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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H7Y3
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 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:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003724 | RNA helicase activity | 3 | 11 |
GO:0003743 | translation initiation factor activity | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004386 | helicase activity | 2 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0008135 | translation factor activity, RNA binding | 3 | 11 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0045182 | translation regulator activity | 1 | 11 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 14 | 18 | PF00656 | 0.509 |
CLV_C14_Caspase3-7 | 282 | 286 | PF00656 | 0.713 |
CLV_C14_Caspase3-7 | 490 | 494 | PF00656 | 0.503 |
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 468 | 470 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 488 | 490 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 528 | 530 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 555 | 557 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 564 | 566 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 596 | 598 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 600 | 602 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 639 | 641 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 649 | 651 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 678 | 680 | PF00675 | 0.613 |
CLV_PCSK_FUR_1 | 303 | 307 | PF00082 | 0.587 |
CLV_PCSK_FUR_1 | 308 | 312 | PF00082 | 0.558 |
CLV_PCSK_FUR_1 | 556 | 560 | PF00082 | 0.572 |
CLV_PCSK_FUR_1 | 675 | 679 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.259 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 546 | 548 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 558 | 560 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 564 | 566 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 600 | 602 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 649 | 651 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 677 | 679 | PF00082 | 0.641 |
CLV_PCSK_PC1ET2_1 | 305 | 307 | PF00082 | 0.572 |
CLV_PCSK_PC1ET2_1 | 310 | 312 | PF00082 | 0.577 |
CLV_PCSK_PC1ET2_1 | 487 | 489 | PF00082 | 0.535 |
CLV_PCSK_PC1ET2_1 | 546 | 548 | PF00082 | 0.636 |
CLV_PCSK_PC1ET2_1 | 558 | 560 | PF00082 | 0.485 |
CLV_PCSK_PC1ET2_1 | 677 | 679 | PF00082 | 0.641 |
CLV_PCSK_PC7_1 | 306 | 312 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 469 | 473 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 635 | 639 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 678 | 682 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.254 |
CLV_Separin_Metazoa | 131 | 135 | PF03568 | 0.382 |
DEG_SCF_FBW7_1 | 274 | 280 | PF00400 | 0.665 |
DOC_CKS1_1 | 169 | 174 | PF01111 | 0.459 |
DOC_CKS1_1 | 274 | 279 | PF01111 | 0.474 |
DOC_CYCLIN_RxL_1 | 131 | 141 | PF00134 | 0.382 |
DOC_CYCLIN_RxL_1 | 370 | 384 | PF00134 | 0.544 |
DOC_CYCLIN_yCln2_LP_2 | 246 | 252 | PF00134 | 0.510 |
DOC_MAPK_gen_1 | 110 | 120 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 262 | 270 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 340 | 349 | PF00069 | 0.312 |
DOC_MAPK_MEF2A_6 | 264 | 272 | PF00069 | 0.327 |
DOC_MAPK_MEF2A_6 | 33 | 41 | PF00069 | 0.484 |
DOC_PP1_RVXF_1 | 31 | 37 | PF00149 | 0.538 |
DOC_PP1_RVXF_1 | 355 | 362 | PF00149 | 0.490 |
DOC_PP2B_PxIxI_1 | 164 | 170 | PF00149 | 0.490 |
DOC_PP4_FxxP_1 | 88 | 91 | PF00568 | 0.459 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.759 |
DOC_USP7_UBL2_3 | 624 | 628 | PF12436 | 0.525 |
DOC_USP7_UBL2_3 | 668 | 672 | PF12436 | 0.665 |
DOC_USP7_UBL2_3 | 673 | 677 | PF12436 | 0.669 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.414 |
LIG_14-3-3_CanoR_1 | 316 | 324 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 363 | 373 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 469 | 475 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 47 | 55 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 622 | 629 | PF00244 | 0.552 |
LIG_BIR_III_2 | 162 | 166 | PF00653 | 0.539 |
LIG_CaM_IQ_9 | 590 | 606 | PF13499 | 0.661 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.471 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.398 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.459 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.434 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.346 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.525 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.539 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.459 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.459 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.526 |
LIG_FHA_1 | 588 | 594 | PF00498 | 0.673 |
LIG_FHA_2 | 12 | 18 | PF00498 | 0.629 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.484 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.391 |
LIG_FHA_2 | 278 | 284 | PF00498 | 0.697 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.679 |
LIG_FHA_2 | 606 | 612 | PF00498 | 0.412 |
LIG_GBD_Chelix_1 | 424 | 432 | PF00786 | 0.311 |
LIG_LIR_Apic_2 | 85 | 91 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 392 | 402 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 244 | 250 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 372 | 378 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 504 | 510 | PF02991 | 0.449 |
LIG_NRBOX | 132 | 138 | PF00104 | 0.562 |
LIG_PCNA_yPIPBox_3 | 123 | 137 | PF02747 | 0.490 |
LIG_SH2_CRK | 430 | 434 | PF00017 | 0.539 |
LIG_SH2_NCK_1 | 430 | 434 | PF00017 | 0.539 |
LIG_SH2_PTP2 | 54 | 57 | PF00017 | 0.505 |
LIG_SH2_STAP1 | 567 | 571 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.476 |
LIG_SH3_1 | 271 | 277 | PF00018 | 0.428 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.490 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.539 |
LIG_SH3_3 | 271 | 277 | PF00018 | 0.428 |
LIG_SUMO_SIM_anti_2 | 191 | 197 | PF11976 | 0.490 |
LIG_SUMO_SIM_anti_2 | 454 | 461 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 116 | 122 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 194 | 200 | PF11976 | 0.470 |
LIG_SUMO_SIM_par_1 | 202 | 208 | PF11976 | 0.444 |
LIG_SUMO_SIM_par_1 | 470 | 475 | PF11976 | 0.460 |
LIG_TRAF2_1 | 333 | 336 | PF00917 | 0.614 |
LIG_TRAF2_1 | 552 | 555 | PF00917 | 0.658 |
LIG_TRAF2_1 | 586 | 589 | PF00917 | 0.600 |
LIG_TRAF2_1 | 608 | 611 | PF00917 | 0.415 |
LIG_TRFH_1 | 430 | 434 | PF08558 | 0.459 |
MOD_CDK_SPK_2 | 298 | 303 | PF00069 | 0.685 |
MOD_CDK_SPxK_1 | 168 | 174 | PF00069 | 0.459 |
MOD_CDK_SPxxK_3 | 298 | 305 | PF00069 | 0.658 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.515 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.621 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.670 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.459 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.459 |
MOD_CK2_1 | 298 | 304 | PF00069 | 0.653 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.599 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.537 |
MOD_CK2_1 | 521 | 527 | PF00069 | 0.534 |
MOD_CK2_1 | 549 | 555 | PF00069 | 0.564 |
MOD_CK2_1 | 605 | 611 | PF00069 | 0.413 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.311 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.259 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.679 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.504 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.276 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.520 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.490 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.459 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.618 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.542 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.421 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.465 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.580 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.470 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.473 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.487 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.419 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.458 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.551 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.494 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.474 |
MOD_PIKK_1 | 27 | 33 | PF00454 | 0.507 |
MOD_PIKK_1 | 521 | 527 | PF00454 | 0.577 |
MOD_PK_1 | 470 | 476 | PF00069 | 0.582 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.621 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.610 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.459 |
MOD_PKB_1 | 363 | 371 | PF00069 | 0.539 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.473 |
MOD_Plk_1 | 571 | 577 | PF00069 | 0.552 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.382 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.473 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.473 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.472 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.388 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.311 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.477 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.616 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.653 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.313 |
MOD_SUMO_for_1 | 545 | 548 | PF00179 | 0.709 |
MOD_SUMO_for_1 | 623 | 626 | PF00179 | 0.642 |
MOD_SUMO_rev_2 | 517 | 524 | PF00179 | 0.529 |
MOD_SUMO_rev_2 | 603 | 608 | PF00179 | 0.618 |
MOD_SUMO_rev_2 | 610 | 614 | PF00179 | 0.575 |
MOD_SUMO_rev_2 | 620 | 629 | PF00179 | 0.470 |
TRG_DiLeu_BaEn_1 | 405 | 410 | PF01217 | 0.539 |
TRG_DiLeu_BaEn_3 | 222 | 228 | PF01217 | 0.382 |
TRG_DiLeu_BaEn_4 | 561 | 567 | PF01217 | 0.621 |
TRG_DiLeu_BaEn_4 | 588 | 594 | PF01217 | 0.528 |
TRG_ER_diArg_1 | 110 | 112 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 268 | 271 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 311 | 313 | PF00400 | 0.619 |
TRG_ER_diArg_1 | 528 | 530 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 564 | 566 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 599 | 601 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 678 | 680 | PF00400 | 0.636 |
TRG_NES_CRM1_1 | 189 | 202 | PF08389 | 0.511 |
TRG_NLS_Bipartite_1 | 627 | 644 | PF00514 | 0.454 |
TRG_NLS_MonoCore_2 | 309 | 314 | PF00514 | 0.651 |
TRG_NLS_MonoExtC_3 | 309 | 315 | PF00514 | 0.642 |
TRG_NLS_MonoExtC_3 | 596 | 601 | PF00514 | 0.587 |
TRG_NLS_MonoExtC_3 | 676 | 681 | PF00514 | 0.656 |
TRG_NLS_MonoExtN_4 | 308 | 314 | PF00514 | 0.636 |
TRG_NLS_MonoExtN_4 | 595 | 601 | PF00514 | 0.592 |
TRG_NLS_MonoExtN_4 | 638 | 644 | PF00514 | 0.467 |
TRG_NLS_MonoExtN_4 | 670 | 676 | PF00514 | 0.631 |
TRG_Pf-PMV_PEXEL_1 | 123 | 128 | PF00026 | 0.259 |
TRG_Pf-PMV_PEXEL_1 | 134 | 138 | PF00026 | 0.259 |
TRG_Pf-PMV_PEXEL_1 | 417 | 422 | PF00026 | 0.339 |
TRG_Pf-PMV_PEXEL_1 | 564 | 568 | PF00026 | 0.628 |
TRG_Pf-PMV_PEXEL_1 | 600 | 605 | PF00026 | 0.403 |
TRG_Pf-PMV_PEXEL_1 | 640 | 644 | PF00026 | 0.637 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5D9 | Leptomonas seymouri | 82% | 89% |
A0A0S4II81 | Bodo saltans | 52% | 78% |
A0A1X0NJH3 | Trypanosomatidae | 26% | 100% |
A0A1X0NU42 | Trypanosomatidae | 63% | 92% |
A0A3R7KKL1 | Trypanosoma rangeli | 64% | 95% |
A0A3S5H6T7 | Leishmania donovani | 88% | 100% |
A0A3S5H7C7 | Leishmania donovani | 22% | 100% |
A0A3S7WQS0 | Leishmania donovani | 23% | 88% |
A0A3S7X5R1 | Leishmania donovani | 29% | 88% |
A0A422P419 | Trypanosoma rangeli | 25% | 100% |
A1A4H6 | Bos taurus | 34% | 89% |
A1CTL8 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 27% | 88% |
A1CTZ6 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 30% | 73% |
A1DNF9 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 29% | 84% |
A2Q9T6 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 29% | 100% |
A2QA23 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 29% | 100% |
A2QFL3 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 30% | 100% |
A2QS00 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 29% | 85% |
A2QWW0 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 28% | 89% |
A2XVF7 | Oryza sativa subsp. indica | 28% | 82% |
A3AVH5 | Oryza sativa subsp. japonica | 28% | 82% |
A3LNL1 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 28% | 100% |
A3LSN3 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 29% | 92% |
A4H5R4 | Leishmania braziliensis | 24% | 88% |
A4HD81 | Leishmania braziliensis | 22% | 100% |
A4HN73 | Leishmania braziliensis | 27% | 99% |
A4HU04 | Leishmania infantum | 23% | 88% |
A4HWB0 | Leishmania infantum | 88% | 100% |
A4I846 | Leishmania infantum | 30% | 88% |
A4REU9 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 29% | 90% |
A5DAR2 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 28% | 91% |
A5DF03 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 29% | 100% |
A5DID7 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 29% | 100% |
A5DKW3 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 31% | 97% |
A5DUB2 | Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) | 26% | 80% |
A6R9U4 | Ajellomyces capsulatus (strain NAm1 / WU24) | 28% | 88% |
A6ZLH6 | Saccharomyces cerevisiae (strain YJM789) | 27% | 80% |
A7A0P8 | Saccharomyces cerevisiae (strain YJM789) | 32% | 91% |
A7TGW7 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 30% | 70% |
A7TJM9 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 32% | 91% |
C9ZNU6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 63% | 100% |
D0A6Z3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
E9AFM8 | Leishmania major | 27% | 100% |
E9AH36 | Leishmania infantum | 22% | 100% |
E9AMT4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 88% |
E9AQ10 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9AWL4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9B304 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 88% |
E9B6T1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 99% |
P0C2N8 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 33% | 82% |
P0CQ84 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 28% | 100% |
P0CQ85 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 28% | 100% |
P21372 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 80% |
P32892 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 91% |
Q03532 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
Q0CI35 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 28% | 88% |
Q0CMM5 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 27% | 85% |
Q0INC5 | Oryza sativa subsp. japonica | 34% | 85% |
Q0U6X2 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 28% | 84% |
Q0UR48 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 29% | 100% |
Q0UZ59 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 25% | 100% |
Q10PV9 | Oryza sativa subsp. japonica | 28% | 100% |
Q1E7Y4 | Coccidioides immitis (strain RS) | 28% | 87% |
Q2UHB7 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 28% | 86% |
Q2UMH8 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 30% | 100% |
Q2UMY7 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 28% | 90% |
Q4IBS2 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 28% | 87% |
Q4JG17 | Penaeus vannamei | 28% | 97% |
Q4P5U4 | Ustilago maydis (strain 521 / FGSC 9021) | 27% | 75% |
Q4P9P3 | Ustilago maydis (strain 521 / FGSC 9021) | 32% | 73% |
Q4PEX7 | Ustilago maydis (strain 521 / FGSC 9021) | 33% | 100% |
Q4Q552 | Leishmania major | 29% | 88% |
Q4QFH1 | Leishmania major | 88% | 100% |
Q4WM60 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 28% | 87% |
Q53RK8 | Oryza sativa subsp. japonica | 29% | 93% |
Q54S03 | Dictyostelium discoideum | 26% | 100% |
Q59N29 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 23% | 100% |
Q59S50 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 29% | 94% |
Q5A4P9 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 25% | 100% |
Q5BCI0 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 30% | 89% |
Q6BH93 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 29% | 100% |
Q6C024 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 28% | 100% |
Q6C7D2 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 26% | 100% |
Q6CCZ1 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 32% | 70% |
Q6CXB7 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 29% | 100% |
Q6DRI7 | Danio rerio | 28% | 100% |
Q6FIL3 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 30% | 100% |
Q6FY67 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 27% | 93% |
Q6H874 | Oryza sativa subsp. japonica | 29% | 100% |
Q6NZQ2 | Mus musculus | 28% | 99% |
Q6P9R1 | Mus musculus | 28% | 100% |
Q74Z73 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 29% | 100% |
Q75F95 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 33% | 93% |
Q761Z9 | Oryza sativa subsp. japonica | 29% | 100% |
Q7S873 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 29% | 84% |
Q921N6 | Mus musculus | 34% | 90% |
Q96GQ7 | Homo sapiens | 34% | 86% |
Q9DF35 | Xenopus laevis | 30% | 90% |
Q9DF36 | Xenopus laevis | 30% | 85% |
Q9H8H2 | Homo sapiens | 29% | 80% |
Q9SB89 | Arabidopsis thaliana | 28% | 100% |
Q9VD51 | Drosophila melanogaster | 27% | 100% |