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: Q4QGH1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 118 | 122 | PF00656 | 0.709 |
CLV_C14_Caspase3-7 | 123 | 127 | PF00656 | 0.701 |
CLV_C14_Caspase3-7 | 168 | 172 | PF00656 | 0.579 |
CLV_C14_Caspase3-7 | 197 | 201 | PF00656 | 0.634 |
CLV_C14_Caspase3-7 | 479 | 483 | PF00656 | 0.583 |
CLV_C14_Caspase3-7 | 498 | 502 | PF00656 | 0.738 |
CLV_C14_Caspase3-7 | 731 | 735 | PF00656 | 0.570 |
CLV_C14_Caspase3-7 | 790 | 794 | PF00656 | 0.479 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.669 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.746 |
CLV_NRD_NRD_1 | 822 | 824 | PF00675 | 0.664 |
CLV_NRD_NRD_1 | 855 | 857 | PF00675 | 0.610 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.758 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 762 | 764 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.746 |
CLV_PCSK_KEX2_1 | 821 | 823 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 857 | 859 | PF00082 | 0.592 |
CLV_PCSK_PC1ET2_1 | 190 | 192 | PF00082 | 0.628 |
CLV_PCSK_PC1ET2_1 | 762 | 764 | PF00082 | 0.577 |
CLV_PCSK_PC1ET2_1 | 857 | 859 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 445 | 449 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 763 | 767 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.733 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 857 | 861 | PF00082 | 0.683 |
DEG_SCF_FBW7_1 | 545 | 552 | PF00400 | 0.544 |
DEG_SPOP_SBC_1 | 549 | 553 | PF00917 | 0.560 |
DEG_SPOP_SBC_1 | 679 | 683 | PF00917 | 0.734 |
DEG_SPOP_SBC_1 | 702 | 706 | PF00917 | 0.506 |
DOC_CYCLIN_RxL_1 | 75 | 83 | PF00134 | 0.740 |
DOC_CYCLIN_yClb1_LxF_4 | 806 | 812 | PF00134 | 0.650 |
DOC_CYCLIN_yCln2_LP_2 | 374 | 380 | PF00134 | 0.727 |
DOC_CYCLIN_yCln2_LP_2 | 398 | 401 | PF00134 | 0.544 |
DOC_MAPK_gen_1 | 762 | 771 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 632 | 641 | PF00069 | 0.511 |
DOC_PP2B_LxvP_1 | 398 | 401 | PF13499 | 0.544 |
DOC_PP2B_LxvP_1 | 639 | 642 | PF13499 | 0.462 |
DOC_PP4_FxxP_1 | 422 | 425 | PF00568 | 0.398 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 500 | 504 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 508 | 512 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 680 | 684 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 701 | 705 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 845 | 849 | PF00917 | 0.732 |
DOC_USP7_UBL2_3 | 217 | 221 | PF12436 | 0.538 |
DOC_USP7_UBL2_3 | 4 | 8 | PF12436 | 0.630 |
DOC_USP7_UBL2_3 | 762 | 766 | PF12436 | 0.532 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.752 |
DOC_WW_Pin1_4 | 421 | 426 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 511 | 516 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 738 | 743 | PF00397 | 0.627 |
LIG_14-3-3_CanoR_1 | 260 | 270 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 607 | 611 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 770 | 776 | PF00244 | 0.507 |
LIG_Actin_WH2_2 | 439 | 456 | PF00022 | 0.504 |
LIG_Actin_WH2_2 | 587 | 605 | PF00022 | 0.553 |
LIG_APCC_ABBA_1 | 867 | 872 | PF00400 | 0.670 |
LIG_CaM_IQ_9 | 226 | 242 | PF13499 | 0.495 |
LIG_deltaCOP1_diTrp_1 | 644 | 652 | PF00928 | 0.431 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.656 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.719 |
LIG_FHA_1 | 584 | 590 | PF00498 | 0.541 |
LIG_FHA_1 | 711 | 717 | PF00498 | 0.481 |
LIG_FHA_1 | 739 | 745 | PF00498 | 0.590 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.736 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.728 |
LIG_FHA_2 | 389 | 395 | PF00498 | 0.495 |
LIG_FHA_2 | 477 | 483 | PF00498 | 0.552 |
LIG_FHA_2 | 496 | 502 | PF00498 | 0.656 |
LIG_FHA_2 | 565 | 571 | PF00498 | 0.603 |
LIG_FHA_2 | 788 | 794 | PF00498 | 0.403 |
LIG_Integrin_isoDGR_2 | 622 | 624 | PF01839 | 0.639 |
LIG_LIR_Apic_2 | 644 | 650 | PF02991 | 0.532 |
LIG_LIR_Apic_2 | 661 | 667 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 12 | 23 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 442 | 451 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 114 | 119 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 161 | 166 | PF02991 | 0.658 |
LIG_LIR_Nem_3 | 431 | 436 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 442 | 446 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 514 | 520 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 646 | 651 | PF02991 | 0.433 |
LIG_LYPXL_yS_3 | 875 | 878 | PF13949 | 0.675 |
LIG_PALB2_WD40_1 | 643 | 651 | PF16756 | 0.532 |
LIG_Pex14_2 | 11 | 15 | PF04695 | 0.500 |
LIG_Pex14_2 | 648 | 652 | PF04695 | 0.429 |
LIG_PROFILIN_1 | 670 | 676 | PF00235 | 0.534 |
LIG_SH2_CRK | 664 | 668 | PF00017 | 0.587 |
LIG_SH2_NCK_1 | 147 | 151 | PF00017 | 0.668 |
LIG_SH2_SRC | 747 | 750 | PF00017 | 0.461 |
LIG_SH2_STAP1 | 747 | 751 | PF00017 | 0.455 |
LIG_SH2_STAT3 | 243 | 246 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.707 |
LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 452 | 455 | PF00017 | 0.594 |
LIG_SH2_STAT5 | 712 | 715 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 727 | 730 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 784 | 787 | PF00017 | 0.543 |
LIG_SH3_1 | 664 | 670 | PF00018 | 0.703 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.577 |
LIG_SH3_3 | 424 | 430 | PF00018 | 0.442 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.549 |
LIG_SH3_3 | 512 | 518 | PF00018 | 0.572 |
LIG_SH3_3 | 559 | 565 | PF00018 | 0.642 |
LIG_SH3_3 | 647 | 653 | PF00018 | 0.441 |
LIG_SH3_3 | 664 | 670 | PF00018 | 0.632 |
LIG_SH3_3 | 671 | 677 | PF00018 | 0.652 |
LIG_SH3_3 | 695 | 701 | PF00018 | 0.708 |
LIG_SUMO_SIM_anti_2 | 394 | 400 | PF11976 | 0.455 |
LIG_TRAF2_1 | 568 | 571 | PF00917 | 0.592 |
LIG_TRFH_1 | 147 | 151 | PF08558 | 0.572 |
LIG_WW_1 | 144 | 147 | PF00397 | 0.745 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.661 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.746 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.623 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.588 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.790 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.624 |
MOD_CK1_1 | 580 | 586 | PF00069 | 0.549 |
MOD_CK1_1 | 681 | 687 | PF00069 | 0.778 |
MOD_CK1_1 | 704 | 710 | PF00069 | 0.617 |
MOD_CK1_1 | 733 | 739 | PF00069 | 0.624 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.656 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.731 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.539 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.509 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.609 |
MOD_CK2_1 | 564 | 570 | PF00069 | 0.616 |
MOD_CK2_1 | 680 | 686 | PF00069 | 0.690 |
MOD_CK2_1 | 691 | 697 | PF00069 | 0.621 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.561 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.550 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.536 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.720 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.657 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.735 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.707 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.756 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.616 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.439 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.576 |
MOD_GlcNHglycan | 509 | 513 | PF01048 | 0.549 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.704 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.558 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.595 |
MOD_GlcNHglycan | 660 | 663 | PF01048 | 0.737 |
MOD_GlcNHglycan | 683 | 686 | PF01048 | 0.696 |
MOD_GlcNHglycan | 693 | 696 | PF01048 | 0.796 |
MOD_GlcNHglycan | 734 | 738 | PF01048 | 0.741 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.713 |
MOD_GlcNHglycan | 833 | 836 | PF01048 | 0.795 |
MOD_GlcNHglycan | 847 | 850 | PF01048 | 0.556 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.597 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.704 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.543 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.539 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.558 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.537 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.721 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.618 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.482 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.569 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.473 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.397 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.662 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.596 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.542 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.595 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.367 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.475 |
MOD_GSK3_1 | 703 | 710 | PF00069 | 0.619 |
MOD_GSK3_1 | 771 | 778 | PF00069 | 0.419 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.659 |
MOD_N-GLC_1 | 472 | 477 | PF02516 | 0.625 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.654 |
MOD_N-GLC_1 | 800 | 805 | PF02516 | 0.559 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.662 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.467 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.426 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.359 |
MOD_NEK2_1 | 581 | 586 | PF00069 | 0.545 |
MOD_NEK2_1 | 610 | 615 | PF00069 | 0.446 |
MOD_NEK2_1 | 643 | 648 | PF00069 | 0.454 |
MOD_NEK2_1 | 771 | 776 | PF00069 | 0.579 |
MOD_PIKK_1 | 347 | 353 | PF00454 | 0.622 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.656 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.563 |
MOD_PKA_2 | 560 | 566 | PF00069 | 0.595 |
MOD_PKA_2 | 606 | 612 | PF00069 | 0.578 |
MOD_PKA_2 | 710 | 716 | PF00069 | 0.542 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.692 |
MOD_Plk_1 | 508 | 514 | PF00069 | 0.685 |
MOD_Plk_1 | 643 | 649 | PF00069 | 0.407 |
MOD_Plk_1 | 800 | 806 | PF00069 | 0.510 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.641 |
MOD_Plk_4 | 577 | 583 | PF00069 | 0.538 |
MOD_Plk_4 | 606 | 612 | PF00069 | 0.533 |
MOD_Plk_4 | 643 | 649 | PF00069 | 0.407 |
MOD_Plk_4 | 747 | 753 | PF00069 | 0.437 |
MOD_Plk_4 | 784 | 790 | PF00069 | 0.407 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.753 |
MOD_ProDKin_1 | 421 | 427 | PF00069 | 0.526 |
MOD_ProDKin_1 | 474 | 480 | PF00069 | 0.667 |
MOD_ProDKin_1 | 511 | 517 | PF00069 | 0.657 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.667 |
MOD_ProDKin_1 | 738 | 744 | PF00069 | 0.612 |
MOD_SUMO_for_1 | 31 | 34 | PF00179 | 0.653 |
MOD_SUMO_rev_2 | 850 | 859 | PF00179 | 0.754 |
TRG_DiLeu_BaEn_1 | 394 | 399 | PF01217 | 0.455 |
TRG_DiLeu_BaEn_1 | 863 | 868 | PF01217 | 0.664 |
TRG_DiLeu_BaLyEn_6 | 369 | 374 | PF01217 | 0.718 |
TRG_DiLeu_BaLyEn_6 | 585 | 590 | PF01217 | 0.472 |
TRG_DiLeu_BaLyEn_6 | 621 | 626 | PF01217 | 0.613 |
TRG_ENDOCYTIC_2 | 875 | 878 | PF00928 | 0.557 |
TRG_ER_diArg_1 | 163 | 165 | PF00400 | 0.679 |
TRG_ER_diArg_1 | 181 | 183 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 76 | 78 | PF00400 | 0.755 |
TRG_ER_diArg_1 | 821 | 823 | PF00400 | 0.748 |
TRG_ER_diArg_1 | 856 | 859 | PF00400 | 0.670 |
TRG_NLS_MonoExtN_4 | 856 | 861 | PF00514 | 0.576 |
TRG_Pf-PMV_PEXEL_1 | 183 | 187 | PF00026 | 0.653 |
TRG_Pf-PMV_PEXEL_1 | 588 | 593 | PF00026 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 624 | 629 | PF00026 | 0.434 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IHU8 | Leishmania donovani | 86% | 100% |
A4H6Z8 | Leishmania braziliensis | 68% | 100% |
C9ZI14 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AGI2 | Leishmania infantum | 86% | 100% |
E9AP18 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |