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: E9AEJ5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 432 | 436 | PF00656 | 0.476 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 524 | 526 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 663 | 665 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 707 | 709 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 715 | 717 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 738 | 740 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 806 | 808 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 834 | 836 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.537 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 391 | 393 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 662 | 664 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 707 | 709 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 715 | 717 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 806 | 808 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 818 | 820 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 876 | 878 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.588 |
CLV_PCSK_PC1ET2_1 | 391 | 393 | PF00082 | 0.505 |
CLV_PCSK_PC1ET2_1 | 662 | 664 | PF00082 | 0.561 |
CLV_PCSK_PC1ET2_1 | 707 | 709 | PF00082 | 0.562 |
CLV_PCSK_PC1ET2_1 | 715 | 717 | PF00082 | 0.566 |
CLV_PCSK_PC1ET2_1 | 818 | 820 | PF00082 | 0.591 |
CLV_PCSK_PC1ET2_1 | 876 | 878 | PF00082 | 0.626 |
CLV_PCSK_PC7_1 | 872 | 878 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 525 | 529 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 757 | 761 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 775 | 779 | PF00082 | 0.535 |
CLV_Separin_Metazoa | 351 | 355 | PF03568 | 0.503 |
CLV_Separin_Metazoa | 669 | 673 | PF03568 | 0.427 |
DEG_APCC_DBOX_1 | 524 | 532 | PF00400 | 0.665 |
DEG_APCC_DBOX_1 | 566 | 574 | PF00400 | 0.476 |
DEG_APCC_DBOX_1 | 756 | 764 | PF00400 | 0.569 |
DEG_APCC_DBOX_1 | 89 | 97 | PF00400 | 0.569 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.444 |
DOC_CYCLIN_RxL_1 | 523 | 533 | PF00134 | 0.567 |
DOC_CYCLIN_RxL_1 | 772 | 782 | PF00134 | 0.522 |
DOC_MAPK_gen_1 | 662 | 670 | PF00069 | 0.456 |
DOC_MAPK_gen_1 | 842 | 849 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 2 | 9 | PF00069 | 0.431 |
DOC_MAPK_MEF2A_6 | 471 | 479 | PF00069 | 0.599 |
DOC_MAPK_MEF2A_6 | 615 | 623 | PF00069 | 0.545 |
DOC_MAPK_MEF2A_6 | 818 | 825 | PF00069 | 0.578 |
DOC_MAPK_NFAT4_5 | 818 | 826 | PF00069 | 0.578 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 675 | 679 | PF00917 | 0.603 |
DOC_USP7_UBL2_3 | 68 | 72 | PF12436 | 0.526 |
LIG_14-3-3_CanoR_1 | 202 | 206 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 268 | 278 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 392 | 398 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 513 | 521 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 525 | 531 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 615 | 623 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 766 | 774 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 835 | 845 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 863 | 871 | PF00244 | 0.638 |
LIG_Actin_WH2_2 | 33 | 50 | PF00022 | 0.601 |
LIG_Actin_WH2_2 | 827 | 844 | PF00022 | 0.498 |
LIG_APCC_ABBA_1 | 845 | 850 | PF00400 | 0.671 |
LIG_BRCT_BRCA1_1 | 656 | 660 | PF00533 | 0.571 |
LIG_BRCT_BRCA1_2 | 656 | 662 | PF00533 | 0.511 |
LIG_Clathr_ClatBox_1 | 384 | 388 | PF01394 | 0.580 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.522 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.533 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.576 |
LIG_FHA_1 | 632 | 638 | PF00498 | 0.472 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.508 |
LIG_FHA_2 | 313 | 319 | PF00498 | 0.574 |
LIG_FHA_2 | 518 | 524 | PF00498 | 0.689 |
LIG_FHA_2 | 638 | 644 | PF00498 | 0.488 |
LIG_FHA_2 | 654 | 660 | PF00498 | 0.501 |
LIG_FHA_2 | 671 | 677 | PF00498 | 0.383 |
LIG_FHA_2 | 771 | 777 | PF00498 | 0.530 |
LIG_GBD_Chelix_1 | 113 | 121 | PF00786 | 0.432 |
LIG_GBD_Chelix_1 | 813 | 821 | PF00786 | 0.588 |
LIG_LIR_Gen_1 | 12 | 22 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 172 | 180 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 371 | 381 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 403 | 411 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 424 | 433 | PF02991 | 0.602 |
LIG_LIR_Gen_1 | 469 | 479 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 73 | 84 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 11 | 16 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 172 | 176 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 371 | 376 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 403 | 408 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 424 | 430 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 469 | 475 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 73 | 79 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 800 | 805 | PF02991 | 0.496 |
LIG_NRBOX | 572 | 578 | PF00104 | 0.551 |
LIG_NRBOX | 773 | 779 | PF00104 | 0.527 |
LIG_PCNA_yPIPBox_3 | 28 | 36 | PF02747 | 0.626 |
LIG_Pex14_2 | 9 | 13 | PF04695 | 0.433 |
LIG_SH2_CRK | 795 | 799 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 173 | 177 | PF00017 | 0.499 |
LIG_SH2_STAP1 | 380 | 384 | PF00017 | 0.469 |
LIG_SH2_STAT3 | 131 | 134 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 721 | 724 | PF00017 | 0.546 |
LIG_SUMO_SIM_anti_2 | 3 | 9 | PF11976 | 0.428 |
LIG_SUMO_SIM_anti_2 | 666 | 674 | PF11976 | 0.459 |
LIG_SUMO_SIM_anti_2 | 697 | 706 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 328 | 336 | PF11976 | 0.575 |
LIG_SUMO_SIM_par_1 | 475 | 481 | PF11976 | 0.346 |
LIG_SUMO_SIM_par_1 | 634 | 641 | PF11976 | 0.469 |
LIG_TRAF2_1 | 429 | 432 | PF00917 | 0.476 |
LIG_TRAF2_1 | 64 | 67 | PF00917 | 0.534 |
LIG_UBA3_1 | 384 | 391 | PF00899 | 0.621 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.428 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.549 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.485 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.568 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.709 |
MOD_CK1_1 | 517 | 523 | PF00069 | 0.671 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.492 |
MOD_CK1_1 | 695 | 701 | PF00069 | 0.548 |
MOD_CK1_1 | 769 | 775 | PF00069 | 0.552 |
MOD_CK1_1 | 826 | 832 | PF00069 | 0.556 |
MOD_CK1_1 | 878 | 884 | PF00069 | 0.733 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.546 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.635 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.708 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.619 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.562 |
MOD_CK2_1 | 517 | 523 | PF00069 | 0.626 |
MOD_CK2_1 | 526 | 532 | PF00069 | 0.528 |
MOD_CK2_1 | 621 | 627 | PF00069 | 0.494 |
MOD_CK2_1 | 637 | 643 | PF00069 | 0.441 |
MOD_CK2_1 | 770 | 776 | PF00069 | 0.509 |
MOD_CK2_1 | 878 | 884 | PF00069 | 0.676 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.441 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.431 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.649 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.728 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.695 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.576 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.687 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.614 |
MOD_GlcNHglycan | 743 | 746 | PF01048 | 0.524 |
MOD_GlcNHglycan | 757 | 760 | PF01048 | 0.370 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.551 |
MOD_GlcNHglycan | 850 | 853 | PF01048 | 0.640 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.562 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.515 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.590 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.619 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.522 |
MOD_GSK3_1 | 621 | 628 | PF00069 | 0.491 |
MOD_GSK3_1 | 633 | 640 | PF00069 | 0.487 |
MOD_GSK3_1 | 654 | 661 | PF00069 | 0.607 |
MOD_GSK3_1 | 698 | 705 | PF00069 | 0.518 |
MOD_GSK3_1 | 762 | 769 | PF00069 | 0.562 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.488 |
MOD_GSK3_1 | 826 | 833 | PF00069 | 0.551 |
MOD_GSK3_1 | 837 | 844 | PF00069 | 0.522 |
MOD_GSK3_1 | 875 | 882 | PF00069 | 0.738 |
MOD_LATS_1 | 390 | 396 | PF00433 | 0.495 |
MOD_LATS_1 | 873 | 879 | PF00433 | 0.733 |
MOD_N-GLC_1 | 220 | 225 | PF02516 | 0.661 |
MOD_N-GLC_1 | 239 | 244 | PF02516 | 0.503 |
MOD_N-GLC_1 | 421 | 426 | PF02516 | 0.585 |
MOD_N-GLC_1 | 594 | 599 | PF02516 | 0.651 |
MOD_N-GLC_1 | 652 | 657 | PF02516 | 0.599 |
MOD_N-GLC_1 | 837 | 842 | PF02516 | 0.572 |
MOD_N-GLC_1 | 864 | 869 | PF02516 | 0.646 |
MOD_N-GLC_2 | 512 | 514 | PF02516 | 0.578 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.613 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.515 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.544 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.600 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.533 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.663 |
MOD_NEK2_1 | 576 | 581 | PF00069 | 0.550 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.565 |
MOD_NEK2_1 | 658 | 663 | PF00069 | 0.574 |
MOD_NEK2_1 | 841 | 846 | PF00069 | 0.627 |
MOD_NEK2_1 | 848 | 853 | PF00069 | 0.684 |
MOD_PIKK_1 | 130 | 136 | PF00454 | 0.442 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.647 |
MOD_PIKK_1 | 360 | 366 | PF00454 | 0.600 |
MOD_PIKK_1 | 530 | 536 | PF00454 | 0.594 |
MOD_PIKK_1 | 692 | 698 | PF00454 | 0.492 |
MOD_PIKK_1 | 823 | 829 | PF00454 | 0.492 |
MOD_PKA_1 | 192 | 198 | PF00069 | 0.522 |
MOD_PKA_1 | 20 | 26 | PF00069 | 0.445 |
MOD_PKA_1 | 391 | 397 | PF00069 | 0.585 |
MOD_PKA_1 | 708 | 714 | PF00069 | 0.534 |
MOD_PKA_1 | 875 | 881 | PF00069 | 0.738 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.593 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.585 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.550 |
MOD_PKA_2 | 514 | 520 | PF00069 | 0.646 |
MOD_PKA_2 | 548 | 554 | PF00069 | 0.580 |
MOD_PKA_2 | 614 | 620 | PF00069 | 0.550 |
MOD_PKA_2 | 876 | 882 | PF00069 | 0.553 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.659 |
MOD_Plk_1 | 337 | 343 | PF00069 | 0.629 |
MOD_Plk_1 | 371 | 377 | PF00069 | 0.571 |
MOD_Plk_1 | 517 | 523 | PF00069 | 0.660 |
MOD_Plk_1 | 594 | 600 | PF00069 | 0.655 |
MOD_Plk_1 | 769 | 775 | PF00069 | 0.544 |
MOD_Plk_1 | 837 | 843 | PF00069 | 0.577 |
MOD_Plk_2-3 | 770 | 776 | PF00069 | 0.506 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.428 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.532 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.649 |
MOD_Plk_4 | 698 | 704 | PF00069 | 0.596 |
MOD_SUMO_for_1 | 117 | 120 | PF00179 | 0.539 |
MOD_SUMO_for_1 | 178 | 181 | PF00179 | 0.363 |
MOD_SUMO_for_1 | 236 | 239 | PF00179 | 0.582 |
MOD_SUMO_for_1 | 71 | 74 | PF00179 | 0.573 |
MOD_SUMO_for_1 | 854 | 857 | PF00179 | 0.672 |
MOD_SUMO_rev_2 | 181 | 187 | PF00179 | 0.367 |
MOD_SUMO_rev_2 | 62 | 71 | PF00179 | 0.589 |
MOD_SUMO_rev_2 | 691 | 701 | PF00179 | 0.481 |
MOD_SUMO_rev_2 | 729 | 738 | PF00179 | 0.559 |
MOD_SUMO_rev_2 | 758 | 765 | PF00179 | 0.572 |
MOD_SUMO_rev_2 | 811 | 820 | PF00179 | 0.595 |
TRG_DiLeu_BaEn_1 | 572 | 577 | PF01217 | 0.551 |
TRG_DiLeu_BaEn_1 | 780 | 785 | PF01217 | 0.500 |
TRG_DiLeu_BaEn_3 | 65 | 71 | PF01217 | 0.405 |
TRG_DiLeu_BaEn_4 | 238 | 244 | PF01217 | 0.585 |
TRG_DiLeu_BaEn_4 | 586 | 592 | PF01217 | 0.681 |
TRG_DiLeu_BaEn_4 | 66 | 72 | PF01217 | 0.403 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 795 | 798 | PF00928 | 0.438 |
TRG_ER_diArg_1 | 107 | 110 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 805 | 807 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 89 | 91 | PF00400 | 0.600 |
TRG_NES_CRM1_1 | 111 | 126 | PF08389 | 0.492 |
TRG_NES_CRM1_1 | 815 | 828 | PF08389 | 0.589 |
TRG_NLS_MonoExtN_4 | 872 | 879 | PF00514 | 0.618 |
TRG_Pf-PMV_PEXEL_1 | 143 | 147 | PF00026 | 0.589 |
TRG_Pf-PMV_PEXEL_1 | 259 | 264 | PF00026 | 0.655 |
TRG_Pf-PMV_PEXEL_1 | 269 | 273 | PF00026 | 0.526 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBM4 | Leptomonas seymouri | 55% | 100% |
A0A1X0NIX3 | Trypanosomatidae | 30% | 100% |
A0A3Q8IHM9 | Leishmania donovani | 91% | 100% |
A0A422N7K6 | Trypanosoma rangeli | 31% | 100% |
A4HM57 | Leishmania braziliensis | 76% | 100% |
A4IAR9 | Leishmania infantum | 91% | 100% |
D0A2E3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9B5Q6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |