Related to both fungal ergosterol C-24 reductases and to a lesser extent, animal delta-14 lanosterol reductases (all preferentially ER-localized).. The highly changed Ser/Arg rich N-terminus might point to a mitochondrial transit signal (ergosterols are essential for Kinetoplastid mitochondria).. Localization: ER (by homology) / Mitochondrial (by feature)
Sterol metabolism/biosynthesis, sterol C-24 reductase
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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
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: A4I8T4
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 9 |
GO:0006694 | steroid biosynthetic process | 5 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0008202 | steroid metabolic process | 4 | 9 |
GO:0008610 | lipid biosynthetic process | 4 | 9 |
GO:0009058 | biosynthetic process | 2 | 9 |
GO:0016125 | sterol metabolic process | 4 | 9 |
GO:0016126 | sterol biosynthetic process | 5 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 9 |
GO:1901576 | organic substance biosynthetic process | 3 | 9 |
GO:1901615 | organic hydroxy compound metabolic process | 3 | 9 |
GO:1901617 | organic hydroxy compound biosynthetic process | 4 | 9 |
GO:0006066 | alcohol metabolic process | 3 | 1 |
GO:0006696 | ergosterol biosynthetic process | 5 | 1 |
GO:0008204 | ergosterol metabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016128 | phytosteroid metabolic process | 4 | 1 |
GO:0016129 | phytosteroid biosynthetic process | 5 | 1 |
GO:0044107 | obsolete cellular alcohol metabolic process | 3 | 1 |
GO:0044108 | obsolete cellular alcohol biosynthetic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0044283 | small molecule biosynthetic process | 3 | 1 |
GO:0046165 | alcohol biosynthetic process | 4 | 1 |
GO:0097384 | cellular lipid biosynthetic process | 4 | 1 |
GO:1902652 | secondary alcohol metabolic process | 4 | 1 |
GO:1902653 | secondary alcohol biosynthetic process | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000246 | delta24(24-1) sterol reductase activity | 5 | 7 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0016491 | oxidoreductase activity | 2 | 9 |
GO:0016627 | oxidoreductase activity, acting on the CH-CH group of donors | 3 | 9 |
GO:0016628 | oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor | 4 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.241 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.259 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.254 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.367 |
CLV_PCSK_FUR_1 | 378 | 382 | PF00082 | 0.263 |
CLV_PCSK_FUR_1 | 464 | 468 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.260 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.263 |
CLV_PCSK_KEX2_1 | 466 | 468 | PF00082 | 0.283 |
CLV_PCSK_PC1ET2_1 | 220 | 222 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.298 |
DEG_APCC_DBOX_1 | 349 | 357 | PF00400 | 0.450 |
DOC_CKS1_1 | 35 | 40 | PF01111 | 0.636 |
DOC_CYCLIN_RxL_1 | 146 | 156 | PF00134 | 0.518 |
DOC_CYCLIN_yCln2_LP_2 | 141 | 147 | PF00134 | 0.374 |
DOC_MAPK_gen_1 | 103 | 112 | PF00069 | 0.351 |
DOC_MAPK_gen_1 | 378 | 388 | PF00069 | 0.518 |
DOC_MAPK_gen_1 | 425 | 433 | PF00069 | 0.527 |
DOC_MAPK_HePTP_8 | 239 | 251 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 242 | 251 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 256 | 264 | PF00069 | 0.265 |
DOC_MAPK_MEF2A_6 | 426 | 435 | PF00069 | 0.443 |
DOC_PP1_RVXF_1 | 107 | 113 | PF00149 | 0.301 |
DOC_PP2B_LxvP_1 | 141 | 144 | PF13499 | 0.349 |
DOC_PP2B_LxvP_1 | 151 | 154 | PF13499 | 0.428 |
DOC_PP4_FxxP_1 | 241 | 244 | PF00568 | 0.443 |
DOC_PP4_FxxP_1 | 63 | 66 | PF00568 | 0.483 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.501 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.476 |
LIG_14-3-3_CanoR_1 | 160 | 164 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 256 | 260 | PF00244 | 0.315 |
LIG_14-3-3_CanoR_1 | 406 | 416 | PF00244 | 0.464 |
LIG_AP2alpha_1 | 416 | 420 | PF02296 | 0.502 |
LIG_APCC_ABBA_1 | 249 | 254 | PF00400 | 0.459 |
LIG_deltaCOP1_diTrp_1 | 55 | 63 | PF00928 | 0.517 |
LIG_eIF4E_1 | 84 | 90 | PF01652 | 0.427 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.304 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.459 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.315 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.552 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.348 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.492 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.566 |
LIG_LIR_Apic_2 | 39 | 45 | PF02991 | 0.560 |
LIG_LIR_Apic_2 | 62 | 66 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 125 | 134 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 169 | 180 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 258 | 267 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 272 | 280 | PF02991 | 0.259 |
LIG_LIR_Gen_1 | 310 | 321 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 481 | 491 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 125 | 129 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 169 | 175 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 258 | 262 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 272 | 277 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 307 | 312 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 40 | 46 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 418 | 423 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 446 | 451 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 481 | 486 | PF02991 | 0.453 |
LIG_NRBOX | 129 | 135 | PF00104 | 0.397 |
LIG_Pex14_1 | 309 | 313 | PF04695 | 0.459 |
LIG_Pex14_1 | 318 | 322 | PF04695 | 0.315 |
LIG_Pex14_2 | 229 | 233 | PF04695 | 0.552 |
LIG_Pex14_2 | 416 | 420 | PF04695 | 0.438 |
LIG_Pex14_2 | 448 | 452 | PF04695 | 0.315 |
LIG_PTB_Apo_2 | 388 | 395 | PF02174 | 0.506 |
LIG_SH2_CRK | 172 | 176 | PF00017 | 0.352 |
LIG_SH2_CRK | 489 | 493 | PF00017 | 0.445 |
LIG_SH2_GRB2like | 294 | 297 | PF00017 | 0.315 |
LIG_SH2_GRB2like | 322 | 325 | PF00017 | 0.315 |
LIG_SH2_NCK_1 | 43 | 47 | PF00017 | 0.612 |
LIG_SH2_PTP2 | 483 | 486 | PF00017 | 0.556 |
LIG_SH2_PTP2 | 84 | 87 | PF00017 | 0.397 |
LIG_SH2_SRC | 294 | 297 | PF00017 | 0.315 |
LIG_SH2_SRC | 43 | 46 | PF00017 | 0.526 |
LIG_SH2_STAP1 | 231 | 235 | PF00017 | 0.459 |
LIG_SH2_STAP1 | 429 | 433 | PF00017 | 0.315 |
LIG_SH2_STAT3 | 332 | 335 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.251 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.315 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.654 |
LIG_SH3_3 | 392 | 398 | PF00018 | 0.459 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.283 |
LIG_SUMO_SIM_anti_2 | 258 | 264 | PF11976 | 0.315 |
LIG_SUMO_SIM_anti_2 | 430 | 435 | PF11976 | 0.327 |
LIG_SUMO_SIM_par_1 | 263 | 268 | PF11976 | 0.321 |
LIG_TRAF2_1 | 37 | 40 | PF00917 | 0.561 |
LIG_TYR_ITIM | 181 | 186 | PF00017 | 0.349 |
LIG_TYR_ITIM | 487 | 492 | PF00017 | 0.459 |
LIG_TYR_ITIM | 80 | 85 | PF00017 | 0.315 |
LIG_WRC_WIRS_1 | 111 | 116 | PF05994 | 0.356 |
LIG_WRC_WIRS_1 | 445 | 450 | PF05994 | 0.259 |
MOD_CDK_SPxK_1 | 26 | 32 | PF00069 | 0.672 |
MOD_CDK_SPxK_1 | 48 | 54 | PF00069 | 0.514 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.744 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.574 |
MOD_Cter_Amidation | 423 | 426 | PF01082 | 0.259 |
MOD_DYRK1A_RPxSP_1 | 26 | 30 | PF00069 | 0.678 |
MOD_DYRK1A_RPxSP_1 | 34 | 38 | PF00069 | 0.595 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.259 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.237 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.274 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.356 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.380 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.488 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.716 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.678 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.673 |
MOD_N-GLC_2 | 324 | 326 | PF02516 | 0.315 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.472 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.349 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.237 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.449 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.330 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.340 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.196 |
MOD_NEK2_2 | 333 | 338 | PF00069 | 0.397 |
MOD_PIKK_1 | 369 | 375 | PF00454 | 0.459 |
MOD_PKA_1 | 20 | 26 | PF00069 | 0.730 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.518 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.459 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.315 |
MOD_PKA_2 | 379 | 385 | PF00069 | 0.487 |
MOD_PKB_1 | 14 | 22 | PF00069 | 0.693 |
MOD_PKB_1 | 26 | 34 | PF00069 | 0.638 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.292 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.315 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.322 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.315 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.277 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.651 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.574 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.479 |
MOD_SUMO_for_1 | 102 | 105 | PF00179 | 0.258 |
TRG_DiLeu_BaEn_1 | 482 | 487 | PF01217 | 0.556 |
TRG_ENDOCYTIC_2 | 172 | 175 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.609 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 476 | 479 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 489 | 492 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.316 |
TRG_ER_diArg_1 | 192 | 194 | PF00400 | 0.283 |
TRG_ER_diArg_1 | 221 | 224 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 32 | 35 | PF00400 | 0.709 |
TRG_ER_diArg_1 | 377 | 380 | PF00400 | 0.512 |
TRG_NLS_MonoExtC_3 | 219 | 224 | PF00514 | 0.463 |
TRG_Pf-PMV_PEXEL_1 | 34 | 39 | PF00026 | 0.400 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3C6 | Leptomonas seymouri | 79% | 99% |
A0A0N1PBH8 | Leptomonas seymouri | 29% | 100% |
A0A0S4IS37 | Bodo saltans | 28% | 100% |
A0A0S4KLN5 | Bodo saltans | 28% | 100% |
A0A1D8PIC7 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 28% | 100% |
A0A1D8PJ25 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 37% | 100% |
A0A1X0NRH6 | Trypanosomatidae | 24% | 100% |
A0A1X0P0Q6 | Trypanosomatidae | 67% | 100% |
A0A3Q8IM20 | Leishmania donovani | 100% | 100% |
A0A3R7KUI7 | Trypanosoma rangeli | 65% | 100% |
A0A3R7N804 | Trypanosoma rangeli | 28% | 100% |
A0A3S7X5R0 | Leishmania donovani | 27% | 100% |
A4HKM3 | Leishmania braziliensis | 27% | 100% |
A4HLA8 | Leishmania braziliensis | 86% | 100% |
A4I855 | Leishmania infantum | 27% | 100% |
D0AAC2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9B312 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B3Q0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
G4SW86 | Methylotuvimicrobium alcaliphilum (strain DSM 19304 / NCIMB 14124 / VKM B-2133 / 20Z) | 31% | 100% |
I1RF79 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 25% | 100% |
I1RR90 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 26% | 100% |
I1RZZ3 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 40% | 83% |
O08984 | Rattus norvegicus | 30% | 80% |
O13597 | Septoria lycopersici | 28% | 97% |
O76062 | Homo sapiens | 32% | 100% |
O88455 | Mus musculus | 26% | 100% |
P23913 | Gallus gallus | 29% | 78% |
P25340 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 100% |
P32462 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 100% |
P36209 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 36% | 100% |
P38670 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 26% | 100% |
P78575 | Ascobolus immersus | 28% | 100% |
Q01447 | Fusarium vanettenii | 27% | 100% |
Q09195 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 100% |
Q14739 | Homo sapiens | 32% | 81% |
Q3U9G9 | Mus musculus | 32% | 79% |
Q4Q4D7 | Leishmania major | 96% | 100% |
Q4Q543 | Leishmania major | 27% | 100% |
Q4WJ59 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 39% | 87% |
Q4WJJ9 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 27% | 96% |
Q4WKA5 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 25% | 100% |
Q4WW43 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 41% | 100% |
Q54PP1 | Dictyostelium discoideum | 31% | 100% |
Q5E9J5 | Bos taurus | 26% | 100% |
Q5R7H4 | Pongo abelii | 32% | 81% |
Q5UQI4 | Acanthamoeba polyphaga mimivirus | 30% | 100% |
Q6P4M0 | Xenopus tropicalis | 26% | 100% |
Q71KT5 | Mus musculus | 32% | 100% |
Q7SXF1 | Danio rerio | 26% | 100% |
Q7ZXH1 | Xenopus laevis | 26% | 100% |
Q8WMV1 | Bos taurus | 32% | 100% |
Q9LDR4 | Arabidopsis thaliana | 27% | 100% |
Q9LDU6 | Arabidopsis thaliana | 28% | 100% |
Q9UBM7 | Homo sapiens | 25% | 100% |
Q9Z2Z8 | Rattus norvegicus | 25% | 100% |
V5BKN3 | Trypanosoma cruzi | 26% | 100% |