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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AFH9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 119 | 123 | PF00656 | 0.651 |
CLV_C14_Caspase3-7 | 527 | 531 | PF00656 | 0.674 |
CLV_C14_Caspase3-7 | 736 | 740 | PF00656 | 0.722 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.695 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.565 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.708 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.565 |
CLV_PCSK_PC1ET2_1 | 175 | 177 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.670 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 745 | 749 | PF00082 | 0.704 |
DEG_APCC_DBOX_1 | 97 | 105 | PF00400 | 0.660 |
DEG_SCF_FBW7_1 | 495 | 502 | PF00400 | 0.814 |
DEG_SPOP_SBC_1 | 601 | 605 | PF00917 | 0.696 |
DOC_CKS1_1 | 686 | 691 | PF01111 | 0.719 |
DOC_CYCLIN_RxL_1 | 81 | 94 | PF00134 | 0.604 |
DOC_MAPK_DCC_7 | 602 | 611 | PF00069 | 0.574 |
DOC_MAPK_gen_1 | 369 | 378 | PF00069 | 0.646 |
DOC_MAPK_MEF2A_6 | 602 | 611 | PF00069 | 0.718 |
DOC_SPAK_OSR1_1 | 13 | 17 | PF12202 | 0.421 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.808 |
DOC_USP7_MATH_1 | 512 | 516 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 528 | 532 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 536 | 540 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 596 | 600 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 607 | 611 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 621 | 625 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 636 | 640 | PF00917 | 0.796 |
DOC_USP7_MATH_1 | 654 | 658 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 673 | 677 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 692 | 696 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 713 | 717 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 731 | 735 | PF00917 | 0.583 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 495 | 500 | PF00397 | 0.777 |
DOC_WW_Pin1_4 | 501 | 506 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 680 | 685 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 688 | 693 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 697 | 702 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 724 | 729 | PF00397 | 0.790 |
LIG_14-3-3_CanoR_1 | 13 | 17 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 234 | 243 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 292 | 298 | PF00244 | 0.631 |
LIG_14-3-3_CanoR_1 | 311 | 316 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 352 | 360 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 602 | 607 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 653 | 659 | PF00244 | 0.793 |
LIG_Actin_WH2_2 | 106 | 123 | PF00022 | 0.650 |
LIG_Actin_WH2_2 | 171 | 188 | PF00022 | 0.634 |
LIG_Actin_WH2_2 | 18 | 33 | PF00022 | 0.561 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.714 |
LIG_BRCT_BRCA1_1 | 430 | 434 | PF00533 | 0.713 |
LIG_BRCT_BRCA1_1 | 520 | 524 | PF00533 | 0.724 |
LIG_DLG_GKlike_1 | 412 | 419 | PF00625 | 0.717 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.657 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.536 |
LIG_FHA_1 | 646 | 652 | PF00498 | 0.746 |
LIG_FHA_2 | 161 | 167 | PF00498 | 0.547 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.675 |
LIG_GBD_Chelix_1 | 260 | 268 | PF00786 | 0.408 |
LIG_LIR_Gen_1 | 223 | 232 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 415 | 422 | PF02991 | 0.724 |
LIG_LIR_Gen_1 | 431 | 441 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 223 | 228 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 415 | 419 | PF02991 | 0.722 |
LIG_LIR_Nem_3 | 584 | 590 | PF02991 | 0.578 |
LIG_MYND_1 | 495 | 499 | PF01753 | 0.599 |
LIG_PCNA_yPIPBox_3 | 17 | 29 | PF02747 | 0.519 |
LIG_Rb_LxCxE_1 | 439 | 454 | PF01857 | 0.664 |
LIG_SH2_NCK_1 | 726 | 730 | PF00017 | 0.818 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.680 |
LIG_SH2_STAT5 | 696 | 699 | PF00017 | 0.728 |
LIG_SH2_STAT5 | 726 | 729 | PF00017 | 0.727 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.659 |
LIG_SH3_3 | 648 | 654 | PF00018 | 0.796 |
LIG_SH3_3 | 683 | 689 | PF00018 | 0.828 |
LIG_SUMO_SIM_anti_2 | 464 | 471 | PF11976 | 0.653 |
LIG_SUMO_SIM_par_1 | 116 | 123 | PF11976 | 0.650 |
LIG_TRAF2_1 | 123 | 126 | PF00917 | 0.490 |
LIG_TRAF2_1 | 159 | 162 | PF00917 | 0.673 |
LIG_TRAF2_2 | 728 | 733 | PF00917 | 0.824 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.569 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.724 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.649 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.699 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.792 |
MOD_CK1_1 | 504 | 510 | PF00069 | 0.825 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.655 |
MOD_CK1_1 | 632 | 638 | PF00069 | 0.823 |
MOD_CK1_1 | 695 | 701 | PF00069 | 0.789 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.562 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.573 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.670 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.595 |
MOD_CK2_1 | 602 | 608 | PF00069 | 0.629 |
MOD_CK2_1 | 654 | 660 | PF00069 | 0.677 |
MOD_CK2_1 | 662 | 668 | PF00069 | 0.600 |
MOD_CK2_1 | 731 | 737 | PF00069 | 0.722 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.400 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.540 |
MOD_GlcNHglycan | 40 | 44 | PF01048 | 0.615 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.738 |
MOD_GlcNHglycan | 444 | 448 | PF01048 | 0.535 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.768 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.636 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.676 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.623 |
MOD_GlcNHglycan | 506 | 509 | PF01048 | 0.748 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.746 |
MOD_GlcNHglycan | 598 | 601 | PF01048 | 0.745 |
MOD_GlcNHglycan | 634 | 637 | PF01048 | 0.814 |
MOD_GlcNHglycan | 640 | 643 | PF01048 | 0.760 |
MOD_GlcNHglycan | 675 | 678 | PF01048 | 0.802 |
MOD_GlcNHglycan | 711 | 714 | PF01048 | 0.772 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.756 |
MOD_GlcNHglycan | 745 | 748 | PF01048 | 0.703 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.411 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.592 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.547 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.648 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.768 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.702 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.814 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.604 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.598 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.784 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.809 |
MOD_GSK3_1 | 630 | 637 | PF00069 | 0.732 |
MOD_GSK3_1 | 654 | 661 | PF00069 | 0.673 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.769 |
MOD_GSK3_1 | 705 | 712 | PF00069 | 0.798 |
MOD_GSK3_1 | 713 | 720 | PF00069 | 0.726 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.528 |
MOD_LATS_1 | 627 | 633 | PF00433 | 0.732 |
MOD_N-GLC_1 | 331 | 336 | PF02516 | 0.678 |
MOD_N-GLC_1 | 420 | 425 | PF02516 | 0.667 |
MOD_N-GLC_1 | 458 | 463 | PF02516 | 0.665 |
MOD_N-GLC_1 | 629 | 634 | PF02516 | 0.758 |
MOD_N-GLC_1 | 731 | 736 | PF02516 | 0.645 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.544 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.568 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.666 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.463 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.603 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.699 |
MOD_NEK2_1 | 517 | 522 | PF00069 | 0.812 |
MOD_NEK2_1 | 705 | 710 | PF00069 | 0.774 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.567 |
MOD_NEK2_2 | 391 | 396 | PF00069 | 0.754 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.661 |
MOD_PIKK_1 | 279 | 285 | PF00454 | 0.410 |
MOD_PIKK_1 | 611 | 617 | PF00454 | 0.805 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.563 |
MOD_PKA_1 | 412 | 418 | PF00069 | 0.703 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.656 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.585 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.566 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.562 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.629 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.591 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.552 |
MOD_PKA_2 | 379 | 385 | PF00069 | 0.639 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.735 |
MOD_PKA_2 | 601 | 607 | PF00069 | 0.689 |
MOD_PKB_1 | 234 | 242 | PF00069 | 0.560 |
MOD_Plk_1 | 399 | 405 | PF00069 | 0.693 |
MOD_Plk_1 | 607 | 613 | PF00069 | 0.712 |
MOD_Plk_1 | 645 | 651 | PF00069 | 0.725 |
MOD_Plk_1 | 91 | 97 | PF00069 | 0.563 |
MOD_Plk_2-3 | 662 | 668 | PF00069 | 0.732 |
MOD_Plk_2-3 | 733 | 739 | PF00069 | 0.814 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.557 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.558 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.765 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.740 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.557 |
MOD_Plk_4 | 645 | 651 | PF00069 | 0.798 |
MOD_Plk_4 | 692 | 698 | PF00069 | 0.721 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.643 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.568 |
MOD_ProDKin_1 | 495 | 501 | PF00069 | 0.781 |
MOD_ProDKin_1 | 680 | 686 | PF00069 | 0.768 |
MOD_ProDKin_1 | 688 | 694 | PF00069 | 0.690 |
MOD_ProDKin_1 | 697 | 703 | PF00069 | 0.641 |
MOD_ProDKin_1 | 724 | 730 | PF00069 | 0.792 |
MOD_SUMO_for_1 | 132 | 135 | PF00179 | 0.668 |
MOD_SUMO_rev_2 | 704 | 710 | PF00179 | 0.774 |
TRG_DiLeu_BaEn_1 | 24 | 29 | PF01217 | 0.546 |
TRG_DiLeu_BaEn_1 | 281 | 286 | PF01217 | 0.652 |
TRG_ENDOCYTIC_2 | 416 | 419 | PF00928 | 0.724 |
TRG_ER_diArg_1 | 127 | 130 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 185 | 187 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 412 | 414 | PF00400 | 0.740 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I179 | Leptomonas seymouri | 40% | 96% |
A0A3Q8IFD3 | Leishmania donovani | 88% | 100% |
A4HN24 | Leishmania braziliensis | 64% | 100% |
A4IBP4 | Leishmania infantum | 88% | 100% |
E9B6N4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |