Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 1 |
Forrest at al. (metacyclic) | no | yes: 3 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 36 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | yes | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 2, no: 103 |
NetGPI | no | yes: 0, no: 105 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0005856 | cytoskeleton | 5 | 1 |
GO:0020016 | ciliary pocket | 2 | 1 |
GO:0020038 | subpellicular network | 2 | 1 |
GO:0030863 | cortical cytoskeleton | 6 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0005929 | cilium | 4 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
Related structures:
AlphaFold database: Q4Q6M4
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 106 |
GO:0006807 | nitrogen compound metabolic process | 2 | 106 |
GO:0008152 | metabolic process | 1 | 106 |
GO:0019538 | protein metabolic process | 3 | 106 |
GO:0043170 | macromolecule metabolic process | 3 | 106 |
GO:0044238 | primary metabolic process | 2 | 106 |
GO:0071704 | organic substance metabolic process | 2 | 106 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 106 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 106 |
GO:0004175 | endopeptidase activity | 4 | 106 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 106 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 106 |
GO:0008233 | peptidase activity | 3 | 106 |
GO:0008234 | cysteine-type peptidase activity | 4 | 106 |
GO:0016787 | hydrolase activity | 2 | 106 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 106 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 646 | 650 | PF00656 | 0.617 |
CLV_C14_Caspase3-7 | 726 | 730 | PF00656 | 0.498 |
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.361 |
CLV_PCSK_FUR_1 | 177 | 181 | PF00082 | 0.696 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.319 |
CLV_PCSK_KEX2_1 | 472 | 474 | PF00082 | 0.352 |
CLV_PCSK_KEX2_1 | 617 | 619 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 798 | 800 | PF00082 | 0.549 |
CLV_PCSK_PC1ET2_1 | 179 | 181 | PF00082 | 0.665 |
CLV_PCSK_PC1ET2_1 | 289 | 291 | PF00082 | 0.473 |
CLV_PCSK_PC1ET2_1 | 617 | 619 | PF00082 | 0.350 |
CLV_PCSK_PC1ET2_1 | 798 | 800 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.722 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 741 | 745 | PF00082 | 0.536 |
DEG_MDM2_SWIB_1 | 643 | 651 | PF02201 | 0.537 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.478 |
DEG_SCF_FBW7_1 | 208 | 214 | PF00400 | 0.252 |
DEG_SCF_FBW7_1 | 58 | 63 | PF00400 | 0.529 |
DEG_SCF_FBW7_2 | 196 | 201 | PF00400 | 0.253 |
DOC_CKS1_1 | 109 | 114 | PF01111 | 0.747 |
DOC_CKS1_1 | 208 | 213 | PF01111 | 0.270 |
DOC_CKS1_1 | 543 | 548 | PF01111 | 0.542 |
DOC_CKS1_1 | 662 | 667 | PF01111 | 0.510 |
DOC_CKS1_1 | 828 | 833 | PF01111 | 0.468 |
DOC_MAPK_FxFP_2 | 82 | 85 | PF00069 | 0.541 |
DOC_MAPK_gen_1 | 472 | 478 | PF00069 | 0.536 |
DOC_MAPK_MEF2A_6 | 223 | 230 | PF00069 | 0.314 |
DOC_PIKK_1 | 298 | 305 | PF02985 | 0.584 |
DOC_PP1_RVXF_1 | 739 | 746 | PF00149 | 0.489 |
DOC_PP1_RVXF_1 | 792 | 798 | PF00149 | 0.431 |
DOC_PP2B_LxvP_1 | 147 | 150 | PF13499 | 0.570 |
DOC_PP4_FxxP_1 | 418 | 421 | PF00568 | 0.553 |
DOC_PP4_FxxP_1 | 765 | 768 | PF00568 | 0.340 |
DOC_PP4_FxxP_1 | 82 | 85 | PF00568 | 0.777 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.789 |
DOC_USP7_MATH_1 | 680 | 684 | PF00917 | 0.449 |
DOC_USP7_UBL2_3 | 122 | 126 | PF12436 | 0.737 |
DOC_USP7_UBL2_3 | 175 | 179 | PF12436 | 0.640 |
DOC_USP7_UBL2_3 | 277 | 281 | PF12436 | 0.382 |
DOC_USP7_UBL2_3 | 481 | 485 | PF12436 | 0.545 |
DOC_USP7_UBL2_3 | 617 | 621 | PF12436 | 0.564 |
DOC_USP7_UBL2_3 | 794 | 798 | PF12436 | 0.393 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.270 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.807 |
DOC_WW_Pin1_4 | 542 | 547 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.821 |
DOC_WW_Pin1_4 | 632 | 637 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 661 | 666 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 759 | 764 | PF00397 | 0.398 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 827 | 832 | PF00397 | 0.442 |
LIG_14-3-3_CanoR_1 | 180 | 186 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 364 | 369 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 419 | 429 | PF00244 | 0.538 |
LIG_APCC_ABBAyCdc20_2 | 290 | 296 | PF00400 | 0.629 |
LIG_BIR_III_4 | 408 | 412 | PF00653 | 0.617 |
LIG_BIR_III_4 | 519 | 523 | PF00653 | 0.440 |
LIG_BRCT_BRCA1_1 | 761 | 765 | PF00533 | 0.466 |
LIG_CSL_BTD_1 | 367 | 370 | PF09270 | 0.590 |
LIG_CSL_BTD_1 | 445 | 448 | PF09270 | 0.602 |
LIG_deltaCOP1_diTrp_1 | 607 | 612 | PF00928 | 0.543 |
LIG_deltaCOP1_diTrp_1 | 646 | 654 | PF00928 | 0.551 |
LIG_eIF4E_1 | 569 | 575 | PF01652 | 0.568 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.515 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.657 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.643 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.429 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.425 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.546 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.615 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.728 |
LIG_FHA_1 | 640 | 646 | PF00498 | 0.575 |
LIG_FHA_2 | 509 | 515 | PF00498 | 0.514 |
LIG_FHA_2 | 543 | 549 | PF00498 | 0.510 |
LIG_FHA_2 | 635 | 641 | PF00498 | 0.553 |
LIG_FHA_2 | 820 | 826 | PF00498 | 0.526 |
LIG_IRF3_LxIS_1 | 24 | 29 | PF10401 | 0.490 |
LIG_LIR_Apic_2 | 416 | 421 | PF02991 | 0.554 |
LIG_LIR_Apic_2 | 762 | 768 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 480 | 491 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 511 | 520 | PF02991 | 0.540 |
LIG_LIR_Gen_1 | 525 | 534 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 566 | 576 | PF02991 | 0.568 |
LIG_LIR_Gen_1 | 585 | 596 | PF02991 | 0.571 |
LIG_LIR_Gen_1 | 692 | 702 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 708 | 719 | PF02991 | 0.456 |
LIG_LIR_LC3C_4 | 255 | 260 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 212 | 218 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 291 | 297 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 344 | 348 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 480 | 486 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 489 | 493 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 503 | 508 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 511 | 516 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 585 | 591 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 616 | 622 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 664 | 669 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 692 | 698 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 708 | 714 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 762 | 767 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 796 | 800 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 849 | 853 | PF02991 | 0.547 |
LIG_LYPXL_yS_3 | 622 | 625 | PF13949 | 0.506 |
LIG_MLH1_MIPbox_1 | 761 | 765 | PF16413 | 0.485 |
LIG_MYND_1 | 114 | 118 | PF01753 | 0.704 |
LIG_Pex14_2 | 442 | 446 | PF04695 | 0.601 |
LIG_Pex14_2 | 643 | 647 | PF04695 | 0.543 |
LIG_PTB_Apo_2 | 624 | 631 | PF02174 | 0.566 |
LIG_PTB_Phospho_1 | 624 | 630 | PF10480 | 0.444 |
LIG_SH2_CRK | 483 | 487 | PF00017 | 0.541 |
LIG_SH2_CRK | 490 | 494 | PF00017 | 0.542 |
LIG_SH2_CRK | 580 | 584 | PF00017 | 0.555 |
LIG_SH2_CRK | 711 | 715 | PF00017 | 0.464 |
LIG_SH2_CRK | 755 | 759 | PF00017 | 0.513 |
LIG_SH2_GRB2like | 151 | 154 | PF00017 | 0.599 |
LIG_SH2_GRB2like | 217 | 220 | PF00017 | 0.494 |
LIG_SH2_GRB2like | 490 | 493 | PF00017 | 0.527 |
LIG_SH2_NCK_1 | 490 | 494 | PF00017 | 0.565 |
LIG_SH2_PTP2 | 140 | 143 | PF00017 | 0.599 |
LIG_SH2_PTP2 | 2 | 5 | PF00017 | 0.476 |
LIG_SH2_PTP2 | 695 | 698 | PF00017 | 0.502 |
LIG_SH2_PTP2 | 88 | 91 | PF00017 | 0.788 |
LIG_SH2_SRC | 140 | 143 | PF00017 | 0.659 |
LIG_SH2_SRC | 490 | 493 | PF00017 | 0.519 |
LIG_SH2_STAP1 | 224 | 228 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 490 | 494 | PF00017 | 0.549 |
LIG_SH2_STAP1 | 513 | 517 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 2 | 5 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 398 | 401 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 587 | 590 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 695 | 698 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 755 | 758 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 764 | 767 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 779 | 782 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 788 | 791 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.777 |
LIG_SH3_2 | 93 | 98 | PF14604 | 0.790 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.802 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.567 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.388 |
LIG_SH3_3 | 495 | 501 | PF00018 | 0.501 |
LIG_SH3_3 | 595 | 601 | PF00018 | 0.512 |
LIG_SH3_3 | 685 | 691 | PF00018 | 0.461 |
LIG_SH3_3 | 733 | 739 | PF00018 | 0.512 |
LIG_SH3_3 | 772 | 778 | PF00018 | 0.579 |
LIG_SH3_3 | 828 | 834 | PF00018 | 0.440 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.689 |
LIG_SH3_4 | 738 | 745 | PF00018 | 0.349 |
LIG_SH3_5 | 665 | 669 | PF00018 | 0.487 |
LIG_SUMO_SIM_par_1 | 24 | 29 | PF11976 | 0.490 |
LIG_SUMO_SIM_par_1 | 447 | 453 | PF11976 | 0.521 |
LIG_TYR_ITIM | 292 | 297 | PF00017 | 0.389 |
LIG_TYR_ITIM | 709 | 714 | PF00017 | 0.542 |
LIG_UBA3_1 | 169 | 175 | PF00899 | 0.416 |
LIG_WRC_WIRS_1 | 513 | 518 | PF05994 | 0.449 |
LIG_WRC_WIRS_1 | 810 | 815 | PF05994 | 0.513 |
LIG_WW_1 | 148 | 151 | PF00397 | 0.601 |
LIG_WW_1 | 85 | 88 | PF00397 | 0.789 |
LIG_WW_3 | 141 | 145 | PF00397 | 0.654 |
MOD_CDC14_SPxK_1 | 63 | 66 | PF00782 | 0.528 |
MOD_CDK_SPK_2 | 827 | 832 | PF00069 | 0.595 |
MOD_CDK_SPxK_1 | 60 | 66 | PF00069 | 0.528 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.704 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.468 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.397 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.432 |
MOD_CK1_1 | 606 | 612 | PF00069 | 0.439 |
MOD_CK1_1 | 689 | 695 | PF00069 | 0.524 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.591 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.393 |
MOD_CK2_1 | 731 | 737 | PF00069 | 0.477 |
MOD_CK2_1 | 819 | 825 | PF00069 | 0.558 |
MOD_CMANNOS | 644 | 647 | PF00535 | 0.387 |
MOD_Cter_Amidation | 722 | 725 | PF01082 | 0.617 |
MOD_DYRK1A_RPxSP_1 | 108 | 112 | PF00069 | 0.803 |
MOD_GlcNHglycan | 253 | 257 | PF01048 | 0.409 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.470 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.372 |
MOD_GlcNHglycan | 408 | 412 | PF01048 | 0.391 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.404 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.393 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.377 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.599 |
MOD_GlcNHglycan | 654 | 657 | PF01048 | 0.396 |
MOD_GlcNHglycan | 688 | 691 | PF01048 | 0.615 |
MOD_GlcNHglycan | 721 | 724 | PF01048 | 0.528 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.695 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.568 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.474 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.482 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.687 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.371 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.583 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.636 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.416 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.685 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.370 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.377 |
MOD_GSK3_1 | 809 | 816 | PF00069 | 0.483 |
MOD_N-GLC_1 | 152 | 157 | PF02516 | 0.609 |
MOD_N-GLC_1 | 170 | 175 | PF02516 | 0.565 |
MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.396 |
MOD_N-GLC_1 | 603 | 608 | PF02516 | 0.436 |
MOD_N-GLC_1 | 686 | 691 | PF02516 | 0.502 |
MOD_N-GLC_1 | 745 | 750 | PF02516 | 0.479 |
MOD_N-GLC_2 | 627 | 629 | PF02516 | 0.494 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.713 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.488 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.470 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.395 |
MOD_NEK2_1 | 714 | 719 | PF00069 | 0.390 |
MOD_NEK2_1 | 728 | 733 | PF00069 | 0.544 |
MOD_NEK2_1 | 753 | 758 | PF00069 | 0.443 |
MOD_NEK2_1 | 784 | 789 | PF00069 | 0.426 |
MOD_NEK2_1 | 813 | 818 | PF00069 | 0.571 |
MOD_NEK2_1 | 819 | 824 | PF00069 | 0.591 |
MOD_NEK2_2 | 343 | 348 | PF00069 | 0.437 |
MOD_PIKK_1 | 384 | 390 | PF00454 | 0.443 |
MOD_PIKK_1 | 696 | 702 | PF00454 | 0.472 |
MOD_PK_1 | 621 | 627 | PF00069 | 0.409 |
MOD_PKA_1 | 617 | 623 | PF00069 | 0.468 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.328 |
MOD_PKA_2 | 617 | 623 | PF00069 | 0.452 |
MOD_PKA_2 | 719 | 725 | PF00069 | 0.502 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.728 |
MOD_Plk_1 | 100 | 106 | PF00069 | 0.696 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.529 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.386 |
MOD_Plk_1 | 479 | 485 | PF00069 | 0.479 |
MOD_Plk_1 | 565 | 571 | PF00069 | 0.490 |
MOD_Plk_1 | 639 | 645 | PF00069 | 0.368 |
MOD_Plk_2-3 | 161 | 167 | PF00069 | 0.491 |
MOD_Plk_2-3 | 317 | 323 | PF00069 | 0.465 |
MOD_Plk_2-3 | 705 | 711 | PF00069 | 0.579 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.663 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.404 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.408 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.417 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.417 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.374 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.405 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.418 |
MOD_Plk_4 | 714 | 720 | PF00069 | 0.439 |
MOD_Plk_4 | 731 | 737 | PF00069 | 0.529 |
MOD_Plk_4 | 753 | 759 | PF00069 | 0.513 |
MOD_Plk_4 | 784 | 790 | PF00069 | 0.455 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.757 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.432 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.270 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.644 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.806 |
MOD_ProDKin_1 | 542 | 548 | PF00069 | 0.407 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.819 |
MOD_ProDKin_1 | 632 | 638 | PF00069 | 0.468 |
MOD_ProDKin_1 | 661 | 667 | PF00069 | 0.524 |
MOD_ProDKin_1 | 759 | 765 | PF00069 | 0.393 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.694 |
MOD_ProDKin_1 | 827 | 833 | PF00069 | 0.448 |
MOD_SUMO_for_1 | 793 | 796 | PF00179 | 0.427 |
MOD_SUMO_rev_2 | 155 | 165 | PF00179 | 0.566 |
MOD_SUMO_rev_2 | 316 | 325 | PF00179 | 0.535 |
TRG_DiLeu_BaEn_1 | 264 | 269 | PF01217 | 0.458 |
TRG_DiLeu_BaEn_1 | 570 | 575 | PF01217 | 0.475 |
TRG_DiLeu_BaEn_1 | 710 | 715 | PF01217 | 0.556 |
TRG_DiLeu_BaLyEn_6 | 591 | 596 | PF01217 | 0.459 |
TRG_ENDOCYTIC_2 | 2 | 5 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 490 | 493 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 513 | 516 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 534 | 537 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 569 | 572 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 580 | 583 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 622 | 625 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 695 | 698 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 711 | 714 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 755 | 758 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 764 | 767 | PF00928 | 0.398 |
TRG_ER_diArg_1 | 143 | 145 | PF00400 | 0.685 |
TRG_ER_diArg_1 | 380 | 382 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 471 | 473 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 596 | 599 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 669 | 672 | PF00400 | 0.386 |
TRG_NES_CRM1_1 | 500 | 514 | PF08389 | 0.409 |
TRG_Pf-PMV_PEXEL_1 | 128 | 133 | PF00026 | 0.741 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 33% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 32% | 87% |
A0A0N1IGQ2 | Leptomonas seymouri | 33% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 34% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 83% | 100% |
A0A0N1P9P1 | Leptomonas seymouri | 33% | 100% |
A0A0N1PCA9 | Leptomonas seymouri | 33% | 100% |
A0A0N1PE91 | Leptomonas seymouri | 27% | 96% |
A0A0N1PFI4 | Leptomonas seymouri | 32% | 100% |
A0A0S4JLK6 | Bodo saltans | 27% | 100% |
A0A0S4JS70 | Bodo saltans | 26% | 100% |
A0A0S4KGT2 | Bodo saltans | 40% | 100% |
A0A1X0NJ19 | Trypanosomatidae | 33% | 70% |
A0A1X0NJK2 | Trypanosomatidae | 31% | 100% |
A0A1X0NJX8 | Trypanosomatidae | 60% | 100% |
A0A1X0NKT7 | Trypanosomatidae | 36% | 100% |
A0A1X0NKX8 | Trypanosomatidae | 34% | 100% |
A0A1X0NMT3 | Trypanosomatidae | 33% | 100% |
A0A1X0NW84 | Trypanosomatidae | 34% | 100% |
A0A1X0NW85 | Trypanosomatidae | 32% | 100% |
A0A1X0NW89 | Trypanosomatidae | 36% | 99% |
A0A1X0NWA6 | Trypanosomatidae | 25% | 98% |
A0A1X0NWW1 | Trypanosomatidae | 37% | 100% |
A0A3Q8IBS3 | Leishmania donovani | 33% | 94% |
A0A3Q8IDD4 | Leishmania donovani | 33% | 100% |
A0A3Q8IJT4 | Leishmania donovani | 28% | 100% |
A0A3S5H5A5 | Leishmania donovani | 31% | 100% |
A0A3S5ISG2 | Trypanosoma rangeli | 33% | 100% |
A0A3S7WW13 | Leishmania donovani | 26% | 77% |
A0A3S7WW18 | Leishmania donovani | 33% | 100% |
A0A3S7WW41 | Leishmania donovani | 30% | 100% |
A0A3S7WW71 | Leishmania donovani | 35% | 100% |
A0A3S7X430 | Leishmania donovani | 99% | 100% |
A0A3S7X438 | Leishmania donovani | 33% | 91% |
A0A3S7X460 | Leishmania donovani | 34% | 100% |
A0A3S7X463 | Leishmania donovani | 29% | 91% |
A0A3S7X470 | Leishmania donovani | 30% | 100% |
A0A422MYU1 | Trypanosoma rangeli | 37% | 93% |
A0A422MYX0 | Trypanosoma rangeli | 35% | 100% |
A4H3W4 | Leishmania braziliensis | 33% | 100% |
A4HE81 | Leishmania braziliensis | 32% | 100% |
A4HJ14 | Leishmania braziliensis | 92% | 100% |
A4HJ21 | Leishmania braziliensis | 28% | 96% |
A4HJ22 | Leishmania braziliensis | 33% | 90% |
A4HJ24 | Leishmania braziliensis | 34% | 100% |
A4HS39 | Leishmania infantum | 31% | 100% |
A4HYN0 | Leishmania infantum | 33% | 100% |
A4HYW1 | Leishmania infantum | 33% | 84% |
A4HYW2 | Leishmania infantum | 35% | 100% |
A4HYW3 | Leishmania infantum | 30% | 100% |
A4HYW4 | Leishmania infantum | 26% | 86% |
A4I1J4 | Leishmania infantum | 33% | 100% |
A4I6E4 | Leishmania infantum | 31% | 100% |
A4I6E6 | Leishmania infantum | 34% | 100% |
A4I6F0 | Leishmania infantum | 33% | 91% |
A4I6K4 | Leishmania infantum | 99% | 100% |
A4I6K5 | Leishmania infantum | 29% | 91% |
A4I6K6 | Leishmania infantum | 28% | 100% |
C9ZIE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 79% |
C9ZIE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZIE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZN52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
C9ZN53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 91% |
E8NHG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E8NHM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AIH1 | Leishmania braziliensis | 35% | 100% |
E9AIH3 | Leishmania braziliensis | 35% | 100% |
E9AIH4 | Leishmania braziliensis | 29% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9AUQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 92% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AXM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B1J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
E9B1J1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 91% |
E9B1J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B1J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
Q4Q6L7 | Leishmania major | 34% | 100% |
Q4Q6L9 | Leishmania major | 29% | 100% |
Q4Q6M0 | Leishmania major | 36% | 100% |
Q4Q6M2 | Leishmania major | 29% | 100% |
Q4Q6M3 | Leishmania major | 30% | 100% |
Q4Q9U3 | Leishmania major | 33% | 100% |
Q4QCS6 | Leishmania major | 30% | 100% |
Q4QCS7 | Leishmania major | 35% | 100% |
Q4QCS8 | Leishmania major | 33% | 100% |
Q4QCS9 | Leishmania major | 33% | 100% |
Q9U0T9 | Leishmania major | 34% | 100% |
V5AYJ1 | Trypanosoma cruzi | 33% | 100% |
V5B5I4 | Trypanosoma cruzi | 37% | 100% |
V5B8W5 | Trypanosoma cruzi | 22% | 83% |
V5BA05 | Trypanosoma cruzi | 37% | 100% |
V5BEL3 | Trypanosoma cruzi | 32% | 100% |
V5BII7 | Trypanosoma cruzi | 35% | 69% |
V5BN20 | Trypanosoma cruzi | 59% | 100% |
V5D5V8 | Trypanosoma cruzi | 28% | 100% |
V5D9Y2 | Trypanosoma cruzi | 33% | 100% |
V5DES7 | Trypanosoma cruzi | 33% | 100% |