A family with high similarity to plant sugar transporters.. Might be an extensive family that already diverged in free-living 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: 0 |
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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 14 |
GO:0110165 | cellular anatomical entity | 1 | 14 |
Related structures:
AlphaFold database: A4HWI5
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 12 |
GO:0022857 | transmembrane transporter activity | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 4 | 8 | PF00656 | 0.647 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.505 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.372 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.617 |
DEG_SCF_TRCP1_1 | 7 | 12 | PF00400 | 0.627 |
DEG_SPOP_SBC_1 | 13 | 17 | PF00917 | 0.608 |
DOC_ANK_TNKS_1 | 392 | 399 | PF00023 | 0.625 |
DOC_CYCLIN_RxL_1 | 20 | 27 | PF00134 | 0.632 |
DOC_CYCLIN_RxL_1 | 362 | 371 | PF00134 | 0.632 |
DOC_CYCLIN_yCln2_LP_2 | 227 | 233 | PF00134 | 0.354 |
DOC_CYCLIN_yCln2_LP_2 | 591 | 597 | PF00134 | 0.334 |
DOC_MAPK_gen_1 | 216 | 226 | PF00069 | 0.268 |
DOC_MAPK_gen_1 | 325 | 334 | PF00069 | 0.648 |
DOC_MAPK_MEF2A_6 | 217 | 226 | PF00069 | 0.270 |
DOC_MAPK_MEF2A_6 | 486 | 495 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 52 | 60 | PF00069 | 0.464 |
DOC_MAPK_NFAT4_5 | 219 | 227 | PF00069 | 0.310 |
DOC_PP1_RVXF_1 | 323 | 329 | PF00149 | 0.640 |
DOC_PP2B_LxvP_1 | 370 | 373 | PF13499 | 0.632 |
DOC_PP2B_LxvP_1 | 591 | 594 | PF13499 | 0.310 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.325 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.332 |
DOC_USP7_MATH_1 | 549 | 553 | PF00917 | 0.322 |
DOC_WW_Pin1_4 | 284 | 289 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 618 | 623 | PF00397 | 0.769 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.600 |
LIG_14-3-3_CanoR_1 | 219 | 225 | PF00244 | 0.310 |
LIG_14-3-3_CanoR_1 | 23 | 31 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 254 | 259 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 325 | 334 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 356 | 365 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 415 | 421 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 544 | 553 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 575 | 579 | PF00244 | 0.275 |
LIG_Actin_WH2_2 | 312 | 329 | PF00022 | 0.662 |
LIG_Actin_WH2_2 | 395 | 412 | PF00022 | 0.616 |
LIG_Actin_WH2_2 | 68 | 86 | PF00022 | 0.308 |
LIG_BIR_III_2 | 330 | 334 | PF00653 | 0.650 |
LIG_BRCT_BRCA1_1 | 376 | 380 | PF00533 | 0.608 |
LIG_eIF4E_1 | 199 | 205 | PF01652 | 0.334 |
LIG_eIF4E_1 | 461 | 467 | PF01652 | 0.277 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.319 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.682 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.347 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.708 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.728 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.778 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.597 |
LIG_FHA_1 | 496 | 502 | PF00498 | 0.309 |
LIG_FHA_1 | 529 | 535 | PF00498 | 0.446 |
LIG_FHA_1 | 579 | 585 | PF00498 | 0.377 |
LIG_FHA_1 | 615 | 621 | PF00498 | 0.648 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.314 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.756 |
LIG_LIR_Gen_1 | 144 | 155 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 2 | 11 | PF02991 | 0.596 |
LIG_LIR_Gen_1 | 59 | 70 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 412 | 417 | PF02991 | 0.643 |
LIG_LIR_Nem_3 | 438 | 444 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.372 |
LIG_PCNA_yPIPBox_3 | 520 | 528 | PF02747 | 0.310 |
LIG_Pex14_2 | 137 | 141 | PF04695 | 0.449 |
LIG_PTB_Apo_2 | 522 | 529 | PF02174 | 0.277 |
LIG_REV1ctd_RIR_1 | 204 | 212 | PF16727 | 0.218 |
LIG_SH2_CRK | 159 | 163 | PF00017 | 0.423 |
LIG_SH2_STAP1 | 70 | 74 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.169 |
LIG_SH2_STAT5 | 567 | 570 | PF00017 | 0.301 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.751 |
LIG_SH3_3 | 437 | 443 | PF00018 | 0.321 |
LIG_SH3_3 | 51 | 57 | PF00018 | 0.454 |
LIG_SH3_3 | 619 | 625 | PF00018 | 0.706 |
LIG_SUMO_SIM_anti_2 | 551 | 557 | PF11976 | 0.294 |
LIG_SUMO_SIM_anti_2 | 85 | 93 | PF11976 | 0.246 |
LIG_SUMO_SIM_par_1 | 260 | 265 | PF11976 | 0.777 |
LIG_SUMO_SIM_par_1 | 428 | 435 | PF11976 | 0.388 |
LIG_SUMO_SIM_par_1 | 500 | 506 | PF11976 | 0.218 |
LIG_SUMO_SIM_par_1 | 614 | 621 | PF11976 | 0.708 |
LIG_SUMO_SIM_par_1 | 85 | 93 | PF11976 | 0.308 |
LIG_TYR_ITIM | 439 | 444 | PF00017 | 0.302 |
LIG_WRC_WIRS_1 | 91 | 96 | PF05994 | 0.277 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.645 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.597 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.705 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.748 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.539 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.307 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.435 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.320 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.323 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.428 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.325 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.719 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.735 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.287 |
MOD_CK2_1 | 545 | 551 | PF00069 | 0.456 |
MOD_CMANNOS | 139 | 142 | PF00535 | 0.260 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.414 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.588 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.526 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.511 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.557 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.370 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.268 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.324 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.437 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.301 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.326 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.640 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.415 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.532 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.809 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.688 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.711 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.672 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.386 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.666 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.369 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.468 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.323 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.207 |
MOD_GSK3_1 | 614 | 621 | PF00069 | 0.780 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.417 |
MOD_N-GLC_1 | 374 | 379 | PF02516 | 0.428 |
MOD_N-GLC_1 | 386 | 391 | PF02516 | 0.389 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.352 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.540 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.685 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.573 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.246 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.330 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.314 |
MOD_NEK2_1 | 578 | 583 | PF00069 | 0.339 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.339 |
MOD_NEK2_1 | 602 | 607 | PF00069 | 0.669 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.386 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.300 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.312 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.621 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.644 |
MOD_PIKK_1 | 294 | 300 | PF00454 | 0.783 |
MOD_PK_1 | 119 | 125 | PF00069 | 0.507 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.739 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.788 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.594 |
MOD_PKA_2 | 574 | 580 | PF00069 | 0.275 |
MOD_PKB_1 | 354 | 362 | PF00069 | 0.615 |
MOD_PKB_1 | 413 | 421 | PF00069 | 0.482 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.707 |
MOD_Plk_1 | 602 | 608 | PF00069 | 0.635 |
MOD_Plk_1 | 614 | 620 | PF00069 | 0.751 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.795 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.687 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.683 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.386 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.393 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.310 |
MOD_Plk_4 | 574 | 580 | PF00069 | 0.351 |
MOD_Plk_4 | 586 | 592 | PF00069 | 0.415 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.419 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.379 |
MOD_ProDKin_1 | 284 | 290 | PF00069 | 0.717 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.454 |
MOD_ProDKin_1 | 618 | 624 | PF00069 | 0.767 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.599 |
TRG_DiLeu_BaEn_1 | 551 | 556 | PF01217 | 0.294 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.288 |
TRG_ER_diArg_1 | 118 | 121 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 215 | 217 | PF00400 | 0.267 |
TRG_ER_diArg_1 | 324 | 327 | PF00400 | 0.641 |
TRG_Pf-PMV_PEXEL_1 | 23 | 28 | PF00026 | 0.442 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5K5 | Leptomonas seymouri | 25% | 100% |
A0A1X0NU64 | Trypanosomatidae | 35% | 100% |
A0A1X0NVK4 | Trypanosomatidae | 32% | 100% |
A0A3Q8IIA5 | Leishmania donovani | 26% | 93% |
A0A3R7L5G2 | Trypanosoma rangeli | 35% | 100% |
A0A3S7WTH9 | Leishmania donovani | 100% | 100% |
A4H859 | Leishmania braziliensis | 70% | 100% |
A4IA48 | Leishmania infantum | 26% | 93% |
E9AQ86 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
E9B562 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
Q4Q2S3 | Leishmania major | 26% | 100% |
Q4QF97 | Leishmania major | 87% | 99% |