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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: A4IA48
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 11 |
GO:0022857 | transmembrane transporter activity | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 264 | 266 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 410 | 412 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 660 | 662 | PF00675 | 0.439 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 481 | 483 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 660 | 662 | PF00082 | 0.422 |
CLV_PCSK_PC1ET2_1 | 229 | 231 | PF00082 | 0.390 |
CLV_PCSK_PC1ET2_1 | 481 | 483 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 524 | 528 | PF00082 | 0.437 |
CLV_Separin_Metazoa | 10 | 14 | PF03568 | 0.522 |
DEG_APCC_DBOX_1 | 158 | 166 | PF00400 | 0.525 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.563 |
DEG_SPOP_SBC_1 | 642 | 646 | PF00917 | 0.654 |
DOC_CDC14_PxL_1 | 22 | 30 | PF14671 | 0.567 |
DOC_CYCLIN_yCln2_LP_2 | 607 | 613 | PF00134 | 0.627 |
DOC_MAPK_gen_1 | 159 | 167 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 107 | 115 | PF00069 | 0.374 |
DOC_PP4_FxxP_1 | 23 | 26 | PF00568 | 0.515 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 553 | 557 | PF00917 | 0.380 |
DOC_USP7_MATH_1 | 619 | 623 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.342 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 630 | 635 | PF00397 | 0.822 |
DOC_WW_Pin1_4 | 636 | 641 | PF00397 | 0.849 |
LIG_14-3-3_CanoR_1 | 13 | 22 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 161 | 166 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 325 | 332 | PF00244 | 0.725 |
LIG_14-3-3_CanoR_1 | 629 | 634 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 660 | 668 | PF00244 | 0.677 |
LIG_Actin_WH2_2 | 139 | 157 | PF00022 | 0.383 |
LIG_BIR_III_4 | 268 | 272 | PF00653 | 0.707 |
LIG_BRCT_BRCA1_1 | 163 | 167 | PF00533 | 0.516 |
LIG_BRCT_BRCA1_1 | 179 | 183 | PF00533 | 0.383 |
LIG_BRCT_BRCA1_1 | 215 | 219 | PF00533 | 0.436 |
LIG_CSL_BTD_1 | 54 | 57 | PF09270 | 0.325 |
LIG_DLG_GKlike_1 | 161 | 169 | PF00625 | 0.496 |
LIG_EH1_1 | 207 | 215 | PF00400 | 0.383 |
LIG_eIF4E_1 | 442 | 448 | PF01652 | 0.296 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.580 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.472 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.615 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.724 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.675 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.704 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.342 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.296 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.437 |
LIG_FHA_1 | 529 | 535 | PF00498 | 0.481 |
LIG_FHA_1 | 591 | 597 | PF00498 | 0.394 |
LIG_FHA_1 | 626 | 632 | PF00498 | 0.806 |
LIG_FHA_1 | 644 | 650 | PF00498 | 0.691 |
LIG_FHA_1 | 654 | 660 | PF00498 | 0.581 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.437 |
LIG_FHA_2 | 391 | 397 | PF00498 | 0.531 |
LIG_GBD_Chelix_1 | 430 | 438 | PF00786 | 0.317 |
LIG_HCF-1_HBM_1 | 399 | 402 | PF13415 | 0.547 |
LIG_LIR_Apic_2 | 21 | 26 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 180 | 188 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 216 | 226 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 497 | 506 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 513 | 523 | PF02991 | 0.213 |
LIG_LIR_Gen_1 | 549 | 557 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 585 | 596 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 21 | 25 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 216 | 222 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 440 | 445 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 497 | 501 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 513 | 519 | PF02991 | 0.210 |
LIG_LIR_Nem_3 | 52 | 58 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 549 | 554 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 585 | 591 | PF02991 | 0.380 |
LIG_PCNA_PIPBox_1 | 8 | 17 | PF02747 | 0.522 |
LIG_Pex14_2 | 215 | 219 | PF04695 | 0.436 |
LIG_Pex14_2 | 582 | 586 | PF04695 | 0.383 |
LIG_Pex14_2 | 587 | 591 | PF04695 | 0.383 |
LIG_PTAP_UEV_1 | 251 | 256 | PF05743 | 0.694 |
LIG_SH2_CRK | 138 | 142 | PF00017 | 0.412 |
LIG_SH2_CRK | 483 | 487 | PF00017 | 0.516 |
LIG_SH2_CRK | 502 | 506 | PF00017 | 0.180 |
LIG_SH2_CRK | 614 | 618 | PF00017 | 0.649 |
LIG_SH2_NCK_1 | 402 | 406 | PF00017 | 0.573 |
LIG_SH2_SRC | 185 | 188 | PF00017 | 0.317 |
LIG_SH2_SRC | 397 | 400 | PF00017 | 0.571 |
LIG_SH2_SRC | 402 | 405 | PF00017 | 0.545 |
LIG_SH2_STAP1 | 15 | 19 | PF00017 | 0.579 |
LIG_SH2_STAP1 | 163 | 167 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 442 | 445 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 521 | 524 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.296 |
LIG_SH3_2 | 252 | 257 | PF14604 | 0.699 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.536 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.688 |
LIG_SH3_3 | 635 | 641 | PF00018 | 0.744 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.496 |
LIG_SUMO_SIM_anti_2 | 236 | 243 | PF11976 | 0.629 |
LIG_SUMO_SIM_anti_2 | 429 | 436 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 236 | 243 | PF11976 | 0.712 |
LIG_SUMO_SIM_par_1 | 429 | 436 | PF11976 | 0.523 |
LIG_SUMO_SIM_par_1 | 609 | 615 | PF11976 | 0.684 |
LIG_TYR_ITIM | 500 | 505 | PF00017 | 0.383 |
LIG_UBA3_1 | 209 | 217 | PF00899 | 0.348 |
LIG_UBA3_1 | 445 | 449 | PF00899 | 0.325 |
LIG_UBA3_1 | 499 | 508 | PF00899 | 0.342 |
LIG_UBA3_1 | 567 | 575 | PF00899 | 0.342 |
LIG_WRC_WIRS_1 | 19 | 24 | PF05994 | 0.515 |
LIG_WRC_WIRS_1 | 464 | 469 | PF05994 | 0.254 |
LIG_WRC_WIRS_1 | 495 | 500 | PF05994 | 0.342 |
LIG_WRC_WIRS_1 | 583 | 588 | PF05994 | 0.383 |
MOD_CDC14_SPxK_1 | 633 | 636 | PF00782 | 0.667 |
MOD_CDK_SPxK_1 | 630 | 636 | PF00069 | 0.666 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.364 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.745 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.691 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.753 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.358 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.374 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.343 |
MOD_CK1_1 | 632 | 638 | PF00069 | 0.725 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.669 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.366 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.719 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.536 |
MOD_CK2_1 | 619 | 625 | PF00069 | 0.713 |
MOD_Cter_Amidation | 479 | 482 | PF01082 | 0.325 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.586 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.480 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.486 |
MOD_GlcNHglycan | 403 | 408 | PF01048 | 0.394 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.348 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.380 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.356 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.383 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.440 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.428 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.380 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.716 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.690 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.760 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.342 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.375 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.366 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.448 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.315 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.364 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.799 |
MOD_N-GLC_1 | 141 | 146 | PF02516 | 0.345 |
MOD_N-GLC_1 | 305 | 310 | PF02516 | 0.501 |
MOD_N-GLC_1 | 451 | 456 | PF02516 | 0.496 |
MOD_N-GLC_1 | 528 | 533 | PF02516 | 0.323 |
MOD_N-GLC_1 | 63 | 68 | PF02516 | 0.525 |
MOD_N-GLC_2 | 307 | 309 | PF02516 | 0.444 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.598 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.399 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.430 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.610 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.655 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.414 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.254 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.389 |
MOD_NEK2_1 | 515 | 520 | PF00069 | 0.343 |
MOD_NEK2_1 | 528 | 533 | PF00069 | 0.361 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.383 |
MOD_NEK2_1 | 590 | 595 | PF00069 | 0.383 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.420 |
MOD_NEK2_1 | 643 | 648 | PF00069 | 0.692 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.479 |
MOD_NEK2_2 | 145 | 150 | PF00069 | 0.525 |
MOD_NEK2_2 | 619 | 624 | PF00069 | 0.630 |
MOD_PKA_1 | 264 | 270 | PF00069 | 0.654 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.654 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.697 |
MOD_PKA_2 | 546 | 552 | PF00069 | 0.516 |
MOD_PKB_1 | 159 | 167 | PF00069 | 0.482 |
MOD_PKB_1 | 627 | 635 | PF00069 | 0.669 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.279 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.296 |
MOD_Plk_1 | 528 | 534 | PF00069 | 0.351 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.525 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.391 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.477 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.629 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.818 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.712 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.428 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.504 |
MOD_Plk_4 | 494 | 500 | PF00069 | 0.430 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.433 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.756 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.701 |
MOD_ProDKin_1 | 630 | 636 | PF00069 | 0.824 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 502 | 505 | PF00928 | 0.180 |
TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.296 |
TRG_ER_diArg_1 | 264 | 266 | PF00400 | 0.695 |
TRG_ER_diArg_1 | 409 | 411 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 659 | 661 | PF00400 | 0.620 |
TRG_Pf-PMV_PEXEL_1 | 536 | 541 | PF00026 | 0.325 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5K5 | Leptomonas seymouri | 56% | 100% |
A0A0S4JGY0 | Bodo saltans | 25% | 100% |
A0A3Q8IIA5 | Leishmania donovani | 100% | 100% |
A0A3S7WTH9 | Leishmania donovani | 26% | 100% |
A4HWI5 | Leishmania infantum | 26% | 100% |
E9AQ86 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B562 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q2S3 | Leishmania major | 87% | 100% |
Q4QF97 | Leishmania major | 26% | 100% |