Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | yes | yes: 2 |
Pissara et al. | yes | yes: 8 |
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 |
Related structures:
AlphaFold database: Q4Q937
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 11 |
GO:0006518 | peptide metabolic process | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043603 | amide metabolic process | 3 | 2 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004175 | endopeptidase activity | 4 | 11 |
GO:0004222 | metalloendopeptidase activity | 5 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008233 | peptidase activity | 3 | 11 |
GO:0008237 | metallopeptidase activity | 4 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 397 | 401 | PF00656 | 0.384 |
CLV_C14_Caspase3-7 | 535 | 539 | PF00656 | 0.280 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 647 | 649 | PF00675 | 0.356 |
CLV_PCSK_FUR_1 | 496 | 500 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.338 |
CLV_PCSK_KEX2_1 | 647 | 649 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.485 |
CLV_PCSK_PC1ET2_1 | 263 | 265 | PF00082 | 0.322 |
CLV_PCSK_PC1ET2_1 | 498 | 500 | PF00082 | 0.334 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.340 |
DEG_APCC_DBOX_1 | 263 | 271 | PF00400 | 0.315 |
DEG_APCC_DBOX_1 | 549 | 557 | PF00400 | 0.315 |
DOC_CYCLIN_RxL_1 | 341 | 351 | PF00134 | 0.444 |
DOC_CYCLIN_RxL_1 | 362 | 369 | PF00134 | 0.315 |
DOC_CYCLIN_RxL_1 | 550 | 562 | PF00134 | 0.393 |
DOC_MAPK_gen_1 | 151 | 157 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 263 | 271 | PF00069 | 0.393 |
DOC_MAPK_gen_1 | 305 | 313 | PF00069 | 0.326 |
DOC_MAPK_gen_1 | 343 | 349 | PF00069 | 0.350 |
DOC_MAPK_gen_1 | 496 | 504 | PF00069 | 0.334 |
DOC_MAPK_MEF2A_6 | 263 | 271 | PF00069 | 0.380 |
DOC_PP1_RVXF_1 | 552 | 559 | PF00149 | 0.315 |
DOC_PP4_FxxP_1 | 566 | 569 | PF00568 | 0.334 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.473 |
DOC_USP7_UBL2_3 | 302 | 306 | PF12436 | 0.440 |
DOC_USP7_UBL2_3 | 540 | 544 | PF12436 | 0.448 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.323 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.319 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.427 |
LIG_14-3-3_CanoR_1 | 111 | 120 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 488 | 493 | PF00244 | 0.407 |
LIG_APCC_ABBA_1 | 463 | 468 | PF00400 | 0.334 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.582 |
LIG_BRCT_BRCA1_1 | 622 | 626 | PF00533 | 0.315 |
LIG_deltaCOP1_diTrp_1 | 510 | 514 | PF00928 | 0.315 |
LIG_EH1_1 | 477 | 485 | PF00400 | 0.334 |
LIG_eIF4E_1 | 409 | 415 | PF01652 | 0.448 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.249 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.316 |
LIG_FHA_1 | 558 | 564 | PF00498 | 0.356 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.346 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.444 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.395 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.467 |
LIG_FHA_2 | 292 | 298 | PF00498 | 0.347 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.249 |
LIG_FHA_2 | 599 | 605 | PF00498 | 0.334 |
LIG_IRF3_LxIS_1 | 276 | 282 | PF10401 | 0.448 |
LIG_LIR_Apic_2 | 331 | 336 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 159 | 168 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 224 | 234 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 275 | 281 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 369 | 379 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 4 | 13 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 470 | 480 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 500 | 509 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 221 | 225 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 275 | 279 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 369 | 374 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 376 | 382 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 4 | 10 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 470 | 476 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 500 | 504 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 581 | 587 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 604 | 610 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 629 | 634 | PF02991 | 0.336 |
LIG_PCNA_yPIPBox_3 | 663 | 672 | PF02747 | 0.400 |
LIG_PDZ_Class_2 | 680 | 685 | PF00595 | 0.317 |
LIG_Pex14_1 | 622 | 626 | PF04695 | 0.315 |
LIG_Pex14_2 | 375 | 379 | PF04695 | 0.315 |
LIG_Pex14_2 | 472 | 476 | PF04695 | 0.344 |
LIG_Pex14_2 | 566 | 570 | PF04695 | 0.315 |
LIG_Pex14_2 | 603 | 607 | PF04695 | 0.315 |
LIG_PTB_Apo_2 | 244 | 251 | PF02174 | 0.393 |
LIG_PTB_Phospho_1 | 244 | 250 | PF10480 | 0.393 |
LIG_Rb_pABgroove_1 | 362 | 370 | PF01858 | 0.315 |
LIG_SH2_CRK | 114 | 118 | PF00017 | 0.442 |
LIG_SH2_CRK | 333 | 337 | PF00017 | 0.448 |
LIG_SH2_NCK_1 | 126 | 130 | PF00017 | 0.414 |
LIG_SH2_NCK_1 | 333 | 337 | PF00017 | 0.358 |
LIG_SH2_PTP2 | 409 | 412 | PF00017 | 0.448 |
LIG_SH2_SRC | 333 | 336 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 126 | 130 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.294 |
LIG_SH2_STAP1 | 561 | 565 | PF00017 | 0.315 |
LIG_SH2_STAT3 | 561 | 564 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 633 | 636 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 649 | 652 | PF00017 | 0.273 |
LIG_SH3_3 | 426 | 432 | PF00018 | 0.315 |
LIG_SH3_3 | 499 | 505 | PF00018 | 0.342 |
LIG_SUMO_SIM_anti_2 | 310 | 315 | PF11976 | 0.332 |
LIG_SUMO_SIM_anti_2 | 74 | 81 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 394 | 400 | PF11976 | 0.397 |
LIG_SUMO_SIM_par_1 | 431 | 437 | PF11976 | 0.431 |
LIG_SUMO_SIM_par_1 | 95 | 101 | PF11976 | 0.397 |
LIG_TRAF2_1 | 158 | 161 | PF00917 | 0.494 |
LIG_TRAF2_1 | 353 | 356 | PF00917 | 0.415 |
LIG_TRFH_1 | 585 | 589 | PF08558 | 0.336 |
LIG_TYR_ITIM | 407 | 412 | PF00017 | 0.448 |
LIG_UBA3_1 | 299 | 306 | PF00899 | 0.321 |
LIG_UBA3_1 | 338 | 344 | PF00899 | 0.358 |
LIG_UBA3_1 | 518 | 527 | PF00899 | 0.315 |
LIG_UBA3_1 | 6 | 15 | PF00899 | 0.523 |
LIG_WRC_WIRS_1 | 273 | 278 | PF05994 | 0.393 |
LIG_WRC_WIRS_1 | 371 | 376 | PF05994 | 0.380 |
LIG_WRC_WIRS_1 | 469 | 474 | PF05994 | 0.315 |
LIG_WRC_WIRS_1 | 489 | 494 | PF05994 | 0.383 |
LIG_WRC_WIRS_1 | 99 | 104 | PF05994 | 0.384 |
MOD_CDC14_SPxK_1 | 83 | 86 | PF00782 | 0.483 |
MOD_CDK_SPxK_1 | 80 | 86 | PF00069 | 0.469 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.461 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.593 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.399 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.430 |
MOD_CK2_1 | 291 | 297 | PF00069 | 0.529 |
MOD_CK2_1 | 598 | 604 | PF00069 | 0.334 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.485 |
MOD_Cter_Amidation | 645 | 648 | PF01082 | 0.321 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.501 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.540 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.517 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.432 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.436 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.359 |
MOD_GlcNHglycan | 604 | 607 | PF01048 | 0.423 |
MOD_GlcNHglycan | 70 | 74 | PF01048 | 0.401 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.488 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.249 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.315 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.455 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.355 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.420 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.373 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.351 |
MOD_GSK3_1 | 598 | 605 | PF00069 | 0.459 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.448 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.430 |
MOD_N-GLC_1 | 347 | 352 | PF02516 | 0.315 |
MOD_N-GLC_1 | 383 | 388 | PF02516 | 0.363 |
MOD_N-GLC_1 | 400 | 405 | PF02516 | 0.269 |
MOD_N-GLC_1 | 8 | 13 | PF02516 | 0.590 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.622 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.301 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.315 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.315 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.315 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.322 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.414 |
MOD_NEK2_1 | 578 | 583 | PF00069 | 0.342 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.395 |
MOD_NEK2_2 | 2 | 7 | PF00069 | 0.500 |
MOD_NEK2_2 | 214 | 219 | PF00069 | 0.446 |
MOD_NEK2_2 | 549 | 554 | PF00069 | 0.334 |
MOD_PIKK_1 | 503 | 509 | PF00454 | 0.315 |
MOD_PIKK_1 | 569 | 575 | PF00454 | 0.499 |
MOD_PIKK_1 | 578 | 584 | PF00454 | 0.450 |
MOD_PIKK_1 | 656 | 662 | PF00454 | 0.444 |
MOD_PKA_1 | 305 | 311 | PF00069 | 0.249 |
MOD_PKA_2 | 549 | 555 | PF00069 | 0.340 |
MOD_PKB_1 | 486 | 494 | PF00069 | 0.407 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.355 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.442 |
MOD_Plk_1 | 360 | 366 | PF00069 | 0.324 |
MOD_Plk_1 | 375 | 381 | PF00069 | 0.315 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.510 |
MOD_Plk_1 | 51 | 57 | PF00069 | 0.518 |
MOD_Plk_1 | 578 | 584 | PF00069 | 0.358 |
MOD_Plk_1 | 8 | 14 | PF00069 | 0.596 |
MOD_Plk_2-3 | 100 | 106 | PF00069 | 0.416 |
MOD_Plk_2-3 | 392 | 398 | PF00069 | 0.428 |
MOD_Plk_2-3 | 63 | 69 | PF00069 | 0.384 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.355 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.533 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.648 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.548 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.368 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.383 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.448 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.537 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.358 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.349 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.323 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.345 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.323 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.453 |
MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.319 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.433 |
MOD_SUMO_rev_2 | 184 | 188 | PF00179 | 0.493 |
MOD_SUMO_rev_2 | 195 | 200 | PF00179 | 0.496 |
MOD_SUMO_rev_2 | 386 | 396 | PF00179 | 0.493 |
MOD_SUMO_rev_2 | 397 | 403 | PF00179 | 0.384 |
MOD_SUMO_rev_2 | 413 | 422 | PF00179 | 0.241 |
MOD_SUMO_rev_2 | 636 | 645 | PF00179 | 0.448 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 371 | 374 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 618 | 621 | PF00928 | 0.315 |
TRG_ER_diArg_1 | 150 | 153 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 486 | 489 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 647 | 649 | PF00400 | 0.366 |
TRG_Pf-PMV_PEXEL_1 | 534 | 538 | PF00026 | 0.469 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6N6 | Leptomonas seymouri | 24% | 100% |
A0A0N1HT30 | Leptomonas seymouri | 24% | 100% |
A0A0N1PBM8 | Leptomonas seymouri | 83% | 100% |
A0A0N1PDB7 | Leptomonas seymouri | 26% | 100% |
A0A0S4JRG5 | Bodo saltans | 58% | 100% |
A0A1X0NTS0 | Trypanosomatidae | 63% | 100% |
A0A1X0P0Z5 | Trypanosomatidae | 23% | 99% |
A0A3Q8IKU0 | Leishmania donovani | 24% | 100% |
A0A3S5H518 | Leishmania donovani | 25% | 100% |
A0A3S7WZY5 | Leishmania donovani | 97% | 100% |
A0A422MUB5 | Trypanosoma rangeli | 61% | 100% |
A0A422P572 | Trypanosoma rangeli | 23% | 100% |
A1CTP5 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 24% | 86% |
A1DMR2 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 23% | 86% |
A2QWM4 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 23% | 86% |
A2VDQ5 | Bos taurus | 33% | 97% |
A3LUT4 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 23% | 84% |
A4HF12 | Leishmania braziliensis | 90% | 100% |
A4HFS7 | Leishmania braziliensis | 27% | 100% |
A4HFS8 | Leishmania braziliensis | 26% | 100% |
A4HG35 | Leishmania braziliensis | 25% | 100% |
A4HG37 | Leishmania braziliensis | 26% | 100% |
A4HPW2 | Leishmania braziliensis | 24% | 100% |
A4HRR9 | Leishmania infantum | 25% | 100% |
A4I291 | Leishmania infantum | 98% | 100% |
A4IDM4 | Leishmania infantum | 24% | 100% |
A4RF25 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 26% | 84% |
A5DI46 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 25% | 87% |
A5E4V6 | Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) | 24% | 84% |
A6SHZ5 | Botryotinia fuckeliana (strain B05.10) | 26% | 90% |
A6ZZI7 | Saccharomyces cerevisiae (strain YJM789) | 27% | 89% |
A7E7L8 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 26% | 87% |
A7TSL2 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 26% | 87% |
A8N2T3 | Coprinopsis cinerea (strain Okayama-7 / 130 / ATCC MYA-4618 / FGSC 9003) | 24% | 88% |
A8QB25 | Malassezia globosa (strain ATCC MYA-4612 / CBS 7966) | 27% | 85% |
B0CRC2 | Laccaria bicolor (strain S238N-H82 / ATCC MYA-4686) | 24% | 89% |
B0Y7Q2 | Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) | 23% | 86% |
C9ZRP1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 92% |
D0A4B0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
E9AC74 | Leishmania major | 24% | 100% |
E9ACE8 | Leishmania major | 24% | 100% |
E9AJN6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9ATM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AYD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
F4HTQ1 | Arabidopsis thaliana | 29% | 96% |
F4KDA5 | Arabidopsis thaliana | 26% | 97% |
P0CQ18 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 27% | 90% |
P0CQ19 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 27% | 90% |
P0CQ20 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 25% | 83% |
P0CQ21 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 25% | 83% |
P24155 | Rattus norvegicus | 34% | 100% |
P24171 | Escherichia coli (strain K12) | 26% | 100% |
P25375 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 96% |
P27236 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 26% | 100% |
P27237 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 28% | 100% |
P27298 | Escherichia coli (strain K12) | 29% | 100% |
P35999 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 89% |
P37932 | Schizophyllum commune | 24% | 88% |
P42675 | Oryctolagus cuniculus | 33% | 97% |
P42676 | Rattus norvegicus | 33% | 97% |
P44573 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 27% | 100% |
P47788 | Sus scrofa | 34% | 100% |
P52888 | Homo sapiens | 34% | 99% |
Q02038 | Sus scrofa | 33% | 97% |
Q0CI79 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 23% | 85% |
Q0TXL7 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 25% | 87% |
Q10415 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 90% |
Q1E8M9 | Coccidioides immitis (strain RS) | 24% | 86% |
Q1JPJ8 | Bos taurus | 35% | 100% |
Q2HFL8 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 25% | 88% |
Q2UN31 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 22% | 86% |
Q4PBS8 | Ustilago maydis (strain 521 / FGSC 9021) | 24% | 77% |
Q4Q0W9 | Leishmania major | 22% | 100% |
Q4WMU9 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 23% | 86% |
Q54DD2 | Dictyostelium discoideum | 30% | 100% |
Q59RK9 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 23% | 87% |
Q5R9V6 | Pongo abelii | 32% | 97% |
Q5RF14 | Pongo abelii | 26% | 96% |
Q6BJ61 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 26% | 86% |
Q6CVF7 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 26% | 88% |
Q6FW88 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 25% | 90% |
Q6VMB4 | Leucoagaricus gongylophorus | 24% | 90% |
Q6Y5M5 | Pleurotus djamor | 25% | 87% |
Q6Y5M6 | Coprinellus disseminatus | 26% | 89% |
Q6Y5M7 | Coprinopsis scobicola | 26% | 89% |
Q753X4 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 26% | 88% |
Q7SDD5 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 24% | 85% |
Q8C1A5 | Mus musculus | 35% | 100% |
Q91YP2 | Mus musculus | 33% | 97% |
Q949P2 | Arabidopsis thaliana | 26% | 98% |
Q94AM1 | Arabidopsis thaliana | 27% | 87% |
Q99797 | Homo sapiens | 26% | 96% |
Q9BYT8 | Homo sapiens | 33% | 97% |
V5B526 | Trypanosoma cruzi | 22% | 100% |