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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 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: A4HL86
Term | Name | Level | Count |
---|---|---|---|
GO:0006479 | protein methylation | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008213 | protein alkylation | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016570 | histone modification | 5 | 1 |
GO:0016571 | histone methylation | 5 | 1 |
GO:0018022 | peptidyl-lysine methylation | 5 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018205 | peptidyl-lysine modification | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032259 | methylation | 2 | 1 |
GO:0034968 | histone lysine methylation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043414 | macromolecule methylation | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0008168 | methyltransferase activity | 4 | 1 |
GO:0008170 | N-methyltransferase activity | 5 | 1 |
GO:0008276 | protein methyltransferase activity | 3 | 1 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 1 |
GO:0016278 | lysine N-methyltransferase activity | 6 | 1 |
GO:0016279 | protein-lysine N-methyltransferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 1 |
GO:0018024 | obsolete histone lysine N-methyltransferase activity | 5 | 1 |
GO:0042054 | histone methyltransferase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 278 | 282 | PF00656 | 0.393 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 592 | 594 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 648 | 650 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 700 | 702 | PF00675 | 0.290 |
CLV_NRD_NRD_1 | 822 | 824 | PF00675 | 0.353 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 317 | 319 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 486 | 488 | PF00082 | 0.288 |
CLV_PCSK_KEX2_1 | 647 | 649 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 700 | 702 | PF00082 | 0.290 |
CLV_PCSK_KEX2_1 | 822 | 824 | PF00082 | 0.353 |
CLV_PCSK_PC1ET2_1 | 486 | 488 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 479 | 483 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 711 | 715 | PF00082 | 0.450 |
DEG_APCC_DBOX_1 | 217 | 225 | PF00400 | 0.537 |
DEG_SCF_FBW7_1 | 125 | 132 | PF00400 | 0.480 |
DEG_SPOP_SBC_1 | 298 | 302 | PF00917 | 0.508 |
DEG_SPOP_SBC_1 | 91 | 95 | PF00917 | 0.471 |
DOC_CDC14_PxL_1 | 444 | 452 | PF14671 | 0.644 |
DOC_CYCLIN_RxL_1 | 708 | 716 | PF00134 | 0.448 |
DOC_MAPK_gen_1 | 216 | 224 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 341 | 351 | PF00069 | 0.515 |
DOC_MAPK_MEF2A_6 | 216 | 224 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 344 | 351 | PF00069 | 0.514 |
DOC_MAPK_MEF2A_6 | 616 | 625 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 78 | 86 | PF00069 | 0.580 |
DOC_PP1_RVXF_1 | 429 | 436 | PF00149 | 0.532 |
DOC_PP2B_LxvP_1 | 49 | 52 | PF13499 | 0.612 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.386 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.389 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 685 | 689 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 691 | 695 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 852 | 856 | PF00917 | 0.367 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.682 |
DOC_USP7_UBL2_3 | 482 | 486 | PF12436 | 0.431 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 529 | 534 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.483 |
LIG_14-3-3_CanoR_1 | 124 | 128 | PF00244 | 0.738 |
LIG_14-3-3_CanoR_1 | 161 | 171 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 198 | 208 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 216 | 221 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 44 | 49 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 660 | 664 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 8 | 13 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 859 | 863 | PF00244 | 0.444 |
LIG_Actin_WH2_2 | 767 | 785 | PF00022 | 0.280 |
LIG_APCC_ABBA_1 | 144 | 149 | PF00400 | 0.562 |
LIG_BIR_III_4 | 99 | 103 | PF00653 | 0.635 |
LIG_BRCT_BRCA1_1 | 227 | 231 | PF00533 | 0.405 |
LIG_Clathr_ClatBox_1 | 526 | 530 | PF01394 | 0.415 |
LIG_Clathr_ClatBox_1 | 702 | 706 | PF01394 | 0.354 |
LIG_CSL_BTD_1 | 13 | 16 | PF09270 | 0.502 |
LIG_deltaCOP1_diTrp_1 | 633 | 638 | PF00928 | 0.429 |
LIG_EVH1_1 | 49 | 53 | PF00568 | 0.666 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.643 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.665 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.411 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.606 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.661 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.417 |
LIG_FHA_1 | 566 | 572 | PF00498 | 0.398 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.600 |
LIG_FHA_1 | 714 | 720 | PF00498 | 0.359 |
LIG_FHA_2 | 111 | 117 | PF00498 | 0.525 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.424 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.466 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.520 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.515 |
LIG_FHA_2 | 750 | 756 | PF00498 | 0.438 |
LIG_FHA_2 | 868 | 874 | PF00498 | 0.432 |
LIG_GBD_Chelix_1 | 663 | 671 | PF00786 | 0.317 |
LIG_GBD_Chelix_1 | 733 | 741 | PF00786 | 0.329 |
LIG_Integrin_isoDGR_2 | 122 | 124 | PF01839 | 0.441 |
LIG_LIR_Gen_1 | 167 | 177 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 632 | 638 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 716 | 725 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 831 | 841 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 11 | 17 | PF02991 | 0.749 |
LIG_LIR_Nem_3 | 116 | 121 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 167 | 172 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 632 | 637 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 716 | 721 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 831 | 836 | PF02991 | 0.377 |
LIG_LYPXL_SIV_4 | 729 | 737 | PF13949 | 0.382 |
LIG_NRBOX | 220 | 226 | PF00104 | 0.540 |
LIG_NRBOX | 361 | 367 | PF00104 | 0.568 |
LIG_PCNA_yPIPBox_3 | 575 | 587 | PF02747 | 0.305 |
LIG_Pex14_1 | 634 | 638 | PF04695 | 0.426 |
LIG_PTAP_UEV_1 | 444 | 449 | PF05743 | 0.581 |
LIG_Rb_LxCxE_1 | 873 | 888 | PF01857 | 0.480 |
LIG_Rb_pABgroove_1 | 109 | 117 | PF01858 | 0.426 |
LIG_SH2_CRK | 497 | 501 | PF00017 | 0.415 |
LIG_SH2_CRK | 730 | 734 | PF00017 | 0.366 |
LIG_SH2_NCK_1 | 147 | 151 | PF00017 | 0.552 |
LIG_SH2_NCK_1 | 730 | 734 | PF00017 | 0.366 |
LIG_SH2_PTP2 | 833 | 836 | PF00017 | 0.391 |
LIG_SH2_SRC | 147 | 150 | PF00017 | 0.559 |
LIG_SH2_SRC | 564 | 567 | PF00017 | 0.408 |
LIG_SH2_STAP1 | 730 | 734 | PF00017 | 0.366 |
LIG_SH2_STAP1 | 860 | 864 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 497 | 500 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 564 | 567 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 773 | 776 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 833 | 836 | PF00017 | 0.394 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.591 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.466 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.489 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.649 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.670 |
LIG_SH3_3 | 813 | 819 | PF00018 | 0.361 |
LIG_SUMO_SIM_anti_2 | 873 | 879 | PF11976 | 0.300 |
LIG_SUMO_SIM_par_1 | 109 | 116 | PF11976 | 0.426 |
LIG_SUMO_SIM_par_1 | 345 | 352 | PF11976 | 0.512 |
LIG_SUMO_SIM_par_1 | 36 | 42 | PF11976 | 0.661 |
LIG_SUMO_SIM_par_1 | 525 | 530 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 701 | 706 | PF11976 | 0.357 |
LIG_TRAF2_1 | 556 | 559 | PF00917 | 0.471 |
LIG_TRAF2_1 | 656 | 659 | PF00917 | 0.391 |
LIG_TRAF2_1 | 752 | 755 | PF00917 | 0.370 |
LIG_WRC_WIRS_1 | 853 | 858 | PF05994 | 0.363 |
LIG_WW_3 | 464 | 468 | PF00397 | 0.635 |
MOD_CDK_SPK_2 | 391 | 396 | PF00069 | 0.531 |
MOD_CDK_SPxK_1 | 529 | 535 | PF00069 | 0.228 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.487 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.538 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.514 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.548 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.586 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.273 |
MOD_CK1_1 | 694 | 700 | PF00069 | 0.313 |
MOD_CK1_1 | 739 | 745 | PF00069 | 0.374 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.459 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.424 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.288 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.537 |
MOD_CK2_1 | 553 | 559 | PF00069 | 0.479 |
MOD_CK2_1 | 571 | 577 | PF00069 | 0.293 |
MOD_CK2_1 | 652 | 658 | PF00069 | 0.424 |
MOD_CK2_1 | 749 | 755 | PF00069 | 0.427 |
MOD_CK2_1 | 867 | 873 | PF00069 | 0.360 |
MOD_CK2_1 | 876 | 882 | PF00069 | 0.387 |
MOD_CMANNOS | 377 | 380 | PF00535 | 0.444 |
MOD_Cter_Amidation | 29 | 32 | PF01082 | 0.535 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.403 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.632 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.475 |
MOD_GlcNHglycan | 27 | 31 | PF01048 | 0.528 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.536 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.636 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.611 |
MOD_GlcNHglycan | 355 | 359 | PF01048 | 0.499 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.602 |
MOD_GlcNHglycan | 504 | 508 | PF01048 | 0.334 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.341 |
MOD_GlcNHglycan | 654 | 657 | PF01048 | 0.467 |
MOD_GlcNHglycan | 686 | 690 | PF01048 | 0.450 |
MOD_GlcNHglycan | 741 | 744 | PF01048 | 0.365 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.531 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.643 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.496 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.494 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.369 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.547 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.647 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.539 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.545 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.558 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.593 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.462 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.305 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.397 |
MOD_GSK3_1 | 629 | 636 | PF00069 | 0.569 |
MOD_GSK3_1 | 709 | 716 | PF00069 | 0.445 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.458 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.573 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.584 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.312 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.398 |
MOD_NEK2_1 | 626 | 631 | PF00069 | 0.482 |
MOD_NEK2_1 | 728 | 733 | PF00069 | 0.412 |
MOD_NEK2_1 | 737 | 742 | PF00069 | 0.339 |
MOD_NEK2_1 | 774 | 779 | PF00069 | 0.385 |
MOD_NEK2_2 | 110 | 115 | PF00069 | 0.426 |
MOD_OFUCOSY | 644 | 651 | PF10250 | 0.509 |
MOD_PIKK_1 | 425 | 431 | PF00454 | 0.509 |
MOD_PIKK_1 | 571 | 577 | PF00454 | 0.399 |
MOD_PK_1 | 386 | 392 | PF00069 | 0.487 |
MOD_PKA_1 | 330 | 336 | PF00069 | 0.550 |
MOD_PKA_1 | 415 | 421 | PF00069 | 0.520 |
MOD_PKA_1 | 647 | 653 | PF00069 | 0.491 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.739 |
MOD_PKA_2 | 395 | 401 | PF00069 | 0.545 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.762 |
MOD_PKA_2 | 647 | 653 | PF00069 | 0.491 |
MOD_PKA_2 | 659 | 665 | PF00069 | 0.368 |
MOD_PKA_2 | 691 | 697 | PF00069 | 0.372 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.518 |
MOD_PKA_2 | 858 | 864 | PF00069 | 0.439 |
MOD_Plk_1 | 148 | 154 | PF00069 | 0.554 |
MOD_Plk_1 | 243 | 249 | PF00069 | 0.454 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.487 |
MOD_Plk_1 | 425 | 431 | PF00069 | 0.502 |
MOD_Plk_1 | 558 | 564 | PF00069 | 0.307 |
MOD_Plk_2-3 | 654 | 660 | PF00069 | 0.402 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.493 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.417 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.578 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.546 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.678 |
MOD_Plk_4 | 544 | 550 | PF00069 | 0.307 |
MOD_Plk_4 | 560 | 566 | PF00069 | 0.307 |
MOD_Plk_4 | 633 | 639 | PF00069 | 0.523 |
MOD_Plk_4 | 691 | 697 | PF00069 | 0.372 |
MOD_Plk_4 | 852 | 858 | PF00069 | 0.420 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.548 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.534 |
MOD_ProDKin_1 | 529 | 535 | PF00069 | 0.375 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.488 |
MOD_SUMO_for_1 | 679 | 682 | PF00179 | 0.531 |
TRG_DiLeu_BaEn_1 | 605 | 610 | PF01217 | 0.433 |
TRG_DiLeu_BaEn_1 | 755 | 760 | PF01217 | 0.397 |
TRG_DiLeu_BaEn_1 | 806 | 811 | PF01217 | 0.430 |
TRG_DiLeu_BaEn_1 | 873 | 878 | PF01217 | 0.375 |
TRG_DiLeu_BaLyEn_6 | 345 | 350 | PF01217 | 0.571 |
TRG_DiLeu_BaLyEn_6 | 762 | 767 | PF01217 | 0.410 |
TRG_ENDOCYTIC_2 | 497 | 500 | PF00928 | 0.228 |
TRG_ENDOCYTIC_2 | 730 | 733 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 773 | 776 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 833 | 836 | PF00928 | 0.391 |
TRG_ER_diArg_1 | 308 | 311 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 31 | 33 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 584 | 587 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 647 | 649 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 699 | 701 | PF00400 | 0.294 |
TRG_ER_diArg_1 | 719 | 722 | PF00400 | 0.323 |
TRG_ER_diArg_1 | 821 | 823 | PF00400 | 0.349 |
TRG_NES_CRM1_1 | 693 | 706 | PF08389 | 0.311 |
TRG_Pf-PMV_PEXEL_1 | 455 | 459 | PF00026 | 0.480 |
TRG_Pf-PMV_PEXEL_1 | 700 | 704 | PF00026 | 0.371 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEX7 | Leptomonas seymouri | 37% | 91% |
A0A3S7X6B7 | Leishmania donovani | 69% | 88% |
A4I8R4 | Leishmania infantum | 69% | 88% |
E9B3M9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
Q4Q4F8 | Leishmania major | 70% | 100% |