Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000407 | phagophore assembly site | 2 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005773 | vacuole | 5 | 2 |
GO:0005776 | autophagosome | 6 | 2 |
GO:0016020 | membrane | 2 | 12 |
GO:0034045 | phagophore assembly site membrane | 3 | 12 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0000502 | proteasome complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1905368 | peptidase complex | 3 | 2 |
GO:1905369 | endopeptidase complex | 4 | 2 |
Related structures:
AlphaFold database: E9AD16
Term | Name | Level | Count |
---|---|---|---|
GO:0000422 | autophagy of mitochondrion | 4 | 2 |
GO:0006810 | transport | 3 | 12 |
GO:0006869 | lipid transport | 5 | 12 |
GO:0006914 | autophagy | 3 | 12 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007005 | mitochondrion organization | 5 | 2 |
GO:0008104 | protein localization | 4 | 2 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009056 | catabolic process | 2 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022411 | cellular component disassembly | 4 | 2 |
GO:0033036 | macromolecule localization | 2 | 2 |
GO:0034497 | protein localization to phagophore assembly site | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044248 | cellular catabolic process | 3 | 12 |
GO:0044804 | autophagy of nucleus | 4 | 2 |
GO:0044805 | late nucleophagy | 5 | 2 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0061726 | mitochondrion disassembly | 6 | 2 |
GO:0061919 | process utilizing autophagic mechanism | 2 | 12 |
GO:0070727 | cellular macromolecule localization | 3 | 2 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:1903008 | organelle disassembly | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 403 | 407 | PF00656 | 0.501 |
CLV_C14_Caspase3-7 | 651 | 655 | PF00656 | 0.517 |
CLV_C14_Caspase3-7 | 749 | 753 | PF00656 | 0.656 |
CLV_MEL_PAP_1 | 516 | 522 | PF00089 | 0.228 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 518 | 520 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 766 | 768 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 800 | 802 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 863 | 865 | PF00675 | 0.514 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 714 | 716 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 800 | 802 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 863 | 865 | PF00082 | 0.527 |
CLV_PCSK_PC1ET2_1 | 33 | 35 | PF00082 | 0.346 |
CLV_PCSK_PC1ET2_1 | 714 | 716 | PF00082 | 0.428 |
CLV_PCSK_PC7_1 | 111 | 117 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.154 |
CLV_PCSK_SKI1_1 | 848 | 852 | PF00082 | 0.469 |
DEG_APCC_DBOX_1 | 114 | 122 | PF00400 | 0.534 |
DEG_SCF_FBW7_2 | 670 | 677 | PF00400 | 0.690 |
DEG_SPOP_SBC_1 | 16 | 20 | PF00917 | 0.534 |
DEG_SPOP_SBC_1 | 828 | 832 | PF00917 | 0.676 |
DOC_CKS1_1 | 298 | 303 | PF01111 | 0.480 |
DOC_CYCLIN_RxL_1 | 111 | 122 | PF00134 | 0.649 |
DOC_CYCLIN_yCln2_LP_2 | 241 | 247 | PF00134 | 0.317 |
DOC_CYCLIN_yCln2_LP_2 | 624 | 630 | PF00134 | 0.343 |
DOC_CYCLIN_yCln2_LP_2 | 702 | 708 | PF00134 | 0.665 |
DOC_MAPK_gen_1 | 158 | 166 | PF00069 | 0.652 |
DOC_MAPK_gen_1 | 610 | 617 | PF00069 | 0.297 |
DOC_MAPK_gen_1 | 714 | 723 | PF00069 | 0.610 |
DOC_MAPK_JIP1_4 | 3 | 9 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 610 | 617 | PF00069 | 0.336 |
DOC_MAPK_MEF2A_6 | 714 | 723 | PF00069 | 0.610 |
DOC_PP2B_LxvP_1 | 125 | 128 | PF13499 | 0.741 |
DOC_PP2B_LxvP_1 | 157 | 160 | PF13499 | 0.627 |
DOC_PP2B_LxvP_1 | 241 | 244 | PF13499 | 0.342 |
DOC_PP2B_LxvP_1 | 624 | 627 | PF13499 | 0.324 |
DOC_PP2B_LxvP_1 | 7 | 10 | PF13499 | 0.666 |
DOC_PP4_FxxP_1 | 28 | 31 | PF00568 | 0.544 |
DOC_PP4_FxxP_1 | 298 | 301 | PF00568 | 0.542 |
DOC_PP4_FxxP_1 | 356 | 359 | PF00568 | 0.542 |
DOC_PP4_FxxP_1 | 533 | 536 | PF00568 | 0.393 |
DOC_PP4_FxxP_1 | 802 | 805 | PF00568 | 0.785 |
DOC_SPAK_OSR1_1 | 801 | 805 | PF12202 | 0.722 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 660 | 664 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 686 | 690 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 695 | 699 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 792 | 796 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 827 | 831 | PF00917 | 0.703 |
DOC_USP7_UBL2_3 | 450 | 454 | PF12436 | 0.392 |
DOC_USP7_UBL2_3 | 714 | 718 | PF12436 | 0.640 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 670 | 675 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 743 | 748 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.527 |
LIG_14-3-3_CanoR_1 | 115 | 121 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 153 | 157 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 161 | 165 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 176 | 185 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 34 | 44 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 426 | 430 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 469 | 479 | PF00244 | 0.288 |
LIG_14-3-3_CanoR_1 | 508 | 514 | PF00244 | 0.320 |
LIG_14-3-3_CanoR_1 | 518 | 527 | PF00244 | 0.186 |
LIG_14-3-3_CanoR_1 | 760 | 765 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 855 | 861 | PF00244 | 0.731 |
LIG_Actin_WH2_2 | 138 | 155 | PF00022 | 0.698 |
LIG_Actin_WH2_2 | 375 | 391 | PF00022 | 0.533 |
LIG_Actin_WH2_2 | 481 | 496 | PF00022 | 0.318 |
LIG_Actin_WH2_2 | 722 | 738 | PF00022 | 0.596 |
LIG_APCC_ABBA_1 | 272 | 277 | PF00400 | 0.398 |
LIG_APCC_ABBA_1 | 479 | 484 | PF00400 | 0.256 |
LIG_APCC_ABBAyCdc20_2 | 478 | 484 | PF00400 | 0.342 |
LIG_BRCT_BRCA1_1 | 24 | 28 | PF00533 | 0.542 |
LIG_BRCT_BRCA1_1 | 352 | 356 | PF00533 | 0.542 |
LIG_BRCT_BRCA1_1 | 63 | 67 | PF00533 | 0.381 |
LIG_BRCT_BRCA1_1 | 679 | 683 | PF00533 | 0.623 |
LIG_Clathr_ClatBox_1 | 372 | 376 | PF01394 | 0.542 |
LIG_deltaCOP1_diTrp_1 | 474 | 479 | PF00928 | 0.280 |
LIG_deltaCOP1_diTrp_1 | 592 | 600 | PF00928 | 0.252 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.531 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.412 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.347 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.440 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.389 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.520 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.204 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.166 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.274 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.366 |
LIG_FHA_1 | 616 | 622 | PF00498 | 0.356 |
LIG_FHA_1 | 818 | 824 | PF00498 | 0.689 |
LIG_FHA_1 | 854 | 860 | PF00498 | 0.683 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.530 |
LIG_FHA_2 | 401 | 407 | PF00498 | 0.554 |
LIG_FHA_2 | 575 | 581 | PF00498 | 0.360 |
LIG_FHA_2 | 649 | 655 | PF00498 | 0.542 |
LIG_FHA_2 | 740 | 746 | PF00498 | 0.709 |
LIG_FHA_2 | 830 | 836 | PF00498 | 0.645 |
LIG_GBD_Chelix_1 | 549 | 557 | PF00786 | 0.406 |
LIG_GBD_Chelix_1 | 616 | 624 | PF00786 | 0.372 |
LIG_LIR_Apic_2 | 25 | 31 | PF02991 | 0.542 |
LIG_LIR_Apic_2 | 295 | 301 | PF02991 | 0.467 |
LIG_LIR_Apic_2 | 353 | 359 | PF02991 | 0.542 |
LIG_LIR_Apic_2 | 532 | 536 | PF02991 | 0.393 |
LIG_LIR_Apic_2 | 799 | 805 | PF02991 | 0.744 |
LIG_LIR_Gen_1 | 141 | 149 | PF02991 | 0.666 |
LIG_LIR_Gen_1 | 205 | 214 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 406 | 415 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 41 | 52 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 431 | 440 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 570 | 579 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 598 | 609 | PF02991 | 0.258 |
LIG_LIR_Gen_1 | 725 | 730 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 141 | 145 | PF02991 | 0.673 |
LIG_LIR_Nem_3 | 205 | 209 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 249 | 255 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 277 | 283 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 320 | 324 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 334 | 340 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 406 | 412 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 41 | 47 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 431 | 435 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 570 | 576 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 598 | 604 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 725 | 729 | PF02991 | 0.481 |
LIG_NRBOX | 120 | 126 | PF00104 | 0.539 |
LIG_Pex14_1 | 256 | 260 | PF04695 | 0.416 |
LIG_Pex14_2 | 162 | 166 | PF04695 | 0.632 |
LIG_Pex14_2 | 202 | 206 | PF04695 | 0.383 |
LIG_Pex14_2 | 215 | 219 | PF04695 | 0.252 |
LIG_Pex14_2 | 247 | 251 | PF04695 | 0.360 |
LIG_Rb_pABgroove_1 | 403 | 411 | PF01858 | 0.456 |
LIG_REV1ctd_RIR_1 | 606 | 616 | PF16727 | 0.342 |
LIG_SH2_CRK | 432 | 436 | PF00017 | 0.381 |
LIG_SH2_CRK | 5 | 9 | PF00017 | 0.609 |
LIG_SH2_CRK | 573 | 577 | PF00017 | 0.293 |
LIG_SH2_NCK_1 | 482 | 486 | PF00017 | 0.267 |
LIG_SH2_NCK_1 | 560 | 564 | PF00017 | 0.429 |
LIG_SH2_NCK_1 | 588 | 592 | PF00017 | 0.362 |
LIG_SH2_NCK_1 | 601 | 605 | PF00017 | 0.299 |
LIG_SH2_PTP2 | 395 | 398 | PF00017 | 0.560 |
LIG_SH2_PTP2 | 446 | 449 | PF00017 | 0.429 |
LIG_SH2_PTP2 | 92 | 95 | PF00017 | 0.166 |
LIG_SH2_SRC | 378 | 381 | PF00017 | 0.522 |
LIG_SH2_SRC | 573 | 576 | PF00017 | 0.333 |
LIG_SH2_SRC | 601 | 604 | PF00017 | 0.360 |
LIG_SH2_STAP1 | 183 | 187 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 270 | 274 | PF00017 | 0.398 |
LIG_SH2_STAP1 | 432 | 436 | PF00017 | 0.369 |
LIG_SH2_STAT3 | 279 | 282 | PF00017 | 0.542 |
LIG_SH2_STAT3 | 307 | 310 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 446 | 449 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.166 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.263 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.166 |
LIG_SH3_1 | 75 | 81 | PF00018 | 0.334 |
LIG_SH3_2 | 127 | 132 | PF14604 | 0.537 |
LIG_SH3_2 | 362 | 367 | PF14604 | 0.542 |
LIG_SH3_3 | 124 | 130 | PF00018 | 0.545 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.520 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.334 |
LIG_SUMO_SIM_anti_2 | 143 | 149 | PF11976 | 0.516 |
LIG_SUMO_SIM_anti_2 | 554 | 559 | PF11976 | 0.344 |
LIG_SUMO_SIM_par_1 | 378 | 384 | PF11976 | 0.542 |
LIG_SUMO_SIM_par_1 | 612 | 618 | PF11976 | 0.334 |
LIG_TYR_ITIM | 430 | 435 | PF00017 | 0.314 |
LIG_TYR_ITIM | 461 | 466 | PF00017 | 0.429 |
LIG_TYR_ITIM | 90 | 95 | PF00017 | 0.166 |
LIG_WRC_WIRS_1 | 203 | 208 | PF05994 | 0.454 |
LIG_WRC_WIRS_1 | 530 | 535 | PF05994 | 0.343 |
LIG_WRC_WIRS_1 | 723 | 728 | PF05994 | 0.349 |
MOD_CDC14_SPxK_1 | 134 | 137 | PF00782 | 0.430 |
MOD_CDK_SPxK_1 | 131 | 137 | PF00069 | 0.434 |
MOD_CDK_SPxxK_3 | 297 | 304 | PF00069 | 0.324 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.545 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.641 |
MOD_CK1_1 | 663 | 669 | PF00069 | 0.464 |
MOD_CK1_1 | 687 | 693 | PF00069 | 0.736 |
MOD_CK1_1 | 722 | 728 | PF00069 | 0.350 |
MOD_CK1_1 | 731 | 737 | PF00069 | 0.424 |
MOD_CK1_1 | 746 | 752 | PF00069 | 0.477 |
MOD_CK1_1 | 776 | 782 | PF00069 | 0.615 |
MOD_CK1_1 | 786 | 792 | PF00069 | 0.645 |
MOD_CK1_1 | 795 | 801 | PF00069 | 0.747 |
MOD_CK1_1 | 842 | 848 | PF00069 | 0.551 |
MOD_CK1_1 | 854 | 860 | PF00069 | 0.617 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.398 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.414 |
MOD_CK2_1 | 574 | 580 | PF00069 | 0.455 |
MOD_CK2_1 | 739 | 745 | PF00069 | 0.680 |
MOD_CK2_1 | 776 | 782 | PF00069 | 0.645 |
MOD_CK2_1 | 829 | 835 | PF00069 | 0.596 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.166 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.590 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.422 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.511 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.429 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.429 |
MOD_GlcNHglycan | 595 | 598 | PF01048 | 0.308 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.406 |
MOD_GlcNHglycan | 674 | 677 | PF01048 | 0.686 |
MOD_GlcNHglycan | 679 | 682 | PF01048 | 0.722 |
MOD_GlcNHglycan | 686 | 689 | PF01048 | 0.727 |
MOD_GlcNHglycan | 696 | 700 | PF01048 | 0.664 |
MOD_GlcNHglycan | 819 | 823 | PF01048 | 0.658 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.398 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.389 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.356 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.404 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.431 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.378 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.335 |
MOD_GSK3_1 | 660 | 667 | PF00069 | 0.481 |
MOD_GSK3_1 | 668 | 675 | PF00069 | 0.591 |
MOD_GSK3_1 | 739 | 746 | PF00069 | 0.648 |
MOD_GSK3_1 | 769 | 776 | PF00069 | 0.578 |
MOD_GSK3_1 | 786 | 793 | PF00069 | 0.628 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.638 |
MOD_GSK3_1 | 839 | 846 | PF00069 | 0.445 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.561 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.566 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.482 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.305 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.331 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.365 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.234 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.320 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.384 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.429 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.365 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.429 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.350 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.468 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.166 |
MOD_NEK2_1 | 620 | 625 | PF00069 | 0.381 |
MOD_NEK2_1 | 647 | 652 | PF00069 | 0.406 |
MOD_NEK2_1 | 839 | 844 | PF00069 | 0.436 |
MOD_NEK2_1 | 851 | 856 | PF00069 | 0.558 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.166 |
MOD_NEK2_2 | 160 | 165 | PF00069 | 0.468 |
MOD_NEK2_2 | 792 | 797 | PF00069 | 0.754 |
MOD_PIKK_1 | 176 | 182 | PF00454 | 0.454 |
MOD_PIKK_1 | 464 | 470 | PF00454 | 0.429 |
MOD_PIKK_1 | 687 | 693 | PF00454 | 0.533 |
MOD_PIKK_1 | 839 | 845 | PF00454 | 0.481 |
MOD_PIKK_1 | 854 | 860 | PF00454 | 0.684 |
MOD_PK_1 | 350 | 356 | PF00069 | 0.429 |
MOD_PKA_1 | 116 | 122 | PF00069 | 0.419 |
MOD_PKA_1 | 518 | 524 | PF00069 | 0.361 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.419 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.636 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.581 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.372 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.429 |
MOD_PKA_2 | 507 | 513 | PF00069 | 0.390 |
MOD_PKA_2 | 518 | 524 | PF00069 | 0.175 |
MOD_PKA_2 | 786 | 792 | PF00069 | 0.705 |
MOD_PKA_2 | 854 | 860 | PF00069 | 0.664 |
MOD_PKB_1 | 492 | 500 | PF00069 | 0.372 |
MOD_Plk_1 | 731 | 737 | PF00069 | 0.575 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.431 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.636 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.632 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.417 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.324 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.369 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.384 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.393 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.364 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.336 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.166 |
MOD_Plk_4 | 529 | 535 | PF00069 | 0.386 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.401 |
MOD_Plk_4 | 604 | 610 | PF00069 | 0.375 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.135 |
MOD_Plk_4 | 697 | 703 | PF00069 | 0.677 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.700 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.395 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.308 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.454 |
MOD_ProDKin_1 | 670 | 676 | PF00069 | 0.684 |
MOD_ProDKin_1 | 743 | 749 | PF00069 | 0.706 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.410 |
TRG_DiLeu_BaEn_2 | 270 | 276 | PF01217 | 0.324 |
TRG_DiLeu_BaLyEn_6 | 609 | 614 | PF01217 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 86 | 91 | PF01217 | 0.166 |
TRG_ENDOCYTIC_2 | 432 | 435 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 446 | 449 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 463 | 466 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 482 | 485 | PF00928 | 0.157 |
TRG_ENDOCYTIC_2 | 573 | 576 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 601 | 604 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.166 |
TRG_ER_diArg_1 | 114 | 117 | PF00400 | 0.419 |
TRG_ER_diArg_1 | 506 | 509 | PF00400 | 0.389 |
TRG_ER_diArg_1 | 517 | 519 | PF00400 | 0.159 |
TRG_ER_diArg_1 | 72 | 75 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 764 | 767 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 800 | 802 | PF00400 | 0.774 |
TRG_NES_CRM1_1 | 364 | 376 | PF08389 | 0.324 |
TRG_Pf-PMV_PEXEL_1 | 402 | 406 | PF00026 | 0.381 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5S4 | Leptomonas seymouri | 69% | 100% |
A0A0S4JRE4 | Bodo saltans | 30% | 100% |
A0A1X0P5B9 | Trypanosomatidae | 36% | 100% |
A0A3S5H7H3 | Leishmania donovani | 97% | 100% |
A0A422NTE4 | Trypanosoma rangeli | 36% | 100% |
D0A5N9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AHC0 | Leishmania infantum | 97% | 100% |
E9AIS5 | Leishmania braziliensis | 81% | 100% |
E9AYU1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
P0CM40 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 20% | 100% |
P0CM41 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 20% | 100% |
V5B7I2 | Trypanosoma cruzi | 34% | 100% |