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:0005739 | mitochondrion | 5 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0000177 | cytoplasmic exosome (RNase complex) | 5 | 1 |
GO:0000178 | exosome (RNase complex) | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0045025 | mitochondrial degradosome | 3 | 1 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1905354 | exoribonuclease complex | 3 | 1 |
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: E9B553
Term | Name | Level | Count |
---|---|---|---|
GO:0000959 | mitochondrial RNA metabolic process | 6 | 1 |
GO:0000963 | mitochondrial RNA processing | 6 | 1 |
GO:0000965 | mitochondrial RNA 3'-end processing | 7 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006401 | RNA catabolic process | 5 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010467 | gene expression | 4 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0019439 | aromatic compound catabolic process | 4 | 1 |
GO:0031123 | RNA 3'-end processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0046700 | heterocycle catabolic process | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:0140053 | mitochondrial gene expression | 5 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
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 | 320 | 324 | PF00656 | 0.492 |
CLV_MEL_PAP_1 | 655 | 661 | PF00089 | 0.262 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.285 |
CLV_NRD_NRD_1 | 506 | 508 | PF00675 | 0.510 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.551 |
CLV_PCSK_PC1ET2_1 | 284 | 286 | PF00082 | 0.454 |
CLV_PCSK_PC7_1 | 137 | 143 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 545 | 549 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 565 | 569 | PF00082 | 0.241 |
CLV_Separin_Metazoa | 555 | 559 | PF03568 | 0.519 |
DEG_APCC_DBOX_1 | 274 | 282 | PF00400 | 0.507 |
DEG_APCC_DBOX_1 | 297 | 305 | PF00400 | 0.285 |
DOC_CYCLIN_RxL_1 | 542 | 552 | PF00134 | 0.472 |
DOC_CYCLIN_RxL_1 | 665 | 675 | PF00134 | 0.547 |
DOC_CYCLIN_yCln2_LP_2 | 16 | 22 | PF00134 | 0.600 |
DOC_MAPK_gen_1 | 186 | 195 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 284 | 291 | PF00069 | 0.409 |
DOC_MAPK_gen_1 | 315 | 321 | PF00069 | 0.550 |
DOC_MAPK_gen_1 | 4 | 12 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 102 | 111 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 284 | 291 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 628 | 635 | PF00069 | 0.619 |
DOC_PP1_RVXF_1 | 416 | 422 | PF00149 | 0.411 |
DOC_PP1_RVXF_1 | 563 | 569 | PF00149 | 0.441 |
DOC_PP2B_LxvP_1 | 246 | 249 | PF13499 | 0.322 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 444 | 448 | PF00917 | 0.532 |
DOC_USP7_UBL2_3 | 119 | 123 | PF12436 | 0.446 |
DOC_USP7_UBL2_3 | 426 | 430 | PF12436 | 0.445 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.331 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.378 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.420 |
LIG_14-3-3_CanoR_1 | 110 | 117 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 354 | 363 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 418 | 427 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 454 | 459 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 460 | 464 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 658 | 664 | PF00244 | 0.436 |
LIG_Actin_WH2_2 | 536 | 551 | PF00022 | 0.452 |
LIG_APCC_ABBA_1 | 495 | 500 | PF00400 | 0.475 |
LIG_BRCT_BRCA1_1 | 446 | 450 | PF00533 | 0.515 |
LIG_BRCT_BRCA1_1 | 534 | 538 | PF00533 | 0.426 |
LIG_BRCT_BRCA1_1 | 655 | 659 | PF00533 | 0.509 |
LIG_BRCT_BRCA1_2 | 655 | 661 | PF00533 | 0.532 |
LIG_deltaCOP1_diTrp_1 | 236 | 241 | PF00928 | 0.344 |
LIG_deltaCOP1_diTrp_1 | 86 | 93 | PF00928 | 0.505 |
LIG_eIF4E_1 | 133 | 139 | PF01652 | 0.507 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.317 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.489 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.455 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.409 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.370 |
LIG_FHA_1 | 561 | 567 | PF00498 | 0.512 |
LIG_FHA_1 | 615 | 621 | PF00498 | 0.640 |
LIG_FHA_1 | 675 | 681 | PF00498 | 0.492 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.480 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.348 |
LIG_FHA_2 | 476 | 482 | PF00498 | 0.415 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.472 |
LIG_FHA_2 | 638 | 644 | PF00498 | 0.388 |
LIG_FHA_2 | 660 | 666 | PF00498 | 0.521 |
LIG_LIR_Apic_2 | 167 | 173 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 112 | 121 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 308 | 318 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 520 | 530 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 650 | 659 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 112 | 117 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 308 | 313 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 518 | 524 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 650 | 655 | PF02991 | 0.435 |
LIG_MYND_1 | 512 | 516 | PF01753 | 0.348 |
LIG_NRBOX | 549 | 555 | PF00104 | 0.228 |
LIG_PCNA_yPIPBox_3 | 351 | 360 | PF02747 | 0.532 |
LIG_PCNA_yPIPBox_3 | 413 | 426 | PF02747 | 0.476 |
LIG_PCNA_yPIPBox_3 | 644 | 655 | PF02747 | 0.501 |
LIG_Pex14_1 | 89 | 93 | PF04695 | 0.484 |
LIG_Pex14_2 | 659 | 663 | PF04695 | 0.441 |
LIG_PTB_Apo_2 | 264 | 271 | PF02174 | 0.459 |
LIG_PTB_Phospho_1 | 264 | 270 | PF10480 | 0.456 |
LIG_SH2_CRK | 170 | 174 | PF00017 | 0.319 |
LIG_SH2_GRB2like | 359 | 362 | PF00017 | 0.492 |
LIG_SH2_SRC | 359 | 362 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 570 | 573 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 652 | 655 | PF00017 | 0.446 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.433 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.301 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.439 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.526 |
LIG_SUMO_SIM_anti_2 | 105 | 110 | PF11976 | 0.407 |
LIG_SUMO_SIM_par_1 | 287 | 292 | PF11976 | 0.382 |
LIG_SUMO_SIM_par_1 | 317 | 323 | PF11976 | 0.547 |
LIG_UBA3_1 | 497 | 505 | PF00899 | 0.516 |
MOD_CDK_SPK_2 | 378 | 383 | PF00069 | 0.228 |
MOD_CDK_SPxK_1 | 393 | 399 | PF00069 | 0.364 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.376 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.628 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.471 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.592 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.445 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.364 |
MOD_CK1_1 | 517 | 523 | PF00069 | 0.530 |
MOD_CK1_1 | 574 | 580 | PF00069 | 0.343 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.505 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.516 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.463 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.452 |
MOD_CK2_1 | 475 | 481 | PF00069 | 0.537 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.410 |
MOD_CK2_1 | 517 | 523 | PF00069 | 0.553 |
MOD_CK2_1 | 637 | 643 | PF00069 | 0.417 |
MOD_CK2_1 | 659 | 665 | PF00069 | 0.441 |
MOD_CMANNOS | 654 | 657 | PF00535 | 0.293 |
MOD_DYRK1A_RPxSP_1 | 26 | 30 | PF00069 | 0.426 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.365 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.335 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.366 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.576 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.395 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.420 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.296 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.505 |
MOD_GlcNHglycan | 575 | 579 | PF01048 | 0.442 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.355 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.445 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.317 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.678 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.172 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.435 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.331 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.339 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.564 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.400 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.420 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.353 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.543 |
MOD_N-GLC_1 | 276 | 281 | PF02516 | 0.452 |
MOD_N-GLC_1 | 94 | 99 | PF02516 | 0.491 |
MOD_N-GLC_2 | 43 | 45 | PF02516 | 0.441 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.471 |
MOD_NEK2_1 | 528 | 533 | PF00069 | 0.404 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.344 |
MOD_NEK2_1 | 659 | 664 | PF00069 | 0.293 |
MOD_NEK2_1 | 672 | 677 | PF00069 | 0.293 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.495 |
MOD_NEK2_2 | 631 | 636 | PF00069 | 0.322 |
MOD_PIKK_1 | 109 | 115 | PF00454 | 0.444 |
MOD_PIKK_1 | 382 | 388 | PF00454 | 0.406 |
MOD_PIKK_1 | 475 | 481 | PF00454 | 0.245 |
MOD_PIKK_1 | 532 | 538 | PF00454 | 0.490 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.421 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.420 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.370 |
MOD_PKB_1 | 298 | 306 | PF00069 | 0.364 |
MOD_Plk_1 | 276 | 282 | PF00069 | 0.502 |
MOD_Plk_1 | 467 | 473 | PF00069 | 0.352 |
MOD_Plk_1 | 558 | 564 | PF00069 | 0.381 |
MOD_Plk_2-3 | 637 | 643 | PF00069 | 0.484 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.469 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.448 |
MOD_Plk_4 | 659 | 665 | PF00069 | 0.320 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.638 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.340 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.490 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.374 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.417 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.263 |
MOD_SUMO_rev_2 | 279 | 286 | PF00179 | 0.482 |
MOD_SUMO_rev_2 | 665 | 675 | PF00179 | 0.442 |
TRG_DiLeu_BaEn_1 | 282 | 287 | PF01217 | 0.426 |
TRG_DiLeu_BaLyEn_6 | 260 | 265 | PF01217 | 0.340 |
TRG_DiLeu_BaLyEn_6 | 69 | 74 | PF01217 | 0.512 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 570 | 573 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 652 | 655 | PF00928 | 0.286 |
TRG_ER_diArg_1 | 139 | 142 | PF00400 | 0.375 |
TRG_ER_diArg_1 | 298 | 301 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 3 | 5 | PF00400 | 0.548 |
TRG_NES_CRM1_1 | 552 | 564 | PF08389 | 0.295 |
TRG_Pf-PMV_PEXEL_1 | 636 | 641 | PF00026 | 0.385 |
TRG_Pf-PMV_PEXEL_1 | 72 | 76 | PF00026 | 0.462 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IL37 | Leptomonas seymouri | 68% | 98% |
A0A0S4JQD9 | Bodo saltans | 44% | 100% |
A0A0S4JTX4 | Bodo saltans | 44% | 100% |
A0A1X0PB30 | Trypanosomatidae | 55% | 100% |
A0A3R7MLZ5 | Trypanosoma rangeli | 52% | 100% |
A0A3S5H7X1 | Leishmania donovani | 91% | 100% |
A4HAX9 | Leishmania braziliensis | 85% | 100% |
A4IA38 | Leishmania infantum | 92% | 100% |
A4IG62 | Danio rerio | 32% | 90% |
C9ZM61 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
F4KFV7 | Arabidopsis thaliana | 33% | 89% |
O74727 | Saccharomyces paradoxus | 31% | 93% |
P32580 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 93% |
Q01IJ3 | Oryza sativa subsp. indica | 35% | 94% |
Q10D00 | Oryza sativa subsp. japonica | 32% | 100% |
Q17828 | Caenorhabditis elegans | 33% | 96% |
Q295E6 | Drosophila pseudoobscura pseudoobscura | 35% | 90% |
Q4Q2T3 | Leishmania major | 92% | 100% |
Q59TB2 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 30% | 95% |
Q5EBA1 | Rattus norvegicus | 34% | 89% |
Q5ZJT0 | Gallus gallus | 33% | 87% |
Q61SU7 | Caenorhabditis briggsae | 33% | 95% |
Q7X745 | Oryza sativa subsp. japonica | 35% | 94% |
Q80YD1 | Mus musculus | 34% | 88% |
Q8IYB8 | Homo sapiens | 34% | 87% |
Q9SMX1 | Arabidopsis thaliana | 31% | 100% |
Q9VN03 | Drosophila melanogaster | 34% | 90% |
V5DLS8 | Trypanosoma cruzi | 52% | 100% |