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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: E9B562
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 10 |
GO:0022857 | transmembrane transporter activity | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 316 | 320 | PF00656 | 0.609 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.347 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 493 | 495 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.347 |
CLV_PCSK_PC1ET2_1 | 241 | 243 | PF00082 | 0.409 |
CLV_PCSK_PC1ET2_1 | 493 | 495 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 536 | 540 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.394 |
DEG_APCC_DBOX_1 | 170 | 178 | PF00400 | 0.509 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.591 |
DOC_CDC14_PxL_1 | 34 | 42 | PF14671 | 0.588 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 470 | 479 | PF00134 | 0.213 |
DOC_CYCLIN_yCln2_LP_2 | 619 | 625 | PF00134 | 0.615 |
DOC_MAPK_gen_1 | 171 | 179 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 421 | 430 | PF00069 | 0.552 |
DOC_MAPK_MEF2A_6 | 119 | 127 | PF00069 | 0.348 |
DOC_MAPK_MEF2A_6 | 423 | 432 | PF00069 | 0.514 |
DOC_PP1_RVXF_1 | 110 | 117 | PF00149 | 0.472 |
DOC_PP4_FxxP_1 | 35 | 38 | PF00568 | 0.533 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 565 | 569 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 631 | 635 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.351 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 643 | 648 | PF00397 | 0.824 |
LIG_14-3-3_CanoR_1 | 173 | 178 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 25 | 35 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 337 | 344 | PF00244 | 0.752 |
LIG_14-3-3_CanoR_1 | 345 | 355 | PF00244 | 0.719 |
LIG_14-3-3_CanoR_1 | 497 | 503 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 659 | 665 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 674 | 681 | PF00244 | 0.674 |
LIG_Actin_WH2_2 | 151 | 169 | PF00022 | 0.357 |
LIG_BRCT_BRCA1_1 | 175 | 179 | PF00533 | 0.509 |
LIG_BRCT_BRCA1_1 | 227 | 231 | PF00533 | 0.357 |
LIG_CSL_BTD_1 | 66 | 69 | PF09270 | 0.309 |
LIG_DLG_GKlike_1 | 173 | 181 | PF00625 | 0.504 |
LIG_EH1_1 | 219 | 227 | PF00400 | 0.357 |
LIG_EH1_1 | 432 | 440 | PF00400 | 0.213 |
LIG_eIF4E_1 | 454 | 460 | PF01652 | 0.304 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.458 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.606 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.766 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.680 |
LIG_FHA_1 | 450 | 456 | PF00498 | 0.351 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.304 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.513 |
LIG_FHA_1 | 541 | 547 | PF00498 | 0.470 |
LIG_FHA_1 | 603 | 609 | PF00498 | 0.397 |
LIG_FHA_1 | 667 | 673 | PF00498 | 0.600 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.416 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.498 |
LIG_FHA_2 | 314 | 320 | PF00498 | 0.610 |
LIG_FHA_2 | 661 | 667 | PF00498 | 0.580 |
LIG_LIR_Gen_1 | 193 | 200 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 509 | 518 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 561 | 569 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 593 | 603 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 93 | 103 | PF02991 | 0.232 |
LIG_LIR_Nem_3 | 193 | 198 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 28 | 34 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 452 | 457 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 509 | 513 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 561 | 566 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 593 | 599 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 93 | 98 | PF02991 | 0.232 |
LIG_Pex14_2 | 227 | 231 | PF04695 | 0.414 |
LIG_Pex14_2 | 31 | 35 | PF04695 | 0.500 |
LIG_Pex14_2 | 594 | 598 | PF04695 | 0.357 |
LIG_Pex14_2 | 91 | 95 | PF04695 | 0.213 |
LIG_PTAP_UEV_1 | 263 | 268 | PF05743 | 0.698 |
LIG_SH2_CRK | 495 | 499 | PF00017 | 0.488 |
LIG_SH2_CRK | 514 | 518 | PF00017 | 0.351 |
LIG_SH2_CRK | 626 | 630 | PF00017 | 0.673 |
LIG_SH2_NCK_1 | 414 | 418 | PF00017 | 0.590 |
LIG_SH2_SRC | 414 | 417 | PF00017 | 0.565 |
LIG_SH2_STAP1 | 175 | 179 | PF00017 | 0.509 |
LIG_SH2_STAP1 | 27 | 31 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 454 | 457 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 533 | 536 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.304 |
LIG_SH3_2 | 264 | 269 | PF14604 | 0.703 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.504 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.754 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.777 |
LIG_SH3_3 | 648 | 654 | PF00018 | 0.829 |
LIG_SUMO_SIM_anti_2 | 248 | 255 | PF11976 | 0.619 |
LIG_SUMO_SIM_anti_2 | 441 | 448 | PF11976 | 0.357 |
LIG_SUMO_SIM_par_1 | 248 | 255 | PF11976 | 0.703 |
LIG_SUMO_SIM_par_1 | 441 | 448 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 621 | 627 | PF11976 | 0.695 |
LIG_SxIP_EBH_1 | 378 | 388 | PF03271 | 0.626 |
LIG_TRAF2_1 | 20 | 23 | PF00917 | 0.496 |
LIG_TYR_ITIM | 512 | 517 | PF00017 | 0.351 |
LIG_TYR_ITIM | 624 | 629 | PF00017 | 0.588 |
LIG_UBA3_1 | 221 | 229 | PF00899 | 0.382 |
LIG_UBA3_1 | 457 | 461 | PF00899 | 0.309 |
LIG_UBA3_1 | 511 | 520 | PF00899 | 0.351 |
LIG_UBA3_1 | 579 | 587 | PF00899 | 0.351 |
LIG_WRC_WIRS_1 | 507 | 512 | PF05994 | 0.351 |
LIG_WRC_WIRS_1 | 595 | 600 | PF05994 | 0.357 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.357 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.666 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.304 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.375 |
MOD_CK1_1 | 568 | 574 | PF00069 | 0.352 |
MOD_CK1_1 | 677 | 683 | PF00069 | 0.672 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.416 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.500 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.677 |
MOD_CK2_1 | 631 | 637 | PF00069 | 0.724 |
MOD_CK2_1 | 660 | 666 | PF00069 | 0.588 |
MOD_Cter_Amidation | 491 | 494 | PF01082 | 0.309 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.578 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.454 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.485 |
MOD_GlcNHglycan | 415 | 420 | PF01048 | 0.441 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.357 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.400 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.395 |
MOD_GlcNHglycan | 605 | 608 | PF01048 | 0.357 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.387 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.405 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.388 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.822 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.680 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.690 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.761 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.743 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.348 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.273 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.351 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.341 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.388 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.206 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.751 |
MOD_N-GLC_1 | 153 | 158 | PF02516 | 0.288 |
MOD_N-GLC_1 | 319 | 324 | PF02516 | 0.482 |
MOD_N-GLC_1 | 463 | 468 | PF02516 | 0.504 |
MOD_N-GLC_1 | 540 | 545 | PF02516 | 0.357 |
MOD_N-GLC_1 | 75 | 80 | PF02516 | 0.509 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.402 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.408 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.570 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.215 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.363 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.372 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.359 |
MOD_NEK2_1 | 540 | 545 | PF00069 | 0.395 |
MOD_NEK2_1 | 594 | 599 | PF00069 | 0.416 |
MOD_NEK2_1 | 602 | 607 | PF00069 | 0.416 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.424 |
MOD_NEK2_2 | 157 | 162 | PF00069 | 0.509 |
MOD_NEK2_2 | 27 | 32 | PF00069 | 0.505 |
MOD_PIKK_1 | 645 | 651 | PF00454 | 0.648 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.540 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.614 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.725 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.725 |
MOD_PKA_2 | 498 | 504 | PF00069 | 0.406 |
MOD_PKA_2 | 558 | 564 | PF00069 | 0.500 |
MOD_PKB_1 | 171 | 179 | PF00069 | 0.509 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.288 |
MOD_Plk_1 | 463 | 469 | PF00069 | 0.304 |
MOD_Plk_1 | 540 | 546 | PF00069 | 0.424 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.525 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.509 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.364 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.466 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.725 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.687 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.513 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.351 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.406 |
MOD_Plk_4 | 590 | 596 | PF00069 | 0.322 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.711 |
MOD_ProDKin_1 | 643 | 649 | PF00069 | 0.824 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 495 | 498 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 514 | 517 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 626 | 629 | PF00928 | 0.611 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.304 |
TRG_ER_diArg_1 | 421 | 423 | PF00400 | 0.589 |
TRG_Pf-PMV_PEXEL_1 | 548 | 553 | PF00026 | 0.309 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5K5 | Leptomonas seymouri | 56% | 100% |
A0A3Q8IIA5 | Leishmania donovani | 85% | 100% |
A0A3S7WTH9 | Leishmania donovani | 26% | 100% |
A4HWI5 | Leishmania infantum | 26% | 100% |
A4IA48 | Leishmania infantum | 85% | 100% |
E9AQ86 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
Q4Q2S3 | Leishmania major | 84% | 100% |
Q4QF97 | Leishmania major | 26% | 100% |