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 |
Related structures:
AlphaFold database: A0A3Q8IT90
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 100 | 104 | PF00656 | 0.548 |
CLV_C14_Caspase3-7 | 458 | 462 | PF00656 | 0.426 |
CLV_C14_Caspase3-7 | 518 | 522 | PF00656 | 0.482 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 548 | 550 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 687 | 689 | PF00675 | 0.549 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 497 | 499 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 548 | 550 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 23 | 25 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 413 | 415 | PF00082 | 0.460 |
CLV_PCSK_PC1ET2_1 | 420 | 422 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 497 | 499 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 527 | 531 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 589 | 593 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 643 | 647 | PF00082 | 0.386 |
DEG_APCC_DBOX_1 | 91 | 99 | PF00400 | 0.592 |
DOC_CKS1_1 | 274 | 279 | PF01111 | 0.453 |
DOC_CYCLIN_RxL_1 | 215 | 224 | PF00134 | 0.427 |
DOC_CYCLIN_RxL_1 | 613 | 625 | PF00134 | 0.441 |
DOC_CYCLIN_yCln2_LP_2 | 321 | 327 | PF00134 | 0.465 |
DOC_MAPK_gen_1 | 670 | 679 | PF00069 | 0.538 |
DOC_MAPK_MEF2A_6 | 255 | 264 | PF00069 | 0.510 |
DOC_PP1_RVXF_1 | 15 | 22 | PF00149 | 0.443 |
DOC_PP1_RVXF_1 | 379 | 386 | PF00149 | 0.421 |
DOC_PP2B_LxvP_1 | 321 | 324 | PF13499 | 0.688 |
DOC_PP2B_LxvP_1 | 512 | 515 | PF13499 | 0.457 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 571 | 575 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 653 | 657 | PF00917 | 0.491 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.414 |
DOC_WW_Pin1_4 | 482 | 487 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.616 |
LIG_14-3-3_CanoR_1 | 107 | 117 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 166 | 171 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 503 | 507 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 527 | 536 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 583 | 589 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 634 | 639 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 643 | 651 | PF00244 | 0.387 |
LIG_Actin_WH2_2 | 428 | 445 | PF00022 | 0.505 |
LIG_BRCT_BRCA1_1 | 605 | 609 | PF00533 | 0.377 |
LIG_CaM_IQ_9 | 77 | 92 | PF13499 | 0.593 |
LIG_Clathr_ClatBox_1 | 608 | 612 | PF01394 | 0.361 |
LIG_EH1_1 | 3 | 11 | PF00400 | 0.551 |
LIG_eIF4E_1 | 363 | 369 | PF01652 | 0.527 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.633 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.610 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.401 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.567 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.572 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.492 |
LIG_FHA_1 | 538 | 544 | PF00498 | 0.383 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.591 |
LIG_FHA_1 | 623 | 629 | PF00498 | 0.425 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.543 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.546 |
LIG_FHA_2 | 526 | 532 | PF00498 | 0.449 |
LIG_FHA_2 | 585 | 591 | PF00498 | 0.454 |
LIG_LIR_Gen_1 | 185 | 196 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 540 | 547 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 623 | 632 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 390 | 396 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 540 | 545 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 623 | 629 | PF02991 | 0.437 |
LIG_NRBOX | 506 | 512 | PF00104 | 0.492 |
LIG_Pex14_2 | 271 | 275 | PF04695 | 0.411 |
LIG_RPA_C_Fungi | 629 | 641 | PF08784 | 0.468 |
LIG_RPA_C_Fungi | 665 | 677 | PF08784 | 0.356 |
LIG_SH2_CRK | 133 | 137 | PF00017 | 0.643 |
LIG_SH2_CRK | 33 | 37 | PF00017 | 0.505 |
LIG_SH2_CRK | 345 | 349 | PF00017 | 0.331 |
LIG_SH2_CRK | 626 | 630 | PF00017 | 0.470 |
LIG_SH2_GRB2like | 207 | 210 | PF00017 | 0.513 |
LIG_SH2_NCK_1 | 170 | 174 | PF00017 | 0.399 |
LIG_SH2_NCK_1 | 33 | 37 | PF00017 | 0.549 |
LIG_SH2_SRC | 343 | 346 | PF00017 | 0.488 |
LIG_SH2_STAP1 | 292 | 296 | PF00017 | 0.415 |
LIG_SH2_STAT3 | 207 | 210 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.589 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 363 | 366 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 578 | 581 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.556 |
LIG_SH3_1 | 133 | 139 | PF00018 | 0.580 |
LIG_SH3_2 | 136 | 141 | PF14604 | 0.577 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.582 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.640 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.382 |
LIG_SUMO_SIM_par_1 | 113 | 121 | PF11976 | 0.526 |
LIG_SUMO_SIM_par_1 | 659 | 665 | PF11976 | 0.373 |
LIG_TRAF2_1 | 158 | 161 | PF00917 | 0.445 |
LIG_TRFH_1 | 440 | 444 | PF08558 | 0.510 |
LIG_UBA3_1 | 379 | 387 | PF00899 | 0.484 |
LIG_UBA3_1 | 9 | 17 | PF00899 | 0.554 |
LIG_WRC_WIRS_1 | 268 | 273 | PF05994 | 0.342 |
MOD_CDK_SPK_2 | 482 | 487 | PF00069 | 0.623 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.748 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.537 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.541 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.456 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.448 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.645 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.678 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.440 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.418 |
MOD_CK2_1 | 525 | 531 | PF00069 | 0.487 |
MOD_CK2_1 | 584 | 590 | PF00069 | 0.476 |
MOD_CK2_1 | 651 | 657 | PF00069 | 0.473 |
MOD_CK2_1 | 681 | 687 | PF00069 | 0.656 |
MOD_GlcNHglycan | 106 | 110 | PF01048 | 0.694 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.453 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.506 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.356 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.578 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.688 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.427 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.631 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.515 |
MOD_GlcNHglycan | 605 | 608 | PF01048 | 0.370 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.670 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.462 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.418 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.536 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.474 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.412 |
MOD_GSK3_1 | 567 | 574 | PF00069 | 0.482 |
MOD_GSK3_1 | 630 | 637 | PF00069 | 0.457 |
MOD_N-GLC_1 | 221 | 226 | PF02516 | 0.526 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.557 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.463 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.682 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.385 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.618 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.515 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.455 |
MOD_NEK2_1 | 520 | 525 | PF00069 | 0.436 |
MOD_NEK2_1 | 621 | 626 | PF00069 | 0.450 |
MOD_NEK2_1 | 630 | 635 | PF00069 | 0.363 |
MOD_NEK2_2 | 584 | 589 | PF00069 | 0.368 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.658 |
MOD_PIKK_1 | 270 | 276 | PF00454 | 0.466 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.592 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.578 |
MOD_PIKK_1 | 40 | 46 | PF00454 | 0.574 |
MOD_PIKK_1 | 537 | 543 | PF00454 | 0.460 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.593 |
MOD_PKA_2 | 442 | 448 | PF00069 | 0.497 |
MOD_PKA_2 | 502 | 508 | PF00069 | 0.358 |
MOD_Plk_1 | 520 | 526 | PF00069 | 0.420 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.464 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.382 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.358 |
MOD_Plk_4 | 520 | 526 | PF00069 | 0.423 |
MOD_Plk_4 | 541 | 547 | PF00069 | 0.386 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.648 |
MOD_Plk_4 | 675 | 681 | PF00069 | 0.529 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.660 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.407 |
MOD_ProDKin_1 | 482 | 488 | PF00069 | 0.680 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.617 |
MOD_SUMO_rev_2 | 684 | 690 | PF00179 | 0.520 |
TRG_DiLeu_BaEn_1 | 73 | 78 | PF01217 | 0.564 |
TRG_DiLeu_BaEn_1 | 94 | 99 | PF01217 | 0.630 |
TRG_DiLeu_BaEn_4 | 73 | 79 | PF01217 | 0.606 |
TRG_DiLeu_BaLyEn_6 | 112 | 117 | PF01217 | 0.529 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 33 | 36 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 626 | 629 | PF00928 | 0.421 |
TRG_ER_diArg_1 | 440 | 443 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 547 | 549 | PF00400 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 206 | 210 | PF00026 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 394 | 398 | PF00026 | 0.521 |
TRG_Pf-PMV_PEXEL_1 | 527 | 531 | PF00026 | 0.454 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE35 | Leptomonas seymouri | 57% | 100% |
A0A1X0NVV3 | Trypanosomatidae | 34% | 100% |
A4I7V9 | Leishmania infantum | 100% | 100% |
D0AA22 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AIV0 | Leishmania braziliensis | 76% | 100% |
E9B2R7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q5E0 | Leishmania major | 88% | 100% |
V5BJJ3 | Trypanosoma cruzi | 35% | 100% |