| 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. | yes | yes: 25 |
| 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. | yes | yes: 8 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 11 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 1 |
| 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 |
Related structures:
AlphaFold database: A0A3Q8IRB8
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006082 | organic acid metabolic process | 3 | 1 |
| GO:0006629 | lipid metabolic process | 3 | 1 |
| GO:0006631 | fatty acid metabolic process | 4 | 1 |
| GO:0006635 | fatty acid beta-oxidation | 6 | 1 |
| GO:0008152 | metabolic process | 1 | 1 |
| GO:0009056 | catabolic process | 2 | 1 |
| GO:0009062 | fatty acid catabolic process | 5 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0016042 | lipid catabolic process | 4 | 1 |
| GO:0016054 | organic acid catabolic process | 4 | 1 |
| GO:0019395 | fatty acid oxidation | 5 | 1 |
| GO:0019752 | carboxylic acid metabolic process | 5 | 1 |
| GO:0030258 | lipid modification | 4 | 1 |
| GO:0032787 | monocarboxylic acid metabolic process | 6 | 1 |
| GO:0034440 | lipid oxidation | 5 | 1 |
| GO:0043436 | oxoacid metabolic process | 4 | 1 |
| GO:0044237 | cellular metabolic process | 2 | 1 |
| GO:0044238 | primary metabolic process | 2 | 1 |
| GO:0044242 | cellular lipid catabolic process | 4 | 1 |
| GO:0044248 | cellular catabolic process | 3 | 1 |
| GO:0044255 | cellular lipid metabolic process | 3 | 1 |
| GO:0044281 | small molecule metabolic process | 2 | 1 |
| GO:0044282 | small molecule catabolic process | 3 | 1 |
| GO:0046395 | carboxylic acid catabolic process | 5 | 1 |
| GO:0071704 | organic substance metabolic process | 2 | 1 |
| GO:0072329 | monocarboxylic acid catabolic process | 6 | 1 |
| GO:1901575 | organic substance catabolic process | 3 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 12 |
| GO:0016740 | transferase activity | 2 | 12 |
| GO:0016746 | acyltransferase activity | 3 | 12 |
| GO:0004095 | carnitine O-palmitoyltransferase activity | 7 | 3 |
| GO:0008374 | O-acyltransferase activity | 5 | 3 |
| GO:0016406 | carnitine O-acyltransferase activity | 6 | 3 |
| GO:0016409 | palmitoyltransferase activity | 5 | 3 |
| GO:0016416 | O-palmitoyltransferase activity | 6 | 3 |
| GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 3 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 350 | 354 | PF00656 | 0.552 |
| CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.489 |
| CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.465 |
| CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.471 |
| CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.484 |
| CLV_PCSK_PC7_1 | 205 | 211 | PF00082 | 0.365 |
| CLV_PCSK_SKI1_1 | 482 | 486 | PF00082 | 0.383 |
| CLV_PCSK_SKI1_1 | 526 | 530 | PF00082 | 0.428 |
| CLV_PCSK_SKI1_1 | 542 | 546 | PF00082 | 0.291 |
| CLV_PCSK_SKI1_1 | 598 | 602 | PF00082 | 0.472 |
| CLV_Separin_Metazoa | 258 | 262 | PF03568 | 0.424 |
| DEG_APCC_DBOX_1 | 31 | 39 | PF00400 | 0.409 |
| DEG_APCC_DBOX_1 | 400 | 408 | PF00400 | 0.445 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.502 |
| DEG_SPOP_SBC_1 | 450 | 454 | PF00917 | 0.518 |
| DEG_SPOP_SBC_1 | 544 | 548 | PF00917 | 0.490 |
| DOC_CKS1_1 | 251 | 256 | PF01111 | 0.378 |
| DOC_CYCLIN_yCln2_LP_2 | 143 | 149 | PF00134 | 0.365 |
| DOC_MAPK_gen_1 | 377 | 386 | PF00069 | 0.378 |
| DOC_MAPK_MEF2A_6 | 214 | 222 | PF00069 | 0.409 |
| DOC_PP1_RVXF_1 | 323 | 329 | PF00149 | 0.466 |
| DOC_PP2B_LxvP_1 | 14 | 17 | PF13499 | 0.446 |
| DOC_PP2B_LxvP_1 | 143 | 146 | PF13499 | 0.471 |
| DOC_PP2B_LxvP_1 | 19 | 22 | PF13499 | 0.340 |
| DOC_PP4_FxxP_1 | 550 | 553 | PF00568 | 0.354 |
| DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.399 |
| DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.490 |
| DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.409 |
| DOC_USP7_MATH_1 | 562 | 566 | PF00917 | 0.409 |
| DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.486 |
| DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.269 |
| DOC_USP7_MATH_2 | 179 | 185 | PF00917 | 0.365 |
| DOC_USP7_UBL2_3 | 425 | 429 | PF12436 | 0.378 |
| DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.359 |
| DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.359 |
| DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.359 |
| DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.359 |
| DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.378 |
| DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.409 |
| DOC_WW_Pin1_4 | 586 | 591 | PF00397 | 0.344 |
| DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.479 |
| LIG_14-3-3_CanoR_1 | 3 | 13 | PF00244 | 0.593 |
| LIG_14-3-3_CanoR_1 | 32 | 36 | PF00244 | 0.496 |
| LIG_14-3-3_CanoR_1 | 362 | 367 | PF00244 | 0.389 |
| LIG_14-3-3_CanoR_1 | 401 | 411 | PF00244 | 0.471 |
| LIG_14-3-3_CanoR_1 | 490 | 499 | PF00244 | 0.396 |
| LIG_14-3-3_CanoR_1 | 542 | 550 | PF00244 | 0.415 |
| LIG_14-3-3_CanoR_1 | 556 | 561 | PF00244 | 0.386 |
| LIG_14-3-3_CanoR_1 | 580 | 590 | PF00244 | 0.344 |
| LIG_APCC_ABBA_1 | 197 | 202 | PF00400 | 0.359 |
| LIG_APCC_ABBA_1 | 260 | 265 | PF00400 | 0.490 |
| LIG_APCC_Cbox_2 | 494 | 500 | PF00515 | 0.409 |
| LIG_CSL_BTD_1 | 38 | 41 | PF09270 | 0.409 |
| LIG_eIF4E_1 | 153 | 159 | PF01652 | 0.365 |
| LIG_FHA_1 | 126 | 132 | PF00498 | 0.464 |
| LIG_FHA_1 | 138 | 144 | PF00498 | 0.361 |
| LIG_FHA_1 | 170 | 176 | PF00498 | 0.444 |
| LIG_FHA_1 | 227 | 233 | PF00498 | 0.407 |
| LIG_FHA_1 | 347 | 353 | PF00498 | 0.413 |
| LIG_FHA_1 | 431 | 437 | PF00498 | 0.477 |
| LIG_FHA_1 | 444 | 450 | PF00498 | 0.302 |
| LIG_FHA_1 | 484 | 490 | PF00498 | 0.513 |
| LIG_FHA_1 | 589 | 595 | PF00498 | 0.409 |
| LIG_FHA_2 | 176 | 182 | PF00498 | 0.399 |
| LIG_FHA_2 | 319 | 325 | PF00498 | 0.490 |
| LIG_FHA_2 | 386 | 392 | PF00498 | 0.386 |
| LIG_FHA_2 | 450 | 456 | PF00498 | 0.499 |
| LIG_FHA_2 | 605 | 611 | PF00498 | 0.568 |
| LIG_FHA_2 | 70 | 76 | PF00498 | 0.507 |
| LIG_FHA_2 | 80 | 86 | PF00498 | 0.477 |
| LIG_LIR_Apic_2 | 547 | 553 | PF02991 | 0.354 |
| LIG_LIR_Gen_1 | 412 | 422 | PF02991 | 0.344 |
| LIG_LIR_LC3C_4 | 265 | 270 | PF02991 | 0.490 |
| LIG_LIR_Nem_3 | 551 | 557 | PF02991 | 0.403 |
| LIG_PCNA_yPIPBox_3 | 252 | 263 | PF02747 | 0.490 |
| LIG_Pex14_1 | 243 | 247 | PF04695 | 0.359 |
| LIG_Pex14_1 | 554 | 558 | PF04695 | 0.378 |
| LIG_Pex14_2 | 550 | 554 | PF04695 | 0.503 |
| LIG_PTB_Apo_2 | 295 | 302 | PF02174 | 0.438 |
| LIG_PTB_Apo_2 | 425 | 432 | PF02174 | 0.365 |
| LIG_PTB_Phospho_1 | 295 | 301 | PF10480 | 0.490 |
| LIG_PTB_Phospho_1 | 425 | 431 | PF10480 | 0.365 |
| LIG_RPA_C_Fungi | 375 | 387 | PF08784 | 0.359 |
| LIG_SH2_SRC | 83 | 86 | PF00017 | 0.378 |
| LIG_SH2_STAP1 | 509 | 513 | PF00017 | 0.409 |
| LIG_SH2_STAT5 | 558 | 561 | PF00017 | 0.419 |
| LIG_SH2_STAT5 | 572 | 575 | PF00017 | 0.276 |
| LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.344 |
| LIG_SH3_3 | 14 | 20 | PF00018 | 0.434 |
| LIG_SH3_3 | 143 | 149 | PF00018 | 0.471 |
| LIG_SH3_3 | 40 | 46 | PF00018 | 0.400 |
| LIG_SUMO_SIM_anti_2 | 184 | 191 | PF11976 | 0.417 |
| LIG_SUMO_SIM_anti_2 | 229 | 236 | PF11976 | 0.415 |
| LIG_SUMO_SIM_anti_2 | 265 | 271 | PF11976 | 0.403 |
| LIG_SUMO_SIM_anti_2 | 334 | 341 | PF11976 | 0.407 |
| LIG_SUMO_SIM_anti_2 | 382 | 391 | PF11976 | 0.440 |
| LIG_SUMO_SIM_par_1 | 184 | 191 | PF11976 | 0.362 |
| LIG_SUMO_SIM_par_1 | 217 | 223 | PF11976 | 0.373 |
| LIG_SUMO_SIM_par_1 | 229 | 236 | PF11976 | 0.393 |
| LIG_TRAF2_1 | 246 | 249 | PF00917 | 0.490 |
| LIG_TRAF2_1 | 292 | 295 | PF00917 | 0.418 |
| LIG_TRAF2_1 | 379 | 382 | PF00917 | 0.490 |
| LIG_TRAF2_1 | 453 | 456 | PF00917 | 0.403 |
| LIG_TRAF2_1 | 97 | 100 | PF00917 | 0.365 |
| LIG_UBA3_1 | 457 | 462 | PF00899 | 0.490 |
| LIG_WRC_WIRS_1 | 557 | 562 | PF05994 | 0.490 |
| MOD_CDK_SPxxK_3 | 175 | 182 | PF00069 | 0.378 |
| MOD_CK1_1 | 125 | 131 | PF00069 | 0.490 |
| MOD_CK1_1 | 169 | 175 | PF00069 | 0.409 |
| MOD_CK1_1 | 230 | 236 | PF00069 | 0.378 |
| MOD_CK1_1 | 320 | 326 | PF00069 | 0.464 |
| MOD_CK1_1 | 345 | 351 | PF00069 | 0.350 |
| MOD_CK1_1 | 371 | 377 | PF00069 | 0.395 |
| MOD_CK1_1 | 543 | 549 | PF00069 | 0.365 |
| MOD_CK1_1 | 584 | 590 | PF00069 | 0.359 |
| MOD_CK1_1 | 604 | 610 | PF00069 | 0.264 |
| MOD_CK2_1 | 175 | 181 | PF00069 | 0.406 |
| MOD_CK2_1 | 2 | 8 | PF00069 | 0.516 |
| MOD_CK2_1 | 279 | 285 | PF00069 | 0.461 |
| MOD_CK2_1 | 289 | 295 | PF00069 | 0.408 |
| MOD_CK2_1 | 385 | 391 | PF00069 | 0.386 |
| MOD_CK2_1 | 429 | 435 | PF00069 | 0.471 |
| MOD_CK2_1 | 449 | 455 | PF00069 | 0.410 |
| MOD_CK2_1 | 501 | 507 | PF00069 | 0.428 |
| MOD_CK2_1 | 543 | 549 | PF00069 | 0.387 |
| MOD_CK2_1 | 604 | 610 | PF00069 | 0.588 |
| MOD_CK2_1 | 69 | 75 | PF00069 | 0.375 |
| MOD_CK2_1 | 79 | 85 | PF00069 | 0.330 |
| MOD_CK2_1 | 94 | 100 | PF00069 | 0.344 |
| MOD_CMANNOS | 328 | 331 | PF00535 | 0.344 |
| MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.490 |
| MOD_GlcNHglycan | 285 | 289 | PF01048 | 0.409 |
| MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.406 |
| MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.597 |
| MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.464 |
| MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.376 |
| MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.336 |
| MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.359 |
| MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.423 |
| MOD_GSK3_1 | 137 | 144 | PF00069 | 0.493 |
| MOD_GSK3_1 | 153 | 160 | PF00069 | 0.320 |
| MOD_GSK3_1 | 162 | 169 | PF00069 | 0.431 |
| MOD_GSK3_1 | 20 | 27 | PF00069 | 0.374 |
| MOD_GSK3_1 | 226 | 233 | PF00069 | 0.406 |
| MOD_GSK3_1 | 342 | 349 | PF00069 | 0.393 |
| MOD_GSK3_1 | 364 | 371 | PF00069 | 0.378 |
| MOD_GSK3_1 | 37 | 44 | PF00069 | 0.359 |
| MOD_GSK3_1 | 387 | 394 | PF00069 | 0.449 |
| MOD_GSK3_1 | 431 | 438 | PF00069 | 0.490 |
| MOD_GSK3_1 | 497 | 504 | PF00069 | 0.514 |
| MOD_GSK3_1 | 540 | 547 | PF00069 | 0.359 |
| MOD_GSK3_1 | 584 | 591 | PF00069 | 0.365 |
| MOD_GSK3_1 | 69 | 76 | PF00069 | 0.370 |
| MOD_GSK3_1 | 88 | 95 | PF00069 | 0.486 |
| MOD_N-GLC_1 | 103 | 108 | PF02516 | 0.420 |
| MOD_N-GLC_1 | 227 | 232 | PF02516 | 0.390 |
| MOD_N-GLC_1 | 55 | 60 | PF02516 | 0.409 |
| MOD_NEK2_1 | 103 | 108 | PF00069 | 0.316 |
| MOD_NEK2_1 | 162 | 167 | PF00069 | 0.392 |
| MOD_NEK2_1 | 174 | 179 | PF00069 | 0.392 |
| MOD_NEK2_1 | 218 | 223 | PF00069 | 0.436 |
| MOD_NEK2_1 | 263 | 268 | PF00069 | 0.490 |
| MOD_NEK2_1 | 318 | 323 | PF00069 | 0.440 |
| MOD_NEK2_1 | 364 | 369 | PF00069 | 0.344 |
| MOD_NEK2_1 | 449 | 454 | PF00069 | 0.490 |
| MOD_NEK2_1 | 537 | 542 | PF00069 | 0.368 |
| MOD_NEK2_1 | 54 | 59 | PF00069 | 0.346 |
| MOD_NEK2_1 | 601 | 606 | PF00069 | 0.480 |
| MOD_NEK2_1 | 88 | 93 | PF00069 | 0.409 |
| MOD_NEK2_2 | 271 | 276 | PF00069 | 0.365 |
| MOD_NEK2_2 | 31 | 36 | PF00069 | 0.434 |
| MOD_PIKK_1 | 116 | 122 | PF00454 | 0.346 |
| MOD_PIKK_1 | 548 | 554 | PF00454 | 0.406 |
| MOD_PK_1 | 362 | 368 | PF00069 | 0.490 |
| MOD_PKA_1 | 2 | 8 | PF00069 | 0.516 |
| MOD_PKA_2 | 2 | 8 | PF00069 | 0.625 |
| MOD_PKA_2 | 31 | 37 | PF00069 | 0.359 |
| MOD_PKA_2 | 489 | 495 | PF00069 | 0.401 |
| MOD_PKA_2 | 579 | 585 | PF00069 | 0.438 |
| MOD_Plk_1 | 103 | 109 | PF00069 | 0.455 |
| MOD_Plk_1 | 279 | 285 | PF00069 | 0.511 |
| MOD_Plk_4 | 103 | 109 | PF00069 | 0.405 |
| MOD_Plk_4 | 230 | 236 | PF00069 | 0.359 |
| MOD_Plk_4 | 263 | 269 | PF00069 | 0.518 |
| MOD_Plk_4 | 334 | 340 | PF00069 | 0.518 |
| MOD_Plk_4 | 368 | 374 | PF00069 | 0.419 |
| MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.359 |
| MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.359 |
| MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.359 |
| MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.359 |
| MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.378 |
| MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.409 |
| MOD_ProDKin_1 | 586 | 592 | PF00069 | 0.344 |
| MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.479 |
| MOD_SUMO_for_1 | 407 | 410 | PF00179 | 0.465 |
| TRG_DiLeu_BaEn_2 | 409 | 415 | PF01217 | 0.465 |
| TRG_DiLeu_BaEn_2 | 532 | 538 | PF01217 | 0.409 |
| TRG_DiLeu_BaEn_4 | 455 | 461 | PF01217 | 0.409 |
| TRG_DiLeu_BaLyEn_6 | 154 | 159 | PF01217 | 0.403 |
| TRG_DiLeu_BaLyEn_6 | 207 | 212 | PF01217 | 0.471 |
| TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.368 |
| TRG_ENDOCYTIC_2 | 557 | 560 | PF00928 | 0.419 |
| TRG_ER_diArg_1 | 209 | 211 | PF00400 | 0.471 |
| TRG_Pf-PMV_PEXEL_1 | 209 | 213 | PF00026 | 0.490 |
| TRG_Pf-PMV_PEXEL_1 | 64 | 68 | PF00026 | 0.490 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P6E3 | Leptomonas seymouri | 75% | 100% |
| A0A0N1I7U1 | Leptomonas seymouri | 23% | 72% |
| A0A0S4JAG1 | Bodo saltans | 27% | 86% |
| A0A0S4JRH6 | Bodo saltans | 27% | 92% |
| A0A0S4JRL8 | Bodo saltans | 24% | 78% |
| A0A0S4JY55 | Bodo saltans | 36% | 100% |
| A0A0S4KE24 | Bodo saltans | 24% | 76% |
| A0A1X0NT49 | Trypanosomatidae | 25% | 85% |
| A0A1X0NT60 | Trypanosomatidae | 25% | 92% |
| A0A1X0NZS6 | Trypanosomatidae | 51% | 100% |
| A0A1X0P523 | Trypanosomatidae | 24% | 83% |
| A0A1X0P5Y2 | Trypanosomatidae | 24% | 79% |
| A0A3R7L2D0 | Trypanosoma rangeli | 49% | 100% |
| A0A3S5IQT1 | Trypanosoma rangeli | 25% | 84% |
| A0A422NAV0 | Trypanosoma rangeli | 23% | 85% |
| A0A422NSK2 | Trypanosoma rangeli | 24% | 93% |
| A4HC81 | Leishmania braziliensis | 22% | 100% |
| A4HHE2 | Leishmania braziliensis | 91% | 100% |
| A4I4I8 | Leishmania infantum | 100% | 100% |
| B2ZGJ1 | Danio rerio | 24% | 98% |
| C9ZL75 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
| C9ZRI9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 94% |
| D0A627 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 81% |
| E9ADY9 | Leishmania major | 98% | 100% |
| E9ALU2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
| F1LN46 | Rattus norvegicus | 24% | 78% |
| O19094 | Bos taurus | 26% | 100% |
| P07668 | Drosophila melanogaster | 23% | 87% |
| P11466 | Rattus norvegicus | 24% | 100% |
| P13222 | Sus scrofa | 23% | 98% |
| P18886 | Rattus norvegicus | 25% | 95% |
| P23786 | Homo sapiens | 25% | 95% |
| P28329 | Homo sapiens | 25% | 84% |
| P32198 | Rattus norvegicus | 26% | 81% |
| P32738 | Rattus norvegicus | 24% | 98% |
| P32756 | Caenorhabditis elegans | 22% | 100% |
| P32796 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 22% | 94% |
| P43155 | Homo sapiens | 26% | 100% |
| P47934 | Mus musculus | 25% | 100% |
| P50416 | Homo sapiens | 26% | 81% |
| P52825 | Mus musculus | 25% | 95% |
| P52826 | Columba livia | 25% | 100% |
| P75448 | Mycoplasma pneumoniae (strain ATCC 29342 / M129 / Subtype 1) | 22% | 100% |
| P80235 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 91% |
| P97742 | Mus musculus | 25% | 81% |
| Q00614 | Candida tropicalis | 23% | 100% |
| Q03059 | Mus musculus | 24% | 98% |
| Q2KJB7 | Bos taurus | 26% | 95% |
| Q58DK1 | Bos taurus | 28% | 81% |
| Q5U3U3 | Danio rerio | 26% | 94% |
| Q60HG9 | Macaca fascicularis | 25% | 95% |
| Q63704 | Rattus norvegicus | 28% | 81% |
| Q68Y62 | Equus caballus | 26% | 81% |
| Q6P4X5 | Xenopus tropicalis | 26% | 95% |
| Q704S8 | Rattus norvegicus | 25% | 100% |
| Q7ZXE1 | Xenopus laevis | 26% | 95% |
| Q8BGD5 | Mus musculus | 25% | 79% |
| Q8HY46 | Sus scrofa | 26% | 81% |
| Q8TCG5 | Homo sapiens | 25% | 78% |
| Q90YJ9 | Gallus gallus | 23% | 98% |
| Q924X2 | Mus musculus | 28% | 81% |
| Q92523 | Homo sapiens | 27% | 81% |
| Q9DC50 | Mus musculus | 23% | 100% |
| Q9UKG9 | Homo sapiens | 25% | 100% |
| V5BH74 | Trypanosoma cruzi | 49% | 100% |
| V5BP17 | Trypanosoma cruzi | 22% | 92% |
| V5BQH8 | Trypanosoma cruzi | 27% | 79% |
| V5D4R1 | Trypanosoma cruzi | 25% | 79% |
| V5DBT5 | Trypanosoma cruzi | 24% | 92% |