Helicases, ATP-dependent RNA helicase
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:0005730 | nucleolus | 5 | 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:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4IBU1
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
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:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003723 | RNA binding | 4 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 304 | 308 | PF00656 | 0.510 |
CLV_C14_Caspase3-7 | 412 | 416 | PF00656 | 0.436 |
CLV_C14_Caspase3-7 | 601 | 605 | PF00656 | 0.763 |
CLV_NRD_NRD_1 | 202 | 204 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 456 | 458 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 477 | 479 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 495 | 497 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 652 | 654 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 679 | 681 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 686 | 688 | PF00675 | 0.505 |
CLV_PCSK_FUR_1 | 454 | 458 | PF00082 | 0.679 |
CLV_PCSK_FUR_1 | 579 | 583 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.249 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.249 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.260 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.260 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 477 | 479 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 554 | 556 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 581 | 583 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 606 | 608 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 652 | 654 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.333 |
CLV_PCSK_PC1ET2_1 | 196 | 198 | PF00082 | 0.260 |
CLV_PCSK_PC1ET2_1 | 320 | 322 | PF00082 | 0.260 |
CLV_PCSK_PC1ET2_1 | 330 | 332 | PF00082 | 0.260 |
CLV_PCSK_PC1ET2_1 | 438 | 440 | PF00082 | 0.577 |
CLV_PCSK_PC1ET2_1 | 477 | 479 | PF00082 | 0.651 |
CLV_PCSK_PC1ET2_1 | 554 | 556 | PF00082 | 0.577 |
CLV_PCSK_PC1ET2_1 | 581 | 583 | PF00082 | 0.553 |
CLV_PCSK_PC1ET2_1 | 606 | 608 | PF00082 | 0.631 |
CLV_PCSK_PC1ET2_1 | 98 | 100 | PF00082 | 0.333 |
CLV_PCSK_PC7_1 | 326 | 332 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 474 | 478 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 479 | 483 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 525 | 529 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 620 | 624 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.260 |
DEG_APCC_DBOX_1 | 187 | 195 | PF00400 | 0.535 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.567 |
DOC_CKS1_1 | 147 | 152 | PF01111 | 0.449 |
DOC_CYCLIN_RxL_1 | 422 | 434 | PF00134 | 0.612 |
DOC_CYCLIN_RxL_1 | 96 | 107 | PF00134 | 0.490 |
DOC_MAPK_DCC_7 | 344 | 353 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 276 | 284 | PF00069 | 0.440 |
DOC_MAPK_gen_1 | 330 | 337 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 375 | 385 | PF00069 | 0.524 |
DOC_MAPK_gen_1 | 554 | 563 | PF00069 | 0.487 |
DOC_MAPK_gen_1 | 612 | 621 | PF00069 | 0.534 |
DOC_MAPK_HePTP_8 | 341 | 353 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 224 | 233 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 276 | 284 | PF00069 | 0.435 |
DOC_MAPK_MEF2A_6 | 344 | 353 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 5 | 13 | PF00069 | 0.435 |
DOC_MAPK_MEF2A_6 | 554 | 563 | PF00069 | 0.430 |
DOC_PP1_RVXF_1 | 179 | 186 | PF00149 | 0.449 |
DOC_PP1_RVXF_1 | 265 | 272 | PF00149 | 0.460 |
DOC_PP1_RVXF_1 | 379 | 386 | PF00149 | 0.437 |
DOC_PP1_RVXF_1 | 97 | 104 | PF00149 | 0.470 |
DOC_PP2B_LxvP_1 | 346 | 349 | PF13499 | 0.449 |
DOC_PP2B_LxvP_1 | 559 | 562 | PF13499 | 0.404 |
DOC_PP2B_LxvP_1 | 82 | 85 | PF13499 | 0.554 |
DOC_PP4_FxxP_1 | 385 | 388 | PF00568 | 0.335 |
DOC_PP4_FxxP_1 | 545 | 548 | PF00568 | 0.301 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 511 | 515 | PF00917 | 0.313 |
DOC_USP7_UBL2_3 | 196 | 200 | PF12436 | 0.438 |
DOC_USP7_UBL2_3 | 664 | 668 | PF12436 | 0.408 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 485 | 490 | PF00397 | 0.388 |
LIG_14-3-3_CanoR_1 | 224 | 230 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 232 | 237 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 260 | 268 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 378 | 384 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 427 | 431 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 510 | 516 | PF00244 | 0.301 |
LIG_14-3-3_CanoR_1 | 607 | 616 | PF00244 | 0.564 |
LIG_BRCT_BRCA1_1 | 252 | 256 | PF00533 | 0.392 |
LIG_BRCT_BRCA1_1 | 381 | 385 | PF00533 | 0.374 |
LIG_Clathr_ClatBox_1 | 173 | 177 | PF01394 | 0.460 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.460 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.482 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.449 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.535 |
LIG_LIR_Apic_2 | 382 | 388 | PF02991 | 0.340 |
LIG_LIR_Apic_2 | 51 | 57 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 169 | 179 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 291 | 301 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 36 | 45 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 390 | 399 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 509 | 519 | PF02991 | 0.190 |
LIG_LIR_Gen_1 | 539 | 548 | PF02991 | 0.295 |
LIG_LIR_Gen_1 | 644 | 651 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 121 | 125 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 253 | 258 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 291 | 297 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 36 | 41 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 390 | 396 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 509 | 515 | PF02991 | 0.181 |
LIG_LIR_Nem_3 | 539 | 545 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 565 | 570 | PF02991 | 0.490 |
LIG_MLH1_MIPbox_1 | 252 | 256 | PF16413 | 0.392 |
LIG_NRBOX | 152 | 158 | PF00104 | 0.460 |
LIG_NRBOX | 190 | 196 | PF00104 | 0.526 |
LIG_NRBOX | 58 | 64 | PF00104 | 0.510 |
LIG_NRBOX | 637 | 643 | PF00104 | 0.566 |
LIG_NRP_CendR_1 | 687 | 690 | PF00754 | 0.579 |
LIG_PCNA_yPIPBox_3 | 629 | 642 | PF02747 | 0.473 |
LIG_PTB_Apo_2 | 73 | 80 | PF02174 | 0.526 |
LIG_Rb_LxCxE_1 | 51 | 73 | PF01857 | 0.474 |
LIG_SH2_CRK | 357 | 361 | PF00017 | 0.460 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.514 |
LIG_SH2_GRB2like | 393 | 396 | PF00017 | 0.465 |
LIG_SH2_SRC | 357 | 360 | PF00017 | 0.449 |
LIG_SH2_SRC | 54 | 57 | PF00017 | 0.509 |
LIG_SH2_STAP1 | 154 | 158 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 38 | 42 | PF00017 | 0.472 |
LIG_SH2_STAT3 | 120 | 123 | PF00017 | 0.449 |
LIG_SH2_STAT3 | 526 | 529 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 526 | 529 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 647 | 650 | PF00017 | 0.434 |
LIG_SH3_1 | 357 | 363 | PF00018 | 0.460 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.510 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.465 |
LIG_SH3_3 | 357 | 363 | PF00018 | 0.460 |
LIG_SUMO_SIM_anti_2 | 172 | 178 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 172 | 178 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 225 | 230 | PF11976 | 0.445 |
LIG_SUMO_SIM_par_1 | 531 | 537 | PF11976 | 0.317 |
LIG_SUMO_SIM_par_1 | 80 | 86 | PF11976 | 0.471 |
LIG_TRAF2_1 | 585 | 588 | PF00917 | 0.609 |
LIG_TRAF2_2 | 403 | 408 | PF00917 | 0.476 |
LIG_TYR_ITSM | 34 | 41 | PF00017 | 0.422 |
LIG_UBA3_1 | 173 | 181 | PF00899 | 0.336 |
LIG_UBA3_1 | 194 | 200 | PF00899 | 0.271 |
LIG_UBA3_1 | 621 | 626 | PF00899 | 0.655 |
LIG_WRC_WIRS_1 | 512 | 517 | PF05994 | 0.301 |
MOD_CDK_SPxK_1 | 146 | 152 | PF00069 | 0.301 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.518 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.494 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.294 |
MOD_CK1_1 | 627 | 633 | PF00069 | 0.618 |
MOD_CK1_1 | 673 | 679 | PF00069 | 0.618 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.422 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.336 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.609 |
MOD_CK2_1 | 622 | 628 | PF00069 | 0.496 |
MOD_CK2_1 | 673 | 679 | PF00069 | 0.513 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.301 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.532 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.371 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.546 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.291 |
MOD_GlcNHglycan | 587 | 592 | PF01048 | 0.574 |
MOD_GlcNHglycan | 675 | 678 | PF01048 | 0.578 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.301 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.301 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.502 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.648 |
MOD_N-GLC_1 | 109 | 114 | PF02516 | 0.408 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.301 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.301 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.502 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.301 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.501 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.288 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.386 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.515 |
MOD_NEK2_1 | 622 | 627 | PF00069 | 0.569 |
MOD_NEK2_1 | 642 | 647 | PF00069 | 0.256 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.448 |
MOD_PIKK_1 | 207 | 213 | PF00454 | 0.301 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.338 |
MOD_PIKK_1 | 469 | 475 | PF00454 | 0.646 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.301 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.352 |
MOD_PKA_2 | 410 | 416 | PF00069 | 0.469 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.486 |
MOD_PKA_2 | 583 | 589 | PF00069 | 0.527 |
MOD_Plk_1 | 670 | 676 | PF00069 | 0.631 |
MOD_Plk_2-3 | 410 | 416 | PF00069 | 0.519 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.301 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.373 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.392 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.301 |
MOD_Plk_4 | 642 | 648 | PF00069 | 0.456 |
MOD_Plk_4 | 670 | 676 | PF00069 | 0.613 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.448 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.301 |
MOD_ProDKin_1 | 485 | 491 | PF00069 | 0.381 |
MOD_SUMO_for_1 | 316 | 319 | PF00179 | 0.317 |
MOD_SUMO_for_1 | 648 | 651 | PF00179 | 0.439 |
MOD_SUMO_rev_2 | 274 | 281 | PF00179 | 0.307 |
MOD_SUMO_rev_2 | 673 | 683 | PF00179 | 0.529 |
MOD_SUMO_rev_2 | 69 | 77 | PF00179 | 0.321 |
TRG_DiLeu_BaEn_1 | 178 | 183 | PF01217 | 0.301 |
TRG_DiLeu_BaEn_1 | 617 | 622 | PF01217 | 0.622 |
TRG_DiLeu_BaEn_1 | 637 | 642 | PF01217 | 0.264 |
TRG_DiLeu_BaEn_2 | 391 | 397 | PF01217 | 0.398 |
TRG_DiLeu_BaEn_2 | 565 | 571 | PF01217 | 0.511 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 393 | 396 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 647 | 650 | PF00928 | 0.580 |
TRG_ER_diArg_1 | 494 | 496 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 555 | 558 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 63 | 66 | PF00400 | 0.422 |
TRG_ER_FFAT_2 | 671 | 679 | PF00635 | 0.560 |
TRG_NES_CRM1_1 | 390 | 400 | PF08389 | 0.387 |
TRG_NES_CRM1_1 | 552 | 565 | PF08389 | 0.420 |
TRG_NES_CRM1_1 | 614 | 628 | PF08389 | 0.643 |
TRG_NLS_Bipartite_1 | 320 | 334 | PF00514 | 0.340 |
TRG_NLS_MonoExtC_3 | 605 | 611 | PF00514 | 0.574 |
TRG_NLS_MonoExtN_4 | 603 | 610 | PF00514 | 0.628 |
TRG_Pf-PMV_PEXEL_1 | 213 | 217 | PF00026 | 0.315 |
TRG_Pf-PMV_PEXEL_1 | 525 | 529 | PF00026 | 0.301 |
TRG_Pf-PMV_PEXEL_1 | 87 | 91 | PF00026 | 0.301 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4X4 | Leptomonas seymouri | 84% | 99% |
A0A0S4IX79 | Bodo saltans | 56% | 95% |
A0A1X0P5E1 | Trypanosomatidae | 65% | 97% |
A0A1X0P9U0 | Trypanosomatidae | 27% | 83% |
A0A3Q8ID91 | Leishmania donovani | 30% | 100% |
A0A3R7M1K3 | Trypanosoma rangeli | 30% | 96% |
A0A3R7NR45 | Trypanosoma rangeli | 28% | 84% |
A0A3S5IQZ7 | Trypanosoma rangeli | 27% | 87% |
A0A3S7X9W0 | Leishmania donovani | 100% | 100% |
A0A3S7XAT8 | Leishmania donovani | 34% | 100% |
A0A422NKE3 | Trypanosoma rangeli | 65% | 95% |
A3LX02 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 31% | 100% |
A4HGR1 | Leishmania braziliensis | 31% | 100% |
A4HK38 | Leishmania braziliensis | 27% | 100% |
A4HN73 | Leishmania braziliensis | 91% | 100% |
A4HP49 | Leishmania braziliensis | 33% | 100% |
A4HT33 | Leishmania infantum | 31% | 100% |
A4HUC1 | Leishmania infantum | 27% | 88% |
A4HZF8 | Leishmania infantum | 26% | 100% |
A4I3T6 | Leishmania infantum | 30% | 100% |
A4IDF6 | Leishmania infantum | 34% | 100% |
A5DAR2 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 27% | 92% |
A6R918 | Ajellomyces capsulatus (strain NAm1 / WU24) | 35% | 100% |
A6RMZ2 | Botryotinia fuckeliana (strain B05.10) | 36% | 100% |
A7F2S3 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 36% | 100% |
C9ZYS3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 68% | 89% |
E9AFM8 | Leishmania major | 95% | 100% |
E9AJG4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9ASV7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B028 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9B6T1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
P0CR08 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 32% | 92% |
P0CR09 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 32% | 92% |
Q1EB38 | Coccidioides immitis (strain RS) | 30% | 74% |
Q4Q1N9 | Leishmania major | 34% | 100% |
Q4Q858 | Leishmania major | 30% | 100% |
Q4QHK6 | Leishmania major | 26% | 93% |
Q59S50 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 27% | 95% |
Q6NZQ2 | Mus musculus | 29% | 100% |
Q873H9 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 33% | 100% |
V5DUK0 | Trypanosoma cruzi | 65% | 90% |