This highly expanded family of Kinetoplastid transporters is likely responsible for the uptake of critical nutrients. Might be a thiamine transporter if relate to human SLC35F proteins.. Localization: Cell surface (by feature)
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 17 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 18 |
GO:0110165 | cellular anatomical entity | 1 | 18 |
Related structures:
AlphaFold database: E9AWV0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.351 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.434 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.352 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 492 | 494 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 176 | 178 | PF00082 | 0.364 |
CLV_PCSK_PC1ET2_1 | 330 | 332 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 492 | 494 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 482 | 486 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.320 |
DEG_APCC_DBOX_1 | 235 | 243 | PF00400 | 0.544 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.581 |
DEG_SCF_FBW7_2 | 319 | 326 | PF00400 | 0.497 |
DOC_CKS1_1 | 320 | 325 | PF01111 | 0.691 |
DOC_CYCLIN_yCln2_LP_2 | 361 | 367 | PF00134 | 0.313 |
DOC_MAPK_gen_1 | 175 | 184 | PF00069 | 0.529 |
DOC_MAPK_HePTP_8 | 456 | 468 | PF00069 | 0.379 |
DOC_MAPK_MEF2A_6 | 28 | 36 | PF00069 | 0.612 |
DOC_MAPK_MEF2A_6 | 344 | 352 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 399 | 408 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 459 | 468 | PF00069 | 0.379 |
DOC_MAPK_NFAT4_5 | 399 | 407 | PF00069 | 0.405 |
DOC_MAPK_RevD_3 | 319 | 332 | PF00069 | 0.483 |
DOC_PP2B_LxvP_1 | 244 | 247 | PF13499 | 0.588 |
DOC_PP4_FxxP_1 | 203 | 206 | PF00568 | 0.376 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 435 | 439 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 498 | 502 | PF00917 | 0.689 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.327 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.782 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.508 |
LIG_14-3-3_CanoR_1 | 28 | 36 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 385 | 389 | PF00244 | 0.363 |
LIG_BIR_III_2 | 366 | 370 | PF00653 | 0.355 |
LIG_BRCT_BRCA1_1 | 180 | 184 | PF00533 | 0.387 |
LIG_BRCT_BRCA1_1 | 224 | 228 | PF00533 | 0.394 |
LIG_BRCT_BRCA1_1 | 386 | 390 | PF00533 | 0.339 |
LIG_BRCT_BRCA1_1 | 55 | 59 | PF00533 | 0.253 |
LIG_Clathr_ClatBox_1 | 309 | 313 | PF01394 | 0.683 |
LIG_eIF4E_1 | 121 | 127 | PF01652 | 0.540 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.692 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.711 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.359 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.355 |
LIG_FHA_2 | 498 | 504 | PF00498 | 0.608 |
LIG_GBD_Chelix_1 | 192 | 200 | PF00786 | 0.369 |
LIG_GBD_Chelix_1 | 349 | 357 | PF00786 | 0.402 |
LIG_GBD_Chelix_1 | 467 | 475 | PF00786 | 0.341 |
LIG_IRF3_LxIS_1 | 51 | 56 | PF10401 | 0.317 |
LIG_LIR_Apic_2 | 201 | 206 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 178 | 186 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 187 | 196 | PF02991 | 0.286 |
LIG_LIR_Gen_1 | 214 | 223 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 359 | 368 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 187 | 191 | PF02991 | 0.225 |
LIG_LIR_Nem_3 | 214 | 220 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 359 | 363 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 394 | 398 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 56 | 62 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 98 | 104 | PF02991 | 0.485 |
LIG_MLH1_MIPbox_1 | 180 | 184 | PF16413 | 0.341 |
LIG_NRBOX | 352 | 358 | PF00104 | 0.405 |
LIG_NRBOX | 480 | 486 | PF00104 | 0.610 |
LIG_Pex14_1 | 120 | 124 | PF04695 | 0.577 |
LIG_Pex14_1 | 166 | 170 | PF04695 | 0.450 |
LIG_Pex14_1 | 217 | 221 | PF04695 | 0.314 |
LIG_Pex14_1 | 60 | 64 | PF04695 | 0.317 |
LIG_Pex14_2 | 184 | 188 | PF04695 | 0.426 |
LIG_Pex14_2 | 392 | 396 | PF04695 | 0.290 |
LIG_Pex14_2 | 408 | 412 | PF04695 | 0.416 |
LIG_Pex14_2 | 41 | 45 | PF04695 | 0.418 |
LIG_Pex14_2 | 9 | 13 | PF04695 | 0.611 |
LIG_REV1ctd_RIR_1 | 6 | 15 | PF16727 | 0.608 |
LIG_SH2_CRK | 101 | 105 | PF00017 | 0.573 |
LIG_SH2_CRK | 400 | 404 | PF00017 | 0.246 |
LIG_SH2_GRB2like | 417 | 420 | PF00017 | 0.480 |
LIG_SH2_SRC | 238 | 241 | PF00017 | 0.523 |
LIG_SH2_SRC | 450 | 453 | PF00017 | 0.434 |
LIG_SH2_STAP1 | 276 | 280 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.516 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.543 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.660 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.730 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.405 |
LIG_SUMO_SIM_anti_2 | 437 | 443 | PF11976 | 0.341 |
LIG_SUMO_SIM_par_1 | 50 | 56 | PF11976 | 0.203 |
LIG_TYR_ITIM | 398 | 403 | PF00017 | 0.228 |
LIG_UBA3_1 | 169 | 176 | PF00899 | 0.588 |
LIG_WRC_WIRS_1 | 185 | 190 | PF05994 | 0.338 |
LIG_WRC_WIRS_1 | 357 | 362 | PF05994 | 0.399 |
LIG_WRC_WIRS_1 | 5 | 10 | PF05994 | 0.563 |
MOD_CDK_SPxK_1 | 262 | 268 | PF00069 | 0.646 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.399 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.459 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.719 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.357 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.463 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.602 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.507 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.485 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.472 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.386 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.577 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.374 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.353 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.384 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.368 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.760 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.687 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.393 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.342 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.320 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.273 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.343 |
MOD_NEK2_2 | 4 | 9 | PF00069 | 0.607 |
MOD_PIKK_1 | 27 | 33 | PF00454 | 0.453 |
MOD_PIKK_1 | 292 | 298 | PF00454 | 0.705 |
MOD_PIKK_1 | 332 | 338 | PF00454 | 0.658 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.351 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.756 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.636 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.383 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.414 |
MOD_Plk_1 | 71 | 77 | PF00069 | 0.351 |
MOD_Plk_2-3 | 274 | 280 | PF00069 | 0.711 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.379 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.475 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.372 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.409 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.319 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.643 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.326 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.447 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.328 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.376 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.325 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.784 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.698 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.701 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.510 |
MOD_SUMO_for_1 | 16 | 19 | PF00179 | 0.430 |
MOD_SUMO_for_1 | 486 | 489 | PF00179 | 0.644 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.558 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.237 |
TRG_ER_diArg_1 | 113 | 116 | PF00400 | 0.608 |
TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.666 |
TRG_NES_CRM1_1 | 355 | 366 | PF08389 | 0.394 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4J6C9 | Bodo saltans | 24% | 100% |
A0A0S4J9G3 | Bodo saltans | 25% | 100% |
A0A0S4JFU7 | Bodo saltans | 25% | 100% |
A0A1X0NW47 | Trypanosomatidae | 48% | 100% |
A0A1X0P8U7 | Trypanosomatidae | 25% | 100% |
A0A3R7KUT2 | Trypanosoma rangeli | 48% | 100% |
A0A3S5H7D1 | Leishmania donovani | 89% | 100% |
A0A422NMM7 | Trypanosoma rangeli | 29% | 99% |
A4H3M6 | Leishmania braziliensis | 26% | 100% |
A4HDG5 | Leishmania braziliensis | 75% | 100% |
A4I0U6 | Leishmania infantum | 90% | 100% |
D0A268 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 98% |
D0A775 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
Q4QAM4 | Leishmania major | 88% | 98% |
V5BAL2 | Trypanosoma cruzi | 53% | 100% |
V5C284 | Trypanosoma cruzi | 28% | 100% |