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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9AEU3
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006396 | RNA processing | 6 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0008380 | RNA splicing | 7 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0003724 | RNA helicase activity | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 11 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.255 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.236 |
CLV_NRD_NRD_1 | 557 | 559 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 590 | 592 | PF00675 | 0.214 |
CLV_NRD_NRD_1 | 630 | 632 | PF00675 | 0.248 |
CLV_NRD_NRD_1 | 685 | 687 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 693 | 695 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.239 |
CLV_PCSK_FUR_1 | 691 | 695 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.248 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 557 | 559 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 590 | 592 | PF00082 | 0.214 |
CLV_PCSK_KEX2_1 | 630 | 632 | PF00082 | 0.248 |
CLV_PCSK_KEX2_1 | 685 | 687 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 693 | 695 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 696 | 698 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.234 |
CLV_PCSK_PC1ET2_1 | 170 | 172 | PF00082 | 0.309 |
CLV_PCSK_PC1ET2_1 | 186 | 188 | PF00082 | 0.489 |
CLV_PCSK_PC1ET2_1 | 696 | 698 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 540 | 544 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 600 | 604 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 619 | 623 | PF00082 | 0.179 |
CLV_PCSK_SKI1_1 | 649 | 653 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 677 | 681 | PF00082 | 0.390 |
CLV_Separin_Metazoa | 387 | 391 | PF03568 | 0.363 |
DEG_APCC_DBOX_1 | 170 | 178 | PF00400 | 0.448 |
DEG_APCC_DBOX_1 | 389 | 397 | PF00400 | 0.355 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.682 |
DOC_CKS1_1 | 343 | 348 | PF01111 | 0.448 |
DOC_CKS1_1 | 486 | 491 | PF01111 | 0.509 |
DOC_CYCLIN_RxL_1 | 554 | 565 | PF00134 | 0.444 |
DOC_MAPK_gen_1 | 170 | 178 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 25 | 32 | PF00069 | 0.403 |
DOC_MAPK_gen_1 | 336 | 344 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 540 | 548 | PF00069 | 0.374 |
DOC_MAPK_gen_1 | 557 | 563 | PF00069 | 0.395 |
DOC_MAPK_gen_1 | 630 | 637 | PF00069 | 0.448 |
DOC_MAPK_HePTP_8 | 89 | 101 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 170 | 178 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 331 | 339 | PF00069 | 0.443 |
DOC_MAPK_MEF2A_6 | 92 | 101 | PF00069 | 0.439 |
DOC_MAPK_RevD_3 | 172 | 187 | PF00069 | 0.448 |
DOC_PP1_RVXF_1 | 617 | 624 | PF00149 | 0.448 |
DOC_PP1_RVXF_1 | 631 | 638 | PF00149 | 0.448 |
DOC_PP1_SILK_1 | 553 | 558 | PF00149 | 0.478 |
DOC_PP2B_LxvP_1 | 559 | 562 | PF13499 | 0.522 |
DOC_PP2B_LxvP_1 | 603 | 606 | PF13499 | 0.448 |
DOC_PP4_FxxP_1 | 413 | 416 | PF00568 | 0.387 |
DOC_PP4_FxxP_1 | 462 | 465 | PF00568 | 0.553 |
DOC_PP4_FxxP_1 | 486 | 489 | PF00568 | 0.459 |
DOC_PP4_FxxP_1 | 504 | 507 | PF00568 | 0.459 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 562 | 566 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.459 |
DOC_USP7_UBL2_3 | 114 | 118 | PF12436 | 0.521 |
DOC_USP7_UBL2_3 | 615 | 619 | PF12436 | 0.448 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 485 | 490 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 660 | 665 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 697 | 702 | PF00397 | 0.709 |
LIG_14-3-3_CanoR_1 | 141 | 145 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 153 | 161 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 19 | 24 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 225 | 233 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 369 | 376 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 649 | 658 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 83 | 93 | PF00244 | 0.462 |
LIG_Actin_WH2_2 | 117 | 133 | PF00022 | 0.448 |
LIG_Actin_WH2_2 | 160 | 177 | PF00022 | 0.448 |
LIG_APCC_ABBA_1 | 518 | 523 | PF00400 | 0.436 |
LIG_APCC_ABBA_1 | 634 | 639 | PF00400 | 0.448 |
LIG_APCC_ABBAyCdc20_2 | 633 | 639 | PF00400 | 0.459 |
LIG_BIR_III_2 | 577 | 581 | PF00653 | 0.425 |
LIG_BRCT_BRCA1_1 | 107 | 111 | PF00533 | 0.489 |
LIG_BRCT_BRCA1_1 | 17 | 21 | PF00533 | 0.529 |
LIG_BRCT_BRCA1_1 | 458 | 462 | PF00533 | 0.534 |
LIG_BRCT_BRCA1_1 | 463 | 467 | PF00533 | 0.534 |
LIG_Clathr_ClatBox_1 | 408 | 412 | PF01394 | 0.401 |
LIG_EH_1 | 483 | 487 | PF12763 | 0.509 |
LIG_eIF4E_1 | 46 | 52 | PF01652 | 0.448 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.496 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.448 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.442 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.440 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.298 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.442 |
LIG_FHA_1 | 674 | 680 | PF00498 | 0.514 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.542 |
LIG_FHA_2 | 161 | 167 | PF00498 | 0.513 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.447 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.452 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.442 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.553 |
LIG_FHA_2 | 382 | 388 | PF00498 | 0.382 |
LIG_FHA_2 | 611 | 617 | PF00498 | 0.447 |
LIG_FHA_2 | 698 | 704 | PF00498 | 0.645 |
LIG_Integrin_RGD_1 | 575 | 577 | PF01839 | 0.452 |
LIG_LIR_Apic_2 | 412 | 416 | PF02991 | 0.392 |
LIG_LIR_Apic_2 | 459 | 465 | PF02991 | 0.553 |
LIG_LIR_Apic_2 | 502 | 507 | PF02991 | 0.506 |
LIG_LIR_Apic_2 | 533 | 539 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 140 | 150 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 18 | 28 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 44 | 52 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 517 | 524 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 384 | 388 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 517 | 521 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 670 | 675 | PF02991 | 0.424 |
LIG_LYPXL_yS_3 | 385 | 388 | PF13949 | 0.384 |
LIG_MLH1_MIPbox_1 | 17 | 21 | PF16413 | 0.529 |
LIG_Pex14_2 | 188 | 192 | PF04695 | 0.381 |
LIG_Pex14_2 | 680 | 684 | PF04695 | 0.538 |
LIG_PTB_Apo_2 | 407 | 414 | PF02174 | 0.410 |
LIG_SH2_CRK | 142 | 146 | PF00017 | 0.448 |
LIG_SH2_CRK | 281 | 285 | PF00017 | 0.448 |
LIG_SH2_CRK | 46 | 50 | PF00017 | 0.448 |
LIG_SH2_CRK | 549 | 553 | PF00017 | 0.357 |
LIG_SH2_GRB2like | 514 | 517 | PF00017 | 0.464 |
LIG_SH2_GRB2like | 536 | 539 | PF00017 | 0.361 |
LIG_SH2_GRB2like | 627 | 630 | PF00017 | 0.534 |
LIG_SH2_PTP2 | 536 | 539 | PF00017 | 0.486 |
LIG_SH2_SRC | 219 | 222 | PF00017 | 0.365 |
LIG_SH2_SRC | 536 | 539 | PF00017 | 0.366 |
LIG_SH2_STAP1 | 107 | 111 | PF00017 | 0.456 |
LIG_SH2_STAP1 | 142 | 146 | PF00017 | 0.448 |
LIG_SH2_STAP1 | 16 | 20 | PF00017 | 0.498 |
LIG_SH2_STAT3 | 567 | 570 | PF00017 | 0.626 |
LIG_SH2_STAT3 | 666 | 669 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 514 | 517 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 536 | 539 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 567 | 570 | PF00017 | 0.626 |
LIG_SH2_STAT5 | 597 | 600 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 627 | 630 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 647 | 650 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 666 | 669 | PF00017 | 0.379 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.459 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.448 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.383 |
LIG_SH3_3 | 449 | 455 | PF00018 | 0.448 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.443 |
LIG_SUMO_SIM_anti_2 | 143 | 149 | PF11976 | 0.448 |
LIG_SUMO_SIM_anti_2 | 48 | 55 | PF11976 | 0.448 |
LIG_SUMO_SIM_par_1 | 143 | 149 | PF11976 | 0.448 |
LIG_SUMO_SIM_par_1 | 48 | 55 | PF11976 | 0.448 |
LIG_TRAF2_1 | 182 | 185 | PF00917 | 0.448 |
LIG_UBA3_1 | 160 | 165 | PF00899 | 0.534 |
LIG_WRC_WIRS_1 | 515 | 520 | PF05994 | 0.420 |
MOD_CDK_SPK_2 | 461 | 466 | PF00069 | 0.553 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.448 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.534 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.446 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.456 |
MOD_CK1_1 | 530 | 536 | PF00069 | 0.434 |
MOD_CK1_1 | 565 | 571 | PF00069 | 0.452 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.447 |
MOD_CK1_1 | 604 | 610 | PF00069 | 0.459 |
MOD_CK1_1 | 662 | 668 | PF00069 | 0.543 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.534 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.448 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.495 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.553 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.392 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.386 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.448 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.543 |
MOD_DYRK1A_RPxSP_1 | 697 | 701 | PF00069 | 0.589 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.242 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.478 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.248 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.223 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.248 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.509 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.248 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.431 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.447 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.448 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.353 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.440 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.497 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.392 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.451 |
MOD_LATS_1 | 151 | 157 | PF00433 | 0.534 |
MOD_N-GLC_1 | 439 | 444 | PF02516 | 0.334 |
MOD_N-GLC_1 | 525 | 530 | PF02516 | 0.469 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.509 |
MOD_NEK2_1 | 640 | 645 | PF00069 | 0.448 |
MOD_NEK2_1 | 659 | 664 | PF00069 | 0.531 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.378 |
MOD_PIKK_1 | 284 | 290 | PF00454 | 0.534 |
MOD_PIKK_1 | 345 | 351 | PF00454 | 0.439 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.425 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.352 |
MOD_PIKK_1 | 76 | 82 | PF00454 | 0.448 |
MOD_PKA_1 | 685 | 691 | PF00069 | 0.359 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.396 |
MOD_PKA_2 | 685 | 691 | PF00069 | 0.511 |
MOD_PKA_2 | 692 | 698 | PF00069 | 0.662 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.505 |
MOD_Plk_1 | 151 | 157 | PF00069 | 0.448 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.489 |
MOD_Plk_1 | 310 | 316 | PF00069 | 0.448 |
MOD_Plk_2-3 | 444 | 450 | PF00069 | 0.386 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.448 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.561 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.439 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.413 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.399 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.440 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.529 |
MOD_Plk_4 | 623 | 629 | PF00069 | 0.448 |
MOD_Plk_4 | 643 | 649 | PF00069 | 0.317 |
MOD_Plk_4 | 662 | 668 | PF00069 | 0.489 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.448 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.459 |
MOD_ProDKin_1 | 485 | 491 | PF00069 | 0.496 |
MOD_ProDKin_1 | 660 | 666 | PF00069 | 0.462 |
MOD_ProDKin_1 | 697 | 703 | PF00069 | 0.712 |
MOD_SUMO_rev_2 | 108 | 116 | PF00179 | 0.534 |
MOD_SUMO_rev_2 | 180 | 188 | PF00179 | 0.500 |
MOD_SUMO_rev_2 | 616 | 621 | PF00179 | 0.459 |
TRG_DiLeu_BaEn_1 | 236 | 241 | PF01217 | 0.473 |
TRG_DiLeu_BaLyEn_6 | 134 | 139 | PF01217 | 0.459 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 385 | 388 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 549 | 552 | PF00928 | 0.363 |
TRG_ER_diArg_1 | 361 | 364 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 498 | 501 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 556 | 558 | PF00400 | 0.359 |
TRG_ER_diArg_1 | 589 | 591 | PF00400 | 0.416 |
TRG_ER_diArg_1 | 630 | 632 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 684 | 686 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.440 |
TRG_NES_CRM1_1 | 471 | 483 | PF08389 | 0.449 |
TRG_NES_CRM1_1 | 510 | 523 | PF08389 | 0.533 |
TRG_NLS_Bipartite_1 | 685 | 700 | PF00514 | 0.532 |
TRG_NLS_MonoExtN_4 | 693 | 700 | PF00514 | 0.632 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5V0 | Leptomonas seymouri | 89% | 100% |
A0A0N0P8Y1 | Leptomonas seymouri | 42% | 91% |
A0A0N0P9D2 | Leptomonas seymouri | 43% | 99% |
A0A0N1IKA7 | Leptomonas seymouri | 37% | 78% |
A0A0N1PEU4 | Leptomonas seymouri | 35% | 74% |
A0A0S4IQ76 | Bodo saltans | 41% | 99% |
A0A0S4IR78 | Bodo saltans | 36% | 80% |
A0A0S4IS51 | Bodo saltans | 38% | 90% |
A0A0S4IWU8 | Bodo saltans | 36% | 83% |
A0A0S4J157 | Bodo saltans | 72% | 100% |
A0A0S4JCY8 | Bodo saltans | 42% | 69% |
A0A1X0NJ46 | Trypanosomatidae | 81% | 99% |
A0A1X0P0D7 | Trypanosomatidae | 39% | 100% |
A0A1X0P872 | Trypanosomatidae | 35% | 80% |
A0A1X0P9K6 | Trypanosomatidae | 44% | 98% |
A0A3Q8II71 | Leishmania donovani | 42% | 87% |
A0A3Q8IJ24 | Leishmania donovani | 36% | 75% |
A0A3Q8IWG4 | Leishmania donovani | 37% | 100% |
A0A3R7MA90 | Trypanosoma rangeli | 79% | 98% |
A0A3R7MM88 | Trypanosoma rangeli | 37% | 100% |
A0A3R7NT42 | Trypanosoma rangeli | 42% | 99% |
A0A3S7X8Z5 | Leishmania donovani | 97% | 100% |
A0A422MXB1 | Trypanosoma rangeli | 43% | 66% |
A0A422N8L3 | Trypanosoma rangeli | 39% | 69% |
A0A422NK53 | Trypanosoma rangeli | 35% | 100% |
A4HAT8 | Leishmania braziliensis | 42% | 93% |
A4HME2 | Leishmania braziliensis | 92% | 100% |
A4HNU7 | Leishmania braziliensis | 36% | 75% |
A4HQ83 | Leishmania braziliensis | 37% | 100% |
A4IA06 | Leishmania infantum | 42% | 87% |
A4IB14 | Leishmania infantum | 98% | 100% |
A4ICP7 | Leishmania infantum | 36% | 75% |
A4IDY1 | Leishmania infantum | 37% | 100% |
C9ZMN0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 95% |
C9ZNP6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 78% | 96% |
D0A2R5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 80% |
D0A3F8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 66% |
D0A429 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 93% |
D0A778 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 67% |
D4A2Z8 | Rattus norvegicus | 28% | 70% |
E9ASK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 82% |
E9AU01 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9B512 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 87% |
E9B5Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
F4IE66 | Arabidopsis thaliana | 39% | 98% |
F4IJV4 | Arabidopsis thaliana | 45% | 67% |
F4ILR7 | Arabidopsis thaliana | 32% | 71% |
F4JMJ3 | Arabidopsis thaliana | 46% | 80% |
F4JRJ6 | Arabidopsis thaliana | 42% | 100% |
O22899 | Arabidopsis thaliana | 53% | 97% |
O35286 | Mus musculus | 51% | 89% |
O42945 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 49% | 96% |
O43143 | Homo sapiens | 51% | 89% |
O45244 | Caenorhabditis elegans | 44% | 70% |
O51767 | Borreliella burgdorferi (strain ATCC 35210 / DSM 4680 / CIP 102532 / B31) | 34% | 86% |
O60231 | Homo sapiens | 45% | 68% |
P0C9A2 | African swine fever virus (isolate Tick/South Africa/Pretoriuskop Pr4/1996) | 30% | 73% |
P0C9A3 | African swine fever virus (isolate Warthog/Namibia/Wart80/1980) | 30% | 73% |
P0C9A4 | African swine fever virus (isolate Pig/Kenya/KEN-50/1950) | 30% | 73% |
P20095 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 41% | 80% |
P36009 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 39% | 96% |
P53131 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 51% | 92% |
Q03319 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 40% | 98% |
Q10752 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 43% | 67% |
Q1EHT7 | Oryza sativa subsp. japonica | 30% | 70% |
Q20875 | Caenorhabditis elegans | 49% | 95% |
Q3ZBE0 | Bos taurus | 33% | 98% |
Q4Q0J4 | Leishmania major | 37% | 100% |
Q4Q1Y9 | Leishmania major | 36% | 75% |
Q4Q2X4 | Leishmania major | 41% | 87% |
Q54NJ4 | Dictyostelium discoideum | 51% | 97% |
Q5R864 | Pongo abelii | 36% | 90% |
Q5RAZ4 | Pongo abelii | 51% | 89% |
Q5RBD4 | Pongo abelii | 43% | 98% |
Q5UQ96 | Acanthamoeba polyphaga mimivirus | 29% | 100% |
Q5XH12 | Xenopus laevis | 33% | 94% |
Q5XI69 | Rattus norvegicus | 35% | 90% |
Q6PE54 | Mus musculus | 36% | 90% |
Q767K6 | Sus scrofa | 46% | 67% |
Q7K3M5 | Drosophila melanogaster | 53% | 97% |
Q7L7V1 | Homo sapiens | 33% | 95% |
Q7YR39 | Pan troglodytes | 45% | 67% |
Q80VY9 | Mus musculus | 39% | 100% |
Q89443 | African swine fever virus (strain Badajoz 1971 Vero-adapted) | 30% | 73% |
Q8BZS9 | Mus musculus | 34% | 95% |
Q8IX18 | Homo sapiens | 36% | 90% |
Q8TE96 | Homo sapiens | 34% | 98% |
Q8V9U2 | African swine fever virus (isolate Tick/Malawi/Lil 20-1/1983) | 30% | 73% |
Q8VHK9 | Mus musculus | 28% | 70% |
Q8VY00 | Arabidopsis thaliana | 47% | 67% |
Q924H9 | Mus musculus | 33% | 98% |
Q93Y16 | Arabidopsis thaliana | 38% | 100% |
Q9BKQ8 | Caenorhabditis elegans | 40% | 96% |
Q9H5Z1 | Homo sapiens | 42% | 100% |
Q9H6R0 | Homo sapiens | 39% | 100% |
Q9HE06 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 36% | 100% |
Q9LZQ9 | Arabidopsis thaliana | 54% | 97% |
V5B3L7 | Trypanosoma cruzi | 38% | 100% |
V5BKH2 | Trypanosoma cruzi | 44% | 92% |
V5BPV3 | Trypanosoma cruzi | 43% | 67% |
V5BV22 | Trypanosoma cruzi | 35% | 79% |
V5C0I9 | Trypanosoma cruzi | 38% | 90% |
V5D886 | Trypanosoma cruzi | 77% | 99% |