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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
Related structures:
AlphaFold database: Q4QF97
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 | 0.674 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.557 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.411 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.597 |
DEG_SCF_TRCP1_1 | 7 | 12 | PF00400 | 0.655 |
DOC_CYCLIN_RxL_1 | 20 | 30 | PF00134 | 0.649 |
DOC_CYCLIN_RxL_1 | 357 | 367 | PF00134 | 0.663 |
DOC_CYCLIN_yCln2_LP_2 | 222 | 228 | PF00134 | 0.377 |
DOC_CYCLIN_yCln2_LP_2 | 586 | 592 | PF00134 | 0.409 |
DOC_MAPK_gen_1 | 211 | 221 | PF00069 | 0.352 |
DOC_MAPK_gen_1 | 320 | 329 | PF00069 | 0.676 |
DOC_MAPK_MEF2A_6 | 212 | 221 | PF00069 | 0.356 |
DOC_MAPK_MEF2A_6 | 47 | 55 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 481 | 490 | PF00069 | 0.503 |
DOC_MAPK_NFAT4_5 | 214 | 222 | PF00069 | 0.360 |
DOC_PP1_RVXF_1 | 318 | 324 | PF00149 | 0.671 |
DOC_PP2B_LxvP_1 | 586 | 589 | PF13499 | 0.413 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.811 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 427 | 431 | PF00917 | 0.355 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.361 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.366 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.283 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 613 | 618 | PF00397 | 0.747 |
LIG_14-3-3_CanoR_1 | 214 | 220 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 23 | 31 | PF00244 | 0.724 |
LIG_14-3-3_CanoR_1 | 249 | 254 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 320 | 329 | PF00244 | 0.795 |
LIG_14-3-3_CanoR_1 | 399 | 405 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 408 | 413 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 539 | 548 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 570 | 574 | PF00244 | 0.305 |
LIG_Actin_WH2_2 | 307 | 324 | PF00022 | 0.671 |
LIG_Actin_WH2_2 | 390 | 407 | PF00022 | 0.650 |
LIG_Actin_WH2_2 | 63 | 81 | PF00022 | 0.418 |
LIG_BIR_III_2 | 325 | 329 | PF00653 | 0.678 |
LIG_eIF4E_1 | 194 | 200 | PF01652 | 0.360 |
LIG_eIF4E_1 | 456 | 462 | PF01652 | 0.317 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.365 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.719 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.427 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.793 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.645 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.649 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.663 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.364 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.498 |
LIG_FHA_1 | 574 | 580 | PF00498 | 0.439 |
LIG_FHA_1 | 610 | 616 | PF00498 | 0.755 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.369 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.789 |
LIG_LIR_Gen_1 | 139 | 150 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 308 | 319 | PF02991 | 0.740 |
LIG_LIR_Gen_1 | 54 | 65 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 139 | 145 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 308 | 314 | PF02991 | 0.742 |
LIG_LIR_Nem_3 | 407 | 412 | PF02991 | 0.735 |
LIG_LIR_Nem_3 | 433 | 439 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 54 | 60 | PF02991 | 0.403 |
LIG_NRBOX | 581 | 587 | PF00104 | 0.218 |
LIG_PCNA_yPIPBox_3 | 515 | 523 | PF02747 | 0.413 |
LIG_Pex14_2 | 132 | 136 | PF04695 | 0.469 |
LIG_Pex14_2 | 437 | 441 | PF04695 | 0.331 |
LIG_PTB_Apo_2 | 517 | 524 | PF02174 | 0.391 |
LIG_SH2_CRK | 154 | 158 | PF00017 | 0.367 |
LIG_SH2_GRB2like | 56 | 59 | PF00017 | 0.229 |
LIG_SH2_STAP1 | 65 | 69 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 2 | 5 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.175 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 562 | 565 | PF00017 | 0.470 |
LIG_SH3_3 | 277 | 283 | PF00018 | 0.764 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.360 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.486 |
LIG_SH3_3 | 614 | 620 | PF00018 | 0.786 |
LIG_SUMO_SIM_anti_2 | 546 | 552 | PF11976 | 0.338 |
LIG_SUMO_SIM_anti_2 | 80 | 88 | PF11976 | 0.276 |
LIG_SUMO_SIM_par_1 | 255 | 260 | PF11976 | 0.751 |
LIG_SUMO_SIM_par_1 | 423 | 430 | PF11976 | 0.378 |
LIG_SUMO_SIM_par_1 | 609 | 616 | PF11976 | 0.783 |
LIG_TRAF2_1 | 239 | 242 | PF00917 | 0.491 |
LIG_TYR_ITIM | 434 | 439 | PF00017 | 0.323 |
LIG_WRC_WIRS_1 | 86 | 91 | PF05994 | 0.317 |
MOD_CDC14_SPxK_1 | 367 | 370 | PF00782 | 0.622 |
MOD_CDK_SPxK_1 | 364 | 370 | PF00069 | 0.621 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.650 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.611 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.487 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.815 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.665 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.451 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.330 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.590 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.374 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.506 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.671 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.403 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.369 |
MOD_CK2_1 | 260 | 266 | PF00069 | 0.726 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.728 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.312 |
MOD_CK2_1 | 540 | 546 | PF00069 | 0.582 |
MOD_CMANNOS | 134 | 137 | PF00535 | 0.295 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.576 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.478 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.399 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.379 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.374 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.467 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.338 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.348 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.683 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.404 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.520 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.813 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.592 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.728 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.727 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.653 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.390 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.437 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.704 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.585 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.373 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.216 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.798 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.295 |
MOD_LATS_1 | 406 | 412 | PF00433 | 0.538 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.437 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.527 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.789 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.621 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.624 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.312 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.369 |
MOD_NEK2_1 | 518 | 523 | PF00069 | 0.356 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.407 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.664 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.444 |
MOD_NEK2_1 | 611 | 616 | PF00069 | 0.682 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.410 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.266 |
MOD_OFUCOSY | 59 | 64 | PF10250 | 0.229 |
MOD_PIKK_1 | 168 | 174 | PF00454 | 0.414 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.643 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.617 |
MOD_PIKK_1 | 289 | 295 | PF00454 | 0.796 |
MOD_PIKK_1 | 372 | 378 | PF00454 | 0.754 |
MOD_PK_1 | 114 | 120 | PF00069 | 0.476 |
MOD_PK_1 | 382 | 388 | PF00069 | 0.637 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.736 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.543 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.808 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.690 |
MOD_PKA_2 | 569 | 575 | PF00069 | 0.305 |
MOD_Plk_1 | 597 | 603 | PF00069 | 0.663 |
MOD_Plk_1 | 609 | 615 | PF00069 | 0.771 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.757 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.809 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.573 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.397 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.378 |
MOD_Plk_4 | 518 | 524 | PF00069 | 0.413 |
MOD_Plk_4 | 546 | 552 | PF00069 | 0.360 |
MOD_Plk_4 | 569 | 575 | PF00069 | 0.413 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.417 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.371 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.657 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.285 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.604 |
MOD_ProDKin_1 | 613 | 619 | PF00069 | 0.748 |
TRG_DiLeu_BaEn_1 | 546 | 551 | PF01217 | 0.338 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 436 | 439 | PF00928 | 0.341 |
TRG_ER_diArg_1 | 113 | 116 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 210 | 212 | PF00400 | 0.303 |
TRG_ER_diArg_1 | 319 | 322 | PF00400 | 0.673 |
TRG_Pf-PMV_PEXEL_1 | 23 | 28 | PF00026 | 0.462 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5K5 | Leptomonas seymouri | 27% | 99% |
A0A0N1ILB5 | Leptomonas seymouri | 47% | 100% |
A0A1X0NVK4 | Trypanosomatidae | 31% | 100% |
A0A3Q8IIA5 | Leishmania donovani | 26% | 92% |
A0A3S7WTH9 | Leishmania donovani | 87% | 99% |
A4H859 | Leishmania braziliensis | 68% | 96% |
A4HWI5 | Leishmania infantum | 87% | 99% |
A4IA48 | Leishmania infantum | 26% | 92% |
E9AQ86 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 93% |
E9B562 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 90% |
Q4Q2S3 | Leishmania major | 25% | 100% |