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: 84 |
NetGPI | no | yes: 0, no: 85 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
GO:0005737 | cytoplasm | 2 | 3 |
GO:0005930 | axoneme | 2 | 1 |
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 |
Related structures:
AlphaFold database: A0A3S7X463
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 86 |
GO:0006807 | nitrogen compound metabolic process | 2 | 86 |
GO:0008152 | metabolic process | 1 | 86 |
GO:0019538 | protein metabolic process | 3 | 86 |
GO:0043170 | macromolecule metabolic process | 3 | 86 |
GO:0044238 | primary metabolic process | 2 | 86 |
GO:0071704 | organic substance metabolic process | 2 | 86 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 86 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 86 |
GO:0004175 | endopeptidase activity | 4 | 86 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 86 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 86 |
GO:0008233 | peptidase activity | 3 | 86 |
GO:0008234 | cysteine-type peptidase activity | 4 | 86 |
GO:0016787 | hydrolase activity | 2 | 86 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 86 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 158 | 162 | PF00656 | 0.457 |
CLV_C14_Caspase3-7 | 752 | 756 | PF00656 | 0.533 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.789 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 572 | 574 | PF00675 | 0.285 |
CLV_NRD_NRD_1 | 685 | 687 | PF00675 | 0.366 |
CLV_NRD_NRD_1 | 736 | 738 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 887 | 889 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.590 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.707 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 371 | 373 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 574 | 576 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 736 | 738 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 887 | 889 | PF00082 | 0.597 |
CLV_PCSK_PC1ET2_1 | 289 | 291 | PF00082 | 0.420 |
CLV_PCSK_PC1ET2_1 | 574 | 576 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 537 | 541 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 719 | 723 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 728 | 732 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.487 |
DEG_APCC_DBOX_1 | 249 | 257 | PF00400 | 0.206 |
DEG_SCF_FBW7_2 | 215 | 221 | PF00400 | 0.192 |
DEG_SPOP_SBC_1 | 817 | 821 | PF00917 | 0.361 |
DOC_CKS1_1 | 185 | 190 | PF01111 | 0.542 |
DOC_CKS1_1 | 215 | 220 | PF01111 | 0.217 |
DOC_CYCLIN_RxL_1 | 532 | 544 | PF00134 | 0.566 |
DOC_CYCLIN_RxL_1 | 85 | 95 | PF00134 | 0.303 |
DOC_CYCLIN_yCln2_LP_2 | 466 | 472 | PF00134 | 0.479 |
DOC_MAPK_gen_1 | 120 | 127 | PF00069 | 0.490 |
DOC_MAPK_gen_1 | 371 | 379 | PF00069 | 0.545 |
DOC_MAPK_gen_1 | 479 | 485 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 573 | 582 | PF00069 | 0.447 |
DOC_MAPK_gen_1 | 686 | 692 | PF00069 | 0.468 |
DOC_MAPK_gen_1 | 726 | 733 | PF00069 | 0.427 |
DOC_MAPK_gen_1 | 734 | 743 | PF00069 | 0.406 |
DOC_MAPK_HePTP_8 | 731 | 743 | PF00069 | 0.367 |
DOC_MAPK_MEF2A_6 | 726 | 733 | PF00069 | 0.354 |
DOC_MAPK_MEF2A_6 | 734 | 743 | PF00069 | 0.370 |
DOC_MAPK_MEF2A_6 | 807 | 815 | PF00069 | 0.507 |
DOC_PP1_RVXF_1 | 47 | 54 | PF00149 | 0.316 |
DOC_PP1_RVXF_1 | 596 | 603 | PF00149 | 0.607 |
DOC_PP2B_LxvP_1 | 827 | 830 | PF13499 | 0.380 |
DOC_PP4_FxxP_1 | 182 | 185 | PF00568 | 0.663 |
DOC_PP4_FxxP_1 | 194 | 197 | PF00568 | 0.296 |
DOC_PP4_FxxP_1 | 425 | 428 | PF00568 | 0.481 |
DOC_PP4_FxxP_1 | 556 | 559 | PF00568 | 0.563 |
DOC_SPAK_OSR1_1 | 862 | 866 | PF12202 | 0.218 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.348 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.325 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 535 | 539 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 640 | 644 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 646 | 650 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 780 | 784 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 817 | 821 | PF00917 | 0.361 |
DOC_USP7_MATH_2 | 901 | 907 | PF00917 | 0.322 |
DOC_USP7_UBL2_3 | 318 | 322 | PF12436 | 0.505 |
DOC_USP7_UBL2_3 | 334 | 338 | PF12436 | 0.266 |
DOC_USP7_UBL2_3 | 488 | 492 | PF12436 | 0.479 |
DOC_USP7_UBL2_3 | 734 | 738 | PF12436 | 0.528 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 554 | 559 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 666 | 671 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 674 | 679 | PF00397 | 0.415 |
LIG_14-3-3_CanoR_1 | 120 | 126 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 205 | 213 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 325 | 333 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 342 | 350 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 426 | 436 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 444 | 448 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 548 | 554 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 573 | 582 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 632 | 637 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 661 | 670 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 671 | 678 | PF00244 | 0.712 |
LIG_14-3-3_CanoR_1 | 887 | 893 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 907 | 914 | PF00244 | 0.413 |
LIG_Actin_WH2_2 | 583 | 600 | PF00022 | 0.536 |
LIG_APCC_ABBAyCdc20_2 | 622 | 628 | PF00400 | 0.400 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.735 |
LIG_BRCT_BRCA1_1 | 188 | 192 | PF00533 | 0.516 |
LIG_BRCT_BRCA1_1 | 879 | 883 | PF00533 | 0.481 |
LIG_deltaCOP1_diTrp_1 | 628 | 636 | PF00928 | 0.539 |
LIG_deltaCOP1_diTrp_1 | 693 | 701 | PF00928 | 0.418 |
LIG_eIF4E_1 | 497 | 503 | PF01652 | 0.374 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.335 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.433 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.693 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.503 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.543 |
LIG_FHA_1 | 550 | 556 | PF00498 | 0.447 |
LIG_FHA_1 | 649 | 655 | PF00498 | 0.444 |
LIG_FHA_1 | 687 | 693 | PF00498 | 0.471 |
LIG_FHA_1 | 742 | 748 | PF00498 | 0.486 |
LIG_FHA_1 | 800 | 806 | PF00498 | 0.468 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.372 |
LIG_FHA_2 | 633 | 639 | PF00498 | 0.606 |
LIG_FHA_2 | 707 | 713 | PF00498 | 0.324 |
LIG_FHA_2 | 747 | 753 | PF00498 | 0.423 |
LIG_IRF3_LxIS_1 | 33 | 40 | PF10401 | 0.411 |
LIG_LIR_Apic_2 | 296 | 300 | PF02991 | 0.442 |
LIG_LIR_Apic_2 | 369 | 373 | PF02991 | 0.475 |
LIG_LIR_Apic_2 | 634 | 640 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 174 | 184 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 359 | 368 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 374 | 382 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 221 | 225 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 359 | 363 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 374 | 379 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 511 | 515 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 533 | 539 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 755 | 760 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 880 | 886 | PF02991 | 0.364 |
LIG_MYND_1 | 830 | 834 | PF01753 | 0.441 |
LIG_PCNA_yPIPBox_3 | 191 | 203 | PF02747 | 0.202 |
LIG_PCNA_yPIPBox_3 | 219 | 233 | PF02747 | 0.417 |
LIG_Pex14_1 | 452 | 456 | PF04695 | 0.377 |
LIG_Pex14_2 | 515 | 519 | PF04695 | 0.477 |
LIG_Pex14_2 | 536 | 540 | PF04695 | 0.530 |
LIG_SH2_NCK_1 | 637 | 641 | PF00017 | 0.651 |
LIG_SH2_PTP2 | 297 | 300 | PF00017 | 0.426 |
LIG_SH2_PTP2 | 376 | 379 | PF00017 | 0.533 |
LIG_SH2_SRC | 461 | 464 | PF00017 | 0.489 |
LIG_SH2_STAP1 | 490 | 494 | PF00017 | 0.508 |
LIG_SH2_STAP1 | 627 | 631 | PF00017 | 0.636 |
LIG_SH2_STAP1 | 633 | 637 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 542 | 545 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 595 | 598 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 633 | 636 | PF00017 | 0.659 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 708 | 711 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 803 | 806 | PF00017 | 0.428 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.722 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.516 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.446 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.532 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.535 |
LIG_SH3_3 | 811 | 817 | PF00018 | 0.478 |
LIG_Sin3_3 | 360 | 367 | PF02671 | 0.374 |
LIG_SUMO_SIM_anti_2 | 231 | 236 | PF11976 | 0.182 |
LIG_SUMO_SIM_anti_2 | 265 | 273 | PF11976 | 0.386 |
LIG_SUMO_SIM_anti_2 | 771 | 777 | PF11976 | 0.453 |
LIG_SUMO_SIM_par_1 | 551 | 557 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 740 | 746 | PF11976 | 0.339 |
LIG_SUMO_SIM_par_1 | 863 | 870 | PF11976 | 0.454 |
LIG_TRAF2_1 | 228 | 231 | PF00917 | 0.182 |
LIG_TYR_ITIM | 65 | 70 | PF00017 | 0.328 |
LIG_UBA3_1 | 211 | 219 | PF00899 | 0.358 |
MOD_CDC14_SPxK_1 | 133 | 136 | PF00782 | 0.483 |
MOD_CDK_SPK_2 | 214 | 219 | PF00069 | 0.182 |
MOD_CDK_SPK_2 | 666 | 671 | PF00069 | 0.720 |
MOD_CDK_SPxK_1 | 130 | 136 | PF00069 | 0.668 |
MOD_CDK_SPxxK_3 | 130 | 137 | PF00069 | 0.678 |
MOD_CDK_SPxxK_3 | 184 | 191 | PF00069 | 0.564 |
MOD_CDK_SPxxK_3 | 37 | 44 | PF00069 | 0.380 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.620 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.532 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.451 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.501 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.467 |
MOD_CK1_1 | 565 | 571 | PF00069 | 0.507 |
MOD_CK1_1 | 649 | 655 | PF00069 | 0.584 |
MOD_CK1_1 | 746 | 752 | PF00069 | 0.431 |
MOD_CK1_1 | 818 | 824 | PF00069 | 0.624 |
MOD_CK1_1 | 835 | 841 | PF00069 | 0.470 |
MOD_CK1_1 | 846 | 852 | PF00069 | 0.604 |
MOD_CK1_1 | 866 | 872 | PF00069 | 0.484 |
MOD_CK1_1 | 906 | 912 | PF00069 | 0.524 |
MOD_CK1_1 | 926 | 932 | PF00069 | 0.461 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.316 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.294 |
MOD_CK2_1 | 470 | 476 | PF00069 | 0.485 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.429 |
MOD_CK2_1 | 746 | 752 | PF00069 | 0.470 |
MOD_CK2_1 | 926 | 932 | PF00069 | 0.467 |
MOD_CMANNOS | 691 | 694 | PF00535 | 0.390 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.667 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.727 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.753 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.366 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.311 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.288 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.288 |
MOD_GlcNHglycan | 644 | 647 | PF01048 | 0.576 |
MOD_GlcNHglycan | 648 | 651 | PF01048 | 0.598 |
MOD_GlcNHglycan | 782 | 785 | PF01048 | 0.466 |
MOD_GlcNHglycan | 833 | 837 | PF01048 | 0.428 |
MOD_GlcNHglycan | 845 | 848 | PF01048 | 0.562 |
MOD_GlcNHglycan | 928 | 931 | PF01048 | 0.501 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.774 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.310 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.378 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.390 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.566 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.453 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.497 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.503 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.621 |
MOD_GSK3_1 | 642 | 649 | PF00069 | 0.576 |
MOD_GSK3_1 | 662 | 669 | PF00069 | 0.426 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.496 |
MOD_GSK3_1 | 795 | 802 | PF00069 | 0.440 |
MOD_GSK3_1 | 843 | 850 | PF00069 | 0.637 |
MOD_GSK3_1 | 882 | 889 | PF00069 | 0.386 |
MOD_GSK3_1 | 891 | 898 | PF00069 | 0.418 |
MOD_GSK3_1 | 919 | 926 | PF00069 | 0.373 |
MOD_N-GLC_1 | 225 | 230 | PF02516 | 0.323 |
MOD_N-GLC_1 | 403 | 408 | PF02516 | 0.355 |
MOD_N-GLC_1 | 780 | 785 | PF02516 | 0.359 |
MOD_N-GLC_1 | 930 | 935 | PF02516 | 0.560 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.678 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.658 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.388 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.728 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.504 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.500 |
MOD_NEK2_1 | 519 | 524 | PF00069 | 0.537 |
MOD_NEK2_1 | 741 | 746 | PF00069 | 0.338 |
MOD_NEK2_1 | 768 | 773 | PF00069 | 0.363 |
MOD_NEK2_1 | 863 | 868 | PF00069 | 0.364 |
MOD_NEK2_1 | 886 | 891 | PF00069 | 0.473 |
MOD_NEK2_1 | 893 | 898 | PF00069 | 0.559 |
MOD_NEK2_2 | 390 | 395 | PF00069 | 0.377 |
MOD_NEK2_2 | 535 | 540 | PF00069 | 0.533 |
MOD_NEK2_2 | 650 | 655 | PF00069 | 0.441 |
MOD_PIKK_1 | 109 | 115 | PF00454 | 0.497 |
MOD_PIKK_1 | 300 | 306 | PF00454 | 0.465 |
MOD_PIKK_1 | 380 | 386 | PF00454 | 0.543 |
MOD_PIKK_1 | 436 | 442 | PF00454 | 0.423 |
MOD_PK_1 | 121 | 127 | PF00069 | 0.745 |
MOD_PK_1 | 807 | 813 | PF00069 | 0.379 |
MOD_PKA_1 | 573 | 579 | PF00069 | 0.479 |
MOD_PKA_1 | 686 | 692 | PF00069 | 0.292 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.537 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.363 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.483 |
MOD_PKA_2 | 443 | 449 | PF00069 | 0.461 |
MOD_PKA_2 | 574 | 580 | PF00069 | 0.516 |
MOD_PKA_2 | 631 | 637 | PF00069 | 0.582 |
MOD_PKA_2 | 787 | 793 | PF00069 | 0.560 |
MOD_PKA_2 | 886 | 892 | PF00069 | 0.441 |
MOD_PKA_2 | 906 | 912 | PF00069 | 0.384 |
MOD_PKA_2 | 926 | 932 | PF00069 | 0.472 |
MOD_PKB_1 | 121 | 129 | PF00069 | 0.488 |
MOD_Plk_1 | 225 | 231 | PF00069 | 0.333 |
MOD_Plk_1 | 262 | 268 | PF00069 | 0.334 |
MOD_Plk_1 | 390 | 396 | PF00069 | 0.537 |
MOD_Plk_1 | 403 | 409 | PF00069 | 0.447 |
MOD_Plk_1 | 807 | 813 | PF00069 | 0.389 |
MOD_Plk_1 | 877 | 883 | PF00069 | 0.458 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.732 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.496 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.490 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.504 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.501 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.518 |
MOD_Plk_4 | 549 | 555 | PF00069 | 0.520 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.570 |
MOD_Plk_4 | 686 | 692 | PF00069 | 0.441 |
MOD_Plk_4 | 706 | 712 | PF00069 | 0.212 |
MOD_Plk_4 | 756 | 762 | PF00069 | 0.673 |
MOD_Plk_4 | 863 | 869 | PF00069 | 0.358 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.685 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.521 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.388 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.448 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.546 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.628 |
MOD_ProDKin_1 | 554 | 560 | PF00069 | 0.492 |
MOD_ProDKin_1 | 666 | 672 | PF00069 | 0.719 |
MOD_ProDKin_1 | 674 | 680 | PF00069 | 0.409 |
MOD_SUMO_for_1 | 218 | 221 | PF00179 | 0.182 |
MOD_SUMO_rev_2 | 132 | 138 | PF00179 | 0.662 |
MOD_SUMO_rev_2 | 679 | 689 | PF00179 | 0.496 |
MOD_SUMO_rev_2 | 926 | 936 | PF00179 | 0.477 |
TRG_DiLeu_BaEn_1 | 149 | 154 | PF01217 | 0.724 |
TRG_DiLeu_BaEn_2 | 390 | 396 | PF01217 | 0.377 |
TRG_DiLeu_BaEn_3 | 271 | 277 | PF01217 | 0.182 |
TRG_DiLeu_BaEn_4 | 374 | 380 | PF01217 | 0.377 |
TRG_DiLeu_BaLyEn_6 | 827 | 832 | PF01217 | 0.492 |
TRG_DiLeu_LyEn_5 | 149 | 154 | PF01217 | 0.403 |
TRG_ENDOCYTIC_2 | 376 | 379 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 542 | 545 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 603 | 606 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.582 |
TRG_ER_diArg_1 | 120 | 123 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 370 | 372 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 478 | 480 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 713 | 716 | PF00400 | 0.351 |
TRG_ER_diArg_1 | 726 | 729 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 886 | 888 | PF00400 | 0.457 |
TRG_NES_CRM1_1 | 227 | 238 | PF08389 | 0.290 |
TRG_NES_CRM1_1 | 507 | 521 | PF08389 | 0.493 |
TRG_Pf-PMV_PEXEL_1 | 152 | 156 | PF00026 | 0.657 |
TRG_Pf-PMV_PEXEL_1 | 479 | 484 | PF00026 | 0.290 |
TRG_Pf-PMV_PEXEL_1 | 88 | 92 | PF00026 | 0.564 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 26% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 30% | 95% |
A0A0N1IGQ2 | Leptomonas seymouri | 24% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 28% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 27% | 100% |
A0A0N1P9P1 | Leptomonas seymouri | 28% | 100% |
A0A0N1PCA9 | Leptomonas seymouri | 27% | 100% |
A0A0S4KGT2 | Bodo saltans | 30% | 100% |
A0A1X0NJ19 | Trypanosomatidae | 39% | 76% |
A0A1X0NJX8 | Trypanosomatidae | 29% | 100% |
A0A1X0NKX8 | Trypanosomatidae | 26% | 100% |
A0A1X0NMT3 | Trypanosomatidae | 27% | 100% |
A0A1X0NW85 | Trypanosomatidae | 26% | 100% |
A0A1X0NW89 | Trypanosomatidae | 26% | 100% |
A0A1X0NWW1 | Trypanosomatidae | 25% | 100% |
A0A3Q8IBS3 | Leishmania donovani | 28% | 100% |
A0A3Q8IDD4 | Leishmania donovani | 28% | 100% |
A0A3S5H5A5 | Leishmania donovani | 30% | 100% |
A0A3S5ISG2 | Trypanosoma rangeli | 26% | 100% |
A0A3S7WW18 | Leishmania donovani | 27% | 100% |
A0A3S7WW41 | Leishmania donovani | 29% | 100% |
A0A3S7WW71 | Leishmania donovani | 26% | 100% |
A0A3S7X430 | Leishmania donovani | 29% | 100% |
A0A3S7X438 | Leishmania donovani | 29% | 100% |
A0A3S7X460 | Leishmania donovani | 27% | 100% |
A0A3S7X470 | Leishmania donovani | 27% | 100% |
A0A422MYU1 | Trypanosoma rangeli | 28% | 100% |
A0A422MYX0 | Trypanosoma rangeli | 26% | 100% |
A4H3W4 | Leishmania braziliensis | 30% | 100% |
A4HE81 | Leishmania braziliensis | 25% | 93% |
A4HJ14 | Leishmania braziliensis | 29% | 100% |
A4HJ22 | Leishmania braziliensis | 30% | 100% |
A4HJ24 | Leishmania braziliensis | 27% | 95% |
A4HS39 | Leishmania infantum | 30% | 100% |
A4HYN0 | Leishmania infantum | 26% | 100% |
A4HYW1 | Leishmania infantum | 27% | 100% |
A4HYW2 | Leishmania infantum | 26% | 100% |
A4HYW3 | Leishmania infantum | 29% | 100% |
A4I1J4 | Leishmania infantum | 28% | 100% |
A4I6E4 | Leishmania infantum | 28% | 100% |
A4I6E6 | Leishmania infantum | 27% | 100% |
A4I6F0 | Leishmania infantum | 29% | 100% |
A4I6K4 | Leishmania infantum | 29% | 100% |
A4I6K5 | Leishmania infantum | 99% | 100% |
C9ZIE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 87% |
C9ZIE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZIE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
C9ZN52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZN53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E8NHG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AIH1 | Leishmania braziliensis | 27% | 100% |
E9AIH3 | Leishmania braziliensis | 26% | 100% |
E9AIH4 | Leishmania braziliensis | 29% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AUQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AUQ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AXM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B1J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B1J1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9B1J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
Q4Q6L7 | Leishmania major | 27% | 100% |
Q4Q6L9 | Leishmania major | 28% | 100% |
Q4Q6M3 | Leishmania major | 94% | 100% |
Q4Q6M4 | Leishmania major | 29% | 100% |
Q4Q9U3 | Leishmania major | 27% | 100% |
Q4QCS6 | Leishmania major | 28% | 100% |
Q4QCS7 | Leishmania major | 27% | 100% |
Q4QCS8 | Leishmania major | 27% | 100% |
Q4QCS9 | Leishmania major | 27% | 100% |
Q9U0T9 | Leishmania major | 29% | 100% |
V5AYJ1 | Trypanosoma cruzi | 27% | 100% |
V5B5I4 | Trypanosoma cruzi | 27% | 100% |
V5BA05 | Trypanosoma cruzi | 28% | 100% |
V5BII7 | Trypanosoma cruzi | 41% | 76% |
V5BN20 | Trypanosoma cruzi | 30% | 100% |
V5DES7 | Trypanosoma cruzi | 27% | 100% |