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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005777 | peroxisome | 6 | 11 |
GO:0042579 | microbody | 5 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: E9AZD5
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:0006635 | fatty acid beta-oxidation | 6 | 10 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009056 | catabolic process | 2 | 10 |
GO:0009062 | fatty acid catabolic process | 5 | 10 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016042 | lipid catabolic process | 4 | 10 |
GO:0016054 | organic acid catabolic process | 4 | 10 |
GO:0019395 | fatty acid oxidation | 5 | 10 |
GO:0019752 | carboxylic acid metabolic process | 5 | 11 |
GO:0030258 | lipid modification | 4 | 10 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 11 |
GO:0034440 | lipid oxidation | 5 | 10 |
GO:0043436 | oxoacid metabolic process | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044242 | cellular lipid catabolic process | 4 | 10 |
GO:0044248 | cellular catabolic process | 3 | 10 |
GO:0044255 | cellular lipid metabolic process | 3 | 11 |
GO:0044281 | small molecule metabolic process | 2 | 11 |
GO:0044282 | small molecule catabolic process | 3 | 10 |
GO:0046395 | carboxylic acid catabolic process | 5 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0072329 | monocarboxylic acid catabolic process | 6 | 10 |
GO:1901575 | organic substance catabolic process | 3 | 10 |
GO:0033540 | fatty acid beta-oxidation using acyl-CoA oxidase | 7 | 1 |
GO:0042592 | homeostatic process | 3 | 1 |
GO:0048878 | chemical homeostasis | 4 | 1 |
GO:0055088 | lipid homeostasis | 5 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0003997 | acyl-CoA oxidase activity | 5 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0016491 | oxidoreductase activity | 2 | 11 |
GO:0016627 | oxidoreductase activity, acting on the CH-CH group of donors | 3 | 11 |
GO:0016634 | oxidoreductase activity, acting on the CH-CH group of donors, oxygen as acceptor | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0050660 | flavin adenine dinucleotide binding | 4 | 11 |
GO:0071949 | FAD binding | 5 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0005504 | fatty acid binding | 3 | 1 |
GO:0008289 | lipid binding | 2 | 1 |
GO:0031406 | carboxylic acid binding | 4 | 1 |
GO:0033293 | monocarboxylic acid binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 148 | 152 | PF00656 | 0.437 |
CLV_C14_Caspase3-7 | 429 | 433 | PF00656 | 0.532 |
CLV_C14_Caspase3-7 | 612 | 616 | PF00656 | 0.355 |
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 525 | 527 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 573 | 575 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 681 | 683 | PF00675 | 0.697 |
CLV_NRD_NRD_1 | 715 | 717 | PF00675 | 0.702 |
CLV_PCSK_FUR_1 | 310 | 314 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 515 | 517 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 525 | 527 | PF00082 | 0.298 |
CLV_PCSK_KEX2_1 | 681 | 683 | PF00082 | 0.692 |
CLV_PCSK_PC1ET2_1 | 515 | 517 | PF00082 | 0.425 |
CLV_PCSK_PC7_1 | 107 | 113 | PF00082 | 0.367 |
CLV_PCSK_PC7_1 | 521 | 527 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 574 | 578 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 643 | 647 | PF00082 | 0.598 |
CLV_Separin_Metazoa | 307 | 311 | PF03568 | 0.517 |
DEG_APCC_DBOX_1 | 573 | 581 | PF00400 | 0.332 |
DEG_APCC_DBOX_1 | 59 | 67 | PF00400 | 0.420 |
DEG_ODPH_VHL_1 | 621 | 634 | PF01847 | 0.355 |
DOC_CYCLIN_RxL_1 | 495 | 507 | PF00134 | 0.444 |
DOC_CYCLIN_yCln2_LP_2 | 281 | 287 | PF00134 | 0.463 |
DOC_CYCLIN_yCln2_LP_2 | 475 | 481 | PF00134 | 0.546 |
DOC_CYCLIN_yCln2_LP_2 | 66 | 69 | PF00134 | 0.325 |
DOC_MAPK_gen_1 | 347 | 355 | PF00069 | 0.536 |
DOC_MAPK_MEF2A_6 | 347 | 355 | PF00069 | 0.545 |
DOC_PP1_RVXF_1 | 450 | 457 | PF00149 | 0.368 |
DOC_PP1_RVXF_1 | 499 | 506 | PF00149 | 0.371 |
DOC_PP1_RVXF_1 | 576 | 583 | PF00149 | 0.355 |
DOC_PP1_RVXF_1 | 590 | 596 | PF00149 | 0.355 |
DOC_PP2B_LxvP_1 | 66 | 69 | PF13499 | 0.495 |
DOC_PP2B_LxvP_1 | 83 | 86 | PF13499 | 0.600 |
DOC_PP4_FxxP_1 | 15 | 18 | PF00568 | 0.448 |
DOC_PP4_FxxP_1 | 383 | 386 | PF00568 | 0.481 |
DOC_PP4_FxxP_1 | 39 | 42 | PF00568 | 0.420 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.373 |
DOC_USP7_MATH_1 | 641 | 645 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 675 | 679 | PF00917 | 0.700 |
DOC_USP7_UBL2_3 | 563 | 567 | PF12436 | 0.405 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.365 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 490 | 495 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 600 | 605 | PF00397 | 0.314 |
DOC_WW_Pin1_4 | 694 | 699 | PF00397 | 0.670 |
LIG_14-3-3_CanoR_1 | 111 | 117 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 246 | 252 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 4 | 11 | PF00244 | 0.699 |
LIG_14-3-3_CanoR_1 | 541 | 546 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 643 | 648 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 666 | 670 | PF00244 | 0.675 |
LIG_Actin_WH2_2 | 700 | 718 | PF00022 | 0.392 |
LIG_ActinCP_TwfCPI_2 | 15 | 22 | PF01115 | 0.450 |
LIG_APCC_ABBA_1 | 380 | 385 | PF00400 | 0.468 |
LIG_deltaCOP1_diTrp_1 | 531 | 540 | PF00928 | 0.312 |
LIG_eIF4E_1 | 135 | 141 | PF01652 | 0.436 |
LIG_EVH1_1 | 67 | 71 | PF00568 | 0.460 |
LIG_EVH1_2 | 70 | 74 | PF00568 | 0.482 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.391 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.504 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.288 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.310 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.523 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.489 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.341 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.517 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.556 |
LIG_FHA_2 | 412 | 418 | PF00498 | 0.498 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.302 |
LIG_FHA_2 | 644 | 650 | PF00498 | 0.614 |
LIG_FHA_2 | 657 | 663 | PF00498 | 0.570 |
LIG_FHA_2 | 666 | 672 | PF00498 | 0.670 |
LIG_FHA_2 | 73 | 79 | PF00498 | 0.675 |
LIG_HP1_1 | 361 | 365 | PF01393 | 0.454 |
LIG_Integrin_RGD_1 | 663 | 665 | PF01839 | 0.609 |
LIG_KLC1_Yacidic_2 | 554 | 559 | PF13176 | 0.424 |
LIG_LIR_Apic_2 | 36 | 42 | PF02991 | 0.435 |
LIG_LIR_Apic_2 | 649 | 655 | PF02991 | 0.630 |
LIG_LIR_Gen_1 | 102 | 110 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 115 | 125 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 369 | 375 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 453 | 463 | PF02991 | 0.295 |
LIG_LIR_Gen_1 | 533 | 540 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 550 | 560 | PF02991 | 0.267 |
LIG_LIR_Gen_1 | 699 | 708 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 102 | 106 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 115 | 120 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 136 | 140 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 369 | 373 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 41 | 47 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 453 | 459 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 533 | 538 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 550 | 555 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 649 | 654 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 699 | 704 | PF02991 | 0.543 |
LIG_LYPXL_yS_3 | 350 | 353 | PF13949 | 0.524 |
LIG_NRBOX | 471 | 477 | PF00104 | 0.546 |
LIG_NRBOX | 592 | 598 | PF00104 | 0.456 |
LIG_OCRL_FandH_1 | 505 | 517 | PF00620 | 0.481 |
LIG_PCNA_yPIPBox_3 | 359 | 368 | PF02747 | 0.451 |
LIG_PTB_Apo_2 | 486 | 493 | PF02174 | 0.514 |
LIG_PTB_Phospho_1 | 486 | 492 | PF10480 | 0.513 |
LIG_REV1ctd_RIR_1 | 503 | 513 | PF16727 | 0.364 |
LIG_RPA_C_Fungi | 308 | 320 | PF08784 | 0.474 |
LIG_SH2_PTP2 | 321 | 324 | PF00017 | 0.411 |
LIG_SH2_PTP2 | 370 | 373 | PF00017 | 0.364 |
LIG_SH2_SRC | 392 | 395 | PF00017 | 0.504 |
LIG_SH2_SRC | 557 | 560 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 117 | 121 | PF00017 | 0.373 |
LIG_SH2_STAP1 | 392 | 396 | PF00017 | 0.436 |
LIG_SH2_STAP1 | 535 | 539 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.649 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 557 | 560 | PF00017 | 0.424 |
LIG_SH3_1 | 65 | 71 | PF00018 | 0.586 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.566 |
LIG_SH3_3 | 271 | 277 | PF00018 | 0.440 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.493 |
LIG_SH3_3 | 475 | 481 | PF00018 | 0.524 |
LIG_SH3_3 | 617 | 623 | PF00018 | 0.312 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.523 |
LIG_SUMO_SIM_par_1 | 407 | 414 | PF11976 | 0.467 |
LIG_TRAF2_1 | 167 | 170 | PF00917 | 0.479 |
LIG_TRAF2_1 | 297 | 300 | PF00917 | 0.613 |
LIG_TRAF2_1 | 38 | 41 | PF00917 | 0.418 |
LIG_TRAF2_1 | 689 | 692 | PF00917 | 0.607 |
LIG_TRAF2_1 | 697 | 700 | PF00917 | 0.561 |
LIG_TYR_ITIM | 555 | 560 | PF00017 | 0.394 |
LIG_WRC_WIRS_1 | 100 | 105 | PF05994 | 0.407 |
LIG_WRC_WIRS_1 | 412 | 417 | PF05994 | 0.435 |
MOD_CDC14_SPxK_1 | 603 | 606 | PF00782 | 0.338 |
MOD_CDK_SPK_2 | 106 | 111 | PF00069 | 0.474 |
MOD_CDK_SPK_2 | 490 | 495 | PF00069 | 0.536 |
MOD_CDK_SPxK_1 | 106 | 112 | PF00069 | 0.488 |
MOD_CDK_SPxK_1 | 600 | 606 | PF00069 | 0.314 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.466 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.418 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.652 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.408 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.516 |
MOD_CK2_1 | 527 | 533 | PF00069 | 0.394 |
MOD_CK2_1 | 643 | 649 | PF00069 | 0.602 |
MOD_CK2_1 | 656 | 662 | PF00069 | 0.554 |
MOD_CK2_1 | 694 | 700 | PF00069 | 0.599 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.666 |
MOD_CMANNOS | 468 | 471 | PF00535 | 0.496 |
MOD_CMANNOS | 534 | 537 | PF00535 | 0.312 |
MOD_Cter_Amidation | 572 | 575 | PF01082 | 0.355 |
MOD_Cter_Amidation | 679 | 682 | PF01082 | 0.697 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.487 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.409 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.634 |
MOD_GlcNHglycan | 385 | 389 | PF01048 | 0.600 |
MOD_GlcNHglycan | 446 | 450 | PF01048 | 0.484 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.669 |
MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.614 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.516 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.341 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.531 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.372 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.468 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.584 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.464 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.332 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.372 |
MOD_GSK3_1 | 650 | 657 | PF00069 | 0.505 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.414 |
MOD_N-GLC_1 | 223 | 228 | PF02516 | 0.487 |
MOD_N-GLC_1 | 257 | 262 | PF02516 | 0.544 |
MOD_N-GLC_1 | 673 | 678 | PF02516 | 0.664 |
MOD_N-GLC_1 | 72 | 77 | PF02516 | 0.595 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.426 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.412 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.573 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.209 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.345 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.489 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.488 |
MOD_NEK2_1 | 595 | 600 | PF00069 | 0.405 |
MOD_NEK2_2 | 145 | 150 | PF00069 | 0.501 |
MOD_PIKK_1 | 298 | 304 | PF00454 | 0.604 |
MOD_PIKK_1 | 72 | 78 | PF00454 | 0.623 |
MOD_PK_1 | 247 | 253 | PF00069 | 0.484 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.659 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.414 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.719 |
MOD_PKA_2 | 665 | 671 | PF00069 | 0.672 |
MOD_PKB_1 | 312 | 320 | PF00069 | 0.418 |
MOD_Plk_1 | 256 | 262 | PF00069 | 0.573 |
MOD_Plk_1 | 416 | 422 | PF00069 | 0.530 |
MOD_Plk_1 | 445 | 451 | PF00069 | 0.377 |
MOD_Plk_2-3 | 411 | 417 | PF00069 | 0.476 |
MOD_Plk_2-3 | 665 | 671 | PF00069 | 0.701 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.389 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.366 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.423 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.540 |
MOD_Plk_4 | 616 | 622 | PF00069 | 0.305 |
MOD_Plk_4 | 643 | 649 | PF00069 | 0.528 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.389 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.545 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.359 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.532 |
MOD_ProDKin_1 | 490 | 496 | PF00069 | 0.532 |
MOD_ProDKin_1 | 600 | 606 | PF00069 | 0.314 |
MOD_ProDKin_1 | 694 | 700 | PF00069 | 0.670 |
MOD_SUMO_rev_2 | 289 | 293 | PF00179 | 0.551 |
TRG_DiLeu_BaEn_4 | 78 | 84 | PF01217 | 0.677 |
TRG_DiLeu_BaLyEn_6 | 375 | 380 | PF01217 | 0.456 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.136 |
TRG_ENDOCYTIC_2 | 535 | 538 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 557 | 560 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 651 | 654 | PF00928 | 0.487 |
TRG_ER_diArg_1 | 11 | 13 | PF00400 | 0.706 |
TRG_ER_diArg_1 | 110 | 112 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 245 | 247 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 309 | 312 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 313 | 315 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 346 | 348 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 540 | 543 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 571 | 574 | PF00400 | 0.312 |
TRG_NES_CRM1_1 | 608 | 624 | PF08389 | 0.415 |
TRG_Pf-PMV_PEXEL_1 | 45 | 49 | PF00026 | 0.390 |
TRG_Pf-PMV_PEXEL_1 | 93 | 98 | PF00026 | 0.453 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2V2 | Leptomonas seymouri | 75% | 92% |
A0A0S4IUE9 | Bodo saltans | 47% | 99% |
A0A1X0NR05 | Trypanosomatidae | 55% | 99% |
A0A3S7X102 | Leishmania donovani | 95% | 100% |
A4HG06 | Leishmania braziliensis | 89% | 100% |
A4I325 | Leishmania infantum | 95% | 100% |
C9ZJJ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 99% |
E9ACU6 | Leishmania major | 95% | 100% |
O64894 | Cucurbita maxima | 23% | 100% |
O65201 | Arabidopsis thaliana | 23% | 100% |
V5ANG8 | Trypanosoma cruzi | 59% | 98% |