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:0005737 | cytoplasm | 2 | 2 |
GO:0005953 | CAAX-protein geranylgeranyltransferase complex | 3 | 2 |
GO:0005965 | protein farnesyltransferase complex | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1990234 | transferase complex | 3 | 2 |
Related structures:
AlphaFold database: E9AE56
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0018342 | protein prenylation | 4 | 11 |
GO:0018343 | protein farnesylation | 5 | 2 |
GO:0018344 | protein geranylgeranylation | 5 | 2 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0097354 | prenylation | 3 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004659 | prenyltransferase activity | 4 | 11 |
GO:0008318 | protein prenyltransferase activity | 3 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016765 | transferase activity, transferring alkyl or aryl (other than methyl) groups | 3 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:0004660 | protein farnesyltransferase activity | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 662 | 666 | PF00656 | 0.432 |
CLV_C14_Caspase3-7 | 701 | 705 | PF00656 | 0.749 |
CLV_C14_Caspase3-7 | 710 | 714 | PF00656 | 0.535 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 670 | 672 | PF00675 | 0.511 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 669 | 671 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 731 | 735 | PF00082 | 0.513 |
DEG_APCC_DBOX_1 | 160 | 168 | PF00400 | 0.549 |
DEG_APCC_DBOX_1 | 223 | 231 | PF00400 | 0.356 |
DEG_APCC_DBOX_1 | 312 | 320 | PF00400 | 0.545 |
DEG_SCF_FBW7_2 | 55 | 60 | PF00400 | 0.605 |
DEG_SPOP_SBC_1 | 442 | 446 | PF00917 | 0.537 |
DEG_SPOP_SBC_1 | 698 | 702 | PF00917 | 0.523 |
DOC_CDC14_PxL_1 | 522 | 530 | PF14671 | 0.564 |
DOC_CKS1_1 | 344 | 349 | PF01111 | 0.503 |
DOC_CKS1_1 | 549 | 554 | PF01111 | 0.568 |
DOC_CYCLIN_RxL_1 | 245 | 252 | PF00134 | 0.475 |
DOC_CYCLIN_RxL_1 | 597 | 608 | PF00134 | 0.504 |
DOC_CYCLIN_yCln2_LP_2 | 150 | 156 | PF00134 | 0.559 |
DOC_CYCLIN_yCln2_LP_2 | 167 | 173 | PF00134 | 0.314 |
DOC_CYCLIN_yCln2_LP_2 | 527 | 530 | PF00134 | 0.525 |
DOC_MAPK_DCC_7 | 161 | 169 | PF00069 | 0.554 |
DOC_MAPK_gen_1 | 300 | 307 | PF00069 | 0.556 |
DOC_MAPK_gen_1 | 742 | 751 | PF00069 | 0.406 |
DOC_MAPK_MEF2A_6 | 124 | 131 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 161 | 169 | PF00069 | 0.554 |
DOC_MAPK_NFAT4_5 | 124 | 132 | PF00069 | 0.458 |
DOC_PP1_RVXF_1 | 219 | 226 | PF00149 | 0.371 |
DOC_PP2B_LxvP_1 | 167 | 170 | PF13499 | 0.505 |
DOC_PP2B_LxvP_1 | 345 | 348 | PF13499 | 0.497 |
DOC_PP2B_LxvP_1 | 527 | 530 | PF13499 | 0.446 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 605 | 609 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 698 | 702 | PF00917 | 0.718 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.521 |
LIG_14-3-3_CanoR_1 | 119 | 127 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 134 | 143 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 198 | 206 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 414 | 423 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 581 | 587 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 611 | 618 | PF00244 | 0.707 |
LIG_14-3-3_CanoR_1 | 632 | 638 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 9 | 19 | PF00244 | 0.702 |
LIG_Actin_WH2_2 | 183 | 200 | PF00022 | 0.602 |
LIG_Actin_WH2_2 | 303 | 319 | PF00022 | 0.548 |
LIG_Actin_WH2_2 | 575 | 592 | PF00022 | 0.485 |
LIG_APCC_ABBA_1 | 423 | 428 | PF00400 | 0.588 |
LIG_APCC_ABBAyCdc20_2 | 422 | 428 | PF00400 | 0.553 |
LIG_BIR_III_2 | 162 | 166 | PF00653 | 0.602 |
LIG_BRCT_BRCA1_1 | 281 | 285 | PF00533 | 0.572 |
LIG_deltaCOP1_diTrp_1 | 210 | 220 | PF00928 | 0.551 |
LIG_deltaCOP1_diTrp_1 | 688 | 695 | PF00928 | 0.581 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.547 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.486 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.636 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.621 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.580 |
LIG_FHA_2 | 292 | 298 | PF00498 | 0.536 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.640 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.619 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.560 |
LIG_FHA_2 | 566 | 572 | PF00498 | 0.418 |
LIG_FHA_2 | 590 | 596 | PF00498 | 0.563 |
LIG_FHA_2 | 626 | 632 | PF00498 | 0.482 |
LIG_FHA_2 | 732 | 738 | PF00498 | 0.559 |
LIG_LIR_Apic_2 | 688 | 692 | PF02991 | 0.628 |
LIG_LIR_Gen_1 | 306 | 314 | PF02991 | 0.553 |
LIG_LIR_Gen_1 | 335 | 345 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 471 | 479 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 571 | 579 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 639 | 649 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 218 | 223 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 282 | 288 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 292 | 298 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 306 | 310 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 335 | 340 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 46 | 51 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 471 | 477 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 571 | 576 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 639 | 644 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 657 | 663 | PF02991 | 0.245 |
LIG_LIR_Nem_3 | 718 | 722 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 80 | 86 | PF02991 | 0.359 |
LIG_MYND_1 | 391 | 395 | PF01753 | 0.541 |
LIG_MYND_1 | 526 | 530 | PF01753 | 0.565 |
LIG_PALB2_WD40_1 | 121 | 129 | PF16756 | 0.497 |
LIG_PCNA_yPIPBox_3 | 577 | 587 | PF02747 | 0.486 |
LIG_Pex14_1 | 419 | 423 | PF04695 | 0.482 |
LIG_PTB_Apo_2 | 747 | 754 | PF02174 | 0.493 |
LIG_PTB_Phospho_1 | 747 | 753 | PF10480 | 0.494 |
LIG_Rb_LxCxE_1 | 37 | 60 | PF01857 | 0.545 |
LIG_SH2_CRK | 86 | 90 | PF00017 | 0.427 |
LIG_SH2_NCK_1 | 722 | 726 | PF00017 | 0.469 |
LIG_SH2_PTP2 | 476 | 479 | PF00017 | 0.502 |
LIG_SH2_SRC | 337 | 340 | PF00017 | 0.473 |
LIG_SH2_SRC | 476 | 479 | PF00017 | 0.502 |
LIG_SH2_SRC | 569 | 572 | PF00017 | 0.489 |
LIG_SH2_STAP1 | 470 | 474 | PF00017 | 0.384 |
LIG_SH2_STAP1 | 722 | 726 | PF00017 | 0.469 |
LIG_SH2_STAT3 | 253 | 256 | PF00017 | 0.513 |
LIG_SH2_STAT3 | 470 | 473 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 476 | 479 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 485 | 488 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 521 | 524 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 569 | 572 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 649 | 652 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.567 |
LIG_SH3_2 | 97 | 102 | PF14604 | 0.469 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.565 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.628 |
LIG_SH3_3 | 388 | 394 | PF00018 | 0.434 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.688 |
LIG_SH3_3 | 523 | 529 | PF00018 | 0.334 |
LIG_SH3_3 | 546 | 552 | PF00018 | 0.619 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.683 |
LIG_SH3_3 | 732 | 738 | PF00018 | 0.504 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.589 |
LIG_SUMO_SIM_anti_2 | 490 | 495 | PF11976 | 0.446 |
LIG_TRFH_1 | 343 | 347 | PF08558 | 0.487 |
LIG_WRC_WIRS_1 | 340 | 345 | PF05994 | 0.279 |
LIG_WRC_WIRS_1 | 45 | 50 | PF05994 | 0.500 |
LIG_WRC_WIRS_1 | 570 | 575 | PF05994 | 0.392 |
LIG_WRC_WIRS_1 | 638 | 643 | PF05994 | 0.536 |
MOD_CDC14_SPxK_1 | 218 | 221 | PF00782 | 0.437 |
MOD_CDK_SPxK_1 | 215 | 221 | PF00069 | 0.539 |
MOD_CDK_SPxxK_3 | 343 | 350 | PF00069 | 0.493 |
MOD_CDK_SPxxK_3 | 548 | 555 | PF00069 | 0.421 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.669 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.437 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.611 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.532 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.485 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.447 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.538 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.560 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.588 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.670 |
MOD_CK2_1 | 565 | 571 | PF00069 | 0.428 |
MOD_CK2_1 | 589 | 595 | PF00069 | 0.507 |
MOD_CK2_1 | 625 | 631 | PF00069 | 0.480 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.435 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.634 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.266 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.681 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.461 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.612 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.521 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.476 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.545 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.575 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.455 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.515 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.619 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.492 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.602 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.639 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.683 |
MOD_N-GLC_1 | 138 | 143 | PF02516 | 0.468 |
MOD_N-GLC_1 | 414 | 419 | PF02516 | 0.282 |
MOD_N-GLC_1 | 468 | 473 | PF02516 | 0.426 |
MOD_N-GLC_1 | 77 | 82 | PF02516 | 0.526 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.606 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.555 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.387 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.492 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.477 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.381 |
MOD_NEK2_1 | 637 | 642 | PF00069 | 0.463 |
MOD_NEK2_1 | 659 | 664 | PF00069 | 0.498 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.772 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.553 |
MOD_PIKK_1 | 198 | 204 | PF00454 | 0.538 |
MOD_PIKK_1 | 27 | 33 | PF00454 | 0.648 |
MOD_PIKK_1 | 631 | 637 | PF00454 | 0.458 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.454 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.576 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.516 |
MOD_PKA_2 | 389 | 395 | PF00069 | 0.543 |
MOD_PKA_2 | 589 | 595 | PF00069 | 0.493 |
MOD_PKA_2 | 610 | 616 | PF00069 | 0.697 |
MOD_PKA_2 | 631 | 637 | PF00069 | 0.498 |
MOD_PKA_2 | 675 | 681 | PF00069 | 0.595 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.750 |
MOD_Plk_1 | 138 | 144 | PF00069 | 0.470 |
MOD_Plk_1 | 225 | 231 | PF00069 | 0.463 |
MOD_Plk_1 | 291 | 297 | PF00069 | 0.515 |
MOD_Plk_1 | 414 | 420 | PF00069 | 0.490 |
MOD_Plk_1 | 468 | 474 | PF00069 | 0.446 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.545 |
MOD_Plk_2-3 | 625 | 631 | PF00069 | 0.548 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.435 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.469 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.431 |
MOD_Plk_4 | 494 | 500 | PF00069 | 0.434 |
MOD_Plk_4 | 565 | 571 | PF00069 | 0.439 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.348 |
MOD_Plk_4 | 625 | 631 | PF00069 | 0.509 |
MOD_Plk_4 | 659 | 665 | PF00069 | 0.488 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.705 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.556 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.465 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.482 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.644 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.458 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.627 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.554 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.595 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.559 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.645 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.528 |
MOD_SUMO_for_1 | 618 | 621 | PF00179 | 0.623 |
MOD_SUMO_rev_2 | 185 | 195 | PF00179 | 0.577 |
MOD_SUMO_rev_2 | 267 | 275 | PF00179 | 0.614 |
MOD_SUMO_rev_2 | 620 | 629 | PF00179 | 0.591 |
MOD_SUMO_rev_2 | 696 | 701 | PF00179 | 0.631 |
TRG_DiLeu_BaEn_1 | 571 | 576 | PF01217 | 0.480 |
TRG_DiLeu_BaLyEn_6 | 284 | 289 | PF01217 | 0.503 |
TRG_DiLeu_BaLyEn_6 | 523 | 528 | PF01217 | 0.567 |
TRG_DiLeu_BaLyEn_6 | 552 | 557 | PF01217 | 0.372 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.376 |
TRG_ER_diArg_1 | 299 | 301 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 557 | 560 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 587 | 590 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 669 | 671 | PF00400 | 0.533 |
TRG_NES_CRM1_1 | 41 | 54 | PF08389 | 0.523 |
TRG_NES_CRM1_1 | 467 | 478 | PF08389 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 188 | 192 | PF00026 | 0.462 |
TRG_Pf-PMV_PEXEL_1 | 351 | 355 | PF00026 | 0.558 |
TRG_Pf-PMV_PEXEL_1 | 432 | 436 | PF00026 | 0.492 |
TRG_Pf-PMV_PEXEL_1 | 627 | 631 | PF00026 | 0.568 |
TRG_Pf-PMV_PEXEL_1 | 87 | 92 | PF00026 | 0.557 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKH9 | Leptomonas seymouri | 50% | 98% |
A0A1X0P015 | Trypanosomatidae | 32% | 100% |
A0A3S5H7L6 | Leishmania donovani | 91% | 100% |
A0A422NNG1 | Trypanosoma rangeli | 32% | 100% |
A4HHJ5 | Leishmania braziliensis | 78% | 92% |
A4I4Q3 | Leishmania infantum | 91% | 100% |
C9ZLE2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9ALM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 95% |
V5DCL7 | Trypanosoma cruzi | 33% | 100% |