Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | yes | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000502 | proteasome complex | 3 | 11 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0140535 | intracellular protein-containing complex | 2 | 11 |
GO:1902494 | catalytic complex | 2 | 11 |
GO:1905368 | peptidase complex | 3 | 11 |
GO:1905369 | endopeptidase complex | 4 | 11 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0008540 | proteasome regulatory particle, base subcomplex | 2 | 1 |
GO:0034515 | proteasome storage granule | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7X246
Term | Name | Level | Count |
---|---|---|---|
GO:0009894 | regulation of catabolic process | 4 | 12 |
GO:0019222 | regulation of metabolic process | 3 | 12 |
GO:0042176 | regulation of protein catabolic process | 5 | 12 |
GO:0050789 | regulation of biological process | 2 | 12 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 12 |
GO:0051246 | regulation of protein metabolic process | 5 | 12 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 12 |
GO:0065007 | biological regulation | 1 | 12 |
GO:0080090 | regulation of primary metabolic process | 4 | 12 |
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030234 | enzyme regulator activity | 2 | 12 |
GO:0098772 | molecular function regulator activity | 1 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 559 | 563 | PF00656 | 0.493 |
CLV_MEL_PAP_1 | 844 | 850 | PF00089 | 0.472 |
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.496 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 664 | 666 | PF00082 | 0.473 |
CLV_PCSK_PC1ET2_1 | 220 | 222 | PF00082 | 0.496 |
CLV_PCSK_PC1ET2_1 | 664 | 666 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.695 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 482 | 486 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 739 | 743 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 753 | 757 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 862 | 866 | PF00082 | 0.354 |
DEG_APCC_KENBOX_2 | 28 | 32 | PF00400 | 0.738 |
DEG_SCF_FBW7_1 | 822 | 827 | PF00400 | 0.522 |
DOC_CKS1_1 | 870 | 875 | PF01111 | 0.414 |
DOC_CYCLIN_RxL_1 | 206 | 217 | PF00134 | 0.434 |
DOC_CYCLIN_yCln2_LP_2 | 484 | 490 | PF00134 | 0.388 |
DOC_MAPK_gen_1 | 111 | 119 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 281 | 289 | PF00069 | 0.408 |
DOC_MAPK_gen_1 | 293 | 300 | PF00069 | 0.369 |
DOC_MAPK_gen_1 | 41 | 50 | PF00069 | 0.588 |
DOC_MAPK_HePTP_8 | 639 | 651 | PF00069 | 0.471 |
DOC_MAPK_JIP1_4 | 281 | 287 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 4 | 12 | PF00069 | 0.688 |
DOC_MAPK_MEF2A_6 | 41 | 50 | PF00069 | 0.533 |
DOC_MAPK_MEF2A_6 | 440 | 449 | PF00069 | 0.612 |
DOC_MAPK_MEF2A_6 | 642 | 651 | PF00069 | 0.441 |
DOC_PP2B_LxvP_1 | 484 | 487 | PF13499 | 0.369 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 713 | 717 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 732 | 736 | PF00917 | 0.368 |
DOC_USP7_MATH_1 | 840 | 844 | PF00917 | 0.567 |
DOC_USP7_UBL2_3 | 15 | 19 | PF12436 | 0.715 |
DOC_USP7_UBL2_3 | 347 | 351 | PF12436 | 0.726 |
DOC_USP7_UBL2_3 | 478 | 482 | PF12436 | 0.414 |
DOC_WW_Pin1_4 | 340 | 345 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 820 | 825 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 869 | 874 | PF00397 | 0.359 |
LIG_14-3-3_CanoR_1 | 322 | 328 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 390 | 400 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 573 | 579 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 73 | 80 | PF00244 | 0.451 |
LIG_Actin_WH2_2 | 86 | 104 | PF00022 | 0.388 |
LIG_BIR_III_4 | 310 | 314 | PF00653 | 0.496 |
LIG_BRCT_BRCA1_1 | 580 | 584 | PF00533 | 0.568 |
LIG_Clathr_ClatBox_1 | 201 | 205 | PF01394 | 0.369 |
LIG_CtBP_PxDLS_1 | 659 | 664 | PF00389 | 0.494 |
LIG_EH_1 | 440 | 444 | PF12763 | 0.548 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.380 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.384 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.436 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.453 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.516 |
LIG_FHA_1 | 562 | 568 | PF00498 | 0.495 |
LIG_FHA_1 | 573 | 579 | PF00498 | 0.428 |
LIG_FHA_1 | 585 | 591 | PF00498 | 0.435 |
LIG_FHA_1 | 634 | 640 | PF00498 | 0.727 |
LIG_FHA_1 | 720 | 726 | PF00498 | 0.589 |
LIG_FHA_1 | 758 | 764 | PF00498 | 0.572 |
LIG_FHA_1 | 821 | 827 | PF00498 | 0.484 |
LIG_FHA_1 | 852 | 858 | PF00498 | 0.360 |
LIG_FHA_1 | 870 | 876 | PF00498 | 0.354 |
LIG_FHA_1 | 877 | 883 | PF00498 | 0.355 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.408 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.328 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.380 |
LIG_FHA_2 | 20 | 26 | PF00498 | 0.748 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.478 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.404 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.313 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.388 |
LIG_FHA_2 | 557 | 563 | PF00498 | 0.489 |
LIG_FHA_2 | 892 | 898 | PF00498 | 0.447 |
LIG_LIR_Apic_2 | 748 | 754 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 118 | 126 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 151 | 160 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 327 | 336 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 595 | 601 | PF02991 | 0.618 |
LIG_LIR_Gen_1 | 767 | 777 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 151 | 155 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 244 | 249 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 536 | 541 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 595 | 600 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 814 | 820 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 886 | 892 | PF02991 | 0.414 |
LIG_LYPXL_S_1 | 93 | 97 | PF13949 | 0.434 |
LIG_LYPXL_yS_3 | 94 | 97 | PF13949 | 0.434 |
LIG_NRBOX | 112 | 118 | PF00104 | 0.496 |
LIG_NRBOX | 67 | 73 | PF00104 | 0.354 |
LIG_PCNA_yPIPBox_3 | 314 | 322 | PF02747 | 0.354 |
LIG_PCNA_yPIPBox_3 | 351 | 362 | PF02747 | 0.624 |
LIG_Pex14_1 | 148 | 152 | PF04695 | 0.354 |
LIG_PTB_Apo_2 | 364 | 371 | PF02174 | 0.430 |
LIG_PTB_Phospho_1 | 364 | 370 | PF10480 | 0.520 |
LIG_REV1ctd_RIR_1 | 381 | 391 | PF16727 | 0.643 |
LIG_SH2_CRK | 219 | 223 | PF00017 | 0.447 |
LIG_SH2_CRK | 693 | 697 | PF00017 | 0.434 |
LIG_SH2_CRK | 751 | 755 | PF00017 | 0.585 |
LIG_SH2_NCK_1 | 504 | 508 | PF00017 | 0.524 |
LIG_SH2_PTP2 | 889 | 892 | PF00017 | 0.434 |
LIG_SH2_SRC | 471 | 474 | PF00017 | 0.369 |
LIG_SH2_SRC | 889 | 892 | PF00017 | 0.384 |
LIG_SH2_STAP1 | 574 | 578 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 416 | 419 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 538 | 541 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 574 | 577 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 889 | 892 | PF00017 | 0.434 |
LIG_SH3_3 | 436 | 442 | PF00018 | 0.465 |
LIG_SH3_3 | 698 | 704 | PF00018 | 0.530 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.739 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.369 |
LIG_SH3_3 | 845 | 851 | PF00018 | 0.480 |
LIG_SH3_3 | 852 | 858 | PF00018 | 0.369 |
LIG_SUMO_SIM_anti_2 | 196 | 203 | PF11976 | 0.356 |
LIG_SUMO_SIM_anti_2 | 44 | 51 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 589 | 595 | PF11976 | 0.599 |
LIG_SUMO_SIM_par_1 | 650 | 657 | PF11976 | 0.445 |
LIG_SUMO_SIM_par_1 | 872 | 877 | PF11976 | 0.373 |
LIG_TRAF2_1 | 324 | 327 | PF00917 | 0.472 |
LIG_TRAF2_1 | 335 | 338 | PF00917 | 0.407 |
LIG_TRAF2_1 | 623 | 626 | PF00917 | 0.848 |
LIG_TRAF2_1 | 631 | 634 | PF00917 | 0.838 |
LIG_TYR_ITIM | 539 | 544 | PF00017 | 0.451 |
LIG_TYR_ITIM | 691 | 696 | PF00017 | 0.430 |
LIG_TYR_ITIM | 887 | 892 | PF00017 | 0.384 |
LIG_WRC_WIRS_1 | 116 | 121 | PF05994 | 0.354 |
MOD_CDK_SPK_2 | 824 | 829 | PF00069 | 0.471 |
MOD_CDK_SPxxK_3 | 340 | 347 | PF00069 | 0.613 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.491 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.339 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.548 |
MOD_CK1_1 | 746 | 752 | PF00069 | 0.595 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.364 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.496 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.745 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.426 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.479 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.447 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.447 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.672 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.388 |
MOD_CK2_1 | 510 | 516 | PF00069 | 0.458 |
MOD_CK2_1 | 891 | 897 | PF00069 | 0.414 |
MOD_GlcNHglycan | 345 | 350 | PF01048 | 0.732 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.352 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.547 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.474 |
MOD_GlcNHglycan | 683 | 686 | PF01048 | 0.511 |
MOD_GlcNHglycan | 696 | 699 | PF01048 | 0.435 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.442 |
MOD_GlcNHglycan | 876 | 879 | PF01048 | 0.403 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.388 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.404 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.369 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.426 |
MOD_GSK3_1 | 713 | 720 | PF00069 | 0.534 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.474 |
MOD_GSK3_1 | 739 | 746 | PF00069 | 0.624 |
MOD_GSK3_1 | 796 | 803 | PF00069 | 0.594 |
MOD_GSK3_1 | 820 | 827 | PF00069 | 0.451 |
MOD_GSK3_1 | 862 | 869 | PF00069 | 0.354 |
MOD_N-GLC_1 | 313 | 318 | PF02516 | 0.297 |
MOD_N-GLC_1 | 621 | 626 | PF02516 | 0.880 |
MOD_N-GLC_1 | 783 | 788 | PF02516 | 0.507 |
MOD_N-GLC_1 | 789 | 794 | PF02516 | 0.418 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.384 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.539 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.395 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.339 |
MOD_NEK2_1 | 561 | 566 | PF00069 | 0.481 |
MOD_NEK2_1 | 584 | 589 | PF00069 | 0.537 |
MOD_NEK2_1 | 660 | 665 | PF00069 | 0.571 |
MOD_NEK2_1 | 672 | 677 | PF00069 | 0.547 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.381 |
MOD_NEK2_1 | 777 | 782 | PF00069 | 0.574 |
MOD_NEK2_1 | 800 | 805 | PF00069 | 0.452 |
MOD_NEK2_1 | 807 | 812 | PF00069 | 0.493 |
MOD_NEK2_2 | 241 | 246 | PF00069 | 0.496 |
MOD_NEK2_2 | 505 | 510 | PF00069 | 0.545 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.434 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.369 |
MOD_PIKK_1 | 866 | 872 | PF00454 | 0.447 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.506 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.419 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.540 |
MOD_PKA_2 | 572 | 578 | PF00069 | 0.468 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.487 |
MOD_PKB_1 | 165 | 173 | PF00069 | 0.297 |
MOD_Plk_1 | 19 | 25 | PF00069 | 0.834 |
MOD_Plk_1 | 193 | 199 | PF00069 | 0.474 |
MOD_Plk_1 | 313 | 319 | PF00069 | 0.297 |
MOD_Plk_1 | 419 | 425 | PF00069 | 0.548 |
MOD_Plk_1 | 789 | 795 | PF00069 | 0.478 |
MOD_Plk_2-3 | 299 | 305 | PF00069 | 0.297 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.354 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.359 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.548 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.465 |
MOD_Plk_4 | 518 | 524 | PF00069 | 0.416 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.487 |
MOD_Plk_4 | 592 | 598 | PF00069 | 0.596 |
MOD_Plk_4 | 667 | 673 | PF00069 | 0.606 |
MOD_Plk_4 | 746 | 752 | PF00069 | 0.476 |
MOD_Plk_4 | 796 | 802 | PF00069 | 0.487 |
MOD_Plk_4 | 807 | 813 | PF00069 | 0.430 |
MOD_Plk_4 | 840 | 846 | PF00069 | 0.597 |
MOD_Plk_4 | 891 | 897 | PF00069 | 0.423 |
MOD_ProDKin_1 | 340 | 346 | PF00069 | 0.640 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.612 |
MOD_ProDKin_1 | 820 | 826 | PF00069 | 0.444 |
MOD_ProDKin_1 | 869 | 875 | PF00069 | 0.359 |
MOD_SUMO_for_1 | 42 | 45 | PF00179 | 0.677 |
MOD_SUMO_for_1 | 629 | 632 | PF00179 | 0.783 |
MOD_SUMO_rev_2 | 273 | 280 | PF00179 | 0.384 |
MOD_SUMO_rev_2 | 30 | 36 | PF00179 | 0.769 |
MOD_SUMO_rev_2 | 343 | 348 | PF00179 | 0.731 |
MOD_SUMO_rev_2 | 479 | 484 | PF00179 | 0.426 |
MOD_SUMO_rev_2 | 491 | 497 | PF00179 | 0.570 |
MOD_SUMO_rev_2 | 528 | 534 | PF00179 | 0.581 |
MOD_SUMO_rev_2 | 632 | 637 | PF00179 | 0.809 |
MOD_SUMO_rev_2 | 880 | 890 | PF00179 | 0.434 |
TRG_DiLeu_BaEn_1 | 303 | 308 | PF01217 | 0.388 |
TRG_DiLeu_BaEn_1 | 44 | 49 | PF01217 | 0.620 |
TRG_DiLeu_BaEn_1 | 493 | 498 | PF01217 | 0.625 |
TRG_DiLeu_BaEn_2 | 150 | 156 | PF01217 | 0.354 |
TRG_DiLeu_BaEn_4 | 303 | 309 | PF01217 | 0.369 |
TRG_DiLeu_BaLyEn_6 | 484 | 489 | PF01217 | 0.496 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 219 | 222 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 541 | 544 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 574 | 577 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 693 | 696 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 889 | 892 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 94 | 97 | PF00928 | 0.369 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.447 |
TRG_NES_CRM1_1 | 115 | 125 | PF08389 | 0.447 |
TRG_NES_CRM1_1 | 203 | 215 | PF08389 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 111 | 115 | PF00026 | 0.222 |
TRG_Pf-PMV_PEXEL_1 | 131 | 135 | PF00026 | 0.222 |
TRG_Pf-PMV_PEXEL_1 | 268 | 273 | PF00026 | 0.397 |
TRG_Pf-PMV_PEXEL_1 | 334 | 338 | PF00026 | 0.485 |
TRG_Pf-PMV_PEXEL_1 | 91 | 96 | PF00026 | 0.426 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCY7 | Leptomonas seymouri | 85% | 100% |
A0A0S4KJP7 | Bodo saltans | 50% | 98% |
A0A1X0NZE4 | Trypanosomatidae | 61% | 100% |
A0A422NUV0 | Trypanosoma rangeli | 60% | 100% |
A4HH20 | Leishmania braziliensis | 92% | 100% |
A4I449 | Leishmania infantum | 100% | 100% |
C9ZKR3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
E9ADL4 | Leishmania major | 98% | 100% |
E9AM67 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
P38764 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 92% |
P56701 | Bos taurus | 36% | 100% |
P87048 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 36% | 100% |
Q13200 | Homo sapiens | 36% | 100% |
Q4FZT9 | Rattus norvegicus | 36% | 100% |
Q54BC6 | Dictyostelium discoideum | 36% | 100% |
Q5R9I6 | Pongo abelii | 36% | 100% |
Q6FPV6 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 33% | 92% |
Q6XJG8 | Arabidopsis thaliana | 37% | 100% |
Q7S8R8 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 34% | 100% |
Q8SS65 | Encephalitozoon cuniculi (strain GB-M1) | 23% | 100% |
Q8VDM4 | Mus musculus | 36% | 100% |
Q9SIV2 | Arabidopsis thaliana | 36% | 100% |
V5DLC9 | Trypanosoma cruzi | 60% | 100% |