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: 98 |
NetGPI | no | yes: 0, no: 99 |
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: A4HJ22
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 100 |
GO:0006807 | nitrogen compound metabolic process | 2 | 100 |
GO:0008152 | metabolic process | 1 | 100 |
GO:0019538 | protein metabolic process | 3 | 100 |
GO:0043170 | macromolecule metabolic process | 3 | 100 |
GO:0044238 | primary metabolic process | 2 | 100 |
GO:0071704 | organic substance metabolic process | 2 | 100 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 100 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 100 |
GO:0004175 | endopeptidase activity | 4 | 100 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 100 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 100 |
GO:0008233 | peptidase activity | 3 | 100 |
GO:0008234 | cysteine-type peptidase activity | 4 | 100 |
GO:0016787 | hydrolase activity | 2 | 100 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 100 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 274 | 278 | PF00656 | 0.266 |
CLV_C14_Caspase3-7 | 32 | 36 | PF00656 | 0.594 |
CLV_C14_Caspase3-7 | 474 | 478 | PF00656 | 0.439 |
CLV_C14_Caspase3-7 | 529 | 533 | PF00656 | 0.379 |
CLV_C14_Caspase3-7 | 752 | 756 | PF00656 | 0.277 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 444 | 446 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 551 | 553 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 809 | 811 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 913 | 915 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.545 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 809 | 811 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 913 | 915 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 693 | 697 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 878 | 882 | PF00082 | 0.430 |
DEG_APCC_DBOX_1 | 631 | 639 | PF00400 | 0.538 |
DEG_APCC_DBOX_1 | 896 | 904 | PF00400 | 0.440 |
DEG_MDM2_SWIB_1 | 593 | 600 | PF02201 | 0.419 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.709 |
DEG_SCF_FBW7_1 | 885 | 892 | PF00400 | 0.527 |
DEG_SPOP_SBC_1 | 30 | 34 | PF00917 | 0.436 |
DEG_SPOP_SBC_1 | 889 | 893 | PF00917 | 0.291 |
DOC_CYCLIN_RxL_1 | 794 | 808 | PF00134 | 0.527 |
DOC_MAPK_gen_1 | 430 | 438 | PF00069 | 0.489 |
DOC_MAPK_gen_1 | 797 | 806 | PF00069 | 0.559 |
DOC_MAPK_gen_1 | 895 | 903 | PF00069 | 0.490 |
DOC_MAPK_JIP1_4 | 800 | 806 | PF00069 | 0.254 |
DOC_MAPK_JIP1_4 | 83 | 89 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 632 | 640 | PF00069 | 0.379 |
DOC_MAPK_MEF2A_6 | 797 | 806 | PF00069 | 0.354 |
DOC_MAPK_MEF2A_6 | 850 | 858 | PF00069 | 0.465 |
DOC_PP1_RVXF_1 | 853 | 859 | PF00149 | 0.442 |
DOC_PP2B_LxvP_1 | 638 | 641 | PF13499 | 0.465 |
DOC_PP4_FxxP_1 | 416 | 419 | PF00568 | 0.532 |
DOC_PP4_FxxP_1 | 498 | 501 | PF00568 | 0.484 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 483 | 487 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 601 | 605 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 607 | 611 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 645 | 649 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 925 | 929 | PF00917 | 0.475 |
DOC_USP7_MATH_2 | 840 | 846 | PF00917 | 0.258 |
DOC_USP7_UBL2_3 | 149 | 153 | PF12436 | 0.523 |
DOC_USP7_UBL2_3 | 561 | 565 | PF12436 | 0.481 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.347 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 613 | 618 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 771 | 776 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 885 | 890 | PF00397 | 0.347 |
DOC_WW_Pin1_4 | 904 | 909 | PF00397 | 0.422 |
LIG_14-3-3_CanoR_1 | 101 | 107 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 213 | 219 | PF00244 | 0.782 |
LIG_14-3-3_CanoR_1 | 272 | 280 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 517 | 521 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 546 | 554 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 750 | 760 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 830 | 840 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 855 | 859 | PF00244 | 0.426 |
LIG_Actin_WH2_2 | 652 | 667 | PF00022 | 0.515 |
LIG_Actin_WH2_2 | 840 | 857 | PF00022 | 0.491 |
LIG_APCC_ABBA_1 | 622 | 627 | PF00400 | 0.363 |
LIG_BIR_III_2 | 772 | 776 | PF00653 | 0.285 |
LIG_BRCT_BRCA1_1 | 121 | 125 | PF00533 | 0.592 |
LIG_BRCT_BRCA1_1 | 278 | 282 | PF00533 | 0.349 |
LIG_BRCT_BRCA1_1 | 906 | 910 | PF00533 | 0.482 |
LIG_deltaCOP1_diTrp_1 | 277 | 282 | PF00928 | 0.254 |
LIG_deltaCOP1_diTrp_1 | 440 | 447 | PF00928 | 0.521 |
LIG_deltaCOP1_diTrp_1 | 723 | 731 | PF00928 | 0.480 |
LIG_EH1_1 | 660 | 668 | PF00400 | 0.508 |
LIG_eIF4E_1 | 661 | 667 | PF01652 | 0.505 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.609 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.433 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.744 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.655 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.430 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.364 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.474 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.546 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.452 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.480 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.683 |
LIG_FHA_1 | 651 | 657 | PF00498 | 0.489 |
LIG_FHA_1 | 752 | 758 | PF00498 | 0.422 |
LIG_FHA_1 | 839 | 845 | PF00498 | 0.524 |
LIG_FHA_1 | 879 | 885 | PF00498 | 0.398 |
LIG_FHA_1 | 916 | 922 | PF00498 | 0.431 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.522 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.545 |
LIG_FHA_2 | 218 | 224 | PF00498 | 0.389 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.266 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.388 |
LIG_FHA_2 | 527 | 533 | PF00498 | 0.492 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.513 |
LIG_FHA_2 | 833 | 839 | PF00498 | 0.467 |
LIG_IBAR_NPY_1 | 239 | 241 | PF08397 | 0.345 |
LIG_LIR_Apic_2 | 234 | 240 | PF02991 | 0.303 |
LIG_LIR_Apic_2 | 351 | 357 | PF02991 | 0.463 |
LIG_LIR_Apic_2 | 440 | 446 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 122 | 132 | PF02991 | 0.611 |
LIG_LIR_Gen_1 | 136 | 146 | PF02991 | 0.620 |
LIG_LIR_Gen_1 | 560 | 571 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 594 | 601 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 620 | 629 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 660 | 667 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 777 | 786 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 136 | 141 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 277 | 283 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 560 | 566 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 569 | 573 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 586 | 591 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 594 | 600 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 620 | 626 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 660 | 664 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 73 | 77 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 777 | 782 | PF02991 | 0.379 |
LIG_LYPXL_yS_3 | 556 | 559 | PF13949 | 0.546 |
LIG_MYND_1 | 236 | 240 | PF01753 | 0.314 |
LIG_NRBOX | 899 | 905 | PF00104 | 0.250 |
LIG_Pex14_1 | 443 | 447 | PF04695 | 0.363 |
LIG_Pex14_2 | 593 | 597 | PF04695 | 0.470 |
LIG_Pex14_2 | 70 | 74 | PF04695 | 0.718 |
LIG_PTB_Apo_2 | 874 | 881 | PF02174 | 0.460 |
LIG_SH2_CRK | 138 | 142 | PF00017 | 0.599 |
LIG_SH2_CRK | 252 | 256 | PF00017 | 0.384 |
LIG_SH2_CRK | 261 | 265 | PF00017 | 0.294 |
LIG_SH2_CRK | 354 | 358 | PF00017 | 0.531 |
LIG_SH2_CRK | 563 | 567 | PF00017 | 0.474 |
LIG_SH2_CRK | 570 | 574 | PF00017 | 0.473 |
LIG_SH2_CRK | 661 | 665 | PF00017 | 0.491 |
LIG_SH2_CRK | 779 | 783 | PF00017 | 0.365 |
LIG_SH2_GRB2like | 237 | 240 | PF00017 | 0.494 |
LIG_SH2_GRB2like | 354 | 357 | PF00017 | 0.556 |
LIG_SH2_NCK_1 | 261 | 265 | PF00017 | 0.420 |
LIG_SH2_NCK_1 | 570 | 574 | PF00017 | 0.496 |
LIG_SH2_PTP2 | 866 | 869 | PF00017 | 0.403 |
LIG_SH2_SRC | 237 | 240 | PF00017 | 0.598 |
LIG_SH2_SRC | 449 | 452 | PF00017 | 0.490 |
LIG_SH2_SRC | 534 | 537 | PF00017 | 0.493 |
LIG_SH2_SRC | 866 | 869 | PF00017 | 0.362 |
LIG_SH2_STAP1 | 289 | 293 | PF00017 | 0.322 |
LIG_SH2_STAP1 | 319 | 323 | PF00017 | 0.332 |
LIG_SH2_STAT3 | 147 | 150 | PF00017 | 0.549 |
LIG_SH2_STAT3 | 23 | 26 | PF00017 | 0.441 |
LIG_SH2_STAT3 | 319 | 322 | PF00017 | 0.420 |
LIG_SH2_STAT3 | 615 | 618 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 534 | 537 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 634 | 637 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 661 | 664 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 779 | 782 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 866 | 869 | PF00017 | 0.361 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.447 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.532 |
LIG_SH3_3 | 464 | 470 | PF00018 | 0.446 |
LIG_SH3_3 | 834 | 840 | PF00018 | 0.548 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.589 |
LIG_SH3_3 | 928 | 934 | PF00018 | 0.359 |
LIG_SUMO_SIM_anti_2 | 329 | 337 | PF11976 | 0.438 |
LIG_SUMO_SIM_anti_2 | 380 | 389 | PF11976 | 0.386 |
LIG_SUMO_SIM_par_1 | 329 | 337 | PF11976 | 0.166 |
LIG_SUMO_SIM_par_1 | 800 | 805 | PF11976 | 0.400 |
LIG_SUMO_SIM_par_1 | 83 | 88 | PF11976 | 0.468 |
LIG_TYR_ITIM | 554 | 559 | PF00017 | 0.546 |
LIG_WRC_WIRS_1 | 588 | 593 | PF05994 | 0.522 |
LIG_WRC_WIRS_1 | 71 | 76 | PF05994 | 0.436 |
LIG_WRC_WIRS_1 | 757 | 762 | PF05994 | 0.500 |
LIG_WRC_WIRS_1 | 926 | 931 | PF05994 | 0.414 |
MOD_CDK_SPxxK_3 | 259 | 266 | PF00069 | 0.384 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.572 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.624 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.587 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.589 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.656 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.311 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.531 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.534 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.440 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.610 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.642 |
MOD_CK1_1 | 610 | 616 | PF00069 | 0.479 |
MOD_CK1_1 | 805 | 811 | PF00069 | 0.429 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.459 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.707 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.528 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.508 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.478 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.487 |
MOD_CK2_1 | 771 | 777 | PF00069 | 0.510 |
MOD_CK2_1 | 808 | 814 | PF00069 | 0.479 |
MOD_CK2_1 | 868 | 874 | PF00069 | 0.372 |
MOD_CK2_1 | 916 | 922 | PF00069 | 0.483 |
MOD_CMANNOS | 721 | 724 | PF00535 | 0.273 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.592 |
MOD_GlcNHglycan | 120 | 124 | PF01048 | 0.499 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.652 |
MOD_GlcNHglycan | 25 | 29 | PF01048 | 0.532 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.374 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.326 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.349 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.287 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.723 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.265 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.780 |
MOD_GlcNHglycan | 685 | 689 | PF01048 | 0.329 |
MOD_GlcNHglycan | 693 | 696 | PF01048 | 0.314 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.626 |
MOD_GlcNHglycan | 892 | 895 | PF01048 | 0.498 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.614 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.608 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.643 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.645 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.614 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.676 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.692 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.373 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.347 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.433 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.469 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.458 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.511 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.519 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.477 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.501 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.674 |
MOD_GSK3_1 | 767 | 774 | PF00069 | 0.555 |
MOD_GSK3_1 | 804 | 811 | PF00069 | 0.350 |
MOD_GSK3_1 | 838 | 845 | PF00069 | 0.393 |
MOD_GSK3_1 | 854 | 861 | PF00069 | 0.387 |
MOD_GSK3_1 | 884 | 891 | PF00069 | 0.464 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.457 |
MOD_N-GLC_1 | 110 | 115 | PF02516 | 0.599 |
MOD_N-GLC_1 | 283 | 288 | PF02516 | 0.326 |
MOD_N-GLC_1 | 342 | 347 | PF02516 | 0.437 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.610 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.604 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.491 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.568 |
MOD_NEK2_1 | 657 | 662 | PF00069 | 0.490 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.526 |
MOD_NEK2_1 | 684 | 689 | PF00069 | 0.488 |
MOD_NEK2_1 | 802 | 807 | PF00069 | 0.356 |
MOD_NEK2_1 | 854 | 859 | PF00069 | 0.393 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.733 |
MOD_NEK2_1 | 884 | 889 | PF00069 | 0.417 |
MOD_NEK2_1 | 903 | 908 | PF00069 | 0.502 |
MOD_NEK2_1 | 916 | 921 | PF00069 | 0.521 |
MOD_NEK2_2 | 307 | 312 | PF00069 | 0.361 |
MOD_NEK2_2 | 424 | 429 | PF00069 | 0.518 |
MOD_PIKK_1 | 183 | 189 | PF00454 | 0.449 |
MOD_PIKK_1 | 283 | 289 | PF00454 | 0.375 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.416 |
MOD_PIKK_1 | 393 | 399 | PF00454 | 0.300 |
MOD_PIKK_1 | 450 | 456 | PF00454 | 0.541 |
MOD_PIKK_1 | 645 | 651 | PF00454 | 0.579 |
MOD_PIKK_1 | 780 | 786 | PF00454 | 0.382 |
MOD_PIKK_1 | 916 | 922 | PF00454 | 0.537 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.491 |
MOD_PKA_2 | 271 | 277 | PF00069 | 0.338 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.389 |
MOD_PKA_2 | 516 | 522 | PF00069 | 0.455 |
MOD_PKA_2 | 545 | 551 | PF00069 | 0.536 |
MOD_PKA_2 | 749 | 755 | PF00069 | 0.379 |
MOD_PKA_2 | 808 | 814 | PF00069 | 0.483 |
MOD_PKA_2 | 849 | 855 | PF00069 | 0.380 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.536 |
MOD_Plk_1 | 350 | 356 | PF00069 | 0.492 |
MOD_Plk_1 | 716 | 722 | PF00069 | 0.470 |
MOD_Plk_2-3 | 116 | 122 | PF00069 | 0.656 |
MOD_Plk_2-3 | 767 | 773 | PF00069 | 0.324 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.561 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.713 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.331 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.288 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.340 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.262 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.399 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.501 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.503 |
MOD_Plk_4 | 659 | 665 | PF00069 | 0.499 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.500 |
MOD_Plk_4 | 716 | 722 | PF00069 | 0.489 |
MOD_Plk_4 | 756 | 762 | PF00069 | 0.404 |
MOD_Plk_4 | 842 | 848 | PF00069 | 0.428 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.619 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.347 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.527 |
MOD_ProDKin_1 | 613 | 619 | PF00069 | 0.546 |
MOD_ProDKin_1 | 771 | 777 | PF00069 | 0.511 |
MOD_ProDKin_1 | 885 | 891 | PF00069 | 0.349 |
MOD_ProDKin_1 | 904 | 910 | PF00069 | 0.380 |
TRG_DiLeu_BaEn_1 | 329 | 334 | PF01217 | 0.397 |
TRG_DiLeu_BaEn_2 | 841 | 847 | PF01217 | 0.398 |
TRG_DiLeu_BaEn_4 | 160 | 166 | PF01217 | 0.431 |
TRG_DiLeu_BaLyEn_6 | 554 | 559 | PF01217 | 0.553 |
TRG_DiLeu_BaLyEn_6 | 670 | 675 | PF01217 | 0.531 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.625 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 556 | 559 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 563 | 566 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 570 | 573 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 588 | 591 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 661 | 664 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 779 | 782 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 865 | 868 | PF00928 | 0.347 |
TRG_ER_diArg_1 | 443 | 445 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 896 | 899 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 937 | 940 | PF00400 | 0.302 |
TRG_ER_diArg_1 | 94 | 96 | PF00400 | 0.395 |
TRG_NES_CRM1_1 | 755 | 768 | PF08389 | 0.492 |
TRG_Pf-PMV_PEXEL_1 | 153 | 157 | PF00026 | 0.615 |
TRG_Pf-PMV_PEXEL_1 | 183 | 187 | PF00026 | 0.668 |
TRG_Pf-PMV_PEXEL_1 | 870 | 874 | PF00026 | 0.442 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 28% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 55% | 96% |
A0A0N1IGQ2 | Leptomonas seymouri | 30% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 31% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 33% | 100% |
A0A0N1P9P1 | Leptomonas seymouri | 32% | 100% |
A0A0N1PCA9 | Leptomonas seymouri | 29% | 100% |
A0A0N1PFI4 | Leptomonas seymouri | 30% | 100% |
A0A0S4JS70 | Bodo saltans | 26% | 100% |
A0A0S4KGT2 | Bodo saltans | 37% | 100% |
A0A1X0NJ19 | Trypanosomatidae | 29% | 77% |
A0A1X0NJK2 | Trypanosomatidae | 27% | 100% |
A0A1X0NJX8 | Trypanosomatidae | 35% | 100% |
A0A1X0NKT7 | Trypanosomatidae | 40% | 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 | 32% | 100% |
A0A3Q8IDD4 | Leishmania donovani | 31% | 100% |
A0A3Q8IJT4 | Leishmania donovani | 28% | 100% |
A0A3S5H5A5 | Leishmania donovani | 30% | 100% |
A0A3S5ISG2 | Trypanosoma rangeli | 31% | 100% |
A0A3S7WW18 | Leishmania donovani | 32% | 100% |
A0A3S7WW41 | Leishmania donovani | 28% | 100% |
A0A3S7WW71 | Leishmania donovani | 30% | 100% |
A0A3S7X430 | Leishmania donovani | 33% | 100% |
A0A3S7X438 | Leishmania donovani | 72% | 100% |
A0A3S7X460 | Leishmania donovani | 30% | 100% |
A0A3S7X463 | Leishmania donovani | 30% | 100% |
A0A3S7X470 | Leishmania donovani | 31% | 100% |
A0A422MYU1 | Trypanosoma rangeli | 30% | 100% |
A0A422MYX0 | Trypanosoma rangeli | 32% | 100% |
A4H3W4 | Leishmania braziliensis | 31% | 100% |
A4HE81 | Leishmania braziliensis | 30% | 100% |
A4HJ14 | Leishmania braziliensis | 33% | 100% |
A4HJ21 | Leishmania braziliensis | 29% | 100% |
A4HJ24 | Leishmania braziliensis | 30% | 100% |
A4HS39 | Leishmania infantum | 30% | 100% |
A4HYN0 | Leishmania infantum | 32% | 100% |
A4HYW1 | Leishmania infantum | 32% | 93% |
A4HYW2 | Leishmania infantum | 30% | 100% |
A4HYW3 | Leishmania infantum | 28% | 100% |
A4I1J4 | Leishmania infantum | 31% | 100% |
A4I6E4 | Leishmania infantum | 31% | 100% |
A4I6E6 | Leishmania infantum | 30% | 100% |
A4I6F0 | Leishmania infantum | 72% | 100% |
A4I6K4 | Leishmania infantum | 33% | 100% |
A4I6K5 | Leishmania infantum | 29% | 100% |
A4I6K6 | Leishmania infantum | 31% | 100% |
C9ZIE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 88% |
C9ZIE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZIE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZN52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZN53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
E8NHG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AIH1 | Leishmania braziliensis | 30% | 100% |
E9AIH3 | Leishmania braziliensis | 30% | 100% |
E9AIH4 | Leishmania braziliensis | 29% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AUQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AUQ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AXM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B1J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B1J1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9B1J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B1J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
Q4Q6L7 | Leishmania major | 30% | 100% |
Q4Q6L9 | Leishmania major | 30% | 100% |
Q4Q6M0 | Leishmania major | 72% | 99% |
Q4Q6M2 | Leishmania major | 29% | 97% |
Q4Q6M3 | Leishmania major | 30% | 100% |
Q4Q6M4 | Leishmania major | 33% | 100% |
Q4Q9U3 | Leishmania major | 31% | 100% |
Q4QCS6 | Leishmania major | 28% | 96% |
Q4QCS7 | Leishmania major | 30% | 95% |
Q4QCS8 | Leishmania major | 32% | 100% |
Q4QCS9 | Leishmania major | 32% | 100% |
Q9U0T9 | Leishmania major | 31% | 100% |
V5AYJ1 | Trypanosoma cruzi | 30% | 100% |
V5B5I4 | Trypanosoma cruzi | 31% | 100% |
V5BA05 | Trypanosoma cruzi | 34% | 100% |
V5BEL3 | Trypanosoma cruzi | 30% | 100% |
V5BII7 | Trypanosoma cruzi | 30% | 77% |
V5BN20 | Trypanosoma cruzi | 33% | 100% |
V5D9Y2 | Trypanosoma cruzi | 31% | 100% |
V5DES7 | Trypanosoma cruzi | 30% | 100% |