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:0016020 | membrane | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0020023 | kinetoplast | 2 | 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: A4HJ86
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:0018022 | peptidyl-lysine methylation | 5 | 1 |
GO:0018026 | peptidyl-lysine monomethylation | 6 | 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: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:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 390 | 394 | PF00656 | 0.530 |
CLV_C14_Caspase3-7 | 574 | 578 | PF00656 | 0.595 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.756 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.197 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.235 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.725 |
CLV_NRD_NRD_1 | 714 | 716 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 755 | 757 | PF00675 | 0.593 |
CLV_PCSK_FUR_1 | 140 | 144 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.782 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.236 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.690 |
CLV_PCSK_KEX2_1 | 714 | 716 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 755 | 757 | PF00082 | 0.599 |
CLV_PCSK_PC1ET2_1 | 193 | 195 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 303 | 305 | PF00082 | 0.273 |
CLV_PCSK_PC1ET2_1 | 438 | 440 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 587 | 591 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.696 |
DOC_CYCLIN_RxL_1 | 415 | 426 | PF00134 | 0.483 |
DOC_CYCLIN_yCln2_LP_2 | 313 | 319 | PF00134 | 0.388 |
DOC_MAPK_DCC_7 | 476 | 485 | PF00069 | 0.388 |
DOC_MAPK_DCC_7 | 549 | 558 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 164 | 175 | PF00069 | 0.525 |
DOC_MAPK_gen_1 | 303 | 313 | PF00069 | 0.533 |
DOC_MAPK_gen_1 | 549 | 558 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 755 | 763 | PF00069 | 0.408 |
DOC_MAPK_HePTP_8 | 546 | 558 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 12 | 21 | PF00069 | 0.367 |
DOC_MAPK_MEF2A_6 | 307 | 315 | PF00069 | 0.499 |
DOC_MAPK_MEF2A_6 | 476 | 485 | PF00069 | 0.388 |
DOC_MAPK_MEF2A_6 | 549 | 558 | PF00069 | 0.494 |
DOC_MAPK_RevD_3 | 180 | 194 | PF00069 | 0.601 |
DOC_MAPK_RevD_3 | 290 | 304 | PF00069 | 0.409 |
DOC_PP2B_LxvP_1 | 313 | 316 | PF13499 | 0.472 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.831 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 670 | 674 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 737 | 741 | PF00917 | 0.684 |
DOC_USP7_UBL2_3 | 193 | 197 | PF12436 | 0.577 |
DOC_USP7_UBL2_3 | 581 | 585 | PF12436 | 0.537 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 653 | 658 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 668 | 673 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 738 | 743 | PF00397 | 0.742 |
LIG_14-3-3_CanoR_1 | 134 | 138 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 142 | 150 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 267 | 276 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 293 | 301 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 32 | 39 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 341 | 350 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 365 | 370 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 404 | 412 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 476 | 481 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 755 | 763 | PF00244 | 0.408 |
LIG_Actin_WH2_2 | 277 | 295 | PF00022 | 0.435 |
LIG_BIR_III_4 | 252 | 256 | PF00653 | 0.531 |
LIG_BIR_III_4 | 577 | 581 | PF00653 | 0.494 |
LIG_BRCT_BRCA1_1 | 208 | 212 | PF00533 | 0.566 |
LIG_BRCT_BRCA1_1 | 396 | 400 | PF00533 | 0.442 |
LIG_BRCT_BRCA1_1 | 523 | 527 | PF00533 | 0.388 |
LIG_BRCT_BRCA1_1 | 670 | 674 | PF00533 | 0.388 |
LIG_EVH1_1 | 182 | 186 | PF00568 | 0.504 |
LIG_FAT_LD_1 | 536 | 544 | PF03623 | 0.388 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.522 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.507 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.394 |
LIG_FHA_1 | 632 | 638 | PF00498 | 0.485 |
LIG_FHA_1 | 648 | 654 | PF00498 | 0.534 |
LIG_FHA_1 | 679 | 685 | PF00498 | 0.535 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.648 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.436 |
LIG_Integrin_RGD_1 | 308 | 310 | PF01839 | 0.265 |
LIG_LIR_Gen_1 | 10 | 21 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 354 | 362 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 671 | 680 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 354 | 358 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 367 | 372 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 397 | 403 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 428 | 433 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 500 | 506 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 671 | 677 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 699 | 705 | PF02991 | 0.331 |
LIG_PDZ_Class_2 | 758 | 763 | PF00595 | 0.409 |
LIG_Pex14_1 | 451 | 455 | PF04695 | 0.454 |
LIG_Pex14_2 | 118 | 122 | PF04695 | 0.515 |
LIG_PTB_Apo_2 | 629 | 636 | PF02174 | 0.535 |
LIG_PTB_Phospho_1 | 629 | 635 | PF10480 | 0.508 |
LIG_SH2_CRK | 23 | 27 | PF00017 | 0.356 |
LIG_SH2_CRK | 355 | 359 | PF00017 | 0.535 |
LIG_SH2_CRK | 503 | 507 | PF00017 | 0.388 |
LIG_SH2_CRK | 707 | 711 | PF00017 | 0.434 |
LIG_SH2_NCK_1 | 342 | 346 | PF00017 | 0.520 |
LIG_SH2_NCK_1 | 455 | 459 | PF00017 | 0.535 |
LIG_SH2_NCK_1 | 698 | 702 | PF00017 | 0.470 |
LIG_SH2_SRC | 591 | 594 | PF00017 | 0.494 |
LIG_SH2_STAP1 | 301 | 305 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 342 | 346 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 455 | 459 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 698 | 702 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 635 | 638 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 694 | 697 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 702 | 705 | PF00017 | 0.292 |
LIG_SH3_2 | 183 | 188 | PF14604 | 0.509 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.576 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.583 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.503 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.485 |
LIG_SH3_3 | 258 | 264 | PF00018 | 0.321 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.426 |
LIG_SH3_3 | 347 | 353 | PF00018 | 0.554 |
LIG_SH3_3 | 395 | 401 | PF00018 | 0.456 |
LIG_SH3_3 | 421 | 427 | PF00018 | 0.441 |
LIG_SH3_3 | 739 | 745 | PF00018 | 0.602 |
LIG_SUMO_SIM_par_1 | 649 | 656 | PF11976 | 0.548 |
LIG_TYR_ITIM | 21 | 26 | PF00017 | 0.350 |
LIG_TYR_ITIM | 553 | 558 | PF00017 | 0.388 |
LIG_UBA3_1 | 17 | 25 | PF00899 | 0.354 |
LIG_UBA3_1 | 482 | 487 | PF00899 | 0.388 |
MOD_CDK_SPK_2 | 218 | 223 | PF00069 | 0.526 |
MOD_CDK_SPxxK_3 | 218 | 225 | PF00069 | 0.494 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.547 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.443 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.520 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.538 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.454 |
MOD_CK1_1 | 507 | 513 | PF00069 | 0.490 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.606 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.456 |
MOD_CK1_1 | 738 | 744 | PF00069 | 0.646 |
MOD_CK1_1 | 746 | 752 | PF00069 | 0.435 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.766 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.517 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.537 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.420 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.424 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.476 |
MOD_CK2_1 | 646 | 652 | PF00069 | 0.572 |
MOD_CK2_1 | 710 | 716 | PF00069 | 0.584 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.703 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.490 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.213 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.335 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.335 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.289 |
MOD_GlcNHglycan | 668 | 671 | PF01048 | 0.267 |
MOD_GlcNHglycan | 737 | 740 | PF01048 | 0.730 |
MOD_GlcNHglycan | 751 | 754 | PF01048 | 0.385 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.624 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.547 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.597 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.582 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.526 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.533 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.533 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.432 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.535 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.705 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.494 |
MOD_GSK3_1 | 664 | 671 | PF00069 | 0.533 |
MOD_GSK3_1 | 696 | 703 | PF00069 | 0.361 |
MOD_GSK3_1 | 737 | 744 | PF00069 | 0.749 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.618 |
MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.535 |
MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.426 |
MOD_N-GLC_1 | 631 | 636 | PF02516 | 0.297 |
MOD_N-GLC_1 | 653 | 658 | PF02516 | 0.268 |
MOD_N-GLC_1 | 88 | 93 | PF02516 | 0.779 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.526 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.475 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.261 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.524 |
MOD_NEK2_1 | 690 | 695 | PF00069 | 0.518 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.555 |
MOD_PIKK_1 | 202 | 208 | PF00454 | 0.574 |
MOD_PIKK_1 | 32 | 38 | PF00454 | 0.601 |
MOD_PIKK_1 | 53 | 59 | PF00454 | 0.623 |
MOD_PK_1 | 476 | 482 | PF00069 | 0.388 |
MOD_PK_1 | 696 | 702 | PF00069 | 0.424 |
MOD_PKA_1 | 142 | 148 | PF00069 | 0.553 |
MOD_PKA_1 | 365 | 371 | PF00069 | 0.426 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.728 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.602 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.778 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.509 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.586 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.465 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.412 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.441 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.501 |
MOD_PKA_2 | 678 | 684 | PF00069 | 0.496 |
MOD_PKB_1 | 140 | 148 | PF00069 | 0.553 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.603 |
MOD_Plk_1 | 631 | 637 | PF00069 | 0.500 |
MOD_Plk_1 | 664 | 670 | PF00069 | 0.436 |
MOD_Plk_1 | 688 | 694 | PF00069 | 0.471 |
MOD_Plk_2-3 | 426 | 432 | PF00069 | 0.408 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.550 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.453 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.388 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.397 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.452 |
MOD_Plk_4 | 690 | 696 | PF00069 | 0.474 |
MOD_Plk_4 | 700 | 706 | PF00069 | 0.288 |
MOD_Plk_4 | 746 | 752 | PF00069 | 0.477 |
MOD_Plk_4 | 757 | 763 | PF00069 | 0.627 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.563 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.542 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.441 |
MOD_ProDKin_1 | 653 | 659 | PF00069 | 0.545 |
MOD_ProDKin_1 | 668 | 674 | PF00069 | 0.500 |
MOD_ProDKin_1 | 738 | 744 | PF00069 | 0.739 |
MOD_SUMO_rev_2 | 510 | 519 | PF00179 | 0.466 |
TRG_DiLeu_BaEn_1 | 285 | 290 | PF01217 | 0.427 |
TRG_DiLeu_BaEn_4 | 685 | 691 | PF01217 | 0.472 |
TRG_DiLeu_BaLyEn_6 | 401 | 406 | PF01217 | 0.497 |
TRG_DiLeu_BaLyEn_6 | 615 | 620 | PF01217 | 0.497 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 355 | 358 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 402 | 405 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 503 | 506 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 555 | 558 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 707 | 710 | PF00928 | 0.443 |
TRG_ER_diArg_1 | 140 | 143 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 306 | 308 | PF00400 | 0.388 |
TRG_ER_diArg_1 | 49 | 51 | PF00400 | 0.700 |
TRG_ER_diArg_1 | 754 | 756 | PF00400 | 0.617 |
TRG_Pf-PMV_PEXEL_1 | 188 | 192 | PF00026 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 50 | 54 | PF00026 | 0.454 |
TRG_Pf-PMV_PEXEL_1 | 596 | 600 | PF00026 | 0.335 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAM8 | Leptomonas seymouri | 50% | 100% |
A0A0S4IKB7 | Bodo saltans | 34% | 100% |
A0A1X0NJ79 | Trypanosomatidae | 41% | 100% |
A0A3S7X4A8 | Leishmania donovani | 77% | 100% |
A4I6N0 | Leishmania infantum | 77% | 100% |
C9ZM67 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9B1Q3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4Q6F7 | Leishmania major | 77% | 100% |
V5BPH7 | Trypanosoma cruzi | 41% | 100% |