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 | 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:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
Related structures:
AlphaFold database: Q4Q0Y6
Term | Name | Level | Count |
---|---|---|---|
GO:0000245 | spliceosomal complex assembly | 7 | 2 |
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:0016043 | cellular component organization | 3 | 2 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0016071 | mRNA metabolic process | 6 | 12 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0065003 | protein-containing complex assembly | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 4 | 8 | PF00656 | 0.697 |
CLV_C14_Caspase3-7 | 606 | 610 | PF00656 | 0.426 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 621 | 623 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 632 | 634 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 758 | 760 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 815 | 817 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.603 |
CLV_PCSK_FUR_1 | 73 | 77 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 483 | 485 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 621 | 623 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 632 | 634 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 758 | 760 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 814 | 816 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.591 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.617 |
CLV_PCSK_PC1ET2_1 | 75 | 77 | PF00082 | 0.477 |
CLV_PCSK_PC1ET2_1 | 814 | 816 | PF00082 | 0.578 |
CLV_PCSK_PC7_1 | 213 | 219 | PF00082 | 0.431 |
CLV_PCSK_PC7_1 | 5 | 11 | PF00082 | 0.677 |
CLV_PCSK_PC7_1 | 628 | 634 | PF00082 | 0.532 |
CLV_PCSK_PC7_1 | 754 | 760 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.198 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 743 | 747 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 811 | 815 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 818 | 822 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.548 |
CLV_Separin_Metazoa | 573 | 577 | PF03568 | 0.549 |
DEG_APCC_DBOX_1 | 742 | 750 | PF00400 | 0.529 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.624 |
DOC_ANK_TNKS_1 | 316 | 323 | PF00023 | 0.518 |
DOC_CKS1_1 | 223 | 228 | PF01111 | 0.498 |
DOC_CYCLIN_RxL_1 | 480 | 490 | PF00134 | 0.536 |
DOC_MAPK_gen_1 | 775 | 784 | PF00069 | 0.501 |
DOC_PP1_RVXF_1 | 757 | 764 | PF00149 | 0.607 |
DOC_PP2B_LxvP_1 | 411 | 414 | PF13499 | 0.579 |
DOC_PP4_FxxP_1 | 223 | 226 | PF00568 | 0.499 |
DOC_PP4_FxxP_1 | 49 | 52 | PF00568 | 0.654 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.673 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 522 | 527 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 702 | 707 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 782 | 787 | PF00397 | 0.381 |
LIG_14-3-3_CanoR_1 | 150 | 159 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 342 | 352 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 445 | 449 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 475 | 485 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 594 | 599 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 710 | 718 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 758 | 762 | PF00244 | 0.592 |
LIG_APCC_ABBA_1 | 118 | 123 | PF00400 | 0.539 |
LIG_APCC_ABBA_1 | 334 | 339 | PF00400 | 0.511 |
LIG_APCC_ABBAyCdc20_2 | 20 | 26 | PF00400 | 0.576 |
LIG_BIR_III_2 | 189 | 193 | PF00653 | 0.547 |
LIG_BRCT_BRCA1_1 | 136 | 140 | PF00533 | 0.568 |
LIG_BRCT_BRCA1_1 | 677 | 681 | PF00533 | 0.555 |
LIG_deltaCOP1_diTrp_1 | 789 | 794 | PF00928 | 0.519 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.470 |
LIG_FHA_1 | 737 | 743 | PF00498 | 0.501 |
LIG_FHA_2 | 585 | 591 | PF00498 | 0.501 |
LIG_FHA_2 | 766 | 772 | PF00498 | 0.595 |
LIG_GBD_Chelix_1 | 328 | 336 | PF00786 | 0.312 |
LIG_LIR_Apic_2 | 221 | 226 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 106 | 114 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 130 | 136 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 311 | 319 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 349 | 358 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 767 | 776 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 789 | 796 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 130 | 134 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 160 | 165 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 228 | 232 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 311 | 315 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 345 | 351 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 353 | 358 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 664 | 669 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 767 | 773 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 778 | 782 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 789 | 794 | PF02991 | 0.364 |
LIG_LRP6_Inhibitor_1 | 90 | 96 | PF00058 | 0.503 |
LIG_LYPXL_S_1 | 657 | 661 | PF13949 | 0.278 |
LIG_MLH1_MIPbox_1 | 677 | 681 | PF16413 | 0.555 |
LIG_PCNA_PIPBox_1 | 33 | 42 | PF02747 | 0.612 |
LIG_PCNA_PIPBox_1 | 651 | 660 | PF02747 | 0.497 |
LIG_PCNA_yPIPBox_3 | 28 | 40 | PF02747 | 0.632 |
LIG_PCNA_yPIPBox_3 | 644 | 658 | PF02747 | 0.512 |
LIG_Pex14_1 | 560 | 564 | PF04695 | 0.452 |
LIG_Pex14_1 | 676 | 680 | PF04695 | 0.518 |
LIG_Pex14_2 | 556 | 560 | PF04695 | 0.413 |
LIG_Pex14_2 | 677 | 681 | PF04695 | 0.555 |
LIG_PTB_Apo_2 | 451 | 458 | PF02174 | 0.523 |
LIG_RPA_C_Fungi | 617 | 629 | PF08784 | 0.551 |
LIG_RPA_C_Fungi | 639 | 651 | PF08784 | 0.350 |
LIG_SH2_CRK | 602 | 606 | PF00017 | 0.497 |
LIG_SH2_GRB2like | 547 | 550 | PF00017 | 0.490 |
LIG_SH2_NCK_1 | 196 | 200 | PF00017 | 0.484 |
LIG_SH2_SRC | 547 | 550 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 196 | 200 | PF00017 | 0.489 |
LIG_SH2_STAP1 | 337 | 341 | PF00017 | 0.469 |
LIG_SH2_STAT3 | 202 | 205 | PF00017 | 0.505 |
LIG_SH2_STAT3 | 358 | 361 | PF00017 | 0.493 |
LIG_SH2_STAT3 | 419 | 422 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 680 | 683 | PF00017 | 0.516 |
LIG_SUMO_SIM_par_1 | 270 | 276 | PF11976 | 0.463 |
LIG_SUMO_SIM_par_1 | 300 | 306 | PF11976 | 0.567 |
LIG_TRAF2_1 | 471 | 474 | PF00917 | 0.516 |
LIG_TRAF2_1 | 649 | 652 | PF00917 | 0.527 |
LIG_TRAF2_1 | 65 | 68 | PF00917 | 0.464 |
LIG_TYR_ITIM | 562 | 567 | PF00017 | 0.482 |
LIG_WRC_WIRS_1 | 585 | 590 | PF05994 | 0.431 |
LIG_WRC_WIRS_1 | 595 | 600 | PF05994 | 0.480 |
LIG_WRC_WIRS_1 | 658 | 663 | PF05994 | 0.276 |
MOD_CDC14_SPxK_1 | 401 | 404 | PF00782 | 0.554 |
MOD_CDK_SPxK_1 | 398 | 404 | PF00069 | 0.599 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.551 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.532 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.415 |
MOD_CK2_1 | 509 | 515 | PF00069 | 0.378 |
MOD_CK2_1 | 525 | 531 | PF00069 | 0.657 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.458 |
MOD_CK2_1 | 745 | 751 | PF00069 | 0.500 |
MOD_CK2_1 | 789 | 795 | PF00069 | 0.516 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.652 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.470 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.592 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.654 |
MOD_GlcNHglycan | 685 | 689 | PF01048 | 0.626 |
MOD_GlcNHglycan | 725 | 728 | PF01048 | 0.506 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.434 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.659 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.627 |
MOD_GSK3_1 | 696 | 703 | PF00069 | 0.621 |
MOD_GSK3_1 | 705 | 712 | PF00069 | 0.526 |
MOD_GSK3_1 | 732 | 739 | PF00069 | 0.662 |
MOD_GSK3_1 | 757 | 764 | PF00069 | 0.571 |
MOD_GSK3_1 | 794 | 801 | PF00069 | 0.548 |
MOD_N-GLC_1 | 343 | 348 | PF02516 | 0.568 |
MOD_N-GLC_1 | 52 | 57 | PF02516 | 0.571 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.722 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.544 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.667 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.626 |
MOD_NEK2_1 | 794 | 799 | PF00069 | 0.453 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.526 |
MOD_NEK2_2 | 350 | 355 | PF00069 | 0.490 |
MOD_PIKK_1 | 487 | 493 | PF00454 | 0.550 |
MOD_PIKK_1 | 765 | 771 | PF00454 | 0.620 |
MOD_PKA_1 | 814 | 820 | PF00069 | 0.585 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.556 |
MOD_PKA_2 | 444 | 450 | PF00069 | 0.566 |
MOD_PKA_2 | 509 | 515 | PF00069 | 0.343 |
MOD_PKA_2 | 709 | 715 | PF00069 | 0.501 |
MOD_PKA_2 | 723 | 729 | PF00069 | 0.505 |
MOD_PKA_2 | 757 | 763 | PF00069 | 0.576 |
MOD_PKA_2 | 814 | 820 | PF00069 | 0.567 |
MOD_PKB_1 | 340 | 348 | PF00069 | 0.567 |
MOD_Plk_1 | 80 | 86 | PF00069 | 0.533 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.417 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.498 |
MOD_Plk_4 | 509 | 515 | PF00069 | 0.343 |
MOD_Plk_4 | 657 | 663 | PF00069 | 0.360 |
MOD_Plk_4 | 745 | 751 | PF00069 | 0.532 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.507 |
MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.582 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.626 |
MOD_ProDKin_1 | 522 | 528 | PF00069 | 0.590 |
MOD_ProDKin_1 | 702 | 708 | PF00069 | 0.498 |
MOD_ProDKin_1 | 782 | 788 | PF00069 | 0.380 |
MOD_SUMO_for_1 | 565 | 568 | PF00179 | 0.371 |
TRG_DiLeu_BaEn_1 | 778 | 783 | PF01217 | 0.506 |
TRG_DiLeu_BaEn_4 | 652 | 658 | PF01217 | 0.539 |
TRG_DiLeu_BaLyEn_6 | 327 | 332 | PF01217 | 0.534 |
TRG_DiLeu_BaLyEn_6 | 481 | 486 | PF01217 | 0.542 |
TRG_DiLeu_BaLyEn_6 | 783 | 788 | PF01217 | 0.483 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 564 | 567 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 602 | 605 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 658 | 661 | PF00928 | 0.367 |
TRG_ER_diArg_1 | 18 | 21 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 483 | 485 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 621 | 624 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 757 | 759 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 815 | 818 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 84 | 86 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.607 |
TRG_NES_CRM1_1 | 108 | 123 | PF08389 | 0.556 |
TRG_NLS_MonoExtC_3 | 1 | 7 | PF00514 | 0.653 |
TRG_NLS_MonoExtC_3 | 813 | 818 | PF00514 | 0.556 |
TRG_NLS_MonoExtN_4 | 811 | 818 | PF00514 | 0.550 |
TRG_Pf-PMV_PEXEL_1 | 184 | 189 | PF00026 | 0.553 |
TRG_Pf-PMV_PEXEL_1 | 330 | 335 | PF00026 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 446 | 450 | PF00026 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 624 | 629 | PF00026 | 0.576 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P767 | Leptomonas seymouri | 74% | 99% |
A0A0S4JKT1 | Bodo saltans | 29% | 95% |
A0A1X0P0C5 | Trypanosomatidae | 43% | 100% |
A0A3Q8IHN6 | Leishmania donovani | 95% | 100% |
A0A3R7P515 | Trypanosoma rangeli | 43% | 100% |
A4HPU7 | Leishmania braziliensis | 87% | 100% |
A4IE46 | Leishmania infantum | 95% | 100% |
D0A493 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9ATL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
P63154 | Mus musculus | 23% | 100% |
P63155 | Rattus norvegicus | 23% | 100% |
P87312 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
Q4PB37 | Ustilago maydis (strain 521 / FGSC 9021) | 28% | 100% |
Q4WT84 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 25% | 100% |
Q5BDX1 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 26% | 100% |
Q5K654 | Paracoccidioides brasiliensis | 25% | 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 | 23% | 97% |
V5B545 | Trypanosoma cruzi | 43% | 100% |