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: 18 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 19 |
GO:0110165 | cellular anatomical entity | 1 | 19 |
Related structures:
AlphaFold database: A0A3S5H7D1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.430 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.428 |
CLV_PCSK_PC1ET2_1 | 176 | 178 | PF00082 | 0.368 |
CLV_PCSK_PC1ET2_1 | 320 | 322 | PF00082 | 0.473 |
CLV_PCSK_PC1ET2_1 | 482 | 484 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 472 | 476 | PF00082 | 0.353 |
DEG_APCC_DBOX_1 | 235 | 243 | PF00400 | 0.544 |
DEG_APCC_DBOX_1 | 471 | 479 | PF00400 | 0.409 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.583 |
DOC_CYCLIN_yCln2_LP_2 | 244 | 250 | PF00134 | 0.669 |
DOC_MAPK_gen_1 | 175 | 184 | PF00069 | 0.532 |
DOC_MAPK_gen_1 | 28 | 36 | PF00069 | 0.556 |
DOC_MAPK_HePTP_8 | 386 | 398 | PF00069 | 0.303 |
DOC_MAPK_HePTP_8 | 446 | 458 | PF00069 | 0.383 |
DOC_MAPK_MEF2A_6 | 28 | 36 | PF00069 | 0.610 |
DOC_MAPK_MEF2A_6 | 334 | 342 | PF00069 | 0.515 |
DOC_MAPK_MEF2A_6 | 389 | 398 | PF00069 | 0.403 |
DOC_MAPK_MEF2A_6 | 449 | 458 | PF00069 | 0.383 |
DOC_MAPK_NFAT4_5 | 389 | 397 | PF00069 | 0.403 |
DOC_PP2B_LxvP_1 | 244 | 247 | PF13499 | 0.561 |
DOC_PP4_FxxP_1 | 203 | 206 | PF00568 | 0.378 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.412 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.328 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 283 | 288 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.503 |
LIG_14-3-3_CanoR_1 | 375 | 379 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 494 | 501 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 506 | 512 | PF00244 | 0.668 |
LIG_BIR_III_2 | 280 | 284 | PF00653 | 0.650 |
LIG_BIR_III_2 | 356 | 360 | PF00653 | 0.359 |
LIG_BRCT_BRCA1_1 | 180 | 184 | PF00533 | 0.395 |
LIG_BRCT_BRCA1_1 | 224 | 228 | PF00533 | 0.397 |
LIG_BRCT_BRCA1_1 | 376 | 380 | PF00533 | 0.336 |
LIG_Clathr_ClatBox_1 | 300 | 304 | PF01394 | 0.668 |
LIG_eIF4E_1 | 121 | 127 | PF01652 | 0.541 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.699 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.353 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.449 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.356 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.575 |
LIG_GBD_Chelix_1 | 192 | 200 | PF00786 | 0.373 |
LIG_GBD_Chelix_1 | 339 | 347 | PF00786 | 0.400 |
LIG_GBD_Chelix_1 | 457 | 465 | PF00786 | 0.339 |
LIG_LIR_Apic_2 | 201 | 206 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 178 | 186 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 187 | 196 | PF02991 | 0.282 |
LIG_LIR_Gen_1 | 214 | 223 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 255 | 261 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 349 | 358 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 384 | 393 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 187 | 191 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 214 | 220 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 255 | 259 | PF02991 | 0.705 |
LIG_LIR_Nem_3 | 349 | 353 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 384 | 388 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 98 | 104 | PF02991 | 0.483 |
LIG_MLH1_MIPbox_1 | 180 | 184 | PF16413 | 0.339 |
LIG_NRBOX | 342 | 348 | PF00104 | 0.455 |
LIG_NRBOX | 470 | 476 | PF00104 | 0.608 |
LIG_Pex14_1 | 120 | 124 | PF04695 | 0.579 |
LIG_Pex14_1 | 166 | 170 | PF04695 | 0.431 |
LIG_Pex14_1 | 217 | 221 | PF04695 | 0.312 |
LIG_Pex14_1 | 60 | 64 | PF04695 | 0.321 |
LIG_Pex14_2 | 184 | 188 | PF04695 | 0.428 |
LIG_Pex14_2 | 398 | 402 | PF04695 | 0.402 |
LIG_Pex14_2 | 9 | 13 | PF04695 | 0.607 |
LIG_REV1ctd_RIR_1 | 6 | 15 | PF16727 | 0.604 |
LIG_SH2_CRK | 101 | 105 | PF00017 | 0.623 |
LIG_SH2_CRK | 256 | 260 | PF00017 | 0.559 |
LIG_SH2_GRB2like | 407 | 410 | PF00017 | 0.487 |
LIG_SH2_NCK_1 | 487 | 491 | PF00017 | 0.653 |
LIG_SH2_SRC | 238 | 241 | PF00017 | 0.522 |
LIG_SH2_SRC | 440 | 443 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.519 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.566 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.718 |
LIG_SH3_3 | 348 | 354 | PF00018 | 0.447 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.412 |
LIG_Sin3_3 | 216 | 223 | PF02671 | 0.459 |
LIG_SUMO_SIM_anti_2 | 427 | 433 | PF11976 | 0.346 |
LIG_TRAF2_1 | 16 | 19 | PF00917 | 0.624 |
LIG_UBA3_1 | 169 | 176 | PF00899 | 0.494 |
LIG_WRC_WIRS_1 | 185 | 190 | PF05994 | 0.343 |
LIG_WRC_WIRS_1 | 347 | 352 | PF05994 | 0.402 |
LIG_WRC_WIRS_1 | 5 | 10 | PF05994 | 0.559 |
MOD_CDK_SPK_2 | 283 | 288 | PF00069 | 0.595 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.402 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.463 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.567 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.362 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.433 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.617 |
MOD_GlcNHglycan | 269 | 274 | PF01048 | 0.494 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.483 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.468 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.385 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.725 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.579 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.395 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.343 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.395 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.363 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.718 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.686 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.401 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.350 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.318 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.354 |
MOD_NEK2_2 | 4 | 9 | PF00069 | 0.605 |
MOD_PIKK_1 | 322 | 328 | PF00454 | 0.656 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.355 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.714 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.631 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.386 |
MOD_PKA_2 | 493 | 499 | PF00069 | 0.685 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.719 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.417 |
MOD_Plk_1 | 71 | 77 | PF00069 | 0.353 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.379 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.472 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.367 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.422 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.191 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.329 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.327 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.640 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.454 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.326 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.381 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.326 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.695 |
MOD_ProDKin_1 | 283 | 289 | PF00069 | 0.658 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.686 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.505 |
MOD_SUMO_for_1 | 476 | 479 | PF00179 | 0.635 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.557 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.695 |
TRG_ER_diArg_1 | 113 | 116 | PF00400 | 0.630 |
TRG_NES_CRM1_1 | 345 | 356 | PF08389 | 0.397 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4ILP9 | Bodo saltans | 21% | 100% |
A0A0S4J6C9 | Bodo saltans | 25% | 100% |
A0A0S4J9G3 | Bodo saltans | 26% | 100% |
A0A0S4JFU7 | Bodo saltans | 25% | 100% |
A0A1X0NW47 | Trypanosomatidae | 49% | 99% |
A0A1X0P8U7 | Trypanosomatidae | 26% | 99% |
A0A3R7KUT2 | Trypanosoma rangeli | 49% | 100% |
A0A422NMM7 | Trypanosoma rangeli | 29% | 97% |
A4H3M6 | Leishmania braziliensis | 25% | 100% |
A4HDG5 | Leishmania braziliensis | 74% | 100% |
A4I0U6 | Leishmania infantum | 100% | 100% |
D0A268 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 96% |
D0A775 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AWV0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QAM4 | Leishmania major | 92% | 100% |
V5BAL2 | Trypanosoma cruzi | 53% | 100% |
V5C284 | Trypanosoma cruzi | 28% | 100% |