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: E9ATL2
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 | 0.674 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 480 | 482 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 618 | 620 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 629 | 631 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 755 | 757 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 812 | 814 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.474 |
CLV_PCSK_FUR_1 | 73 | 77 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 480 | 482 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 618 | 620 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 629 | 631 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 755 | 757 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 811 | 813 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.350 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.570 |
CLV_PCSK_PC1ET2_1 | 75 | 77 | PF00082 | 0.424 |
CLV_PCSK_PC1ET2_1 | 811 | 813 | PF00082 | 0.558 |
CLV_PCSK_PC7_1 | 213 | 219 | PF00082 | 0.374 |
CLV_PCSK_PC7_1 | 625 | 631 | PF00082 | 0.471 |
CLV_PCSK_PC7_1 | 751 | 757 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 740 | 744 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 808 | 812 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 815 | 819 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.513 |
CLV_Separin_Metazoa | 570 | 574 | PF03568 | 0.419 |
DEG_APCC_DBOX_1 | 640 | 648 | PF00400 | 0.502 |
DEG_APCC_DBOX_1 | 739 | 747 | PF00400 | 0.505 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.575 |
DOC_ANK_TNKS_1 | 316 | 323 | PF00023 | 0.494 |
DOC_CKS1_1 | 223 | 228 | PF01111 | 0.390 |
DOC_CYCLIN_RxL_1 | 477 | 487 | PF00134 | 0.491 |
DOC_MAPK_gen_1 | 772 | 781 | PF00069 | 0.494 |
DOC_PP1_RVXF_1 | 754 | 761 | PF00149 | 0.616 |
DOC_PP2B_LxvP_1 | 408 | 411 | PF13499 | 0.549 |
DOC_PP4_FxxP_1 | 223 | 226 | PF00568 | 0.393 |
DOC_PP4_FxxP_1 | 49 | 52 | PF00568 | 0.631 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.377 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.647 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 519 | 524 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 699 | 704 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 779 | 784 | PF00397 | 0.327 |
LIG_14-3-3_CanoR_1 | 150 | 159 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 288 | 292 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 342 | 352 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 366 | 374 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 442 | 446 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 591 | 596 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 707 | 715 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 755 | 759 | PF00244 | 0.602 |
LIG_APCC_ABBA_1 | 118 | 123 | PF00400 | 0.507 |
LIG_APCC_ABBA_1 | 334 | 339 | PF00400 | 0.525 |
LIG_APCC_ABBA_1 | 493 | 498 | PF00400 | 0.433 |
LIG_APCC_ABBAyCdc20_2 | 20 | 26 | PF00400 | 0.521 |
LIG_BIR_III_2 | 189 | 193 | PF00653 | 0.514 |
LIG_BRCT_BRCA1_1 | 136 | 140 | PF00533 | 0.443 |
LIG_BRCT_BRCA1_1 | 674 | 678 | PF00533 | 0.434 |
LIG_deltaCOP1_diTrp_1 | 786 | 791 | PF00928 | 0.365 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.465 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.758 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.410 |
LIG_FHA_1 | 734 | 740 | PF00498 | 0.407 |
LIG_FHA_2 | 432 | 438 | PF00498 | 0.279 |
LIG_FHA_2 | 582 | 588 | PF00498 | 0.340 |
LIG_FHA_2 | 644 | 650 | PF00498 | 0.434 |
LIG_FHA_2 | 763 | 769 | PF00498 | 0.588 |
LIG_LIR_Apic_2 | 221 | 226 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 106 | 114 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 130 | 136 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 311 | 319 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 349 | 358 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 764 | 773 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 786 | 793 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 130 | 134 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 160 | 165 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 228 | 232 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 311 | 315 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 345 | 351 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 661 | 666 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 764 | 770 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 775 | 779 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 786 | 791 | PF02991 | 0.383 |
LIG_LRP6_Inhibitor_1 | 90 | 96 | PF00058 | 0.472 |
LIG_MLH1_MIPbox_1 | 674 | 678 | PF16413 | 0.434 |
LIG_PCNA_PIPBox_1 | 33 | 42 | PF02747 | 0.488 |
LIG_PCNA_PIPBox_1 | 648 | 657 | PF02747 | 0.461 |
LIG_PCNA_yPIPBox_3 | 28 | 40 | PF02747 | 0.510 |
LIG_PCNA_yPIPBox_3 | 641 | 655 | PF02747 | 0.466 |
LIG_Pex14_1 | 557 | 561 | PF04695 | 0.410 |
LIG_Pex14_1 | 673 | 677 | PF04695 | 0.490 |
LIG_Pex14_2 | 553 | 557 | PF04695 | 0.371 |
LIG_Pex14_2 | 674 | 678 | PF04695 | 0.434 |
LIG_PTB_Apo_2 | 448 | 455 | PF02174 | 0.490 |
LIG_RPA_C_Fungi | 614 | 626 | PF08784 | 0.427 |
LIG_SH2_CRK | 599 | 603 | PF00017 | 0.467 |
LIG_SH2_CRK | 655 | 659 | PF00017 | 0.418 |
LIG_SH2_GRB2like | 544 | 547 | PF00017 | 0.462 |
LIG_SH2_NCK_1 | 196 | 200 | PF00017 | 0.446 |
LIG_SH2_SRC | 544 | 547 | PF00017 | 0.462 |
LIG_SH2_STAP1 | 196 | 200 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 337 | 341 | PF00017 | 0.454 |
LIG_SH2_STAP1 | 655 | 659 | PF00017 | 0.355 |
LIG_SH2_STAT3 | 202 | 205 | PF00017 | 0.473 |
LIG_SH2_STAT3 | 358 | 361 | PF00017 | 0.462 |
LIG_SH2_STAT3 | 416 | 419 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 536 | 539 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 677 | 680 | PF00017 | 0.490 |
LIG_SH3_2 | 396 | 401 | PF14604 | 0.310 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.527 |
LIG_SUMO_SIM_par_1 | 270 | 276 | PF11976 | 0.413 |
LIG_TRAF2_1 | 468 | 471 | PF00917 | 0.479 |
LIG_TRAF2_1 | 646 | 649 | PF00917 | 0.487 |
LIG_TRAF2_1 | 65 | 68 | PF00917 | 0.406 |
LIG_TYR_ITIM | 559 | 564 | PF00017 | 0.448 |
LIG_WRC_WIRS_1 | 582 | 587 | PF05994 | 0.372 |
LIG_WRC_WIRS_1 | 592 | 597 | PF05994 | 0.429 |
MOD_CDC14_SPxK_1 | 398 | 401 | PF00782 | 0.532 |
MOD_CDK_SPxK_1 | 395 | 401 | PF00069 | 0.574 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.519 |
MOD_CK1_1 | 699 | 705 | PF00069 | 0.565 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.374 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.278 |
MOD_CK2_1 | 522 | 528 | PF00069 | 0.644 |
MOD_CK2_1 | 581 | 587 | PF00069 | 0.502 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.401 |
MOD_CK2_1 | 643 | 649 | PF00069 | 0.443 |
MOD_CK2_1 | 742 | 748 | PF00069 | 0.463 |
MOD_CK2_1 | 786 | 792 | PF00069 | 0.455 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.392 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.543 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.620 |
MOD_GlcNHglycan | 682 | 686 | PF01048 | 0.600 |
MOD_GlcNHglycan | 722 | 725 | PF01048 | 0.485 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.461 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.381 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.415 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.666 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.634 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.589 |
MOD_GSK3_1 | 693 | 700 | PF00069 | 0.620 |
MOD_GSK3_1 | 702 | 709 | PF00069 | 0.495 |
MOD_GSK3_1 | 750 | 757 | PF00069 | 0.497 |
MOD_GSK3_1 | 758 | 765 | PF00069 | 0.551 |
MOD_GSK3_1 | 791 | 798 | PF00069 | 0.480 |
MOD_N-GLC_1 | 343 | 348 | PF02516 | 0.450 |
MOD_N-GLC_1 | 52 | 57 | PF02516 | 0.521 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.697 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.524 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.425 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.652 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.295 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.298 |
MOD_NEK2_1 | 791 | 796 | PF00069 | 0.421 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.492 |
MOD_NEK2_2 | 287 | 292 | PF00069 | 0.255 |
MOD_PIKK_1 | 474 | 480 | PF00454 | 0.471 |
MOD_PIKK_1 | 762 | 768 | PF00454 | 0.533 |
MOD_PKA_1 | 342 | 348 | PF00069 | 0.394 |
MOD_PKA_1 | 811 | 817 | PF00069 | 0.559 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.409 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.522 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.446 |
MOD_PKA_2 | 706 | 712 | PF00069 | 0.492 |
MOD_PKA_2 | 720 | 726 | PF00069 | 0.568 |
MOD_PKA_2 | 750 | 756 | PF00069 | 0.538 |
MOD_PKA_2 | 811 | 817 | PF00069 | 0.540 |
MOD_PKB_1 | 340 | 348 | PF00069 | 0.454 |
MOD_PKB_1 | 366 | 374 | PF00069 | 0.426 |
MOD_Plk_1 | 496 | 502 | PF00069 | 0.226 |
MOD_Plk_1 | 80 | 86 | PF00069 | 0.498 |
MOD_Plk_2-3 | 643 | 649 | PF00069 | 0.369 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.389 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.474 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.239 |
MOD_Plk_4 | 654 | 660 | PF00069 | 0.336 |
MOD_Plk_4 | 742 | 748 | PF00069 | 0.421 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.476 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.710 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.589 |
MOD_ProDKin_1 | 519 | 525 | PF00069 | 0.491 |
MOD_ProDKin_1 | 699 | 705 | PF00069 | 0.459 |
MOD_ProDKin_1 | 779 | 785 | PF00069 | 0.330 |
MOD_SUMO_for_1 | 562 | 565 | PF00179 | 0.318 |
TRG_DiLeu_BaEn_1 | 775 | 780 | PF01217 | 0.484 |
TRG_DiLeu_BaEn_4 | 649 | 655 | PF01217 | 0.405 |
TRG_DiLeu_BaLyEn_6 | 300 | 305 | PF01217 | 0.521 |
TRG_DiLeu_BaLyEn_6 | 478 | 483 | PF01217 | 0.494 |
TRG_DiLeu_BaLyEn_6 | 780 | 785 | PF01217 | 0.456 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 561 | 564 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 599 | 602 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 655 | 658 | PF00928 | 0.303 |
TRG_ER_diArg_1 | 18 | 21 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.373 |
TRG_ER_diArg_1 | 480 | 482 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 618 | 621 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 754 | 756 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 812 | 815 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 84 | 86 | PF00400 | 0.513 |
TRG_NES_CRM1_1 | 108 | 123 | PF08389 | 0.430 |
TRG_NLS_MonoExtC_3 | 1 | 7 | PF00514 | 0.611 |
TRG_NLS_MonoExtC_3 | 810 | 815 | PF00514 | 0.534 |
TRG_NLS_MonoExtN_4 | 808 | 815 | PF00514 | 0.527 |
TRG_Pf-PMV_PEXEL_1 | 184 | 189 | PF00026 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 443 | 447 | PF00026 | 0.516 |
TRG_Pf-PMV_PEXEL_1 | 621 | 626 | PF00026 | 0.533 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P767 | Leptomonas seymouri | 74% | 99% |
A0A0S4JKT1 | Bodo saltans | 29% | 94% |
A0A1X0P0C5 | Trypanosomatidae | 43% | 100% |
A0A3Q8IHN6 | Leishmania donovani | 93% | 100% |
A0A3R7P515 | Trypanosoma rangeli | 42% | 100% |
A4HPU7 | Leishmania braziliensis | 87% | 100% |
A4IE46 | Leishmania infantum | 93% | 100% |
D0A493 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
P63154 | Mus musculus | 25% | 100% |
P63155 | Rattus norvegicus | 25% | 100% |
Q4PB37 | Ustilago maydis (strain 521 / FGSC 9021) | 28% | 100% |
Q4Q0Y6 | Leishmania major | 92% | 100% |
Q4WT84 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 27% | 100% |
Q527H0 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 25% | 100% |
Q5BDX1 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 27% | 100% |
Q5K654 | Paracoccidioides brasiliensis | 26% | 100% |
Q6CJK2 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 22% | 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% |