Fatty acid metabolism, long-chain-fatty-acid-CoA ligase (Fragment)
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: 15 |
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: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I3J3
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:0006633 | fatty acid biosynthetic process | 5 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008610 | lipid biosynthetic process | 4 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016053 | organic acid biosynthetic process | 4 | 1 |
GO:0019752 | carboxylic acid metabolic process | 5 | 1 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 1 |
GO:0043436 | oxoacid metabolic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary 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:0046394 | carboxylic acid biosynthetic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0072330 | monocarboxylic acid biosynthetic process | 6 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 17 |
GO:0004467 | long-chain fatty acid-CoA ligase activity | 3 | 5 |
GO:0015645 | fatty acid ligase activity | 2 | 5 |
GO:0016405 | CoA-ligase activity | 4 | 10 |
GO:0016874 | ligase activity | 2 | 17 |
GO:0016877 | ligase activity, forming carbon-sulfur bonds | 3 | 10 |
GO:0016878 | acid-thiol ligase activity | 4 | 10 |
GO:0140657 | ATP-dependent activity | 1 | 5 |
GO:0031957 | very long-chain fatty acid-CoA ligase activity | 3 | 1 |
GO:0016207 | 4-coumarate-CoA ligase activity | 5 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.367 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.721 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.353 |
CLV_PCSK_PC1ET2_1 | 229 | 231 | PF00082 | 0.428 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 673 | 677 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 695 | 699 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 718 | 722 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 727 | 731 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.436 |
CLV_Separin_Metazoa | 715 | 719 | PF03568 | 0.353 |
DEG_APCC_DBOX_1 | 33 | 41 | PF00400 | 0.321 |
DEG_ODPH_VHL_1 | 701 | 713 | PF01847 | 0.288 |
DOC_CKS1_1 | 135 | 140 | PF01111 | 0.330 |
DOC_CYCLIN_yCln2_LP_2 | 135 | 141 | PF00134 | 0.358 |
DOC_CYCLIN_yCln2_LP_2 | 507 | 513 | PF00134 | 0.289 |
DOC_MAPK_gen_1 | 144 | 152 | PF00069 | 0.370 |
DOC_MAPK_gen_1 | 337 | 347 | PF00069 | 0.289 |
DOC_MAPK_gen_1 | 622 | 631 | PF00069 | 0.374 |
DOC_MAPK_gen_1 | 694 | 700 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 726 | 735 | PF00069 | 0.472 |
DOC_PP1_RVXF_1 | 671 | 678 | PF00149 | 0.288 |
DOC_PP2B_LxvP_1 | 478 | 481 | PF13499 | 0.289 |
DOC_PP2B_LxvP_1 | 700 | 703 | PF13499 | 0.288 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.337 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.314 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 561 | 565 | PF00917 | 0.275 |
DOC_USP7_MATH_1 | 602 | 606 | PF00917 | 0.289 |
DOC_USP7_UBL2_3 | 229 | 233 | PF12436 | 0.645 |
DOC_USP7_UBL2_3 | 267 | 271 | PF12436 | 0.426 |
DOC_USP7_UBL2_3 | 723 | 727 | PF12436 | 0.398 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.323 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.256 |
DOC_WW_Pin1_4 | 521 | 526 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.595 |
LIG_14-3-3_CanoR_1 | 497 | 507 | PF00244 | 0.270 |
LIG_14-3-3_CanoR_1 | 613 | 617 | PF00244 | 0.289 |
LIG_14-3-3_CanoR_1 | 673 | 678 | PF00244 | 0.395 |
LIG_APCC_ABBAyCdc20_2 | 638 | 644 | PF00400 | 0.313 |
LIG_BRCT_BRCA1_1 | 207 | 211 | PF00533 | 0.469 |
LIG_Clathr_ClatBox_1 | 312 | 316 | PF01394 | 0.288 |
LIG_deltaCOP1_diTrp_1 | 375 | 379 | PF00928 | 0.335 |
LIG_EH1_1 | 391 | 399 | PF00400 | 0.289 |
LIG_eIF4E_1 | 217 | 223 | PF01652 | 0.418 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.378 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.320 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.543 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.426 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.558 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.358 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.325 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.334 |
LIG_FHA_1 | 684 | 690 | PF00498 | 0.364 |
LIG_FHA_1 | 719 | 725 | PF00498 | 0.289 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.451 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.322 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.463 |
LIG_FHA_2 | 412 | 418 | PF00498 | 0.289 |
LIG_FHA_2 | 491 | 497 | PF00498 | 0.274 |
LIG_FHA_2 | 574 | 580 | PF00498 | 0.289 |
LIG_FHA_2 | 674 | 680 | PF00498 | 0.400 |
LIG_GBD_Chelix_1 | 397 | 405 | PF00786 | 0.200 |
LIG_LIR_Apic_2 | 241 | 245 | PF02991 | 0.530 |
LIG_LIR_Apic_2 | 76 | 82 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 15 | 24 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 175 | 183 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 432 | 442 | PF02991 | 0.295 |
LIG_LIR_Gen_1 | 549 | 560 | PF02991 | 0.295 |
LIG_LIR_Gen_1 | 605 | 616 | PF02991 | 0.246 |
LIG_LIR_Gen_1 | 708 | 717 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 15 | 19 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 175 | 179 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 432 | 437 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 439 | 444 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 46 | 50 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 549 | 555 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 563 | 569 | PF02991 | 0.221 |
LIG_LIR_Nem_3 | 605 | 611 | PF02991 | 0.218 |
LIG_LIR_Nem_3 | 708 | 713 | PF02991 | 0.333 |
LIG_PCNA_yPIPBox_3 | 17 | 30 | PF02747 | 0.338 |
LIG_Pex14_2 | 566 | 570 | PF04695 | 0.270 |
LIG_SH2_CRK | 10 | 14 | PF00017 | 0.337 |
LIG_SH2_CRK | 120 | 124 | PF00017 | 0.286 |
LIG_SH2_CRK | 331 | 335 | PF00017 | 0.397 |
LIG_SH2_CRK | 47 | 51 | PF00017 | 0.352 |
LIG_SH2_CRK | 608 | 612 | PF00017 | 0.401 |
LIG_SH2_CRK | 704 | 708 | PF00017 | 0.295 |
LIG_SH2_GRB2like | 569 | 572 | PF00017 | 0.401 |
LIG_SH2_NCK_1 | 331 | 335 | PF00017 | 0.236 |
LIG_SH2_NCK_1 | 552 | 556 | PF00017 | 0.266 |
LIG_SH2_PTP2 | 441 | 444 | PF00017 | 0.236 |
LIG_SH2_PTP2 | 710 | 713 | PF00017 | 0.348 |
LIG_SH2_SRC | 552 | 555 | PF00017 | 0.290 |
LIG_SH2_STAP1 | 10 | 14 | PF00017 | 0.325 |
LIG_SH2_STAP1 | 110 | 114 | PF00017 | 0.358 |
LIG_SH2_STAP1 | 120 | 124 | PF00017 | 0.244 |
LIG_SH2_STAP1 | 176 | 180 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 217 | 221 | PF00017 | 0.328 |
LIG_SH2_STAP1 | 341 | 345 | PF00017 | 0.288 |
LIG_SH2_STAP1 | 643 | 647 | PF00017 | 0.401 |
LIG_SH2_STAT3 | 532 | 535 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 608 | 611 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 710 | 713 | PF00017 | 0.348 |
LIG_SH3_1 | 192 | 198 | PF00018 | 0.454 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.469 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.398 |
LIG_SH3_3 | 507 | 513 | PF00018 | 0.324 |
LIG_SH3_3 | 519 | 525 | PF00018 | 0.283 |
LIG_SH3_3 | 530 | 536 | PF00018 | 0.253 |
LIG_SH3_3 | 595 | 601 | PF00018 | 0.278 |
LIG_SH3_3 | 711 | 717 | PF00018 | 0.270 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.439 |
LIG_SH3_5 | 99 | 103 | PF00018 | 0.377 |
LIG_SUMO_SIM_anti_2 | 614 | 621 | PF11976 | 0.313 |
LIG_SUMO_SIM_anti_2 | 657 | 664 | PF11976 | 0.330 |
LIG_TRAF2_1 | 282 | 285 | PF00917 | 0.506 |
LIG_TYR_ITIM | 8 | 13 | PF00017 | 0.336 |
LIG_WRC_WIRS_1 | 413 | 418 | PF05994 | 0.423 |
MOD_CDK_SPxxK_3 | 450 | 457 | PF00069 | 0.348 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.487 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.644 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.330 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.267 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.265 |
MOD_CK2_1 | 490 | 496 | PF00069 | 0.289 |
MOD_CK2_1 | 543 | 549 | PF00069 | 0.421 |
MOD_CK2_1 | 573 | 579 | PF00069 | 0.289 |
MOD_CK2_1 | 624 | 630 | PF00069 | 0.357 |
MOD_CK2_1 | 673 | 679 | PF00069 | 0.400 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.431 |
MOD_GlcNHglycan | 154 | 158 | PF01048 | 0.448 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.692 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.564 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.416 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.391 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.334 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.320 |
MOD_GlcNHglycan | 488 | 492 | PF01048 | 0.354 |
MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.485 |
MOD_GlcNHglycan | 571 | 574 | PF01048 | 0.328 |
MOD_GlcNHglycan | 604 | 607 | PF01048 | 0.261 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.345 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.481 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.261 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.460 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.620 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.423 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.316 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.309 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.346 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.161 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.236 |
MOD_GSK3_1 | 683 | 690 | PF00069 | 0.399 |
MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.537 |
MOD_N-GLC_1 | 718 | 723 | PF02516 | 0.319 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.368 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.388 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.421 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.299 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.449 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.334 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.323 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.274 |
MOD_NEK2_1 | 611 | 616 | PF00069 | 0.270 |
MOD_NEK2_2 | 429 | 434 | PF00069 | 0.401 |
MOD_NEK2_2 | 464 | 469 | PF00069 | 0.288 |
MOD_NEK2_2 | 561 | 566 | PF00069 | 0.326 |
MOD_NEK2_2 | 9 | 14 | PF00069 | 0.330 |
MOD_PIKK_1 | 139 | 145 | PF00454 | 0.414 |
MOD_PIKK_1 | 505 | 511 | PF00454 | 0.344 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.311 |
MOD_PKA_2 | 379 | 385 | PF00069 | 0.353 |
MOD_PKA_2 | 612 | 618 | PF00069 | 0.289 |
MOD_PKB_1 | 289 | 297 | PF00069 | 0.520 |
MOD_PKB_1 | 671 | 679 | PF00069 | 0.227 |
MOD_Plk_1 | 429 | 435 | PF00069 | 0.293 |
MOD_Plk_1 | 631 | 637 | PF00069 | 0.253 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.368 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.385 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.293 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.530 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.355 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.324 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.268 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.274 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.321 |
MOD_Plk_4 | 561 | 567 | PF00069 | 0.272 |
MOD_Plk_4 | 606 | 612 | PF00069 | 0.415 |
MOD_Plk_4 | 631 | 637 | PF00069 | 0.431 |
MOD_Plk_4 | 655 | 661 | PF00069 | 0.347 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.327 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.327 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.434 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.256 |
MOD_ProDKin_1 | 521 | 527 | PF00069 | 0.387 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.586 |
MOD_SUMO_rev_2 | 158 | 168 | PF00179 | 0.454 |
MOD_SUMO_rev_2 | 225 | 235 | PF00179 | 0.577 |
MOD_SUMO_rev_2 | 264 | 269 | PF00179 | 0.481 |
MOD_SUMO_rev_2 | 691 | 696 | PF00179 | 0.304 |
TRG_DiLeu_BaEn_1 | 466 | 471 | PF01217 | 0.416 |
TRG_ENDOCYTIC_2 | 10 | 13 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.253 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.272 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.270 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 552 | 555 | PF00928 | 0.256 |
TRG_ENDOCYTIC_2 | 608 | 611 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 710 | 713 | PF00928 | 0.318 |
TRG_ER_diArg_1 | 191 | 193 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 287 | 289 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 62 | 64 | PF00400 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 166 | 170 | PF00026 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 273 | 278 | PF00026 | 0.661 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IL67 | Bodo saltans | 42% | 95% |
A0A0S4J3H6 | Bodo saltans | 24% | 100% |
A0A1X0NYK4 | Trypanosomatidae | 51% | 100% |
A0A3Q8ID29 | Leishmania donovani | 99% | 99% |
A0A3R7KRF3 | Trypanosoma rangeli | 51% | 100% |
A0A3S7WVG2 | Leishmania donovani | 24% | 100% |
A0A3S7WVH9 | Leishmania donovani | 20% | 100% |
A0A3S7WVL1 | Leishmania donovani | 24% | 100% |
A4HA52 | Leishmania braziliensis | 21% | 100% |
A4HGG0 | Leishmania braziliensis | 82% | 100% |
A4HYA8 | Leishmania infantum | 24% | 100% |
A4HYB7 | Leishmania infantum | 20% | 100% |
D0A7V2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E9AGS6 | Leishmania infantum | 24% | 100% |
E9AZT3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
P14912 | Petroselinum crispum | 22% | 100% |
Q4Q8F1 | Leishmania major | 92% | 100% |
Q4QDB5 | Leishmania major | 21% | 100% |
Q4QDB6 | Leishmania major | 23% | 100% |
V5AUI9 | Trypanosoma cruzi | 52% | 100% |