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:0031251 | PAN complex | 2 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0000932 | P-body | 5 | 1 |
GO:0035770 | ribonucleoprotein granule | 3 | 1 |
GO:0036464 | cytoplasmic ribonucleoprotein granule | 4 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HK53
Term | Name | Level | Count |
---|---|---|---|
GO:0000289 | nuclear-transcribed mRNA poly(A) tail shortening | 8 | 12 |
GO:0000956 | nuclear-transcribed mRNA catabolic process | 7 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006397 | mRNA processing | 7 | 12 |
GO:0006401 | RNA catabolic process | 5 | 12 |
GO:0006402 | mRNA catabolic process | 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:0009056 | catabolic process | 2 | 12 |
GO:0009057 | macromolecule catabolic process | 4 | 12 |
GO:0009892 | negative regulation of metabolic process | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0010468 | regulation of gene expression | 5 | 12 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 12 |
GO:0010629 | negative regulation of gene expression | 6 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0016071 | mRNA metabolic process | 6 | 12 |
GO:0019222 | regulation of metabolic process | 3 | 12 |
GO:0019439 | aromatic compound catabolic process | 4 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044248 | cellular catabolic process | 3 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 12 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0046700 | heterocycle catabolic process | 4 | 12 |
GO:0048519 | negative regulation of biological process | 3 | 12 |
GO:0050789 | regulation of biological process | 2 | 12 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 12 |
GO:0065007 | biological regulation | 1 | 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:1901361 | organic cyclic compound catabolic process | 4 | 12 |
GO:1901575 | organic substance catabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003727 | single-stranded RNA binding | 5 | 1 |
GO:0008143 | poly(A) binding | 7 | 1 |
GO:0070717 | poly-purine tract binding | 6 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.270 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.566 |
CLV_PCSK_FUR_1 | 79 | 83 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.270 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.219 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.441 |
DEG_APCC_DBOX_1 | 448 | 456 | PF00400 | 0.454 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.578 |
DEG_SCF_FBW7_1 | 55 | 61 | PF00400 | 0.560 |
DOC_CKS1_1 | 52 | 57 | PF01111 | 0.478 |
DOC_CKS1_1 | 72 | 77 | PF01111 | 0.332 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 284 | 293 | PF00134 | 0.460 |
DOC_CYCLIN_yCln2_LP_2 | 372 | 378 | PF00134 | 0.512 |
DOC_MAPK_gen_1 | 133 | 140 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 153 | 163 | PF00069 | 0.190 |
DOC_MAPK_gen_1 | 360 | 370 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 133 | 140 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 360 | 368 | PF00069 | 0.408 |
DOC_MAPK_NFAT4_5 | 363 | 371 | PF00069 | 0.450 |
DOC_PP1_RVXF_1 | 365 | 371 | PF00149 | 0.408 |
DOC_PP4_FxxP_1 | 22 | 25 | PF00568 | 0.623 |
DOC_PP4_FxxP_1 | 63 | 66 | PF00568 | 0.505 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.431 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.371 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.318 |
LIG_14-3-3_CanoR_1 | 201 | 209 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 260 | 265 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 333 | 337 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 473 | 477 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 69 | 75 | PF00244 | 0.487 |
LIG_Actin_RPEL_3 | 238 | 257 | PF02755 | 0.424 |
LIG_AP2alpha_2 | 49 | 51 | PF02296 | 0.613 |
LIG_BRCT_BRCA1_1 | 18 | 22 | PF00533 | 0.641 |
LIG_BRCT_BRCA1_1 | 305 | 309 | PF00533 | 0.343 |
LIG_BRCT_BRCA1_1 | 59 | 63 | PF00533 | 0.429 |
LIG_BRCT_BRCA1_1 | 88 | 92 | PF00533 | 0.352 |
LIG_eIF4E_1 | 155 | 161 | PF01652 | 0.318 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.341 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.285 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.255 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.395 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.653 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.534 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.483 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.342 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.579 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.383 |
LIG_FHA_2 | 313 | 319 | PF00498 | 0.439 |
LIG_FHA_2 | 465 | 471 | PF00498 | 0.608 |
LIG_Integrin_isoDGR_2 | 358 | 360 | PF01839 | 0.208 |
LIG_LIR_Apic_2 | 19 | 25 | PF02991 | 0.588 |
LIG_LIR_Apic_2 | 60 | 66 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 308 | 317 | PF02991 | 0.309 |
LIG_LIR_Gen_1 | 444 | 452 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 453 | 463 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 93 | 101 | PF02991 | 0.417 |
LIG_LIR_LC3C_4 | 439 | 443 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 182 | 186 | PF02991 | 0.208 |
LIG_LIR_Nem_3 | 306 | 312 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 410 | 414 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 444 | 448 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 453 | 459 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 54 | 59 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 89 | 95 | PF02991 | 0.332 |
LIG_MYND_1 | 158 | 162 | PF01753 | 0.294 |
LIG_NRBOX | 214 | 220 | PF00104 | 0.407 |
LIG_NRBOX | 252 | 258 | PF00104 | 0.433 |
LIG_PCNA_yPIPBox_3 | 354 | 365 | PF02747 | 0.408 |
LIG_Pex14_1 | 411 | 415 | PF04695 | 0.408 |
LIG_Pex14_2 | 305 | 309 | PF04695 | 0.347 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.246 |
LIG_SH2_CRK | 415 | 419 | PF00017 | 0.475 |
LIG_SH2_CRK | 56 | 60 | PF00017 | 0.415 |
LIG_SH2_CRK | 95 | 99 | PF00017 | 0.333 |
LIG_SH2_NCK_1 | 56 | 60 | PF00017 | 0.415 |
LIG_SH2_NCK_1 | 95 | 99 | PF00017 | 0.333 |
LIG_SH2_STAP1 | 95 | 99 | PF00017 | 0.352 |
LIG_SH2_STAT3 | 29 | 32 | PF00017 | 0.609 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.243 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.624 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.333 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.492 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.574 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.574 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.526 |
LIG_SUMO_SIM_anti_2 | 439 | 444 | PF11976 | 0.410 |
LIG_SUMO_SIM_par_1 | 434 | 444 | PF11976 | 0.417 |
LIG_TRAF2_1 | 168 | 171 | PF00917 | 0.458 |
LIG_TYR_ITIM | 443 | 448 | PF00017 | 0.408 |
LIG_TYR_ITSM | 52 | 59 | PF00017 | 0.480 |
LIG_WRC_WIRS_1 | 208 | 213 | PF05994 | 0.263 |
LIG_WRC_WIRS_1 | 219 | 224 | PF05994 | 0.268 |
LIG_WRC_WIRS_1 | 293 | 298 | PF05994 | 0.535 |
MOD_CDK_SPxxK_3 | 62 | 69 | PF00069 | 0.430 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.542 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.481 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.518 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.596 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.401 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.422 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.448 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.437 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.475 |
MOD_Cter_Amidation | 199 | 202 | PF01082 | 0.500 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.438 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.384 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.420 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.450 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.415 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.429 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.358 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.548 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.436 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.404 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.250 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.542 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.366 |
MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.644 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.281 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.353 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.281 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.270 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.539 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.313 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.301 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.454 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.442 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.484 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.453 |
MOD_NEK2_2 | 58 | 63 | PF00069 | 0.512 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.433 |
MOD_PIKK_1 | 303 | 309 | PF00454 | 0.487 |
MOD_PIKK_1 | 347 | 353 | PF00454 | 0.432 |
MOD_PKA_1 | 201 | 207 | PF00069 | 0.392 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.361 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.333 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.408 |
MOD_PKA_2 | 472 | 478 | PF00069 | 0.580 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.529 |
MOD_Plk_1 | 425 | 431 | PF00069 | 0.528 |
MOD_Plk_2-3 | 332 | 338 | PF00069 | 0.408 |
MOD_Plk_2-3 | 422 | 428 | PF00069 | 0.401 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.334 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.576 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.410 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.499 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.318 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.413 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.472 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.490 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.355 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.566 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.512 |
MOD_ProDKin_1 | 474 | 480 | PF00069 | 0.543 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.503 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.368 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.323 |
MOD_SUMO_for_1 | 140 | 143 | PF00179 | 0.484 |
MOD_SUMO_for_1 | 291 | 294 | PF00179 | 0.449 |
MOD_SUMO_rev_2 | 102 | 108 | PF00179 | 0.441 |
TRG_DiLeu_BaEn_1 | 427 | 432 | PF01217 | 0.408 |
TRG_DiLeu_BaLyEn_6 | 360 | 365 | PF01217 | 0.503 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 415 | 418 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 445 | 448 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.318 |
TRG_ER_diArg_1 | 132 | 134 | PF00400 | 0.270 |
TRG_ER_diArg_1 | 78 | 81 | PF00400 | 0.553 |
TRG_NES_CRM1_1 | 129 | 144 | PF08389 | 0.451 |
TRG_NES_CRM1_1 | 325 | 337 | PF08389 | 0.450 |
TRG_Pf-PMV_PEXEL_1 | 190 | 194 | PF00026 | 0.368 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9X4 | Leptomonas seymouri | 91% | 100% |
A0A0S4KIQ3 | Bodo saltans | 49% | 88% |
A0A1X0NUP4 | Trypanosomatidae | 58% | 95% |
A0A3Q8IFR4 | Leishmania donovani | 96% | 100% |
A0A422NJH8 | Trypanosoma rangeli | 57% | 95% |
A1CP31 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 26% | 73% |
A1D1Y5 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 26% | 73% |
A2QAQ3 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 27% | 72% |
A3LQL9 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 28% | 76% |
A4I7N9 | Leishmania infantum | 96% | 100% |
A5DCP8 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 28% | 78% |
D0A9U0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 94% |
E9B2J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
G0S0Y3 | Chaetomium thermophilum (strain DSM 1495 / CBS 144.50 / IMI 039719) | 27% | 75% |
O13865 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 71% |
P0CP50 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 26% | 70% |
P0CP51 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 26% | 70% |
P34653 | Caenorhabditis elegans | 24% | 76% |
P36102 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 71% |
Q0D0A1 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 27% | 74% |
Q0V0I4 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 24% | 72% |
Q1E2S2 | Coccidioides immitis (strain RS) | 27% | 73% |
Q2H401 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 27% | 74% |
Q2KFH6 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 25% | 71% |
Q2U0M4 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 27% | 73% |
Q4Q5L0 | Leishmania major | 96% | 100% |
Q5AK10 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 25% | 69% |
Q5BFB1 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 26% | 73% |
Q6BRV5 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 27% | 73% |
Q6CBZ0 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 26% | 72% |
Q6CP23 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 24% | 73% |
Q6FKP2 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 28% | 67% |
Q6MY57 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 25% | 73% |
Q75BU9 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 25% | 79% |
Q7SDP4 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 26% | 73% |
Q9UST1 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 82% |
V5BAR3 | Trypanosoma cruzi | 57% | 95% |