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:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0005794 | Golgi apparatus | 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 |
Related structures:
AlphaFold database: A4HI71
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 1 |
GO:0006605 | protein targeting | 5 | 1 |
GO:0006612 | protein targeting to membrane | 5 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018198 | peptidyl-cysteine modification | 6 | 1 |
GO:0018230 | peptidyl-L-cysteine S-palmitoylation | 7 | 1 |
GO:0018231 | peptidyl-S-diacylglycerol-L-cysteine biosynthetic process from peptidyl-cysteine | 7 | 1 |
GO:0018345 | protein palmitoylation | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043543 | protein acylation | 5 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0051668 | localization within membrane | 3 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0072657 | protein localization to membrane | 4 | 1 |
GO:0090150 | establishment of protein localization to membrane | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0016409 | palmitoyltransferase activity | 5 | 7 |
GO:0016417 | S-acyltransferase activity | 5 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016746 | acyltransferase activity | 3 | 7 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 7 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 7 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 105 | 109 | PF00656 | 0.775 |
CLV_C14_Caspase3-7 | 24 | 28 | PF00656 | 0.680 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 478 | 480 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 716 | 718 | PF00675 | 0.445 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 674 | 676 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 749 | 751 | PF00082 | 0.470 |
CLV_PCSK_PC1ET2_1 | 674 | 676 | PF00082 | 0.339 |
CLV_PCSK_PC1ET2_1 | 749 | 751 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 671 | 675 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.479 |
CLV_Separin_Metazoa | 741 | 745 | PF03568 | 0.727 |
DEG_APCC_DBOX_1 | 397 | 405 | PF00400 | 0.687 |
DEG_APCC_DBOX_1 | 478 | 486 | PF00400 | 0.590 |
DEG_APCC_KENBOX_2 | 253 | 257 | PF00400 | 0.803 |
DEG_COP1_1 | 504 | 513 | PF00400 | 0.694 |
DOC_ANK_TNKS_1 | 204 | 211 | PF00023 | 0.658 |
DOC_CKS1_1 | 168 | 173 | PF01111 | 0.669 |
DOC_CYCLIN_RxL_1 | 133 | 143 | PF00134 | 0.673 |
DOC_CYCLIN_yCln2_LP_2 | 513 | 519 | PF00134 | 0.640 |
DOC_MAPK_FxFP_2 | 10 | 13 | PF00069 | 0.674 |
DOC_MAPK_FxFP_2 | 621 | 624 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 599 | 609 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 407 | 415 | PF00069 | 0.736 |
DOC_MAPK_MEF2A_6 | 602 | 611 | PF00069 | 0.346 |
DOC_PP1_RVXF_1 | 703 | 709 | PF00149 | 0.641 |
DOC_PP2B_LxvP_1 | 11 | 14 | PF13499 | 0.668 |
DOC_PP2B_LxvP_1 | 508 | 511 | PF13499 | 0.675 |
DOC_PP4_FxxP_1 | 10 | 13 | PF00568 | 0.674 |
DOC_PP4_FxxP_1 | 390 | 393 | PF00568 | 0.593 |
DOC_PP4_FxxP_1 | 621 | 624 | PF00568 | 0.411 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.842 |
DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.711 |
DOC_USP7_UBL2_3 | 644 | 648 | PF12436 | 0.546 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.797 |
LIG_14-3-3_CanoR_1 | 172 | 177 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 22 | 30 | PF00244 | 0.834 |
LIG_14-3-3_CanoR_1 | 247 | 253 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 259 | 264 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 340 | 345 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 478 | 483 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 502 | 510 | PF00244 | 0.707 |
LIG_14-3-3_CanoR_1 | 744 | 748 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 83 | 88 | PF00244 | 0.808 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.817 |
LIG_BRCT_BRCA1_1 | 313 | 317 | PF00533 | 0.772 |
LIG_BRCT_BRCA1_1 | 48 | 52 | PF00533 | 0.752 |
LIG_BRCT_BRCA1_1 | 565 | 569 | PF00533 | 0.512 |
LIG_BRCT_BRCA1_1 | 649 | 653 | PF00533 | 0.674 |
LIG_CtBP_PxDLS_1 | 191 | 195 | PF00389 | 0.655 |
LIG_deltaCOP1_diTrp_1 | 365 | 375 | PF00928 | 0.418 |
LIG_eIF4E_1 | 562 | 568 | PF01652 | 0.411 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.655 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.794 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.701 |
LIG_FHA_1 | 592 | 598 | PF00498 | 0.402 |
LIG_FHA_1 | 738 | 744 | PF00498 | 0.552 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.661 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.635 |
LIG_FHA_2 | 636 | 642 | PF00498 | 0.538 |
LIG_HCF-1_HBM_1 | 662 | 665 | PF13415 | 0.528 |
LIG_Integrin_RGD_1 | 407 | 409 | PF01839 | 0.579 |
LIG_IRF3_LxIS_1 | 621 | 628 | PF10401 | 0.265 |
LIG_LIR_Apic_2 | 9 | 13 | PF02991 | 0.676 |
LIG_LIR_Gen_1 | 273 | 282 | PF02991 | 0.627 |
LIG_LIR_Gen_1 | 381 | 390 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 566 | 577 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 594 | 603 | PF02991 | 0.242 |
LIG_LIR_Gen_1 | 662 | 673 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 273 | 279 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 365 | 371 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 381 | 387 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 512 | 518 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 558 | 563 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 566 | 572 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 594 | 598 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 614 | 618 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 650 | 656 | PF02991 | 0.672 |
LIG_LIR_Nem_3 | 662 | 668 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 689 | 695 | PF02991 | 0.644 |
LIG_LYPXL_S_1 | 353 | 357 | PF13949 | 0.411 |
LIG_MLH1_MIPbox_1 | 565 | 569 | PF16413 | 0.512 |
LIG_MLH1_MIPbox_1 | 649 | 653 | PF16413 | 0.674 |
LIG_MYND_3 | 510 | 514 | PF01753 | 0.641 |
LIG_Pex14_1 | 342 | 346 | PF04695 | 0.411 |
LIG_Pex14_2 | 515 | 519 | PF04695 | 0.631 |
LIG_Pex14_2 | 564 | 568 | PF04695 | 0.512 |
LIG_SH2_CRK | 276 | 280 | PF00017 | 0.681 |
LIG_SH2_CRK | 348 | 352 | PF00017 | 0.411 |
LIG_SH2_CRK | 576 | 580 | PF00017 | 0.411 |
LIG_SH2_CRK | 605 | 609 | PF00017 | 0.346 |
LIG_SH2_CRK | 665 | 669 | PF00017 | 0.615 |
LIG_SH2_GRB2like | 665 | 668 | PF00017 | 0.669 |
LIG_SH2_NCK_1 | 276 | 280 | PF00017 | 0.631 |
LIG_SH2_SRC | 590 | 593 | PF00017 | 0.394 |
LIG_SH2_SRC | 603 | 606 | PF00017 | 0.282 |
LIG_SH2_SRC | 665 | 668 | PF00017 | 0.669 |
LIG_SH2_STAP1 | 276 | 280 | PF00017 | 0.631 |
LIG_SH2_STAP1 | 456 | 460 | PF00017 | 0.753 |
LIG_SH2_STAP1 | 576 | 580 | PF00017 | 0.512 |
LIG_SH2_STAP1 | 669 | 673 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.713 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.758 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.683 |
LIG_SH2_STAT5 | 562 | 565 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 590 | 593 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 612 | 615 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 652 | 655 | PF00017 | 0.670 |
LIG_SH2_STAT5 | 669 | 672 | PF00017 | 0.516 |
LIG_SH3_1 | 495 | 501 | PF00018 | 0.643 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.700 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.702 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.770 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.683 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.657 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.810 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.687 |
LIG_SH3_3 | 495 | 501 | PF00018 | 0.631 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.739 |
LIG_SUMO_SIM_anti_2 | 378 | 384 | PF11976 | 0.512 |
LIG_SUMO_SIM_anti_2 | 409 | 414 | PF11976 | 0.680 |
LIG_SUMO_SIM_par_1 | 188 | 195 | PF11976 | 0.658 |
LIG_SUMO_SIM_par_1 | 235 | 242 | PF11976 | 0.695 |
LIG_SUMO_SIM_par_1 | 623 | 628 | PF11976 | 0.265 |
LIG_SxIP_EBH_1 | 259 | 272 | PF03271 | 0.737 |
LIG_TRAF2_1 | 271 | 274 | PF00917 | 0.625 |
LIG_TRAF2_1 | 713 | 716 | PF00917 | 0.643 |
LIG_TYR_ITIM | 574 | 579 | PF00017 | 0.411 |
LIG_UBA3_1 | 518 | 527 | PF00899 | 0.265 |
LIG_WRC_WIRS_1 | 612 | 617 | PF05994 | 0.411 |
MOD_CDK_SPK_2 | 167 | 172 | PF00069 | 0.584 |
MOD_CDK_SPxK_1 | 241 | 247 | PF00069 | 0.579 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.642 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.570 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.630 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.563 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.469 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.411 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.758 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.685 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.692 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.587 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.768 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.626 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.545 |
MOD_CK2_1 | 635 | 641 | PF00069 | 0.400 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.652 |
MOD_GlcNHglycan | 143 | 147 | PF01048 | 0.746 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.571 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.804 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.386 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.605 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.629 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.710 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.489 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.820 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.653 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.510 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.683 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.567 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.847 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.812 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.593 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.788 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.628 |
MOD_N-GLC_1 | 402 | 407 | PF02516 | 0.633 |
MOD_N-GLC_1 | 451 | 456 | PF02516 | 0.633 |
MOD_N-GLC_2 | 552 | 554 | PF02516 | 0.485 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.586 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.584 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.611 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.609 |
MOD_NEK2_1 | 563 | 568 | PF00069 | 0.352 |
MOD_NEK2_1 | 625 | 630 | PF00069 | 0.409 |
MOD_NEK2_2 | 451 | 456 | PF00069 | 0.488 |
MOD_OFUCOSY | 548 | 554 | PF10250 | 0.265 |
MOD_PIKK_1 | 432 | 438 | PF00454 | 0.651 |
MOD_PIKK_1 | 657 | 663 | PF00454 | 0.632 |
MOD_PK_1 | 172 | 178 | PF00069 | 0.574 |
MOD_PKA_1 | 478 | 484 | PF00069 | 0.580 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.844 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.563 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.508 |
MOD_PKA_2 | 477 | 483 | PF00069 | 0.627 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.749 |
MOD_PKA_2 | 743 | 749 | PF00069 | 0.420 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.623 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.573 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.643 |
MOD_Plk_4 | 378 | 384 | PF00069 | 0.404 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.721 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.598 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.627 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.411 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.588 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.584 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.677 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.521 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.710 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.763 |
MOD_SUMO_rev_2 | 292 | 300 | PF00179 | 0.605 |
MOD_SUMO_rev_2 | 322 | 331 | PF00179 | 0.502 |
MOD_SUMO_rev_2 | 702 | 706 | PF00179 | 0.540 |
MOD_SUMO_rev_2 | 715 | 720 | PF00179 | 0.552 |
TRG_DiLeu_BaLyEn_6 | 596 | 601 | PF01217 | 0.265 |
TRG_DiLeu_BaLyEn_6 | 605 | 610 | PF01217 | 0.228 |
TRG_DiLeu_BaLyEn_6 | 621 | 626 | PF01217 | 0.199 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 354 | 357 | PF00928 | 0.183 |
TRG_ENDOCYTIC_2 | 560 | 563 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 576 | 579 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 612 | 615 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 665 | 668 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 669 | 672 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 692 | 695 | PF00928 | 0.541 |
TRG_ER_diArg_1 | 309 | 311 | PF00400 | 0.679 |
TRG_ER_diArg_1 | 397 | 400 | PF00400 | 0.592 |
TRG_NLS_MonoExtC_3 | 643 | 648 | PF00514 | 0.294 |
TRG_NLS_MonoExtN_4 | 644 | 649 | PF00514 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 428 | 432 | PF00026 | 0.478 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P984 | Leptomonas seymouri | 63% | 100% |
A0A3Q8IHU7 | Leishmania donovani | 72% | 100% |
A4I5E8 | Leishmania infantum | 72% | 100% |
E9B0P6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4Q7I6 | Leishmania major | 79% | 100% |