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: A4HIA7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 237 | 241 | PF00656 | 0.568 |
CLV_C14_Caspase3-7 | 302 | 306 | PF00656 | 0.496 |
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.782 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 452 | 454 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 524 | 526 | PF00675 | 0.749 |
CLV_NRD_NRD_1 | 589 | 591 | PF00675 | 0.431 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.782 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 524 | 526 | PF00082 | 0.706 |
CLV_PCSK_KEX2_1 | 589 | 591 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 603 | 605 | PF00082 | 0.514 |
CLV_PCSK_PC1ET2_1 | 603 | 605 | PF00082 | 0.587 |
CLV_PCSK_PC7_1 | 155 | 161 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.556 |
CLV_Separin_Metazoa | 152 | 156 | PF03568 | 0.329 |
CLV_Separin_Metazoa | 544 | 548 | PF03568 | 0.567 |
CLV_Separin_Metazoa | 654 | 658 | PF03568 | 0.609 |
DEG_APCC_DBOX_1 | 196 | 204 | PF00400 | 0.585 |
DEG_APCC_DBOX_1 | 251 | 259 | PF00400 | 0.413 |
DEG_APCC_DBOX_1 | 401 | 409 | PF00400 | 0.472 |
DEG_APCC_DBOX_1 | 603 | 611 | PF00400 | 0.725 |
DEG_MDM2_SWIB_1 | 463 | 471 | PF02201 | 0.495 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.699 |
DOC_CYCLIN_RxL_1 | 589 | 602 | PF00134 | 0.534 |
DOC_MAPK_DCC_7 | 239 | 248 | PF00069 | 0.375 |
DOC_MAPK_gen_1 | 475 | 481 | PF00069 | 0.346 |
DOC_MAPK_gen_1 | 603 | 610 | PF00069 | 0.675 |
DOC_MAPK_MEF2A_6 | 262 | 270 | PF00069 | 0.286 |
DOC_MAPK_MEF2A_6 | 464 | 473 | PF00069 | 0.459 |
DOC_PP1_RVXF_1 | 172 | 179 | PF00149 | 0.510 |
DOC_PP1_RVXF_1 | 404 | 410 | PF00149 | 0.571 |
DOC_PP1_RVXF_1 | 462 | 468 | PF00149 | 0.419 |
DOC_PP2B_LxvP_1 | 351 | 354 | PF13499 | 0.472 |
DOC_PP2B_LxvP_1 | 408 | 411 | PF13499 | 0.495 |
DOC_PP4_FxxP_1 | 277 | 280 | PF00568 | 0.791 |
DOC_PP4_FxxP_1 | 514 | 517 | PF00568 | 0.747 |
DOC_SPAK_OSR1_1 | 571 | 575 | PF12202 | 0.508 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.757 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.374 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 678 | 683 | PF00397 | 0.711 |
LIG_14-3-3_CanoR_1 | 135 | 144 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 160 | 170 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 2 | 6 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 262 | 267 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 390 | 398 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 425 | 434 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 464 | 468 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 478 | 487 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 519 | 523 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 620 | 626 | PF00244 | 0.713 |
LIG_Actin_RPEL_3 | 200 | 219 | PF02755 | 0.308 |
LIG_Actin_WH2_2 | 374 | 392 | PF00022 | 0.404 |
LIG_BIR_III_2 | 240 | 244 | PF00653 | 0.400 |
LIG_BRCT_BRCA1_1 | 375 | 379 | PF00533 | 0.501 |
LIG_BRCT_BRCA1_1 | 482 | 486 | PF00533 | 0.342 |
LIG_BRCT_BRCA1_2 | 482 | 488 | PF00533 | 0.280 |
LIG_Clathr_ClatBox_1 | 607 | 611 | PF01394 | 0.473 |
LIG_CSL_BTD_1 | 408 | 411 | PF09270 | 0.551 |
LIG_deltaCOP1_diTrp_1 | 568 | 572 | PF00928 | 0.518 |
LIG_eIF4E_1 | 457 | 463 | PF01652 | 0.532 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.589 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.410 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.519 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.315 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.480 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.488 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.392 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.388 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.550 |
LIG_FHA_1 | 557 | 563 | PF00498 | 0.546 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.446 |
LIG_IRF3_LxIS_1 | 359 | 364 | PF10401 | 0.382 |
LIG_LIR_Apic_2 | 275 | 280 | PF02991 | 0.771 |
LIG_LIR_Apic_2 | 513 | 517 | PF02991 | 0.648 |
LIG_LIR_Apic_2 | 664 | 669 | PF02991 | 0.625 |
LIG_LIR_Gen_1 | 265 | 274 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 369 | 379 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 482 | 492 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 265 | 270 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 369 | 375 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 376 | 382 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 482 | 487 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 567 | 572 | PF02991 | 0.447 |
LIG_NRP_CendR_1 | 693 | 696 | PF00754 | 0.544 |
LIG_PAM2_1 | 268 | 280 | PF00658 | 0.436 |
LIG_Pex14_2 | 463 | 467 | PF04695 | 0.481 |
LIG_SH2_CRK | 398 | 402 | PF00017 | 0.539 |
LIG_SH2_CRK | 484 | 488 | PF00017 | 0.500 |
LIG_SH2_STAP1 | 670 | 674 | PF00017 | 0.496 |
LIG_SH2_STAT3 | 412 | 415 | PF00017 | 0.666 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.244 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.700 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.748 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.554 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.553 |
LIG_SH3_3 | 576 | 582 | PF00018 | 0.512 |
LIG_SH3_3 | 671 | 677 | PF00018 | 0.457 |
LIG_SUMO_SIM_anti_2 | 244 | 250 | PF11976 | 0.372 |
LIG_SUMO_SIM_anti_2 | 311 | 317 | PF11976 | 0.383 |
LIG_SUMO_SIM_anti_2 | 33 | 39 | PF11976 | 0.555 |
LIG_SUMO_SIM_par_1 | 606 | 611 | PF11976 | 0.471 |
LIG_TRAF2_1 | 527 | 530 | PF00917 | 0.489 |
LIG_TYR_ITIM | 370 | 375 | PF00017 | 0.366 |
LIG_WRC_WIRS_1 | 154 | 159 | PF05994 | 0.496 |
LIG_WRC_WIRS_1 | 511 | 516 | PF05994 | 0.513 |
MOD_CDK_SPK_2 | 268 | 273 | PF00069 | 0.374 |
MOD_CDK_SPxxK_3 | 678 | 685 | PF00069 | 0.667 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.580 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.469 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.588 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.674 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.476 |
MOD_CK1_1 | 630 | 636 | PF00069 | 0.789 |
MOD_CK1_1 | 643 | 649 | PF00069 | 0.531 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.594 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.588 |
MOD_Cter_Amidation | 693 | 696 | PF01082 | 0.544 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.599 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.401 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.437 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.508 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.394 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.711 |
MOD_GlcNHglycan | 355 | 359 | PF01048 | 0.616 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.593 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.459 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.640 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.469 |
MOD_GlcNHglycan | 629 | 632 | PF01048 | 0.759 |
MOD_GlcNHglycan | 645 | 649 | PF01048 | 0.691 |
MOD_GlcNHglycan | 82 | 86 | PF01048 | 0.631 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.705 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.643 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.344 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.554 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.449 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.712 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.587 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.634 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.635 |
MOD_GSK3_1 | 612 | 619 | PF00069 | 0.668 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.762 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.719 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.719 |
MOD_LATS_1 | 317 | 323 | PF00433 | 0.574 |
MOD_N-GLC_1 | 234 | 239 | PF02516 | 0.466 |
MOD_N-GLC_1 | 275 | 280 | PF02516 | 0.497 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.651 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.420 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.486 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.319 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.533 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.524 |
MOD_PIKK_1 | 40 | 46 | PF00454 | 0.675 |
MOD_PIKK_1 | 499 | 505 | PF00454 | 0.627 |
MOD_PIKK_1 | 640 | 646 | PF00454 | 0.510 |
MOD_PKA_1 | 110 | 116 | PF00069 | 0.772 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.627 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.785 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.510 |
MOD_PKA_2 | 389 | 395 | PF00069 | 0.496 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.476 |
MOD_PKA_2 | 518 | 524 | PF00069 | 0.674 |
MOD_PKA_2 | 616 | 622 | PF00069 | 0.665 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.492 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.759 |
MOD_Plk_2-3 | 234 | 240 | PF00069 | 0.584 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.564 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.343 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.514 |
MOD_Plk_4 | 557 | 563 | PF00069 | 0.686 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.507 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.383 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.476 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.566 |
MOD_ProDKin_1 | 678 | 684 | PF00069 | 0.714 |
TRG_DiLeu_BaEn_1 | 33 | 38 | PF01217 | 0.558 |
TRG_DiLeu_BaEn_1 | 369 | 374 | PF01217 | 0.481 |
TRG_DiLeu_BaEn_2 | 531 | 537 | PF01217 | 0.461 |
TRG_DiLeu_BaLyEn_6 | 333 | 338 | PF01217 | 0.486 |
TRG_DiLeu_BaLyEn_6 | 403 | 408 | PF01217 | 0.437 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.617 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.269 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.528 |
TRG_ENDOCYTIC_2 | 484 | 487 | PF00928 | 0.493 |
TRG_ER_diArg_1 | 110 | 112 | PF00400 | 0.782 |
TRG_ER_diArg_1 | 158 | 160 | PF00400 | 0.365 |
TRG_ER_diArg_1 | 384 | 387 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 451 | 453 | PF00400 | 0.660 |
TRG_ER_diArg_1 | 523 | 525 | PF00400 | 0.718 |
TRG_ER_diArg_1 | 589 | 591 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 688 | 691 | PF00400 | 0.675 |
TRG_NES_CRM1_1 | 365 | 377 | PF08389 | 0.265 |
TRG_Pf-PMV_PEXEL_1 | 336 | 340 | PF00026 | 0.522 |
TRG_Pf-PMV_PEXEL_1 | 453 | 458 | PF00026 | 0.586 |
TRG_Pf-PMV_PEXEL_1 | 657 | 661 | PF00026 | 0.603 |
TRG_Pf-PMV_PEXEL_1 | 66 | 70 | PF00026 | 0.692 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PA41 | Leptomonas seymouri | 45% | 95% |
A0A1X0P203 | Trypanosomatidae | 28% | 100% |
A0A422P4Y6 | Trypanosoma rangeli | 25% | 100% |
A4I5J1 | Leishmania infantum | 75% | 100% |
C9ZQS6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9B0T6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
Q4Q7E2 | Leishmania major | 74% | 100% |
V5BU74 | Trypanosoma cruzi | 25% | 100% |