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 |
Related structures:
AlphaFold database: E9AQQ7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 102 | 106 | PF00656 | 0.560 |
CLV_C14_Caspase3-7 | 648 | 652 | PF00656 | 0.720 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 506 | 508 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 602 | 604 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 690 | 692 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 701 | 703 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 711 | 713 | PF00675 | 0.604 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 480 | 482 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 506 | 508 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 602 | 604 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 690 | 692 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 701 | 703 | PF00082 | 0.572 |
CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.683 |
CLV_PCSK_PC1ET2_1 | 480 | 482 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.647 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.708 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.672 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.468 |
CLV_Separin_Metazoa | 283 | 287 | PF03568 | 0.677 |
DEG_APCC_DBOX_1 | 332 | 340 | PF00400 | 0.661 |
DEG_APCC_DBOX_1 | 60 | 68 | PF00400 | 0.570 |
DOC_CYCLIN_RxL_1 | 19 | 29 | PF00134 | 0.669 |
DOC_MAPK_gen_1 | 19 | 27 | PF00069 | 0.539 |
DOC_MAPK_gen_1 | 275 | 284 | PF00069 | 0.615 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 726 | 730 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.716 |
DOC_USP7_UBL2_3 | 155 | 159 | PF12436 | 0.568 |
LIG_14-3-3_CanoR_1 | 161 | 169 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 333 | 341 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 379 | 383 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 442 | 446 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 681 | 689 | PF00244 | 0.583 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.567 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.518 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.578 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.652 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.490 |
LIG_FHA_1 | 672 | 678 | PF00498 | 0.549 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.634 |
LIG_FHA_2 | 161 | 167 | PF00498 | 0.533 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.504 |
LIG_FHA_2 | 681 | 687 | PF00498 | 0.608 |
LIG_LIR_Gen_1 | 69 | 75 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 69 | 74 | PF02991 | 0.580 |
LIG_NRBOX | 23 | 29 | PF00104 | 0.521 |
LIG_RPA_C_Fungi | 451 | 463 | PF08784 | 0.621 |
LIG_SH2_STAP1 | 515 | 519 | PF00017 | 0.346 |
LIG_SH2_STAP1 | 71 | 75 | PF00017 | 0.582 |
LIG_SH2_STAT3 | 42 | 45 | PF00017 | 0.499 |
LIG_SH2_STAT3 | 515 | 518 | PF00017 | 0.344 |
LIG_SH2_STAT3 | 663 | 666 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.533 |
LIG_SUMO_SIM_anti_2 | 23 | 29 | PF11976 | 0.661 |
LIG_SUMO_SIM_anti_2 | 281 | 286 | PF11976 | 0.601 |
LIG_SUMO_SIM_par_1 | 23 | 29 | PF11976 | 0.545 |
LIG_TRAF2_1 | 130 | 133 | PF00917 | 0.633 |
LIG_TRAF2_1 | 163 | 166 | PF00917 | 0.609 |
LIG_TRAF2_1 | 228 | 231 | PF00917 | 0.673 |
LIG_TRAF2_1 | 444 | 447 | PF00917 | 0.555 |
LIG_TRAF2_1 | 684 | 687 | PF00917 | 0.597 |
LIG_TRAF2_1 | 81 | 84 | PF00917 | 0.461 |
MOD_CK1_1 | 618 | 624 | PF00069 | 0.696 |
MOD_CK1_1 | 680 | 686 | PF00069 | 0.648 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.545 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.601 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.694 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.550 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.496 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.619 |
MOD_CK2_1 | 638 | 644 | PF00069 | 0.690 |
MOD_CK2_1 | 680 | 686 | PF00069 | 0.648 |
MOD_Cter_Amidation | 710 | 713 | PF01082 | 0.590 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.725 |
MOD_GlcNHglycan | 635 | 638 | PF01048 | 0.751 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.647 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.709 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.638 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.585 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.541 |
MOD_GSK3_1 | 676 | 683 | PF00069 | 0.587 |
MOD_N-GLC_1 | 93 | 98 | PF02516 | 0.474 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.677 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.602 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.533 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.539 |
MOD_NEK2_1 | 615 | 620 | PF00069 | 0.601 |
MOD_NEK2_1 | 671 | 676 | PF00069 | 0.543 |
MOD_NEK2_1 | 677 | 682 | PF00069 | 0.561 |
MOD_NEK2_1 | 696 | 701 | PF00069 | 0.560 |
MOD_PIKK_1 | 137 | 143 | PF00454 | 0.646 |
MOD_PIKK_1 | 344 | 350 | PF00454 | 0.708 |
MOD_PIKK_1 | 401 | 407 | PF00454 | 0.530 |
MOD_PIKK_1 | 408 | 414 | PF00454 | 0.445 |
MOD_PIKK_1 | 615 | 621 | PF00454 | 0.610 |
MOD_PIKK_1 | 627 | 633 | PF00454 | 0.570 |
MOD_PK_1 | 232 | 238 | PF00069 | 0.725 |
MOD_PKA_1 | 179 | 185 | PF00069 | 0.643 |
MOD_PKA_1 | 212 | 218 | PF00069 | 0.677 |
MOD_PKA_1 | 362 | 368 | PF00069 | 0.727 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.636 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.397 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.647 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.583 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.580 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.727 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.607 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.635 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.602 |
MOD_PKA_2 | 471 | 477 | PF00069 | 0.563 |
MOD_PKA_2 | 680 | 686 | PF00069 | 0.648 |
MOD_PKB_1 | 311 | 319 | PF00069 | 0.611 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.708 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.615 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.531 |
MOD_Plk_1 | 55 | 61 | PF00069 | 0.503 |
MOD_Plk_1 | 561 | 567 | PF00069 | 0.481 |
MOD_Plk_1 | 627 | 633 | PF00069 | 0.742 |
MOD_Plk_2-3 | 181 | 187 | PF00069 | 0.601 |
MOD_Plk_2-3 | 214 | 220 | PF00069 | 0.693 |
MOD_Plk_2-3 | 378 | 384 | PF00069 | 0.569 |
MOD_Plk_2-3 | 441 | 447 | PF00069 | 0.635 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.617 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.454 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.599 |
MOD_Plk_4 | 705 | 711 | PF00069 | 0.581 |
MOD_SUMO_for_1 | 67 | 70 | PF00179 | 0.613 |
MOD_SUMO_rev_2 | 208 | 218 | PF00179 | 0.572 |
MOD_SUMO_rev_2 | 29 | 36 | PF00179 | 0.529 |
MOD_SUMO_rev_2 | 484 | 492 | PF00179 | 0.593 |
TRG_DiLeu_BaEn_1 | 23 | 28 | PF01217 | 0.655 |
TRG_DiLeu_BaEn_1 | 471 | 476 | PF01217 | 0.333 |
TRG_DiLeu_BaEn_4 | 187 | 193 | PF01217 | 0.613 |
TRG_DiLeu_BaEn_4 | 440 | 446 | PF01217 | 0.596 |
TRG_DiLeu_BaEn_4 | 570 | 576 | PF01217 | 0.563 |
TRG_DiLeu_BaEn_4 | 588 | 594 | PF01217 | 0.571 |
TRG_DiLeu_BaEn_4 | 83 | 89 | PF01217 | 0.625 |
TRG_DiLeu_BaLyEn_6 | 673 | 678 | PF01217 | 0.611 |
TRG_ENDOCYTIC_2 | 71 | 74 | PF00928 | 0.624 |
TRG_ER_diArg_1 | 178 | 180 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 285 | 288 | PF00400 | 0.673 |
TRG_ER_diArg_1 | 450 | 452 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 506 | 508 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 601 | 603 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 689 | 691 | PF00400 | 0.565 |
TRG_ER_diArg_1 | 701 | 703 | PF00400 | 0.569 |
TRG_Pf-PMV_PEXEL_1 | 22 | 26 | PF00026 | 0.674 |
TRG_Pf-PMV_PEXEL_1 | 422 | 426 | PF00026 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 443 | 447 | PF00026 | 0.550 |
TRG_Pf-PMV_PEXEL_1 | 450 | 454 | PF00026 | 0.568 |
TRG_Pf-PMV_PEXEL_1 | 485 | 489 | PF00026 | 0.594 |
TRG_Pf-PMV_PEXEL_1 | 506 | 510 | PF00026 | 0.651 |
TRG_Pf-PMV_PEXEL_1 | 517 | 521 | PF00026 | 0.575 |
TRG_Pf-PMV_PEXEL_1 | 627 | 631 | PF00026 | 0.657 |
TRG_Pf-PMV_PEXEL_1 | 701 | 705 | PF00026 | 0.583 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4JQ17 | Bodo saltans | 33% | 83% |
A0A3R7LSL7 | Trypanosoma rangeli | 41% | 78% |
A4H8M2 | Leishmania braziliensis | 85% | 100% |
A4HWZ3 | Leishmania infantum | 97% | 75% |
C9ZW08 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 78% |
Q4QES2 | Leishmania major | 95% | 100% |
V5B8F4 | Trypanosoma cruzi | 41% | 78% |