E.A. Skomorokhova, L.V. Puchkova, and M. Broggini. (2019). CRISP-R/Cas9 Mediated Deletion of Copper Transport Genes CTR1 and DMT1 in NSCLC Cell Line H1299. Biological and Pharmacological Consequences. Cells 8:.

Jung, H.I., S.R. Gayomba, M.A. Rutzke, E. Craft, L.V. Kochian, and O.K. Vatamaniuk. (2012). COPT6 Is a Plasma Membrane Transporter That Functions in Copper Homeostasis in Arabidopsis and Is a Novel Target of SQUAMOSA Promoter-binding Protein-like 7. J. Biol. Chem. 287: 33252-33267.

Kadioglu, O., J. Serly, E.J. Seo, I. Vincze, C. Somlai, M.E. Saeed, J. Molnár, and T. Efferth. (2015). Molecular Docking Analysis of Steroid-based Copper Transporter 1 Inhibitors. Anticancer Res 35: 6505-6508.

Kaplan, J.H. and S. Lutsenko. (2009). Copper transport in mammalian cells: special care for a metal with special needs. J. Biol. Chem. 284: 25461-25465.

Klaumann, S., S.D. Nickolaus, S.H. Fürst, S. Starck, S. Schneider, H. Ekkehard Neuhaus, and O. Trentmann. (2011). The tonoplast copper transporter COPT5 acts as an exporter and is required for interorgan allocation of copper in Arabidopsis thaliana. New Phytol 192: 393-404.

Kuo, Y.-M., B. Zhou, D. Cosco, and J. Gitschier. (2001). The copper transporter CTR1 provides an essential function in mammalian embryonic development. Proc. Natl. Acad. Sci. USA 98: 6836-6841.

Larson, C.A., P.L. Adams, B.G. Blair, R. Safaei, and S.B. Howell. (2010). The role of the methionines and histidines in the transmembrane domain of mammalian copper transporter 1 in the cellular accumulation of cisplatin. Mol Pharmacol 78: 333-339.

Lee, J., J.R. Prohaska, and D.J. Thiele. (2001). Essential role for mammalian copper transporter Ctr1 in copper homeostasis and embryonic development. Proc. Natl. Acad. Sci. USA 98: 6842-6847.

Lee, J., M.M.O. Peña, Y. Nose, and D.J. Thiele. (2002). Biochemical characterization of the human copper transporter Ctr1. J. Biol. Chem. 277: 4380-4387.

Lee, S., S.B. Howell, and S.J. Opella. (2007). NMR and mutagenesis of human copper transporter 1 (hCtr1) show that Cys-189 is required for correct folding and dimerization. Biochim. Biophys. Acta. 1768: 3127-3134.

Martins, V., M. Hanana, E. Blumwald, and H. Gerós. (2012). Copper transport and compartmentation in grape cells. Plant Cell Physiol. 53: 1866-1880.

Marvin, M.E., R.P. Mason, and A.M. Cashmore. (2004). The CaCTR1 gene is required for high-affinity iron uptake and is transcriptionally controlled by a copper-sensing transactivator encoded by CaMAC1. Microbiology 150: 2197-2208.

Maryon EB., Molloy SA., Ivy K., Yu H. and Kaplan JH. (2013). Rate and regulation of copper transport by human copper transporter 1 (hCTR1). J Biol Chem. 288(25):18035-46.

Molloy, S.A. and J.H. Kaplan. (2009). Copper-dependent recycling of hCTR1, the human high affinity copper transporter. J. Biol. Chem. 284: 29704-29713.

Nose, Y., E.M. Rees, and D.J. Thiele. (2006). Structure of the Ctr1 copper trans'PORE'ter reveals novel architecture. Trends Biochem. Sci. 31: 604-607.

Okada, M., S. Kajimoto, and T. Nakabayashi. (2018). Embedding a Metal Binding Motif for Copper Transporter into a Lipid Bilayer by Cu(I) Binding. J Phys Chem B. [Epub: Ahead of Print]

Page, M.D., J. Kropat, P.P. Hamel, and S.S. Merchant. (2009). Two Chlamydomonas CTR Copper Transporters with a Novel Cys-Met Motif Are Localized to the Plasma Membrane and Function in Copper Assimilation. Plant Cell 21: 928-943.

Park YS., Lian H., Chang M., Kang CM. and Yun CW. (2014). Identification of high-affinity copper transporters in Aspergillus fumigatus. Fungal Genet Biol. 73:29-38.

Puig, S., J. Lee, M. Lau, and D.J. Thiele. (2002). Biochemical and genetic analyses of yeast and human high affinity copper transporters suggest a conserved mechanism for copper uptake. J. Biol. Chem. 277: 26021-26030.

Rees, E.M. and D.J. Thiele. (2007). Identification of a vacuole-associated metalloreductase and its role in Ctr2-mediated intracellular copper mobilization. J. Biol. Chem. 282: 21629-21638.

Rubino, J.T., M.P. Chenkin, M. Keller, P. Riggs-Gelasco, and K.J. Franz. (2011). A comparison of methionine, histidine and cysteine in copper(I)-binding peptides reveals differences relevant to copper uptake by organisms in diverse environments. Metallomics 3: 61-73.

Rubino, J.T., P. Riggs-Gelasco, and K.J. Franz. (2010). Methionine motifs of copper transport proteins provide general and flexible thioether-only binding sites for Cu(I) and Ag(I). J Biol Inorg Chem 15: 1033-1049.

Sancenón, V., S. Puig, I. Nateu-Andrés, E. Dorcey, D.J. Thiele, and L. Peñarrubia. (2004). The Arabidopsis copper transporter COPT1 functions in root elongation and pollen development. J. Biol. Chem. 279: 15348-15355.

Sinani, D., D.J. Adle, H. Kim, and J. Lee. (2007). Distinct mechanisms for Ctr1-mediated copper and cisplatin transport. J. Biol. Chem. 282: 26775-26785.

Soll, S.J., S.J. Neil, and P.D. Bieniasz. (2010). Identification of a receptor for an extinct virus. Proc. Natl. Acad. Sci. USA 107: 19496-19501.

Turski, M.L., and D.J. Thiele. (2007). Drosophila Ctr1A functions as a copper transporter essential for development. J. Biol. Chem. 282: 24017-24026.

Vatansever, R., I.I. Ozyigit, and E. Filiz. (2016). Genome-Wide Identification and Comparative Analysis of Copper Transporter Genes in Plants. Interdiscip Sci. [Epub: Ahead of Print]

Wang, X., P. Jiang, P. Wang, C.S. Yang, X. Wang, and Q. Feng. (2015). EGCG Enhances Cisplatin Sensitivity by Regulating Expression of the Copper and Cisplatin Influx Transporter CTR1 in Ovary Cancer. PLoS One 10: e0125402.

Wee, N.K., D.C. Weinstein, S.T. Fraser, and S.J. Assinder. (2013). The mammalian copper transporters CTR1 and CTR2 and their roles in development and disease. Int J Biochem. Cell Biol. 45: 960-963.

Wu, X., D. Sinani, H. Kim, and J. Lee. (2009). Copper transport activity of yeast Ctr1 is down-regulated via its C terminus in response to excess copper. J. Biol. Chem. 284: 4112-4122.

Yang L., Huang Z. and Li F. (2012). Structural insights into the transmembrane domains of human copper transporter 1. J Pept Sci. 18(7):449-55.

Zhang H., Yang J., Wang W., Li D., Hu X., Wang H., Wei M., Liu Q., Wang Z. and Li C. (2015). Genome-wide identification and expression profiling of the copper transporter gene family in Populus trichocarpa. Plant Physiol Biochem. 97:451-60.

Zhou H., K.M. Cadigan, D.J. Thiele. (2003) A copper-regulated transporter required for copper acquisition, pigmentation, and specific stages of development in Drosophila melanogaster. J. Biol. Chem. 278:48210-48218.

Zhou, B. and J. Gitschier. (1997). hCTR1: a human gene for copper uptake identified by complementation in yeast. Proc. Natl. Acad. Sci. USA 94: 7481-7486.

Zhou, H. and D.J. Thiele. (2001). Identification of a novel high affinity copper transport complex in the fission yeast Schizosaccharomyces pombe. J. Biol. Chem. 276: 20529-20535.

Zimnicka, A.M., E.B. Maryon, and J.H. Kaplan. (2007). Human copper transporter hCTR1 mediates basolateral uptake of copper into enterocytes: implications for copper homeostasis. J. Biol. Chem. 282: 26471-26480.

Examples:

TC#NameOrganismal TypeExample
1.A.56.1.1

Plasma membrane copper uptake transporter; takes up Cu2+ into the cytoplasm (Andrés-Colás et al. 2010).  Met-rich motifs in the N-terminal region, an MXXXM motif in TMS-2, and a GXXXG motif in TMS-3 could be essential for Cu transport since they are highly conserved in all analyzed species (Vatansever et al. 2016).

Plants

CopT1 of Arabidopsis thaliana

 
1.A.56.1.10The vacuolar copper transporter, Ctr2 (Involved in spore germination and pathogenesis (Barhoom et al., 2008))FungiCtr2 of Colletotrichum gloeosporioides (A9XIK8)
 
1.A.56.1.11

Vacuolar/tonoplast copper transporter 5 (AtCOPT5).  It exports copper from the vacuole to the cytoplasm and is required for photosynthetic electron transport under comditions of copper deficiency.  It also promotes interorgan allocation of copper (Garcia-Molina et al. 2011; Klaumann et al. 2011).

Plants

COPT5 of Arabidopsis thaliana

 
1.A.56.1.12Putative copper transporter 5.2 (OsCOPT5.2)PlantsCOPT5.2 of Oryza sativa subsp. japonica
 
1.A.56.1.13Copper transporter 3 (OsCOPT3)PlantsCOPT3 of Oryza sativa subsp. japonica
 
1.A.56.1.14

Copper uptake system, COPT6. Interacts with itself and its homologue, COPT1. Regulated by copper availability by using SPL7 (Jung et al., 2012). 

Plants

COPT6 of Arabidopsis thaliana (Q8GWP3)

 
1.A.56.1.15

Copper transporter, PF14_0369 (Choveaux et al. 2012). Binds Cu+ and is present in both the erythrocyte and parasite plasma membranes (Choveaux et al. 2012).

Alveolata

Copper transporter of Plasmodium falciparum

 
1.A.56.1.16

Plasma membrane copper uptake channel of 257 aas, CtrC (Park et al. 2014).

Fungi

CtrC of Neosartorya fumigata (Aspergillus fumigatus)

 
1.A.56.1.17

Grape vacuolar copper transporter, Ctr1 (Martins et al. 2012).

Plants

Ctr1 of Vitis vinifera

 
1.A.56.1.18

Putative copper uptake transporter of 242 aas, CtrB (Park et al. 2014).

Fungi

CtrB of Neosartorya fumigata (Aspergillus fumigatus)

 
1.A.56.1.2

High affinity copper (Cu+) and silver (Ag+) uptake transporter, Ctr1 of 190 aas and 3 TMSs.  The trimeric channel (Eisses and Kaplan, 2005) forms an oligomeric pore with each subunit displaying 3 TMSs and 2 metal binding motifs (Lee et al., 2007). TMS2 is sufficient to form the trimer, and the MXXM motif bind Ag+ (Dong et al. 2015). Ctr1 mediates basolateral uptakes of Cu+ in enterocytes (Zimnicka et al., 2007) and shows copper-dependent internalization and recycling which provides a reversible mechanism for the regulation of cellular copper entry (Molloy and Kaplan, 2009). It acts as a receptor for the two extinct viruses, CERV1 and CERV2 (Soll et al., 2010). Ctr1 takes up platinum anticancer drugs, cisplatin and carboplatin (Du et al., 2012). The 3-d structure is known (Yang et al., 2012).  Ctr1 has a low turn over number of about 10 ions/second/trimer (Maryon et al. 2013).  Methionine and histidine residues in the transmembrane domain are essential for transport of copper, but when mutated, they stimulated uptake of cisplatin (Larson et al. 2010).  Plays important roles in the developing embryo as well as in adult ionic homeostasis (Wee et al. 2013). (-)-Epigallocatechin-3-gallate (EGCG), a major polyphenol from green tea, can enhance CTR1 mRNA and protein expression in ovarian cancer cells. EGCG inhibits the rapid degradation of CTR1 induced by cisplatin (cDDP). The combination of EGCG and cDDP increases the accumulation of cDDP and DNA-Pt adducts, and subsequently enhances the sensitivity of ovarian cancer (Wang et al. 2015). Steroid inhibitors may be able to overcome cycplatin resistance (Kadioglu et al. 2015).  ctr1 is upregulated in colorectal cancer cells (Barresi et al. 2016). The N-terminus of CTR1 binds Cu2+ following transfer from blood copper carriers such as human serum albumin to the transporter (Bossak et al. 2018). Once in the cytosol, enzyme-specific chaperones receive copper from the CTR1 C-terminal domain and deliver it to their apoenzymes (Ilyechova et al. 2019).

Animals

SLC31A1 or Ctr1 of Homo sapiens

 
1.A.56.1.3Vacuolar copper transporter (exports Cu+ from the vacuole to the cytoplasm; acts with Fre6 (Q12473: TC# 5.B.1.7.1) (metalo-reductase that reduces Cu2+ to Cu+ in the vacuole) (Rees and Thiele, 2007). YeastCtr2p of Saccharomyces cerevisiae
 
1.A.56.1.4Copper uptake transporterYeastCtr3p of Saccharomyces cerevisiae
 
1.A.56.1.5

The heterodimeric high affinity copper uptake transporter, Ctr4/Ctr5. The Ctr4 central domain may mediate Cu2+ transport in this hetero-complex, whereas the Ctr5 carboxyl-terminal domain functions in the regulation of trafficking of the Cu2+ transport complex to the cell surface (Beaudoin et al., 2011).

Yeast

Ctr4/Ctr5 of Schizosaccharomyces pombe
Ctr4
Ctr5

 
1.A.56.1.6

Vacuolar, trimeric copper release protein (Beaudoin et al. 2013).

Yeast

Ctr6 of Schizosaccharomyces pombe

 
1.A.56.1.7The CtrlB Copper transporter (expressed during late embryonic and larval stages of development in response to copper deprivation (Zhou et al., 2003).AnimalsCtrlB of Drosophila melanogaster
(Q9VHS6)
 
1.A.56.1.8The plasma membrane copper import transporter, Ctr1A (3 isoforms in Drosophila, Ctr1A, 1B and 1C; Ctr1A but not Ctr1B is required for development) (Turski and Thiele, 2007)AnimalsCtr1A of Drosophila melanogaster (Q9W3X9)
 
1.A.56.1.9

Probable low affinity copper uptake protein 2 (Ctr2) (present in the plasma membrane and interbal membranes where it stimulates copper uptake into the cytoplasm) (Bertinato et al., 2007; Wee et al. 2013).

Animals

SLC31A2 of Homo sapiens

 
Examples:

TC#NameOrganismal TypeExample
1.A.56.2.1Plasma membrane high affinity copper transporter, Ctr1p (Puig et al., 2002); acts with Fre1 (P32791: TC# 5.B.1.5.1) (metalo-reductase that reduces Cu2+ to Cu+ at the cell surface (Rees and Thiele, 2007). YeastCtr1p of Saccharomyces cerevisiae
 
1.A.56.2.2High affinity copper transporter, Ctr1p (Marvin et al., 2004)YeastCtr1p of Candida albicans (CAB878806)
 
Examples:

TC#NameOrganismal TypeExample
1.A.56.3.1Ctr1 assimilatory copper transporter (has a Cx2(Mx2)2 (C-x)5 motif) (Page et al. 2009).

Green algae

Ctr1 of Chlamydomonas reinhardtii (Q4U0V9)

 
1.A.56.3.2

Copper uptake porter, CtrA2 (Park et al. 2014).

Fungi

CtrA2 of Neosartorya fumigata (Aspergillus fumigatus)

 
1.A.56.3.3

Uncharacterized protein of 244 aas and 3 TMSs

UP of Vitrella brassicaformis