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: 13 |
NetGPI | no | yes: 0, no: 13 |
Related structures:
AlphaFold database: Q4Q2X4
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006396 | RNA processing | 6 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0008380 | RNA splicing | 7 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016070 | RNA metabolic process | 5 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 14 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0003724 | RNA helicase activity | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 14 |
GO:0004386 | helicase activity | 2 | 14 |
GO:0005488 | binding | 1 | 14 |
GO:0005524 | ATP binding | 5 | 14 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 7 |
GO:0016787 | hydrolase activity | 2 | 14 |
GO:0017076 | purine nucleotide binding | 4 | 14 |
GO:0030554 | adenyl nucleotide binding | 5 | 14 |
GO:0032553 | ribonucleotide binding | 3 | 14 |
GO:0032555 | purine ribonucleotide binding | 4 | 14 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 14 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 14 |
GO:0036094 | small molecule binding | 2 | 14 |
GO:0043167 | ion binding | 2 | 14 |
GO:0043168 | anion binding | 3 | 14 |
GO:0097159 | organic cyclic compound binding | 2 | 14 |
GO:0097367 | carbohydrate derivative binding | 2 | 14 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 7 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 14 |
GO:0140657 | ATP-dependent activity | 1 | 14 |
GO:1901265 | nucleoside phosphate binding | 3 | 14 |
GO:1901363 | heterocyclic compound binding | 2 | 14 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 140 | 144 | PF00656 | 0.210 |
CLV_C14_Caspase3-7 | 599 | 603 | PF00656 | 0.466 |
CLV_C14_Caspase3-7 | 709 | 713 | PF00656 | 0.470 |
CLV_C14_Caspase3-7 | 775 | 779 | PF00656 | 0.409 |
CLV_NRD_NRD_1 | 155 | 157 | PF00675 | 0.293 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.251 |
CLV_NRD_NRD_1 | 541 | 543 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 647 | 649 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 673 | 675 | PF00675 | 0.251 |
CLV_NRD_NRD_1 | 786 | 788 | PF00675 | 0.501 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 238 | 240 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 541 | 543 | PF00082 | 0.315 |
CLV_PCSK_KEX2_1 | 623 | 625 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 647 | 649 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 786 | 788 | PF00082 | 0.484 |
CLV_PCSK_PC1ET2_1 | 106 | 108 | PF00082 | 0.479 |
CLV_PCSK_PC1ET2_1 | 238 | 240 | PF00082 | 0.389 |
CLV_PCSK_PC1ET2_1 | 41 | 43 | PF00082 | 0.692 |
CLV_PCSK_PC1ET2_1 | 623 | 625 | PF00082 | 0.533 |
CLV_PCSK_PC1ET2_1 | 66 | 68 | PF00082 | 0.725 |
CLV_PCSK_PC7_1 | 239 | 245 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.745 |
CLV_PCSK_SKI1_1 | 465 | 469 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 554 | 558 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 675 | 679 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 711 | 715 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.561 |
CLV_Separin_Metazoa | 482 | 486 | PF03568 | 0.368 |
DEG_APCC_DBOX_1 | 242 | 250 | PF00400 | 0.388 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.578 |
DEG_SPOP_SBC_1 | 72 | 76 | PF00917 | 0.627 |
DOC_CKS1_1 | 358 | 363 | PF01111 | 0.589 |
DOC_CKS1_1 | 687 | 692 | PF01111 | 0.552 |
DOC_CYCLIN_RxL_1 | 235 | 242 | PF00134 | 0.426 |
DOC_CYCLIN_RxL_1 | 89 | 97 | PF00134 | 0.473 |
DOC_CYCLIN_yCln2_LP_2 | 10 | 16 | PF00134 | 0.485 |
DOC_MAPK_DCC_7 | 541 | 550 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 155 | 162 | PF00069 | 0.333 |
DOC_MAPK_gen_1 | 243 | 251 | PF00069 | 0.337 |
DOC_MAPK_gen_1 | 541 | 548 | PF00069 | 0.518 |
DOC_MAPK_gen_1 | 647 | 655 | PF00069 | 0.427 |
DOC_MAPK_HePTP_8 | 162 | 174 | PF00069 | 0.305 |
DOC_MAPK_MEF2A_6 | 115 | 123 | PF00069 | 0.333 |
DOC_MAPK_MEF2A_6 | 165 | 174 | PF00069 | 0.318 |
DOC_MAPK_MEF2A_6 | 367 | 376 | PF00069 | 0.353 |
DOC_MAPK_MEF2A_6 | 541 | 550 | PF00069 | 0.382 |
DOC_MAPK_MEF2A_6 | 648 | 657 | PF00069 | 0.489 |
DOC_PP2B_LxvP_1 | 283 | 286 | PF13499 | 0.542 |
DOC_PP2B_LxvP_1 | 557 | 560 | PF13499 | 0.534 |
DOC_PP2B_LxvP_1 | 653 | 656 | PF13499 | 0.502 |
DOC_PP4_FxxP_1 | 508 | 511 | PF00568 | 0.376 |
DOC_PP4_FxxP_1 | 581 | 584 | PF00568 | 0.467 |
DOC_PP4_FxxP_1 | 687 | 690 | PF00568 | 0.494 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 406 | 410 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 656 | 660 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.656 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 686 | 691 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.529 |
LIG_14-3-3_CanoR_1 | 465 | 475 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 632 | 637 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 647 | 657 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 705 | 711 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 720 | 724 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 753 | 762 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 84 | 94 | PF00244 | 0.432 |
LIG_Actin_WH2_2 | 190 | 206 | PF00022 | 0.293 |
LIG_Actin_WH2_2 | 25 | 43 | PF00022 | 0.401 |
LIG_BRCT_BRCA1_1 | 468 | 472 | PF00533 | 0.435 |
LIG_BRCT_BRCA1_1 | 517 | 521 | PF00533 | 0.460 |
LIG_BRCT_BRCA1_1 | 747 | 751 | PF00533 | 0.554 |
LIG_deltaCOP1_diTrp_1 | 759 | 769 | PF00928 | 0.470 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.344 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.197 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.283 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.318 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.292 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.509 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.682 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.428 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.450 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.398 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.346 |
LIG_FHA_1 | 668 | 674 | PF00498 | 0.390 |
LIG_FHA_1 | 701 | 707 | PF00498 | 0.531 |
LIG_FHA_1 | 733 | 739 | PF00498 | 0.500 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.440 |
LIG_FHA_2 | 358 | 364 | PF00498 | 0.698 |
LIG_FHA_2 | 466 | 472 | PF00498 | 0.396 |
LIG_FHA_2 | 477 | 483 | PF00498 | 0.327 |
LIG_FHA_2 | 707 | 713 | PF00498 | 0.450 |
LIG_GBD_Chelix_1 | 232 | 240 | PF00786 | 0.426 |
LIG_LIR_Apic_2 | 436 | 440 | PF02991 | 0.470 |
LIG_LIR_Apic_2 | 505 | 511 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 3 | 11 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 469 | 476 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 519 | 530 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 679 | 690 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 735 | 744 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 767 | 777 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 143 | 148 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 3 | 7 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 469 | 475 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 505 | 509 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 518 | 524 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 679 | 685 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 704 | 710 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 735 | 739 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 767 | 773 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 88 | 94 | PF02991 | 0.409 |
LIG_NRBOX | 236 | 242 | PF00104 | 0.426 |
LIG_PCNA_TLS_4 | 675 | 682 | PF02747 | 0.483 |
LIG_PDZ_Class_3 | 800 | 805 | PF00595 | 0.700 |
LIG_Pex14_2 | 612 | 616 | PF04695 | 0.348 |
LIG_RPA_C_Fungi | 715 | 727 | PF08784 | 0.399 |
LIG_SH2_CRK | 215 | 219 | PF00017 | 0.372 |
LIG_SH2_CRK | 377 | 381 | PF00017 | 0.293 |
LIG_SH2_CRK | 522 | 526 | PF00017 | 0.387 |
LIG_SH2_CRK | 643 | 647 | PF00017 | 0.381 |
LIG_SH2_CRK | 707 | 711 | PF00017 | 0.426 |
LIG_SH2_CRK | 91 | 95 | PF00017 | 0.409 |
LIG_SH2_GRB2like | 627 | 630 | PF00017 | 0.476 |
LIG_SH2_SRC | 292 | 295 | PF00017 | 0.371 |
LIG_SH2_STAP1 | 215 | 219 | PF00017 | 0.372 |
LIG_SH2_STAP1 | 627 | 631 | PF00017 | 0.493 |
LIG_SH2_STAT3 | 423 | 426 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.113 |
LIG_SH2_STAT5 | 526 | 529 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 615 | 618 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 630 | 633 | PF00017 | 0.267 |
LIG_SH2_STAT5 | 661 | 664 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 667 | 670 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 770 | 773 | PF00017 | 0.492 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.419 |
LIG_SH3_3 | 263 | 269 | PF00018 | 0.400 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.383 |
LIG_SH3_3 | 497 | 503 | PF00018 | 0.372 |
LIG_SH3_3 | 687 | 693 | PF00018 | 0.438 |
LIG_SH3_5 | 288 | 292 | PF00018 | 0.411 |
LIG_Sin3_3 | 247 | 254 | PF02671 | 0.421 |
LIG_SUMO_SIM_anti_2 | 216 | 222 | PF11976 | 0.309 |
LIG_SUMO_SIM_anti_2 | 279 | 284 | PF11976 | 0.430 |
LIG_SUMO_SIM_anti_2 | 369 | 375 | PF11976 | 0.444 |
LIG_SUMO_SIM_anti_2 | 491 | 497 | PF11976 | 0.366 |
LIG_SUMO_SIM_par_1 | 119 | 126 | PF11976 | 0.316 |
LIG_SUMO_SIM_par_1 | 216 | 222 | PF11976 | 0.293 |
LIG_SUMO_SIM_par_1 | 491 | 497 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 762 | 768 | PF11976 | 0.356 |
LIG_TRAF2_1 | 381 | 384 | PF00917 | 0.381 |
LIG_UBA3_1 | 20 | 28 | PF00899 | 0.487 |
LIG_UBA3_1 | 37 | 41 | PF00899 | 0.591 |
LIG_UBA3_1 | 555 | 561 | PF00899 | 0.426 |
MOD_CDK_SPxxK_3 | 77 | 84 | PF00069 | 0.449 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.283 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.396 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.289 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.535 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.332 |
MOD_CK2_1 | 476 | 482 | PF00069 | 0.370 |
MOD_CK2_1 | 753 | 759 | PF00069 | 0.351 |
MOD_Cter_Amidation | 539 | 542 | PF01082 | 0.396 |
MOD_Cter_Amidation | 621 | 624 | PF01082 | 0.532 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.283 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.348 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.523 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.637 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.290 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.441 |
MOD_GlcNHglycan | 714 | 717 | PF01048 | 0.363 |
MOD_GlcNHglycan | 747 | 750 | PF01048 | 0.397 |
MOD_GlcNHglycan | 755 | 758 | PF01048 | 0.345 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.591 |
MOD_GlcNHglycan | 792 | 796 | PF01048 | 0.541 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.514 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.358 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.209 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.668 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.713 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.322 |
MOD_GSK3_1 | 579 | 586 | PF00069 | 0.366 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.587 |
MOD_GSK3_1 | 747 | 754 | PF00069 | 0.369 |
MOD_GSK3_1 | 764 | 771 | PF00069 | 0.300 |
MOD_LATS_1 | 181 | 187 | PF00433 | 0.372 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.586 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.648 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.331 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.414 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.710 |
MOD_NEK2_1 | 714 | 719 | PF00069 | 0.395 |
MOD_NEK2_1 | 751 | 756 | PF00069 | 0.393 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.478 |
MOD_PIKK_1 | 129 | 135 | PF00454 | 0.293 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.113 |
MOD_PIKK_1 | 345 | 351 | PF00454 | 0.490 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.719 |
MOD_PIKK_1 | 648 | 654 | PF00454 | 0.428 |
MOD_PIKK_1 | 680 | 686 | PF00454 | 0.307 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.513 |
MOD_PKA_2 | 719 | 725 | PF00069 | 0.360 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.370 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.296 |
MOD_Plk_1 | 293 | 299 | PF00069 | 0.433 |
MOD_Plk_1 | 406 | 412 | PF00069 | 0.292 |
MOD_Plk_2-3 | 205 | 211 | PF00069 | 0.359 |
MOD_Plk_2-3 | 471 | 477 | PF00069 | 0.434 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.336 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.351 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.497 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.655 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.305 |
MOD_Plk_4 | 488 | 494 | PF00069 | 0.376 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.643 |
MOD_Plk_4 | 657 | 663 | PF00069 | 0.521 |
MOD_Plk_4 | 719 | 725 | PF00069 | 0.315 |
MOD_Plk_4 | 732 | 738 | PF00069 | 0.253 |
MOD_Plk_4 | 747 | 753 | PF00069 | 0.256 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.709 |
MOD_ProDKin_1 | 686 | 692 | PF00069 | 0.396 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.524 |
TRG_DiLeu_BaEn_1 | 105 | 110 | PF01217 | 0.485 |
TRG_DiLeu_BaEn_1 | 759 | 764 | PF01217 | 0.372 |
TRG_DiLeu_BaLyEn_6 | 236 | 241 | PF01217 | 0.314 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 377 | 380 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 522 | 525 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 643 | 646 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 707 | 710 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 770 | 773 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.402 |
TRG_ER_diArg_1 | 154 | 156 | PF00400 | 0.293 |
TRG_ER_diArg_1 | 243 | 245 | PF00400 | 0.333 |
TRG_ER_diArg_1 | 457 | 460 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 541 | 543 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 646 | 648 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 785 | 787 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 98 | 101 | PF00400 | 0.502 |
TRG_NES_CRM1_1 | 535 | 549 | PF08389 | 0.366 |
TRG_Pf-PMV_PEXEL_1 | 107 | 111 | PF00026 | 0.480 |
TRG_Pf-PMV_PEXEL_1 | 647 | 652 | PF00026 | 0.490 |
TRG_Pf-PMV_PEXEL_1 | 92 | 96 | PF00026 | 0.491 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5V0 | Leptomonas seymouri | 41% | 100% |
A0A0N0P8Y1 | Leptomonas seymouri | 74% | 100% |
A0A0N0P9D2 | Leptomonas seymouri | 38% | 100% |
A0A0N1I0Z0 | Leptomonas seymouri | 35% | 74% |
A0A0N1IKA7 | Leptomonas seymouri | 34% | 89% |
A0A0N1IMH3 | Leptomonas seymouri | 26% | 67% |
A0A0N1PEU4 | Leptomonas seymouri | 35% | 85% |
A0A0S4IQ76 | Bodo saltans | 48% | 100% |
A0A0S4IR78 | Bodo saltans | 36% | 91% |
A0A0S4IS51 | Bodo saltans | 36% | 100% |
A0A0S4ITR4 | Bodo saltans | 34% | 75% |
A0A0S4IWU8 | Bodo saltans | 36% | 94% |
A0A0S4J157 | Bodo saltans | 42% | 100% |
A0A0S4JCY8 | Bodo saltans | 36% | 79% |
A0A1X0NJ46 | Trypanosomatidae | 44% | 100% |
A0A1X0NKY7 | Trypanosomatidae | 34% | 75% |
A0A1X0NVG5 | Trypanosomatidae | 35% | 75% |
A0A1X0P0D7 | Trypanosomatidae | 34% | 100% |
A0A1X0P872 | Trypanosomatidae | 38% | 91% |
A0A1X0P9K6 | Trypanosomatidae | 56% | 100% |
A0A3Q8IEC9 | Leishmania donovani | 32% | 74% |
A0A3Q8II71 | Leishmania donovani | 96% | 100% |
A0A3Q8IJ24 | Leishmania donovani | 36% | 85% |
A0A3Q8IWG4 | Leishmania donovani | 32% | 100% |
A0A3R7MA90 | Trypanosoma rangeli | 43% | 100% |
A0A3R7MM88 | Trypanosoma rangeli | 32% | 100% |
A0A3R7NT42 | Trypanosoma rangeli | 57% | 100% |
A0A3S7WYA1 | Leishmania donovani | 35% | 74% |
A0A3S7X8Z5 | Leishmania donovani | 42% | 100% |
A0A3S7XB01 | Leishmania donovani | 34% | 74% |
A0A422MXB1 | Trypanosoma rangeli | 35% | 76% |
A0A422N8L3 | Trypanosoma rangeli | 35% | 79% |
A0A422NK53 | Trypanosoma rangeli | 37% | 100% |
A4HAT8 | Leishmania braziliensis | 87% | 100% |
A4HDG6 | Leishmania braziliensis | 35% | 74% |
A4HME2 | Leishmania braziliensis | 42% | 100% |
A4HNU7 | Leishmania braziliensis | 36% | 85% |
A4HPE9 | Leishmania braziliensis | 34% | 75% |
A4HQ83 | Leishmania braziliensis | 36% | 100% |
A4I009 | Leishmania infantum | 32% | 74% |
A4I0U7 | Leishmania infantum | 35% | 74% |
A4IA06 | Leishmania infantum | 95% | 100% |
A4IB14 | Leishmania infantum | 42% | 100% |
A4ICJ0 | Leishmania infantum | 34% | 74% |
A4ICP7 | Leishmania infantum | 36% | 85% |
A4IDY1 | Leishmania infantum | 32% | 100% |
C9ZMN0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
C9ZNP6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
D0A2R5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 91% |
D0A3F8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 76% |
D0A429 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A778 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 77% |
D4A2Z8 | Rattus norvegicus | 29% | 80% |
E9AEU3 | Leishmania major | 41% | 96% |
E9AIQ7 | Leishmania braziliensis | 31% | 74% |
E9ASK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 94% |
E9AT60 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 74% |
E9AU01 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9AVY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 74% |
E9B512 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9B5Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
F4HYJ7 | Arabidopsis thaliana | 33% | 67% |
F4IE66 | Arabidopsis thaliana | 34% | 100% |
F4IJV4 | Arabidopsis thaliana | 37% | 77% |
F4ILR7 | Arabidopsis thaliana | 34% | 81% |
F4IM84 | Arabidopsis thaliana | 32% | 72% |
F4JMJ3 | Arabidopsis thaliana | 37% | 91% |
F4JRJ6 | Arabidopsis thaliana | 38% | 100% |
O22899 | Arabidopsis thaliana | 43% | 100% |
O35286 | Mus musculus | 40% | 100% |
O42643 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 37% | 69% |
O42945 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 42% | 100% |
O43143 | Homo sapiens | 40% | 100% |
O45244 | Caenorhabditis elegans | 39% | 80% |
O51767 | Borreliella burgdorferi (strain ATCC 35210 / DSM 4680 / CIP 102532 / B31) | 31% | 98% |
O60231 | Homo sapiens | 39% | 77% |
P15938 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 75% |
P20095 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 92% |
P24384 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 37% | 70% |
P34305 | Caenorhabditis elegans | 30% | 70% |
P34498 | Caenorhabditis elegans | 35% | 71% |
P36009 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 100% |
P53131 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 41% | 100% |
Q03319 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 100% |
Q05B79 | Bos taurus | 30% | 80% |
Q09530 | Caenorhabditis elegans | 37% | 67% |
Q10752 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 37% | 76% |
Q14147 | Homo sapiens | 36% | 70% |
Q20875 | Caenorhabditis elegans | 41% | 100% |
Q38953 | Arabidopsis thaliana | 39% | 69% |
Q3ZBE0 | Bos taurus | 29% | 100% |
Q4Q0J4 | Leishmania major | 33% | 100% |
Q4Q1D7 | Leishmania major | 34% | 74% |
Q4Q1Y9 | Leishmania major | 36% | 85% |
Q4QAM3 | Leishmania major | 35% | 71% |
Q4QBJ7 | Leishmania major | 32% | 74% |
Q54F05 | Dictyostelium discoideum | 38% | 69% |
Q54MH3 | Dictyostelium discoideum | 39% | 73% |
Q54NJ4 | Dictyostelium discoideum | 41% | 100% |
Q5BJS0 | Rattus norvegicus | 29% | 67% |
Q5R607 | Pongo abelii | 29% | 67% |
Q5R864 | Pongo abelii | 35% | 100% |
Q5RAZ4 | Pongo abelii | 40% | 100% |
Q5RBD4 | Pongo abelii | 37% | 100% |
Q5UQ96 | Acanthamoeba polyphaga mimivirus | 25% | 100% |
Q5XH12 | Xenopus laevis | 27% | 100% |
Q5XI69 | Rattus norvegicus | 34% | 100% |
Q6PE54 | Mus musculus | 34% | 100% |
Q767K6 | Sus scrofa | 39% | 77% |
Q7K3M5 | Drosophila melanogaster | 41% | 100% |
Q7L2E3 | Homo sapiens | 29% | 67% |
Q7L7V1 | Homo sapiens | 29% | 100% |
Q7YR39 | Pan troglodytes | 39% | 77% |
Q80VY9 | Mus musculus | 36% | 100% |
Q8BZS9 | Mus musculus | 28% | 100% |
Q8IX18 | Homo sapiens | 35% | 100% |
Q8TE96 | Homo sapiens | 30% | 100% |
Q8VHK9 | Mus musculus | 30% | 80% |
Q8VY00 | Arabidopsis thaliana | 38% | 77% |
Q924H9 | Mus musculus | 30% | 100% |
Q93Y16 | Arabidopsis thaliana | 36% | 100% |
Q99PU8 | Mus musculus | 29% | 66% |
Q9BKQ8 | Caenorhabditis elegans | 36% | 100% |
Q9DBV3 | Mus musculus | 35% | 70% |
Q9H2U1 | Homo sapiens | 29% | 80% |
Q9H5Z1 | Homo sapiens | 37% | 100% |
Q9H6R0 | Homo sapiens | 36% | 100% |
Q9HDY4 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 68% |
Q9HE06 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 100% |
Q9LZQ9 | Arabidopsis thaliana | 43% | 100% |
Q9P774 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 36% | 69% |
V5B3L7 | Trypanosoma cruzi | 36% | 100% |
V5B7H6 | Trypanosoma cruzi | 32% | 74% |
V5BKH2 | Trypanosoma cruzi | 56% | 100% |
V5BPV3 | Trypanosoma cruzi | 34% | 76% |
V5BV22 | Trypanosoma cruzi | 34% | 91% |
V5C0I9 | Trypanosoma cruzi | 35% | 100% |
V5D886 | Trypanosoma cruzi | 43% | 100% |