Fatty acid metabolism, enoyl-CoA hydratase/Enoyl-CoA isomerase/3-hydroxyacyl-CoA dehydrogenase
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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005777 | peroxisome | 6 | 1 |
GO:0020015 | glycosome | 7 | 1 |
GO:0042579 | microbody | 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: A4I9A0
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 11 |
GO:0006629 | lipid metabolic process | 3 | 11 |
GO:0006631 | fatty acid metabolic process | 4 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0019752 | carboxylic acid metabolic process | 5 | 11 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 11 |
GO:0043436 | oxoacid metabolic process | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044255 | cellular lipid metabolic process | 3 | 11 |
GO:0044281 | small molecule metabolic process | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0006635 | fatty acid beta-oxidation | 6 | 9 |
GO:0009056 | catabolic process | 2 | 9 |
GO:0009062 | fatty acid catabolic process | 5 | 9 |
GO:0016042 | lipid catabolic process | 4 | 9 |
GO:0016054 | organic acid catabolic process | 4 | 9 |
GO:0019395 | fatty acid oxidation | 5 | 9 |
GO:0030258 | lipid modification | 4 | 9 |
GO:0034440 | lipid oxidation | 5 | 9 |
GO:0044242 | cellular lipid catabolic process | 4 | 9 |
GO:0044248 | cellular catabolic process | 3 | 9 |
GO:0044282 | small molecule catabolic process | 3 | 9 |
GO:0046395 | carboxylic acid catabolic process | 5 | 9 |
GO:0072329 | monocarboxylic acid catabolic process | 6 | 9 |
GO:1901575 | organic substance catabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0003857 | 3-hydroxyacyl-CoA dehydrogenase activity | 5 | 7 |
GO:0004300 | enoyl-CoA hydratase activity | 5 | 6 |
GO:0005488 | binding | 1 | 11 |
GO:0016491 | oxidoreductase activity | 2 | 11 |
GO:0016614 | oxidoreductase activity, acting on CH-OH group of donors | 3 | 11 |
GO:0016616 | oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor | 4 | 11 |
GO:0016829 | lyase activity | 2 | 6 |
GO:0016835 | carbon-oxygen lyase activity | 3 | 6 |
GO:0016836 | hydro-lyase activity | 4 | 6 |
GO:0016853 | isomerase activity | 2 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0051287 | NAD binding | 4 | 11 |
GO:0070403 | NAD+ binding | 4 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 46 | 50 | PF00656 | 0.518 |
CLV_C14_Caspase3-7 | 487 | 491 | PF00656 | 0.624 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.332 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 443 | 445 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 553 | 555 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 557 | 559 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 623 | 625 | PF00675 | 0.279 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.497 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 551 | 553 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 557 | 559 | PF00082 | 0.400 |
CLV_PCSK_PC1ET2_1 | 251 | 253 | PF00082 | 0.368 |
CLV_PCSK_PC1ET2_1 | 404 | 406 | PF00082 | 0.604 |
CLV_PCSK_PC1ET2_1 | 551 | 553 | PF00082 | 0.499 |
CLV_PCSK_PC7_1 | 32 | 38 | PF00082 | 0.483 |
CLV_PCSK_PC7_1 | 553 | 559 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 452 | 456 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 568 | 572 | PF00082 | 0.122 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 651 | 655 | PF00082 | 0.286 |
DEG_APCC_DBOX_1 | 135 | 143 | PF00400 | 0.335 |
DEG_APCC_DBOX_1 | 332 | 340 | PF00400 | 0.383 |
DEG_APCC_DBOX_1 | 524 | 532 | PF00400 | 0.461 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.458 |
DOC_CDC14_PxL_1 | 316 | 324 | PF14671 | 0.328 |
DOC_CKS1_1 | 400 | 405 | PF01111 | 0.459 |
DOC_CKS1_1 | 453 | 458 | PF01111 | 0.481 |
DOC_CYCLIN_RxL_1 | 361 | 374 | PF00134 | 0.383 |
DOC_CYCLIN_RxL_1 | 56 | 64 | PF00134 | 0.564 |
DOC_CYCLIN_yClb3_PxF_3 | 424 | 430 | PF00134 | 0.271 |
DOC_MAPK_FxFP_2 | 600 | 603 | PF00069 | 0.328 |
DOC_MAPK_gen_1 | 523 | 531 | PF00069 | 0.394 |
DOC_MAPK_HePTP_8 | 271 | 283 | PF00069 | 0.307 |
DOC_MAPK_MEF2A_6 | 108 | 116 | PF00069 | 0.499 |
DOC_MAPK_MEF2A_6 | 160 | 168 | PF00069 | 0.318 |
DOC_MAPK_MEF2A_6 | 18 | 27 | PF00069 | 0.576 |
DOC_MAPK_MEF2A_6 | 274 | 283 | PF00069 | 0.307 |
DOC_MAPK_MEF2A_6 | 523 | 531 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 97 | 104 | PF00069 | 0.531 |
DOC_PP1_RVXF_1 | 566 | 572 | PF00149 | 0.270 |
DOC_PP2B_LxvP_1 | 66 | 69 | PF13499 | 0.526 |
DOC_PP4_FxxP_1 | 283 | 286 | PF00568 | 0.268 |
DOC_PP4_FxxP_1 | 430 | 433 | PF00568 | 0.426 |
DOC_PP4_FxxP_1 | 600 | 603 | PF00568 | 0.455 |
DOC_PP4_FxxP_1 | 638 | 641 | PF00568 | 0.270 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 527 | 531 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 632 | 636 | PF00917 | 0.445 |
DOC_USP7_UBL2_3 | 621 | 625 | PF12436 | 0.364 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.261 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 509 | 514 | PF00397 | 0.692 |
LIG_14-3-3_CanoR_1 | 108 | 116 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 160 | 168 | PF00244 | 0.255 |
LIG_14-3-3_CanoR_1 | 297 | 306 | PF00244 | 0.304 |
LIG_14-3-3_CanoR_1 | 333 | 343 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 35 | 40 | PF00244 | 0.690 |
LIG_14-3-3_CanoR_1 | 385 | 389 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 6 | 10 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 79 | 86 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 90 | 100 | PF00244 | 0.564 |
LIG_Actin_WH2_2 | 147 | 162 | PF00022 | 0.360 |
LIG_BRCT_BRCA1_1 | 29 | 33 | PF00533 | 0.545 |
LIG_BRCT_BRCA1_1 | 634 | 638 | PF00533 | 0.328 |
LIG_Clathr_ClatBox_1 | 369 | 373 | PF01394 | 0.404 |
LIG_eIF4E_1 | 329 | 335 | PF01652 | 0.279 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.569 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.274 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.383 |
LIG_FHA_1 | 509 | 515 | PF00498 | 0.693 |
LIG_FHA_2 | 453 | 459 | PF00498 | 0.457 |
LIG_FHA_2 | 485 | 491 | PF00498 | 0.663 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.612 |
LIG_HP1_1 | 527 | 531 | PF01393 | 0.450 |
LIG_LIR_Apic_2 | 419 | 425 | PF02991 | 0.430 |
LIG_LIR_Apic_2 | 635 | 641 | PF02991 | 0.271 |
LIG_LIR_Gen_1 | 563 | 574 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 654 | 659 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 317 | 322 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 337 | 343 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 448 | 454 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 524 | 529 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 541 | 547 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 563 | 569 | PF02991 | 0.419 |
LIG_LYPXL_SIV_4 | 53 | 61 | PF13949 | 0.521 |
LIG_LYPXL_yS_3 | 319 | 322 | PF13949 | 0.328 |
LIG_LYPXL_yS_3 | 526 | 529 | PF13949 | 0.379 |
LIG_PCNA_TLS_4 | 180 | 187 | PF02747 | 0.328 |
LIG_Pex14_2 | 655 | 659 | PF04695 | 0.342 |
LIG_SH2_CRK | 451 | 455 | PF00017 | 0.398 |
LIG_SH2_NCK_1 | 54 | 58 | PF00017 | 0.571 |
LIG_SH2_SRC | 612 | 615 | PF00017 | 0.315 |
LIG_SH2_STAP1 | 540 | 544 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 612 | 616 | PF00017 | 0.252 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.478 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.498 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.647 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.393 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.639 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.681 |
LIG_SH3_3 | 422 | 428 | PF00018 | 0.363 |
LIG_SUMO_SIM_anti_2 | 152 | 158 | PF11976 | 0.284 |
LIG_SUMO_SIM_anti_2 | 162 | 168 | PF11976 | 0.255 |
LIG_SUMO_SIM_par_1 | 165 | 170 | PF11976 | 0.283 |
LIG_SUMO_SIM_par_1 | 320 | 325 | PF11976 | 0.429 |
LIG_SUMO_SIM_par_1 | 527 | 533 | PF11976 | 0.468 |
LIG_TRAF2_1 | 455 | 458 | PF00917 | 0.428 |
LIG_TYR_ITIM | 542 | 547 | PF00017 | 0.342 |
LIG_UBA3_1 | 242 | 251 | PF00899 | 0.383 |
LIG_UBA3_1 | 312 | 318 | PF00899 | 0.381 |
MOD_CDK_SPK_2 | 399 | 404 | PF00069 | 0.464 |
MOD_CDK_SPxK_1 | 399 | 405 | PF00069 | 0.461 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.706 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.702 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.603 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.518 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.639 |
MOD_CK1_1 | 530 | 536 | PF00069 | 0.372 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.523 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.311 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.328 |
MOD_CK2_1 | 411 | 417 | PF00069 | 0.574 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.440 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.628 |
MOD_Cter_Amidation | 442 | 445 | PF01082 | 0.365 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.629 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.585 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.311 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.566 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.557 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.562 |
MOD_GlcNHglycan | 490 | 494 | PF01048 | 0.623 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.571 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.620 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.626 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.391 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.444 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.588 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.554 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.508 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.658 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.474 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.568 |
MOD_N-GLC_1 | 287 | 292 | PF02516 | 0.383 |
MOD_N-GLC_1 | 538 | 543 | PF02516 | 0.442 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.322 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.252 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.339 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.453 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.395 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.436 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.587 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.557 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.536 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.481 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.374 |
MOD_PIKK_1 | 269 | 275 | PF00454 | 0.364 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.582 |
MOD_PIKK_1 | 78 | 84 | PF00454 | 0.589 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.447 |
MOD_PK_1 | 35 | 41 | PF00069 | 0.495 |
MOD_PKA_1 | 251 | 257 | PF00069 | 0.328 |
MOD_PKA_1 | 35 | 41 | PF00069 | 0.495 |
MOD_PKA_1 | 553 | 559 | PF00069 | 0.450 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.520 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.255 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.269 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.237 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.405 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.675 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.406 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.525 |
MOD_PKA_2 | 443 | 449 | PF00069 | 0.434 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.618 |
MOD_PKA_2 | 553 | 559 | PF00069 | 0.528 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.475 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.456 |
MOD_Plk_1 | 538 | 544 | PF00069 | 0.335 |
MOD_Plk_2-3 | 127 | 133 | PF00069 | 0.538 |
MOD_Plk_2-3 | 543 | 549 | PF00069 | 0.409 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.282 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.219 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.328 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.497 |
MOD_Plk_4 | 501 | 507 | PF00069 | 0.708 |
MOD_Plk_4 | 530 | 536 | PF00069 | 0.510 |
MOD_Plk_4 | 654 | 660 | PF00069 | 0.438 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.632 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.261 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.500 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.482 |
MOD_ProDKin_1 | 509 | 515 | PF00069 | 0.691 |
MOD_SUMO_rev_2 | 85 | 93 | PF00179 | 0.684 |
TRG_DiLeu_BaEn_1 | 63 | 68 | PF01217 | 0.512 |
TRG_DiLeu_BaLyEn_6 | 330 | 335 | PF01217 | 0.330 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.658 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 451 | 454 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 526 | 529 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 544 | 547 | PF00928 | 0.471 |
TRG_ER_diArg_1 | 187 | 190 | PF00400 | 0.330 |
TRG_ER_diArg_1 | 207 | 210 | PF00400 | 0.122 |
TRG_ER_diArg_1 | 35 | 37 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 463 | 466 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 552 | 554 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 557 | 559 | PF00400 | 0.417 |
TRG_NLS_MonoCore_2 | 550 | 555 | PF00514 | 0.436 |
TRG_Pf-PMV_PEXEL_1 | 367 | 371 | PF00026 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 59 | 63 | PF00026 | 0.556 |
TRG_Pf-PMV_PEXEL_1 | 631 | 636 | PF00026 | 0.330 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVX9 | Leptomonas seymouri | 56% | 71% |
A0A1X0NSP5 | Trypanosomatidae | 30% | 83% |
A0A3R7KS65 | Trypanosoma rangeli | 31% | 83% |
A0A3S7X716 | Leishmania donovani | 99% | 71% |
A4HLX1 | Leishmania braziliensis | 77% | 100% |
C9ZJC6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 82% |
E9B4A0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
P76083 | Escherichia coli (strain K12) | 27% | 100% |
Q4Q3S6 | Leishmania major | 92% | 100% |
V5B7W6 | Trypanosoma cruzi | 24% | 81% |
V5BN63 | Trypanosoma cruzi | 30% | 78% |