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: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 3 |
GO:0005829 | cytosol | 2 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: Q4QCH5
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 15 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 15 |
GO:0006807 | nitrogen compound metabolic process | 2 | 15 |
GO:0008152 | metabolic process | 1 | 15 |
GO:0009056 | catabolic process | 2 | 15 |
GO:0009057 | macromolecule catabolic process | 4 | 15 |
GO:0009987 | cellular process | 1 | 15 |
GO:0016579 | protein deubiquitination | 6 | 15 |
GO:0019538 | protein metabolic process | 3 | 15 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 15 |
GO:0036211 | protein modification process | 4 | 15 |
GO:0043170 | macromolecule metabolic process | 3 | 15 |
GO:0043412 | macromolecule modification | 4 | 15 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 15 |
GO:0044237 | cellular metabolic process | 2 | 15 |
GO:0044238 | primary metabolic process | 2 | 15 |
GO:0044248 | cellular catabolic process | 3 | 15 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 15 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 15 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 15 |
GO:0070646 | protein modification by small protein removal | 5 | 15 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 15 |
GO:0071704 | organic substance metabolic process | 2 | 15 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 15 |
GO:1901575 | organic substance catabolic process | 3 | 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 15 |
GO:0004175 | endopeptidase activity | 4 | 3 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 3 |
GO:0004843 | cysteine-type deubiquitinase activity | 5 | 15 |
GO:0008233 | peptidase activity | 3 | 15 |
GO:0008234 | cysteine-type peptidase activity | 4 | 15 |
GO:0016787 | hydrolase activity | 2 | 15 |
GO:0019783 | ubiquitin-like protein peptidase activity | 4 | 15 |
GO:0101005 | deubiquitinase activity | 5 | 15 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 15 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 139 | 143 | PF00656 | 0.617 |
CLV_C14_Caspase3-7 | 541 | 545 | PF00656 | 0.358 |
CLV_NRD_NRD_1 | 580 | 582 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 623 | 625 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.721 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 490 | 492 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 580 | 582 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 623 | 625 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.726 |
CLV_PCSK_PC1ET2_1 | 140 | 142 | PF00082 | 0.541 |
CLV_PCSK_PC1ET2_1 | 490 | 492 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 470 | 474 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 636 | 640 | PF00082 | 0.452 |
DEG_APCC_DBOX_1 | 228 | 236 | PF00400 | 0.282 |
DEG_APCC_DBOX_1 | 579 | 587 | PF00400 | 0.374 |
DEG_APCC_KENBOX_2 | 362 | 366 | PF00400 | 0.232 |
DEG_SCF_FBW7_1 | 38 | 45 | PF00400 | 0.515 |
DEG_SPOP_SBC_1 | 545 | 549 | PF00917 | 0.386 |
DEG_SPOP_SBC_1 | 651 | 655 | PF00917 | 0.294 |
DOC_MAPK_gen_1 | 340 | 347 | PF00069 | 0.324 |
DOC_MAPK_gen_1 | 503 | 510 | PF00069 | 0.258 |
DOC_MAPK_HePTP_8 | 421 | 433 | PF00069 | 0.374 |
DOC_MAPK_HePTP_8 | 500 | 512 | PF00069 | 0.247 |
DOC_MAPK_MEF2A_6 | 424 | 433 | PF00069 | 0.278 |
DOC_MAPK_MEF2A_6 | 503 | 512 | PF00069 | 0.329 |
DOC_MAPK_MEF2A_6 | 57 | 65 | PF00069 | 0.546 |
DOC_MAPK_RevD_3 | 475 | 491 | PF00069 | 0.281 |
DOC_PP4_FxxP_1 | 448 | 451 | PF00568 | 0.258 |
DOC_PP4_FxxP_1 | 642 | 645 | PF00568 | 0.374 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.322 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 545 | 549 | PF00917 | 0.313 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.675 |
DOC_USP7_UBL2_3 | 279 | 283 | PF12436 | 0.360 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 396 | 401 | PF00397 | 0.327 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 565 | 570 | PF00397 | 0.339 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.636 |
LIG_14-3-3_CanoR_1 | 132 | 137 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 44 | 49 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 73 | 82 | PF00244 | 0.768 |
LIG_14-3-3_CanoR_1 | 93 | 101 | PF00244 | 0.664 |
LIG_APCC_ABBAyCdc20_2 | 424 | 430 | PF00400 | 0.374 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.462 |
LIG_BIR_III_4 | 647 | 651 | PF00653 | 0.374 |
LIG_BRCT_BRCA1_1 | 175 | 179 | PF00533 | 0.464 |
LIG_BRCT_BRCA1_1 | 343 | 347 | PF00533 | 0.357 |
LIG_BRCT_BRCA1_1 | 76 | 80 | PF00533 | 0.737 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.464 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.500 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.322 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.303 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.232 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.374 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.792 |
LIG_FHA_1 | 594 | 600 | PF00498 | 0.374 |
LIG_FHA_1 | 653 | 659 | PF00498 | 0.270 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.660 |
LIG_FHA_2 | 374 | 380 | PF00498 | 0.357 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.343 |
LIG_FHA_2 | 519 | 525 | PF00498 | 0.374 |
LIG_FHA_2 | 630 | 636 | PF00498 | 0.317 |
LIG_LIR_Apic_2 | 32 | 38 | PF02991 | 0.627 |
LIG_LIR_Apic_2 | 446 | 451 | PF02991 | 0.302 |
LIG_LIR_Gen_1 | 194 | 204 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 306 | 315 | PF02991 | 0.241 |
LIG_LIR_Gen_1 | 425 | 436 | PF02991 | 0.275 |
LIG_LIR_Gen_1 | 654 | 665 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 194 | 199 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 234 | 239 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 306 | 310 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 425 | 431 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 654 | 660 | PF02991 | 0.297 |
LIG_PCNA_PIPBox_1 | 513 | 522 | PF02747 | 0.374 |
LIG_PTB_Apo_2 | 208 | 215 | PF02174 | 0.253 |
LIG_PTB_Phospho_1 | 208 | 214 | PF10480 | 0.238 |
LIG_SH2_CRK | 35 | 39 | PF00017 | 0.642 |
LIG_SH2_CRK | 483 | 487 | PF00017 | 0.258 |
LIG_SH2_NCK_1 | 661 | 665 | PF00017 | 0.307 |
LIG_SH2_PTP2 | 657 | 660 | PF00017 | 0.258 |
LIG_SH2_SRC | 27 | 30 | PF00017 | 0.591 |
LIG_SH2_STAP1 | 335 | 339 | PF00017 | 0.398 |
LIG_SH2_STAP1 | 483 | 487 | PF00017 | 0.311 |
LIG_SH2_STAP1 | 661 | 665 | PF00017 | 0.364 |
LIG_SH2_STAT3 | 617 | 620 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.691 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 611 | 614 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 641 | 644 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 657 | 660 | PF00017 | 0.239 |
LIG_SH3_2 | 88 | 93 | PF14604 | 0.636 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.638 |
LIG_SH3_3 | 505 | 511 | PF00018 | 0.309 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.665 |
LIG_SUMO_SIM_anti_2 | 259 | 265 | PF11976 | 0.327 |
LIG_SUMO_SIM_par_1 | 112 | 120 | PF11976 | 0.660 |
LIG_TRAF2_1 | 423 | 426 | PF00917 | 0.425 |
LIG_TRAF2_1 | 575 | 578 | PF00917 | 0.365 |
LIG_TYR_ITIM | 659 | 664 | PF00017 | 0.292 |
LIG_UBA3_1 | 260 | 266 | PF00899 | 0.294 |
LIG_UBA3_1 | 485 | 490 | PF00899 | 0.253 |
MOD_CDC14_SPxK_1 | 90 | 93 | PF00782 | 0.571 |
MOD_CDK_SPxK_1 | 38 | 44 | PF00069 | 0.515 |
MOD_CDK_SPxK_1 | 87 | 93 | PF00069 | 0.569 |
MOD_CDK_SPxxK_3 | 122 | 129 | PF00069 | 0.529 |
MOD_CDK_SPxxK_3 | 4 | 11 | PF00069 | 0.534 |
MOD_CDK_SPxxK_3 | 87 | 94 | PF00069 | 0.571 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.560 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.631 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.579 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.617 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.492 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.319 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.540 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.349 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.635 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.289 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.290 |
MOD_CK1_1 | 568 | 574 | PF00069 | 0.308 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.622 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.548 |
MOD_CK2_1 | 358 | 364 | PF00069 | 0.364 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.373 |
MOD_CK2_1 | 518 | 524 | PF00069 | 0.371 |
MOD_CK2_1 | 629 | 635 | PF00069 | 0.295 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.559 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.609 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.661 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.353 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.590 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.331 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.317 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.386 |
MOD_GlcNHglycan | 607 | 610 | PF01048 | 0.323 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.563 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.554 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.583 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.636 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.557 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.611 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.501 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.354 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.478 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.284 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.318 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.609 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.388 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.280 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.364 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.194 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.370 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.590 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.550 |
MOD_N-GLC_1 | 110 | 115 | PF02516 | 0.766 |
MOD_N-GLC_1 | 268 | 273 | PF02516 | 0.385 |
MOD_N-GLC_1 | 419 | 424 | PF02516 | 0.317 |
MOD_N-GLC_1 | 552 | 557 | PF02516 | 0.453 |
MOD_N-GLC_1 | 563 | 568 | PF02516 | 0.290 |
MOD_N-GLC_1 | 99 | 104 | PF02516 | 0.788 |
MOD_N-GLC_2 | 211 | 213 | PF02516 | 0.253 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.589 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.681 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.548 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.639 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.446 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.349 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.688 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.407 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.342 |
MOD_NEK2_1 | 593 | 598 | PF00069 | 0.258 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.626 |
MOD_NEK2_2 | 152 | 157 | PF00069 | 0.512 |
MOD_NEK2_2 | 209 | 214 | PF00069 | 0.258 |
MOD_NEK2_2 | 335 | 340 | PF00069 | 0.239 |
MOD_NEK2_2 | 471 | 476 | PF00069 | 0.357 |
MOD_PIKK_1 | 534 | 540 | PF00454 | 0.319 |
MOD_PIKK_1 | 55 | 61 | PF00454 | 0.697 |
MOD_PIKK_1 | 65 | 71 | PF00454 | 0.671 |
MOD_PKA_1 | 341 | 347 | PF00069 | 0.357 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.705 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.278 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.370 |
MOD_Plk_1 | 335 | 341 | PF00069 | 0.477 |
MOD_Plk_1 | 367 | 373 | PF00069 | 0.296 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.530 |
MOD_Plk_1 | 429 | 435 | PF00069 | 0.255 |
MOD_Plk_1 | 526 | 532 | PF00069 | 0.450 |
MOD_Plk_1 | 626 | 632 | PF00069 | 0.301 |
MOD_Plk_2-3 | 518 | 524 | PF00069 | 0.374 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.393 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.258 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.265 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.614 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.282 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.581 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.436 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.588 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.515 |
MOD_ProDKin_1 | 396 | 402 | PF00069 | 0.327 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.695 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.464 |
MOD_ProDKin_1 | 565 | 571 | PF00069 | 0.339 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.636 |
MOD_SUMO_for_1 | 291 | 294 | PF00179 | 0.232 |
MOD_SUMO_for_1 | 333 | 336 | PF00179 | 0.232 |
MOD_SUMO_rev_2 | 23 | 33 | PF00179 | 0.490 |
MOD_SUMO_rev_2 | 463 | 468 | PF00179 | 0.425 |
TRG_DiLeu_BaEn_2 | 305 | 311 | PF01217 | 0.258 |
TRG_DiLeu_BaEn_2 | 593 | 599 | PF01217 | 0.374 |
TRG_DiLeu_BaLyEn_6 | 228 | 233 | PF01217 | 0.282 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 641 | 644 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 657 | 660 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 661 | 664 | PF00928 | 0.353 |
TRG_ER_diArg_1 | 228 | 231 | PF00400 | 0.266 |
TRG_ER_diArg_1 | 579 | 581 | PF00400 | 0.276 |
TRG_ER_diArg_1 | 622 | 624 | PF00400 | 0.374 |
TRG_NLS_MonoExtC_3 | 241 | 246 | PF00514 | 0.271 |
TRG_NLS_MonoExtN_4 | 580 | 585 | PF00514 | 0.261 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2Z2 | Leptomonas seymouri | 23% | 83% |
A0A0N0P852 | Leptomonas seymouri | 68% | 88% |
A0A0S4IVV7 | Bodo saltans | 22% | 100% |
A0A3Q8IB18 | Leishmania donovani | 95% | 92% |
A0A422MZT5 | Trypanosoma rangeli | 42% | 100% |
A4HBN8 | Leishmania braziliensis | 79% | 90% |
A4HZ39 | Leishmania infantum | 95% | 92% |
A4IBF1 | Leishmania infantum | 24% | 100% |
D0A1P0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AV07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9AWQ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 82% |
P39944 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 22% | 83% |
Q4QAS1 | Leishmania major | 22% | 82% |
V5DGZ8 | Trypanosoma cruzi | 40% | 100% |