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: 97 |
NetGPI | no | yes: 0, no: 98 |
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: Q4Q6M0
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 99 |
GO:0006807 | nitrogen compound metabolic process | 2 | 99 |
GO:0008152 | metabolic process | 1 | 99 |
GO:0019538 | protein metabolic process | 3 | 99 |
GO:0043170 | macromolecule metabolic process | 3 | 99 |
GO:0044238 | primary metabolic process | 2 | 99 |
GO:0071704 | organic substance metabolic process | 2 | 99 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 99 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 99 |
GO:0004175 | endopeptidase activity | 4 | 99 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 99 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 99 |
GO:0008233 | peptidase activity | 3 | 99 |
GO:0008234 | cysteine-type peptidase activity | 4 | 99 |
GO:0016787 | hydrolase activity | 2 | 99 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 99 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 130 | 134 | PF00656 | 0.492 |
CLV_C14_Caspase3-7 | 187 | 191 | PF00656 | 0.433 |
CLV_C14_Caspase3-7 | 519 | 523 | PF00656 | 0.376 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 541 | 543 | PF00675 | 0.283 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 741 | 745 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 869 | 873 | PF00082 | 0.458 |
DEG_APCC_DBOX_1 | 622 | 630 | PF00400 | 0.539 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.692 |
DEG_SPOP_SBC_1 | 67 | 71 | PF00917 | 0.458 |
DOC_CKS1_1 | 253 | 258 | PF01111 | 0.455 |
DOC_CKS1_1 | 828 | 833 | PF01111 | 0.464 |
DOC_CYCLIN_yCln2_LP_2 | 105 | 111 | PF00134 | 0.636 |
DOC_MAPK_gen_1 | 420 | 428 | PF00069 | 0.497 |
DOC_MAPK_gen_1 | 656 | 665 | PF00069 | 0.484 |
DOC_MAPK_gen_1 | 788 | 797 | PF00069 | 0.574 |
DOC_MAPK_gen_1 | 886 | 894 | PF00069 | 0.507 |
DOC_MAPK_JIP1_4 | 791 | 797 | PF00069 | 0.253 |
DOC_MAPK_MEF2A_6 | 623 | 631 | PF00069 | 0.376 |
DOC_MAPK_MEF2A_6 | 788 | 797 | PF00069 | 0.367 |
DOC_MAPK_MEF2A_6 | 841 | 849 | PF00069 | 0.477 |
DOC_PP1_RVXF_1 | 844 | 850 | PF00149 | 0.456 |
DOC_PP2B_LxvP_1 | 105 | 108 | PF13499 | 0.597 |
DOC_PP2B_LxvP_1 | 629 | 632 | PF13499 | 0.467 |
DOC_PP4_FxxP_1 | 23 | 26 | PF00568 | 0.451 |
DOC_PP4_FxxP_1 | 406 | 409 | PF00568 | 0.525 |
DOC_PP4_FxxP_1 | 488 | 491 | PF00568 | 0.481 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.389 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 588 | 592 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 597 | 601 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 895 | 899 | PF00917 | 0.509 |
DOC_USP7_UBL2_3 | 148 | 152 | PF12436 | 0.518 |
DOC_USP7_UBL2_3 | 551 | 555 | PF12436 | 0.478 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.351 |
DOC_WW_Pin1_4 | 564 | 569 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 603 | 608 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 762 | 767 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 779 | 784 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 827 | 832 | PF00397 | 0.492 |
LIG_14-3-3_CanoR_1 | 265 | 274 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 507 | 516 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 536 | 544 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 598 | 605 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 821 | 831 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 846 | 850 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 904 | 912 | PF00244 | 0.496 |
LIG_Actin_WH2_2 | 640 | 658 | PF00022 | 0.515 |
LIG_Actin_WH2_2 | 831 | 848 | PF00022 | 0.508 |
LIG_APCC_ABBA_1 | 227 | 232 | PF00400 | 0.370 |
LIG_BRCT_BRCA1_1 | 120 | 124 | PF00533 | 0.589 |
LIG_BRCT_BRCA1_1 | 271 | 275 | PF00533 | 0.352 |
LIG_BRCT_BRCA1_1 | 69 | 73 | PF00533 | 0.693 |
LIG_BRCT_BRCA1_1 | 897 | 901 | PF00533 | 0.478 |
LIG_CtBP_PxDLS_1 | 108 | 112 | PF00389 | 0.438 |
LIG_deltaCOP1_diTrp_1 | 270 | 275 | PF00928 | 0.252 |
LIG_deltaCOP1_diTrp_1 | 585 | 592 | PF00928 | 0.492 |
LIG_deltaCOP1_diTrp_1 | 714 | 722 | PF00928 | 0.480 |
LIG_EH1_1 | 651 | 659 | PF00400 | 0.510 |
LIG_eIF4E_1 | 652 | 658 | PF01652 | 0.507 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.668 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.587 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.598 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.432 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.635 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.347 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.446 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.479 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.450 |
LIG_FHA_1 | 670 | 676 | PF00498 | 0.537 |
LIG_FHA_1 | 708 | 714 | PF00498 | 0.507 |
LIG_FHA_1 | 830 | 836 | PF00498 | 0.528 |
LIG_FHA_1 | 882 | 888 | PF00498 | 0.477 |
LIG_FHA_1 | 907 | 913 | PF00498 | 0.431 |
LIG_FHA_2 | 115 | 121 | PF00498 | 0.528 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.683 |
LIG_FHA_2 | 517 | 523 | PF00498 | 0.476 |
LIG_FHA_2 | 612 | 618 | PF00498 | 0.374 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.664 |
LIG_FHA_2 | 824 | 830 | PF00498 | 0.474 |
LIG_LIR_Apic_2 | 21 | 26 | PF02991 | 0.456 |
LIG_LIR_Apic_2 | 345 | 350 | PF02991 | 0.460 |
LIG_LIR_Apic_2 | 430 | 436 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 121 | 131 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 135 | 145 | PF02991 | 0.584 |
LIG_LIR_Gen_1 | 550 | 561 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 610 | 620 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 651 | 658 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 768 | 777 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 121 | 127 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 135 | 140 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 550 | 556 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 559 | 563 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 576 | 581 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 603 | 608 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 610 | 616 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 651 | 655 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 768 | 773 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 853 | 859 | PF02991 | 0.381 |
LIG_LYPXL_yS_3 | 546 | 549 | PF13949 | 0.547 |
LIG_PCNA_PIPBox_1 | 247 | 256 | PF02747 | 0.180 |
LIG_PCNA_yPIPBox_3 | 244 | 254 | PF02747 | 0.192 |
LIG_PDZ_Class_1 | 933 | 938 | PF00595 | 0.475 |
LIG_Pex14_1 | 732 | 736 | PF04695 | 0.229 |
LIG_Pex14_2 | 583 | 587 | PF04695 | 0.470 |
LIG_Pex14_2 | 871 | 875 | PF04695 | 0.472 |
LIG_REV1ctd_RIR_1 | 741 | 748 | PF16727 | 0.524 |
LIG_SH2_CRK | 137 | 141 | PF00017 | 0.590 |
LIG_SH2_CRK | 245 | 249 | PF00017 | 0.374 |
LIG_SH2_CRK | 264 | 268 | PF00017 | 0.236 |
LIG_SH2_CRK | 347 | 351 | PF00017 | 0.537 |
LIG_SH2_CRK | 553 | 557 | PF00017 | 0.476 |
LIG_SH2_CRK | 560 | 564 | PF00017 | 0.475 |
LIG_SH2_CRK | 605 | 609 | PF00017 | 0.529 |
LIG_SH2_CRK | 652 | 656 | PF00017 | 0.492 |
LIG_SH2_CRK | 770 | 774 | PF00017 | 0.367 |
LIG_SH2_GRB2like | 347 | 350 | PF00017 | 0.561 |
LIG_SH2_NCK_1 | 254 | 258 | PF00017 | 0.422 |
LIG_SH2_NCK_1 | 560 | 564 | PF00017 | 0.497 |
LIG_SH2_PTP2 | 857 | 860 | PF00017 | 0.426 |
LIG_SH2_SRC | 439 | 442 | PF00017 | 0.492 |
LIG_SH2_SRC | 524 | 527 | PF00017 | 0.493 |
LIG_SH2_SRC | 857 | 860 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 172 | 176 | PF00017 | 0.478 |
LIG_SH2_STAP1 | 282 | 286 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 312 | 316 | PF00017 | 0.335 |
LIG_SH2_STAP1 | 584 | 588 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 736 | 740 | PF00017 | 0.350 |
LIG_SH2_STAT3 | 146 | 149 | PF00017 | 0.556 |
LIG_SH2_STAT3 | 312 | 315 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 625 | 628 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 770 | 773 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 837 | 840 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 857 | 860 | PF00017 | 0.380 |
LIG_SH3_2 | 783 | 788 | PF14604 | 0.569 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.523 |
LIG_SH3_3 | 454 | 460 | PF00018 | 0.447 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.738 |
LIG_SH3_3 | 780 | 786 | PF00018 | 0.569 |
LIG_SH3_3 | 825 | 831 | PF00018 | 0.505 |
LIG_SH3_3 | 889 | 895 | PF00018 | 0.442 |
LIG_SUMO_SIM_anti_2 | 322 | 329 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 107 | 112 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 750 | 756 | PF11976 | 0.404 |
LIG_SUMO_SIM_par_1 | 791 | 796 | PF11976 | 0.404 |
LIG_TRAF2_1 | 615 | 618 | PF00917 | 0.374 |
LIG_TYR_ITIM | 262 | 267 | PF00017 | 0.348 |
LIG_TYR_ITIM | 544 | 549 | PF00017 | 0.547 |
LIG_UBA3_1 | 612 | 619 | PF00899 | 0.484 |
LIG_WRC_WIRS_1 | 578 | 583 | PF05994 | 0.523 |
LIG_WRC_WIRS_1 | 748 | 753 | PF05994 | 0.478 |
MOD_CDK_SPxxK_3 | 252 | 259 | PF00069 | 0.387 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.611 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.316 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.520 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.543 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.476 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.540 |
MOD_CK1_1 | 600 | 606 | PF00069 | 0.474 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.655 |
MOD_CK1_1 | 760 | 766 | PF00069 | 0.527 |
MOD_CK1_1 | 796 | 802 | PF00069 | 0.418 |
MOD_CK1_1 | 906 | 912 | PF00069 | 0.482 |
MOD_CK2_1 | 564 | 570 | PF00069 | 0.510 |
MOD_CK2_1 | 611 | 617 | PF00069 | 0.517 |
MOD_CK2_1 | 762 | 768 | PF00069 | 0.480 |
MOD_CK2_1 | 827 | 833 | PF00069 | 0.429 |
MOD_CK2_1 | 859 | 865 | PF00069 | 0.398 |
MOD_CMANNOS | 712 | 715 | PF00535 | 0.273 |
MOD_GlcNHglycan | 119 | 123 | PF01048 | 0.508 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.571 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.752 |
MOD_GlcNHglycan | 199 | 203 | PF01048 | 0.554 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.639 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.167 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.340 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.509 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.463 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.547 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.390 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.720 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.262 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.288 |
MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.260 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.698 |
MOD_GlcNHglycan | 684 | 687 | PF01048 | 0.317 |
MOD_GlcNHglycan | 762 | 765 | PF01048 | 0.592 |
MOD_GlcNHglycan | 876 | 879 | PF01048 | 0.449 |
MOD_GlcNHglycan | 897 | 900 | PF01048 | 0.418 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.576 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.680 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.742 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.720 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.646 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.400 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.374 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.330 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.454 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.657 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.457 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.513 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.475 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.488 |
MOD_GSK3_1 | 753 | 760 | PF00069 | 0.465 |
MOD_GSK3_1 | 823 | 830 | PF00069 | 0.395 |
MOD_GSK3_1 | 845 | 852 | PF00069 | 0.396 |
MOD_N-GLC_1 | 276 | 281 | PF02516 | 0.325 |
MOD_N-GLC_1 | 335 | 340 | PF02516 | 0.423 |
MOD_N-GLC_1 | 343 | 348 | PF02516 | 0.485 |
MOD_N-GLC_1 | 373 | 378 | PF02516 | 0.478 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.427 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.741 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.681 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.303 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.750 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.629 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.448 |
MOD_NEK2_1 | 556 | 561 | PF00069 | 0.487 |
MOD_NEK2_1 | 648 | 653 | PF00069 | 0.492 |
MOD_NEK2_1 | 793 | 798 | PF00069 | 0.356 |
MOD_NEK2_1 | 845 | 850 | PF00069 | 0.402 |
MOD_NEK2_2 | 300 | 305 | PF00069 | 0.354 |
MOD_NEK2_2 | 414 | 419 | PF00069 | 0.509 |
MOD_PIKK_1 | 440 | 446 | PF00454 | 0.539 |
MOD_PIKK_1 | 771 | 777 | PF00454 | 0.391 |
MOD_PK_1 | 659 | 665 | PF00069 | 0.597 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.380 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.452 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.537 |
MOD_PKA_2 | 597 | 603 | PF00069 | 0.509 |
MOD_PKA_2 | 840 | 846 | PF00069 | 0.395 |
MOD_PKA_2 | 903 | 909 | PF00069 | 0.489 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.336 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.476 |
MOD_Plk_1 | 373 | 379 | PF00069 | 0.390 |
MOD_Plk_1 | 429 | 435 | PF00069 | 0.540 |
MOD_Plk_1 | 588 | 594 | PF00069 | 0.522 |
MOD_Plk_1 | 600 | 606 | PF00069 | 0.553 |
MOD_Plk_1 | 753 | 759 | PF00069 | 0.380 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.404 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.264 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.342 |
MOD_Plk_4 | 373 | 379 | PF00069 | 0.391 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.494 |
MOD_Plk_4 | 516 | 522 | PF00069 | 0.496 |
MOD_Plk_4 | 707 | 713 | PF00069 | 0.486 |
MOD_Plk_4 | 747 | 753 | PF00069 | 0.391 |
MOD_Plk_4 | 811 | 817 | PF00069 | 0.595 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.618 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.712 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.351 |
MOD_ProDKin_1 | 564 | 570 | PF00069 | 0.496 |
MOD_ProDKin_1 | 603 | 609 | PF00069 | 0.547 |
MOD_ProDKin_1 | 762 | 768 | PF00069 | 0.498 |
MOD_ProDKin_1 | 779 | 785 | PF00069 | 0.481 |
MOD_ProDKin_1 | 827 | 833 | PF00069 | 0.502 |
MOD_SUMO_rev_2 | 615 | 620 | PF00179 | 0.546 |
TRG_DiLeu_BaEn_1 | 322 | 327 | PF01217 | 0.387 |
TRG_DiLeu_BaLyEn_6 | 544 | 549 | PF01217 | 0.539 |
TRG_DiLeu_BaLyEn_6 | 661 | 666 | PF01217 | 0.532 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.586 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 546 | 549 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 553 | 556 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 560 | 563 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 605 | 608 | PF00928 | 0.542 |
TRG_ENDOCYTIC_2 | 652 | 655 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 770 | 773 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 856 | 859 | PF00928 | 0.368 |
TRG_ER_diArg_1 | 433 | 435 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 860 | 863 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 887 | 890 | PF00400 | 0.473 |
TRG_NES_CRM1_1 | 746 | 758 | PF08389 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 360 | 364 | PF00026 | 0.576 |
TRG_Pf-PMV_PEXEL_1 | 7 | 11 | PF00026 | 0.447 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 30% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 53% | 95% |
A0A0N1IGQ2 | Leptomonas seymouri | 30% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 30% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 34% | 100% |
A0A0N1P9P1 | Leptomonas seymouri | 32% | 100% |
A0A0N1PCA9 | Leptomonas seymouri | 29% | 100% |
A0A0N1PE91 | Leptomonas seymouri | 28% | 100% |
A0A0N1PFI4 | Leptomonas seymouri | 31% | 100% |
A0A0S4JS70 | Bodo saltans | 25% | 100% |
A0A0S4KGT2 | Bodo saltans | 36% | 100% |
A0A0S4KKP7 | Bodo saltans | 25% | 100% |
A0A1X0NJ19 | Trypanosomatidae | 28% | 76% |
A0A1X0NJK2 | Trypanosomatidae | 27% | 100% |
A0A1X0NJX8 | Trypanosomatidae | 35% | 100% |
A0A1X0NKT7 | Trypanosomatidae | 39% | 100% |
A0A1X0NKX8 | Trypanosomatidae | 29% | 100% |
A0A1X0NMT3 | Trypanosomatidae | 30% | 100% |
A0A1X0NW84 | Trypanosomatidae | 31% | 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 | 29% | 100% |
A0A3Q8IJT4 | Leishmania donovani | 28% | 100% |
A0A3S5H5A5 | Leishmania donovani | 31% | 100% |
A0A3S5ISG2 | Trypanosoma rangeli | 30% | 100% |
A0A3S7WW18 | Leishmania donovani | 30% | 100% |
A0A3S7WW41 | Leishmania donovani | 29% | 100% |
A0A3S7WW71 | Leishmania donovani | 31% | 100% |
A0A3S7X430 | Leishmania donovani | 35% | 100% |
A0A3S7X438 | Leishmania donovani | 90% | 100% |
A0A3S7X460 | Leishmania donovani | 31% | 100% |
A0A3S7X470 | Leishmania donovani | 31% | 100% |
A0A422MYU1 | Trypanosoma rangeli | 30% | 100% |
A0A422MYX0 | Trypanosoma rangeli | 31% | 100% |
A4H3W4 | Leishmania braziliensis | 33% | 100% |
A4HE81 | Leishmania braziliensis | 29% | 100% |
A4HJ14 | Leishmania braziliensis | 35% | 100% |
A4HJ21 | Leishmania braziliensis | 27% | 100% |
A4HJ22 | Leishmania braziliensis | 72% | 99% |
A4HJ24 | Leishmania braziliensis | 30% | 100% |
A4HS39 | Leishmania infantum | 31% | 100% |
A4HYN0 | Leishmania infantum | 31% | 100% |
A4HYW1 | Leishmania infantum | 31% | 93% |
A4HYW2 | Leishmania infantum | 31% | 100% |
A4HYW3 | Leishmania infantum | 30% | 100% |
A4I1J4 | Leishmania infantum | 29% | 100% |
A4I6E4 | Leishmania infantum | 31% | 100% |
A4I6E6 | Leishmania infantum | 31% | 100% |
A4I6F0 | Leishmania infantum | 90% | 100% |
A4I6K4 | Leishmania infantum | 35% | 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) | 30% | 100% |
C9ZIE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 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) | 31% | 100% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 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 | 30% | 100% |
E9AIH3 | Leishmania braziliensis | 31% | 100% |
E9AIH4 | Leishmania braziliensis | 29% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 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) | 31% | 100% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AXM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B1J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 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 | 30% | 100% |
Q4Q6L9 | Leishmania major | 30% | 100% |
Q4Q6M2 | Leishmania major | 28% | 100% |
Q4Q6M4 | Leishmania major | 36% | 100% |
Q4Q9U3 | Leishmania major | 29% | 98% |
Q4QCS6 | Leishmania major | 29% | 100% |
Q4QCS7 | Leishmania major | 31% | 100% |
Q4QCS8 | Leishmania major | 31% | 100% |
Q4QCS9 | Leishmania major | 31% | 100% |
Q9U0T9 | Leishmania major | 33% | 100% |
V5AYJ1 | Trypanosoma cruzi | 30% | 100% |
V5B5I4 | Trypanosoma cruzi | 31% | 100% |
V5BA05 | Trypanosoma cruzi | 31% | 100% |
V5BEL3 | Trypanosoma cruzi | 31% | 100% |
V5BII7 | Trypanosoma cruzi | 29% | 76% |
V5BN20 | Trypanosoma cruzi | 33% | 100% |
V5D9Y2 | Trypanosoma cruzi | 31% | 100% |
V5DES7 | Trypanosoma cruzi | 29% | 100% |