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 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A4HDU0
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:0019538 | protein metabolic process | 3 | 12 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
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:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:1901575 | organic substance catabolic process | 3 | 12 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0005515 | protein binding | 2 | 12 |
GO:0019899 | enzyme binding | 3 | 12 |
GO:0031625 | ubiquitin protein ligase binding | 5 | 12 |
GO:0044389 | ubiquitin-like protein ligase binding | 4 | 12 |
GO:0030674 | protein-macromolecule adaptor activity | 2 | 1 |
GO:0060090 | molecular adaptor activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 259 | 263 | PF00656 | 0.529 |
CLV_MEL_PAP_1 | 705 | 711 | PF00089 | 0.294 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 622 | 624 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 647 | 649 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 673 | 675 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 689 | 691 | PF00675 | 0.250 |
CLV_NRD_NRD_1 | 725 | 727 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.430 |
CLV_PCSK_FUR_1 | 645 | 649 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 647 | 649 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 689 | 691 | PF00082 | 0.273 |
CLV_PCSK_KEX2_1 | 725 | 727 | PF00082 | 0.316 |
CLV_PCSK_PC1ET2_1 | 206 | 208 | PF00082 | 0.370 |
CLV_PCSK_PC7_1 | 237 | 243 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 549 | 553 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 619 | 623 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 627 | 631 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 684 | 688 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 714 | 718 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.276 |
CLV_Separin_Metazoa | 536 | 540 | PF03568 | 0.560 |
DEG_APCC_DBOX_1 | 5 | 13 | PF00400 | 0.537 |
DEG_COP1_1 | 520 | 530 | PF00400 | 0.518 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.466 |
DEG_SPOP_SBC_1 | 380 | 384 | PF00917 | 0.551 |
DOC_CKS1_1 | 591 | 596 | PF01111 | 0.560 |
DOC_CYCLIN_RxL_1 | 153 | 161 | PF00134 | 0.541 |
DOC_MAPK_gen_1 | 298 | 305 | PF00069 | 0.497 |
DOC_MAPK_gen_1 | 623 | 632 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 518 | 527 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 708 | 715 | PF00069 | 0.532 |
DOC_PP1_RVXF_1 | 441 | 447 | PF00149 | 0.394 |
DOC_PP1_RVXF_1 | 547 | 554 | PF00149 | 0.455 |
DOC_PP4_FxxP_1 | 197 | 200 | PF00568 | 0.469 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.380 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 656 | 660 | PF00917 | 0.601 |
DOC_USP7_UBL2_3 | 104 | 108 | PF12436 | 0.466 |
DOC_USP7_UBL2_3 | 156 | 160 | PF12436 | 0.541 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 498 | 503 | PF00397 | 0.380 |
DOC_WW_Pin1_4 | 586 | 591 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 610 | 615 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 707 | 712 | PF00397 | 0.456 |
LIG_14-3-3_CanoR_1 | 165 | 174 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 241 | 247 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 251 | 260 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 418 | 424 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 431 | 440 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 49 | 57 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 518 | 526 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 549 | 554 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 600 | 606 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 657 | 661 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 689 | 693 | PF00244 | 0.480 |
LIG_APCC_ABBA_1 | 135 | 140 | PF00400 | 0.455 |
LIG_APCC_ABBA_1 | 198 | 203 | PF00400 | 0.516 |
LIG_APCC_ABBA_1 | 390 | 395 | PF00400 | 0.516 |
LIG_APCC_Cbox_2 | 430 | 436 | PF00515 | 0.541 |
LIG_BRCT_BRCA1_1 | 352 | 356 | PF00533 | 0.496 |
LIG_BRCT_BRCA1_1 | 484 | 488 | PF00533 | 0.516 |
LIG_BRCT_BRCA1_1 | 705 | 709 | PF00533 | 0.480 |
LIG_Clathr_ClatBox_1 | 629 | 633 | PF01394 | 0.560 |
LIG_Clathr_ClatBox_1 | 65 | 69 | PF01394 | 0.496 |
LIG_CtBP_PxDLS_1 | 652 | 656 | PF00389 | 0.586 |
LIG_deltaCOP1_diTrp_1 | 481 | 488 | PF00928 | 0.561 |
LIG_EH1_1 | 502 | 510 | PF00400 | 0.541 |
LIG_eIF4E_1 | 60 | 66 | PF01652 | 0.480 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.449 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.541 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.470 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.466 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.440 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.460 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.530 |
LIG_FHA_2 | 252 | 258 | PF00498 | 0.469 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.509 |
LIG_FHA_2 | 433 | 439 | PF00498 | 0.462 |
LIG_FHA_2 | 635 | 641 | PF00498 | 0.560 |
LIG_GBD_Chelix_1 | 149 | 157 | PF00786 | 0.341 |
LIG_LIR_Apic_2 | 195 | 200 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 15 | 23 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 208 | 213 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 604 | 612 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 69 | 78 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 113 | 117 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 15 | 19 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 208 | 212 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 25 | 30 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 346 | 351 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 56 | 60 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 604 | 608 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 98 | 103 | PF02991 | 0.461 |
LIG_LYPXL_S_1 | 347 | 351 | PF13949 | 0.341 |
LIG_LYPXL_yS_3 | 348 | 351 | PF13949 | 0.541 |
LIG_PCNA_yPIPBox_3 | 71 | 82 | PF02747 | 0.455 |
LIG_PCNA_yPIPBox_3 | 731 | 742 | PF02747 | 0.501 |
LIG_PDZ_Class_2 | 738 | 743 | PF00595 | 0.391 |
LIG_Pex14_1 | 396 | 400 | PF04695 | 0.541 |
LIG_Pex14_2 | 212 | 216 | PF04695 | 0.547 |
LIG_Pex14_2 | 356 | 360 | PF04695 | 0.541 |
LIG_PTB_Apo_2 | 21 | 28 | PF02174 | 0.474 |
LIG_PTB_Apo_2 | 290 | 297 | PF02174 | 0.560 |
LIG_PTB_Apo_2 | 399 | 406 | PF02174 | 0.560 |
LIG_REV1ctd_RIR_1 | 293 | 303 | PF16727 | 0.541 |
LIG_SH2_CRK | 103 | 107 | PF00017 | 0.466 |
LIG_SH2_CRK | 40 | 44 | PF00017 | 0.455 |
LIG_SH2_CRK | 739 | 743 | PF00017 | 0.482 |
LIG_SH2_GRB2like | 400 | 403 | PF00017 | 0.541 |
LIG_SH2_NCK_1 | 40 | 44 | PF00017 | 0.455 |
LIG_SH2_SRC | 400 | 403 | PF00017 | 0.459 |
LIG_SH2_STAP1 | 209 | 213 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 425 | 428 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 542 | 545 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 611 | 614 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 728 | 731 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.511 |
LIG_SH3_3 | 258 | 264 | PF00018 | 0.541 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.541 |
LIG_SH3_3 | 531 | 537 | PF00018 | 0.553 |
LIG_SH3_3 | 588 | 594 | PF00018 | 0.560 |
LIG_SH3_4 | 127 | 134 | PF00018 | 0.480 |
LIG_SUMO_SIM_anti_2 | 300 | 307 | PF11976 | 0.541 |
LIG_SUMO_SIM_anti_2 | 331 | 336 | PF11976 | 0.546 |
LIG_SUMO_SIM_anti_2 | 580 | 585 | PF11976 | 0.380 |
LIG_SUMO_SIM_par_1 | 95 | 101 | PF11976 | 0.541 |
LIG_TRAF2_2 | 594 | 599 | PF00917 | 0.560 |
LIG_UBA3_1 | 305 | 312 | PF00899 | 0.541 |
LIG_WRC_WIRS_1 | 111 | 116 | PF05994 | 0.516 |
LIG_WRC_WIRS_1 | 30 | 35 | PF05994 | 0.565 |
LIG_WRC_WIRS_1 | 527 | 532 | PF05994 | 0.478 |
MOD_CDK_SPxxK_3 | 260 | 267 | PF00069 | 0.540 |
MOD_CDK_SPxxK_3 | 610 | 617 | PF00069 | 0.539 |
MOD_CDK_SPxxK_3 | 707 | 714 | PF00069 | 0.494 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.496 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.447 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.480 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.487 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.452 |
MOD_CK1_1 | 517 | 523 | PF00069 | 0.560 |
MOD_CK1_1 | 707 | 713 | PF00069 | 0.531 |
MOD_CK1_1 | 730 | 736 | PF00069 | 0.380 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.549 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.547 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.458 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.484 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.406 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.541 |
MOD_CK2_1 | 498 | 504 | PF00069 | 0.496 |
MOD_CK2_1 | 555 | 561 | PF00069 | 0.541 |
MOD_Cter_Amidation | 687 | 690 | PF01082 | 0.341 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.302 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.316 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.343 |
MOD_GlcNHglycan | 546 | 549 | PF01048 | 0.321 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.217 |
MOD_GlcNHglycan | 624 | 627 | PF01048 | 0.341 |
MOD_GlcNHglycan | 83 | 87 | PF01048 | 0.343 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.541 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.512 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.523 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.536 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.427 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.492 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.450 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.503 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.500 |
MOD_GSK3_1 | 656 | 663 | PF00069 | 0.585 |
MOD_GSK3_1 | 703 | 710 | PF00069 | 0.458 |
MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.329 |
MOD_N-GLC_1 | 586 | 591 | PF02516 | 0.303 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.459 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.487 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.532 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.546 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.483 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.532 |
MOD_NEK2_1 | 615 | 620 | PF00069 | 0.479 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.503 |
MOD_NEK2_2 | 484 | 489 | PF00069 | 0.482 |
MOD_PIKK_1 | 151 | 157 | PF00454 | 0.464 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.541 |
MOD_PIKK_1 | 567 | 573 | PF00454 | 0.541 |
MOD_PKA_1 | 298 | 304 | PF00069 | 0.541 |
MOD_PKA_1 | 567 | 573 | PF00069 | 0.541 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.517 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.466 |
MOD_PKA_2 | 517 | 523 | PF00069 | 0.541 |
MOD_PKA_2 | 622 | 628 | PF00069 | 0.516 |
MOD_PKA_2 | 656 | 662 | PF00069 | 0.592 |
MOD_PKA_2 | 664 | 670 | PF00069 | 0.520 |
MOD_PKA_2 | 688 | 694 | PF00069 | 0.541 |
MOD_PKA_2 | 730 | 736 | PF00069 | 0.476 |
MOD_PKB_1 | 617 | 625 | PF00069 | 0.560 |
MOD_PKB_1 | 80 | 88 | PF00069 | 0.560 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.491 |
MOD_Plk_1 | 256 | 262 | PF00069 | 0.500 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.534 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.506 |
MOD_Plk_1 | 634 | 640 | PF00069 | 0.555 |
MOD_Plk_2-3 | 328 | 334 | PF00069 | 0.530 |
MOD_Plk_2-3 | 634 | 640 | PF00069 | 0.541 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.483 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.516 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.485 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.506 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.466 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.486 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.465 |
MOD_Plk_4 | 577 | 583 | PF00069 | 0.552 |
MOD_Plk_4 | 656 | 662 | PF00069 | 0.570 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.529 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.514 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.516 |
MOD_ProDKin_1 | 498 | 504 | PF00069 | 0.380 |
MOD_ProDKin_1 | 586 | 592 | PF00069 | 0.505 |
MOD_ProDKin_1 | 610 | 616 | PF00069 | 0.539 |
MOD_ProDKin_1 | 707 | 713 | PF00069 | 0.456 |
MOD_SUMO_for_1 | 325 | 328 | PF00179 | 0.541 |
MOD_SUMO_rev_2 | 164 | 174 | PF00179 | 0.505 |
MOD_SUMO_rev_2 | 667 | 677 | PF00179 | 0.466 |
MOD_SUMO_rev_2 | 706 | 716 | PF00179 | 0.456 |
TRG_DiLeu_BaEn_1 | 504 | 509 | PF01217 | 0.560 |
TRG_DiLeu_BaEn_1 | 693 | 698 | PF01217 | 0.433 |
TRG_DiLeu_BaEn_2 | 427 | 433 | PF01217 | 0.541 |
TRG_DiLeu_BaLyEn_6 | 611 | 616 | PF01217 | 0.480 |
TRG_ENDOCYTIC_2 | 103 | 106 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 739 | 742 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.475 |
TRG_ER_diArg_1 | 241 | 243 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 281 | 284 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 35 | 37 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 463 | 466 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 616 | 619 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 645 | 648 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 724 | 726 | PF00400 | 0.516 |
TRG_NLS_MonoExtC_3 | 9 | 15 | PF00514 | 0.560 |
TRG_Pf-PMV_PEXEL_1 | 211 | 215 | PF00026 | 0.322 |
TRG_Pf-PMV_PEXEL_1 | 457 | 461 | PF00026 | 0.296 |
TRG_Pf-PMV_PEXEL_1 | 82 | 87 | PF00026 | 0.316 |
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 | 92% | 100% |
A0A3R7K785 | Trypanosoma rangeli | 45% | 100% |
A0A3R7K7T8 | Trypanosoma rangeli | 21% | 92% |
A2A432 | Mus musculus | 24% | 77% |
A4I137 | Leishmania infantum | 91% | 100% |
A4IHP4 | Xenopus tropicalis | 25% | 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) | 91% | 100% |
O13790 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 97% |
O14122 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 21% | 100% |
O60999 | Dictyostelium discoideum | 24% | 96% |
P0CH31 | Arabidopsis thaliana | 25% | 100% |
Q09760 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 95% |
Q12018 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 21% | 91% |
Q13616 | Homo sapiens | 24% | 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 | 25% | 96% |
Q21346 | Caenorhabditis elegans | 25% | 100% |
Q23639 | Caenorhabditis elegans | 21% | 97% |
Q24311 | Drosophila melanogaster | 23% | 96% |
Q29425 | Oryctolagus cuniculus | 21% | 95% |
Q3TCH7 | Mus musculus | 23% | 98% |
Q4QAA1 | Leishmania major | 92% | 100% |
Q54CS2 | Dictyostelium discoideum | 23% | 93% |
Q54NZ5 | Dictyostelium discoideum | 22% | 97% |
Q54XF7 | Dictyostelium discoideum | 21% | 99% |
Q5R4G6 | Pongo abelii | 24% | 96% |
Q5RB36 | Pongo abelii | 21% | 95% |
Q5RCF3 | Pongo abelii | 22% | 100% |
Q5ZC88 | Oryza sativa subsp. japonica | 26% | 100% |
Q6DE95 | Xenopus laevis | 25% | 97% |
Q6GPF3 | Xenopus laevis | 25% | 97% |
Q8LGH4 | Arabidopsis thaliana | 24% | 94% |
Q93034 | Homo sapiens | 22% | 95% |
Q94AH6 | Arabidopsis thaliana | 27% | 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 | 27% | 100% |
Q9WTX6 | Mus musculus | 24% | 96% |
Q9XZJ3 | Dictyostelium discoideum | 22% | 96% |
Q9ZVH4 | Arabidopsis thaliana | 24% | 100% |
V5APS6 | Trypanosoma cruzi | 45% | 100% |