Proteases, mitochondrial intermediate peptidase
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:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4IDM4
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:0006518 | peptide metabolic process | 4 | 1 |
GO:0043603 | amide metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004175 | endopeptidase activity | 4 | 12 |
GO:0004222 | metalloendopeptidase activity | 5 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008233 | peptidase activity | 3 | 12 |
GO:0008237 | metallopeptidase activity | 4 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 61 | 65 | PF00656 | 0.438 |
CLV_C14_Caspase3-7 | 95 | 99 | PF00656 | 0.327 |
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.347 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.370 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 624 | 626 | PF00675 | 0.260 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.164 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.076 |
CLV_PCSK_KEX2_1 | 514 | 516 | PF00082 | 0.260 |
CLV_PCSK_KEX2_1 | 560 | 562 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 624 | 626 | PF00082 | 0.260 |
CLV_PCSK_PC1ET2_1 | 124 | 126 | PF00082 | 0.427 |
CLV_PCSK_PC1ET2_1 | 361 | 363 | PF00082 | 0.329 |
CLV_PCSK_PC1ET2_1 | 406 | 408 | PF00082 | 0.317 |
CLV_PCSK_PC1ET2_1 | 514 | 516 | PF00082 | 0.260 |
CLV_PCSK_PC1ET2_1 | 560 | 562 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.276 |
DEG_APCC_DBOX_1 | 143 | 151 | PF00400 | 0.335 |
DEG_APCC_DBOX_1 | 226 | 234 | PF00400 | 0.294 |
DEG_MDM2_SWIB_1 | 493 | 501 | PF02201 | 0.260 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.533 |
DEG_SPOP_SBC_1 | 38 | 42 | PF00917 | 0.637 |
DOC_MAPK_gen_1 | 124 | 131 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 190 | 198 | PF00069 | 0.357 |
DOC_MAPK_gen_1 | 361 | 369 | PF00069 | 0.407 |
DOC_MAPK_gen_1 | 403 | 413 | PF00069 | 0.306 |
DOC_MAPK_MEF2A_6 | 361 | 368 | PF00069 | 0.260 |
DOC_MAPK_MEF2A_6 | 406 | 414 | PF00069 | 0.270 |
DOC_PP2B_LxvP_1 | 402 | 405 | PF13499 | 0.260 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.700 |
DOC_USP7_UBL2_3 | 82 | 86 | PF12436 | 0.508 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.491 |
LIG_14-3-3_CanoR_1 | 125 | 130 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 190 | 198 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 297 | 303 | PF00244 | 0.257 |
LIG_14-3-3_CanoR_1 | 3 | 12 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 515 | 522 | PF00244 | 0.410 |
LIG_Actin_WH2_2 | 67 | 84 | PF00022 | 0.441 |
LIG_APCC_ABBA_1 | 354 | 359 | PF00400 | 0.294 |
LIG_APCC_ABBAyCdc20_2 | 353 | 359 | PF00400 | 0.260 |
LIG_BIR_III_2 | 305 | 309 | PF00653 | 0.275 |
LIG_BRCT_BRCA1_1 | 127 | 131 | PF00533 | 0.358 |
LIG_BRCT_BRCA1_1 | 328 | 332 | PF00533 | 0.260 |
LIG_BRCT_BRCA1_1 | 480 | 484 | PF00533 | 0.294 |
LIG_BRCT_BRCA1_1 | 489 | 493 | PF00533 | 0.334 |
LIG_BRCT_BRCA1_2 | 127 | 133 | PF00533 | 0.343 |
LIG_BRCT_BRCA1_2 | 489 | 495 | PF00533 | 0.345 |
LIG_Clathr_ClatBox_1 | 233 | 237 | PF01394 | 0.294 |
LIG_deltaCOP1_diTrp_1 | 253 | 258 | PF00928 | 0.329 |
LIG_EH_1 | 214 | 218 | PF12763 | 0.391 |
LIG_eIF4E_1 | 228 | 234 | PF01652 | 0.294 |
LIG_FHA_1 | 383 | 389 | PF00498 | 0.260 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.260 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.149 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.385 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.338 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.286 |
LIG_FHA_2 | 245 | 251 | PF00498 | 0.294 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.380 |
LIG_FHA_2 | 48 | 54 | PF00498 | 0.494 |
LIG_FHA_2 | 560 | 566 | PF00498 | 0.392 |
LIG_FHA_2 | 668 | 674 | PF00498 | 0.486 |
LIG_HP1_1 | 410 | 414 | PF01393 | 0.260 |
LIG_LIR_Gen_1 | 146 | 154 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 253 | 263 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 445 | 455 | PF02991 | 0.260 |
LIG_LIR_Gen_1 | 478 | 488 | PF02991 | 0.260 |
LIG_LIR_Gen_1 | 490 | 501 | PF02991 | 0.260 |
LIG_LIR_Gen_1 | 600 | 611 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 146 | 151 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 253 | 259 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 313 | 317 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 445 | 451 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 47 | 51 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 478 | 483 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 490 | 496 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 508 | 512 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 600 | 606 | PF02991 | 0.260 |
LIG_LYPXL_yS_3 | 409 | 412 | PF13949 | 0.260 |
LIG_NRBOX | 103 | 109 | PF00104 | 0.294 |
LIG_NRBOX | 219 | 225 | PF00104 | 0.275 |
LIG_NRBOX | 229 | 235 | PF00104 | 0.275 |
LIG_PCNA_PIPBox_1 | 252 | 261 | PF02747 | 0.260 |
LIG_PCNA_TLS_4 | 658 | 665 | PF02747 | 0.380 |
LIG_PCNA_yPIPBox_3 | 245 | 259 | PF02747 | 0.260 |
LIG_PDZ_Class_2 | 671 | 676 | PF00595 | 0.371 |
LIG_PDZ_Wminus1_1 | 674 | 676 | PF00595 | 0.367 |
LIG_Pex14_1 | 627 | 631 | PF04695 | 0.260 |
LIG_Pex14_2 | 480 | 484 | PF04695 | 0.275 |
LIG_Pex14_2 | 493 | 497 | PF04695 | 0.313 |
LIG_PTB_Apo_2 | 22 | 29 | PF02174 | 0.596 |
LIG_PTB_Apo_2 | 53 | 60 | PF02174 | 0.407 |
LIG_SH2_CRK | 148 | 152 | PF00017 | 0.338 |
LIG_SH2_CRK | 48 | 52 | PF00017 | 0.571 |
LIG_SH2_CRK | 614 | 618 | PF00017 | 0.260 |
LIG_SH2_GRB2like | 372 | 375 | PF00017 | 0.317 |
LIG_SH2_NCK_1 | 228 | 232 | PF00017 | 0.345 |
LIG_SH2_SRC | 357 | 360 | PF00017 | 0.380 |
LIG_SH2_SRC | 616 | 619 | PF00017 | 0.260 |
LIG_SH2_STAP1 | 432 | 436 | PF00017 | 0.193 |
LIG_SH2_STAP1 | 618 | 622 | PF00017 | 0.260 |
LIG_SH2_STAT3 | 222 | 225 | PF00017 | 0.345 |
LIG_SH2_STAT3 | 239 | 242 | PF00017 | 0.294 |
LIG_SH2_STAT3 | 266 | 269 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 476 | 479 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 616 | 619 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 664 | 667 | PF00017 | 0.260 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.325 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.648 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.559 |
LIG_SH3_3 | 545 | 551 | PF00018 | 0.365 |
LIG_SH3_3 | 580 | 586 | PF00018 | 0.360 |
LIG_Sin3_3 | 577 | 584 | PF02671 | 0.451 |
LIG_SUMO_SIM_par_1 | 365 | 370 | PF11976 | 0.260 |
LIG_SUMO_SIM_par_1 | 409 | 415 | PF11976 | 0.260 |
LIG_SUMO_SIM_par_1 | 585 | 591 | PF11976 | 0.379 |
LIG_SUMO_SIM_par_1 | 71 | 78 | PF11976 | 0.337 |
LIG_TRAF2_1 | 392 | 395 | PF00917 | 0.294 |
LIG_TYR_ITIM | 312 | 317 | PF00017 | 0.380 |
LIG_UBA3_1 | 80 | 88 | PF00899 | 0.368 |
LIG_WRC_WIRS_1 | 477 | 482 | PF05994 | 0.260 |
MOD_CDC14_SPxK_1 | 10 | 13 | PF00782 | 0.534 |
MOD_CDK_SPK_2 | 39 | 44 | PF00069 | 0.496 |
MOD_CDK_SPxK_1 | 7 | 13 | PF00069 | 0.526 |
MOD_CDK_SPxxK_3 | 86 | 93 | PF00069 | 0.487 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.380 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.301 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.544 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.260 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.260 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.275 |
MOD_CK2_1 | 585 | 591 | PF00069 | 0.371 |
MOD_Cter_Amidation | 158 | 161 | PF01082 | 0.433 |
MOD_Cter_Amidation | 558 | 561 | PF01082 | 0.381 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.274 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.540 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.667 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.383 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.187 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.299 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.432 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.579 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.355 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.348 |
MOD_N-GLC_1 | 288 | 293 | PF02516 | 0.264 |
MOD_N-GLC_1 | 32 | 37 | PF02516 | 0.664 |
MOD_N-GLC_1 | 347 | 352 | PF02516 | 0.380 |
MOD_N-GLC_1 | 667 | 672 | PF02516 | 0.416 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.260 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.260 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.643 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.260 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.260 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.294 |
MOD_NEK2_2 | 216 | 221 | PF00069 | 0.339 |
MOD_NEK2_2 | 454 | 459 | PF00069 | 0.260 |
MOD_PIKK_1 | 459 | 465 | PF00454 | 0.370 |
MOD_PIKK_1 | 478 | 484 | PF00454 | 0.098 |
MOD_PK_1 | 585 | 591 | PF00069 | 0.480 |
MOD_PKA_1 | 514 | 520 | PF00069 | 0.329 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.260 |
MOD_PKA_2 | 470 | 476 | PF00069 | 0.260 |
MOD_PKA_2 | 514 | 520 | PF00069 | 0.410 |
MOD_PKA_2 | 657 | 663 | PF00069 | 0.407 |
MOD_PKB_1 | 295 | 303 | PF00069 | 0.329 |
MOD_Plk_1 | 347 | 353 | PF00069 | 0.400 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.277 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.278 |
MOD_Plk_2-3 | 505 | 511 | PF00069 | 0.260 |
MOD_Plk_2-3 | 667 | 673 | PF00069 | 0.490 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.450 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.260 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.275 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.262 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.076 |
MOD_Plk_4 | 544 | 550 | PF00069 | 0.373 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.411 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.614 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.401 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.539 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.490 |
MOD_SUMO_for_1 | 334 | 337 | PF00179 | 0.345 |
MOD_SUMO_rev_2 | 358 | 363 | PF00179 | 0.312 |
TRG_DiLeu_BaEn_1 | 229 | 234 | PF01217 | 0.317 |
TRG_DiLeu_BaEn_2 | 358 | 364 | PF01217 | 0.260 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.260 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.260 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.583 |
TRG_ENDOCYTIC_2 | 614 | 617 | PF00928 | 0.260 |
TRG_ER_diArg_1 | 12 | 15 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 284 | 287 | PF00400 | 0.263 |
TRG_ER_diArg_1 | 294 | 297 | PF00400 | 0.258 |
TRG_ER_diArg_1 | 302 | 304 | PF00400 | 0.248 |
TRG_ER_diArg_1 | 426 | 428 | PF00400 | 0.345 |
TRG_ER_diArg_1 | 624 | 626 | PF00400 | 0.260 |
TRG_NES_CRM1_1 | 325 | 338 | PF08389 | 0.260 |
TRG_NES_CRM1_1 | 345 | 359 | PF08389 | 0.076 |
TRG_NES_CRM1_1 | 64 | 78 | PF08389 | 0.449 |
TRG_Pf-PMV_PEXEL_1 | 145 | 149 | PF00026 | 0.356 |
TRG_Pf-PMV_PEXEL_1 | 206 | 210 | PF00026 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 221 | 225 | PF00026 | 0.260 |
TRG_Pf-PMV_PEXEL_1 | 561 | 565 | PF00026 | 0.394 |
TRG_Pf-PMV_PEXEL_1 | 578 | 582 | PF00026 | 0.341 |
TRG_Pf-PMV_PEXEL_1 | 642 | 646 | PF00026 | 0.294 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6N6 | Leptomonas seymouri | 87% | 100% |
A0A0N1PBM8 | Leptomonas seymouri | 25% | 99% |
A0A0N1PDB7 | Leptomonas seymouri | 23% | 100% |
A0A0S4JRG5 | Bodo saltans | 22% | 99% |
A0A0S4JWM4 | Bodo saltans | 67% | 100% |
A0A1X0P0Z5 | Trypanosomatidae | 75% | 98% |
A0A3Q8IKU0 | Leishmania donovani | 100% | 100% |
A0A3S7WZY5 | Leishmania donovani | 24% | 99% |
A0A422MUB5 | Trypanosoma rangeli | 26% | 99% |
A0A422P572 | Trypanosoma rangeli | 73% | 99% |
A1CTP5 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 26% | 84% |
A1DMR2 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 26% | 84% |
A2QWM4 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 26% | 85% |
A3LUT4 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 24% | 83% |
A4HF12 | Leishmania braziliensis | 25% | 100% |
A4HPW2 | Leishmania braziliensis | 91% | 100% |
A4I291 | Leishmania infantum | 24% | 100% |
A4RF25 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 23% | 83% |
A5DI46 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 24% | 86% |
A6H611 | Mus musculus | 24% | 95% |
A6SHZ5 | Botryotinia fuckeliana (strain B05.10) | 27% | 89% |
A6ZZI7 | Saccharomyces cerevisiae (strain YJM789) | 23% | 88% |
A7E7L8 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 27% | 86% |
A7TSL2 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 28% | 86% |
A8N2T3 | Coprinopsis cinerea (strain Okayama-7 / 130 / ATCC MYA-4618 / FGSC 9003) | 31% | 87% |
A8QB25 | Malassezia globosa (strain ATCC MYA-4612 / CBS 7966) | 28% | 84% |
B0CRC2 | Laccaria bicolor (strain S238N-H82 / ATCC MYA-4686) | 24% | 88% |
B0Y7Q2 | Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) | 26% | 84% |
D0A4B0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 74% | 100% |
E9ATM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
E9AYD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
F4HTQ1 | Arabidopsis thaliana | 25% | 95% |
F4KDA5 | Arabidopsis thaliana | 25% | 96% |
P0CQ18 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 27% | 89% |
P0CQ19 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 27% | 89% |
P0CQ20 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 24% | 82% |
P0CQ21 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 24% | 82% |
P24155 | Rattus norvegicus | 26% | 98% |
P25375 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 95% |
P27237 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 27% | 99% |
P27298 | Escherichia coli (strain K12) | 27% | 99% |
P35999 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 88% |
P37932 | Schizophyllum commune | 27% | 87% |
P44573 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 25% | 99% |
P47788 | Sus scrofa | 26% | 98% |
P52888 | Homo sapiens | 25% | 98% |
Q01992 | Rattus norvegicus | 24% | 95% |
Q0CI79 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 27% | 84% |
Q0TXL7 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 26% | 86% |
Q10415 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 89% |
Q1E8M9 | Coccidioides immitis (strain RS) | 26% | 85% |
Q1JPJ8 | Bos taurus | 26% | 98% |
Q2HFL8 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 25% | 87% |
Q2UN31 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 25% | 84% |
Q4PBS8 | Ustilago maydis (strain 521 / FGSC 9021) | 26% | 76% |
Q4Q0W9 | Leishmania major | 97% | 100% |
Q4Q937 | Leishmania major | 24% | 100% |
Q4WMU9 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 26% | 84% |
Q54DD2 | Dictyostelium discoideum | 24% | 100% |
Q59RK9 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 26% | 86% |
Q5RF14 | Pongo abelii | 25% | 95% |
Q6BJ61 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 28% | 85% |
Q6CHD6 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 27% | 87% |
Q6CVF7 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 25% | 87% |
Q6FW88 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 25% | 89% |
Q6VMB4 | Leucoagaricus gongylophorus | 24% | 89% |
Q6Y5M5 | Pleurotus djamor | 27% | 86% |
Q6Y5M6 | Coprinellus disseminatus | 24% | 87% |
Q6Y5M7 | Coprinopsis scobicola | 25% | 88% |
Q753X4 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 25% | 87% |
Q7SDD5 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 24% | 84% |
Q8C1A5 | Mus musculus | 26% | 98% |
Q949P2 | Arabidopsis thaliana | 25% | 96% |
Q94AM1 | Arabidopsis thaliana | 25% | 85% |
Q99797 | Homo sapiens | 25% | 95% |
V5B526 | Trypanosoma cruzi | 74% | 99% |