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:0005737 | cytoplasm | 2 | 2 |
GO:0005886 | plasma membrane | 3 | 24 |
GO:0016020 | membrane | 2 | 24 |
GO:0020016 | ciliary pocket | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 24 |
Related structures:
AlphaFold database: Q4Q1K0
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0051179 | localization | 1 | 3 |
GO:0051234 | establishment of localization | 2 | 3 |
GO:0055085 | transmembrane transport | 2 | 3 |
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 | 3 | 7 | PF00656 | 0.576 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.217 |
CLV_PCSK_PC1ET2_1 | 295 | 297 | PF00082 | 0.395 |
CLV_PCSK_PC1ET2_1 | 372 | 374 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.316 |
DEG_MDM2_SWIB_1 | 174 | 182 | PF02201 | 0.364 |
DEG_MDM2_SWIB_1 | 253 | 261 | PF02201 | 0.310 |
DEG_MDM2_SWIB_1 | 58 | 66 | PF02201 | 0.555 |
DEG_MDM2_SWIB_1 | 73 | 80 | PF02201 | 0.334 |
DEG_SPOP_SBC_1 | 297 | 301 | PF00917 | 0.297 |
DOC_CKS1_1 | 260 | 265 | PF01111 | 0.388 |
DOC_MAPK_MEF2A_6 | 159 | 168 | PF00069 | 0.309 |
DOC_MAPK_MEF2A_6 | 204 | 213 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 354 | 362 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 416 | 424 | PF00069 | 0.297 |
DOC_PP4_FxxP_1 | 435 | 438 | PF00568 | 0.435 |
DOC_SPAK_OSR1_1 | 52 | 56 | PF12202 | 0.469 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.308 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.316 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.216 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.443 |
LIG_14-3-3_CanoR_1 | 198 | 204 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 296 | 305 | PF00244 | 0.229 |
LIG_14-3-3_CanoR_1 | 373 | 378 | PF00244 | 0.400 |
LIG_Actin_WH2_2 | 179 | 196 | PF00022 | 0.273 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.595 |
LIG_BIR_III_2 | 88 | 92 | PF00653 | 0.269 |
LIG_BIR_III_4 | 472 | 476 | PF00653 | 0.604 |
LIG_BIR_III_4 | 6 | 10 | PF00653 | 0.584 |
LIG_BRCT_BRCA1_1 | 303 | 307 | PF00533 | 0.224 |
LIG_BRCT_BRCA1_1 | 403 | 407 | PF00533 | 0.381 |
LIG_BRCT_BRCA1_1 | 432 | 436 | PF00533 | 0.366 |
LIG_deltaCOP1_diTrp_1 | 60 | 67 | PF00928 | 0.431 |
LIG_EH1_1 | 245 | 253 | PF00400 | 0.407 |
LIG_EH1_1 | 424 | 432 | PF00400 | 0.311 |
LIG_eIF4E_1 | 386 | 392 | PF01652 | 0.440 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.473 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.423 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.229 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.431 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.294 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.445 |
LIG_GBD_Chelix_1 | 247 | 255 | PF00786 | 0.276 |
LIG_GBD_Chelix_1 | 401 | 409 | PF00786 | 0.358 |
LIG_GBD_Chelix_1 | 426 | 434 | PF00786 | 0.225 |
LIG_LIR_Apic_2 | 433 | 438 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 145 | 155 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 217 | 228 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 404 | 413 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 444 | 454 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 60 | 70 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 74 | 85 | PF02991 | 0.279 |
LIG_LIR_LC3C_4 | 309 | 312 | PF02991 | 0.245 |
LIG_LIR_Nem_3 | 145 | 150 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 20 | 26 | PF02991 | 0.677 |
LIG_LIR_Nem_3 | 215 | 221 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 299 | 305 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 350 | 355 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 404 | 410 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 433 | 439 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 444 | 450 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 60 | 65 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 74 | 80 | PF02991 | 0.283 |
LIG_MLH1_MIPbox_1 | 432 | 436 | PF16413 | 0.245 |
LIG_NRBOX | 333 | 339 | PF00104 | 0.367 |
LIG_Pex14_2 | 174 | 178 | PF04695 | 0.318 |
LIG_Pex14_2 | 253 | 257 | PF04695 | 0.289 |
LIG_Pex14_2 | 383 | 387 | PF04695 | 0.446 |
LIG_Pex14_2 | 58 | 62 | PF04695 | 0.592 |
LIG_Pex14_2 | 73 | 77 | PF04695 | 0.300 |
LIG_SH2_CRK | 23 | 27 | PF00017 | 0.663 |
LIG_SH2_CRK | 244 | 248 | PF00017 | 0.369 |
LIG_SH2_CRK | 355 | 359 | PF00017 | 0.440 |
LIG_SH2_CRK | 465 | 469 | PF00017 | 0.496 |
LIG_SH2_GRB2like | 329 | 332 | PF00017 | 0.409 |
LIG_SH2_GRB2like | 351 | 354 | PF00017 | 0.434 |
LIG_SH2_GRB2like | 386 | 389 | PF00017 | 0.440 |
LIG_SH2_PTP2 | 107 | 110 | PF00017 | 0.321 |
LIG_SH2_PTP2 | 220 | 223 | PF00017 | 0.407 |
LIG_SH2_SRC | 329 | 332 | PF00017 | 0.409 |
LIG_SH2_SRC | 367 | 370 | PF00017 | 0.455 |
LIG_SH2_STAT3 | 236 | 239 | PF00017 | 0.188 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.440 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.366 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.653 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.240 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.498 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.566 |
LIG_Sin3_3 | 189 | 196 | PF02671 | 0.464 |
LIG_SUMO_SIM_par_1 | 399 | 404 | PF11976 | 0.348 |
LIG_TYR_ITIM | 105 | 110 | PF00017 | 0.258 |
LIG_WRC_WIRS_1 | 291 | 296 | PF05994 | 0.218 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.370 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.446 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.292 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.509 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.291 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.439 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.457 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.415 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.511 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.389 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.321 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.520 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.480 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.319 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.275 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.212 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.547 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.402 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.503 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.279 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.255 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.265 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.294 |
MOD_N-GLC_1 | 473 | 478 | PF02516 | 0.311 |
MOD_N-GLC_2 | 388 | 390 | PF02516 | 0.325 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.338 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.458 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.525 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.314 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.239 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.158 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.293 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.487 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.277 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.305 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.523 |
MOD_NEK2_2 | 442 | 447 | PF00069 | 0.442 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.703 |
MOD_PIKK_1 | 256 | 262 | PF00454 | 0.248 |
MOD_PIKK_1 | 90 | 96 | PF00454 | 0.396 |
MOD_PKA_1 | 295 | 301 | PF00069 | 0.203 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.254 |
MOD_PKA_2 | 457 | 463 | PF00069 | 0.589 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.574 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.332 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.399 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.437 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.280 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.289 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.503 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.347 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.315 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.394 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.300 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.388 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.618 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.216 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 195 | 200 | PF01217 | 0.409 |
TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.670 |
TRG_ENDOCYTIC_2 | 244 | 247 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 355 | 358 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 465 | 468 | PF00928 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 319 | 323 | PF00026 | 0.294 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9D8 | Leptomonas seymouri | 63% | 96% |
A0A0N1PA24 | Leptomonas seymouri | 33% | 82% |
A0A0S4IW21 | Bodo saltans | 37% | 90% |
A0A0S4KHP0 | Bodo saltans | 43% | 97% |
A0A1X0P8J3 | Trypanosomatidae | 46% | 99% |
A0A3Q8I9V7 | Leishmania donovani | 34% | 80% |
A0A3R7MAJ2 | Trypanosoma rangeli | 33% | 96% |
A0A3S5IRA1 | Trypanosoma rangeli | 47% | 99% |
A0A3S7XAV8 | Leishmania donovani | 92% | 95% |
A4H7J7 | Leishmania braziliensis | 36% | 80% |
A4HP90 | Leishmania braziliensis | 76% | 95% |
A4HVY0 | Leishmania infantum | 34% | 80% |
A4IDJ5 | Leishmania infantum | 92% | 95% |
A5PMW0 | Danio rerio | 24% | 69% |
D0A390 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 99% |
D0A391 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 99% |
D0A392 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 96% |
D0A393 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 94% |
E9APN1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 80% |
E9ASZ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 95% |
P0CM92 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 32% | 88% |
P0CM93 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 32% | 88% |
Q12412 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 90% |
Q4I8E9 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 28% | 90% |
Q4PIP8 | Ustilago maydis (strain 521 / FGSC 9021) | 26% | 91% |
Q4QFU7 | Leishmania major | 36% | 80% |
Q4WYG7 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 28% | 90% |
Q54IJ2 | Dictyostelium discoideum | 25% | 88% |
Q5AB93 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 27% | 93% |
Q6BIV4 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 30% | 94% |
Q6C938 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 27% | 85% |
Q6CY85 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 26% | 88% |
Q6FLC9 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 27% | 87% |
Q75EG5 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 27% | 88% |
Q870V7 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 28% | 87% |
V5AWF7 | Trypanosoma cruzi | 47% | 100% |
V5BMB4 | Trypanosoma cruzi | 34% | 99% |