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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000177 | cytoplasmic exosome (RNase complex) | 5 | 2 |
GO:0000178 | exosome (RNase complex) | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0045025 | mitochondrial degradosome | 3 | 2 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1905354 | exoribonuclease complex | 3 | 2 |
GO:0005739 | mitochondrion | 5 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005759 | mitochondrial matrix | 5 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
Related structures:
AlphaFold database: Q4Q2T3
Term | Name | Level | Count |
---|---|---|---|
GO:0000959 | mitochondrial RNA metabolic process | 6 | 2 |
GO:0000963 | mitochondrial RNA processing | 6 | 2 |
GO:0000965 | mitochondrial RNA 3'-end processing | 7 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006401 | RNA catabolic process | 5 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010467 | gene expression | 4 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0019439 | aromatic compound catabolic process | 4 | 2 |
GO:0031123 | RNA 3'-end processing | 7 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 2 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0046700 | heterocycle catabolic process | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:0140053 | mitochondrial gene expression | 5 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003724 | RNA helicase activity | 3 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004386 | helicase activity | 2 | 13 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 13 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 13 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 13 |
GO:0140657 | ATP-dependent activity | 1 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
GO:0016887 | ATP hydrolysis activity | 7 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 287 | 291 | PF00656 | 0.399 |
CLV_MEL_PAP_1 | 623 | 629 | PF00089 | 0.241 |
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 391 | 393 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.468 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.420 |
CLV_PCSK_PC1ET2_1 | 251 | 253 | PF00082 | 0.431 |
CLV_PCSK_PC7_1 | 104 | 110 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 512 | 516 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 532 | 536 | PF00082 | 0.232 |
CLV_Separin_Metazoa | 522 | 526 | PF03568 | 0.506 |
DEG_APCC_DBOX_1 | 241 | 249 | PF00400 | 0.497 |
DEG_APCC_DBOX_1 | 288 | 296 | PF00400 | 0.433 |
DOC_CYCLIN_RxL_1 | 509 | 519 | PF00134 | 0.467 |
DOC_CYCLIN_RxL_1 | 522 | 531 | PF00134 | 0.450 |
DOC_CYCLIN_RxL_1 | 633 | 643 | PF00134 | 0.504 |
DOC_MAPK_gen_1 | 153 | 162 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 251 | 258 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 282 | 288 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 251 | 258 | PF00069 | 0.395 |
DOC_MAPK_MEF2A_6 | 474 | 483 | PF00069 | 0.529 |
DOC_PP1_RVXF_1 | 530 | 536 | PF00149 | 0.420 |
DOC_PP2B_LxvP_1 | 213 | 216 | PF13499 | 0.299 |
DOC_SPAK_OSR1_1 | 567 | 571 | PF12202 | 0.435 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.345 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.436 |
DOC_USP7_UBL2_3 | 393 | 397 | PF12436 | 0.411 |
DOC_USP7_UBL2_3 | 86 | 90 | PF12436 | 0.523 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.320 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.435 |
LIG_14-3-3_CanoR_1 | 385 | 394 | PF00244 | 0.345 |
LIG_14-3-3_CanoR_1 | 427 | 431 | PF00244 | 0.345 |
LIG_14-3-3_CanoR_1 | 474 | 479 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 525 | 530 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 626 | 632 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 77 | 84 | PF00244 | 0.499 |
LIG_Actin_WH2_2 | 503 | 518 | PF00022 | 0.442 |
LIG_APCC_ABBA_1 | 462 | 467 | PF00400 | 0.496 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.315 |
LIG_BRCT_BRCA1_1 | 413 | 417 | PF00533 | 0.491 |
LIG_BRCT_BRCA1_1 | 501 | 505 | PF00533 | 0.400 |
LIG_BRCT_BRCA1_1 | 56 | 60 | PF00533 | 0.265 |
LIG_BRCT_BRCA1_1 | 623 | 627 | PF00533 | 0.494 |
LIG_BRCT_BRCA1_2 | 623 | 629 | PF00533 | 0.522 |
LIG_deltaCOP1_diTrp_1 | 203 | 208 | PF00928 | 0.313 |
LIG_deltaCOP1_diTrp_1 | 53 | 60 | PF00928 | 0.503 |
LIG_eIF4E_1 | 100 | 106 | PF01652 | 0.463 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.289 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.439 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.422 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.293 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.373 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.362 |
LIG_FHA_1 | 528 | 534 | PF00498 | 0.496 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.475 |
LIG_FHA_1 | 643 | 649 | PF00498 | 0.459 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.463 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.341 |
LIG_FHA_2 | 606 | 612 | PF00498 | 0.367 |
LIG_FHA_2 | 628 | 634 | PF00498 | 0.522 |
LIG_LIR_Apic_2 | 134 | 140 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 275 | 285 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 487 | 497 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 618 | 627 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 79 | 88 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 275 | 280 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 300 | 304 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 487 | 491 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 618 | 623 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 79 | 84 | PF02991 | 0.512 |
LIG_PCNA_yPIPBox_3 | 318 | 327 | PF02747 | 0.487 |
LIG_PCNA_yPIPBox_3 | 380 | 393 | PF02747 | 0.372 |
LIG_PCNA_yPIPBox_3 | 612 | 623 | PF02747 | 0.484 |
LIG_Pex14_1 | 56 | 60 | PF04695 | 0.480 |
LIG_Pex14_2 | 627 | 631 | PF04695 | 0.424 |
LIG_PTB_Apo_2 | 231 | 238 | PF02174 | 0.446 |
LIG_PTB_Phospho_1 | 231 | 237 | PF10480 | 0.442 |
LIG_SH2_CRK | 137 | 141 | PF00017 | 0.307 |
LIG_SH2_GRB2like | 326 | 329 | PF00017 | 0.415 |
LIG_SH2_SRC | 326 | 329 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 537 | 540 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 620 | 623 | PF00017 | 0.424 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.458 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.352 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.385 |
LIG_SUMO_SIM_anti_2 | 72 | 77 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 254 | 259 | PF11976 | 0.422 |
LIG_SUMO_SIM_par_1 | 284 | 290 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 477 | 484 | PF11976 | 0.526 |
LIG_UBA3_1 | 464 | 472 | PF00899 | 0.502 |
LIG_WRC_WIRS_1 | 298 | 303 | PF05994 | 0.238 |
MOD_CDK_SPxK_1 | 360 | 366 | PF00069 | 0.533 |
MOD_CDK_SPxxK_3 | 256 | 263 | PF00069 | 0.502 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.344 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.463 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.513 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.766 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.626 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.598 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.629 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.469 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.316 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.508 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.391 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.487 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.712 |
MOD_CK2_1 | 484 | 490 | PF00069 | 0.575 |
MOD_CK2_1 | 495 | 501 | PF00069 | 0.513 |
MOD_CK2_1 | 605 | 611 | PF00069 | 0.389 |
MOD_CK2_1 | 627 | 633 | PF00069 | 0.382 |
MOD_CMANNOS | 622 | 625 | PF00535 | 0.264 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.589 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.335 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.332 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.314 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.590 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.373 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.499 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.526 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.516 |
MOD_GlcNHglycan | 482 | 486 | PF01048 | 0.567 |
MOD_GlcNHglycan | 542 | 546 | PF01048 | 0.382 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.325 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.527 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.577 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.534 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.569 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.403 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.442 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.547 |
MOD_GSK3_1 | 642 | 649 | PF00069 | 0.326 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.473 |
MOD_N-GLC_1 | 243 | 248 | PF02516 | 0.410 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.537 |
MOD_N-GLC_1 | 338 | 343 | PF02516 | 0.719 |
MOD_N-GLC_1 | 525 | 530 | PF02516 | 0.337 |
MOD_N-GLC_2 | 10 | 12 | PF02516 | 0.393 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.432 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.475 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.591 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.403 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.532 |
MOD_NEK2_1 | 627 | 632 | PF00069 | 0.271 |
MOD_NEK2_1 | 640 | 645 | PF00069 | 0.367 |
MOD_PIKK_1 | 499 | 505 | PF00454 | 0.473 |
MOD_PIKK_1 | 66 | 72 | PF00454 | 0.373 |
MOD_PIKK_1 | 76 | 82 | PF00454 | 0.447 |
MOD_PKA_1 | 474 | 480 | PF00069 | 0.462 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.688 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.349 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.482 |
MOD_PKB_1 | 265 | 273 | PF00069 | 0.419 |
MOD_Plk_1 | 243 | 249 | PF00069 | 0.414 |
MOD_Plk_1 | 525 | 531 | PF00069 | 0.378 |
MOD_Plk_2-3 | 605 | 611 | PF00069 | 0.426 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.463 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.432 |
MOD_Plk_4 | 627 | 633 | PF00069 | 0.306 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.331 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.386 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.747 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.592 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.439 |
MOD_SUMO_rev_2 | 246 | 253 | PF00179 | 0.468 |
MOD_SUMO_rev_2 | 633 | 643 | PF00179 | 0.382 |
TRG_DiLeu_BaEn_1 | 249 | 254 | PF01217 | 0.408 |
TRG_DiLeu_BaLyEn_6 | 227 | 232 | PF01217 | 0.313 |
TRG_DiLeu_BaLyEn_6 | 36 | 41 | PF01217 | 0.513 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 537 | 540 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 620 | 623 | PF00928 | 0.275 |
TRG_ER_diArg_1 | 106 | 109 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 130 | 133 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 262 | 265 | PF00400 | 0.571 |
TRG_NES_CRM1_1 | 519 | 531 | PF08389 | 0.266 |
TRG_Pf-PMV_PEXEL_1 | 39 | 43 | PF00026 | 0.450 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IL37 | Leptomonas seymouri | 68% | 94% |
A0A0S4JQD9 | Bodo saltans | 43% | 100% |
A0A0S4JTX4 | Bodo saltans | 43% | 100% |
A0A1X0PB30 | Trypanosomatidae | 55% | 100% |
A0A3R7MLZ5 | Trypanosoma rangeli | 52% | 100% |
A0A3S5H7X1 | Leishmania donovani | 94% | 95% |
A4HAX9 | Leishmania braziliensis | 84% | 95% |
A4IA38 | Leishmania infantum | 94% | 95% |
A4IG62 | Danio rerio | 32% | 86% |
C9ZM61 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9B553 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 95% |
F4KFV7 | Arabidopsis thaliana | 32% | 84% |
O74727 | Saccharomyces paradoxus | 30% | 89% |
O94445 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |
P32580 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 89% |
Q01IJ3 | Oryza sativa subsp. indica | 34% | 89% |
Q10D00 | Oryza sativa subsp. japonica | 32% | 100% |
Q17828 | Caenorhabditis elegans | 34% | 91% |
Q295E6 | Drosophila pseudoobscura pseudoobscura | 35% | 86% |
Q59TB2 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 30% | 91% |
Q5EBA1 | Rattus norvegicus | 34% | 84% |
Q5ZJT0 | Gallus gallus | 32% | 82% |
Q61SU7 | Caenorhabditis briggsae | 33% | 91% |
Q7X745 | Oryza sativa subsp. japonica | 34% | 89% |
Q80YD1 | Mus musculus | 34% | 84% |
Q8IYB8 | Homo sapiens | 34% | 83% |
Q9SMX1 | Arabidopsis thaliana | 32% | 100% |
Q9VN03 | Drosophila melanogaster | 34% | 86% |
V5DLS8 | Trypanosoma cruzi | 52% | 100% |