Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 1 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 24 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 81 |
NetGPI | no | yes: 0, no: 82 |
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: A4HJ21
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 83 |
GO:0006807 | nitrogen compound metabolic process | 2 | 83 |
GO:0008152 | metabolic process | 1 | 83 |
GO:0019538 | protein metabolic process | 3 | 83 |
GO:0043170 | macromolecule metabolic process | 3 | 83 |
GO:0044238 | primary metabolic process | 2 | 83 |
GO:0071704 | organic substance metabolic process | 2 | 83 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 83 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 83 |
GO:0004175 | endopeptidase activity | 4 | 83 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 83 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 83 |
GO:0008233 | peptidase activity | 3 | 83 |
GO:0008234 | cysteine-type peptidase activity | 4 | 83 |
GO:0016787 | hydrolase activity | 2 | 83 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 83 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 320 | 324 | PF00656 | 0.547 |
CLV_C14_Caspase3-7 | 496 | 500 | PF00656 | 0.475 |
CLV_C14_Caspase3-7 | 568 | 572 | PF00656 | 0.567 |
CLV_C14_Caspase3-7 | 725 | 729 | PF00656 | 0.458 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.298 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.326 |
CLV_NRD_NRD_1 | 596 | 598 | PF00675 | 0.264 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.290 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 512 | 514 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 584 | 586 | PF00082 | 0.347 |
CLV_PCSK_KEX2_1 | 596 | 598 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 402 | 404 | PF00082 | 0.323 |
CLV_PCSK_PC1ET2_1 | 512 | 514 | PF00082 | 0.285 |
CLV_PCSK_PC1ET2_1 | 584 | 586 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 512 | 516 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 804 | 808 | PF00082 | 0.490 |
DEG_SCF_FBW7_1 | 204 | 209 | PF00400 | 0.194 |
DEG_SCF_FBW7_1 | 792 | 799 | PF00400 | 0.679 |
DEG_SPOP_SBC_1 | 118 | 122 | PF00917 | 0.780 |
DEG_SPOP_SBC_1 | 273 | 277 | PF00917 | 0.574 |
DEG_SPOP_SBC_1 | 796 | 800 | PF00917 | 0.354 |
DEG_SPOP_SBC_1 | 870 | 874 | PF00917 | 0.501 |
DOC_CKS1_1 | 793 | 798 | PF01111 | 0.560 |
DOC_CYCLIN_RxL_1 | 506 | 519 | PF00134 | 0.523 |
DOC_CYCLIN_yCln2_LP_2 | 468 | 474 | PF00134 | 0.380 |
DOC_CYCLIN_yCln2_LP_2 | 87 | 93 | PF00134 | 0.429 |
DOC_MAPK_gen_1 | 301 | 310 | PF00069 | 0.308 |
DOC_MAPK_gen_1 | 596 | 603 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 301 | 310 | PF00069 | 0.271 |
DOC_MAPK_MEF2A_6 | 656 | 664 | PF00069 | 0.388 |
DOC_PP1_RVXF_1 | 299 | 306 | PF00149 | 0.344 |
DOC_PP1_RVXF_1 | 444 | 450 | PF00149 | 0.556 |
DOC_PP2B_LxvP_1 | 138 | 141 | PF13499 | 0.305 |
DOC_PP2B_LxvP_1 | 468 | 471 | PF13499 | 0.363 |
DOC_PP2B_LxvP_1 | 87 | 90 | PF13499 | 0.428 |
DOC_PP4_FxxP_1 | 325 | 328 | PF00568 | 0.473 |
DOC_PP4_FxxP_1 | 392 | 395 | PF00568 | 0.479 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 587 | 591 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 639 | 643 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 764 | 768 | PF00917 | 0.218 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 796 | 800 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 870 | 874 | PF00917 | 0.579 |
DOC_USP7_UBL2_3 | 455 | 459 | PF12436 | 0.475 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.375 |
DOC_WW_Pin1_4 | 726 | 731 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 792 | 797 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 837 | 842 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 871 | 876 | PF00397 | 0.641 |
LIG_14-3-3_CanoR_1 | 146 | 151 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 173 | 181 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 188 | 193 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 286 | 295 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 333 | 339 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 45 | 49 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 516 | 526 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 577 | 587 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 671 | 677 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 787 | 793 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 835 | 841 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 846 | 855 | PF00244 | 0.448 |
LIG_Actin_WH2_2 | 349 | 365 | PF00022 | 0.363 |
LIG_Actin_WH2_2 | 483 | 500 | PF00022 | 0.372 |
LIG_BRCT_BRCA1_1 | 718 | 722 | PF00533 | 0.300 |
LIG_Clathr_ClatBox_1 | 450 | 454 | PF01394 | 0.363 |
LIG_deltaCOP1_diTrp_1 | 180 | 183 | PF00928 | 0.263 |
LIG_deltaCOP1_diTrp_1 | 589 | 595 | PF00928 | 0.471 |
LIG_eIF4E_1 | 760 | 766 | PF01652 | 0.195 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.572 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.496 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.416 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.346 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.469 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.476 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.429 |
LIG_FHA_1 | 559 | 565 | PF00498 | 0.494 |
LIG_FHA_1 | 668 | 674 | PF00498 | 0.457 |
LIG_FHA_1 | 686 | 692 | PF00498 | 0.554 |
LIG_FHA_1 | 776 | 782 | PF00498 | 0.398 |
LIG_FHA_1 | 798 | 804 | PF00498 | 0.501 |
LIG_FHA_1 | 854 | 860 | PF00498 | 0.349 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.495 |
LIG_FHA_2 | 566 | 572 | PF00498 | 0.494 |
LIG_FHA_2 | 614 | 620 | PF00498 | 0.438 |
LIG_FHA_2 | 688 | 694 | PF00498 | 0.589 |
LIG_GBD_Chelix_1 | 773 | 781 | PF00786 | 0.237 |
LIG_IRF3_LxIS_1 | 330 | 337 | PF10401 | 0.363 |
LIG_LIR_Apic_2 | 323 | 329 | PF02991 | 0.474 |
LIG_LIR_Apic_2 | 416 | 422 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 275 | 285 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 463 | 472 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 505 | 515 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 589 | 598 | PF02991 | 0.526 |
LIG_LIR_Gen_1 | 619 | 629 | PF02991 | 0.497 |
LIG_LIR_LC3C_4 | 778 | 783 | PF02991 | 0.221 |
LIG_LIR_Nem_3 | 180 | 184 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 275 | 281 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 463 | 467 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 505 | 510 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 547 | 553 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 589 | 594 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 619 | 625 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 812 | 818 | PF02991 | 0.474 |
LIG_NRBOX | 447 | 453 | PF00104 | 0.363 |
LIG_NRBOX | 706 | 712 | PF00104 | 0.223 |
LIG_Pex14_1 | 528 | 532 | PF04695 | 0.538 |
LIG_Pex14_2 | 475 | 479 | PF04695 | 0.372 |
LIG_PTB_Apo_2 | 367 | 374 | PF02174 | 0.364 |
LIG_SH2_CRK | 153 | 157 | PF00017 | 0.384 |
LIG_SH2_CRK | 172 | 176 | PF00017 | 0.254 |
LIG_SH2_CRK | 464 | 468 | PF00017 | 0.473 |
LIG_SH2_CRK | 761 | 765 | PF00017 | 0.438 |
LIG_SH2_NCK_1 | 278 | 282 | PF00017 | 0.621 |
LIG_SH2_PTP2 | 326 | 329 | PF00017 | 0.575 |
LIG_SH2_SRC | 278 | 281 | PF00017 | 0.335 |
LIG_SH2_SRC | 326 | 329 | PF00017 | 0.551 |
LIG_SH2_STAP1 | 190 | 194 | PF00017 | 0.317 |
LIG_SH2_STAP1 | 278 | 282 | PF00017 | 0.627 |
LIG_SH2_STAP1 | 464 | 468 | PF00017 | 0.492 |
LIG_SH2_STAP1 | 743 | 747 | PF00017 | 0.497 |
LIG_SH2_STAP1 | 775 | 779 | PF00017 | 0.385 |
LIG_SH2_STAT3 | 190 | 193 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 631 | 634 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 751 | 754 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 775 | 778 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 879 | 882 | PF00017 | 0.609 |
LIG_SH3_3 | 278 | 284 | PF00018 | 0.611 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.444 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.637 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.601 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.534 |
LIG_SUMO_SIM_anti_2 | 854 | 859 | PF11976 | 0.258 |
LIG_SUMO_SIM_par_1 | 449 | 454 | PF11976 | 0.363 |
LIG_SUMO_SIM_par_1 | 672 | 677 | PF11976 | 0.322 |
LIG_SUMO_SIM_par_1 | 687 | 696 | PF11976 | 0.584 |
LIG_TRAF2_1 | 217 | 220 | PF00917 | 0.399 |
LIG_TRAF2_1 | 256 | 259 | PF00917 | 0.500 |
LIG_TRFH_1 | 751 | 755 | PF08558 | 0.363 |
LIG_TYR_ITIM | 170 | 175 | PF00017 | 0.321 |
LIG_TYR_ITSM | 185 | 192 | PF00017 | 0.194 |
LIG_TYR_ITSM | 274 | 281 | PF00017 | 0.616 |
LIG_UBA3_1 | 450 | 455 | PF00899 | 0.335 |
MOD_CDC14_SPxK_1 | 840 | 843 | PF00782 | 0.279 |
MOD_CDK_SPxK_1 | 837 | 843 | PF00069 | 0.267 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.595 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.329 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.344 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.508 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.505 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.333 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.460 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.685 |
MOD_CK1_1 | 687 | 693 | PF00069 | 0.607 |
MOD_CK1_1 | 713 | 719 | PF00069 | 0.480 |
MOD_CK1_1 | 767 | 773 | PF00069 | 0.439 |
MOD_CK1_1 | 786 | 792 | PF00069 | 0.714 |
MOD_CK1_1 | 799 | 805 | PF00069 | 0.442 |
MOD_CK1_1 | 831 | 837 | PF00069 | 0.578 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.487 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.406 |
MOD_CK2_1 | 823 | 829 | PF00069 | 0.513 |
MOD_CK2_1 | 882 | 888 | PF00069 | 0.799 |
MOD_CMANNOS | 420 | 423 | PF00535 | 0.166 |
MOD_Cter_Amidation | 400 | 403 | PF01082 | 0.279 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.697 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.368 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.370 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.321 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.391 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.352 |
MOD_GlcNHglycan | 534 | 537 | PF01048 | 0.335 |
MOD_GlcNHglycan | 715 | 718 | PF01048 | 0.522 |
MOD_GlcNHglycan | 829 | 833 | PF01048 | 0.555 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.618 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.688 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.512 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.373 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.330 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.427 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.348 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.343 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.307 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.331 |
MOD_GSK3_1 | 613 | 620 | PF00069 | 0.369 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.604 |
MOD_GSK3_1 | 722 | 729 | PF00069 | 0.459 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.576 |
MOD_GSK3_1 | 764 | 771 | PF00069 | 0.337 |
MOD_GSK3_1 | 792 | 799 | PF00069 | 0.635 |
MOD_GSK3_1 | 805 | 812 | PF00069 | 0.396 |
MOD_GSK3_1 | 824 | 831 | PF00069 | 0.460 |
MOD_GSK3_1 | 847 | 854 | PF00069 | 0.372 |
MOD_GSK3_1 | 877 | 884 | PF00069 | 0.698 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.557 |
MOD_N-GLC_1 | 184 | 189 | PF02516 | 0.321 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.492 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.557 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.351 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.349 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.411 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.422 |
MOD_NEK2_1 | 662 | 667 | PF00069 | 0.436 |
MOD_NEK2_1 | 672 | 677 | PF00069 | 0.382 |
MOD_NEK2_1 | 681 | 686 | PF00069 | 0.548 |
MOD_NEK2_1 | 710 | 715 | PF00069 | 0.444 |
MOD_NEK2_1 | 722 | 727 | PF00069 | 0.456 |
MOD_NEK2_1 | 765 | 770 | PF00069 | 0.466 |
MOD_NEK2_1 | 805 | 810 | PF00069 | 0.476 |
MOD_NEK2_1 | 823 | 828 | PF00069 | 0.486 |
MOD_NEK2_1 | 847 | 852 | PF00069 | 0.440 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.636 |
MOD_NEK2_2 | 321 | 326 | PF00069 | 0.414 |
MOD_NEK2_2 | 565 | 570 | PF00069 | 0.222 |
MOD_NEK2_2 | 810 | 815 | PF00069 | 0.397 |
MOD_PIKK_1 | 536 | 542 | PF00454 | 0.468 |
MOD_PIKK_1 | 651 | 657 | PF00454 | 0.535 |
MOD_PIKK_1 | 674 | 680 | PF00454 | 0.395 |
MOD_PK_1 | 656 | 662 | PF00069 | 0.266 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.552 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.509 |
MOD_PKA_2 | 497 | 503 | PF00069 | 0.372 |
MOD_PKA_2 | 517 | 523 | PF00069 | 0.430 |
MOD_PKA_2 | 578 | 584 | PF00069 | 0.362 |
MOD_PKA_2 | 786 | 792 | PF00069 | 0.563 |
MOD_PKA_2 | 823 | 829 | PF00069 | 0.487 |
MOD_PKA_2 | 882 | 888 | PF00069 | 0.477 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.436 |
MOD_Plk_1 | 184 | 190 | PF00069 | 0.327 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.453 |
MOD_Plk_1 | 693 | 699 | PF00069 | 0.719 |
MOD_Plk_1 | 824 | 830 | PF00069 | 0.464 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.450 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.359 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.358 |
MOD_Plk_4 | 521 | 527 | PF00069 | 0.345 |
MOD_Plk_4 | 558 | 564 | PF00069 | 0.370 |
MOD_Plk_4 | 587 | 593 | PF00069 | 0.458 |
MOD_Plk_4 | 617 | 623 | PF00069 | 0.344 |
MOD_Plk_4 | 656 | 662 | PF00069 | 0.426 |
MOD_Plk_4 | 693 | 699 | PF00069 | 0.622 |
MOD_Plk_4 | 810 | 816 | PF00069 | 0.508 |
MOD_Plk_4 | 853 | 859 | PF00069 | 0.424 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.711 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.559 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.375 |
MOD_ProDKin_1 | 726 | 732 | PF00069 | 0.531 |
MOD_ProDKin_1 | 792 | 798 | PF00069 | 0.546 |
MOD_ProDKin_1 | 837 | 843 | PF00069 | 0.413 |
MOD_ProDKin_1 | 871 | 877 | PF00069 | 0.640 |
MOD_SUMO_for_1 | 691 | 694 | PF00179 | 0.437 |
MOD_SUMO_rev_2 | 224 | 233 | PF00179 | 0.385 |
TRG_DiLeu_BaEn_1 | 605 | 610 | PF01217 | 0.194 |
TRG_DiLeu_BaEn_3 | 228 | 234 | PF01217 | 0.166 |
TRG_DiLeu_BaEn_4 | 258 | 264 | PF01217 | 0.420 |
TRG_DiLeu_BaLyEn_6 | 510 | 515 | PF01217 | 0.375 |
TRG_DiLeu_BaLyEn_6 | 668 | 673 | PF01217 | 0.237 |
TRG_ENDOCYTIC_2 | 172 | 175 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.519 |
TRG_ENDOCYTIC_2 | 464 | 467 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 550 | 553 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 760 | 763 | PF00928 | 0.319 |
TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.370 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 515 | 518 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 576 | 579 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 585 | 587 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 595 | 597 | PF00400 | 0.385 |
TRG_NES_CRM1_1 | 443 | 454 | PF08389 | 0.166 |
TRG_NES_CRM1_1 | 544 | 556 | PF08389 | 0.170 |
TRG_NLS_MonoExtC_3 | 5 | 11 | PF00514 | 0.401 |
TRG_NLS_MonoExtN_4 | 4 | 10 | PF00514 | 0.417 |
TRG_Pf-PMV_PEXEL_1 | 173 | 177 | PF00026 | 0.256 |
TRG_Pf-PMV_PEXEL_1 | 485 | 489 | PF00026 | 0.166 |
TRG_Pf-PMV_PEXEL_1 | 513 | 517 | PF00026 | 0.415 |
TRG_Pf-PMV_PEXEL_1 | 679 | 683 | PF00026 | 0.435 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 25% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 30% | 90% |
A0A0N1ILF1 | Leptomonas seymouri | 25% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 28% | 100% |
A0A0N1P9P1 | Leptomonas seymouri | 28% | 100% |
A0A0N1PCA9 | Leptomonas seymouri | 25% | 100% |
A0A0N1PE91 | Leptomonas seymouri | 48% | 100% |
A0A0N1PFI4 | Leptomonas seymouri | 27% | 100% |
A0A0S4JLK6 | Bodo saltans | 25% | 100% |
A0A0S4JS70 | Bodo saltans | 22% | 100% |
A0A0S4KGT2 | Bodo saltans | 27% | 100% |
A0A1X0NJX8 | Trypanosomatidae | 28% | 100% |
A0A1X0NKX8 | Trypanosomatidae | 28% | 100% |
A0A1X0NMT3 | Trypanosomatidae | 28% | 100% |
A0A1X0NW84 | Trypanosomatidae | 25% | 100% |
A0A1X0NW85 | Trypanosomatidae | 25% | 100% |
A0A1X0NW89 | Trypanosomatidae | 28% | 100% |
A0A1X0NWW1 | Trypanosomatidae | 26% | 100% |
A0A3Q8IDD4 | Leishmania donovani | 25% | 100% |
A0A3Q8IJT4 | Leishmania donovani | 75% | 100% |
A0A3S5H5A5 | Leishmania donovani | 28% | 100% |
A0A3S5ISG2 | Trypanosoma rangeli | 26% | 100% |
A0A3S7WW41 | Leishmania donovani | 26% | 100% |
A0A3S7WW71 | Leishmania donovani | 25% | 100% |
A0A3S7X430 | Leishmania donovani | 28% | 100% |
A0A3S7X438 | Leishmania donovani | 28% | 95% |
A0A3S7X460 | Leishmania donovani | 25% | 100% |
A0A3S7X470 | Leishmania donovani | 26% | 100% |
A0A422MYU1 | Trypanosoma rangeli | 26% | 97% |
A0A422MYX0 | Trypanosoma rangeli | 26% | 100% |
A4H3W4 | Leishmania braziliensis | 29% | 100% |
A4HE81 | Leishmania braziliensis | 24% | 100% |
A4HJ14 | Leishmania braziliensis | 28% | 100% |
A4HJ22 | Leishmania braziliensis | 29% | 94% |
A4HJ24 | Leishmania braziliensis | 25% | 100% |
A4HS39 | Leishmania infantum | 28% | 100% |
A4HYW2 | Leishmania infantum | 25% | 100% |
A4HYW3 | Leishmania infantum | 26% | 100% |
A4I1J4 | Leishmania infantum | 24% | 100% |
A4I6E4 | Leishmania infantum | 26% | 100% |
A4I6E6 | Leishmania infantum | 25% | 100% |
A4I6F0 | Leishmania infantum | 28% | 95% |
A4I6K4 | Leishmania infantum | 28% | 100% |
A4I6K6 | Leishmania infantum | 76% | 100% |
C9ZIE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 83% |
C9ZIE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 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) | 24% | 100% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 95% |
E8NHG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AIH3 | Leishmania braziliensis | 25% | 100% |
E9AIH4 | Leishmania braziliensis | 26% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AXM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9B1J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B1J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
E9B1J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
Q4Q6L7 | Leishmania major | 25% | 100% |
Q4Q6L9 | Leishmania major | 26% | 100% |
Q4Q6M0 | Leishmania major | 27% | 100% |
Q4Q6M2 | Leishmania major | 75% | 100% |
Q4Q6M4 | Leishmania major | 28% | 100% |
Q4Q9U3 | Leishmania major | 24% | 100% |
Q4QCS6 | Leishmania major | 25% | 100% |
Q4QCS7 | Leishmania major | 25% | 93% |
Q9U0T9 | Leishmania major | 28% | 100% |
V5AYJ1 | Trypanosoma cruzi | 23% | 100% |
V5BA05 | Trypanosoma cruzi | 26% | 100% |
V5BEL3 | Trypanosoma cruzi | 26% | 100% |
V5BII7 | Trypanosoma cruzi | 28% | 72% |
V5BN20 | Trypanosoma cruzi | 28% | 100% |
V5D9Y2 | Trypanosoma cruzi | 27% | 100% |
V5DES7 | Trypanosoma cruzi | 26% | 100% |