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: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: A4H3Z2
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 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.254 |
CLV_NRD_NRD_1 | 448 | 450 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 500 | 502 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 545 | 547 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 549 | 551 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 567 | 569 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 580 | 582 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 588 | 590 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 642 | 644 | PF00675 | 0.520 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.249 |
CLV_PCSK_KEX2_1 | 544 | 546 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 574 | 576 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 642 | 644 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.249 |
CLV_PCSK_PC1ET2_1 | 10 | 12 | PF00082 | 0.435 |
CLV_PCSK_PC1ET2_1 | 306 | 308 | PF00082 | 0.535 |
CLV_PCSK_PC1ET2_1 | 574 | 576 | PF00082 | 0.525 |
CLV_PCSK_PC1ET2_1 | 95 | 97 | PF00082 | 0.343 |
CLV_PCSK_PC7_1 | 638 | 644 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.183 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.224 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.224 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.213 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 546 | 550 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 609 | 613 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 651 | 655 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.323 |
DOC_CYCLIN_RxL_1 | 315 | 325 | PF00134 | 0.345 |
DOC_MAPK_gen_1 | 524 | 533 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 581 | 587 | PF00069 | 0.453 |
DOC_PP1_RVXF_1 | 210 | 216 | PF00149 | 0.249 |
DOC_PP1_RVXF_1 | 244 | 251 | PF00149 | 0.265 |
DOC_PP1_RVXF_1 | 320 | 327 | PF00149 | 0.480 |
DOC_PP1_RVXF_1 | 68 | 75 | PF00149 | 0.265 |
DOC_PP4_FxxP_1 | 150 | 153 | PF00568 | 0.249 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.409 |
DOC_USP7_UBL2_3 | 10 | 14 | PF12436 | 0.441 |
DOC_USP7_UBL2_3 | 652 | 656 | PF12436 | 0.499 |
DOC_USP7_UBL2_3 | 663 | 667 | PF12436 | 0.489 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.265 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.367 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 558 | 563 | PF00397 | 0.390 |
LIG_14-3-3_CanoR_1 | 117 | 121 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 322 | 327 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 517 | 525 | PF00244 | 0.481 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.590 |
LIG_BRCT_BRCA1_1 | 34 | 38 | PF00533 | 0.249 |
LIG_Clathr_ClatBox_1 | 249 | 253 | PF01394 | 0.284 |
LIG_Clathr_ClatBox_1 | 30 | 34 | PF01394 | 0.265 |
LIG_EH1_1 | 445 | 453 | PF00400 | 0.376 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.271 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.225 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.249 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.459 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.426 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.397 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.563 |
LIG_FHA_1 | 536 | 542 | PF00498 | 0.516 |
LIG_FHA_2 | 121 | 127 | PF00498 | 0.265 |
LIG_GLEBS_BUB3_1 | 471 | 479 | PF00400 | 0.430 |
LIG_IBAR_NPY_1 | 660 | 662 | PF08397 | 0.475 |
LIG_KLC1_Yacidic_2 | 239 | 243 | PF13176 | 0.249 |
LIG_LIR_Apic_2 | 378 | 382 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 193 | 204 | PF02991 | 0.249 |
LIG_LIR_Gen_1 | 236 | 245 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 193 | 199 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 236 | 240 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 319 | 324 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 455 | 459 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 659 | 665 | PF02991 | 0.521 |
LIG_MYND_1 | 365 | 369 | PF01753 | 0.424 |
LIG_PCNA_PIPBox_1 | 231 | 240 | PF02747 | 0.309 |
LIG_PCNA_yPIPBox_3 | 224 | 238 | PF02747 | 0.309 |
LIG_PTB_Apo_2 | 450 | 457 | PF02174 | 0.439 |
LIG_PTB_Phospho_1 | 450 | 456 | PF10480 | 0.435 |
LIG_RPA_C_Fungi | 540 | 552 | PF08784 | 0.505 |
LIG_SH2_CRK | 148 | 152 | PF00017 | 0.249 |
LIG_SH2_CRK | 596 | 600 | PF00017 | 0.432 |
LIG_SH2_CRK | 662 | 666 | PF00017 | 0.469 |
LIG_SH2_NCK_1 | 456 | 460 | PF00017 | 0.476 |
LIG_SH2_PTP2 | 232 | 235 | PF00017 | 0.249 |
LIG_SH2_PTP2 | 379 | 382 | PF00017 | 0.249 |
LIG_SH2_SRC | 440 | 443 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 204 | 208 | PF00017 | 0.297 |
LIG_SH2_STAP1 | 221 | 225 | PF00017 | 0.167 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.249 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.204 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.255 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.249 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.249 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.249 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.251 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.353 |
LIG_SH3_3 | 476 | 482 | PF00018 | 0.656 |
LIG_SH3_3 | 512 | 518 | PF00018 | 0.674 |
LIG_SH3_4 | 503 | 510 | PF00018 | 0.631 |
LIG_TRAF2_1 | 473 | 476 | PF00917 | 0.547 |
LIG_WRC_WIRS_1 | 234 | 239 | PF05994 | 0.339 |
MOD_CDK_SPxxK_3 | 149 | 156 | PF00069 | 0.343 |
MOD_CDK_SPxxK_3 | 558 | 565 | PF00069 | 0.385 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.260 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.249 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.524 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.362 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.355 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.249 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.249 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.249 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.434 |
MOD_CK2_1 | 470 | 476 | PF00069 | 0.514 |
MOD_CK2_1 | 490 | 496 | PF00069 | 0.598 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.358 |
MOD_Cter_Amidation | 649 | 652 | PF01082 | 0.563 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.265 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.555 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.544 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.516 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.474 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.265 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.569 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.299 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.335 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.249 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.384 |
MOD_N-GLC_1 | 355 | 360 | PF02516 | 0.265 |
MOD_N-GLC_2 | 342 | 344 | PF02516 | 0.384 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.343 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.269 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.284 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.523 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.265 |
MOD_NEK2_2 | 195 | 200 | PF00069 | 0.265 |
MOD_PKA_1 | 568 | 574 | PF00069 | 0.521 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.349 |
MOD_PKA_2 | 556 | 562 | PF00069 | 0.523 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.279 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.265 |
MOD_Plk_1 | 488 | 494 | PF00069 | 0.491 |
MOD_Plk_2-3 | 470 | 476 | PF00069 | 0.529 |
MOD_Plk_2-3 | 509 | 515 | PF00069 | 0.626 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.265 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.249 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.284 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.262 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.265 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.371 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.347 |
MOD_ProDKin_1 | 558 | 564 | PF00069 | 0.385 |
MOD_SUMO_for_1 | 12 | 15 | PF00179 | 0.265 |
MOD_SUMO_for_1 | 155 | 158 | PF00179 | 0.175 |
MOD_SUMO_for_1 | 208 | 211 | PF00179 | 0.343 |
MOD_SUMO_for_1 | 250 | 253 | PF00179 | 0.284 |
MOD_SUMO_rev_2 | 104 | 109 | PF00179 | 0.262 |
MOD_SUMO_rev_2 | 152 | 157 | PF00179 | 0.393 |
MOD_SUMO_rev_2 | 302 | 308 | PF00179 | 0.581 |
MOD_SUMO_rev_2 | 457 | 466 | PF00179 | 0.475 |
MOD_SUMO_rev_2 | 629 | 634 | PF00179 | 0.532 |
TRG_DiLeu_BaEn_1 | 447 | 452 | PF01217 | 0.382 |
TRG_DiLeu_BaEn_1 | 71 | 76 | PF01217 | 0.265 |
TRG_DiLeu_BaEn_2 | 242 | 248 | PF01217 | 0.249 |
TRG_DiLeu_BaLyEn_6 | 26 | 31 | PF01217 | 0.265 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.277 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.122 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 456 | 459 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 596 | 599 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 662 | 665 | PF00928 | 0.476 |
TRG_ER_diArg_1 | 212 | 215 | PF00400 | 0.249 |
TRG_ER_diArg_1 | 38 | 40 | PF00400 | 0.249 |
TRG_ER_diArg_1 | 544 | 546 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 642 | 645 | PF00400 | 0.517 |
TRG_NES_CRM1_1 | 243 | 255 | PF08389 | 0.339 |
TRG_NLS_Bipartite_1 | 4 | 22 | PF00514 | 0.265 |
TRG_NLS_Bipartite_1 | 574 | 593 | PF00514 | 0.476 |
TRG_NLS_MonoExtC_3 | 9 | 14 | PF00514 | 0.438 |
TRG_NLS_MonoExtN_4 | 16 | 22 | PF00514 | 0.265 |
TRG_Pf-PMV_PEXEL_1 | 29 | 34 | PF00026 | 0.249 |
TRG_Pf-PMV_PEXEL_1 | 307 | 311 | PF00026 | 0.550 |
TRG_Pf-PMV_PEXEL_1 | 651 | 655 | PF00026 | 0.526 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2Q9 | Leptomonas seymouri | 84% | 100% |
A0A0S4JN88 | Bodo saltans | 61% | 100% |
A0A1X0NKV4 | Trypanosomatidae | 69% | 100% |
A0A3R7LRI0 | Trypanosoma rangeli | 69% | 100% |
A0A3S5H5C9 | Leishmania donovani | 92% | 100% |
A1CHD1 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 30% | 99% |
A1CXF4 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 30% | 99% |
A4H3Z2 | Leishmania braziliensis | 100% | 100% |
A4HS78 | Leishmania infantum | 92% | 100% |
A4RLI4 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 30% | 99% |
A5DGY0 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 31% | 100% |
A5DYS6 | Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) | 30% | 100% |
A6SK81 | Botryotinia fuckeliana (strain B05.10) | 29% | 99% |
A7EGB5 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 31% | 99% |
A7TSA8 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 33% | 100% |
A8N1X3 | Coprinopsis cinerea (strain Okayama-7 / 130 / ATCC MYA-4618 / FGSC 9003) | 30% | 100% |
A9URZ4 | Monosiga brevicollis | 30% | 100% |
B0CQL7 | Laccaria bicolor (strain S238N-H82 / ATCC MYA-4686) | 31% | 100% |
B0Y612 | Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) | 30% | 99% |
B2WBA7 | Pyrenophora tritici-repentis (strain Pt-1C-BFP) | 29% | 99% |
C9ZY72 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 67% | 100% |
E9AK64 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
O60164 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |
O97209 | Leishmania major | 92% | 100% |
P0CP58 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 29% | 100% |
P0CP59 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 29% | 100% |
Q0CLP9 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 31% | 99% |
Q0V577 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 29% | 99% |
Q1DLJ4 | Coccidioides immitis (strain RS) | 30% | 97% |
Q2HCV1 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 29% | 100% |
Q2UGQ8 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 31% | 98% |
Q4WP65 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 30% | 99% |
Q59X38 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 31% | 100% |
Q5B6K3 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 31% | 99% |
Q6CDK0 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 31% | 100% |
Q6CQQ1 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 31% | 100% |
Q6FSU1 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 32% | 100% |
Q75EI5 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 31% | 100% |
Q7R7N4 | Plasmodium yoelii yoelii | 23% | 100% |
Q851S7 | Oryza sativa subsp. japonica | 32% | 100% |
Q9LYK7 | Arabidopsis thaliana | 33% | 100% |
V5AY93 | Trypanosoma cruzi | 69% | 100% |