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. | yes | yes: 36 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 26 |
NetGPI | no | yes: 0, no: 26 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 27 |
GO:0110165 | cellular anatomical entity | 1 | 27 |
GO:0005635 | nuclear envelope | 4 | 4 |
GO:0005783 | endoplasmic reticulum | 5 | 4 |
GO:0031967 | organelle envelope | 3 | 4 |
GO:0031975 | envelope | 2 | 4 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 4 |
Related structures:
AlphaFold database: A0A3Q8IV37
Term | Name | Level | Count |
---|---|---|---|
GO:0006486 | protein glycosylation | 4 | 27 |
GO:0006807 | nitrogen compound metabolic process | 2 | 27 |
GO:0008152 | metabolic process | 1 | 27 |
GO:0019538 | protein metabolic process | 3 | 27 |
GO:0036211 | protein modification process | 4 | 27 |
GO:0043170 | macromolecule metabolic process | 3 | 27 |
GO:0043412 | macromolecule modification | 4 | 27 |
GO:0043413 | macromolecule glycosylation | 3 | 27 |
GO:0044238 | primary metabolic process | 2 | 27 |
GO:0070085 | glycosylation | 2 | 27 |
GO:0071704 | organic substance metabolic process | 2 | 27 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 27 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 27 |
GO:0004576 | oligosaccharyl transferase activity | 5 | 27 |
GO:0004579 | dolichyl-diphosphooligosaccharide-protein glycotransferase activity | 6 | 27 |
GO:0005488 | binding | 1 | 27 |
GO:0016740 | transferase activity | 2 | 27 |
GO:0016757 | glycosyltransferase activity | 3 | 27 |
GO:0016758 | hexosyltransferase activity | 4 | 27 |
GO:0043167 | ion binding | 2 | 27 |
GO:0043169 | cation binding | 3 | 27 |
GO:0046872 | metal ion binding | 4 | 27 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 633 | 637 | PF00656 | 0.276 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 502 | 504 | PF00675 | 0.294 |
CLV_NRD_NRD_1 | 815 | 817 | PF00675 | 0.651 |
CLV_NRD_NRD_1 | 829 | 831 | PF00675 | 0.614 |
CLV_PCSK_FUR_1 | 500 | 504 | PF00082 | 0.163 |
CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 829 | 831 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 454 | 458 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 537 | 541 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 589 | 593 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 650 | 654 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 736 | 740 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 757 | 761 | PF00082 | 0.601 |
DEG_MDM2_SWIB_1 | 541 | 548 | PF02201 | 0.364 |
DEG_ODPH_VHL_1 | 363 | 376 | PF01847 | 0.367 |
DEG_SCF_FBW7_1 | 26 | 33 | PF00400 | 0.535 |
DEG_SCF_TRCP1_1 | 10 | 16 | PF00400 | 0.579 |
DEG_SPOP_SBC_1 | 120 | 124 | PF00917 | 0.474 |
DOC_AGCK_PIF_2 | 105 | 110 | PF00069 | 0.302 |
DOC_CKS1_1 | 27 | 32 | PF01111 | 0.535 |
DOC_CYCLIN_RxL_1 | 374 | 384 | PF00134 | 0.264 |
DOC_CYCLIN_RxL_1 | 451 | 459 | PF00134 | 0.266 |
DOC_MAPK_FxFP_2 | 40 | 43 | PF00069 | 0.490 |
DOC_MAPK_gen_1 | 225 | 234 | PF00069 | 0.363 |
DOC_MAPK_gen_1 | 329 | 336 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 337 | 346 | PF00069 | 0.513 |
DOC_MAPK_HePTP_8 | 336 | 348 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 339 | 348 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 537 | 544 | PF00069 | 0.498 |
DOC_PP1_RVXF_1 | 433 | 439 | PF00149 | 0.505 |
DOC_PP1_RVXF_1 | 535 | 542 | PF00149 | 0.364 |
DOC_PP1_RVXF_1 | 612 | 619 | PF00149 | 0.289 |
DOC_PP4_FxxP_1 | 40 | 43 | PF00568 | 0.495 |
DOC_SPAK_OSR1_1 | 48 | 52 | PF12202 | 0.385 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.338 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.276 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.277 |
DOC_USP7_MATH_1 | 561 | 565 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 568 | 572 | PF00917 | 0.312 |
DOC_USP7_MATH_1 | 674 | 678 | PF00917 | 0.460 |
DOC_USP7_UBL2_3 | 813 | 817 | PF12436 | 0.548 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.289 |
DOC_WW_Pin1_4 | 527 | 532 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 606 | 611 | PF00397 | 0.277 |
DOC_WW_Pin1_4 | 651 | 656 | PF00397 | 0.310 |
DOC_WW_Pin1_4 | 680 | 685 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 715 | 720 | PF00397 | 0.329 |
LIG_14-3-3_CanoR_1 | 225 | 231 | PF00244 | 0.311 |
LIG_14-3-3_CanoR_1 | 271 | 275 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 280 | 285 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 347 | 352 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 48 | 54 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 631 | 635 | PF00244 | 0.301 |
LIG_14-3-3_CanoR_1 | 688 | 694 | PF00244 | 0.323 |
LIG_14-3-3_CanoR_1 | 70 | 75 | PF00244 | 0.289 |
LIG_14-3-3_CanoR_1 | 722 | 726 | PF00244 | 0.377 |
LIG_AP2alpha_2 | 85 | 87 | PF02296 | 0.289 |
LIG_BRCT_BRCA1_1 | 101 | 105 | PF00533 | 0.380 |
LIG_BRCT_BRCA1_1 | 40 | 44 | PF00533 | 0.528 |
LIG_BRCT_BRCA1_1 | 433 | 437 | PF00533 | 0.439 |
LIG_BRCT_BRCA1_1 | 556 | 560 | PF00533 | 0.337 |
LIG_BRCT_BRCA1_1 | 563 | 567 | PF00533 | 0.292 |
LIG_deltaCOP1_diTrp_1 | 403 | 408 | PF00928 | 0.232 |
LIG_eIF4E_1 | 431 | 437 | PF01652 | 0.385 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.379 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.386 |
LIG_FHA_1 | 548 | 554 | PF00498 | 0.391 |
LIG_FHA_1 | 651 | 657 | PF00498 | 0.315 |
LIG_FHA_1 | 733 | 739 | PF00498 | 0.392 |
LIG_FHA_2 | 27 | 33 | PF00498 | 0.571 |
LIG_FHA_2 | 471 | 477 | PF00498 | 0.278 |
LIG_FHA_2 | 520 | 526 | PF00498 | 0.431 |
LIG_FHA_2 | 564 | 570 | PF00498 | 0.341 |
LIG_FHA_2 | 607 | 613 | PF00498 | 0.266 |
LIG_LIR_Apic_2 | 366 | 371 | PF02991 | 0.314 |
LIG_LIR_Apic_2 | 713 | 717 | PF02991 | 0.379 |
LIG_LIR_Apic_2 | 785 | 789 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 187 | 196 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 216 | 224 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 403 | 414 | PF02991 | 0.236 |
LIG_LIR_Gen_1 | 601 | 610 | PF02991 | 0.262 |
LIG_LIR_Gen_1 | 62 | 71 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 668 | 674 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 692 | 702 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 743 | 753 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 98 | 108 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 106 | 110 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 112 | 116 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 187 | 191 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 216 | 221 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 283 | 288 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 302 | 307 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 33 | 39 | PF02991 | 0.660 |
LIG_LIR_Nem_3 | 366 | 372 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 403 | 409 | PF02991 | 0.224 |
LIG_LIR_Nem_3 | 41 | 47 | PF02991 | 0.659 |
LIG_LIR_Nem_3 | 426 | 431 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 434 | 440 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 601 | 605 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 62 | 67 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 668 | 672 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 692 | 697 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 743 | 748 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 750 | 756 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 98 | 104 | PF02991 | 0.287 |
LIG_LYPXL_yS_3 | 125 | 128 | PF13949 | 0.387 |
LIG_MLH1_MIPbox_1 | 101 | 105 | PF16413 | 0.380 |
LIG_NRBOX | 309 | 315 | PF00104 | 0.389 |
LIG_NRBOX | 435 | 441 | PF00104 | 0.369 |
LIG_Pex14_1 | 101 | 105 | PF04695 | 0.289 |
LIG_Pex14_1 | 45 | 49 | PF04695 | 0.488 |
LIG_Pex14_1 | 619 | 623 | PF04695 | 0.277 |
LIG_Pex14_2 | 104 | 108 | PF04695 | 0.215 |
LIG_Pex14_2 | 36 | 40 | PF04695 | 0.642 |
LIG_Pex14_2 | 541 | 545 | PF04695 | 0.500 |
LIG_Pex14_2 | 556 | 560 | PF04695 | 0.232 |
LIG_Pex14_2 | 84 | 88 | PF04695 | 0.267 |
LIG_PTB_Apo_2 | 688 | 695 | PF02174 | 0.327 |
LIG_PTB_Phospho_1 | 688 | 694 | PF10480 | 0.323 |
LIG_SH2_CRK | 714 | 718 | PF00017 | 0.370 |
LIG_SH2_CRK | 753 | 757 | PF00017 | 0.305 |
LIG_SH2_CRK | 77 | 81 | PF00017 | 0.302 |
LIG_SH2_NCK_1 | 714 | 718 | PF00017 | 0.328 |
LIG_SH2_PTP2 | 250 | 253 | PF00017 | 0.364 |
LIG_SH2_PTP2 | 602 | 605 | PF00017 | 0.173 |
LIG_SH2_PTP2 | 669 | 672 | PF00017 | 0.292 |
LIG_SH2_SRC | 431 | 434 | PF00017 | 0.364 |
LIG_SH2_SRC | 79 | 82 | PF00017 | 0.313 |
LIG_SH2_STAP1 | 282 | 286 | PF00017 | 0.364 |
LIG_SH2_STAP1 | 749 | 753 | PF00017 | 0.365 |
LIG_SH2_STAT3 | 621 | 624 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 447 | 450 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 598 | 601 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 602 | 605 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 669 | 672 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.351 |
LIG_SH3_2 | 43 | 48 | PF14604 | 0.480 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.387 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.567 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.414 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.444 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.202 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.489 |
LIG_SH3_3 | 696 | 702 | PF00018 | 0.406 |
LIG_SH3_3 | 769 | 775 | PF00018 | 0.372 |
LIG_SH3_3 | 776 | 782 | PF00018 | 0.374 |
LIG_SUMO_SIM_par_1 | 420 | 427 | PF11976 | 0.224 |
LIG_SUMO_SIM_par_1 | 454 | 459 | PF11976 | 0.218 |
LIG_SxIP_EBH_1 | 184 | 197 | PF03271 | 0.349 |
LIG_TYR_ITSM | 214 | 221 | PF00017 | 0.329 |
LIG_UBA3_1 | 23 | 28 | PF00899 | 0.556 |
LIG_UBA3_1 | 725 | 734 | PF00899 | 0.401 |
LIG_WRC_WIRS_1 | 214 | 219 | PF05994 | 0.329 |
LIG_WRC_WIRS_1 | 405 | 410 | PF05994 | 0.185 |
LIG_WRC_WIRS_1 | 425 | 430 | PF05994 | 0.199 |
MOD_CDC14_SPxK_1 | 302 | 305 | PF00782 | 0.380 |
MOD_CDK_SPxK_1 | 299 | 305 | PF00069 | 0.289 |
MOD_CDK_SPxxK_3 | 715 | 722 | PF00069 | 0.377 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.720 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.433 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.307 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.364 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.498 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.422 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.350 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.318 |
MOD_CK1_1 | 715 | 721 | PF00069 | 0.334 |
MOD_CK1_1 | 765 | 771 | PF00069 | 0.345 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.256 |
MOD_CK2_1 | 470 | 476 | PF00069 | 0.355 |
MOD_CK2_1 | 563 | 569 | PF00069 | 0.341 |
MOD_CK2_1 | 819 | 825 | PF00069 | 0.534 |
MOD_Cter_Amidation | 1 | 4 | PF01082 | 0.521 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.436 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.570 |
MOD_GlcNHglycan | 173 | 177 | PF01048 | 0.506 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.315 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.170 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.196 |
MOD_GlcNHglycan | 676 | 679 | PF01048 | 0.579 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.355 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.631 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.529 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.306 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.560 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.518 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.415 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.318 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.384 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.349 |
MOD_N-GLC_1 | 629 | 634 | PF02516 | 0.476 |
MOD_N-GLC_1 | 762 | 767 | PF02516 | 0.541 |
MOD_N-GLC_2 | 205 | 207 | PF02516 | 0.289 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.345 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.375 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.368 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.222 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.258 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.310 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.337 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.214 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.400 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.419 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.183 |
MOD_NEK2_1 | 721 | 726 | PF00069 | 0.327 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.578 |
MOD_NEK2_2 | 220 | 225 | PF00069 | 0.329 |
MOD_PK_1 | 347 | 353 | PF00069 | 0.426 |
MOD_PK_1 | 70 | 76 | PF00069 | 0.322 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.323 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.539 |
MOD_PKA_2 | 584 | 590 | PF00069 | 0.304 |
MOD_PKA_2 | 630 | 636 | PF00069 | 0.277 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.226 |
MOD_PKA_2 | 721 | 727 | PF00069 | 0.372 |
MOD_PKB_1 | 345 | 353 | PF00069 | 0.513 |
MOD_Plk_1 | 629 | 635 | PF00069 | 0.276 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.289 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.329 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.432 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.432 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.355 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.331 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.326 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.494 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.281 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.272 |
MOD_Plk_4 | 658 | 664 | PF00069 | 0.351 |
MOD_Plk_4 | 689 | 695 | PF00069 | 0.313 |
MOD_Plk_4 | 721 | 727 | PF00069 | 0.365 |
MOD_Plk_4 | 740 | 746 | PF00069 | 0.271 |
MOD_Plk_4 | 782 | 788 | PF00069 | 0.377 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.589 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.641 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.289 |
MOD_ProDKin_1 | 527 | 533 | PF00069 | 0.573 |
MOD_ProDKin_1 | 606 | 612 | PF00069 | 0.277 |
MOD_ProDKin_1 | 651 | 657 | PF00069 | 0.316 |
MOD_ProDKin_1 | 680 | 686 | PF00069 | 0.348 |
MOD_ProDKin_1 | 715 | 721 | PF00069 | 0.324 |
TRG_DiLeu_BaEn_1 | 658 | 663 | PF01217 | 0.330 |
TRG_DiLeu_BaLyEn_6 | 451 | 456 | PF01217 | 0.295 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 602 | 605 | PF00928 | 0.273 |
TRG_ENDOCYTIC_2 | 669 | 672 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 694 | 697 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 753 | 756 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.302 |
TRG_ER_diArg_1 | 224 | 227 | PF00400 | 0.376 |
TRG_ER_diArg_1 | 328 | 331 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 336 | 339 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 344 | 347 | PF00400 | 0.355 |
TRG_ER_diArg_1 | 374 | 377 | PF00400 | 0.257 |
TRG_ER_diArg_1 | 500 | 503 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 828 | 830 | PF00400 | 0.417 |
TRG_NES_CRM1_1 | 308 | 323 | PF08389 | 0.380 |
TRG_Pf-PMV_PEXEL_1 | 377 | 382 | PF00026 | 0.478 |
TRG_Pf-PMV_PEXEL_1 | 521 | 525 | PF00026 | 0.177 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IZ72 | Bodo saltans | 51% | 100% |
A0A1X0NFU7 | Trypanosomatidae | 55% | 99% |
A0A3Q8IHT0 | Leishmania donovani | 75% | 100% |
A0A3Q8II34 | Leishmania donovani | 57% | 100% |
A0A3Q8ILY7 | Leishmania donovani | 75% | 99% |
A0A422MX14 | Trypanosoma rangeli | 55% | 100% |
A4HFF9 | Leishmania braziliensis | 71% | 100% |
A4HMD5 | Leishmania braziliensis | 71% | 100% |
A4HMD6 | Leishmania braziliensis | 55% | 100% |
A4HMD7 | Leishmania braziliensis | 81% | 100% |
A4IB08 | Leishmania infantum | 75% | 100% |
A4IB09 | Leishmania infantum | 75% | 99% |
A4IB10 | Leishmania infantum | 58% | 100% |
C9ZNL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
C9ZQ40 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E2RG47 | Canis lupus familiaris | 30% | 100% |
E9AET6 | Leishmania major | 74% | 100% |
E9AET7 | Leishmania major | 75% | 100% |
E9AET8 | Leishmania major | 57% | 100% |
E9AET9 | Leishmania major | 91% | 100% |
E9AHU4 | Leishmania infantum | 100% | 100% |
E9B5Z2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
E9B5Z3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
E9B5Z4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 100% |
E9B5Z5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
F1PJP5 | Canis lupus familiaris | 29% | 100% |
O94335 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 100% |
P39007 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
P46975 | Caenorhabditis elegans | 30% | 100% |
P46977 | Homo sapiens | 29% | 100% |
P46978 | Mus musculus | 29% | 100% |
Q2KJI2 | Bos taurus | 29% | 100% |
Q3TDQ1 | Mus musculus | 30% | 100% |
Q54NM9 | Dictyostelium discoideum | 31% | 100% |
Q5RCE2 | Pongo abelii | 29% | 100% |
Q6F2Z1 | Oryza sativa subsp. japonica | 29% | 100% |
Q7XQ88 | Oryza sativa subsp. japonica | 32% | 100% |
Q8TCJ2 | Homo sapiens | 30% | 100% |
Q93ZY3 | Arabidopsis thaliana | 31% | 100% |
Q9FX21 | Arabidopsis thaliana | 32% | 100% |
V5BDM6 | Trypanosoma cruzi | 57% | 100% |