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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0031248 | protein acetyltransferase complex | 3 | 2 |
GO:0031414 | N-terminal protein acetyltransferase complex | 4 | 2 |
GO:0031416 | NatB complex | 5 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902493 | acetyltransferase complex | 4 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1990234 | transferase complex | 3 | 2 |
Related structures:
AlphaFold database: Q4Q7Q4
Term | Name | Level | Count |
---|---|---|---|
GO:0006473 | protein acetylation | 6 | 2 |
GO:0006474 | N-terminal protein amino acid acetylation | 5 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0017196 | N-terminal peptidyl-methionine acetylation | 6 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018206 | peptidyl-methionine modification | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0031365 | N-terminal protein amino acid modification | 5 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043543 | protein acylation | 5 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0051604 | protein maturation | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0016740 | transferase activity | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 12 | 16 | PF00656 | 0.377 |
CLV_C14_Caspase3-7 | 638 | 642 | PF00656 | 0.340 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.236 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.216 |
CLV_NRD_NRD_1 | 679 | 681 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 710 | 712 | PF00675 | 0.630 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.248 |
CLV_PCSK_KEX2_1 | 485 | 487 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 679 | 681 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.230 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 610 | 614 | PF00082 | 0.229 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 682 | 686 | PF00082 | 0.407 |
DEG_APCC_DBOX_1 | 507 | 515 | PF00400 | 0.430 |
DEG_APCC_DBOX_1 | 681 | 689 | PF00400 | 0.408 |
DEG_APCC_DBOX_1 | 774 | 782 | PF00400 | 0.394 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.515 |
DEG_SCF_FBW7_1 | 733 | 739 | PF00400 | 0.450 |
DEG_SCF_FBW7_1 | 847 | 854 | PF00400 | 0.479 |
DEG_SPOP_SBC_1 | 463 | 467 | PF00917 | 0.367 |
DOC_CKS1_1 | 366 | 371 | PF01111 | 0.510 |
DOC_CKS1_1 | 733 | 738 | PF01111 | 0.451 |
DOC_CYCLIN_RxL_1 | 679 | 687 | PF00134 | 0.427 |
DOC_MAPK_FxFP_2 | 795 | 798 | PF00069 | 0.294 |
DOC_MAPK_gen_1 | 355 | 363 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 54 | 63 | PF00069 | 0.411 |
DOC_PP4_FxxP_1 | 366 | 369 | PF00568 | 0.510 |
DOC_PP4_FxxP_1 | 795 | 798 | PF00568 | 0.294 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.354 |
DOC_USP7_MATH_1 | 427 | 431 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 695 | 699 | PF00917 | 0.373 |
DOC_USP7_MATH_1 | 705 | 709 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 736 | 740 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 765 | 769 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 851 | 855 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 857 | 861 | PF00917 | 0.517 |
DOC_USP7_UBL2_3 | 162 | 166 | PF12436 | 0.365 |
DOC_USP7_UBL2_3 | 317 | 321 | PF12436 | 0.510 |
DOC_USP7_UBL2_3 | 613 | 617 | PF12436 | 0.430 |
DOC_USP7_UBL2_3 | 814 | 818 | PF12436 | 0.461 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.318 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 732 | 737 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 847 | 852 | PF00397 | 0.539 |
LIG_14-3-3_CanoR_1 | 104 | 111 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 132 | 137 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 231 | 238 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 240 | 250 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 288 | 292 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 432 | 440 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 629 | 633 | PF00244 | 0.394 |
LIG_14-3-3_CanoR_1 | 682 | 691 | PF00244 | 0.293 |
LIG_14-3-3_CanoR_1 | 838 | 844 | PF00244 | 0.517 |
LIG_APCC_ABBA_1 | 253 | 258 | PF00400 | 0.427 |
LIG_BRCT_BRCA1_1 | 685 | 689 | PF00533 | 0.288 |
LIG_Clathr_ClatBox_2 | 542 | 547 | PF01394 | 0.461 |
LIG_deltaCOP1_diTrp_1 | 248 | 253 | PF00928 | 0.307 |
LIG_deltaCOP1_diTrp_1 | 621 | 627 | PF00928 | 0.552 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.365 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.341 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.510 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.471 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.436 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.449 |
LIG_FHA_1 | 584 | 590 | PF00498 | 0.417 |
LIG_FHA_1 | 598 | 604 | PF00498 | 0.487 |
LIG_FHA_1 | 641 | 647 | PF00498 | 0.341 |
LIG_FHA_1 | 769 | 775 | PF00498 | 0.374 |
LIG_FHA_1 | 867 | 873 | PF00498 | 0.422 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.438 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.443 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.382 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.448 |
LIG_FHA_2 | 464 | 470 | PF00498 | 0.430 |
LIG_FHA_2 | 606 | 612 | PF00498 | 0.474 |
LIG_FHA_2 | 636 | 642 | PF00498 | 0.481 |
LIG_IRF3_LxIS_1 | 357 | 364 | PF10401 | 0.461 |
LIG_LIR_Apic_2 | 351 | 357 | PF02991 | 0.549 |
LIG_LIR_Apic_2 | 364 | 369 | PF02991 | 0.448 |
LIG_LIR_Apic_2 | 793 | 798 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 113 | 121 | PF02991 | 0.236 |
LIG_LIR_Gen_1 | 186 | 192 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 247 | 256 | PF02991 | 0.302 |
LIG_LIR_Gen_1 | 358 | 367 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 447 | 457 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 467 | 477 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 837 | 847 | PF02991 | 0.579 |
LIG_LIR_Gen_1 | 93 | 100 | PF02991 | 0.375 |
LIG_LIR_LC3C_4 | 666 | 670 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 186 | 190 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 247 | 253 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 358 | 363 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 447 | 452 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 467 | 473 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 491 | 495 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 549 | 554 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 837 | 843 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 93 | 97 | PF02991 | 0.347 |
LIG_NRBOX | 802 | 808 | PF00104 | 0.353 |
LIG_PCNA_yPIPBox_3 | 343 | 356 | PF02747 | 0.461 |
LIG_Pex14_1 | 547 | 551 | PF04695 | 0.461 |
LIG_PTB_Apo_2 | 47 | 54 | PF02174 | 0.370 |
LIG_PTB_Phospho_1 | 47 | 53 | PF10480 | 0.364 |
LIG_SH2_CRK | 120 | 124 | PF00017 | 0.386 |
LIG_SH2_CRK | 354 | 358 | PF00017 | 0.510 |
LIG_SH2_CRK | 470 | 474 | PF00017 | 0.510 |
LIG_SH2_NCK_1 | 120 | 124 | PF00017 | 0.350 |
LIG_SH2_PTP2 | 187 | 190 | PF00017 | 0.302 |
LIG_SH2_PTP2 | 449 | 452 | PF00017 | 0.428 |
LIG_SH2_SRC | 187 | 190 | PF00017 | 0.311 |
LIG_SH2_SRC | 360 | 363 | PF00017 | 0.492 |
LIG_SH2_SRC | 742 | 745 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 197 | 201 | PF00017 | 0.400 |
LIG_SH2_STAP1 | 470 | 474 | PF00017 | 0.510 |
LIG_SH2_STAP1 | 495 | 499 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 729 | 733 | PF00017 | 0.367 |
LIG_SH2_STAT3 | 552 | 555 | PF00017 | 0.510 |
LIG_SH2_STAT3 | 590 | 593 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 569 | 572 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 742 | 745 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 756 | 759 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 777 | 780 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 883 | 886 | PF00017 | 0.441 |
LIG_SH3_3 | 666 | 672 | PF00018 | 0.368 |
LIG_SUMO_SIM_anti_2 | 186 | 192 | PF11976 | 0.432 |
LIG_SUMO_SIM_anti_2 | 276 | 282 | PF11976 | 0.375 |
LIG_SUMO_SIM_anti_2 | 330 | 336 | PF11976 | 0.458 |
LIG_SUMO_SIM_anti_2 | 43 | 49 | PF11976 | 0.332 |
LIG_SUMO_SIM_anti_2 | 475 | 481 | PF11976 | 0.461 |
LIG_SUMO_SIM_anti_2 | 666 | 673 | PF11976 | 0.347 |
LIG_SUMO_SIM_par_1 | 666 | 673 | PF11976 | 0.388 |
LIG_TRAF2_1 | 407 | 410 | PF00917 | 0.529 |
LIG_TRAF2_1 | 553 | 556 | PF00917 | 0.560 |
LIG_TYR_ITIM | 527 | 532 | PF00017 | 0.445 |
LIG_UBA3_1 | 159 | 166 | PF00899 | 0.365 |
LIG_UBA3_1 | 802 | 808 | PF00899 | 0.408 |
LIG_WRC_WIRS_1 | 363 | 368 | PF05994 | 0.510 |
MOD_CDK_SPxxK_3 | 281 | 288 | PF00069 | 0.316 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.388 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.510 |
MOD_CK1_1 | 768 | 774 | PF00069 | 0.384 |
MOD_CK1_1 | 785 | 791 | PF00069 | 0.426 |
MOD_CK1_1 | 839 | 845 | PF00069 | 0.283 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.393 |
MOD_CK2_1 | 273 | 279 | PF00069 | 0.523 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.447 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.501 |
MOD_CK2_1 | 550 | 556 | PF00069 | 0.491 |
MOD_CK2_1 | 696 | 702 | PF00069 | 0.480 |
MOD_CK2_1 | 756 | 762 | PF00069 | 0.500 |
MOD_CMANNOS | 544 | 547 | PF00535 | 0.310 |
MOD_CMANNOS | 624 | 627 | PF00535 | 0.426 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.368 |
MOD_GlcNHglycan | 274 | 278 | PF01048 | 0.475 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.373 |
MOD_GlcNHglycan | 721 | 724 | PF01048 | 0.658 |
MOD_GlcNHglycan | 736 | 739 | PF01048 | 0.620 |
MOD_GlcNHglycan | 768 | 771 | PF01048 | 0.506 |
MOD_GlcNHglycan | 786 | 790 | PF01048 | 0.463 |
MOD_GlcNHglycan | 803 | 806 | PF01048 | 0.307 |
MOD_GlcNHglycan | 853 | 856 | PF01048 | 0.575 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.390 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.416 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.479 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.489 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.510 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.450 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.461 |
MOD_GSK3_1 | 728 | 735 | PF00069 | 0.466 |
MOD_GSK3_1 | 773 | 780 | PF00069 | 0.424 |
MOD_GSK3_1 | 834 | 841 | PF00069 | 0.513 |
MOD_GSK3_1 | 843 | 850 | PF00069 | 0.490 |
MOD_N-GLC_1 | 567 | 572 | PF02516 | 0.310 |
MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.447 |
MOD_N-GLC_2 | 83 | 85 | PF02516 | 0.435 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.316 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.322 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.408 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.510 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.420 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.560 |
MOD_NEK2_1 | 567 | 572 | PF00069 | 0.487 |
MOD_NEK2_1 | 664 | 669 | PF00069 | 0.373 |
MOD_NEK2_1 | 684 | 689 | PF00069 | 0.146 |
MOD_NEK2_1 | 728 | 733 | PF00069 | 0.475 |
MOD_NEK2_1 | 843 | 848 | PF00069 | 0.586 |
MOD_NEK2_2 | 251 | 256 | PF00069 | 0.310 |
MOD_NEK2_2 | 883 | 888 | PF00069 | 0.366 |
MOD_PIKK_1 | 241 | 247 | PF00454 | 0.399 |
MOD_PIKK_1 | 605 | 611 | PF00454 | 0.462 |
MOD_PKA_1 | 355 | 361 | PF00069 | 0.430 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.428 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.441 |
MOD_PKA_2 | 520 | 526 | PF00069 | 0.510 |
MOD_PKA_2 | 628 | 634 | PF00069 | 0.405 |
MOD_PKA_2 | 678 | 684 | PF00069 | 0.430 |
MOD_PKA_2 | 824 | 830 | PF00069 | 0.353 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.514 |
MOD_Plk_1 | 291 | 297 | PF00069 | 0.314 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.450 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.454 |
MOD_Plk_1 | 468 | 474 | PF00069 | 0.553 |
MOD_Plk_1 | 557 | 563 | PF00069 | 0.416 |
MOD_Plk_1 | 567 | 573 | PF00069 | 0.415 |
MOD_Plk_2-3 | 478 | 484 | PF00069 | 0.445 |
MOD_Plk_2-3 | 550 | 556 | PF00069 | 0.461 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.410 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.459 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.440 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.415 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.461 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.466 |
MOD_Plk_4 | 488 | 494 | PF00069 | 0.412 |
MOD_Plk_4 | 557 | 563 | PF00069 | 0.442 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.517 |
MOD_Plk_4 | 635 | 641 | PF00069 | 0.465 |
MOD_Plk_4 | 647 | 653 | PF00069 | 0.392 |
MOD_Plk_4 | 664 | 670 | PF00069 | 0.253 |
MOD_Plk_4 | 684 | 690 | PF00069 | 0.146 |
MOD_Plk_4 | 777 | 783 | PF00069 | 0.421 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.315 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.510 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.510 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.512 |
MOD_ProDKin_1 | 732 | 738 | PF00069 | 0.464 |
MOD_ProDKin_1 | 847 | 853 | PF00069 | 0.532 |
MOD_SUMO_for_1 | 870 | 873 | PF00179 | 0.382 |
MOD_SUMO_for_1 | 887 | 890 | PF00179 | 0.218 |
MOD_SUMO_rev_2 | 309 | 319 | PF00179 | 0.496 |
MOD_SUMO_rev_2 | 605 | 615 | PF00179 | 0.430 |
TRG_DiLeu_BaEn_1 | 475 | 480 | PF01217 | 0.512 |
TRG_DiLeu_BaLyEn_6 | 528 | 533 | PF01217 | 0.490 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.182 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 449 | 452 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 470 | 473 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 529 | 532 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 94 | 97 | PF00928 | 0.377 |
TRG_ER_diArg_1 | 396 | 398 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 485 | 487 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 678 | 680 | PF00400 | 0.472 |
TRG_NLS_MonoExtN_4 | 709 | 715 | PF00514 | 0.547 |
TRG_Pf-PMV_PEXEL_1 | 104 | 108 | PF00026 | 0.413 |
TRG_Pf-PMV_PEXEL_1 | 17 | 21 | PF00026 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 240 | 245 | PF00026 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 308 | 312 | PF00026 | 0.310 |
TRG_Pf-PMV_PEXEL_1 | 418 | 423 | PF00026 | 0.332 |
TRG_Pf-PMV_PEXEL_1 | 432 | 436 | PF00026 | 0.199 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I184 | Leptomonas seymouri | 66% | 98% |
A0A1X0P396 | Trypanosomatidae | 44% | 100% |
A0A3S5IR93 | Trypanosoma rangeli | 43% | 100% |
A0A3S7X316 | Leishmania donovani | 96% | 100% |
A4HI03 | Leishmania braziliensis | 85% | 100% |
A4I580 | Leishmania infantum | 96% | 100% |
C9ZQK9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9B0H7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q17DK2 | Aedes aegypti | 22% | 95% |
Q294E0 | Drosophila pseudoobscura pseudoobscura | 22% | 93% |
Q6QI44 | Rattus norvegicus | 23% | 92% |
Q7PYI4 | Anopheles gambiae | 21% | 91% |
Q8BWZ3 | Mus musculus | 23% | 92% |
Q9VDQ7 | Drosophila melanogaster | 22% | 95% |
V5BGT7 | Trypanosoma cruzi | 47% | 100% |