Homologous to bacterial FtsH and Eukaryotic AFG3 proteins. Probably involved in mitochondrial protein processing.. Localization: Mitochondrial (by homology)
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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 20 |
NetGPI | no | yes: 0, no: 20 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 17 |
GO:0110165 | cellular anatomical entity | 1 | 18 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0005745 | m-AAA complex | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0098796 | membrane protein complex | 2 | 2 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 2 |
GO:0098800 | inner mitochondrial membrane protein complex | 3 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1905368 | peptidase complex | 3 | 2 |
Related structures:
AlphaFold database: E9B1M1
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 20 |
GO:0006807 | nitrogen compound metabolic process | 2 | 20 |
GO:0008152 | metabolic process | 1 | 20 |
GO:0019538 | protein metabolic process | 3 | 20 |
GO:0043170 | macromolecule metabolic process | 3 | 20 |
GO:0044238 | primary metabolic process | 2 | 20 |
GO:0071704 | organic substance metabolic process | 2 | 20 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 20 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016485 | protein processing | 5 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0034982 | mitochondrial protein processing | 6 | 2 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0051604 | protein maturation | 4 | 2 |
GO:0065003 | protein-containing complex assembly | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 21 |
GO:0003824 | catalytic activity | 1 | 21 |
GO:0004175 | endopeptidase activity | 4 | 20 |
GO:0004176 | ATP-dependent peptidase activity | 2 | 20 |
GO:0004222 | metalloendopeptidase activity | 5 | 20 |
GO:0005488 | binding | 1 | 21 |
GO:0005524 | ATP binding | 5 | 21 |
GO:0008233 | peptidase activity | 3 | 20 |
GO:0008237 | metallopeptidase activity | 4 | 20 |
GO:0016462 | pyrophosphatase activity | 5 | 21 |
GO:0016787 | hydrolase activity | 2 | 21 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 21 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 21 |
GO:0016887 | ATP hydrolysis activity | 7 | 21 |
GO:0017076 | purine nucleotide binding | 4 | 21 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 21 |
GO:0030554 | adenyl nucleotide binding | 5 | 21 |
GO:0032553 | ribonucleotide binding | 3 | 21 |
GO:0032555 | purine ribonucleotide binding | 4 | 21 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 21 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 21 |
GO:0036094 | small molecule binding | 2 | 21 |
GO:0043167 | ion binding | 2 | 21 |
GO:0043168 | anion binding | 3 | 21 |
GO:0097159 | organic cyclic compound binding | 2 | 21 |
GO:0097367 | carbohydrate derivative binding | 2 | 21 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 20 |
GO:0140657 | ATP-dependent activity | 1 | 20 |
GO:1901265 | nucleoside phosphate binding | 3 | 21 |
GO:1901363 | heterocyclic compound binding | 2 | 21 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 213 | 217 | PF00656 | 0.473 |
CLV_C14_Caspase3-7 | 431 | 435 | PF00656 | 0.450 |
CLV_C14_Caspase3-7 | 460 | 464 | PF00656 | 0.450 |
CLV_C14_Caspase3-7 | 541 | 545 | PF00656 | 0.710 |
CLV_C14_Caspase3-7 | 751 | 755 | PF00656 | 0.463 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.329 |
CLV_NRD_NRD_1 | 469 | 471 | PF00675 | 0.342 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 629 | 631 | PF00675 | 0.290 |
CLV_NRD_NRD_1 | 781 | 783 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 825 | 827 | PF00675 | 0.342 |
CLV_NRD_NRD_1 | 880 | 882 | PF00675 | 0.442 |
CLV_PCSK_FUR_1 | 627 | 631 | PF00082 | 0.246 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.239 |
CLV_PCSK_KEX2_1 | 469 | 471 | PF00082 | 0.263 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 629 | 631 | PF00082 | 0.290 |
CLV_PCSK_KEX2_1 | 825 | 827 | PF00082 | 0.342 |
CLV_PCSK_PC1ET2_1 | 173 | 175 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 439 | 441 | PF00082 | 0.239 |
CLV_PCSK_PC1ET2_1 | 585 | 587 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 618 | 622 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 747 | 751 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 783 | 787 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 810 | 814 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 825 | 829 | PF00082 | 0.263 |
DEG_APCC_DBOX_1 | 139 | 147 | PF00400 | 0.450 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.606 |
DEG_SCF_FBW7_1 | 502 | 508 | PF00400 | 0.612 |
DOC_ANK_TNKS_1 | 86 | 93 | PF00023 | 0.617 |
DOC_CKS1_1 | 34 | 39 | PF01111 | 0.723 |
DOC_CKS1_1 | 502 | 507 | PF01111 | 0.611 |
DOC_CYCLIN_RxL_1 | 412 | 420 | PF00134 | 0.471 |
DOC_CYCLIN_yCln2_LP_2 | 811 | 817 | PF00134 | 0.542 |
DOC_MAPK_gen_1 | 314 | 322 | PF00069 | 0.595 |
DOC_MAPK_gen_1 | 422 | 430 | PF00069 | 0.471 |
DOC_MAPK_gen_1 | 469 | 476 | PF00069 | 0.463 |
DOC_MAPK_gen_1 | 492 | 502 | PF00069 | 0.450 |
DOC_MAPK_gen_1 | 750 | 760 | PF00069 | 0.524 |
DOC_MAPK_JIP1_4 | 256 | 262 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 140 | 149 | PF00069 | 0.272 |
DOC_MAPK_MEF2A_6 | 256 | 264 | PF00069 | 0.347 |
DOC_MAPK_MEF2A_6 | 717 | 726 | PF00069 | 0.462 |
DOC_MAPK_MEF2A_6 | 753 | 760 | PF00069 | 0.463 |
DOC_PP2B_LxvP_1 | 372 | 375 | PF13499 | 0.439 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.641 |
DOC_USP7_UBL2_3 | 312 | 316 | PF12436 | 0.622 |
DOC_USP7_UBL2_3 | 339 | 343 | PF12436 | 0.537 |
DOC_USP7_UBL2_3 | 360 | 364 | PF12436 | 0.615 |
DOC_USP7_UBL2_3 | 419 | 423 | PF12436 | 0.524 |
DOC_USP7_UBL2_3 | 846 | 850 | PF12436 | 0.521 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.430 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 501 | 506 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 557 | 562 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 602 | 607 | PF00397 | 0.660 |
LIG_14-3-3_CanoR_1 | 267 | 275 | PF00244 | 0.263 |
LIG_14-3-3_CanoR_1 | 35 | 41 | PF00244 | 0.756 |
LIG_14-3-3_CanoR_1 | 48 | 53 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 691 | 700 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 877 | 885 | PF00244 | 0.710 |
LIG_Actin_WH2_2 | 509 | 524 | PF00022 | 0.517 |
LIG_Actin_WH2_2 | 766 | 784 | PF00022 | 0.463 |
LIG_APCC_ABBA_1 | 188 | 193 | PF00400 | 0.397 |
LIG_APCC_ABBAyCdc20_2 | 425 | 431 | PF00400 | 0.439 |
LIG_BIR_III_4 | 434 | 438 | PF00653 | 0.450 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.398 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.306 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.504 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.513 |
LIG_FHA_1 | 502 | 508 | PF00498 | 0.594 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.724 |
LIG_FHA_1 | 807 | 813 | PF00498 | 0.450 |
LIG_FHA_1 | 836 | 842 | PF00498 | 0.430 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.578 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.516 |
LIG_FHA_2 | 452 | 458 | PF00498 | 0.455 |
LIG_FHA_2 | 526 | 532 | PF00498 | 0.696 |
LIG_FHA_2 | 578 | 584 | PF00498 | 0.763 |
LIG_FHA_2 | 746 | 752 | PF00498 | 0.450 |
LIG_FHA_2 | 861 | 867 | PF00498 | 0.450 |
LIG_Integrin_RGD_1 | 470 | 472 | PF01839 | 0.250 |
LIG_LIR_Apic_2 | 134 | 139 | PF02991 | 0.688 |
LIG_LIR_Apic_2 | 799 | 804 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 141 | 151 | PF02991 | 0.291 |
LIG_LIR_Gen_1 | 166 | 175 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 18 | 25 | PF02991 | 0.765 |
LIG_LIR_Gen_1 | 185 | 195 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 356 | 366 | PF02991 | 0.584 |
LIG_LIR_Gen_1 | 400 | 409 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 80 | 91 | PF02991 | 0.602 |
LIG_LIR_Gen_1 | 863 | 871 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 166 | 171 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 18 | 23 | PF02991 | 0.783 |
LIG_LIR_Nem_3 | 185 | 190 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 330 | 335 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 356 | 361 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 400 | 405 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 614 | 620 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 80 | 86 | PF02991 | 0.707 |
LIG_LIR_Nem_3 | 863 | 867 | PF02991 | 0.450 |
LIG_NRBOX | 454 | 460 | PF00104 | 0.439 |
LIG_PCNA_PIPBox_1 | 849 | 858 | PF02747 | 0.450 |
LIG_Pex14_1 | 282 | 286 | PF04695 | 0.274 |
LIG_Pex14_2 | 288 | 292 | PF04695 | 0.274 |
LIG_PTAP_UEV_1 | 552 | 557 | PF05743 | 0.638 |
LIG_PTB_Apo_2 | 739 | 746 | PF02174 | 0.433 |
LIG_SH2_CRK | 20 | 24 | PF00017 | 0.768 |
LIG_SH2_CRK | 358 | 362 | PF00017 | 0.528 |
LIG_SH2_CRK | 789 | 793 | PF00017 | 0.463 |
LIG_SH2_GRB2like | 184 | 187 | PF00017 | 0.323 |
LIG_SH2_NCK_1 | 20 | 24 | PF00017 | 0.749 |
LIG_SH2_SRC | 789 | 792 | PF00017 | 0.506 |
LIG_SH2_SRC | 864 | 867 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 184 | 188 | PF00017 | 0.333 |
LIG_SH2_STAP1 | 306 | 310 | PF00017 | 0.694 |
LIG_SH2_STAP1 | 52 | 56 | PF00017 | 0.585 |
LIG_SH2_STAP1 | 613 | 617 | PF00017 | 0.549 |
LIG_SH2_STAP1 | 635 | 639 | PF00017 | 0.518 |
LIG_SH2_STAP1 | 736 | 740 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 835 | 839 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 864 | 868 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.720 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.710 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 739 | 742 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 791 | 794 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 870 | 873 | PF00017 | 0.541 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.740 |
LIG_SH3_3 | 499 | 505 | PF00018 | 0.462 |
LIG_SH3_3 | 547 | 553 | PF00018 | 0.718 |
LIG_SH3_3 | 797 | 803 | PF00018 | 0.488 |
LIG_SUMO_SIM_anti_2 | 472 | 479 | PF11976 | 0.462 |
LIG_SUMO_SIM_anti_2 | 837 | 843 | PF11976 | 0.542 |
LIG_SUMO_SIM_par_1 | 147 | 152 | PF11976 | 0.341 |
LIG_SUMO_SIM_par_1 | 837 | 843 | PF11976 | 0.542 |
LIG_TRAF2_1 | 580 | 583 | PF00917 | 0.786 |
LIG_TYR_ITIM | 862 | 867 | PF00017 | 0.481 |
LIG_WRC_WIRS_1 | 792 | 797 | PF05994 | 0.463 |
MOD_CDK_SPK_2 | 30 | 35 | PF00069 | 0.598 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.719 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.689 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.568 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.634 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.682 |
MOD_CK1_1 | 560 | 566 | PF00069 | 0.755 |
MOD_CK1_1 | 602 | 608 | PF00069 | 0.773 |
MOD_CK1_1 | 806 | 812 | PF00069 | 0.490 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.452 |
MOD_CK2_1 | 577 | 583 | PF00069 | 0.730 |
MOD_CK2_1 | 608 | 614 | PF00069 | 0.676 |
MOD_CK2_1 | 622 | 628 | PF00069 | 0.548 |
MOD_CK2_1 | 670 | 676 | PF00069 | 0.454 |
MOD_CK2_1 | 691 | 697 | PF00069 | 0.450 |
MOD_CK2_1 | 745 | 751 | PF00069 | 0.450 |
MOD_Cter_Amidation | 110 | 113 | PF01082 | 0.422 |
MOD_Cter_Amidation | 467 | 470 | PF01082 | 0.281 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.592 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.254 |
MOD_GlcNHglycan | 531 | 535 | PF01048 | 0.554 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.444 |
MOD_GlcNHglycan | 67 | 72 | PF01048 | 0.538 |
MOD_GlcNHglycan | 731 | 734 | PF01048 | 0.250 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.461 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.386 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.501 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.499 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.661 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.625 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.631 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.464 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.661 |
MOD_GSK3_1 | 557 | 564 | PF00069 | 0.677 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.684 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.682 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.563 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.674 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.688 |
MOD_GSK3_1 | 752 | 759 | PF00069 | 0.452 |
MOD_GSK3_1 | 771 | 778 | PF00069 | 0.370 |
MOD_GSK3_1 | 872 | 879 | PF00069 | 0.629 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.697 |
MOD_N-GLC_1 | 608 | 613 | PF02516 | 0.542 |
MOD_N-GLC_1 | 670 | 675 | PF02516 | 0.204 |
MOD_N-GLC_1 | 743 | 748 | PF02516 | 0.346 |
MOD_N-GLC_1 | 806 | 811 | PF02516 | 0.301 |
MOD_N-GLC_2 | 527 | 529 | PF02516 | 0.354 |
MOD_N-GLC_2 | 641 | 643 | PF02516 | 0.290 |
MOD_N-GLC_2 | 653 | 655 | PF02516 | 0.208 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.483 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.281 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.395 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.447 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.691 |
MOD_NEK2_1 | 722 | 727 | PF00069 | 0.461 |
MOD_NEK2_1 | 745 | 750 | PF00069 | 0.534 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.644 |
MOD_PIKK_1 | 204 | 210 | PF00454 | 0.377 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.655 |
MOD_PIKK_1 | 294 | 300 | PF00454 | 0.553 |
MOD_PIKK_1 | 457 | 463 | PF00454 | 0.450 |
MOD_PIKK_1 | 568 | 574 | PF00454 | 0.770 |
MOD_PIKK_1 | 73 | 79 | PF00454 | 0.601 |
MOD_PKA_1 | 48 | 54 | PF00069 | 0.688 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.455 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.764 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.519 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.670 |
MOD_PKA_2 | 637 | 643 | PF00069 | 0.523 |
MOD_PKA_2 | 752 | 758 | PF00069 | 0.463 |
MOD_PKA_2 | 873 | 879 | PF00069 | 0.571 |
MOD_PKB_1 | 689 | 697 | PF00069 | 0.506 |
MOD_Plk_1 | 260 | 266 | PF00069 | 0.436 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.450 |
MOD_Plk_1 | 564 | 570 | PF00069 | 0.781 |
MOD_Plk_1 | 587 | 593 | PF00069 | 0.759 |
MOD_Plk_1 | 608 | 614 | PF00069 | 0.595 |
MOD_Plk_1 | 670 | 676 | PF00069 | 0.433 |
MOD_Plk_1 | 806 | 812 | PF00069 | 0.532 |
MOD_Plk_2-3 | 577 | 583 | PF00069 | 0.721 |
MOD_Plk_2-3 | 860 | 866 | PF00069 | 0.450 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.450 |
MOD_Plk_4 | 564 | 570 | PF00069 | 0.728 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.777 |
MOD_Plk_4 | 722 | 728 | PF00069 | 0.492 |
MOD_Plk_4 | 796 | 802 | PF00069 | 0.506 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.433 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.753 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.745 |
MOD_ProDKin_1 | 501 | 507 | PF00069 | 0.577 |
MOD_ProDKin_1 | 557 | 563 | PF00069 | 0.651 |
MOD_ProDKin_1 | 602 | 608 | PF00069 | 0.657 |
MOD_SUMO_for_1 | 341 | 344 | PF00179 | 0.539 |
MOD_SUMO_for_1 | 573 | 576 | PF00179 | 0.773 |
MOD_SUMO_for_1 | 857 | 860 | PF00179 | 0.506 |
MOD_SUMO_rev_2 | 124 | 133 | PF00179 | 0.706 |
MOD_SUMO_rev_2 | 193 | 197 | PF00179 | 0.345 |
MOD_SUMO_rev_2 | 595 | 601 | PF00179 | 0.792 |
MOD_SUMO_rev_2 | 847 | 852 | PF00179 | 0.542 |
TRG_DiLeu_BaEn_2 | 346 | 352 | PF01217 | 0.496 |
TRG_DiLeu_BaLyEn_6 | 627 | 632 | PF01217 | 0.503 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.767 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.550 |
TRG_ENDOCYTIC_2 | 406 | 409 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 789 | 792 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 864 | 867 | PF00928 | 0.481 |
TRG_ER_diArg_1 | 412 | 415 | PF00400 | 0.431 |
TRG_ER_diArg_1 | 47 | 49 | PF00400 | 0.654 |
TRG_ER_diArg_1 | 629 | 631 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 689 | 692 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 86 | 89 | PF00400 | 0.710 |
TRG_ER_diLys_1 | 882 | 885 | PF00400 | 0.672 |
TRG_NES_CRM1_1 | 404 | 416 | PF08389 | 0.439 |
TRG_NLS_MonoExtN_4 | 419 | 426 | PF00514 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 415 | 420 | PF00026 | 0.250 |
TRG_Pf-PMV_PEXEL_1 | 618 | 623 | PF00026 | 0.425 |
TRG_Pf-PMV_PEXEL_1 | 629 | 633 | PF00026 | 0.337 |
TRG_Pf-PMV_PEXEL_1 | 691 | 695 | PF00026 | 0.342 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PGD9 | Leptomonas seymouri | 70% | 89% |
A0A0S4JGG9 | Bodo saltans | 30% | 100% |
A0A0S4JTL4 | Bodo saltans | 55% | 100% |
A0A1X0NJP5 | Trypanosomatidae | 59% | 100% |
A0A1X0NW32 | Trypanosomatidae | 32% | 100% |
A0A3Q8ICE7 | Leishmania donovani | 93% | 100% |
A0A3Q8IFG3 | Leishmania donovani | 33% | 100% |
A0A3R7L0P7 | Trypanosoma rangeli | 33% | 100% |
A0A422NQX8 | Trypanosoma rangeli | 62% | 98% |
A4HJ48 | Leishmania braziliensis | 82% | 100% |
A4HKD8 | Leishmania braziliensis | 32% | 100% |
A4I6G4 | Leishmania infantum | 93% | 100% |
A4I809 | Leishmania infantum | 33% | 100% |
C9ZN81 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
E9B2S6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
Q4Q5D1 | Leishmania major | 33% | 100% |
Q4Q6J3 | Leishmania major | 92% | 100% |
V5B3P7 | Trypanosoma cruzi | 55% | 100% |
V5BP04 | Trypanosoma cruzi | 33% | 100% |