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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: E9B6K3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 597 | 601 | PF00656 | 0.787 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.666 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 616 | 618 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 640 | 642 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 704 | 706 | PF00675 | 0.754 |
CLV_NRD_NRD_1 | 730 | 732 | PF00675 | 0.683 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 500 | 502 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 616 | 618 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 640 | 642 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 703 | 705 | PF00082 | 0.791 |
CLV_PCSK_KEX2_1 | 730 | 732 | PF00082 | 0.681 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.574 |
CLV_PCSK_PC1ET2_1 | 425 | 427 | PF00082 | 0.614 |
CLV_PCSK_PC7_1 | 612 | 618 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 674 | 678 | PF00082 | 0.736 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.617 |
CLV_Separin_Metazoa | 577 | 581 | PF03568 | 0.775 |
DEG_APCC_DBOX_1 | 140 | 148 | PF00400 | 0.631 |
DEG_APCC_DBOX_1 | 189 | 197 | PF00400 | 0.574 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.631 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 401 | 410 | PF00134 | 0.593 |
DOC_MAPK_gen_1 | 260 | 268 | PF00069 | 0.477 |
DOC_MAPK_gen_1 | 730 | 738 | PF00069 | 0.716 |
DOC_MIT_MIM_1 | 369 | 377 | PF04212 | 0.443 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 570 | 574 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 598 | 602 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 719 | 723 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 724 | 728 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 752 | 756 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 758 | 762 | PF00917 | 0.606 |
DOC_USP7_UBL2_3 | 105 | 109 | PF12436 | 0.631 |
DOC_WW_Pin1_4 | 601 | 606 | PF00397 | 0.476 |
LIG_14-3-3_CanoR_1 | 261 | 267 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 55 | 59 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 563 | 571 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 572 | 577 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 696 | 702 | PF00244 | 0.815 |
LIG_APCC_ABBAyCdc20_2 | 263 | 269 | PF00400 | 0.494 |
LIG_BRCT_BRCA1_1 | 721 | 725 | PF00533 | 0.486 |
LIG_Clathr_ClatBox_1 | 193 | 197 | PF01394 | 0.577 |
LIG_deltaCOP1_diTrp_1 | 429 | 438 | PF00928 | 0.448 |
LIG_deltaCOP1_diTrp_1 | 772 | 782 | PF00928 | 0.718 |
LIG_DLG_GKlike_1 | 572 | 579 | PF00625 | 0.430 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.580 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.660 |
LIG_FHA_1 | 594 | 600 | PF00498 | 0.735 |
LIG_FHA_1 | 781 | 787 | PF00498 | 0.600 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.550 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.698 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.579 |
LIG_FHA_2 | 595 | 601 | PF00498 | 0.745 |
LIG_KLC1_Yacidic_2 | 223 | 228 | PF13176 | 0.502 |
LIG_LIR_Gen_1 | 170 | 179 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 781 | 788 | PF02991 | 0.643 |
LIG_LIR_Nem_3 | 170 | 174 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 484 | 488 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 781 | 785 | PF02991 | 0.642 |
LIG_NRBOX | 86 | 92 | PF00104 | 0.633 |
LIG_PCNA_PIPBox_1 | 293 | 302 | PF02747 | 0.612 |
LIG_Pex14_1 | 431 | 435 | PF04695 | 0.444 |
LIG_RPA_C_Fungi | 50 | 62 | PF08784 | 0.551 |
LIG_SH2_SRC | 226 | 229 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 171 | 175 | PF00017 | 0.567 |
LIG_SH2_STAP1 | 345 | 349 | PF00017 | 0.634 |
LIG_SH2_STAP1 | 574 | 578 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 66 | 70 | PF00017 | 0.507 |
LIG_SH2_STAT3 | 440 | 443 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.617 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.297 |
LIG_SH3_3 | 581 | 587 | PF00018 | 0.785 |
LIG_SH3_3 | 713 | 719 | PF00018 | 0.692 |
LIG_TRAF2_1 | 208 | 211 | PF00917 | 0.577 |
LIG_TRAF2_1 | 283 | 286 | PF00917 | 0.540 |
LIG_TRAF2_1 | 301 | 304 | PF00917 | 0.363 |
LIG_TRAF2_1 | 316 | 319 | PF00917 | 0.515 |
LIG_TRAF2_1 | 418 | 421 | PF00917 | 0.597 |
LIG_TRAF2_1 | 448 | 451 | PF00917 | 0.522 |
LIG_TRAF2_1 | 80 | 83 | PF00917 | 0.461 |
MOD_CK1_1 | 601 | 607 | PF00069 | 0.555 |
MOD_CK1_1 | 765 | 771 | PF00069 | 0.658 |
MOD_CK1_1 | 778 | 784 | PF00069 | 0.739 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.539 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.563 |
MOD_CK2_1 | 31 | 37 | PF00069 | 0.547 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.478 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.570 |
MOD_CK2_1 | 424 | 430 | PF00069 | 0.517 |
MOD_CK2_1 | 768 | 774 | PF00069 | 0.761 |
MOD_Cter_Amidation | 351 | 354 | PF01082 | 0.460 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.478 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.537 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.550 |
MOD_GlcNHglycan | 30 | 36 | PF01048 | 0.505 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.788 |
MOD_GlcNHglycan | 635 | 638 | PF01048 | 0.761 |
MOD_GlcNHglycan | 667 | 670 | PF01048 | 0.676 |
MOD_GlcNHglycan | 721 | 724 | PF01048 | 0.645 |
MOD_GlcNHglycan | 777 | 780 | PF01048 | 0.716 |
MOD_GlcNHglycan | 92 | 96 | PF01048 | 0.714 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.513 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.594 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.551 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.790 |
MOD_GSK3_1 | 719 | 726 | PF00069 | 0.498 |
MOD_GSK3_1 | 753 | 760 | PF00069 | 0.650 |
MOD_GSK3_1 | 786 | 793 | PF00069 | 0.642 |
MOD_N-GLC_1 | 601 | 606 | PF02516 | 0.618 |
MOD_N-GLC_1 | 762 | 767 | PF02516 | 0.742 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.586 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.601 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.549 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.561 |
MOD_NEK2_1 | 631 | 636 | PF00069 | 0.490 |
MOD_NEK2_1 | 665 | 670 | PF00069 | 0.658 |
MOD_NEK2_1 | 677 | 682 | PF00069 | 0.717 |
MOD_NEK2_1 | 791 | 796 | PF00069 | 0.678 |
MOD_PIKK_1 | 205 | 211 | PF00454 | 0.575 |
MOD_PIKK_1 | 377 | 383 | PF00454 | 0.584 |
MOD_PIKK_1 | 394 | 400 | PF00454 | 0.448 |
MOD_PIKK_1 | 40 | 46 | PF00454 | 0.630 |
MOD_PIKK_1 | 518 | 524 | PF00454 | 0.581 |
MOD_PIKK_1 | 564 | 570 | PF00454 | 0.634 |
MOD_PIKK_1 | 762 | 768 | PF00454 | 0.670 |
MOD_PIKK_1 | 792 | 798 | PF00454 | 0.651 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.588 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.607 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.429 |
MOD_PKA_2 | 611 | 617 | PF00069 | 0.781 |
MOD_PKA_2 | 697 | 703 | PF00069 | 0.777 |
MOD_PKA_2 | 729 | 735 | PF00069 | 0.754 |
MOD_Plk_1 | 196 | 202 | PF00069 | 0.600 |
MOD_Plk_1 | 245 | 251 | PF00069 | 0.601 |
MOD_Plk_1 | 411 | 417 | PF00069 | 0.568 |
MOD_Plk_1 | 708 | 714 | PF00069 | 0.724 |
MOD_Plk_1 | 762 | 768 | PF00069 | 0.694 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.627 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.495 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.327 |
MOD_ProDKin_1 | 601 | 607 | PF00069 | 0.481 |
MOD_SUMO_for_1 | 62 | 65 | PF00179 | 0.537 |
MOD_SUMO_rev_2 | 30 | 35 | PF00179 | 0.541 |
MOD_SUMO_rev_2 | 65 | 71 | PF00179 | 0.546 |
TRG_DiLeu_BaEn_1 | 143 | 148 | PF01217 | 0.536 |
TRG_DiLeu_BaEn_1 | 189 | 194 | PF01217 | 0.572 |
TRG_DiLeu_BaEn_1 | 236 | 241 | PF01217 | 0.565 |
TRG_DiLeu_BaEn_1 | 366 | 371 | PF01217 | 0.442 |
TRG_DiLeu_BaEn_4 | 82 | 88 | PF01217 | 0.340 |
TRG_DiLeu_LyEn_5 | 189 | 194 | PF01217 | 0.572 |
TRG_DiLeu_LyEn_5 | 236 | 241 | PF01217 | 0.591 |
TRG_ENDOCYTIC_2 | 171 | 174 | PF00928 | 0.568 |
TRG_ER_diArg_1 | 120 | 122 | PF00400 | 0.661 |
TRG_ER_diArg_1 | 22 | 24 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 260 | 263 | PF00400 | 0.610 |
TRG_ER_diArg_1 | 435 | 437 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 499 | 502 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 616 | 618 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 702 | 705 | PF00400 | 0.782 |
TRG_ER_diArg_1 | 730 | 733 | PF00400 | 0.693 |
TRG_ER_diArg_1 | 738 | 741 | PF00400 | 0.728 |
TRG_NES_CRM1_1 | 455 | 470 | PF08389 | 0.547 |
TRG_NES_CRM1_1 | 553 | 568 | PF08389 | 0.616 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.625 |
TRG_Pf-PMV_PEXEL_1 | 192 | 197 | PF00026 | 0.541 |
TRG_Pf-PMV_PEXEL_1 | 239 | 244 | PF00026 | 0.571 |
TRG_Pf-PMV_PEXEL_1 | 408 | 412 | PF00026 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 472 | 477 | PF00026 | 0.549 |
TRG_Pf-PMV_PEXEL_1 | 652 | 656 | PF00026 | 0.619 |
TRG_Pf-PMV_PEXEL_1 | 88 | 92 | PF00026 | 0.645 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJW5 | Leptomonas seymouri | 58% | 82% |
A0A0S4IKJ1 | Bodo saltans | 33% | 100% |
A0A1X0P6F2 | Trypanosomatidae | 36% | 92% |
A0A3Q8IIH8 | Leishmania donovani | 90% | 100% |
A0A422MWV3 | Trypanosoma rangeli | 33% | 95% |
A4HMZ1 | Leishmania braziliensis | 77% | 100% |
A4IBL5 | Leishmania infantum | 89% | 100% |
C9ZZ25 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 92% |
E9AFE8 | Leishmania major | 88% | 100% |
V5BCX8 | Trypanosoma cruzi | 32% | 95% |