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. | no | yes: 38 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 101 |
NetGPI | no | yes: 0, no: 102 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
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 | 1 |
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 |
Related structures:
AlphaFold database: E8NHG7
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 103 |
GO:0006807 | nitrogen compound metabolic process | 2 | 103 |
GO:0008152 | metabolic process | 1 | 103 |
GO:0019538 | protein metabolic process | 3 | 103 |
GO:0043170 | macromolecule metabolic process | 3 | 103 |
GO:0044238 | primary metabolic process | 2 | 103 |
GO:0071704 | organic substance metabolic process | 2 | 103 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 103 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 103 |
GO:0004175 | endopeptidase activity | 4 | 103 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 103 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 103 |
GO:0008233 | peptidase activity | 3 | 103 |
GO:0008234 | cysteine-type peptidase activity | 4 | 103 |
GO:0016787 | hydrolase activity | 2 | 103 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 103 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 132 | 136 | PF00656 | 0.529 |
CLV_C14_Caspase3-7 | 522 | 526 | PF00656 | 0.604 |
CLV_C14_Caspase3-7 | 589 | 593 | PF00656 | 0.463 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 544 | 546 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 907 | 909 | PF00675 | 0.571 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 907 | 909 | PF00082 | 0.595 |
CLV_PCSK_PC1ET2_1 | 367 | 369 | PF00082 | 0.399 |
CLV_PCSK_PC7_1 | 363 | 369 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 744 | 748 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 872 | 876 | PF00082 | 0.451 |
DEG_APCC_DBOX_1 | 664 | 672 | PF00400 | 0.540 |
DEG_MDM2_SWIB_1 | 586 | 594 | PF02201 | 0.421 |
DEG_SPOP_SBC_1 | 70 | 74 | PF00917 | 0.459 |
DOC_CKS1_1 | 256 | 261 | PF01111 | 0.450 |
DOC_CKS1_1 | 831 | 836 | PF01111 | 0.461 |
DOC_CYCLIN_RxL_1 | 788 | 802 | PF00134 | 0.533 |
DOC_MAPK_gen_1 | 423 | 431 | PF00069 | 0.484 |
DOC_MAPK_gen_1 | 662 | 671 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 791 | 800 | PF00069 | 0.576 |
DOC_MAPK_gen_1 | 889 | 897 | PF00069 | 0.508 |
DOC_MAPK_JIP1_4 | 794 | 800 | PF00069 | 0.259 |
DOC_MAPK_MEF2A_6 | 626 | 634 | PF00069 | 0.377 |
DOC_MAPK_MEF2A_6 | 791 | 800 | PF00069 | 0.366 |
DOC_MAPK_MEF2A_6 | 844 | 852 | PF00069 | 0.487 |
DOC_PP2B_LxvP_1 | 195 | 198 | PF13499 | 0.648 |
DOC_PP2B_LxvP_1 | 26 | 29 | PF13499 | 0.434 |
DOC_PP2B_LxvP_1 | 632 | 635 | PF13499 | 0.468 |
DOC_PP4_FxxP_1 | 25 | 28 | PF00568 | 0.439 |
DOC_PP4_FxxP_1 | 256 | 259 | PF00568 | 0.314 |
DOC_PP4_FxxP_1 | 409 | 412 | PF00568 | 0.526 |
DOC_PP4_FxxP_1 | 491 | 494 | PF00568 | 0.482 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.391 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 593 | 597 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 600 | 604 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.686 |
DOC_USP7_MATH_2 | 639 | 645 | PF00917 | 0.367 |
DOC_USP7_UBL2_3 | 554 | 558 | PF12436 | 0.479 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.350 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 606 | 611 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 765 | 770 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 830 | 835 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 898 | 903 | PF00397 | 0.446 |
LIG_14-3-3_CanoR_1 | 27 | 33 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 356 | 365 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 510 | 519 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 539 | 547 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 601 | 608 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 824 | 834 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 849 | 853 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 907 | 915 | PF00244 | 0.461 |
LIG_Actin_WH2_2 | 643 | 661 | PF00022 | 0.524 |
LIG_Actin_WH2_2 | 834 | 851 | PF00022 | 0.508 |
LIG_APCC_ABBA_1 | 230 | 235 | PF00400 | 0.357 |
LIG_BRCT_BRCA1_1 | 122 | 126 | PF00533 | 0.588 |
LIG_BRCT_BRCA1_1 | 274 | 278 | PF00533 | 0.354 |
LIG_BRCT_BRCA1_1 | 71 | 75 | PF00533 | 0.467 |
LIG_BRCT_BRCA1_1 | 900 | 904 | PF00533 | 0.490 |
LIG_CtBP_PxDLS_1 | 110 | 114 | PF00389 | 0.451 |
LIG_deltaCOP1_diTrp_1 | 717 | 725 | PF00928 | 0.480 |
LIG_EH1_1 | 654 | 662 | PF00400 | 0.511 |
LIG_eIF4E_1 | 655 | 661 | PF01652 | 0.508 |
LIG_EVH1_2 | 28 | 32 | PF00568 | 0.439 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.551 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.350 |
LIG_FHA_1 | 483 | 489 | PF00498 | 0.452 |
LIG_FHA_1 | 518 | 524 | PF00498 | 0.483 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.710 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.451 |
LIG_FHA_1 | 673 | 679 | PF00498 | 0.519 |
LIG_FHA_1 | 833 | 839 | PF00498 | 0.539 |
LIG_FHA_1 | 885 | 891 | PF00498 | 0.470 |
LIG_FHA_1 | 910 | 916 | PF00498 | 0.443 |
LIG_FHA_2 | 117 | 123 | PF00498 | 0.535 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.741 |
LIG_FHA_2 | 380 | 386 | PF00498 | 0.361 |
LIG_FHA_2 | 520 | 526 | PF00498 | 0.461 |
LIG_FHA_2 | 615 | 621 | PF00498 | 0.374 |
LIG_FHA_2 | 827 | 833 | PF00498 | 0.476 |
LIG_Integrin_RGD_1 | 804 | 806 | PF01839 | 0.457 |
LIG_LIR_Apic_2 | 23 | 28 | PF02991 | 0.436 |
LIG_LIR_Apic_2 | 348 | 353 | PF02991 | 0.454 |
LIG_LIR_Apic_2 | 433 | 439 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 123 | 133 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 553 | 564 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 771 | 780 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 123 | 129 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 275 | 279 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 553 | 559 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 562 | 566 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 579 | 584 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 606 | 611 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 654 | 658 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 771 | 776 | PF02991 | 0.408 |
LIG_LYPXL_yS_3 | 549 | 552 | PF13949 | 0.548 |
LIG_PCNA_PIPBox_1 | 250 | 259 | PF02747 | 0.180 |
LIG_PCNA_yPIPBox_3 | 247 | 257 | PF02747 | 0.197 |
LIG_Pex14_2 | 586 | 590 | PF04695 | 0.473 |
LIG_Pex14_2 | 874 | 878 | PF04695 | 0.466 |
LIG_PTB_Apo_2 | 344 | 351 | PF02174 | 0.269 |
LIG_PTB_Apo_2 | 868 | 875 | PF02174 | 0.472 |
LIG_PTB_Phospho_1 | 344 | 350 | PF10480 | 0.265 |
LIG_REV1ctd_RIR_1 | 744 | 751 | PF16727 | 0.527 |
LIG_SH2_CRK | 139 | 143 | PF00017 | 0.568 |
LIG_SH2_CRK | 248 | 252 | PF00017 | 0.375 |
LIG_SH2_CRK | 267 | 271 | PF00017 | 0.234 |
LIG_SH2_CRK | 350 | 354 | PF00017 | 0.524 |
LIG_SH2_CRK | 556 | 560 | PF00017 | 0.475 |
LIG_SH2_CRK | 563 | 567 | PF00017 | 0.474 |
LIG_SH2_CRK | 608 | 612 | PF00017 | 0.530 |
LIG_SH2_CRK | 655 | 659 | PF00017 | 0.493 |
LIG_SH2_CRK | 773 | 777 | PF00017 | 0.369 |
LIG_SH2_GRB2like | 350 | 353 | PF00017 | 0.543 |
LIG_SH2_NCK_1 | 257 | 261 | PF00017 | 0.424 |
LIG_SH2_NCK_1 | 563 | 567 | PF00017 | 0.498 |
LIG_SH2_PTP2 | 860 | 863 | PF00017 | 0.430 |
LIG_SH2_SRC | 442 | 445 | PF00017 | 0.485 |
LIG_SH2_SRC | 527 | 530 | PF00017 | 0.496 |
LIG_SH2_SRC | 860 | 863 | PF00017 | 0.389 |
LIG_SH2_STAP1 | 315 | 319 | PF00017 | 0.337 |
LIG_SH2_STAT3 | 148 | 151 | PF00017 | 0.562 |
LIG_SH2_STAT3 | 315 | 318 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 442 | 445 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 628 | 631 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 773 | 776 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 840 | 843 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 860 | 863 | PF00017 | 0.383 |
LIG_SH3_2 | 786 | 791 | PF14604 | 0.564 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.525 |
LIG_SH3_3 | 457 | 463 | PF00018 | 0.448 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.677 |
LIG_SH3_3 | 783 | 789 | PF00018 | 0.562 |
LIG_SH3_3 | 828 | 834 | PF00018 | 0.506 |
LIG_SH3_3 | 892 | 898 | PF00018 | 0.448 |
LIG_SUMO_SIM_anti_2 | 325 | 332 | PF11976 | 0.440 |
LIG_SUMO_SIM_par_1 | 109 | 114 | PF11976 | 0.654 |
LIG_SUMO_SIM_par_1 | 753 | 759 | PF11976 | 0.403 |
LIG_SUMO_SIM_par_1 | 794 | 799 | PF11976 | 0.411 |
LIG_TRAF2_1 | 618 | 621 | PF00917 | 0.374 |
LIG_TYR_ITIM | 265 | 270 | PF00017 | 0.349 |
LIG_TYR_ITIM | 547 | 552 | PF00017 | 0.423 |
LIG_WRC_WIRS_1 | 751 | 756 | PF05994 | 0.479 |
MOD_CDK_SPxxK_3 | 255 | 262 | PF00069 | 0.388 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.601 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.585 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.312 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.634 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.496 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.530 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.510 |
MOD_CK1_1 | 603 | 609 | PF00069 | 0.322 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.747 |
MOD_CK1_1 | 763 | 769 | PF00069 | 0.542 |
MOD_CK1_1 | 799 | 805 | PF00069 | 0.427 |
MOD_CK1_1 | 909 | 915 | PF00069 | 0.492 |
MOD_CK2_1 | 567 | 573 | PF00069 | 0.372 |
MOD_CK2_1 | 614 | 620 | PF00069 | 0.383 |
MOD_CK2_1 | 765 | 771 | PF00069 | 0.500 |
MOD_CK2_1 | 830 | 836 | PF00069 | 0.416 |
MOD_CMANNOS | 715 | 718 | PF00535 | 0.320 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.501 |
MOD_GlcNHglycan | 121 | 125 | PF01048 | 0.571 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.590 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.695 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.668 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.342 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.473 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.349 |
MOD_GlcNHglycan | 4 | 8 | PF01048 | 0.518 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.305 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.460 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.338 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.307 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.431 |
MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.258 |
MOD_GlcNHglycan | 680 | 683 | PF01048 | 0.400 |
MOD_GlcNHglycan | 685 | 688 | PF01048 | 0.388 |
MOD_GlcNHglycan | 765 | 768 | PF01048 | 0.617 |
MOD_GlcNHglycan | 816 | 820 | PF01048 | 0.520 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.591 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.458 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.710 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.645 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.681 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.332 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.390 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.556 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.526 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.292 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.377 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.366 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.650 |
MOD_GSK3_1 | 756 | 763 | PF00069 | 0.457 |
MOD_GSK3_1 | 826 | 833 | PF00069 | 0.399 |
MOD_GSK3_1 | 848 | 855 | PF00069 | 0.408 |
MOD_GSK3_1 | 878 | 885 | PF00069 | 0.473 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.505 |
MOD_N-GLC_1 | 272 | 277 | PF02516 | 0.326 |
MOD_N-GLC_1 | 279 | 284 | PF02516 | 0.326 |
MOD_N-GLC_1 | 338 | 343 | PF02516 | 0.404 |
MOD_N-GLC_1 | 346 | 351 | PF02516 | 0.466 |
MOD_N-GLC_1 | 376 | 381 | PF02516 | 0.478 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.425 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.302 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.594 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.704 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.442 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.585 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.286 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.338 |
MOD_NEK2_1 | 651 | 656 | PF00069 | 0.352 |
MOD_NEK2_1 | 683 | 688 | PF00069 | 0.341 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.464 |
MOD_NEK2_1 | 796 | 801 | PF00069 | 0.361 |
MOD_NEK2_1 | 848 | 853 | PF00069 | 0.412 |
MOD_NEK2_1 | 878 | 883 | PF00069 | 0.424 |
MOD_NEK2_2 | 417 | 422 | PF00069 | 0.370 |
MOD_NEK2_2 | 71 | 76 | PF00069 | 0.450 |
MOD_PIKK_1 | 305 | 311 | PF00454 | 0.310 |
MOD_PIKK_1 | 443 | 449 | PF00454 | 0.416 |
MOD_PIKK_1 | 482 | 488 | PF00454 | 0.476 |
MOD_PIKK_1 | 774 | 780 | PF00454 | 0.388 |
MOD_PIKK_1 | 852 | 858 | PF00454 | 0.375 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.503 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.384 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.417 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.410 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.357 |
MOD_PKA_2 | 843 | 849 | PF00069 | 0.392 |
MOD_PKA_2 | 906 | 912 | PF00069 | 0.500 |
MOD_PKB_1 | 354 | 362 | PF00069 | 0.417 |
MOD_Plk_1 | 180 | 186 | PF00069 | 0.598 |
MOD_Plk_1 | 346 | 352 | PF00069 | 0.453 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.390 |
MOD_Plk_1 | 432 | 438 | PF00069 | 0.415 |
MOD_Plk_1 | 603 | 609 | PF00069 | 0.433 |
MOD_Plk_1 | 756 | 762 | PF00069 | 0.380 |
MOD_Plk_2-3 | 117 | 123 | PF00069 | 0.655 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.348 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.266 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.392 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.353 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.350 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.306 |
MOD_Plk_4 | 750 | 756 | PF00069 | 0.389 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.694 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.350 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.581 |
MOD_ProDKin_1 | 606 | 612 | PF00069 | 0.423 |
MOD_ProDKin_1 | 765 | 771 | PF00069 | 0.509 |
MOD_ProDKin_1 | 830 | 836 | PF00069 | 0.521 |
MOD_ProDKin_1 | 898 | 904 | PF00069 | 0.404 |
MOD_SUMO_rev_2 | 616 | 623 | PF00179 | 0.421 |
TRG_DiLeu_BaEn_1 | 325 | 330 | PF01217 | 0.388 |
TRG_DiLeu_BaLyEn_6 | 547 | 552 | PF01217 | 0.413 |
TRG_DiLeu_BaLyEn_6 | 664 | 669 | PF01217 | 0.395 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.590 |
TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 549 | 552 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 556 | 559 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 563 | 566 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 608 | 611 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 655 | 658 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 773 | 776 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 859 | 862 | PF00928 | 0.374 |
TRG_ER_diArg_1 | 353 | 356 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 436 | 438 | PF00400 | 0.362 |
TRG_ER_diArg_1 | 890 | 893 | PF00400 | 0.479 |
TRG_NES_CRM1_1 | 749 | 761 | PF08389 | 0.473 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 30% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 54% | 96% |
A0A0N1IGQ2 | Leptomonas seymouri | 29% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 30% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 33% | 100% |
A0A0N1P9P1 | Leptomonas seymouri | 33% | 100% |
A0A0N1PCA9 | Leptomonas seymouri | 30% | 100% |
A0A0N1PE91 | Leptomonas seymouri | 28% | 100% |
A0A0N1PFI4 | Leptomonas seymouri | 31% | 100% |
A0A0S4JS70 | Bodo saltans | 26% | 100% |
A0A0S4KGT2 | Bodo saltans | 36% | 100% |
A0A0S4KKP7 | Bodo saltans | 25% | 100% |
A0A1X0NJ19 | Trypanosomatidae | 27% | 77% |
A0A1X0NJK2 | Trypanosomatidae | 28% | 100% |
A0A1X0NJX8 | Trypanosomatidae | 35% | 100% |
A0A1X0NKT7 | Trypanosomatidae | 38% | 100% |
A0A1X0NKX8 | Trypanosomatidae | 29% | 100% |
A0A1X0NMT3 | Trypanosomatidae | 31% | 100% |
A0A1X0NW84 | Trypanosomatidae | 30% | 100% |
A0A1X0NW85 | Trypanosomatidae | 31% | 100% |
A0A1X0NW89 | Trypanosomatidae | 30% | 100% |
A0A1X0NWA6 | Trypanosomatidae | 25% | 100% |
A0A1X0NWW1 | Trypanosomatidae | 30% | 100% |
A0A3Q8IBS3 | Leishmania donovani | 31% | 100% |
A0A3Q8IDD4 | Leishmania donovani | 28% | 100% |
A0A3Q8IJT4 | Leishmania donovani | 28% | 100% |
A0A3S5H5A5 | Leishmania donovani | 33% | 100% |
A0A3S5ISG2 | Trypanosoma rangeli | 30% | 100% |
A0A3S7WW18 | Leishmania donovani | 31% | 100% |
A0A3S7WW41 | Leishmania donovani | 30% | 100% |
A0A3S7WW71 | Leishmania donovani | 30% | 100% |
A0A3S7X430 | Leishmania donovani | 34% | 100% |
A0A3S7X438 | Leishmania donovani | 87% | 100% |
A0A3S7X460 | Leishmania donovani | 31% | 100% |
A0A3S7X463 | Leishmania donovani | 27% | 100% |
A0A3S7X470 | Leishmania donovani | 32% | 100% |
A0A422MYU1 | Trypanosoma rangeli | 30% | 100% |
A0A422MYX0 | Trypanosoma rangeli | 30% | 100% |
A4H3W4 | Leishmania braziliensis | 34% | 100% |
A4HE81 | Leishmania braziliensis | 27% | 95% |
A4HJ14 | Leishmania braziliensis | 34% | 100% |
A4HJ21 | Leishmania braziliensis | 28% | 100% |
A4HJ22 | Leishmania braziliensis | 72% | 100% |
A4HJ24 | Leishmania braziliensis | 30% | 98% |
A4HS39 | Leishmania infantum | 33% | 100% |
A4HYN0 | Leishmania infantum | 31% | 100% |
A4HYW1 | Leishmania infantum | 31% | 93% |
A4HYW2 | Leishmania infantum | 30% | 100% |
A4HYW3 | Leishmania infantum | 30% | 100% |
A4I1J4 | Leishmania infantum | 29% | 100% |
A4I6E4 | Leishmania infantum | 32% | 100% |
A4I6E6 | Leishmania infantum | 31% | 100% |
A4I6F0 | Leishmania infantum | 87% | 100% |
A4I6K4 | Leishmania infantum | 34% | 100% |
A4I6K5 | Leishmania infantum | 27% | 100% |
A4I6K6 | Leishmania infantum | 28% | 100% |
C9ZIE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 87% |
C9ZIE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZIE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZN52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZN53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E8NHG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AIH1 | Leishmania braziliensis | 29% | 100% |
E9AIH3 | Leishmania braziliensis | 30% | 94% |
E9AIH4 | Leishmania braziliensis | 30% | 96% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AUQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AUQ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AXM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B1J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B1J1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B1J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9B1J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
Q4Q6L7 | Leishmania major | 31% | 99% |
Q4Q6L9 | Leishmania major | 31% | 100% |
Q4Q6M0 | Leishmania major | 85% | 100% |
Q4Q6M2 | Leishmania major | 29% | 97% |
Q4Q6M3 | Leishmania major | 28% | 100% |
Q4Q6M4 | Leishmania major | 34% | 100% |
Q4Q9U3 | Leishmania major | 28% | 98% |
Q4QCS6 | Leishmania major | 30% | 96% |
Q4QCS7 | Leishmania major | 30% | 94% |
Q4QCS8 | Leishmania major | 31% | 100% |
Q4QCS9 | Leishmania major | 31% | 100% |
Q9U0T9 | Leishmania major | 34% | 100% |
V5AYJ1 | Trypanosoma cruzi | 28% | 100% |
V5B5I4 | Trypanosoma cruzi | 32% | 100% |
V5BA05 | Trypanosoma cruzi | 32% | 100% |
V5BEL3 | Trypanosoma cruzi | 30% | 100% |
V5BII7 | Trypanosoma cruzi | 30% | 76% |
V5BN20 | Trypanosoma cruzi | 33% | 100% |
V5D5V8 | Trypanosoma cruzi | 27% | 100% |
V5D9Y2 | Trypanosoma cruzi | 31% | 100% |
V5DES7 | Trypanosoma cruzi | 30% | 100% |