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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: E9AS92
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 12 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 12 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 12 |
GO:0022857 | transmembrane transporter activity | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 463 | 467 | PF00656 | 0.590 |
CLV_C14_Caspase3-7 | 590 | 594 | PF00656 | 0.754 |
CLV_NRD_NRD_1 | 104 | 106 | PF00675 | 0.298 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 391 | 393 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.424 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.268 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 552 | 556 | PF00082 | 0.427 |
DEG_SPOP_SBC_1 | 478 | 482 | PF00917 | 0.632 |
DEG_SPOP_SBC_1 | 7 | 11 | PF00917 | 0.765 |
DOC_CYCLIN_RxL_1 | 244 | 254 | PF00134 | 0.368 |
DOC_MAPK_gen_1 | 105 | 117 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 392 | 400 | PF00069 | 0.595 |
DOC_MAPK_gen_1 | 45 | 55 | PF00069 | 0.493 |
DOC_MAPK_HePTP_8 | 390 | 402 | PF00069 | 0.632 |
DOC_MAPK_MEF2A_6 | 393 | 402 | PF00069 | 0.626 |
DOC_PP1_RVXF_1 | 245 | 252 | PF00149 | 0.368 |
DOC_PP4_FxxP_1 | 541 | 544 | PF00568 | 0.662 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.368 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.773 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 591 | 595 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 608 | 612 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.310 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 374 | 379 | PF00397 | 0.803 |
DOC_WW_Pin1_4 | 490 | 495 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 511 | 516 | PF00397 | 0.735 |
LIG_14-3-3_CanoR_1 | 438 | 442 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 530 | 536 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 546 | 550 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 552 | 557 | PF00244 | 0.576 |
LIG_Actin_WH2_2 | 333 | 348 | PF00022 | 0.644 |
LIG_APCC_ABBA_1 | 220 | 225 | PF00400 | 0.303 |
LIG_BRCT_BRCA1_1 | 497 | 501 | PF00533 | 0.689 |
LIG_deltaCOP1_diTrp_1 | 276 | 285 | PF00928 | 0.169 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.640 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.311 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.348 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.398 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.572 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.619 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.760 |
LIG_FHA_1 | 540 | 546 | PF00498 | 0.706 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.576 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.417 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.273 |
LIG_FHA_2 | 588 | 594 | PF00498 | 0.664 |
LIG_LIR_Apic_2 | 540 | 544 | PF02991 | 0.619 |
LIG_LIR_Gen_1 | 216 | 223 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 445 | 452 | PF02991 | 0.583 |
LIG_LIR_Gen_1 | 537 | 545 | PF02991 | 0.665 |
LIG_LIR_Gen_1 | 83 | 93 | PF02991 | 0.240 |
LIG_LIR_Gen_1 | 97 | 103 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 323 | 327 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 445 | 450 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 537 | 541 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 83 | 88 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 97 | 101 | PF02991 | 0.275 |
LIG_Pex14_2 | 397 | 401 | PF04695 | 0.631 |
LIG_SH2_GRB2like | 327 | 330 | PF00017 | 0.639 |
LIG_SH2_NCK_1 | 418 | 422 | PF00017 | 0.652 |
LIG_SH2_PTP2 | 98 | 101 | PF00017 | 0.346 |
LIG_SH2_SRC | 327 | 330 | PF00017 | 0.639 |
LIG_SH2_STAP1 | 223 | 227 | PF00017 | 0.337 |
LIG_SH2_STAP1 | 409 | 413 | PF00017 | 0.542 |
LIG_SH2_STAT3 | 46 | 49 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.756 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.310 |
LIG_SUMO_SIM_anti_2 | 150 | 157 | PF11976 | 0.162 |
LIG_SUMO_SIM_anti_2 | 77 | 83 | PF11976 | 0.248 |
LIG_SUMO_SIM_par_1 | 150 | 157 | PF11976 | 0.290 |
LIG_SUMO_SIM_par_1 | 413 | 420 | PF11976 | 0.584 |
LIG_SUMO_SIM_par_1 | 448 | 454 | PF11976 | 0.682 |
LIG_SUMO_SIM_par_1 | 550 | 561 | PF11976 | 0.486 |
LIG_TRAF2_1 | 202 | 205 | PF00917 | 0.495 |
LIG_TRAF2_1 | 534 | 537 | PF00917 | 0.658 |
LIG_TRAF2_1 | 548 | 551 | PF00917 | 0.490 |
LIG_TYR_ITIM | 416 | 421 | PF00017 | 0.642 |
LIG_TYR_ITIM | 96 | 101 | PF00017 | 0.274 |
LIG_WRC_WIRS_1 | 538 | 543 | PF05994 | 0.617 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.559 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.714 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.757 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.672 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.719 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.592 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.639 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.642 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.668 |
MOD_CK1_1 | 603 | 609 | PF00069 | 0.787 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.247 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.591 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.440 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.684 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.678 |
MOD_CK2_1 | 531 | 537 | PF00069 | 0.654 |
MOD_CK2_1 | 545 | 551 | PF00069 | 0.476 |
MOD_CK2_1 | 567 | 573 | PF00069 | 0.673 |
MOD_GlcNHglycan | 121 | 125 | PF01048 | 0.368 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.761 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.275 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.581 |
MOD_GlcNHglycan | 331 | 336 | PF01048 | 0.356 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.539 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.389 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.454 |
MOD_GlcNHglycan | 473 | 478 | PF01048 | 0.465 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.518 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.425 |
MOD_GlcNHglycan | 508 | 512 | PF01048 | 0.465 |
MOD_GlcNHglycan | 580 | 583 | PF01048 | 0.439 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.503 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.522 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.504 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.311 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.548 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.586 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.763 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.770 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.667 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.688 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.666 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.616 |
MOD_GSK3_1 | 578 | 585 | PF00069 | 0.591 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.650 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.310 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.712 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.690 |
MOD_N-GLC_1 | 454 | 459 | PF02516 | 0.495 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.511 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.320 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.438 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.288 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.459 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.705 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.338 |
MOD_PIKK_1 | 356 | 362 | PF00454 | 0.589 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.721 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.432 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.588 |
MOD_PKA_2 | 545 | 551 | PF00069 | 0.666 |
MOD_Plk_1 | 331 | 337 | PF00069 | 0.606 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.695 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.703 |
MOD_Plk_1 | 550 | 556 | PF00069 | 0.660 |
MOD_Plk_1 | 566 | 572 | PF00069 | 0.619 |
MOD_Plk_2-3 | 150 | 156 | PF00069 | 0.214 |
MOD_Plk_2-3 | 567 | 573 | PF00069 | 0.646 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.358 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.344 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.429 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.540 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.620 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.543 |
MOD_ProDKin_1 | 374 | 380 | PF00069 | 0.806 |
MOD_ProDKin_1 | 490 | 496 | PF00069 | 0.623 |
MOD_ProDKin_1 | 511 | 517 | PF00069 | 0.737 |
MOD_SUMO_rev_2 | 467 | 477 | PF00179 | 0.588 |
TRG_DiLeu_BaEn_1 | 428 | 433 | PF01217 | 0.650 |
TRG_DiLeu_BaLyEn_6 | 512 | 517 | PF01217 | 0.573 |
TRG_DiLeu_BaLyEn_6 | 575 | 580 | PF01217 | 0.567 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 418 | 421 | PF00928 | 0.668 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.274 |
TRG_ER_diArg_1 | 255 | 257 | PF00400 | 0.549 |
TRG_NES_CRM1_1 | 142 | 156 | PF08389 | 0.162 |
TRG_NLS_MonoExtC_3 | 104 | 109 | PF00514 | 0.491 |
TRG_Pf-PMV_PEXEL_1 | 439 | 444 | PF00026 | 0.408 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHD4 | Leptomonas seymouri | 62% | 97% |
A0A0S4IWL9 | Bodo saltans | 36% | 100% |
A0A1X0P615 | Trypanosomatidae | 49% | 100% |
A0A3Q8IBF0 | Leishmania donovani | 92% | 100% |
A0A3R7MPI1 | Trypanosoma rangeli | 44% | 100% |
A4HA88 | Leishmania braziliensis | 79% | 100% |
A4HYG8 | Leishmania infantum | 91% | 100% |
D0A0T8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
Q4QD72 | Leishmania major | 91% | 100% |
V5B132 | Trypanosoma cruzi | 45% | 100% |