Elongation of fatty acids protein, responsible for very long carbon chain llipid biosynthesis (conserved in Eukaryota).. This group of enzymes has expanded heavily in kinetoplastids.. Localization: ER (by homology)
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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 68 |
NetGPI | no | yes: 0, no: 69 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 60 |
GO:0110165 | cellular anatomical entity | 1 | 63 |
GO:0005737 | cytoplasm | 2 | 3 |
Related structures:
AlphaFold database: E9APR8
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 70 |
GO:0006629 | lipid metabolic process | 3 | 70 |
GO:0006631 | fatty acid metabolic process | 4 | 70 |
GO:0006633 | fatty acid biosynthetic process | 5 | 70 |
GO:0008152 | metabolic process | 1 | 70 |
GO:0008610 | lipid biosynthetic process | 4 | 70 |
GO:0009058 | biosynthetic process | 2 | 70 |
GO:0009987 | cellular process | 1 | 70 |
GO:0016053 | organic acid biosynthetic process | 4 | 70 |
GO:0019752 | carboxylic acid metabolic process | 5 | 70 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 70 |
GO:0043436 | oxoacid metabolic process | 4 | 70 |
GO:0044237 | cellular metabolic process | 2 | 70 |
GO:0044238 | primary metabolic process | 2 | 70 |
GO:0044249 | cellular biosynthetic process | 3 | 70 |
GO:0044255 | cellular lipid metabolic process | 3 | 70 |
GO:0044281 | small molecule metabolic process | 2 | 70 |
GO:0044283 | small molecule biosynthetic process | 3 | 70 |
GO:0046394 | carboxylic acid biosynthetic process | 5 | 70 |
GO:0071704 | organic substance metabolic process | 2 | 70 |
GO:0072330 | monocarboxylic acid biosynthetic process | 6 | 70 |
GO:1901576 | organic substance biosynthetic process | 3 | 70 |
GO:0000038 | very long-chain fatty acid metabolic process | 5 | 10 |
GO:0006643 | membrane lipid metabolic process | 4 | 10 |
GO:0006665 | sphingolipid metabolic process | 4 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0019367 | fatty acid elongation, saturated fatty acid | 7 | 10 |
GO:0019368 | fatty acid elongation, unsaturated fatty acid | 7 | 10 |
GO:0030148 | sphingolipid biosynthetic process | 5 | 10 |
GO:0030497 | fatty acid elongation | 6 | 10 |
GO:0034625 | fatty acid elongation, monounsaturated fatty acid | 8 | 10 |
GO:0034626 | fatty acid elongation, polyunsaturated fatty acid | 8 | 10 |
GO:0042761 | very long-chain fatty acid biosynthetic process | 6 | 10 |
GO:0046467 | membrane lipid biosynthetic process | 4 | 10 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 10 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 10 |
GO:0001676 | long-chain fatty acid metabolic process | 5 | 2 |
GO:0042759 | long-chain fatty acid biosynthetic process | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 70 |
GO:0004312 | fatty acid synthase activity | 5 | 70 |
GO:0009922 | fatty acid elongase activity | 6 | 70 |
GO:0016740 | transferase activity | 2 | 70 |
GO:0016746 | acyltransferase activity | 3 | 70 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 70 |
GO:0102756 | very-long-chain 3-ketoacyl-CoA synthase activity | 5 | 70 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.279 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.322 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.326 |
CLV_PCSK_PC1ET2_1 | 357 | 359 | PF00082 | 0.313 |
CLV_PCSK_PC1ET2_1 | 376 | 378 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.644 |
DOC_CKS1_1 | 12 | 17 | PF01111 | 0.242 |
DOC_CKS1_1 | 169 | 174 | PF01111 | 0.476 |
DOC_CYCLIN_RxL_1 | 348 | 356 | PF00134 | 0.350 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 65 | 74 | PF00134 | 0.366 |
DOC_MAPK_MEF2A_6 | 243 | 251 | PF00069 | 0.492 |
DOC_MAPK_RevD_3 | 40 | 55 | PF00069 | 0.189 |
DOC_PP1_RVXF_1 | 183 | 190 | PF00149 | 0.467 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.332 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.208 |
DOC_USP7_UBL2_3 | 95 | 99 | PF12436 | 0.155 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.401 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.357 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.615 |
LIG_14-3-3_CanoR_1 | 142 | 147 | PF00244 | 0.244 |
LIG_14-3-3_CanoR_1 | 159 | 169 | PF00244 | 0.225 |
LIG_14-3-3_CanoR_1 | 184 | 190 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 368 | 373 | PF00244 | 0.582 |
LIG_Actin_WH2_2 | 226 | 241 | PF00022 | 0.441 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.310 |
LIG_BIR_III_2 | 28 | 32 | PF00653 | 0.171 |
LIG_BRCT_BRCA1_1 | 109 | 113 | PF00533 | 0.167 |
LIG_BRCT_BRCA1_1 | 318 | 322 | PF00533 | 0.215 |
LIG_CORNRBOX | 40 | 48 | PF00104 | 0.151 |
LIG_deltaCOP1_diTrp_1 | 6 | 11 | PF00928 | 0.463 |
LIG_eIF4E_1 | 228 | 234 | PF01652 | 0.373 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.336 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.323 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.226 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.688 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.554 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.287 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.294 |
LIG_GBD_Chelix_1 | 196 | 204 | PF00786 | 0.205 |
LIG_GBD_Chelix_1 | 70 | 78 | PF00786 | 0.183 |
LIG_KLC1_Yacidic_2 | 352 | 356 | PF13176 | 0.405 |
LIG_LIR_Apic_2 | 152 | 158 | PF02991 | 0.273 |
LIG_LIR_Gen_1 | 100 | 107 | PF02991 | 0.150 |
LIG_LIR_Gen_1 | 163 | 174 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 176 | 187 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 198 | 209 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 225 | 234 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 264 | 273 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 341 | 350 | PF02991 | 0.316 |
LIG_LIR_Gen_1 | 80 | 88 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 100 | 105 | PF02991 | 0.159 |
LIG_LIR_Nem_3 | 163 | 169 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 176 | 182 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 198 | 204 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 225 | 231 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 264 | 269 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 280 | 285 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 291 | 297 | PF02991 | 0.175 |
LIG_LIR_Nem_3 | 32 | 36 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 341 | 345 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 80 | 84 | PF02991 | 0.388 |
LIG_Pex14_1 | 203 | 207 | PF04695 | 0.451 |
LIG_Pex14_2 | 222 | 226 | PF04695 | 0.435 |
LIG_Pex14_2 | 346 | 350 | PF04695 | 0.328 |
LIG_Pex14_2 | 88 | 92 | PF04695 | 0.331 |
LIG_PTB_Apo_2 | 117 | 124 | PF02174 | 0.171 |
LIG_PTB_Apo_2 | 289 | 296 | PF02174 | 0.175 |
LIG_PTB_Phospho_1 | 117 | 123 | PF10480 | 0.171 |
LIG_PTB_Phospho_1 | 289 | 295 | PF10480 | 0.184 |
LIG_REV1ctd_RIR_1 | 280 | 288 | PF16727 | 0.190 |
LIG_SH2_CRK | 102 | 106 | PF00017 | 0.341 |
LIG_SH2_CRK | 155 | 159 | PF00017 | 0.294 |
LIG_SH2_CRK | 162 | 166 | PF00017 | 0.370 |
LIG_SH2_CRK | 342 | 346 | PF00017 | 0.231 |
LIG_SH2_CRK | 36 | 40 | PF00017 | 0.352 |
LIG_SH2_CRK | 81 | 85 | PF00017 | 0.305 |
LIG_SH2_PTP2 | 201 | 204 | PF00017 | 0.467 |
LIG_SH2_PTP2 | 262 | 265 | PF00017 | 0.464 |
LIG_SH2_SRC | 123 | 126 | PF00017 | 0.347 |
LIG_SH2_SRC | 41 | 44 | PF00017 | 0.461 |
LIG_SH2_STAP1 | 146 | 150 | PF00017 | 0.243 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.255 |
LIG_SH2_STAP1 | 36 | 40 | PF00017 | 0.387 |
LIG_SH2_STAP1 | 5 | 9 | PF00017 | 0.286 |
LIG_SH2_STAT3 | 146 | 149 | PF00017 | 0.177 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.202 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.580 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.454 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.369 |
LIG_SUMO_SIM_anti_2 | 73 | 80 | PF11976 | 0.189 |
LIG_TRFH_1 | 271 | 275 | PF08558 | 0.210 |
LIG_TYR_ITIM | 39 | 44 | PF00017 | 0.275 |
LIG_UBA3_1 | 165 | 170 | PF00899 | 0.378 |
LIG_UBA3_1 | 178 | 185 | PF00899 | 0.336 |
LIG_UBA3_1 | 235 | 240 | PF00899 | 0.399 |
LIG_UBA3_1 | 345 | 351 | PF00899 | 0.323 |
LIG_UBA3_1 | 87 | 95 | PF00899 | 0.315 |
LIG_WRC_WIRS_1 | 223 | 228 | PF05994 | 0.218 |
MOD_CDK_SPxxK_3 | 369 | 376 | PF00069 | 0.662 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.207 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.318 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.380 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.543 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.469 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.349 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.348 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.426 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.392 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.340 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.288 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.274 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.336 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.414 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.345 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.525 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.358 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.305 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.327 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.502 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.336 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.253 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.325 |
MOD_NEK2_2 | 103 | 108 | PF00069 | 0.359 |
MOD_OFUCOSY | 325 | 331 | PF10250 | 0.396 |
MOD_PKA_1 | 108 | 114 | PF00069 | 0.150 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.344 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.251 |
MOD_PKA_2 | 238 | 244 | PF00069 | 0.419 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.157 |
MOD_Plk_1 | 360 | 366 | PF00069 | 0.694 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.474 |
MOD_Plk_1 | 93 | 99 | PF00069 | 0.299 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.290 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.468 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.295 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.275 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.307 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.277 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.207 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.680 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.331 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.255 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.404 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.357 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.476 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.615 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.263 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 207 | 210 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 262 | 265 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 342 | 345 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.342 |
TRG_ER_diArg_1 | 107 | 109 | PF00400 | 0.164 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5E5 | Leptomonas seymouri | 34% | 100% |
A0A0N0P7D1 | Leptomonas seymouri | 29% | 100% |
A0A0N0P7D6 | Leptomonas seymouri | 27% | 100% |
A0A0N0P7R2 | Leptomonas seymouri | 32% | 100% |
A0A0N1HZJ8 | Leptomonas seymouri | 30% | 100% |
A0A0N1I9H5 | Leptomonas seymouri | 30% | 100% |
A0A0N1PDR8 | Leptomonas seymouri | 30% | 100% |
A0A0S4IS29 | Bodo saltans | 31% | 100% |
A0A0S4IVS6 | Bodo saltans | 29% | 100% |
A0A0S4IW98 | Bodo saltans | 30% | 100% |
A0A1X0NNK7 | Trypanosomatidae | 32% | 100% |
A0A1X0NNM4 | Trypanosomatidae | 27% | 100% |
A0A1X0NNM5 | Trypanosomatidae | 31% | 100% |
A0A1X0NP89 | Trypanosomatidae | 32% | 100% |
A0A3Q8I8T7 | Leishmania donovani | 90% | 98% |
A0A3Q8I9T2 | Leishmania donovani | 67% | 100% |
A0A3Q8I9U9 | Leishmania donovani | 32% | 100% |
A0A3Q8I9X8 | Leishmania donovani | 30% | 100% |
A0A3Q8IC05 | Leishmania donovani | 35% | 100% |
A0A3Q8ID51 | Leishmania donovani | 67% | 97% |
A0A3Q8IIA9 | Leishmania donovani | 28% | 100% |
A0A3R7KG78 | Trypanosoma rangeli | 33% | 100% |
A0A3S7WSY8 | Leishmania donovani | 28% | 100% |
A0A3S7WSZ1 | Leishmania donovani | 32% | 100% |
A0A3S7WT03 | Leishmania donovani | 31% | 100% |
A0A3S7WT16 | Leishmania donovani | 30% | 100% |
A0A422NNP1 | Trypanosoma rangeli | 28% | 100% |
A4H7M2 | Leishmania braziliensis | 29% | 100% |
A4H7M4 | Leishmania braziliensis | 27% | 100% |
A4H7M6 | Leishmania braziliensis | 31% | 81% |
A4H7M7 | Leishmania braziliensis | 29% | 93% |
A4H7M8 | Leishmania braziliensis | 62% | 100% |
A4H7M9 | Leishmania braziliensis | 78% | 100% |
A4H7N0 | Leishmania braziliensis | 36% | 78% |
A4HW07 | Leishmania infantum | 28% | 100% |
A4HW09 | Leishmania infantum | 28% | 100% |
A4HW12 | Leishmania infantum | 31% | 100% |
A4HW13 | Leishmania infantum | 32% | 100% |
A4HW14 | Leishmania infantum | 30% | 100% |
A4HW15 | Leishmania infantum | 67% | 100% |
A4HW16 | Leishmania infantum | 66% | 100% |
A4HW17 | Leishmania infantum | 88% | 98% |
A4HW18 | Leishmania infantum | 35% | 100% |
C9ZT16 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E8NHR2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
E8NHR3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
E9AGL0 | Leishmania infantum | 31% | 100% |
E9AGL2 | Leishmania infantum | 32% | 100% |
E9APQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9APR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9APR3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 88% |
E9APR4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 88% |
E9APR5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 91% |
E9APR6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 90% |
E9APR7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 97% |
E9APR9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
Q20300 | Caenorhabditis elegans | 26% | 100% |
Q4QFQ9 | Leishmania major | 34% | 81% |
Q4QFR0 | Leishmania major | 87% | 100% |
Q4QFR1 | Leishmania major | 67% | 100% |
Q4QFR2 | Leishmania major | 68% | 100% |
Q4QFR3 | Leishmania major | 30% | 97% |
Q4QFR4 | Leishmania major | 29% | 91% |
Q4QFR5 | Leishmania major | 31% | 100% |
Q4QFR6 | Leishmania major | 32% | 88% |
Q4QFR8 | Leishmania major | 28% | 100% |
Q4QFS0 | Leishmania major | 28% | 100% |
Q9VV87 | Drosophila melanogaster | 25% | 100% |
Q9XVQ9 | Caenorhabditis elegans | 26% | 100% |
V5BE99 | Trypanosoma cruzi | 33% | 100% |
V5BND3 | Trypanosoma cruzi | 33% | 100% |
V5DF68 | Trypanosoma cruzi | 28% | 100% |