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: A4HP90
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 | 19 | 23 | PF00656 | 0.551 |
CLV_C14_Caspase3-7 | 476 | 480 | PF00656 | 0.528 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.239 |
CLV_PCSK_PC1ET2_1 | 319 | 321 | PF00082 | 0.415 |
CLV_PCSK_PC1ET2_1 | 396 | 398 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.178 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.422 |
DEG_APCC_DBOX_1 | 358 | 366 | PF00400 | 0.485 |
DEG_MDM2_SWIB_1 | 198 | 206 | PF02201 | 0.388 |
DEG_MDM2_SWIB_1 | 277 | 285 | PF02201 | 0.339 |
DEG_MDM2_SWIB_1 | 82 | 89 | PF02201 | 0.562 |
DEG_MDM2_SWIB_1 | 97 | 104 | PF02201 | 0.351 |
DEG_ODPH_VHL_1 | 416 | 429 | PF01847 | 0.159 |
DEG_SPOP_SBC_1 | 144 | 148 | PF00917 | 0.426 |
DEG_SPOP_SBC_1 | 321 | 325 | PF00917 | 0.328 |
DOC_ANK_TNKS_1 | 439 | 446 | PF00023 | 0.189 |
DOC_CYCLIN_RxL_1 | 356 | 363 | PF00134 | 0.548 |
DOC_MAPK_MEF2A_6 | 183 | 192 | PF00069 | 0.312 |
DOC_MAPK_MEF2A_6 | 228 | 237 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 378 | 386 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 440 | 448 | PF00069 | 0.314 |
DOC_PP1_RVXF_1 | 126 | 132 | PF00149 | 0.296 |
DOC_PP2B_LxvP_1 | 415 | 418 | PF13499 | 0.159 |
DOC_PP4_FxxP_1 | 459 | 462 | PF00568 | 0.445 |
DOC_SPAK_OSR1_1 | 76 | 80 | PF12202 | 0.494 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.326 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.345 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.635 |
LIG_14-3-3_CanoR_1 | 118 | 127 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 218 | 224 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 320 | 329 | PF00244 | 0.251 |
LIG_Actin_WH2_2 | 203 | 220 | PF00022 | 0.303 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.680 |
LIG_BIR_III_4 | 496 | 500 | PF00653 | 0.652 |
LIG_BRCT_BRCA1_1 | 327 | 331 | PF00533 | 0.251 |
LIG_BRCT_BRCA1_1 | 33 | 37 | PF00533 | 0.538 |
LIG_BRCT_BRCA1_1 | 456 | 460 | PF00533 | 0.442 |
LIG_BRCT_BRCA1_1 | 87 | 91 | PF00533 | 0.421 |
LIG_deltaCOP1_diTrp_1 | 84 | 91 | PF00928 | 0.452 |
LIG_EH1_1 | 269 | 277 | PF00400 | 0.424 |
LIG_EH1_1 | 448 | 456 | PF00400 | 0.341 |
LIG_eIF4E_1 | 410 | 416 | PF01652 | 0.462 |
LIG_FAT_LD_1 | 362 | 370 | PF03623 | 0.348 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.468 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.263 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.453 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.467 |
LIG_FHA_2 | 17 | 23 | PF00498 | 0.574 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.500 |
LIG_LIR_Apic_2 | 457 | 462 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 196 | 206 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 241 | 252 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 428 | 438 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 44 | 55 | PF02991 | 0.638 |
LIG_LIR_Gen_1 | 468 | 478 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 487 | 497 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 84 | 94 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 98 | 109 | PF02991 | 0.303 |
LIG_LIR_LC3C_4 | 333 | 336 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 196 | 201 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 241 | 247 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 323 | 329 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.647 |
LIG_LIR_Nem_3 | 428 | 434 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.670 |
LIG_LIR_Nem_3 | 457 | 463 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 468 | 474 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 487 | 492 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 84 | 89 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 98 | 104 | PF02991 | 0.310 |
LIG_LYPXL_S_1 | 60 | 64 | PF13949 | 0.255 |
LIG_LYPXL_yS_3 | 61 | 64 | PF13949 | 0.463 |
LIG_MLH1_MIPbox_1 | 456 | 460 | PF16413 | 0.285 |
LIG_NRBOX | 357 | 363 | PF00104 | 0.559 |
LIG_Pex14_2 | 198 | 202 | PF04695 | 0.351 |
LIG_Pex14_2 | 277 | 281 | PF04695 | 0.319 |
LIG_Pex14_2 | 407 | 411 | PF04695 | 0.468 |
LIG_Pex14_2 | 82 | 86 | PF04695 | 0.606 |
LIG_Pex14_2 | 97 | 101 | PF04695 | 0.311 |
LIG_REV1ctd_RIR_1 | 201 | 210 | PF16727 | 0.337 |
LIG_SH2_CRK | 268 | 272 | PF00017 | 0.392 |
LIG_SH2_CRK | 379 | 383 | PF00017 | 0.462 |
LIG_SH2_CRK | 431 | 435 | PF00017 | 0.372 |
LIG_SH2_CRK | 489 | 493 | PF00017 | 0.532 |
LIG_SH2_GRB2like | 353 | 356 | PF00017 | 0.438 |
LIG_SH2_GRB2like | 375 | 378 | PF00017 | 0.456 |
LIG_SH2_GRB2like | 410 | 413 | PF00017 | 0.462 |
LIG_SH2_NCK_1 | 431 | 435 | PF00017 | 0.159 |
LIG_SH2_NCK_1 | 489 | 493 | PF00017 | 0.475 |
LIG_SH2_PTP2 | 244 | 247 | PF00017 | 0.424 |
LIG_SH2_SRC | 353 | 356 | PF00017 | 0.438 |
LIG_SH2_SRC | 391 | 394 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 33 | 37 | PF00017 | 0.679 |
LIG_SH2_STAP1 | 431 | 435 | PF00017 | 0.159 |
LIG_SH2_STAP1 | 489 | 493 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.735 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.390 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.241 |
LIG_SUMO_SIM_anti_2 | 146 | 154 | PF11976 | 0.208 |
LIG_TYR_ITIM | 242 | 247 | PF00017 | 0.439 |
LIG_TYR_ITIM | 429 | 434 | PF00017 | 0.159 |
LIG_TYR_ITIM | 59 | 64 | PF00017 | 0.454 |
LIG_WRC_WIRS_1 | 315 | 320 | PF05994 | 0.233 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.401 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.372 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.308 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.522 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.461 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.437 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.384 |
MOD_CK2_1 | 481 | 487 | PF00069 | 0.528 |
MOD_GlcNHglycan | 114 | 118 | PF01048 | 0.567 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.632 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.190 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.380 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.324 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.244 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.336 |
MOD_GlcNHglycan | 347 | 351 | PF01048 | 0.275 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.234 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.470 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.311 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.423 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.486 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.296 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.295 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.324 |
MOD_N-GLC_1 | 16 | 21 | PF02516 | 0.348 |
MOD_N-GLC_1 | 497 | 502 | PF02516 | 0.373 |
MOD_N-GLC_2 | 412 | 414 | PF02516 | 0.337 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.350 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.473 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.458 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.268 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.225 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.375 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.281 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.494 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.292 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.335 |
MOD_NEK2_2 | 466 | 471 | PF00069 | 0.464 |
MOD_PIKK_1 | 280 | 286 | PF00454 | 0.278 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.526 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.605 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.590 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.354 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.418 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.338 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.446 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.311 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.298 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.411 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.335 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.410 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.532 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.474 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.636 |
TRG_DiLeu_BaLyEn_6 | 219 | 224 | PF01217 | 0.519 |
TRG_ENDOCYTIC_2 | 244 | 247 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.666 |
TRG_ENDOCYTIC_2 | 489 | 492 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.463 |
TRG_ER_diArg_1 | 77 | 80 | PF00400 | 0.609 |
TRG_Pf-PMV_PEXEL_1 | 343 | 347 | PF00026 | 0.312 |
TRG_Pf-PMV_PEXEL_1 | 359 | 363 | PF00026 | 0.312 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9D8 | Leptomonas seymouri | 64% | 100% |
A0A0N1PA24 | Leptomonas seymouri | 34% | 86% |
A0A0S4IW21 | Bodo saltans | 35% | 94% |
A0A0S4KHP0 | Bodo saltans | 41% | 100% |
A0A1X0P8J3 | Trypanosomatidae | 48% | 100% |
A0A3Q8I9V7 | Leishmania donovani | 36% | 84% |
A0A3R7MAJ2 | Trypanosoma rangeli | 30% | 100% |
A0A3S5IRA1 | Trypanosoma rangeli | 45% | 100% |
A0A3S7XAV8 | Leishmania donovani | 75% | 99% |
A4H7J7 | Leishmania braziliensis | 36% | 84% |
A4HVY0 | Leishmania infantum | 36% | 84% |
A4IDJ5 | Leishmania infantum | 75% | 99% |
A5PMW0 | Danio rerio | 27% | 72% |
D0A390 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
D0A391 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
D0A392 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
D0A393 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 98% |
E9APN1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 84% |
E9ASZ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
Q12412 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 94% |
Q4I8E9 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 28% | 94% |
Q4PIP8 | Ustilago maydis (strain 521 / FGSC 9021) | 29% | 96% |
Q4Q1K0 | Leishmania major | 76% | 100% |
Q4QFU7 | Leishmania major | 37% | 84% |
Q4WYG7 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 27% | 95% |
Q54IJ2 | Dictyostelium discoideum | 25% | 93% |
Q5AB93 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 27% | 98% |
Q6BIV4 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 27% | 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) | 25% | 92% |
Q6FLC9 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 27% | 91% |
Q75EG5 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 27% | 92% |
Q870V7 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 30% | 92% |
Q921V7 | Mus musculus | 23% | 77% |
V5AWF7 | Trypanosoma cruzi | 47% | 100% |
V5BMB4 | Trypanosoma cruzi | 33% | 100% |