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: 45 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | yes | yes: 1, no: 31 |
| NetGPI | no | yes: 0, no: 32 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0016020 | membrane | 2 | 29 |
| GO:0110165 | cellular anatomical entity | 1 | 30 |
| GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: E9APQ9
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006082 | organic acid metabolic process | 3 | 33 |
| GO:0006629 | lipid metabolic process | 3 | 33 |
| GO:0006631 | fatty acid metabolic process | 4 | 33 |
| GO:0006633 | fatty acid biosynthetic process | 5 | 33 |
| GO:0008152 | metabolic process | 1 | 33 |
| GO:0008610 | lipid biosynthetic process | 4 | 33 |
| GO:0009058 | biosynthetic process | 2 | 33 |
| GO:0009987 | cellular process | 1 | 33 |
| GO:0016053 | organic acid biosynthetic process | 4 | 33 |
| GO:0019752 | carboxylic acid metabolic process | 5 | 33 |
| GO:0032787 | monocarboxylic acid metabolic process | 6 | 33 |
| GO:0043436 | oxoacid metabolic process | 4 | 33 |
| GO:0044237 | cellular metabolic process | 2 | 33 |
| GO:0044238 | primary metabolic process | 2 | 33 |
| GO:0044249 | cellular biosynthetic process | 3 | 33 |
| GO:0044255 | cellular lipid metabolic process | 3 | 33 |
| GO:0044281 | small molecule metabolic process | 2 | 33 |
| GO:0044283 | small molecule biosynthetic process | 3 | 33 |
| GO:0046394 | carboxylic acid biosynthetic process | 5 | 33 |
| GO:0071704 | organic substance metabolic process | 2 | 33 |
| GO:0072330 | monocarboxylic acid biosynthetic process | 6 | 33 |
| GO:1901576 | organic substance biosynthetic process | 3 | 33 |
| GO:0000038 | very long-chain fatty acid metabolic process | 5 | 4 |
| GO:0001676 | long-chain fatty acid metabolic process | 5 | 3 |
| GO:0006643 | membrane lipid metabolic process | 4 | 4 |
| GO:0006665 | sphingolipid metabolic process | 4 | 4 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 4 |
| GO:0019367 | fatty acid elongation, saturated fatty acid | 7 | 4 |
| GO:0019368 | fatty acid elongation, unsaturated fatty acid | 7 | 4 |
| GO:0030148 | sphingolipid biosynthetic process | 5 | 4 |
| GO:0030497 | fatty acid elongation | 6 | 4 |
| GO:0034625 | fatty acid elongation, monounsaturated fatty acid | 8 | 4 |
| GO:0034626 | fatty acid elongation, polyunsaturated fatty acid | 8 | 4 |
| GO:0042759 | long-chain fatty acid biosynthetic process | 6 | 3 |
| GO:0042761 | very long-chain fatty acid biosynthetic process | 6 | 4 |
| GO:0046467 | membrane lipid biosynthetic process | 4 | 4 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 4 |
| GO:1901566 | organonitrogen compound biosynthetic process | 4 | 4 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 33 |
| GO:0004312 | fatty acid synthase activity | 5 | 33 |
| GO:0009922 | fatty acid elongase activity | 6 | 33 |
| GO:0016740 | transferase activity | 2 | 33 |
| GO:0016746 | acyltransferase activity | 3 | 33 |
| GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 33 |
| GO:0102756 | very-long-chain 3-ketoacyl-CoA synthase activity | 5 | 33 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.286 |
| CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.484 |
| CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.512 |
| CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.477 |
| CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.462 |
| CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.465 |
| CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.455 |
| CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.534 |
| CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.482 |
| CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.462 |
| CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.465 |
| CLV_PCSK_PC1ET2_1 | 373 | 375 | PF00082 | 0.554 |
| CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.339 |
| CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.529 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.382 |
| DOC_AGCK_PIF_1 | 247 | 252 | PF00069 | 0.413 |
| DOC_CYCLIN_RxL_1 | 57 | 68 | PF00134 | 0.311 |
| DOC_CYCLIN_yCln2_LP_2 | 287 | 293 | PF00134 | 0.532 |
| DOC_CYCLIN_yCln2_LP_2 | 75 | 81 | PF00134 | 0.257 |
| DOC_MAPK_gen_1 | 285 | 295 | PF00069 | 0.420 |
| DOC_MAPK_gen_1 | 59 | 66 | PF00069 | 0.312 |
| DOC_MAPK_MEF2A_6 | 2 | 9 | PF00069 | 0.374 |
| DOC_MAPK_MEF2A_6 | 289 | 297 | PF00069 | 0.453 |
| DOC_MAPK_MEF2A_6 | 335 | 342 | PF00069 | 0.298 |
| DOC_MAPK_MEF2A_6 | 59 | 66 | PF00069 | 0.312 |
| DOC_MAPK_NFAT4_5 | 59 | 67 | PF00069 | 0.310 |
| DOC_PP1_RVXF_1 | 202 | 208 | PF00149 | 0.321 |
| DOC_PP1_RVXF_1 | 230 | 236 | PF00149 | 0.517 |
| DOC_PP1_RVXF_1 | 71 | 78 | PF00149 | 0.277 |
| DOC_PP2B_LxvP_1 | 19 | 22 | PF13499 | 0.373 |
| DOC_PP4_FxxP_1 | 135 | 138 | PF00568 | 0.332 |
| DOC_PP4_FxxP_1 | 15 | 18 | PF00568 | 0.371 |
| DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.216 |
| DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.715 |
| DOC_USP7_UBL2_3 | 285 | 289 | PF12436 | 0.486 |
| DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.164 |
| DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.660 |
| LIG_14-3-3_CanoR_1 | 33 | 37 | PF00244 | 0.322 |
| LIG_14-3-3_CanoR_1 | 48 | 56 | PF00244 | 0.303 |
| LIG_14-3-3_CanoR_1 | 73 | 78 | PF00244 | 0.272 |
| LIG_Actin_WH2_2 | 159 | 176 | PF00022 | 0.440 |
| LIG_APCC_ABBA_1 | 345 | 350 | PF00400 | 0.382 |
| LIG_BRCT_BRCA1_1 | 348 | 352 | PF00533 | 0.284 |
| LIG_BRCT_BRCA1_2 | 348 | 354 | PF00533 | 0.367 |
| LIG_EH1_1 | 266 | 274 | PF00400 | 0.345 |
| LIG_EVH1_1 | 17 | 21 | PF00568 | 0.367 |
| LIG_FHA_1 | 200 | 206 | PF00498 | 0.225 |
| LIG_FHA_1 | 221 | 227 | PF00498 | 0.310 |
| LIG_FHA_1 | 241 | 247 | PF00498 | 0.265 |
| LIG_FHA_1 | 299 | 305 | PF00498 | 0.417 |
| LIG_FHA_1 | 334 | 340 | PF00498 | 0.412 |
| LIG_FHA_1 | 65 | 71 | PF00498 | 0.303 |
| LIG_FHA_2 | 192 | 198 | PF00498 | 0.281 |
| LIG_FHA_2 | 63 | 69 | PF00498 | 0.308 |
| LIG_FHA_2 | 89 | 95 | PF00498 | 0.425 |
| LIG_HCF-1_HBM_1 | 104 | 107 | PF13415 | 0.248 |
| LIG_LIR_Gen_1 | 222 | 233 | PF02991 | 0.473 |
| LIG_LIR_Gen_1 | 237 | 247 | PF02991 | 0.406 |
| LIG_LIR_Gen_1 | 271 | 282 | PF02991 | 0.355 |
| LIG_LIR_Gen_1 | 43 | 54 | PF02991 | 0.310 |
| LIG_LIR_Nem_3 | 165 | 170 | PF02991 | 0.296 |
| LIG_LIR_Nem_3 | 237 | 242 | PF02991 | 0.331 |
| LIG_LIR_Nem_3 | 244 | 250 | PF02991 | 0.300 |
| LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.317 |
| LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.463 |
| LIG_LIR_Nem_3 | 43 | 49 | PF02991 | 0.314 |
| LIG_LIR_Nem_3 | 53 | 58 | PF02991 | 0.308 |
| LIG_LIR_Nem_3 | 76 | 82 | PF02991 | 0.254 |
| LIG_PCNA_yPIPBox_3 | 113 | 126 | PF02747 | 0.146 |
| LIG_PCNA_yPIPBox_3 | 59 | 70 | PF02747 | 0.309 |
| LIG_Pex14_1 | 98 | 102 | PF04695 | 0.368 |
| LIG_Pex14_2 | 235 | 239 | PF04695 | 0.383 |
| LIG_Pex14_2 | 348 | 352 | PF04695 | 0.274 |
| LIG_PTAP_UEV_1 | 21 | 26 | PF05743 | 0.385 |
| LIG_REV1ctd_RIR_1 | 53 | 64 | PF16727 | 0.312 |
| LIG_SH2_PTP2 | 294 | 297 | PF00017 | 0.333 |
| LIG_SH2_PTP2 | 356 | 359 | PF00017 | 0.548 |
| LIG_SH2_STAP1 | 201 | 205 | PF00017 | 0.247 |
| LIG_SH2_STAP1 | 274 | 278 | PF00017 | 0.224 |
| LIG_SH2_STAT3 | 250 | 253 | PF00017 | 0.321 |
| LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.298 |
| LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.299 |
| LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.287 |
| LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.295 |
| LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.362 |
| LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.302 |
| LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.424 |
| LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.265 |
| LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.314 |
| LIG_SH2_STAT5 | 346 | 349 | PF00017 | 0.299 |
| LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.431 |
| LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.323 |
| LIG_SH3_3 | 15 | 21 | PF00018 | 0.371 |
| LIG_SH3_3 | 172 | 178 | PF00018 | 0.348 |
| LIG_SH3_3 | 22 | 28 | PF00018 | 0.393 |
| LIG_SH3_3 | 319 | 325 | PF00018 | 0.199 |
| LIG_SH3_3 | 363 | 369 | PF00018 | 0.611 |
| LIG_UBA3_1 | 140 | 148 | PF00899 | 0.488 |
| LIG_UBA3_1 | 211 | 216 | PF00899 | 0.329 |
| LIG_UBA3_1 | 347 | 354 | PF00899 | 0.309 |
| LIG_WRC_WIRS_1 | 192 | 197 | PF05994 | 0.302 |
| MOD_CDC14_SPxK_1 | 370 | 373 | PF00782 | 0.715 |
| MOD_CDK_SPxK_1 | 367 | 373 | PF00069 | 0.690 |
| MOD_CDK_SPxxK_3 | 367 | 374 | PF00069 | 0.718 |
| MOD_CK1_1 | 165 | 171 | PF00069 | 0.249 |
| MOD_CK1_1 | 50 | 56 | PF00069 | 0.306 |
| MOD_CK2_1 | 191 | 197 | PF00069 | 0.308 |
| MOD_CMANNOS | 157 | 160 | PF00535 | 0.397 |
| MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.513 |
| MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.307 |
| MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.365 |
| MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.528 |
| MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.504 |
| MOD_GSK3_1 | 268 | 275 | PF00069 | 0.435 |
| MOD_GSK3_1 | 316 | 323 | PF00069 | 0.261 |
| MOD_GSK3_1 | 329 | 336 | PF00069 | 0.296 |
| MOD_NEK2_1 | 133 | 138 | PF00069 | 0.304 |
| MOD_NEK2_1 | 162 | 167 | PF00069 | 0.292 |
| MOD_NEK2_1 | 188 | 193 | PF00069 | 0.258 |
| MOD_NEK2_1 | 200 | 205 | PF00069 | 0.227 |
| MOD_NEK2_1 | 212 | 217 | PF00069 | 0.312 |
| MOD_NEK2_1 | 220 | 225 | PF00069 | 0.321 |
| MOD_NEK2_1 | 226 | 231 | PF00069 | 0.455 |
| MOD_NEK2_1 | 268 | 273 | PF00069 | 0.299 |
| MOD_NEK2_1 | 293 | 298 | PF00069 | 0.485 |
| MOD_NEK2_1 | 307 | 312 | PF00069 | 0.272 |
| MOD_NEK2_1 | 62 | 67 | PF00069 | 0.310 |
| MOD_PIKK_1 | 298 | 304 | PF00454 | 0.369 |
| MOD_PIKK_1 | 32 | 38 | PF00454 | 0.322 |
| MOD_PIKK_1 | 333 | 339 | PF00454 | 0.375 |
| MOD_PKA_1 | 316 | 322 | PF00069 | 0.140 |
| MOD_PKA_1 | 73 | 79 | PF00069 | 0.270 |
| MOD_PKA_1 | 86 | 92 | PF00069 | 0.257 |
| MOD_PKA_2 | 32 | 38 | PF00069 | 0.322 |
| MOD_PKA_2 | 47 | 53 | PF00069 | 0.302 |
| MOD_PKA_2 | 73 | 79 | PF00069 | 0.270 |
| MOD_Plk_4 | 162 | 168 | PF00069 | 0.245 |
| MOD_Plk_4 | 220 | 226 | PF00069 | 0.302 |
| MOD_Plk_4 | 234 | 240 | PF00069 | 0.292 |
| MOD_Plk_4 | 241 | 247 | PF00069 | 0.283 |
| MOD_Plk_4 | 254 | 260 | PF00069 | 0.193 |
| MOD_Plk_4 | 268 | 274 | PF00069 | 0.271 |
| MOD_Plk_4 | 50 | 56 | PF00069 | 0.306 |
| MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.164 |
| MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.661 |
| TRG_DiLeu_BaLyEn_6 | 175 | 180 | PF01217 | 0.435 |
| TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.293 |
| TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.372 |
| TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.327 |
| TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.133 |
| TRG_ER_diArg_1 | 366 | 368 | PF00400 | 0.752 |
| TRG_ER_diArg_1 | 72 | 74 | PF00400 | 0.290 |
| TRG_NES_CRM1_1 | 337 | 350 | PF08389 | 0.433 |
| TRG_Pf-PMV_PEXEL_1 | 181 | 186 | PF00026 | 0.545 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P5E5 | Leptomonas seymouri | 33% | 100% |
| A0A0N0P7D1 | Leptomonas seymouri | 32% | 100% |
| A0A0N0P7D6 | Leptomonas seymouri | 44% | 100% |
| A0A0N1HZJ8 | Leptomonas seymouri | 29% | 100% |
| A0A0N1I9H5 | Leptomonas seymouri | 72% | 100% |
| A0A0N1ILQ4 | Leptomonas seymouri | 38% | 100% |
| A0A0N1IM10 | Leptomonas seymouri | 50% | 100% |
| A0A0N1PDR8 | Leptomonas seymouri | 32% | 100% |
| A0A0S4IS29 | Bodo saltans | 35% | 100% |
| A0A0S4IVJ6 | Bodo saltans | 29% | 100% |
| A0A0S4IVS6 | Bodo saltans | 32% | 100% |
| A0A0S4IW98 | Bodo saltans | 34% | 100% |
| A0A0S4J4C4 | Bodo saltans | 24% | 100% |
| A0A1X0NNK7 | Trypanosomatidae | 33% | 100% |
| A0A1X0NNL0 | Trypanosomatidae | 45% | 100% |
| A0A1X0NNM4 | Trypanosomatidae | 40% | 100% |
| A0A1X0NNM5 | Trypanosomatidae | 30% | 100% |
| A0A3Q8I8T7 | Leishmania donovani | 28% | 96% |
| A0A3Q8I9T2 | Leishmania donovani | 31% | 100% |
| A0A3Q8I9U9 | Leishmania donovani | 31% | 100% |
| A0A3Q8I9X8 | Leishmania donovani | 32% | 100% |
| A0A3Q8IC05 | Leishmania donovani | 30% | 100% |
| A0A3Q8ID51 | Leishmania donovani | 30% | 94% |
| A0A3Q8IIA9 | Leishmania donovani | 61% | 100% |
| A0A3R7KG78 | Trypanosoma rangeli | 29% | 100% |
| A0A3R7MJR2 | Trypanosoma rangeli | 41% | 100% |
| A0A3R7NSQ3 | Trypanosoma rangeli | 47% | 100% |
| A0A3S5H6R7 | Leishmania donovani | 53% | 100% |
| A0A3S5H6R8 | Leishmania donovani | 35% | 100% |
| A0A3S7WSY8 | Leishmania donovani | 92% | 100% |
| A0A3S7WSZ1 | Leishmania donovani | 32% | 100% |
| A0A3S7WT03 | Leishmania donovani | 32% | 100% |
| A0A3S7WT16 | Leishmania donovani | 30% | 100% |
| A0A422NNP1 | Trypanosoma rangeli | 30% | 100% |
| A4H7M2 | Leishmania braziliensis | 82% | 100% |
| A4H7M3 | Leishmania braziliensis | 54% | 100% |
| A4H7M4 | Leishmania braziliensis | 59% | 100% |
| A4H7M5 | Leishmania braziliensis | 35% | 100% |
| A4H7M6 | Leishmania braziliensis | 31% | 100% |
| A4H7M7 | Leishmania braziliensis | 31% | 100% |
| A4H7M8 | Leishmania braziliensis | 31% | 100% |
| A4H7M9 | Leishmania braziliensis | 29% | 92% |
| A4H7N0 | Leishmania braziliensis | 34% | 100% |
| A4HW07 | Leishmania infantum | 92% | 100% |
| A4HW08 | Leishmania infantum | 53% | 100% |
| A4HW09 | Leishmania infantum | 61% | 100% |
| A4HW10 | Leishmania infantum | 35% | 100% |
| A4HW12 | Leishmania infantum | 32% | 100% |
| A4HW13 | Leishmania infantum | 31% | 100% |
| A4HW14 | Leishmania infantum | 30% | 100% |
| A4HW15 | Leishmania infantum | 31% | 100% |
| A4HW16 | Leishmania infantum | 30% | 100% |
| A4HW17 | Leishmania infantum | 29% | 96% |
| A4HW18 | Leishmania infantum | 31% | 100% |
| C9ZT13 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
| C9ZT15 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
| C9ZT16 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
| E8NHR2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
| E8NHR3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
| E9AGL0 | Leishmania infantum | 32% | 100% |
| E9AGL2 | Leishmania infantum | 32% | 100% |
| E9APR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 53% | 100% |
| E9APR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 100% |
| E9APR2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
| E9APR3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
| E9APR4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
| E9APR5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
| E9APR6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
| E9APR7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
| E9APR8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 97% |
| E9APR9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
| G5EEE5 | Caenorhabditis elegans | 27% | 100% |
| P39540 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 100% |
| Q4QFQ9 | Leishmania major | 31% | 100% |
| Q4QFR0 | Leishmania major | 28% | 100% |
| Q4QFR2 | Leishmania major | 31% | 100% |
| Q4QFR3 | Leishmania major | 30% | 100% |
| Q4QFR4 | Leishmania major | 31% | 100% |
| Q4QFR5 | Leishmania major | 32% | 100% |
| Q4QFR6 | Leishmania major | 34% | 100% |
| Q4QFR7 | Leishmania major | 37% | 99% |
| Q4QFR8 | Leishmania major | 59% | 100% |
| Q4QFR9 | Leishmania major | 53% | 100% |
| Q4QFS0 | Leishmania major | 92% | 100% |
| Q5ZJR8 | Gallus gallus | 34% | 100% |
| Q6PC64 | Danio rerio | 34% | 100% |
| Q920L5 | Mus musculus | 35% | 100% |
| Q9H5J4 | Homo sapiens | 34% | 100% |
| Q9VV87 | Drosophila melanogaster | 32% | 100% |
| V5BE99 | Trypanosoma cruzi | 30% | 100% |
| V5BIX9 | Trypanosoma cruzi | 41% | 100% |
| V5BND3 | Trypanosoma cruzi | 31% | 100% |
| V5DF68 | Trypanosoma cruzi | 46% | 100% |