Highly homologous to other eukaryotic choline transporters. The protein family expanded in parazitic kinetoplastids.
Transporters, Plasma-membrane choline transporter
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | yes | yes: 6 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | yes | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 23 |
NetGPI | no | yes: 0, no: 23 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 24 |
GO:0016020 | membrane | 2 | 24 |
GO:0110165 | cellular anatomical entity | 1 | 24 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0020016 | ciliary pocket | 2 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4IDJ5
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0055085 | transmembrane transport | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 24 |
GO:0022857 | transmembrane transporter activity | 2 | 24 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 30 | 34 | PF00656 | 0.564 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.215 |
CLV_PCSK_PC1ET2_1 | 322 | 324 | PF00082 | 0.391 |
CLV_PCSK_PC1ET2_1 | 399 | 401 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.297 |
DEG_MDM2_SWIB_1 | 100 | 107 | PF02201 | 0.338 |
DEG_MDM2_SWIB_1 | 201 | 209 | PF02201 | 0.365 |
DEG_MDM2_SWIB_1 | 280 | 288 | PF02201 | 0.316 |
DEG_MDM2_SWIB_1 | 85 | 93 | PF02201 | 0.536 |
DEG_SPOP_SBC_1 | 324 | 328 | PF00917 | 0.305 |
DOC_ANK_TNKS_1 | 442 | 449 | PF00023 | 0.166 |
DOC_CKS1_1 | 287 | 292 | PF01111 | 0.387 |
DOC_MAPK_MEF2A_6 | 186 | 195 | PF00069 | 0.288 |
DOC_MAPK_MEF2A_6 | 231 | 240 | PF00069 | 0.481 |
DOC_MAPK_MEF2A_6 | 381 | 389 | PF00069 | 0.513 |
DOC_PP4_FxxP_1 | 462 | 465 | PF00568 | 0.421 |
DOC_SPAK_OSR1_1 | 79 | 83 | PF12202 | 0.504 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.302 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.321 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.223 |
LIG_14-3-3_CanoR_1 | 221 | 227 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 323 | 332 | PF00244 | 0.227 |
LIG_Actin_WH2_2 | 206 | 223 | PF00022 | 0.280 |
LIG_Actin_WH2_2 | 357 | 372 | PF00022 | 0.352 |
LIG_APCC_ABBA_1 | 61 | 66 | PF00400 | 0.564 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.648 |
LIG_BIR_III_4 | 33 | 37 | PF00653 | 0.570 |
LIG_BIR_III_4 | 499 | 503 | PF00653 | 0.603 |
LIG_BRCT_BRCA1_1 | 1 | 5 | PF00533 | 0.551 |
LIG_BRCT_BRCA1_1 | 330 | 334 | PF00533 | 0.228 |
LIG_BRCT_BRCA1_1 | 430 | 434 | PF00533 | 0.379 |
LIG_BRCT_BRCA1_1 | 459 | 463 | PF00533 | 0.418 |
LIG_deltaCOP1_diTrp_1 | 87 | 94 | PF00928 | 0.430 |
LIG_EH1_1 | 187 | 195 | PF00400 | 0.248 |
LIG_EH1_1 | 272 | 280 | PF00400 | 0.400 |
LIG_EH1_1 | 451 | 459 | PF00400 | 0.317 |
LIG_eIF4E_1 | 413 | 419 | PF01652 | 0.439 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.227 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.467 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.419 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.239 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.430 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.278 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.443 |
LIG_GBD_Chelix_1 | 453 | 461 | PF00786 | 0.235 |
LIG_LIR_Apic_2 | 460 | 465 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 101 | 112 | PF02991 | 0.263 |
LIG_LIR_Gen_1 | 244 | 255 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 431 | 441 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 471 | 481 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 87 | 97 | PF02991 | 0.425 |
LIG_LIR_LC3C_4 | 336 | 339 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 242 | 248 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 326 | 332 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 377 | 382 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 431 | 437 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 460 | 466 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.673 |
LIG_LIR_Nem_3 | 471 | 477 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 87 | 92 | PF02991 | 0.422 |
LIG_MLH1_MIPbox_1 | 459 | 463 | PF16413 | 0.262 |
LIG_Pex14_2 | 100 | 104 | PF04695 | 0.250 |
LIG_Pex14_2 | 201 | 205 | PF04695 | 0.324 |
LIG_Pex14_2 | 280 | 284 | PF04695 | 0.296 |
LIG_Pex14_2 | 410 | 414 | PF04695 | 0.444 |
LIG_Pex14_2 | 85 | 89 | PF04695 | 0.574 |
LIG_Rb_LxCxE_1 | 366 | 377 | PF01857 | 0.407 |
LIG_SH2_CRK | 382 | 386 | PF00017 | 0.439 |
LIG_SH2_CRK | 492 | 496 | PF00017 | 0.492 |
LIG_SH2_CRK | 50 | 54 | PF00017 | 0.660 |
LIG_SH2_GRB2like | 356 | 359 | PF00017 | 0.414 |
LIG_SH2_GRB2like | 378 | 381 | PF00017 | 0.433 |
LIG_SH2_GRB2like | 413 | 416 | PF00017 | 0.439 |
LIG_SH2_PTP2 | 134 | 137 | PF00017 | 0.310 |
LIG_SH2_PTP2 | 247 | 250 | PF00017 | 0.400 |
LIG_SH2_PTP2 | 271 | 274 | PF00017 | 0.174 |
LIG_SH2_SRC | 356 | 359 | PF00017 | 0.414 |
LIG_SH2_SRC | 394 | 397 | PF00017 | 0.453 |
LIG_SH2_STAT3 | 263 | 266 | PF00017 | 0.187 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.248 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 394 | 397 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.439 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.367 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.222 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.646 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.527 |
LIG_SUMO_SIM_par_1 | 426 | 431 | PF11976 | 0.350 |
LIG_TYR_ITIM | 132 | 137 | PF00017 | 0.261 |
LIG_TYR_ITIM | 48 | 53 | PF00017 | 0.669 |
LIG_WRC_WIRS_1 | 318 | 323 | PF05994 | 0.209 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.446 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.349 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.442 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.285 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.498 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.438 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.414 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.502 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.629 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.167 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.327 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.222 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.499 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.313 |
MOD_GlcNHglycan | 350 | 354 | PF01048 | 0.252 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.210 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.475 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.290 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.399 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.465 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.273 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.258 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.271 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.301 |
MOD_N-GLC_1 | 10 | 15 | PF02516 | 0.498 |
MOD_N-GLC_1 | 500 | 505 | PF02516 | 0.323 |
MOD_N-GLC_2 | 415 | 417 | PF02516 | 0.313 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.342 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.449 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.435 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.342 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.245 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.201 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.351 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.471 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.269 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.218 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.699 |
MOD_NEK2_1 | 491 | 496 | PF00069 | 0.479 |
MOD_NEK2_2 | 469 | 474 | PF00069 | 0.441 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.389 |
MOD_PIKK_1 | 283 | 289 | PF00454 | 0.255 |
MOD_PIKK_1 | 38 | 44 | PF00454 | 0.684 |
MOD_PKA_1 | 322 | 328 | PF00069 | 0.200 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.502 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.691 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.252 |
MOD_PKA_2 | 484 | 490 | PF00069 | 0.575 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.607 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.330 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.393 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.431 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.287 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.274 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.495 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.348 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.312 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.386 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.294 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.446 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.387 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.223 |
TRG_DiLeu_BaLyEn_6 | 222 | 227 | PF01217 | 0.522 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.286 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 492 | 495 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.666 |
TRG_ER_diArg_1 | 209 | 212 | PF00400 | 0.369 |
TRG_Pf-PMV_PEXEL_1 | 346 | 350 | PF00026 | 0.288 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9D8 | Leptomonas seymouri | 62% | 100% |
A0A0N1PA24 | Leptomonas seymouri | 33% | 87% |
A0A0S4IW21 | Bodo saltans | 37% | 95% |
A0A0S4KHP0 | Bodo saltans | 43% | 100% |
A0A1X0P8J3 | Trypanosomatidae | 47% | 100% |
A0A3Q8I9V7 | Leishmania donovani | 34% | 84% |
A0A3R7MAJ2 | Trypanosoma rangeli | 33% | 100% |
A0A3S5IRA1 | Trypanosoma rangeli | 46% | 100% |
A0A3S7XAV8 | Leishmania donovani | 100% | 100% |
A4H7J7 | Leishmania braziliensis | 36% | 84% |
A4HP90 | Leishmania braziliensis | 75% | 99% |
A4HVY0 | Leishmania infantum | 34% | 84% |
A5PMW0 | Danio rerio | 24% | 73% |
D0A390 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
D0A391 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
D0A392 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
D0A393 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 99% |
E9APN1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 84% |
E9ASZ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
P0CM92 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 30% | 93% |
P0CM93 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 30% | 93% |
Q12412 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 95% |
Q20026 | Caenorhabditis elegans | 24% | 66% |
Q4I8E9 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 28% | 95% |
Q4PIP8 | Ustilago maydis (strain 521 / FGSC 9021) | 28% | 97% |
Q4Q1K0 | Leishmania major | 92% | 100% |
Q4QFU7 | Leishmania major | 36% | 84% |
Q4WYG7 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 28% | 95% |
Q53GD3 | Homo sapiens | 23% | 72% |
Q54IJ2 | Dictyostelium discoideum | 25% | 93% |
Q5AB93 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 28% | 99% |
Q6BIV4 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 29% | 100% |
Q6C938 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 27% | 89% |
Q6CY85 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 26% | 92% |
Q6FLC9 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 27% | 92% |
Q6GN42 | Xenopus laevis | 23% | 72% |
Q75EG5 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 28% | 92% |
Q870V7 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 28% | 92% |
V5AWF7 | Trypanosoma cruzi | 46% | 100% |
V5BMB4 | Trypanosoma cruzi | 34% | 100% |