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: Q4QAM4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 484 | 486 | PF00675 | 0.437 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 483 | 485 | PF00082 | 0.437 |
CLV_PCSK_PC1ET2_1 | 176 | 178 | PF00082 | 0.338 |
CLV_PCSK_PC1ET2_1 | 321 | 323 | PF00082 | 0.466 |
CLV_PCSK_PC1ET2_1 | 483 | 485 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.332 |
DEG_APCC_DBOX_1 | 235 | 243 | PF00400 | 0.514 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.533 |
DOC_CYCLIN_yCln2_LP_2 | 244 | 250 | PF00134 | 0.674 |
DOC_MAPK_gen_1 | 175 | 184 | PF00069 | 0.499 |
DOC_MAPK_HePTP_8 | 387 | 399 | PF00069 | 0.239 |
DOC_MAPK_HePTP_8 | 447 | 459 | PF00069 | 0.332 |
DOC_MAPK_MEF2A_6 | 28 | 36 | PF00069 | 0.577 |
DOC_MAPK_MEF2A_6 | 335 | 343 | PF00069 | 0.480 |
DOC_MAPK_MEF2A_6 | 390 | 399 | PF00069 | 0.309 |
DOC_MAPK_MEF2A_6 | 450 | 459 | PF00069 | 0.332 |
DOC_MAPK_NFAT4_5 | 390 | 398 | PF00069 | 0.300 |
DOC_PP2B_LxvP_1 | 244 | 247 | PF13499 | 0.520 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.412 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.286 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 410 | 415 | PF00397 | 0.487 |
LIG_14-3-3_CanoR_1 | 28 | 36 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 376 | 380 | PF00244 | 0.365 |
LIG_BIR_III_2 | 280 | 284 | PF00653 | 0.604 |
LIG_BIR_III_2 | 357 | 361 | PF00653 | 0.324 |
LIG_BRCT_BRCA1_1 | 180 | 184 | PF00533 | 0.417 |
LIG_BRCT_BRCA1_1 | 224 | 228 | PF00533 | 0.371 |
LIG_BRCT_BRCA1_1 | 377 | 381 | PF00533 | 0.310 |
LIG_Clathr_ClatBox_1 | 300 | 304 | PF01394 | 0.621 |
LIG_eIF4E_1 | 121 | 127 | PF01652 | 0.515 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.623 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.346 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.457 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.317 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.547 |
LIG_FHA_2 | 290 | 296 | PF00498 | 0.712 |
LIG_GBD_Chelix_1 | 192 | 200 | PF00786 | 0.320 |
LIG_GBD_Chelix_1 | 340 | 348 | PF00786 | 0.298 |
LIG_GBD_Chelix_1 | 458 | 466 | PF00786 | 0.261 |
LIG_LIR_Gen_1 | 178 | 186 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 187 | 196 | PF02991 | 0.281 |
LIG_LIR_Gen_1 | 214 | 223 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 350 | 359 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 385 | 394 | PF02991 | 0.295 |
LIG_LIR_Gen_1 | 87 | 97 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 187 | 191 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 214 | 220 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 350 | 354 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 385 | 389 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 98 | 104 | PF02991 | 0.387 |
LIG_MLH1_MIPbox_1 | 180 | 184 | PF16413 | 0.261 |
LIG_NRBOX | 343 | 349 | PF00104 | 0.300 |
LIG_NRBOX | 471 | 477 | PF00104 | 0.594 |
LIG_Pex14_1 | 120 | 124 | PF04695 | 0.550 |
LIG_Pex14_1 | 166 | 170 | PF04695 | 0.428 |
LIG_Pex14_1 | 217 | 221 | PF04695 | 0.265 |
LIG_Pex14_1 | 60 | 64 | PF04695 | 0.285 |
LIG_Pex14_2 | 184 | 188 | PF04695 | 0.426 |
LIG_Pex14_2 | 399 | 403 | PF04695 | 0.378 |
LIG_Pex14_2 | 9 | 13 | PF04695 | 0.542 |
LIG_REV1ctd_RIR_1 | 6 | 15 | PF16727 | 0.537 |
LIG_SH2_CRK | 101 | 105 | PF00017 | 0.366 |
LIG_SH2_GRB2like | 408 | 411 | PF00017 | 0.454 |
LIG_SH2_SRC | 238 | 241 | PF00017 | 0.490 |
LIG_SH2_SRC | 441 | 444 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.497 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.533 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.638 |
LIG_SH3_3 | 349 | 355 | PF00018 | 0.422 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.412 |
LIG_Sin3_3 | 216 | 223 | PF02671 | 0.441 |
LIG_SUMO_SIM_anti_2 | 428 | 434 | PF11976 | 0.291 |
LIG_SUMO_SIM_par_1 | 82 | 87 | PF11976 | 0.229 |
LIG_TRAF2_1 | 16 | 19 | PF00917 | 0.617 |
LIG_UBA3_1 | 169 | 176 | PF00899 | 0.572 |
LIG_WRC_WIRS_1 | 185 | 190 | PF05994 | 0.288 |
LIG_WRC_WIRS_1 | 348 | 353 | PF05994 | 0.356 |
LIG_WRC_WIRS_1 | 5 | 10 | PF05994 | 0.509 |
LIG_WRC_WIRS_1 | 85 | 90 | PF05994 | 0.204 |
MOD_CDC14_SPxK_1 | 265 | 268 | PF00782 | 0.574 |
MOD_CDK_SPxK_1 | 262 | 268 | PF00069 | 0.592 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.356 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.404 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.700 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.548 |
MOD_CK2_1 | 289 | 295 | PF00069 | 0.714 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.321 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.474 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.592 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.484 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.486 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.390 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.288 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.579 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.563 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.372 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.354 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.378 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.319 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.715 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.630 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.362 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.297 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.270 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.271 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.653 |
MOD_NEK2_2 | 4 | 9 | PF00069 | 0.536 |
MOD_PIKK_1 | 283 | 289 | PF00454 | 0.658 |
MOD_PIKK_1 | 323 | 329 | PF00454 | 0.650 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.330 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.605 |
MOD_PKA_2 | 375 | 381 | PF00069 | 0.364 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.352 |
MOD_Plk_1 | 71 | 77 | PF00069 | 0.330 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.343 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.485 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.324 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.397 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.287 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.305 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.558 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.474 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.293 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.343 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.286 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.765 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.681 |
MOD_ProDKin_1 | 410 | 416 | PF00069 | 0.489 |
MOD_SUMO_for_1 | 477 | 480 | PF00179 | 0.555 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.482 |
TRG_ER_diArg_1 | 113 | 116 | PF00400 | 0.529 |
TRG_NES_CRM1_1 | 346 | 357 | PF08389 | 0.350 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4J6C9 | Bodo saltans | 24% | 100% |
A0A0S4J9G3 | Bodo saltans | 26% | 100% |
A0A0S4JFU7 | Bodo saltans | 26% | 100% |
A0A1X0NW47 | Trypanosomatidae | 48% | 99% |
A0A1X0P8U7 | Trypanosomatidae | 26% | 99% |
A0A3R7KUT2 | Trypanosoma rangeli | 48% | 100% |
A0A3S5H7D1 | Leishmania donovani | 92% | 100% |
A0A422NMM7 | Trypanosoma rangeli | 28% | 97% |
A4H3M6 | Leishmania braziliensis | 27% | 67% |
A4HDG5 | Leishmania braziliensis | 73% | 89% |
A4I0U6 | Leishmania infantum | 92% | 100% |
D0A268 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 96% |
D0A775 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9AWV0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 98% |
V5BAL2 | Trypanosoma cruzi | 52% | 100% |
V5C284 | Trypanosoma cruzi | 29% | 100% |