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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000151 | ubiquitin ligase complex | 3 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1990234 | transferase complex | 3 | 2 |
Related structures:
AlphaFold database: Q4QAA1
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 12 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009056 | catabolic process | 2 | 12 |
GO:0009057 | macromolecule catabolic process | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016567 | protein ubiquitination | 7 | 2 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 12 |
GO:0032446 | protein modification by small protein conjugation | 6 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044248 | cellular catabolic process | 3 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 12 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 12 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:1901575 | organic substance catabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0005515 | protein binding | 2 | 12 |
GO:0019899 | enzyme binding | 3 | 12 |
GO:0030674 | protein-macromolecule adaptor activity | 2 | 2 |
GO:0031625 | ubiquitin protein ligase binding | 5 | 12 |
GO:0044389 | ubiquitin-like protein ligase binding | 4 | 12 |
GO:0060090 | molecular adaptor activity | 1 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 706 | 712 | PF00089 | 0.275 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.265 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 623 | 625 | PF00675 | 0.330 |
CLV_NRD_NRD_1 | 648 | 650 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 674 | 676 | PF00675 | 0.254 |
CLV_NRD_NRD_1 | 690 | 692 | PF00675 | 0.229 |
CLV_NRD_NRD_1 | 726 | 728 | PF00675 | 0.236 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.403 |
CLV_PCSK_FUR_1 | 646 | 650 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 648 | 650 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 690 | 692 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 726 | 728 | PF00082 | 0.299 |
CLV_PCSK_PC1ET2_1 | 206 | 208 | PF00082 | 0.369 |
CLV_PCSK_PC7_1 | 237 | 243 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 550 | 554 | PF00082 | 0.244 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 620 | 624 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 628 | 632 | PF00082 | 0.202 |
CLV_PCSK_SKI1_1 | 685 | 689 | PF00082 | 0.234 |
CLV_PCSK_SKI1_1 | 715 | 719 | PF00082 | 0.234 |
CLV_Separin_Metazoa | 537 | 541 | PF03568 | 0.518 |
DEG_APCC_DBOX_1 | 5 | 13 | PF00400 | 0.524 |
DEG_COP1_1 | 521 | 531 | PF00400 | 0.502 |
DEG_MDM2_SWIB_1 | 212 | 219 | PF02201 | 0.472 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.438 |
DEG_SPOP_SBC_1 | 379 | 383 | PF00917 | 0.516 |
DOC_CKS1_1 | 592 | 597 | PF01111 | 0.518 |
DOC_CYCLIN_RxL_1 | 153 | 161 | PF00134 | 0.530 |
DOC_MAPK_gen_1 | 298 | 305 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 568 | 575 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 502 | 510 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 519 | 528 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 709 | 716 | PF00069 | 0.530 |
DOC_PP1_RVXF_1 | 548 | 555 | PF00149 | 0.434 |
DOC_PP4_FxxP_1 | 197 | 200 | PF00568 | 0.448 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 545 | 549 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 657 | 661 | PF00917 | 0.576 |
DOC_USP7_UBL2_3 | 104 | 108 | PF12436 | 0.445 |
DOC_USP7_UBL2_3 | 156 | 160 | PF12436 | 0.530 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 587 | 592 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 708 | 713 | PF00397 | 0.454 |
LIG_14-3-3_CanoR_1 | 165 | 174 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 22 | 30 | PF00244 | 0.394 |
LIG_14-3-3_CanoR_1 | 242 | 252 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 419 | 425 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 432 | 441 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 49 | 57 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 519 | 527 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 550 | 555 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 601 | 607 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 658 | 662 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 690 | 694 | PF00244 | 0.459 |
LIG_APCC_ABBA_1 | 135 | 140 | PF00400 | 0.434 |
LIG_APCC_ABBA_1 | 198 | 203 | PF00400 | 0.499 |
LIG_APCC_ABBA_1 | 391 | 396 | PF00400 | 0.499 |
LIG_APCC_Cbox_2 | 431 | 437 | PF00515 | 0.530 |
LIG_BRCT_BRCA1_1 | 352 | 356 | PF00533 | 0.477 |
LIG_BRCT_BRCA1_1 | 485 | 489 | PF00533 | 0.499 |
LIG_BRCT_BRCA1_1 | 706 | 710 | PF00533 | 0.459 |
LIG_Clathr_ClatBox_1 | 630 | 634 | PF01394 | 0.518 |
LIG_Clathr_ClatBox_1 | 65 | 69 | PF01394 | 0.477 |
LIG_CtBP_PxDLS_1 | 653 | 657 | PF00389 | 0.552 |
LIG_deltaCOP1_diTrp_1 | 482 | 489 | PF00928 | 0.557 |
LIG_EH1_1 | 503 | 511 | PF00400 | 0.530 |
LIG_eIF4E_1 | 60 | 66 | PF01652 | 0.459 |
LIG_eIF4E_2 | 612 | 618 | PF01652 | 0.472 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.530 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.446 |
LIG_FHA_1 | 501 | 507 | PF00498 | 0.524 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.439 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.517 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.489 |
LIG_FHA_2 | 252 | 258 | PF00498 | 0.463 |
LIG_FHA_2 | 426 | 432 | PF00498 | 0.492 |
LIG_FHA_2 | 434 | 440 | PF00498 | 0.439 |
LIG_FHA_2 | 636 | 642 | PF00498 | 0.561 |
LIG_GBD_Chelix_1 | 149 | 157 | PF00786 | 0.330 |
LIG_LIR_Apic_2 | 195 | 200 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 15 | 23 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 208 | 213 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 215 | 224 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 486 | 496 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 605 | 614 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 69 | 78 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 91 | 99 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 113 | 117 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 15 | 19 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 208 | 212 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 215 | 219 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 25 | 30 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 346 | 351 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 56 | 60 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 605 | 609 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 91 | 96 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 98 | 103 | PF02991 | 0.444 |
LIG_LYPXL_S_1 | 347 | 351 | PF13949 | 0.330 |
LIG_LYPXL_yS_3 | 348 | 351 | PF13949 | 0.530 |
LIG_PCNA_yPIPBox_3 | 71 | 82 | PF02747 | 0.434 |
LIG_PDZ_Class_2 | 739 | 744 | PF00595 | 0.368 |
LIG_Pex14_1 | 397 | 401 | PF04695 | 0.530 |
LIG_Pex14_2 | 212 | 216 | PF04695 | 0.538 |
LIG_Pex14_2 | 356 | 360 | PF04695 | 0.530 |
LIG_PTB_Apo_2 | 290 | 297 | PF02174 | 0.518 |
LIG_PTB_Apo_2 | 400 | 407 | PF02174 | 0.518 |
LIG_REV1ctd_RIR_1 | 293 | 303 | PF16727 | 0.530 |
LIG_SH2_CRK | 103 | 107 | PF00017 | 0.445 |
LIG_SH2_CRK | 40 | 44 | PF00017 | 0.434 |
LIG_SH2_CRK | 740 | 744 | PF00017 | 0.465 |
LIG_SH2_GRB2like | 401 | 404 | PF00017 | 0.530 |
LIG_SH2_NCK_1 | 40 | 44 | PF00017 | 0.434 |
LIG_SH2_SRC | 401 | 404 | PF00017 | 0.437 |
LIG_SH2_SRC | 612 | 615 | PF00017 | 0.472 |
LIG_SH2_STAP1 | 209 | 213 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 612 | 615 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 729 | 732 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.493 |
LIG_SH3_3 | 258 | 264 | PF00018 | 0.530 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.530 |
LIG_SH3_3 | 532 | 538 | PF00018 | 0.545 |
LIG_SH3_3 | 589 | 595 | PF00018 | 0.518 |
LIG_SH3_4 | 127 | 134 | PF00018 | 0.459 |
LIG_SUMO_SIM_anti_2 | 300 | 307 | PF11976 | 0.530 |
LIG_SUMO_SIM_anti_2 | 331 | 336 | PF11976 | 0.536 |
LIG_SUMO_SIM_anti_2 | 505 | 510 | PF11976 | 0.488 |
LIG_SUMO_SIM_par_1 | 95 | 101 | PF11976 | 0.530 |
LIG_TRAF2_1 | 88 | 91 | PF00917 | 0.520 |
LIG_TRAF2_2 | 595 | 600 | PF00917 | 0.518 |
LIG_UBA3_1 | 153 | 160 | PF00899 | 0.382 |
LIG_UBA3_1 | 305 | 312 | PF00899 | 0.530 |
LIG_UBA3_1 | 445 | 451 | PF00899 | 0.455 |
LIG_WRC_WIRS_1 | 111 | 116 | PF05994 | 0.499 |
LIG_WRC_WIRS_1 | 30 | 35 | PF05994 | 0.556 |
LIG_WRC_WIRS_1 | 528 | 533 | PF05994 | 0.457 |
MOD_CDK_SPxxK_3 | 260 | 267 | PF00069 | 0.527 |
MOD_CDK_SPxxK_3 | 708 | 715 | PF00069 | 0.475 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.477 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.459 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.466 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.555 |
MOD_CK1_1 | 708 | 714 | PF00069 | 0.517 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.540 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.459 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.451 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.508 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.450 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.532 |
MOD_CK2_1 | 556 | 562 | PF00069 | 0.515 |
MOD_CK2_1 | 657 | 663 | PF00069 | 0.596 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.485 |
MOD_Cter_Amidation | 688 | 691 | PF01082 | 0.330 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.285 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.299 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.333 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.291 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.235 |
MOD_GlcNHglycan | 625 | 628 | PF01048 | 0.330 |
MOD_GlcNHglycan | 83 | 87 | PF01048 | 0.332 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.530 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.527 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.473 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.444 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.492 |
MOD_GSK3_1 | 657 | 664 | PF00069 | 0.563 |
MOD_GSK3_1 | 704 | 711 | PF00069 | 0.456 |
MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.315 |
MOD_N-GLC_1 | 587 | 592 | PF02516 | 0.293 |
MOD_N-GLC_2 | 238 | 240 | PF02516 | 0.182 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.437 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.477 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.495 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.536 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.477 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.518 |
MOD_NEK2_1 | 563 | 568 | PF00069 | 0.536 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.485 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.530 |
MOD_PIKK_1 | 243 | 249 | PF00454 | 0.472 |
MOD_PIKK_1 | 568 | 574 | PF00454 | 0.535 |
MOD_PKA_1 | 298 | 304 | PF00069 | 0.530 |
MOD_PKA_1 | 450 | 456 | PF00069 | 0.520 |
MOD_PKA_1 | 568 | 574 | PF00069 | 0.530 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.501 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.445 |
MOD_PKA_2 | 518 | 524 | PF00069 | 0.532 |
MOD_PKA_2 | 623 | 629 | PF00069 | 0.499 |
MOD_PKA_2 | 657 | 663 | PF00069 | 0.569 |
MOD_PKA_2 | 689 | 695 | PF00069 | 0.530 |
MOD_PKB_1 | 618 | 626 | PF00069 | 0.518 |
MOD_PKB_1 | 80 | 88 | PF00069 | 0.518 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.532 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.489 |
MOD_Plk_1 | 635 | 641 | PF00069 | 0.549 |
MOD_Plk_2-3 | 328 | 334 | PF00069 | 0.509 |
MOD_Plk_2-3 | 635 | 641 | PF00069 | 0.530 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.470 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.422 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.499 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.483 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.445 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.465 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.462 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.515 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.494 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.459 |
MOD_ProDKin_1 | 587 | 593 | PF00069 | 0.487 |
MOD_ProDKin_1 | 708 | 714 | PF00069 | 0.454 |
MOD_SUMO_for_1 | 310 | 313 | PF00179 | 0.559 |
MOD_SUMO_for_1 | 325 | 328 | PF00179 | 0.491 |
MOD_SUMO_rev_2 | 164 | 174 | PF00179 | 0.472 |
MOD_SUMO_rev_2 | 668 | 678 | PF00179 | 0.438 |
MOD_SUMO_rev_2 | 707 | 717 | PF00179 | 0.438 |
TRG_DiLeu_BaEn_1 | 505 | 510 | PF01217 | 0.518 |
TRG_DiLeu_BaEn_2 | 428 | 434 | PF01217 | 0.530 |
TRG_DiLeu_BaLyEn_6 | 612 | 617 | PF01217 | 0.459 |
TRG_ENDOCYTIC_2 | 103 | 106 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 740 | 743 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.454 |
TRG_ER_diArg_1 | 241 | 243 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 281 | 284 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 35 | 37 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 464 | 467 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 617 | 620 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 646 | 649 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 725 | 727 | PF00400 | 0.499 |
TRG_NLS_MonoExtC_3 | 9 | 15 | PF00514 | 0.506 |
TRG_Pf-PMV_PEXEL_1 | 211 | 215 | PF00026 | 0.311 |
TRG_Pf-PMV_PEXEL_1 | 268 | 272 | PF00026 | 0.272 |
TRG_Pf-PMV_PEXEL_1 | 458 | 462 | PF00026 | 0.320 |
TRG_Pf-PMV_PEXEL_1 | 82 | 87 | PF00026 | 0.299 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I048 | Leptomonas seymouri | 82% | 100% |
A0A0S4J5R6 | Bodo saltans | 23% | 90% |
A0A0S4KHD2 | Bodo saltans | 22% | 100% |
A0A0S4KHS5 | Bodo saltans | 33% | 100% |
A0A1X0NXD6 | Trypanosomatidae | 45% | 100% |
A0A3Q8IF31 | Leishmania donovani | 97% | 100% |
A0A3R7K785 | Trypanosoma rangeli | 45% | 100% |
A0A3R7K7T8 | Trypanosoma rangeli | 23% | 92% |
A2A432 | Mus musculus | 24% | 77% |
A4HDU0 | Leishmania braziliensis | 92% | 100% |
A4I137 | Leishmania infantum | 96% | 100% |
A4IHP4 | Xenopus tropicalis | 26% | 97% |
B5DF89 | Rattus norvegicus | 25% | 97% |
C9ZW70 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AX75 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
O13790 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 97% |
O14122 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 100% |
O60999 | Dictyostelium discoideum | 24% | 97% |
P0CH31 | Arabidopsis thaliana | 24% | 100% |
Q09760 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 95% |
Q12018 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 20% | 91% |
Q13616 | Homo sapiens | 25% | 96% |
Q13617 | Homo sapiens | 22% | 100% |
Q13618 | Homo sapiens | 25% | 97% |
Q13619 | Homo sapiens | 24% | 98% |
Q13620 | Homo sapiens | 24% | 81% |
Q17389 | Caenorhabditis elegans | 24% | 95% |
Q17390 | Caenorhabditis elegans | 22% | 94% |
Q17391 | Caenorhabditis elegans | 26% | 96% |
Q21346 | Caenorhabditis elegans | 24% | 100% |
Q23639 | Caenorhabditis elegans | 23% | 97% |
Q24311 | Drosophila melanogaster | 23% | 96% |
Q29425 | Oryctolagus cuniculus | 21% | 95% |
Q3TCH7 | Mus musculus | 24% | 98% |
Q54CS2 | Dictyostelium discoideum | 22% | 93% |
Q54NZ5 | Dictyostelium discoideum | 23% | 97% |
Q54XF7 | Dictyostelium discoideum | 22% | 99% |
Q5R4G6 | Pongo abelii | 25% | 96% |
Q5RB36 | Pongo abelii | 21% | 95% |
Q5RCF3 | Pongo abelii | 22% | 100% |
Q5ZC88 | Oryza sativa subsp. japonica | 26% | 100% |
Q6DE95 | Xenopus laevis | 26% | 97% |
Q6GPF3 | Xenopus laevis | 26% | 97% |
Q8LGH4 | Arabidopsis thaliana | 23% | 94% |
Q93034 | Homo sapiens | 21% | 95% |
Q94AH6 | Arabidopsis thaliana | 26% | 100% |
Q9C9L0 | Arabidopsis thaliana | 24% | 100% |
Q9D4H8 | Mus musculus | 23% | 100% |
Q9D5V5 | Mus musculus | 22% | 95% |
Q9JJ31 | Rattus norvegicus | 22% | 95% |
Q9JLV5 | Mus musculus | 25% | 97% |
Q9SRZ0 | Arabidopsis thaliana | 26% | 100% |
Q9WTX6 | Mus musculus | 25% | 96% |
Q9XZJ3 | Dictyostelium discoideum | 21% | 96% |
Q9ZVH4 | Arabidopsis thaliana | 24% | 100% |
V5APS6 | Trypanosoma cruzi | 45% | 100% |