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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000974 | Prp19 complex | 2 | 1 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0005684 | U2-type spliceosomal complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0071007 | U2-type catalytic step 2 spliceosome | 4 | 1 |
GO:0071013 | catalytic step 2 spliceosome | 3 | 1 |
GO:0071014 | post-mRNA release spliceosomal complex | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A4HD39
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 11 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 11 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 11 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006396 | RNA processing | 6 | 11 |
GO:0006397 | mRNA processing | 7 | 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:0016071 | mRNA metabolic process | 6 | 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 |
GO:0000349 | generation of catalytic spliceosome for first transesterification step | 7 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 410 | 414 | PF00656 | 0.530 |
CLV_C14_Caspase3-7 | 475 | 479 | PF00656 | 0.552 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 691 | 693 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 698 | 700 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 776 | 778 | PF00675 | 0.445 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 494 | 496 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 727 | 729 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 775 | 777 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 786 | 788 | PF00082 | 0.542 |
CLV_PCSK_PC1ET2_1 | 149 | 151 | PF00082 | 0.421 |
CLV_PCSK_PC1ET2_1 | 331 | 333 | PF00082 | 0.331 |
CLV_PCSK_PC1ET2_1 | 375 | 377 | PF00082 | 0.376 |
CLV_PCSK_PC1ET2_1 | 494 | 496 | PF00082 | 0.675 |
CLV_PCSK_PC1ET2_1 | 727 | 729 | PF00082 | 0.472 |
CLV_PCSK_PC1ET2_1 | 786 | 788 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.192 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 612 | 616 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 717 | 721 | PF00082 | 0.364 |
CLV_Separin_Metazoa | 118 | 122 | PF03568 | 0.555 |
DEG_APCC_DBOX_1 | 281 | 289 | PF00400 | 0.431 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.641 |
DOC_CKS1_1 | 620 | 625 | PF01111 | 0.494 |
DOC_MAPK_gen_1 | 146 | 156 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 179 | 187 | PF00069 | 0.487 |
DOC_MAPK_gen_1 | 255 | 264 | PF00069 | 0.514 |
DOC_MAPK_gen_1 | 669 | 677 | PF00069 | 0.560 |
DOC_MAPK_gen_1 | 775 | 784 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 257 | 266 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 564 | 572 | PF00069 | 0.459 |
DOC_PP1_RVXF_1 | 214 | 221 | PF00149 | 0.475 |
DOC_PP2B_LxvP_1 | 202 | 205 | PF13499 | 0.550 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 534 | 538 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.505 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.407 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 542 | 547 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 619 | 624 | PF00397 | 0.476 |
LIG_14-3-3_CanoR_1 | 121 | 125 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 167 | 173 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 388 | 392 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 56 | 65 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 6 | 14 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 728 | 738 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 777 | 783 | PF00244 | 0.347 |
LIG_Actin_WH2_2 | 351 | 366 | PF00022 | 0.501 |
LIG_APCC_ABBAyCdc20_2 | 216 | 222 | PF00400 | 0.311 |
LIG_BIR_III_2 | 290 | 294 | PF00653 | 0.321 |
LIG_BIR_III_4 | 740 | 744 | PF00653 | 0.578 |
LIG_BRCT_BRCA1_1 | 264 | 268 | PF00533 | 0.456 |
LIG_BRCT_BRCA1_1 | 544 | 548 | PF00533 | 0.503 |
LIG_BRCT_BRCA1_1 | 684 | 688 | PF00533 | 0.429 |
LIG_BRCT_BRCA1_1 | 780 | 784 | PF00533 | 0.479 |
LIG_BRCT_BRCA1_1 | 82 | 86 | PF00533 | 0.305 |
LIG_BRCT_BRCA1_2 | 780 | 786 | PF00533 | 0.462 |
LIG_Clathr_ClatBox_1 | 588 | 592 | PF01394 | 0.466 |
LIG_CtBP_PxDLS_1 | 261 | 265 | PF00389 | 0.487 |
LIG_deltaCOP1_diTrp_1 | 442 | 449 | PF00928 | 0.355 |
LIG_deltaCOP1_diTrp_1 | 754 | 760 | PF00928 | 0.508 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.431 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.459 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.545 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.431 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.470 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.383 |
LIG_FHA_2 | 22 | 28 | PF00498 | 0.569 |
LIG_FHA_2 | 388 | 394 | PF00498 | 0.510 |
LIG_FHA_2 | 685 | 691 | PF00498 | 0.445 |
LIG_FHA_2 | 763 | 769 | PF00498 | 0.499 |
LIG_GBD_Chelix_1 | 705 | 713 | PF00786 | 0.540 |
LIG_LIR_Apic_2 | 442 | 448 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 109 | 116 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 181 | 187 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 191 | 200 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 224 | 233 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 24 | 33 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 265 | 273 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 389 | 398 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 533 | 542 | PF02991 | 0.282 |
LIG_LIR_Gen_1 | 592 | 600 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 613 | 623 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 672 | 682 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 768 | 774 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 83 | 93 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 109 | 113 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 181 | 186 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 191 | 195 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 217 | 223 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 24 | 28 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 327 | 333 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 353 | 357 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 389 | 394 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 533 | 538 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 592 | 597 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 613 | 618 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 672 | 677 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 754 | 759 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 768 | 773 | PF02991 | 0.359 |
LIG_LYPXL_SIV_4 | 641 | 649 | PF13949 | 0.525 |
LIG_NRBOX | 284 | 290 | PF00104 | 0.462 |
LIG_NRBOX | 457 | 463 | PF00104 | 0.504 |
LIG_Pex14_1 | 445 | 449 | PF04695 | 0.357 |
LIG_Pex14_2 | 611 | 615 | PF04695 | 0.519 |
LIG_RPA_C_Fungi | 25 | 37 | PF08784 | 0.484 |
LIG_SH2_CRK | 330 | 334 | PF00017 | 0.441 |
LIG_SH2_CRK | 695 | 699 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 51 | 55 | PF00017 | 0.360 |
LIG_SH2_STAP1 | 93 | 97 | PF00017 | 0.359 |
LIG_SH2_STAT3 | 71 | 74 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 446 | 449 | PF00017 | 0.250 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 561 | 564 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 594 | 597 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 599 | 602 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 674 | 677 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 701 | 704 | PF00017 | 0.352 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.379 |
LIG_SH3_3 | 508 | 514 | PF00018 | 0.495 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.389 |
LIG_Sin3_3 | 354 | 361 | PF02671 | 0.482 |
LIG_SUMO_SIM_anti_2 | 566 | 572 | PF11976 | 0.475 |
LIG_SUMO_SIM_anti_2 | 659 | 664 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 260 | 265 | PF11976 | 0.489 |
LIG_SUMO_SIM_par_1 | 434 | 442 | PF11976 | 0.266 |
LIG_SUMO_SIM_par_1 | 472 | 478 | PF11976 | 0.552 |
LIG_SUMO_SIM_par_1 | 622 | 628 | PF11976 | 0.459 |
LIG_TRAF2_1 | 766 | 769 | PF00917 | 0.475 |
LIG_Vh1_VBS_1 | 447 | 465 | PF01044 | 0.506 |
LIG_Vh1_VBS_1 | 649 | 667 | PF01044 | 0.481 |
LIG_WRC_WIRS_1 | 169 | 174 | PF05994 | 0.513 |
LIG_WRC_WIRS_1 | 313 | 318 | PF05994 | 0.529 |
LIG_WRC_WIRS_1 | 594 | 599 | PF05994 | 0.470 |
MOD_CDK_SPK_2 | 18 | 23 | PF00069 | 0.619 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.494 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.544 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.702 |
MOD_CK1_1 | 729 | 735 | PF00069 | 0.536 |
MOD_CK1_1 | 762 | 768 | PF00069 | 0.435 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.577 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.438 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.421 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.443 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.433 |
MOD_CK2_1 | 684 | 690 | PF00069 | 0.449 |
MOD_CK2_1 | 762 | 768 | PF00069 | 0.440 |
MOD_CMANNOS | 517 | 520 | PF00535 | 0.461 |
MOD_CMANNOS | 757 | 760 | PF00535 | 0.391 |
MOD_Cter_Amidation | 784 | 787 | PF01082 | 0.396 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.503 |
MOD_GlcNHglycan | 17 | 21 | PF01048 | 0.595 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.526 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.265 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.499 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.570 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.598 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.426 |
MOD_GlcNHglycan | 630 | 633 | PF01048 | 0.470 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.550 |
MOD_GlcNHglycan | 728 | 731 | PF01048 | 0.514 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.568 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.513 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.400 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.479 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.335 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.626 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.411 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.393 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.438 |
MOD_GSK3_1 | 742 | 749 | PF00069 | 0.487 |
MOD_GSK3_1 | 759 | 766 | PF00069 | 0.273 |
MOD_GSK3_1 | 786 | 793 | PF00069 | 0.579 |
MOD_N-GLC_1 | 530 | 535 | PF02516 | 0.378 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.449 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.371 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.468 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.433 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.343 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.402 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.569 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.355 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.459 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.392 |
MOD_NEK2_1 | 649 | 654 | PF00069 | 0.297 |
MOD_NEK2_1 | 682 | 687 | PF00069 | 0.254 |
MOD_NEK2_1 | 759 | 764 | PF00069 | 0.384 |
MOD_PIKK_1 | 136 | 142 | PF00454 | 0.392 |
MOD_PIKK_1 | 742 | 748 | PF00454 | 0.427 |
MOD_PK_1 | 564 | 570 | PF00069 | 0.485 |
MOD_PKA_1 | 786 | 792 | PF00069 | 0.542 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.386 |
MOD_PKA_2 | 238 | 244 | PF00069 | 0.481 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.503 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.514 |
MOD_PKA_2 | 482 | 488 | PF00069 | 0.585 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.598 |
MOD_PKA_2 | 786 | 792 | PF00069 | 0.667 |
MOD_Plk_1 | 221 | 227 | PF00069 | 0.401 |
MOD_Plk_1 | 262 | 268 | PF00069 | 0.471 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.367 |
MOD_Plk_1 | 530 | 536 | PF00069 | 0.294 |
MOD_Plk_1 | 658 | 664 | PF00069 | 0.513 |
MOD_Plk_1 | 682 | 688 | PF00069 | 0.378 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.407 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.495 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.454 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.548 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.403 |
MOD_Plk_4 | 593 | 599 | PF00069 | 0.455 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.612 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.407 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.518 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.542 |
MOD_ProDKin_1 | 542 | 548 | PF00069 | 0.531 |
MOD_ProDKin_1 | 619 | 625 | PF00069 | 0.470 |
TRG_DiLeu_BaEn_1 | 214 | 219 | PF01217 | 0.557 |
TRG_DiLeu_BaEn_1 | 284 | 289 | PF01217 | 0.527 |
TRG_DiLeu_BaEn_1 | 613 | 618 | PF01217 | 0.480 |
TRG_DiLeu_BaLyEn_6 | 352 | 357 | PF01217 | 0.455 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 169 | 172 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 446 | 449 | PF00928 | 0.250 |
TRG_ENDOCYTIC_2 | 594 | 597 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 674 | 677 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 695 | 698 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 756 | 759 | PF00928 | 0.504 |
TRG_ER_diArg_1 | 668 | 671 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 77 | 79 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 775 | 777 | PF00400 | 0.540 |
TRG_NES_CRM1_1 | 243 | 256 | PF08389 | 0.368 |
TRG_NES_CRM1_1 | 296 | 310 | PF08389 | 0.499 |
TRG_Pf-PMV_PEXEL_1 | 95 | 99 | PF00026 | 0.434 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCJ1 | Leptomonas seymouri | 69% | 100% |
A0A1X0NWW2 | Trypanosomatidae | 39% | 100% |
A0A3Q8IBX9 | Leishmania donovani | 89% | 100% |
A0A422NJT0 | Trypanosoma rangeli | 39% | 100% |
C9ZNR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 87% |
E9AH17 | Leishmania infantum | 90% | 100% |
E9AWI7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QAY3 | Leishmania major | 88% | 100% |
Q4WVF4 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 23% | 95% |
Q52DF3 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 23% | 95% |
Q54Z08 | Dictyostelium discoideum | 22% | 93% |
Q5BH69 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 23% | 93% |
Q7SAK5 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 23% | 96% |
Q9P7R9 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 20% | 100% |
V5ARA5 | Trypanosoma cruzi | 40% | 100% |