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: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 15 |
GO:0016020 | membrane | 2 | 15 |
GO:0110165 | cellular anatomical entity | 1 | 15 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0020016 | ciliary pocket | 2 | 1 |
Related structures:
AlphaFold database: E9APN1
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 | 15 |
GO:0022857 | transmembrane transporter activity | 2 | 15 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 442 | 446 | PF00656 | 0.501 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.249 |
CLV_NRD_NRD_1 | 594 | 596 | PF00675 | 0.397 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.249 |
CLV_PCSK_KEX2_1 | 594 | 596 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.250 |
DEG_SPOP_SBC_1 | 230 | 234 | PF00917 | 0.346 |
DEG_SPOP_SBC_1 | 302 | 306 | PF00917 | 0.413 |
DEG_SPOP_SBC_1 | 38 | 42 | PF00917 | 0.548 |
DEG_SPOP_SBC_1 | 412 | 416 | PF00917 | 0.316 |
DEG_SPOP_SBC_1 | 440 | 444 | PF00917 | 0.422 |
DOC_CKS1_1 | 91 | 96 | PF01111 | 0.616 |
DOC_CYCLIN_RxL_1 | 316 | 325 | PF00134 | 0.492 |
DOC_MAPK_gen_1 | 316 | 326 | PF00069 | 0.449 |
DOC_PP1_RVXF_1 | 220 | 227 | PF00149 | 0.260 |
DOC_PP2B_PxIxI_1 | 362 | 368 | PF00149 | 0.241 |
DOC_PP4_FxxP_1 | 196 | 199 | PF00568 | 0.324 |
DOC_PP4_FxxP_1 | 551 | 554 | PF00568 | 0.404 |
DOC_PP4_FxxP_1 | 91 | 94 | PF00568 | 0.622 |
DOC_SPAK_OSR1_1 | 434 | 438 | PF12202 | 0.435 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.272 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.220 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.312 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.407 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.241 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.655 |
LIG_14-3-3_CanoR_1 | 17 | 27 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 300 | 308 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 316 | 322 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 411 | 420 | PF00244 | 0.261 |
LIG_14-3-3_CanoR_1 | 441 | 450 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 48 | 56 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 88 | 92 | PF00244 | 0.605 |
LIG_Actin_WH2_2 | 168 | 185 | PF00022 | 0.333 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.638 |
LIG_BRCT_BRCA1_1 | 331 | 335 | PF00533 | 0.272 |
LIG_BRCT_BRCA1_1 | 499 | 503 | PF00533 | 0.470 |
LIG_BRCT_BRCA1_1 | 547 | 551 | PF00533 | 0.395 |
LIG_deltaCOP1_diTrp_1 | 102 | 106 | PF00928 | 0.643 |
LIG_deltaCOP1_diTrp_1 | 113 | 120 | PF00928 | 0.455 |
LIG_EH1_1 | 540 | 548 | PF00400 | 0.305 |
LIG_eIF4E_1 | 239 | 245 | PF01652 | 0.317 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.179 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.382 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.232 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.249 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.501 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.705 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.454 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.306 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.236 |
LIG_FHA_1 | 559 | 565 | PF00498 | 0.474 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.567 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.543 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.297 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.615 |
LIG_GBD_Chelix_1 | 535 | 543 | PF00786 | 0.201 |
LIG_LIR_Apic_2 | 194 | 199 | PF02991 | 0.308 |
LIG_LIR_Apic_2 | 548 | 554 | PF02991 | 0.475 |
LIG_LIR_Apic_2 | 90 | 94 | PF02991 | 0.616 |
LIG_LIR_Gen_1 | 113 | 123 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 332 | 341 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 431 | 440 | PF02991 | 0.272 |
LIG_LIR_Gen_1 | 447 | 458 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 489 | 499 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 500 | 511 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 531 | 540 | PF02991 | 0.263 |
LIG_LIR_Gen_1 | 561 | 571 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 579 | 589 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 113 | 118 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 332 | 336 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 359 | 365 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 414 | 420 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 431 | 435 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 447 | 453 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 489 | 494 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 500 | 506 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 531 | 535 | PF02991 | 0.243 |
LIG_LIR_Nem_3 | 549 | 555 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 561 | 566 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 576 | 580 | PF02991 | 0.504 |
LIG_LYPXL_yS_3 | 362 | 365 | PF13949 | 0.272 |
LIG_NRBOX | 521 | 527 | PF00104 | 0.241 |
LIG_Pex14_1 | 115 | 119 | PF04695 | 0.368 |
LIG_Pex14_2 | 368 | 372 | PF04695 | 0.344 |
LIG_Pex14_2 | 499 | 503 | PF04695 | 0.449 |
LIG_SH2_CRK | 239 | 243 | PF00017 | 0.351 |
LIG_SH2_CRK | 471 | 475 | PF00017 | 0.449 |
LIG_SH2_CRK | 552 | 556 | PF00017 | 0.351 |
LIG_SH2_CRK | 581 | 585 | PF00017 | 0.506 |
LIG_SH2_GRB2like | 467 | 470 | PF00017 | 0.449 |
LIG_SH2_NCK_1 | 552 | 556 | PF00017 | 0.329 |
LIG_SH2_SRC | 483 | 486 | PF00017 | 0.467 |
LIG_SH2_STAP1 | 581 | 585 | PF00017 | 0.502 |
LIG_SH2_STAT3 | 248 | 251 | PF00017 | 0.484 |
LIG_SH2_STAT3 | 295 | 298 | PF00017 | 0.372 |
LIG_SH2_STAT3 | 467 | 470 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.636 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.237 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.608 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.340 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.593 |
LIG_SH3_3 | 398 | 404 | PF00018 | 0.249 |
LIG_SUMO_SIM_anti_2 | 144 | 149 | PF11976 | 0.347 |
LIG_SUMO_SIM_anti_2 | 240 | 246 | PF11976 | 0.306 |
LIG_SUMO_SIM_anti_2 | 311 | 316 | PF11976 | 0.425 |
LIG_SUMO_SIM_par_1 | 322 | 328 | PF11976 | 0.226 |
LIG_SUMO_SIM_par_1 | 521 | 527 | PF11976 | 0.353 |
LIG_TYR_ITIM | 237 | 242 | PF00017 | 0.340 |
LIG_TYR_ITIM | 360 | 365 | PF00017 | 0.241 |
LIG_TYR_ITIM | 550 | 555 | PF00017 | 0.329 |
LIG_UBA3_1 | 147 | 155 | PF00899 | 0.260 |
LIG_Vh1_VBS_1 | 366 | 384 | PF01044 | 0.234 |
LIG_WRC_WIRS_1 | 429 | 434 | PF05994 | 0.272 |
LIG_WRC_WIRS_1 | 514 | 519 | PF05994 | 0.226 |
MOD_CDC14_SPxK_1 | 42 | 45 | PF00782 | 0.576 |
MOD_CDK_SPxK_1 | 39 | 45 | PF00069 | 0.561 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.636 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.479 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.365 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.351 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.319 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.273 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.658 |
MOD_CK2_1 | 573 | 579 | PF00069 | 0.497 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.671 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.464 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.343 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.348 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.331 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.457 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.317 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.249 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.271 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.566 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.444 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.351 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.358 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.291 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.291 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.455 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.797 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.299 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.263 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.278 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.533 |
MOD_N-GLC_1 | 18 | 23 | PF02516 | 0.462 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.587 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.270 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.719 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.406 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.388 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.503 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.262 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.376 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.490 |
MOD_NEK2_1 | 541 | 546 | PF00069 | 0.337 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.498 |
MOD_NEK2_2 | 167 | 172 | PF00069 | 0.390 |
MOD_NEK2_2 | 558 | 563 | PF00069 | 0.462 |
MOD_NEK2_2 | 596 | 601 | PF00069 | 0.510 |
MOD_PIKK_1 | 589 | 595 | PF00454 | 0.524 |
MOD_PKA_2 | 410 | 416 | PF00069 | 0.332 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.435 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.668 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.646 |
MOD_Plk_1 | 596 | 602 | PF00069 | 0.530 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.308 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.351 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.400 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.514 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.454 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.269 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.291 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.291 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.525 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.362 |
MOD_Plk_4 | 541 | 547 | PF00069 | 0.317 |
MOD_Plk_4 | 558 | 564 | PF00069 | 0.429 |
MOD_Plk_4 | 596 | 602 | PF00069 | 0.574 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.648 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.403 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.241 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.581 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.652 |
TRG_DiLeu_BaEn_1 | 489 | 494 | PF01217 | 0.492 |
TRG_DiLeu_BaLyEn_6 | 287 | 292 | PF01217 | 0.272 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 362 | 365 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 471 | 474 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 552 | 555 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 581 | 584 | PF00928 | 0.479 |
TRG_ER_diArg_1 | 106 | 109 | PF00400 | 0.635 |
TRG_ER_diArg_1 | 315 | 317 | PF00400 | 0.561 |
TRG_NES_CRM1_1 | 359 | 374 | PF08389 | 0.196 |
TRG_Pf-PMV_PEXEL_1 | 434 | 438 | PF00026 | 0.329 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9D8 | Leptomonas seymouri | 33% | 100% |
A0A0N1PA24 | Leptomonas seymouri | 56% | 100% |
A0A1X0P8J3 | Trypanosomatidae | 36% | 100% |
A0A3Q8I9V7 | Leishmania donovani | 88% | 100% |
A0A3S7XAV8 | Leishmania donovani | 37% | 100% |
A4H7J7 | Leishmania braziliensis | 77% | 100% |
A4HP90 | Leishmania braziliensis | 38% | 100% |
A4HVY0 | Leishmania infantum | 88% | 100% |
A4IDJ5 | Leishmania infantum | 37% | 100% |
D0A391 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9ASZ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
Q4I8E9 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 29% | 100% |
Q4Q1K0 | Leishmania major | 36% | 100% |
Q4QFU7 | Leishmania major | 87% | 100% |
Q870V7 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 28% | 100% |