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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 11 |
GO:0005730 | nucleolus | 5 | 12 |
GO:0030684 | preribosome | 3 | 11 |
GO:0030687 | preribosome, large subunit precursor | 4 | 11 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0043226 | organelle | 2 | 12 |
GO:0043228 | non-membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:1990904 | ribonucleoprotein complex | 2 | 11 |
GO:0070545 | PeBoW complex | 3 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A4H6F7
Term | Name | Level | Count |
---|---|---|---|
GO:0000460 | maturation of 5.8S rRNA | 9 | 11 |
GO:0000463 | maturation of LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 11 |
GO:0000466 | maturation of 5.8S rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 11 |
GO:0000470 | maturation of LSU-rRNA | 9 | 11 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006364 | rRNA processing | 8 | 12 |
GO:0006396 | RNA processing | 6 | 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:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0016072 | rRNA metabolic process | 7 | 12 |
GO:0034470 | ncRNA processing | 7 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 11 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 11 |
GO:0044877 | protein-containing complex binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 27 | 31 | PF00656 | 0.709 |
CLV_C14_Caspase3-7 | 484 | 488 | PF00656 | 0.697 |
CLV_C14_Caspase3-7 | 510 | 514 | PF00656 | 0.435 |
CLV_C14_Caspase3-7 | 70 | 74 | PF00656 | 0.565 |
CLV_C14_Caspase3-7 | 8 | 12 | PF00656 | 0.625 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.332 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 573 | 575 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 612 | 614 | PF00675 | 0.376 |
CLV_PCSK_FUR_1 | 505 | 509 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.194 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 507 | 509 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 612 | 614 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 655 | 657 | PF00082 | 0.374 |
CLV_PCSK_PC1ET2_1 | 403 | 405 | PF00082 | 0.396 |
CLV_PCSK_PC1ET2_1 | 507 | 509 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 566 | 568 | PF00082 | 0.394 |
CLV_PCSK_PC1ET2_1 | 655 | 657 | PF00082 | 0.374 |
CLV_PCSK_PC7_1 | 288 | 294 | PF00082 | 0.194 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 479 | 483 | PF00082 | 0.724 |
CLV_PCSK_SKI1_1 | 567 | 571 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 612 | 616 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 701 | 705 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 709 | 713 | PF00082 | 0.228 |
DEG_APCC_DBOX_1 | 111 | 119 | PF00400 | 0.315 |
DEG_APCC_DBOX_1 | 587 | 595 | PF00400 | 0.239 |
DOC_CDC14_PxL_1 | 453 | 461 | PF14671 | 0.586 |
DOC_CYCLIN_yClb1_LxF_4 | 356 | 361 | PF00134 | 0.299 |
DOC_CYCLIN_yCln2_LP_2 | 704 | 710 | PF00134 | 0.375 |
DOC_MAPK_DCC_7 | 701 | 710 | PF00069 | 0.379 |
DOC_MAPK_gen_1 | 317 | 326 | PF00069 | 0.299 |
DOC_MAPK_gen_1 | 329 | 337 | PF00069 | 0.299 |
DOC_MAPK_gen_1 | 517 | 525 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 555 | 564 | PF00069 | 0.352 |
DOC_MAPK_HePTP_8 | 314 | 326 | PF00069 | 0.299 |
DOC_MAPK_MEF2A_6 | 317 | 326 | PF00069 | 0.293 |
DOC_MAPK_MEF2A_6 | 519 | 527 | PF00069 | 0.375 |
DOC_MAPK_MEF2A_6 | 555 | 564 | PF00069 | 0.352 |
DOC_MAPK_MEF2A_6 | 701 | 710 | PF00069 | 0.379 |
DOC_MAPK_NFAT4_5 | 557 | 565 | PF00069 | 0.466 |
DOC_PP1_RVXF_1 | 356 | 362 | PF00149 | 0.299 |
DOC_PP2B_LxvP_1 | 454 | 457 | PF13499 | 0.431 |
DOC_PP2B_LxvP_1 | 704 | 707 | PF13499 | 0.369 |
DOC_PP4_FxxP_1 | 435 | 438 | PF00568 | 0.318 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.194 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.325 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.495 |
DOC_USP7_UBL2_3 | 105 | 109 | PF12436 | 0.381 |
DOC_USP7_UBL2_3 | 202 | 206 | PF12436 | 0.299 |
DOC_USP7_UBL2_3 | 551 | 555 | PF12436 | 0.398 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.472 |
LIG_14-3-3_CanoR_1 | 155 | 163 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 371 | 376 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 479 | 486 | PF00244 | 0.739 |
LIG_14-3-3_CanoR_1 | 656 | 664 | PF00244 | 0.381 |
LIG_APCC_ABBA_1 | 352 | 357 | PF00400 | 0.299 |
LIG_APCC_ABBA_1 | 37 | 42 | PF00400 | 0.542 |
LIG_APCC_ABBA_1 | 624 | 629 | PF00400 | 0.343 |
LIG_BIR_III_4 | 28 | 32 | PF00653 | 0.705 |
LIG_BRCT_BRCA1_1 | 431 | 435 | PF00533 | 0.336 |
LIG_CSL_BTD_1 | 721 | 724 | PF09270 | 0.458 |
LIG_eIF4E_1 | 699 | 705 | PF01652 | 0.400 |
LIG_EVH1_2 | 261 | 265 | PF00568 | 0.420 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.374 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.299 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.447 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.383 |
LIG_FHA_1 | 494 | 500 | PF00498 | 0.656 |
LIG_FHA_1 | 557 | 563 | PF00498 | 0.345 |
LIG_FHA_1 | 595 | 601 | PF00498 | 0.332 |
LIG_FHA_1 | 619 | 625 | PF00498 | 0.353 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.569 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.313 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.299 |
LIG_FHA_2 | 382 | 388 | PF00498 | 0.443 |
LIG_FHA_2 | 482 | 488 | PF00498 | 0.599 |
LIG_FHA_2 | 489 | 495 | PF00498 | 0.612 |
LIG_FHA_2 | 729 | 735 | PF00498 | 0.452 |
LIG_Integrin_isoDGR_2 | 57 | 59 | PF01839 | 0.656 |
LIG_LIR_Apic_2 | 266 | 271 | PF02991 | 0.299 |
LIG_LIR_Apic_2 | 432 | 438 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 130 | 138 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 300 | 309 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 430 | 438 | PF02991 | 0.335 |
LIG_LIR_LC3C_4 | 333 | 337 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 161 | 166 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 173 | 179 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 246 | 251 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 264 | 268 | PF02991 | 0.150 |
LIG_LIR_Nem_3 | 300 | 304 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 430 | 434 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 673 | 679 | PF02991 | 0.383 |
LIG_NRBOX | 114 | 120 | PF00104 | 0.299 |
LIG_Pex14_2 | 645 | 649 | PF04695 | 0.496 |
LIG_SH2_CRK | 132 | 136 | PF00017 | 0.315 |
LIG_SH2_CRK | 166 | 170 | PF00017 | 0.194 |
LIG_SH2_CRK | 268 | 272 | PF00017 | 0.314 |
LIG_SH2_CRK | 431 | 435 | PF00017 | 0.336 |
LIG_SH2_GRB2like | 250 | 253 | PF00017 | 0.356 |
LIG_SH2_NCK_1 | 431 | 435 | PF00017 | 0.336 |
LIG_SH2_SRC | 274 | 277 | PF00017 | 0.299 |
LIG_SH2_STAP1 | 431 | 435 | PF00017 | 0.336 |
LIG_SH2_STAP1 | 718 | 722 | PF00017 | 0.458 |
LIG_SH2_STAT3 | 394 | 397 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.716 |
LIG_SH2_STAT5 | 544 | 547 | PF00017 | 0.344 |
LIG_SH3_1 | 341 | 347 | PF00018 | 0.315 |
LIG_SH3_1 | 584 | 590 | PF00018 | 0.367 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.420 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.304 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.299 |
LIG_SH3_3 | 341 | 347 | PF00018 | 0.299 |
LIG_SH3_3 | 566 | 572 | PF00018 | 0.375 |
LIG_SH3_3 | 584 | 590 | PF00018 | 0.183 |
LIG_TRAF2_1 | 223 | 226 | PF00917 | 0.359 |
LIG_TYR_ITIM | 429 | 434 | PF00017 | 0.359 |
LIG_UBA3_1 | 342 | 350 | PF00899 | 0.334 |
LIG_UBA3_1 | 560 | 568 | PF00899 | 0.357 |
LIG_WRC_WIRS_1 | 437 | 442 | PF05994 | 0.409 |
LIG_WW_1 | 271 | 274 | PF00397 | 0.315 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.278 |
MOD_CK1_1 | 640 | 646 | PF00069 | 0.458 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.555 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.315 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.695 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.414 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.555 |
MOD_CK2_1 | 728 | 734 | PF00069 | 0.307 |
MOD_Cter_Amidation | 103 | 106 | PF01082 | 0.294 |
MOD_GlcNHglycan | 111 | 115 | PF01048 | 0.316 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.294 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.383 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.614 |
MOD_GlcNHglycan | 513 | 517 | PF01048 | 0.439 |
MOD_GlcNHglycan | 616 | 619 | PF01048 | 0.526 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.420 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.321 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.415 |
MOD_GSK3_1 | 614 | 621 | PF00069 | 0.393 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.349 |
MOD_LATS_1 | 362 | 368 | PF00433 | 0.420 |
MOD_N-GLC_1 | 155 | 160 | PF02516 | 0.299 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.420 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.356 |
MOD_NEK2_1 | 512 | 517 | PF00069 | 0.450 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.352 |
MOD_NEK2_1 | 593 | 598 | PF00069 | 0.352 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.493 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.569 |
MOD_NEK2_1 | 678 | 683 | PF00069 | 0.345 |
MOD_NEK2_2 | 127 | 132 | PF00069 | 0.299 |
MOD_PIKK_1 | 479 | 485 | PF00454 | 0.592 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.533 |
MOD_PK_1 | 371 | 377 | PF00069 | 0.334 |
MOD_PKA_1 | 574 | 580 | PF00069 | 0.421 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.420 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.329 |
MOD_PKA_2 | 556 | 562 | PF00069 | 0.351 |
MOD_Plk_1 | 110 | 116 | PF00069 | 0.375 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.420 |
MOD_Plk_1 | 429 | 435 | PF00069 | 0.339 |
MOD_Plk_1 | 447 | 453 | PF00069 | 0.379 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.432 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.420 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.327 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.351 |
MOD_Plk_4 | 640 | 646 | PF00069 | 0.434 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.334 |
MOD_SUMO_for_1 | 108 | 111 | PF00179 | 0.315 |
MOD_SUMO_rev_2 | 101 | 107 | PF00179 | 0.370 |
MOD_SUMO_rev_2 | 133 | 142 | PF00179 | 0.299 |
MOD_SUMO_rev_2 | 214 | 220 | PF00179 | 0.341 |
MOD_SUMO_rev_2 | 90 | 98 | PF00179 | 0.400 |
TRG_DiLeu_BaEn_1 | 103 | 108 | PF01217 | 0.294 |
TRG_DiLeu_BaEn_2 | 588 | 594 | PF01217 | 0.354 |
TRG_DiLeu_BaEn_2 | 628 | 634 | PF01217 | 0.368 |
TRG_DiLeu_BaLyEn_6 | 114 | 119 | PF01217 | 0.315 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.705 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 603 | 606 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 654 | 657 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 676 | 679 | PF00928 | 0.363 |
TRG_ER_diArg_1 | 208 | 210 | PF00400 | 0.301 |
TRG_ER_diArg_1 | 332 | 335 | PF00400 | 0.299 |
TRG_ER_diArg_1 | 612 | 614 | PF00400 | 0.380 |
TRG_NLS_MonoExtN_4 | 652 | 659 | PF00514 | 0.390 |
TRG_Pf-PMV_PEXEL_1 | 129 | 133 | PF00026 | 0.299 |
TRG_Pf-PMV_PEXEL_1 | 209 | 214 | PF00026 | 0.386 |
TRG_Pf-PMV_PEXEL_1 | 341 | 345 | PF00026 | 0.327 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I232 | Leptomonas seymouri | 90% | 90% |
A0A0S4IU17 | Bodo saltans | 69% | 93% |
A0A1X0NV50 | Trypanosomatidae | 77% | 91% |
A0A3S5H6I3 | Leishmania donovani | 94% | 92% |
A0A422NYV3 | Trypanosoma rangeli | 78% | 95% |
A0JMQ0 | Danio rerio | 34% | 96% |
A1CQI9 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 33% | 94% |
A1D3F5 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 33% | 94% |
A2QPZ4 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 33% | 94% |
A3LXF0 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 34% | 92% |
A4H6F7 | Leishmania braziliensis | 100% | 100% |
A4HUV2 | Leishmania infantum | 93% | 92% |
A4IHS2 | Xenopus tropicalis | 35% | 100% |
A4R0Q1 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 33% | 96% |
A5DBG1 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 34% | 94% |
A5DWF4 | Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) | 32% | 85% |
A6QX61 | Ajellomyces capsulatus (strain NAm1 / WU24) | 32% | 94% |
A6RRD4 | Botryotinia fuckeliana (strain B05.10) | 32% | 97% |
A6ZMA9 | Saccharomyces cerevisiae (strain YJM789) | 32% | 92% |
A8NWR2 | Coprinopsis cinerea (strain Okayama-7 / 130 / ATCC MYA-4618 / FGSC 9003) | 31% | 99% |
A8PWB6 | Brugia malayi | 29% | 100% |
A8QD31 | Malassezia globosa (strain ATCC MYA-4612 / CBS 7966) | 33% | 86% |
A8XYW9 | Caenorhabditis briggsae | 31% | 100% |
A9UZS7 | Monosiga brevicollis | 35% | 93% |
B0WC36 | Culex quinquefasciatus | 32% | 86% |
B0XQ42 | Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) | 33% | 93% |
B2AY28 | Podospora anserina (strain S / ATCC MYA-4624 / DSM 980 / FGSC 10383) | 32% | 95% |
B2VR76 | Pyrenophora tritici-repentis (strain Pt-1C-BFP) | 33% | 95% |
B3MHX6 | Drosophila ananassae | 33% | 94% |
B3NLK7 | Drosophila erecta | 34% | 95% |
B4GIU9 | Drosophila persimilis | 34% | 95% |
B4HN85 | Drosophila sechellia | 34% | 95% |
B4J9K1 | Drosophila grimshawi | 32% | 95% |
B4KQU8 | Drosophila mojavensis | 33% | 94% |
B4LKS9 | Drosophila virilis | 33% | 95% |
B4MYI5 | Drosophila willistoni | 33% | 96% |
B4P528 | Drosophila yakuba | 34% | 95% |
D0A7K2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 78% | 95% |
E9ANI7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 88% |
F4IH25 | Arabidopsis thaliana | 32% | 99% |
G0SCK6 | Chaetomium thermophilum (strain DSM 1495 / CBS 144.50 / IMI 039719) | 31% | 93% |
O74399 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 100% |
P0CS34 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 34% | 90% |
P0CS35 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 34% | 90% |
P97452 | Mus musculus | 34% | 100% |
Q04660 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 92% |
Q0CCP0 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 34% | 95% |
Q0D6V7 | Oryza sativa subsp. japonica | 35% | 100% |
Q0UN56 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 33% | 95% |
Q14137 | Homo sapiens | 34% | 100% |
Q17LZ2 | Aedes aegypti | 33% | 86% |
Q1DRB6 | Coccidioides immitis (strain RS) | 32% | 88% |
Q28XF0 | Drosophila pseudoobscura pseudoobscura | 34% | 95% |
Q2HDW0 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 32% | 95% |
Q2UPK0 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 32% | 95% |
Q4P2E9 | Ustilago maydis (strain 521 / FGSC 9021) | 31% | 80% |
Q4QH39 | Leishmania major | 93% | 100% |
Q4WTI3 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 33% | 93% |
Q54TD8 | Dictyostelium discoideum | 33% | 89% |
Q562C2 | Rattus norvegicus | 34% | 100% |
Q59VP7 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 32% | 88% |
Q5BDL3 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 33% | 94% |
Q6BRG6 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 33% | 92% |
Q6C4I9 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 34% | 91% |
Q6CIH3 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 32% | 94% |
Q6FLA4 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 32% | 92% |
Q75DC5 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 32% | 90% |
Q7K0Y1 | Drosophila melanogaster | 34% | 95% |
Q7PTC5 | Anopheles gambiae | 32% | 86% |
Q7SEM3 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 32% | 95% |
Q7T0W1 | Xenopus laevis | 35% | 100% |
Q7ZXX9 | Xenopus laevis | 34% | 100% |
Q9U2A9 | Caenorhabditis elegans | 30% | 100% |
V5BRK9 | Trypanosoma cruzi | 77% | 93% |