| 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: 8 |
| NetGPI | no | yes: 0, no: 8 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0016020 | membrane | 2 | 8 |
| GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: Q4QFV2
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003333 | amino acid transmembrane transport | 5 | 2 |
| GO:0006810 | transport | 3 | 2 |
| GO:0006865 | amino acid transport | 5 | 2 |
| GO:0009987 | cellular process | 1 | 2 |
| GO:0015849 | organic acid transport | 5 | 2 |
| GO:0051179 | localization | 1 | 2 |
| GO:0051234 | establishment of localization | 2 | 2 |
| GO:0055085 | transmembrane transport | 2 | 2 |
| GO:0071702 | organic substance transport | 4 | 2 |
| GO:0071705 | nitrogen compound transport | 4 | 2 |
| GO:1903825 | organic acid transmembrane transport | 3 | 2 |
| GO:1905039 | carboxylic acid transmembrane transport | 4 | 2 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005215 | transporter activity | 1 | 2 |
| GO:0005342 | organic acid transmembrane transporter activity | 3 | 2 |
| GO:0015171 | amino acid transmembrane transporter activity | 5 | 2 |
| GO:0022857 | transmembrane transporter activity | 2 | 2 |
| GO:0046943 | carboxylic acid transmembrane transporter activity | 4 | 2 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 180 | 184 | PF00656 | 0.415 |
| CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.783 |
| CLV_NRD_NRD_1 | 592 | 594 | PF00675 | 0.407 |
| CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.783 |
| CLV_PCSK_KEX2_1 | 592 | 594 | PF00082 | 0.408 |
| CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.576 |
| CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.518 |
| CLV_PCSK_SKI1_1 | 524 | 528 | PF00082 | 0.314 |
| CLV_PCSK_SKI1_1 | 592 | 596 | PF00082 | 0.416 |
| DEG_COP1_1 | 264 | 273 | PF00400 | 0.444 |
| DEG_Kelch_Keap1_1 | 115 | 120 | PF01344 | 0.454 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.565 |
| DEG_SCF_FBW7_1 | 24 | 31 | PF00400 | 0.552 |
| DEG_SPOP_SBC_1 | 262 | 266 | PF00917 | 0.503 |
| DEG_SPOP_SBC_1 | 33 | 37 | PF00917 | 0.450 |
| DEG_SPOP_SBC_1 | 412 | 416 | PF00917 | 0.491 |
| DOC_CDC14_PxL_1 | 295 | 303 | PF14671 | 0.484 |
| DOC_CKS1_1 | 110 | 115 | PF01111 | 0.620 |
| DOC_CKS1_1 | 25 | 30 | PF01111 | 0.588 |
| DOC_CKS1_1 | 335 | 340 | PF01111 | 0.221 |
| DOC_CYCLIN_RxL_1 | 313 | 323 | PF00134 | 0.336 |
| DOC_CYCLIN_RxL_1 | 518 | 532 | PF00134 | 0.560 |
| DOC_CYCLIN_yCln2_LP_2 | 335 | 341 | PF00134 | 0.301 |
| DOC_MAPK_gen_1 | 481 | 488 | PF00069 | 0.221 |
| DOC_MAPK_gen_1 | 524 | 533 | PF00069 | 0.510 |
| DOC_MAPK_MEF2A_6 | 393 | 400 | PF00069 | 0.540 |
| DOC_MAPK_MEF2A_6 | 524 | 533 | PF00069 | 0.490 |
| DOC_MAPK_RevD_3 | 579 | 593 | PF00069 | 0.450 |
| DOC_PIKK_1 | 177 | 185 | PF02985 | 0.502 |
| DOC_PP2B_LxvP_1 | 26 | 29 | PF13499 | 0.525 |
| DOC_PP2B_LxvP_1 | 437 | 440 | PF13499 | 0.391 |
| DOC_PP4_FxxP_1 | 22 | 25 | PF00568 | 0.554 |
| DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.551 |
| DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.554 |
| DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.482 |
| DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.571 |
| DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.400 |
| DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.554 |
| DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.438 |
| DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.388 |
| DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.388 |
| DOC_USP7_UBL2_3 | 371 | 375 | PF12436 | 0.518 |
| DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.572 |
| DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.620 |
| DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.573 |
| DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.221 |
| DOC_WW_Pin1_4 | 489 | 494 | PF00397 | 0.362 |
| DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.583 |
| DOC_WW_Pin1_4 | 604 | 609 | PF00397 | 0.560 |
| LIG_14-3-3_CanoR_1 | 252 | 262 | PF00244 | 0.409 |
| LIG_14-3-3_CanoR_1 | 530 | 534 | PF00244 | 0.386 |
| LIG_14-3-3_CanoR_1 | 569 | 578 | PF00244 | 0.349 |
| LIG_14-3-3_CanoR_1 | 599 | 606 | PF00244 | 0.666 |
| LIG_Actin_WH2_2 | 554 | 571 | PF00022 | 0.358 |
| LIG_BIR_III_4 | 218 | 222 | PF00653 | 0.395 |
| LIG_BRCT_BRCA1_1 | 233 | 237 | PF00533 | 0.550 |
| LIG_BRCT_BRCA1_1 | 322 | 326 | PF00533 | 0.405 |
| LIG_BRCT_BRCA1_1 | 335 | 339 | PF00533 | 0.360 |
| LIG_BRCT_BRCA1_1 | 493 | 497 | PF00533 | 0.397 |
| LIG_Clathr_ClatBox_1 | 473 | 477 | PF01394 | 0.438 |
| LIG_EH1_1 | 401 | 409 | PF00400 | 0.391 |
| LIG_eIF4E_1 | 402 | 408 | PF01652 | 0.255 |
| LIG_eIF4E_1 | 87 | 93 | PF01652 | 0.441 |
| LIG_FHA_1 | 116 | 122 | PF00498 | 0.503 |
| LIG_FHA_1 | 281 | 287 | PF00498 | 0.506 |
| LIG_FHA_1 | 330 | 336 | PF00498 | 0.341 |
| LIG_FHA_1 | 463 | 469 | PF00498 | 0.427 |
| LIG_FHA_1 | 511 | 517 | PF00498 | 0.438 |
| LIG_FHA_1 | 553 | 559 | PF00498 | 0.316 |
| LIG_FHA_1 | 605 | 611 | PF00498 | 0.566 |
| LIG_FHA_1 | 88 | 94 | PF00498 | 0.581 |
| LIG_FHA_2 | 192 | 198 | PF00498 | 0.499 |
| LIG_FHA_2 | 94 | 100 | PF00498 | 0.602 |
| LIG_HP1_1 | 446 | 450 | PF01393 | 0.438 |
| LIG_LIR_Gen_1 | 354 | 363 | PF02991 | 0.430 |
| LIG_LIR_Gen_1 | 494 | 505 | PF02991 | 0.326 |
| LIG_LIR_LC3C_4 | 300 | 303 | PF02991 | 0.415 |
| LIG_LIR_Nem_3 | 323 | 329 | PF02991 | 0.390 |
| LIG_LIR_Nem_3 | 354 | 358 | PF02991 | 0.430 |
| LIG_LIR_Nem_3 | 494 | 500 | PF02991 | 0.362 |
| LIG_LIR_Nem_3 | 536 | 540 | PF02991 | 0.399 |
| LIG_LIR_Nem_3 | 546 | 551 | PF02991 | 0.357 |
| LIG_LIR_Nem_3 | 601 | 606 | PF02991 | 0.690 |
| LIG_LYPXL_yS_3 | 395 | 398 | PF13949 | 0.525 |
| LIG_MAD2 | 379 | 387 | PF02301 | 0.560 |
| LIG_MLH1_MIPbox_1 | 493 | 497 | PF16413 | 0.397 |
| LIG_MYND_1 | 24 | 28 | PF01753 | 0.550 |
| LIG_PDZ_Class_1 | 611 | 616 | PF00595 | 0.580 |
| LIG_Pex14_1 | 391 | 395 | PF04695 | 0.530 |
| LIG_Pex14_2 | 105 | 109 | PF04695 | 0.540 |
| LIG_Pex14_2 | 322 | 326 | PF04695 | 0.405 |
| LIG_PTB_Apo_2 | 396 | 403 | PF02174 | 0.560 |
| LIG_PTB_Phospho_1 | 396 | 402 | PF10480 | 0.560 |
| LIG_REV1ctd_RIR_1 | 327 | 335 | PF16727 | 0.221 |
| LIG_SH2_CRK | 402 | 406 | PF00017 | 0.373 |
| LIG_SH2_STAP1 | 362 | 366 | PF00017 | 0.392 |
| LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.531 |
| LIG_SH2_STAT5 | 525 | 528 | PF00017 | 0.508 |
| LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.564 |
| LIG_SH3_3 | 22 | 28 | PF00018 | 0.604 |
| LIG_SH3_3 | 48 | 54 | PF00018 | 0.585 |
| LIG_SH3_3 | 516 | 522 | PF00018 | 0.560 |
| LIG_SH3_3 | 528 | 534 | PF00018 | 0.560 |
| LIG_Sin3_3 | 572 | 579 | PF02671 | 0.491 |
| LIG_SUMO_SIM_anti_2 | 441 | 446 | PF11976 | 0.244 |
| LIG_SUMO_SIM_anti_2 | 470 | 475 | PF11976 | 0.419 |
| LIG_SUMO_SIM_anti_2 | 580 | 585 | PF11976 | 0.391 |
| LIG_SUMO_SIM_par_1 | 349 | 354 | PF11976 | 0.434 |
| LIG_SUMO_SIM_par_1 | 457 | 463 | PF11976 | 0.525 |
| LIG_SUMO_SIM_par_1 | 512 | 517 | PF11976 | 0.491 |
| LIG_SUMO_SIM_par_1 | 559 | 565 | PF11976 | 0.320 |
| LIG_SUMO_SIM_par_1 | 582 | 588 | PF11976 | 0.244 |
| LIG_SUMO_SIM_par_1 | 61 | 66 | PF11976 | 0.444 |
| LIG_TRAF2_1 | 194 | 197 | PF00917 | 0.498 |
| LIG_TRFH_1 | 53 | 57 | PF08558 | 0.559 |
| LIG_TYR_ITSM | 599 | 606 | PF00017 | 0.671 |
| LIG_UBA3_1 | 421 | 428 | PF00899 | 0.397 |
| LIG_WRC_WIRS_1 | 326 | 331 | PF05994 | 0.371 |
| LIG_WRC_WIRS_1 | 352 | 357 | PF05994 | 0.380 |
| MOD_CDK_SPK_2 | 15 | 20 | PF00069 | 0.531 |
| MOD_CDK_SPxxK_3 | 109 | 116 | PF00069 | 0.611 |
| MOD_CK1_1 | 115 | 121 | PF00069 | 0.523 |
| MOD_CK1_1 | 275 | 281 | PF00069 | 0.498 |
| MOD_CK1_1 | 512 | 518 | PF00069 | 0.491 |
| MOD_CK1_1 | 557 | 563 | PF00069 | 0.336 |
| MOD_CK2_1 | 114 | 120 | PF00069 | 0.594 |
| MOD_CK2_1 | 160 | 166 | PF00069 | 0.580 |
| MOD_CK2_1 | 191 | 197 | PF00069 | 0.469 |
| MOD_CK2_1 | 489 | 495 | PF00069 | 0.303 |
| MOD_CK2_1 | 582 | 588 | PF00069 | 0.494 |
| MOD_CMANNOS | 391 | 394 | PF00535 | 0.360 |
| MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.787 |
| MOD_GlcNHglycan | 177 | 182 | PF01048 | 0.753 |
| MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.667 |
| MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.496 |
| MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.363 |
| MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.417 |
| MOD_GlcNHglycan | 564 | 567 | PF01048 | 0.396 |
| MOD_GlcNHglycan | 572 | 575 | PF01048 | 0.336 |
| MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.807 |
| MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.715 |
| MOD_GSK3_1 | 108 | 115 | PF00069 | 0.528 |
| MOD_GSK3_1 | 20 | 27 | PF00069 | 0.575 |
| MOD_GSK3_1 | 272 | 279 | PF00069 | 0.447 |
| MOD_GSK3_1 | 28 | 35 | PF00069 | 0.415 |
| MOD_GSK3_1 | 305 | 312 | PF00069 | 0.368 |
| MOD_GSK3_1 | 325 | 332 | PF00069 | 0.366 |
| MOD_GSK3_1 | 357 | 364 | PF00069 | 0.425 |
| MOD_GSK3_1 | 408 | 415 | PF00069 | 0.331 |
| MOD_GSK3_1 | 487 | 494 | PF00069 | 0.356 |
| MOD_GSK3_1 | 505 | 512 | PF00069 | 0.339 |
| MOD_GSK3_1 | 529 | 536 | PF00069 | 0.548 |
| MOD_GSK3_1 | 69 | 76 | PF00069 | 0.563 |
| MOD_N-GLC_1 | 123 | 128 | PF02516 | 0.785 |
| MOD_N-GLC_1 | 155 | 160 | PF02516 | 0.705 |
| MOD_N-GLC_1 | 39 | 44 | PF02516 | 0.734 |
| MOD_N-GLC_1 | 552 | 557 | PF02516 | 0.568 |
| MOD_NEK2_1 | 254 | 259 | PF00069 | 0.445 |
| MOD_NEK2_1 | 280 | 285 | PF00069 | 0.395 |
| MOD_NEK2_1 | 322 | 327 | PF00069 | 0.352 |
| MOD_NEK2_1 | 329 | 334 | PF00069 | 0.295 |
| MOD_NEK2_1 | 34 | 39 | PF00069 | 0.520 |
| MOD_NEK2_1 | 413 | 418 | PF00069 | 0.318 |
| MOD_NEK2_1 | 427 | 432 | PF00069 | 0.292 |
| MOD_NEK2_1 | 449 | 454 | PF00069 | 0.552 |
| MOD_NEK2_1 | 462 | 467 | PF00069 | 0.376 |
| MOD_NEK2_1 | 500 | 505 | PF00069 | 0.414 |
| MOD_NEK2_1 | 529 | 534 | PF00069 | 0.506 |
| MOD_NEK2_1 | 543 | 548 | PF00069 | 0.335 |
| MOD_NEK2_1 | 559 | 564 | PF00069 | 0.254 |
| MOD_NEK2_1 | 577 | 582 | PF00069 | 0.162 |
| MOD_NEK2_1 | 595 | 600 | PF00069 | 0.725 |
| MOD_NEK2_1 | 611 | 616 | PF00069 | 0.605 |
| MOD_NEK2_1 | 63 | 68 | PF00069 | 0.593 |
| MOD_NEK2_1 | 88 | 93 | PF00069 | 0.528 |
| MOD_NEK2_2 | 101 | 106 | PF00069 | 0.448 |
| MOD_PIKK_1 | 452 | 458 | PF00454 | 0.525 |
| MOD_PKA_2 | 138 | 144 | PF00069 | 0.582 |
| MOD_PKA_2 | 191 | 197 | PF00069 | 0.541 |
| MOD_PKA_2 | 529 | 535 | PF00069 | 0.525 |
| MOD_PKA_2 | 598 | 604 | PF00069 | 0.672 |
| MOD_PKA_2 | 73 | 79 | PF00069 | 0.550 |
| MOD_Plk_1 | 476 | 482 | PF00069 | 0.491 |
| MOD_Plk_4 | 132 | 138 | PF00069 | 0.584 |
| MOD_Plk_4 | 241 | 247 | PF00069 | 0.414 |
| MOD_Plk_4 | 264 | 270 | PF00069 | 0.533 |
| MOD_Plk_4 | 351 | 357 | PF00069 | 0.354 |
| MOD_Plk_4 | 438 | 444 | PF00069 | 0.391 |
| MOD_Plk_4 | 467 | 473 | PF00069 | 0.418 |
| MOD_Plk_4 | 500 | 506 | PF00069 | 0.494 |
| MOD_Plk_4 | 554 | 560 | PF00069 | 0.325 |
| MOD_Plk_4 | 579 | 585 | PF00069 | 0.450 |
| MOD_Plk_4 | 88 | 94 | PF00069 | 0.511 |
| MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.573 |
| MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.621 |
| MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.573 |
| MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.221 |
| MOD_ProDKin_1 | 489 | 495 | PF00069 | 0.362 |
| MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.586 |
| MOD_ProDKin_1 | 604 | 610 | PF00069 | 0.560 |
| TRG_DiLeu_BaLyEn_6 | 170 | 175 | PF01217 | 0.416 |
| TRG_DiLeu_BaLyEn_6 | 384 | 389 | PF01217 | 0.505 |
| TRG_DiLeu_BaLyEn_6 | 393 | 398 | PF01217 | 0.456 |
| TRG_DiLeu_BaLyEn_6 | 58 | 63 | PF01217 | 0.526 |
| TRG_DiLeu_BaLyEn_6 | 590 | 595 | PF01217 | 0.578 |
| TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.466 |
| TRG_ENDOCYTIC_2 | 395 | 398 | PF00928 | 0.499 |
| TRG_ENDOCYTIC_2 | 402 | 405 | PF00928 | 0.357 |
| TRG_ENDOCYTIC_2 | 525 | 528 | PF00928 | 0.501 |
| TRG_ENDOCYTIC_2 | 603 | 606 | PF00928 | 0.642 |
| TRG_ER_diArg_1 | 592 | 594 | PF00400 | 0.608 |
| TRG_Pf-PMV_PEXEL_1 | 173 | 177 | PF00026 | 0.786 |
| TRG_PTS1 | 613 | 616 | PF00515 | 0.584 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P3C5 | Leptomonas seymouri | 62% | 84% |
| A0A0N1PBG3 | Leptomonas seymouri | 30% | 73% |
| A0A0S4ISI1 | Bodo saltans | 43% | 100% |
| A0A3S7WST2 | Leishmania donovani | 87% | 87% |
| A4H7J2 | Leishmania braziliensis | 69% | 86% |
| A4HVX5 | Leishmania infantum | 88% | 87% |
| E9APM6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 88% |