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:0000974 | Prp19 complex | 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:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A4HPU7
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 12 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 12 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006397 | mRNA processing | 7 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0008380 | RNA splicing | 7 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0016071 | mRNA metabolic process | 6 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0000245 | spliceosomal complex assembly | 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 | 4 | 8 | PF00656 | 0.666 |
CLV_C14_Caspase3-7 | 635 | 639 | PF00656 | 0.450 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 444 | 446 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 620 | 622 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 757 | 759 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 814 | 816 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.473 |
CLV_PCSK_FUR_1 | 363 | 367 | PF00082 | 0.358 |
CLV_PCSK_FUR_1 | 73 | 77 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 620 | 622 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 757 | 759 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 813 | 815 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.318 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.566 |
CLV_PCSK_PC1ET2_1 | 75 | 77 | PF00082 | 0.448 |
CLV_PCSK_PC1ET2_1 | 813 | 815 | PF00082 | 0.552 |
CLV_PCSK_PC7_1 | 213 | 219 | PF00082 | 0.384 |
CLV_PCSK_PC7_1 | 753 | 759 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.202 |
CLV_PCSK_SKI1_1 | 482 | 486 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 562 | 566 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 742 | 746 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 810 | 814 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 817 | 821 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.512 |
CLV_Separin_Metazoa | 572 | 576 | PF03568 | 0.435 |
CLV_Separin_Metazoa | 652 | 656 | PF03568 | 0.245 |
DEG_APCC_DBOX_1 | 642 | 650 | PF00400 | 0.380 |
DEG_APCC_DBOX_1 | 741 | 749 | PF00400 | 0.506 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.572 |
DEG_SPOP_SBC_1 | 520 | 524 | PF00917 | 0.400 |
DOC_ANK_TNKS_1 | 316 | 323 | PF00023 | 0.476 |
DOC_CKS1_1 | 223 | 228 | PF01111 | 0.394 |
DOC_CKS1_1 | 731 | 736 | PF01111 | 0.392 |
DOC_CYCLIN_RxL_1 | 479 | 489 | PF00134 | 0.515 |
DOC_CYCLIN_yCln2_LP_2 | 392 | 398 | PF00134 | 0.433 |
DOC_MAPK_gen_1 | 774 | 783 | PF00069 | 0.493 |
DOC_PP1_RVXF_1 | 756 | 763 | PF00149 | 0.611 |
DOC_PP2B_LxvP_1 | 410 | 413 | PF13499 | 0.556 |
DOC_PP4_FxxP_1 | 223 | 226 | PF00568 | 0.398 |
DOC_PP4_FxxP_1 | 49 | 52 | PF00568 | 0.617 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.269 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.630 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 701 | 706 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 730 | 735 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 781 | 786 | PF00397 | 0.329 |
LIG_14-3-3_CanoR_1 | 116 | 121 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 150 | 159 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 342 | 352 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 365 | 373 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 444 | 448 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 507 | 516 | PF00244 | 0.301 |
LIG_14-3-3_CanoR_1 | 593 | 598 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 709 | 717 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 757 | 761 | PF00244 | 0.612 |
LIG_APCC_ABBA_1 | 118 | 123 | PF00400 | 0.505 |
LIG_APCC_ABBA_1 | 334 | 339 | PF00400 | 0.485 |
LIG_APCC_ABBAyCdc20_2 | 20 | 26 | PF00400 | 0.513 |
LIG_BIR_III_2 | 189 | 193 | PF00653 | 0.510 |
LIG_BRCT_BRCA1_1 | 136 | 140 | PF00533 | 0.436 |
LIG_BRCT_BRCA1_1 | 452 | 456 | PF00533 | 0.277 |
LIG_BRCT_BRCA1_1 | 676 | 680 | PF00533 | 0.443 |
LIG_deltaCOP1_diTrp_1 | 788 | 793 | PF00928 | 0.365 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.457 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.432 |
LIG_FHA_2 | 444 | 450 | PF00498 | 0.388 |
LIG_FHA_2 | 646 | 652 | PF00498 | 0.466 |
LIG_FHA_2 | 765 | 771 | PF00498 | 0.596 |
LIG_LIR_Apic_2 | 221 | 226 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 106 | 114 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 130 | 136 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 310 | 318 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 349 | 358 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 766 | 775 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 788 | 795 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 160 | 165 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 228 | 232 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 310 | 315 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 345 | 351 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 353 | 358 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 663 | 668 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 766 | 772 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 777 | 781 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 788 | 793 | PF02991 | 0.384 |
LIG_LRP6_Inhibitor_1 | 90 | 96 | PF00058 | 0.472 |
LIG_MLH1_MIPbox_1 | 676 | 680 | PF16413 | 0.443 |
LIG_PCNA_PIPBox_1 | 33 | 42 | PF02747 | 0.483 |
LIG_PCNA_PIPBox_1 | 650 | 659 | PF02747 | 0.448 |
LIG_PCNA_yPIPBox_3 | 28 | 40 | PF02747 | 0.504 |
LIG_PCNA_yPIPBox_3 | 643 | 657 | PF02747 | 0.462 |
LIG_Pex14_1 | 559 | 563 | PF04695 | 0.414 |
LIG_Pex14_1 | 675 | 679 | PF04695 | 0.493 |
LIG_Pex14_2 | 555 | 559 | PF04695 | 0.359 |
LIG_Pex14_2 | 676 | 680 | PF04695 | 0.443 |
LIG_RPA_C_Fungi | 616 | 628 | PF08784 | 0.425 |
LIG_SH2_CRK | 601 | 605 | PF00017 | 0.472 |
LIG_SH2_CRK | 657 | 661 | PF00017 | 0.421 |
LIG_SH2_GRB2like | 546 | 549 | PF00017 | 0.461 |
LIG_SH2_SRC | 546 | 549 | PF00017 | 0.461 |
LIG_SH2_STAP1 | 243 | 247 | PF00017 | 0.322 |
LIG_SH2_STAP1 | 337 | 341 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 657 | 661 | PF00017 | 0.349 |
LIG_SH2_STAT3 | 202 | 205 | PF00017 | 0.475 |
LIG_SH2_STAT3 | 358 | 361 | PF00017 | 0.456 |
LIG_SH2_STAT3 | 418 | 421 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 538 | 541 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 679 | 682 | PF00017 | 0.475 |
LIG_SUMO_SIM_par_1 | 270 | 276 | PF11976 | 0.416 |
LIG_SUMO_SIM_par_1 | 300 | 306 | PF11976 | 0.553 |
LIG_TRAF2_1 | 470 | 473 | PF00917 | 0.482 |
LIG_TRAF2_1 | 648 | 651 | PF00917 | 0.484 |
LIG_TRAF2_1 | 65 | 68 | PF00917 | 0.403 |
LIG_TYR_ITIM | 561 | 566 | PF00017 | 0.456 |
LIG_WRC_WIRS_1 | 584 | 589 | PF05994 | 0.382 |
LIG_WRC_WIRS_1 | 594 | 599 | PF05994 | 0.428 |
MOD_CDC14_SPxK_1 | 400 | 403 | PF00782 | 0.517 |
MOD_CDK_SPxK_1 | 397 | 403 | PF00069 | 0.564 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.262 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.517 |
MOD_CK1_1 | 701 | 707 | PF00069 | 0.564 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.265 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.376 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.287 |
MOD_CK2_1 | 524 | 530 | PF00069 | 0.664 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.401 |
MOD_CK2_1 | 645 | 651 | PF00069 | 0.471 |
MOD_CK2_1 | 744 | 750 | PF00069 | 0.458 |
MOD_CK2_1 | 788 | 794 | PF00069 | 0.455 |
MOD_GlcNHglycan | 135 | 140 | PF01048 | 0.511 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.309 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.393 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.625 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.650 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.566 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.526 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.400 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.636 |
MOD_GlcNHglycan | 634 | 637 | PF01048 | 0.400 |
MOD_GlcNHglycan | 684 | 688 | PF01048 | 0.600 |
MOD_GlcNHglycan | 735 | 738 | PF01048 | 0.358 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.372 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.570 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.587 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.575 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.554 |
MOD_GSK3_1 | 695 | 702 | PF00069 | 0.617 |
MOD_GSK3_1 | 704 | 711 | PF00069 | 0.493 |
MOD_GSK3_1 | 744 | 751 | PF00069 | 0.444 |
MOD_GSK3_1 | 756 | 763 | PF00069 | 0.534 |
MOD_GSK3_1 | 793 | 800 | PF00069 | 0.478 |
MOD_N-GLC_1 | 343 | 348 | PF02516 | 0.449 |
MOD_N-GLC_1 | 52 | 57 | PF02516 | 0.508 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.713 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.531 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.680 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.360 |
MOD_NEK2_1 | 793 | 798 | PF00069 | 0.420 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.505 |
MOD_NEK2_1 | 818 | 823 | PF00069 | 0.556 |
MOD_NEK2_2 | 350 | 355 | PF00069 | 0.459 |
MOD_PIKK_1 | 476 | 482 | PF00454 | 0.482 |
MOD_PIKK_1 | 486 | 492 | PF00454 | 0.549 |
MOD_PIKK_1 | 521 | 527 | PF00454 | 0.399 |
MOD_PIKK_1 | 764 | 770 | PF00454 | 0.536 |
MOD_PK_1 | 116 | 122 | PF00069 | 0.305 |
MOD_PKA_1 | 342 | 348 | PF00069 | 0.389 |
MOD_PKA_1 | 365 | 371 | PF00069 | 0.392 |
MOD_PKA_1 | 813 | 819 | PF00069 | 0.556 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.589 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.686 |
MOD_PKA_2 | 443 | 449 | PF00069 | 0.450 |
MOD_PKA_2 | 592 | 598 | PF00069 | 0.406 |
MOD_PKA_2 | 708 | 714 | PF00069 | 0.485 |
MOD_PKA_2 | 756 | 762 | PF00069 | 0.599 |
MOD_PKA_2 | 813 | 819 | PF00069 | 0.536 |
MOD_PKB_1 | 340 | 348 | PF00069 | 0.449 |
MOD_PKB_1 | 363 | 371 | PF00069 | 0.401 |
MOD_Plk_1 | 644 | 650 | PF00069 | 0.393 |
MOD_Plk_1 | 80 | 86 | PF00069 | 0.496 |
MOD_Plk_2-3 | 645 | 651 | PF00069 | 0.371 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.266 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.416 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.469 |
MOD_Plk_4 | 744 | 750 | PF00069 | 0.420 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.479 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.677 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.618 |
MOD_ProDKin_1 | 701 | 707 | PF00069 | 0.450 |
MOD_ProDKin_1 | 730 | 736 | PF00069 | 0.397 |
MOD_ProDKin_1 | 781 | 787 | PF00069 | 0.331 |
MOD_SUMO_for_1 | 564 | 567 | PF00179 | 0.329 |
MOD_SUMO_rev_2 | 449 | 454 | PF00179 | 0.528 |
TRG_DiLeu_BaEn_1 | 777 | 782 | PF01217 | 0.492 |
TRG_DiLeu_BaEn_3 | 135 | 141 | PF01217 | 0.266 |
TRG_DiLeu_BaEn_4 | 651 | 657 | PF01217 | 0.408 |
TRG_DiLeu_BaLyEn_6 | 299 | 304 | PF01217 | 0.497 |
TRG_DiLeu_BaLyEn_6 | 480 | 485 | PF01217 | 0.517 |
TRG_DiLeu_BaLyEn_6 | 782 | 787 | PF01217 | 0.457 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 563 | 566 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 601 | 604 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 657 | 660 | PF00928 | 0.307 |
TRG_ER_diArg_1 | 18 | 21 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.382 |
TRG_ER_diArg_1 | 365 | 367 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 482 | 484 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 620 | 623 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 756 | 758 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 814 | 817 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 84 | 86 | PF00400 | 0.511 |
TRG_NES_CRM1_1 | 108 | 123 | PF08389 | 0.429 |
TRG_NLS_MonoExtC_3 | 1 | 7 | PF00514 | 0.603 |
TRG_NLS_MonoExtC_3 | 812 | 817 | PF00514 | 0.532 |
TRG_NLS_MonoExtN_4 | 810 | 817 | PF00514 | 0.526 |
TRG_Pf-PMV_PEXEL_1 | 184 | 189 | PF00026 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 445 | 449 | PF00026 | 0.530 |
TRG_Pf-PMV_PEXEL_1 | 623 | 628 | PF00026 | 0.524 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P767 | Leptomonas seymouri | 73% | 99% |
A0A0S4JKT1 | Bodo saltans | 28% | 94% |
A0A1X0P0C5 | Trypanosomatidae | 42% | 100% |
A0A3Q8IHN6 | Leishmania donovani | 88% | 100% |
A0A3R7P515 | Trypanosoma rangeli | 43% | 100% |
A4IE46 | Leishmania infantum | 88% | 100% |
D0A493 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9ATL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
P63154 | Mus musculus | 25% | 100% |
P63155 | Rattus norvegicus | 25% | 100% |
P87312 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
Q4PB37 | Ustilago maydis (strain 521 / FGSC 9021) | 28% | 100% |
Q4Q0Y6 | Leishmania major | 87% | 100% |
Q4WT84 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 26% | 100% |
Q5BDX1 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 27% | 100% |
Q5K654 | Paracoccidioides brasiliensis | 26% | 100% |
Q6C186 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 24% | 100% |
Q6CJK2 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 23% | 100% |
Q7SGD2 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 25% | 100% |
Q9BZJ0 | Homo sapiens | 25% | 97% |
V5B545 | Trypanosoma cruzi | 43% | 100% |