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 | 2 |
GO:0005654 | nucleoplasm | 2 | 2 |
GO:0005681 | spliceosomal complex | 3 | 2 |
GO:0005684 | U2-type spliceosomal complex | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0071007 | U2-type catalytic step 2 spliceosome | 4 | 2 |
GO:0071013 | catalytic step 2 spliceosome | 3 | 2 |
GO:0071014 | post-mRNA release spliceosomal complex | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
Related structures:
AlphaFold database: Q4QAY3
Term | Name | Level | Count |
---|---|---|---|
GO:0000349 | generation of catalytic spliceosome for first transesterification step | 7 | 2 |
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:0016043 | cellular component organization | 3 | 2 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0016071 | mRNA metabolic process | 6 | 11 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0065003 | protein-containing complex assembly | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 410 | 414 | PF00656 | 0.543 |
CLV_C14_Caspase3-7 | 475 | 479 | PF00656 | 0.541 |
CLV_NRD_NRD_1 | 692 | 694 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 776 | 778 | PF00675 | 0.440 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 494 | 496 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 692 | 694 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 727 | 729 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 775 | 777 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 786 | 788 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 149 | 151 | PF00082 | 0.423 |
CLV_PCSK_PC1ET2_1 | 179 | 181 | PF00082 | 0.480 |
CLV_PCSK_PC1ET2_1 | 375 | 377 | PF00082 | 0.376 |
CLV_PCSK_PC1ET2_1 | 494 | 496 | PF00082 | 0.652 |
CLV_PCSK_PC1ET2_1 | 727 | 729 | PF00082 | 0.471 |
CLV_PCSK_PC1ET2_1 | 786 | 788 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.194 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 612 | 616 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 717 | 721 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.509 |
CLV_Separin_Metazoa | 118 | 122 | PF03568 | 0.557 |
DEG_APCC_DBOX_1 | 281 | 289 | PF00400 | 0.421 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.673 |
DOC_CKS1_1 | 620 | 625 | PF01111 | 0.497 |
DOC_MAPK_gen_1 | 146 | 156 | PF00069 | 0.504 |
DOC_MAPK_gen_1 | 179 | 187 | PF00069 | 0.487 |
DOC_MAPK_gen_1 | 246 | 253 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 255 | 264 | PF00069 | 0.512 |
DOC_MAPK_gen_1 | 349 | 358 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 429 | 439 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 669 | 677 | PF00069 | 0.580 |
DOC_MAPK_gen_1 | 775 | 784 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 163 | 172 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 257 | 266 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 564 | 572 | PF00069 | 0.494 |
DOC_PP1_RVXF_1 | 161 | 168 | PF00149 | 0.280 |
DOC_PP2B_LxvP_1 | 202 | 205 | PF13499 | 0.530 |
DOC_PP4_FxxP_1 | 470 | 473 | PF00568 | 0.352 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 526 | 530 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 541 | 545 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.505 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 542 | 547 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 619 | 624 | PF00397 | 0.477 |
LIG_14-3-3_CanoR_1 | 121 | 125 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 388 | 392 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 56 | 66 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 6 | 14 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 693 | 699 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 728 | 738 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 95 | 104 | PF00244 | 0.468 |
LIG_Actin_WH2_2 | 243 | 259 | PF00022 | 0.508 |
LIG_Actin_WH2_2 | 351 | 366 | PF00022 | 0.506 |
LIG_BIR_III_4 | 740 | 744 | PF00653 | 0.580 |
LIG_BRCT_BRCA1_1 | 264 | 268 | PF00533 | 0.457 |
LIG_BRCT_BRCA1_1 | 544 | 548 | PF00533 | 0.505 |
LIG_BRCT_BRCA1_1 | 684 | 688 | PF00533 | 0.437 |
LIG_BRCT_BRCA1_1 | 780 | 784 | PF00533 | 0.460 |
LIG_BRCT_BRCA1_2 | 780 | 786 | PF00533 | 0.438 |
LIG_Clathr_ClatBox_1 | 588 | 592 | PF01394 | 0.470 |
LIG_CtBP_PxDLS_1 | 261 | 265 | PF00389 | 0.486 |
LIG_deltaCOP1_diTrp_1 | 442 | 449 | PF00928 | 0.361 |
LIG_deltaCOP1_diTrp_1 | 754 | 760 | PF00928 | 0.512 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.486 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.470 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.441 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.497 |
LIG_FHA_1 | 663 | 669 | PF00498 | 0.463 |
LIG_FHA_2 | 22 | 28 | PF00498 | 0.572 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.550 |
LIG_FHA_2 | 388 | 394 | PF00498 | 0.514 |
LIG_FHA_2 | 685 | 691 | PF00498 | 0.451 |
LIG_FHA_2 | 763 | 769 | PF00498 | 0.503 |
LIG_GBD_Chelix_1 | 705 | 713 | PF00786 | 0.543 |
LIG_LIR_Apic_2 | 442 | 448 | PF02991 | 0.474 |
LIG_LIR_Apic_2 | 469 | 473 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 109 | 116 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 181 | 187 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 224 | 233 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 24 | 33 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 265 | 273 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 389 | 398 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 592 | 600 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 613 | 623 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 768 | 774 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 84 | 93 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 109 | 113 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 181 | 186 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 191 | 195 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 24 | 28 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 327 | 333 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 353 | 357 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 389 | 394 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 592 | 597 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 613 | 618 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 754 | 759 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 768 | 773 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 84 | 89 | PF02991 | 0.346 |
LIG_LYPXL_SIV_4 | 329 | 337 | PF13949 | 0.472 |
LIG_LYPXL_SIV_4 | 641 | 649 | PF13949 | 0.530 |
LIG_NRBOX | 284 | 290 | PF00104 | 0.458 |
LIG_NRBOX | 457 | 463 | PF00104 | 0.510 |
LIG_PCNA_yPIPBox_3 | 331 | 345 | PF02747 | 0.431 |
LIG_Pex14_1 | 445 | 449 | PF04695 | 0.363 |
LIG_Pex14_2 | 611 | 615 | PF04695 | 0.523 |
LIG_SH2_CRK | 330 | 334 | PF00017 | 0.430 |
LIG_SH2_CRK | 695 | 699 | PF00017 | 0.510 |
LIG_SH2_NCK_1 | 527 | 531 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 51 | 55 | PF00017 | 0.367 |
LIG_SH2_STAP1 | 93 | 97 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 561 | 564 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 594 | 597 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 637 | 640 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 701 | 704 | PF00017 | 0.369 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.395 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.414 |
LIG_Sin3_3 | 354 | 361 | PF02671 | 0.487 |
LIG_SUMO_SIM_anti_2 | 434 | 442 | PF11976 | 0.438 |
LIG_SUMO_SIM_anti_2 | 566 | 572 | PF11976 | 0.478 |
LIG_SUMO_SIM_anti_2 | 659 | 665 | PF11976 | 0.487 |
LIG_SUMO_SIM_par_1 | 260 | 265 | PF11976 | 0.489 |
LIG_SUMO_SIM_par_1 | 472 | 478 | PF11976 | 0.546 |
LIG_SUMO_SIM_par_1 | 622 | 628 | PF11976 | 0.461 |
LIG_TRAF2_1 | 212 | 215 | PF00917 | 0.570 |
LIG_Vh1_VBS_1 | 447 | 465 | PF01044 | 0.512 |
LIG_Vh1_VBS_1 | 649 | 667 | PF01044 | 0.489 |
LIG_WRC_WIRS_1 | 169 | 174 | PF05994 | 0.507 |
LIG_WRC_WIRS_1 | 313 | 318 | PF05994 | 0.530 |
LIG_WRC_WIRS_1 | 467 | 472 | PF05994 | 0.337 |
LIG_WRC_WIRS_1 | 594 | 599 | PF05994 | 0.474 |
MOD_CDK_SPK_2 | 18 | 23 | PF00069 | 0.631 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.495 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.445 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.395 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.582 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.693 |
MOD_CK1_1 | 729 | 735 | PF00069 | 0.536 |
MOD_CK1_1 | 762 | 768 | PF00069 | 0.439 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.289 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.578 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.429 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.415 |
MOD_CK2_1 | 684 | 690 | PF00069 | 0.478 |
MOD_CK2_1 | 762 | 768 | PF00069 | 0.464 |
MOD_CMANNOS | 517 | 520 | PF00535 | 0.423 |
MOD_CMANNOS | 757 | 760 | PF00535 | 0.394 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.503 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.535 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.538 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.522 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.567 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.582 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.519 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.425 |
MOD_GlcNHglycan | 630 | 633 | PF01048 | 0.479 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.590 |
MOD_GlcNHglycan | 728 | 731 | PF01048 | 0.541 |
MOD_GlcNHglycan | 788 | 791 | PF01048 | 0.456 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.510 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.536 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.396 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.354 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.473 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.454 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.615 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.372 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.487 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.457 |
MOD_GSK3_1 | 742 | 749 | PF00069 | 0.494 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.282 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.445 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.383 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.481 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.442 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.344 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.547 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.487 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.406 |
MOD_NEK2_1 | 649 | 654 | PF00069 | 0.303 |
MOD_NEK2_1 | 662 | 667 | PF00069 | 0.408 |
MOD_NEK2_1 | 682 | 687 | PF00069 | 0.262 |
MOD_NEK2_1 | 759 | 764 | PF00069 | 0.387 |
MOD_NEK2_2 | 158 | 163 | PF00069 | 0.475 |
MOD_NEK2_2 | 694 | 699 | PF00069 | 0.496 |
MOD_PIKK_1 | 136 | 142 | PF00454 | 0.393 |
MOD_PIKK_1 | 742 | 748 | PF00454 | 0.429 |
MOD_PK_1 | 564 | 570 | PF00069 | 0.487 |
MOD_PKA_1 | 786 | 792 | PF00069 | 0.499 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.388 |
MOD_PKA_2 | 238 | 244 | PF00069 | 0.476 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.558 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.505 |
MOD_PKA_2 | 482 | 488 | PF00069 | 0.585 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.632 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.336 |
MOD_PKA_2 | 786 | 792 | PF00069 | 0.649 |
MOD_PKB_1 | 72 | 80 | PF00069 | 0.332 |
MOD_Plk_1 | 221 | 227 | PF00069 | 0.411 |
MOD_Plk_1 | 262 | 268 | PF00069 | 0.472 |
MOD_Plk_1 | 658 | 664 | PF00069 | 0.523 |
MOD_Plk_1 | 682 | 688 | PF00069 | 0.386 |
MOD_Plk_1 | 74 | 80 | PF00069 | 0.467 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.289 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.398 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.484 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.502 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.554 |
MOD_Plk_4 | 593 | 599 | PF00069 | 0.477 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.624 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.402 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.521 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.540 |
MOD_ProDKin_1 | 542 | 548 | PF00069 | 0.531 |
MOD_ProDKin_1 | 619 | 625 | PF00069 | 0.471 |
MOD_SUMO_for_1 | 178 | 181 | PF00179 | 0.463 |
TRG_DiLeu_BaEn_1 | 214 | 219 | PF01217 | 0.537 |
TRG_DiLeu_BaEn_1 | 284 | 289 | PF01217 | 0.516 |
TRG_DiLeu_BaEn_1 | 294 | 299 | PF01217 | 0.507 |
TRG_DiLeu_BaEn_1 | 353 | 358 | PF01217 | 0.481 |
TRG_DiLeu_BaEn_1 | 613 | 618 | PF01217 | 0.483 |
TRG_DiLeu_BaLyEn_6 | 352 | 357 | PF01217 | 0.463 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 169 | 172 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.290 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 594 | 597 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 695 | 698 | PF00928 | 0.511 |
TRG_ENDOCYTIC_2 | 756 | 759 | PF00928 | 0.507 |
TRG_ER_diArg_1 | 668 | 671 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 71 | 74 | PF00400 | 0.368 |
TRG_ER_diArg_1 | 775 | 777 | PF00400 | 0.535 |
TRG_NES_CRM1_1 | 296 | 310 | PF08389 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 286 | 290 | PF00026 | 0.510 |
TRG_Pf-PMV_PEXEL_1 | 323 | 327 | PF00026 | 0.550 |
TRG_Pf-PMV_PEXEL_1 | 95 | 99 | PF00026 | 0.434 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCJ1 | Leptomonas seymouri | 71% | 100% |
A0A1X0NWW2 | Trypanosomatidae | 41% | 100% |
A0A3Q8IBX9 | Leishmania donovani | 94% | 100% |
A0A422NJT0 | Trypanosoma rangeli | 39% | 100% |
A4HD39 | Leishmania braziliensis | 88% | 100% |
C9ZNR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 87% |
E9AH17 | Leishmania infantum | 95% | 100% |
E9AWI7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 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) | 24% | 93% |
Q7SAK5 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 23% | 96% |
Q99PK0 | Rattus norvegicus | 23% | 93% |
Q9DCD2 | Mus musculus | 23% | 93% |
Q9HCS7 | Homo sapiens | 23% | 93% |
Q9P7R9 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 21% | 100% |
V5ARA5 | Trypanosoma cruzi | 40% | 100% |