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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HZX6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 115 | 119 | PF00656 | 0.404 |
CLV_C14_Caspase3-7 | 135 | 139 | PF00656 | 0.260 |
CLV_MEL_PAP_1 | 203 | 209 | PF00089 | 0.530 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.791 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 613 | 615 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 648 | 650 | PF00675 | 0.780 |
CLV_NRD_NRD_1 | 658 | 660 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.475 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.706 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 594 | 596 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 613 | 615 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 648 | 650 | PF00082 | 0.780 |
CLV_PCSK_KEX2_1 | 658 | 660 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.415 |
CLV_PCSK_PC1ET2_1 | 155 | 157 | PF00082 | 0.407 |
CLV_PCSK_PC1ET2_1 | 3 | 5 | PF00082 | 0.609 |
CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.444 |
CLV_PCSK_PC1ET2_1 | 594 | 596 | PF00082 | 0.723 |
CLV_PCSK_PC1ET2_1 | 80 | 82 | PF00082 | 0.415 |
CLV_PCSK_PC7_1 | 590 | 596 | PF00082 | 0.692 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 521 | 525 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 628 | 632 | PF00082 | 0.763 |
CLV_PCSK_SKI1_1 | 658 | 662 | PF00082 | 0.720 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.431 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.642 |
DEG_SPOP_SBC_1 | 619 | 623 | PF00917 | 0.744 |
DOC_MAPK_gen_1 | 166 | 175 | PF00069 | 0.576 |
DOC_MAPK_gen_1 | 352 | 359 | PF00069 | 0.524 |
DOC_MAPK_gen_1 | 362 | 369 | PF00069 | 0.422 |
DOC_MAPK_MEF2A_6 | 188 | 196 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 90 | 99 | PF00069 | 0.537 |
DOC_PP1_RVXF_1 | 104 | 110 | PF00149 | 0.381 |
DOC_PP4_FxxP_1 | 160 | 163 | PF00568 | 0.457 |
DOC_PP4_FxxP_1 | 583 | 586 | PF00568 | 0.592 |
DOC_SPAK_OSR1_1 | 206 | 210 | PF12202 | 0.537 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 619 | 623 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 647 | 651 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 652 | 656 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 668 | 672 | PF00917 | 0.510 |
DOC_USP7_UBL2_3 | 235 | 239 | PF12436 | 0.548 |
DOC_USP7_UBL2_3 | 295 | 299 | PF12436 | 0.564 |
DOC_USP7_UBL2_3 | 503 | 507 | PF12436 | 0.634 |
DOC_USP7_UBL2_3 | 80 | 84 | PF12436 | 0.412 |
DOC_WW_Pin1_4 | 613 | 618 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 630 | 635 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 640 | 645 | PF00397 | 0.751 |
LIG_14-3-3_CanoR_1 | 188 | 193 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 269 | 275 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 314 | 322 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 384 | 392 | PF00244 | 0.708 |
LIG_14-3-3_CanoR_1 | 4 | 8 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 658 | 667 | PF00244 | 0.644 |
LIG_14-3-3_CterR_2 | 676 | 678 | PF00244 | 0.677 |
LIG_Actin_WH2_2 | 299 | 315 | PF00022 | 0.593 |
LIG_Actin_WH2_2 | 8 | 23 | PF00022 | 0.459 |
LIG_Actin_WH2_2 | 96 | 113 | PF00022 | 0.374 |
LIG_AP2alpha_2 | 471 | 473 | PF02296 | 0.523 |
LIG_BRCT_BRCA1_1 | 243 | 247 | PF00533 | 0.547 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.552 |
LIG_FHA_1 | 565 | 571 | PF00498 | 0.561 |
LIG_FHA_1 | 607 | 613 | PF00498 | 0.694 |
LIG_FHA_1 | 662 | 668 | PF00498 | 0.722 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.546 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.488 |
LIG_FHA_2 | 316 | 322 | PF00498 | 0.501 |
LIG_FHA_2 | 428 | 434 | PF00498 | 0.657 |
LIG_LIR_Apic_2 | 157 | 163 | PF02991 | 0.446 |
LIG_LIR_Apic_2 | 467 | 472 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 112 | 121 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 24 | 30 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 470 | 481 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 112 | 117 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 30 | 35 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 37 | 43 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 470 | 476 | PF02991 | 0.630 |
LIG_LIR_Nem_3 | 486 | 490 | PF02991 | 0.636 |
LIG_LIR_Nem_3 | 553 | 558 | PF02991 | 0.695 |
LIG_RPA_C_Fungi | 129 | 141 | PF08784 | 0.541 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.479 |
LIG_SH2_CRK | 487 | 491 | PF00017 | 0.628 |
LIG_SH2_NCK_1 | 469 | 473 | PF00017 | 0.538 |
LIG_SH2_SRC | 469 | 472 | PF00017 | 0.538 |
LIG_SH2_STAP1 | 237 | 241 | PF00017 | 0.558 |
LIG_SH2_STAP1 | 491 | 495 | PF00017 | 0.544 |
LIG_SH2_STAP1 | 574 | 578 | PF00017 | 0.676 |
LIG_SH2_STAT3 | 341 | 344 | PF00017 | 0.592 |
LIG_SH2_STAT3 | 505 | 508 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 505 | 508 | PF00017 | 0.703 |
LIG_SH2_STAT5 | 554 | 557 | PF00017 | 0.581 |
LIG_SH3_3 | 559 | 565 | PF00018 | 0.703 |
LIG_SUMO_SIM_anti_2 | 301 | 308 | PF11976 | 0.505 |
LIG_SUMO_SIM_par_1 | 95 | 101 | PF11976 | 0.517 |
LIG_TRAF2_1 | 318 | 321 | PF00917 | 0.654 |
LIG_TRAF2_1 | 430 | 433 | PF00917 | 0.566 |
LIG_UBA3_1 | 587 | 594 | PF00899 | 0.659 |
MOD_CDC14_SPxK_1 | 633 | 636 | PF00782 | 0.714 |
MOD_CDK_SPxK_1 | 630 | 636 | PF00069 | 0.703 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.370 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.532 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.446 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.562 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.748 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.655 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.682 |
MOD_CK1_1 | 608 | 614 | PF00069 | 0.647 |
MOD_CK1_1 | 622 | 628 | PF00069 | 0.750 |
MOD_CK1_1 | 671 | 677 | PF00069 | 0.589 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.490 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.527 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.405 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.545 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.482 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.503 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.697 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.455 |
MOD_Cter_Amidation | 381 | 384 | PF01082 | 0.608 |
MOD_Cter_Amidation | 501 | 504 | PF01082 | 0.582 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.430 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.460 |
MOD_GlcNHglycan | 242 | 246 | PF01048 | 0.511 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.553 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.663 |
MOD_GlcNHglycan | 393 | 397 | PF01048 | 0.651 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.690 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.658 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.574 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.645 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.792 |
MOD_GlcNHglycan | 624 | 627 | PF01048 | 0.718 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.506 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.696 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.608 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.680 |
MOD_GSK3_1 | 613 | 620 | PF00069 | 0.645 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.650 |
MOD_GSK3_1 | 667 | 674 | PF00069 | 0.544 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.580 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.495 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.458 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.365 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.559 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.666 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.592 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.639 |
MOD_NEK2_1 | 618 | 623 | PF00069 | 0.752 |
MOD_NEK2_2 | 472 | 477 | PF00069 | 0.558 |
MOD_NEK2_2 | 527 | 532 | PF00069 | 0.656 |
MOD_PIKK_1 | 112 | 118 | PF00454 | 0.393 |
MOD_PIKK_1 | 382 | 388 | PF00454 | 0.733 |
MOD_PIKK_1 | 414 | 420 | PF00454 | 0.648 |
MOD_PK_1 | 3 | 9 | PF00069 | 0.439 |
MOD_PKA_1 | 3 | 9 | PF00069 | 0.439 |
MOD_PKA_1 | 503 | 509 | PF00069 | 0.596 |
MOD_PKA_1 | 658 | 664 | PF00069 | 0.648 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.512 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.476 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.499 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.559 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.724 |
MOD_PKA_2 | 647 | 653 | PF00069 | 0.759 |
MOD_PKA_2 | 658 | 664 | PF00069 | 0.578 |
MOD_Plk_1 | 171 | 177 | PF00069 | 0.642 |
MOD_Plk_1 | 652 | 658 | PF00069 | 0.555 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.455 |
MOD_Plk_4 | 538 | 544 | PF00069 | 0.672 |
MOD_Plk_4 | 662 | 668 | PF00069 | 0.605 |
MOD_ProDKin_1 | 613 | 619 | PF00069 | 0.638 |
MOD_ProDKin_1 | 630 | 636 | PF00069 | 0.547 |
MOD_ProDKin_1 | 640 | 646 | PF00069 | 0.753 |
MOD_SUMO_for_1 | 221 | 224 | PF00179 | 0.561 |
MOD_SUMO_for_1 | 298 | 301 | PF00179 | 0.605 |
MOD_SUMO_for_1 | 363 | 366 | PF00179 | 0.569 |
MOD_SUMO_for_1 | 593 | 596 | PF00179 | 0.655 |
MOD_SUMO_rev_2 | 569 | 578 | PF00179 | 0.662 |
MOD_SUMO_rev_2 | 86 | 92 | PF00179 | 0.575 |
TRG_DiLeu_BaEn_1 | 279 | 284 | PF01217 | 0.522 |
TRG_DiLeu_BaEn_4 | 320 | 326 | PF01217 | 0.558 |
TRG_DiLeu_BaLyEn_6 | 583 | 588 | PF01217 | 0.697 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.563 |
TRG_ENDOCYTIC_2 | 487 | 490 | PF00928 | 0.594 |
TRG_ER_diArg_1 | 106 | 109 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 19 | 22 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 312 | 314 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 612 | 614 | PF00400 | 0.650 |
TRG_ER_diArg_1 | 648 | 651 | PF00400 | 0.788 |
TRG_ER_diArg_1 | 658 | 660 | PF00400 | 0.693 |
TRG_NES_CRM1_1 | 198 | 213 | PF08389 | 0.537 |
TRG_NES_CRM1_1 | 358 | 371 | PF08389 | 0.581 |
TRG_NLS_MonoExtC_3 | 79 | 84 | PF00514 | 0.461 |
TRG_NLS_MonoExtN_4 | 454 | 460 | PF00514 | 0.457 |
TRG_NLS_MonoExtN_4 | 80 | 85 | PF00514 | 0.549 |
TRG_Pf-PMV_PEXEL_1 | 108 | 112 | PF00026 | 0.495 |
TRG_Pf-PMV_PEXEL_1 | 134 | 138 | PF00026 | 0.547 |
TRG_Pf-PMV_PEXEL_1 | 346 | 350 | PF00026 | 0.634 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8W6 | Leptomonas seymouri | 66% | 100% |
A0A0S4KMX4 | Bodo saltans | 45% | 100% |
A0A1X0NU00 | Trypanosomatidae | 54% | 100% |
A0A3S7WXA7 | Leishmania donovani | 99% | 100% |
A0A422MU25 | Trypanosoma rangeli | 54% | 100% |
A4HCC0 | Leishmania braziliensis | 83% | 99% |
C9ZSL5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E9AVT6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QBP3 | Leishmania major | 95% | 100% |