Highly homologous to other eukaryotic choline transporters. The protein family expanded in parazitic kinetoplastids.
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) | no | 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. | no | 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 |
Related structures:
AlphaFold database: E9ASZ8
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_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.239 |
CLV_PCSK_PC1ET2_1 | 321 | 323 | PF00082 | 0.415 |
CLV_PCSK_PC1ET2_1 | 398 | 400 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.321 |
DEG_MDM2_SWIB_1 | 200 | 208 | PF02201 | 0.389 |
DEG_MDM2_SWIB_1 | 279 | 287 | PF02201 | 0.340 |
DEG_MDM2_SWIB_1 | 99 | 106 | PF02201 | 0.351 |
DEG_SPOP_SBC_1 | 323 | 327 | PF00917 | 0.328 |
DEG_SPOP_SBC_1 | 348 | 352 | PF00917 | 0.411 |
DOC_CKS1_1 | 286 | 291 | PF01111 | 0.410 |
DOC_MAPK_MEF2A_6 | 185 | 194 | PF00069 | 0.312 |
DOC_MAPK_MEF2A_6 | 230 | 239 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 380 | 388 | PF00069 | 0.537 |
DOC_MAPK_NFAT4_5 | 230 | 238 | PF00069 | 0.334 |
DOC_PP4_FxxP_1 | 123 | 126 | PF00568 | 0.265 |
DOC_PP4_FxxP_1 | 461 | 464 | PF00568 | 0.445 |
DOC_SPAK_OSR1_1 | 78 | 82 | PF12202 | 0.486 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.326 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.345 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.410 |
DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.246 |
LIG_14-3-3_CanoR_1 | 220 | 226 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 322 | 331 | PF00244 | 0.251 |
LIG_Actin_WH2_2 | 205 | 222 | PF00022 | 0.303 |
LIG_Actin_WH2_2 | 356 | 371 | PF00022 | 0.376 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.675 |
LIG_BIR_III_4 | 498 | 502 | PF00653 | 0.625 |
LIG_BRCT_BRCA1_1 | 1 | 5 | PF00533 | 0.578 |
LIG_BRCT_BRCA1_1 | 329 | 333 | PF00533 | 0.251 |
LIG_BRCT_BRCA1_1 | 429 | 433 | PF00533 | 0.403 |
LIG_BRCT_BRCA1_1 | 458 | 462 | PF00533 | 0.442 |
LIG_deltaCOP1_diTrp_1 | 86 | 93 | PF00928 | 0.453 |
LIG_EH1_1 | 271 | 279 | PF00400 | 0.424 |
LIG_EH1_1 | 450 | 458 | PF00400 | 0.341 |
LIG_eIF4E_1 | 412 | 418 | PF01652 | 0.462 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.490 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.443 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.263 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.454 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.467 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.496 |
LIG_GBD_Chelix_1 | 452 | 460 | PF00786 | 0.259 |
LIG_LIR_Apic_2 | 121 | 126 | PF02991 | 0.270 |
LIG_LIR_Apic_2 | 459 | 464 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 100 | 111 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 171 | 181 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 243 | 254 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 430 | 440 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 470 | 480 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 489 | 499 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 86 | 96 | PF02991 | 0.451 |
LIG_LIR_LC3C_4 | 335 | 338 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 100 | 106 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 171 | 176 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 243 | 249 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 325 | 331 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 376 | 381 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 430 | 436 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 459 | 465 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 470 | 476 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 489 | 494 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 86 | 91 | PF02991 | 0.449 |
LIG_MLH1_MIPbox_1 | 458 | 462 | PF16413 | 0.285 |
LIG_PCNA_yPIPBox_3 | 361 | 373 | PF02747 | 0.334 |
LIG_Pex14_2 | 200 | 204 | PF04695 | 0.351 |
LIG_Pex14_2 | 279 | 283 | PF04695 | 0.320 |
LIG_Pex14_2 | 409 | 413 | PF04695 | 0.468 |
LIG_Pex14_2 | 84 | 88 | PF04695 | 0.603 |
LIG_Pex14_2 | 99 | 103 | PF04695 | 0.311 |
LIG_PTB_Apo_2 | 8 | 15 | PF02174 | 0.546 |
LIG_Rb_LxCxE_1 | 365 | 376 | PF01857 | 0.431 |
LIG_SH2_CRK | 381 | 385 | PF00017 | 0.462 |
LIG_SH2_CRK | 491 | 495 | PF00017 | 0.524 |
LIG_SH2_GRB2like | 355 | 358 | PF00017 | 0.438 |
LIG_SH2_GRB2like | 377 | 380 | PF00017 | 0.456 |
LIG_SH2_GRB2like | 412 | 415 | PF00017 | 0.462 |
LIG_SH2_PTP2 | 133 | 136 | PF00017 | 0.334 |
LIG_SH2_PTP2 | 246 | 249 | PF00017 | 0.424 |
LIG_SH2_PTP2 | 270 | 273 | PF00017 | 0.198 |
LIG_SH2_SRC | 355 | 358 | PF00017 | 0.438 |
LIG_SH2_SRC | 393 | 396 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 49 | 53 | PF00017 | 0.501 |
LIG_SH2_STAT3 | 262 | 265 | PF00017 | 0.210 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 304 | 307 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.462 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.392 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.390 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.242 |
LIG_SUMO_SIM_par_1 | 148 | 154 | PF11976 | 0.189 |
LIG_SUMO_SIM_par_1 | 274 | 280 | PF11976 | 0.178 |
LIG_TYR_ITIM | 131 | 136 | PF00017 | 0.287 |
LIG_WRC_WIRS_1 | 241 | 246 | PF05994 | 0.201 |
LIG_WRC_WIRS_1 | 317 | 322 | PF05994 | 0.233 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.462 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.372 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.466 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.308 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.522 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.461 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.438 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.526 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.518 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.643 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.190 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.324 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.245 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.534 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.337 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.234 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.305 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.423 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.489 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.296 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.295 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.324 |
MOD_N-GLC_1 | 499 | 504 | PF02516 | 0.342 |
MOD_N-GLC_2 | 414 | 416 | PF02516 | 0.337 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.350 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.473 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.459 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.268 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.225 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.375 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.281 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.494 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.292 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.510 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.187 |
MOD_NEK2_2 | 468 | 473 | PF00069 | 0.464 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.278 |
MOD_PIKK_1 | 305 | 311 | PF00454 | 0.139 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.713 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.526 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.595 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.354 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.284 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.419 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.446 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.311 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.298 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.519 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.372 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.336 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.410 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.532 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.464 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.410 |
MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.246 |
TRG_DiLeu_BaLyEn_6 | 127 | 132 | PF01217 | 0.242 |
TRG_DiLeu_BaLyEn_6 | 221 | 226 | PF01217 | 0.519 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 491 | 494 | PF00928 | 0.516 |
TRG_ER_diArg_1 | 208 | 211 | PF00400 | 0.392 |
TRG_Pf-PMV_PEXEL_1 | 345 | 349 | PF00026 | 0.312 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9D8 | Leptomonas seymouri | 63% | 100% |
A0A0N1PA24 | Leptomonas seymouri | 30% | 86% |
A0A0S4IW21 | Bodo saltans | 36% | 94% |
A0A0S4KHP0 | Bodo saltans | 43% | 100% |
A0A1X0P8J3 | Trypanosomatidae | 47% | 100% |
A0A3Q8I9V7 | Leishmania donovani | 36% | 84% |
A0A3R7MAJ2 | Trypanosoma rangeli | 32% | 100% |
A0A3S5IRA1 | Trypanosoma rangeli | 45% | 100% |
A0A3S7XAV8 | Leishmania donovani | 88% | 100% |
A4H7J7 | Leishmania braziliensis | 36% | 84% |
A4HP90 | Leishmania braziliensis | 74% | 100% |
A4HVY0 | Leishmania infantum | 36% | 84% |
A4IDJ5 | Leishmania infantum | 88% | 100% |
A5PMW0 | Danio rerio | 26% | 73% |
B0JZD0 | Xenopus tropicalis | 25% | 71% |
D0A390 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
D0A391 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
D0A392 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
D0A393 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 99% |
E9APN1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 84% |
P0CM92 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 29% | 93% |
P0CM93 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 29% | 93% |
Q12412 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 95% |
Q20026 | Caenorhabditis elegans | 23% | 66% |
Q4I8E9 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 27% | 95% |
Q4PIP8 | Ustilago maydis (strain 521 / FGSC 9021) | 29% | 96% |
Q4Q1K0 | Leishmania major | 87% | 100% |
Q4QFU7 | Leishmania major | 37% | 84% |
Q4WYG7 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 27% | 95% |
Q53GD3 | Homo sapiens | 24% | 72% |
Q54IJ2 | Dictyostelium discoideum | 24% | 93% |
Q5AB93 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 28% | 98% |
Q6BIV4 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 29% | 99% |
Q6C938 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 28% | 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) | 29% | 92% |
Q6GN42 | Xenopus laevis | 23% | 72% |
Q75EG5 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 26% | 92% |
Q7T2B0 | Danio rerio | 24% | 71% |
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 | 33% | 100% |