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: 8 |
NetGPI | no | yes: 0, no: 8 |
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: E9AX20
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 | 180 | 184 | PF00656 | 0.604 |
CLV_C14_Caspase3-7 | 373 | 377 | PF00656 | 0.481 |
CLV_C14_Caspase3-7 | 579 | 583 | PF00656 | 0.641 |
CLV_C14_Caspase3-7 | 92 | 96 | PF00656 | 0.494 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.727 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 712 | 714 | PF00675 | 0.451 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.740 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 711 | 713 | PF00082 | 0.427 |
CLV_PCSK_PC1ET2_1 | 296 | 298 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 527 | 531 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 713 | 717 | PF00082 | 0.524 |
DEG_APCC_DBOX_1 | 296 | 304 | PF00400 | 0.510 |
DEG_APCC_DBOX_1 | 390 | 398 | PF00400 | 0.439 |
DEG_APCC_DBOX_1 | 435 | 443 | PF00400 | 0.563 |
DEG_COP1_1 | 406 | 415 | PF00400 | 0.316 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.474 |
DOC_ANK_TNKS_1 | 574 | 581 | PF00023 | 0.503 |
DOC_CKS1_1 | 281 | 286 | PF01111 | 0.684 |
DOC_CYCLIN_RxL_1 | 398 | 409 | PF00134 | 0.555 |
DOC_MAPK_gen_1 | 386 | 394 | PF00069 | 0.459 |
DOC_MAPK_MEF2A_6 | 391 | 399 | PF00069 | 0.406 |
DOC_PP1_RVXF_1 | 399 | 406 | PF00149 | 0.517 |
DOC_PP1_RVXF_1 | 420 | 427 | PF00149 | 0.496 |
DOC_PP1_RVXF_1 | 58 | 64 | PF00149 | 0.509 |
DOC_PP4_FxxP_1 | 281 | 284 | PF00568 | 0.619 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 514 | 518 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 578 | 582 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 602 | 606 | PF00917 | 0.612 |
DOC_USP7_MATH_2 | 80 | 86 | PF00917 | 0.691 |
DOC_USP7_UBL2_3 | 94 | 98 | PF12436 | 0.708 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.776 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 496 | 501 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 510 | 515 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 561 | 566 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 632 | 637 | PF00397 | 0.544 |
LIG_14-3-3_CanoR_1 | 131 | 138 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 191 | 197 | PF00244 | 0.673 |
LIG_14-3-3_CanoR_1 | 248 | 257 | PF00244 | 0.748 |
LIG_14-3-3_CanoR_1 | 264 | 273 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 404 | 408 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 463 | 467 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 74 | 80 | PF00244 | 0.437 |
LIG_Actin_WH2_1 | 391 | 406 | PF00022 | 0.441 |
LIG_Actin_WH2_2 | 388 | 406 | PF00022 | 0.509 |
LIG_Actin_WH2_2 | 447 | 465 | PF00022 | 0.524 |
LIG_BIR_III_4 | 582 | 586 | PF00653 | 0.743 |
LIG_BRCT_BRCA1_1 | 30 | 34 | PF00533 | 0.608 |
LIG_BRCT_BRCA1_1 | 537 | 541 | PF00533 | 0.469 |
LIG_CSL_BTD_1 | 497 | 500 | PF09270 | 0.560 |
LIG_FAT_LD_1 | 182 | 190 | PF03623 | 0.640 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.770 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.666 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.679 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.443 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.625 |
LIG_FHA_1 | 528 | 534 | PF00498 | 0.535 |
LIG_FHA_1 | 584 | 590 | PF00498 | 0.552 |
LIG_FHA_1 | 668 | 674 | PF00498 | 0.390 |
LIG_FHA_1 | 689 | 695 | PF00498 | 0.508 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.620 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.577 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.771 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.589 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.473 |
LIG_FHA_2 | 517 | 523 | PF00498 | 0.647 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.699 |
LIG_GBD_Chelix_1 | 395 | 403 | PF00786 | 0.405 |
LIG_HP1_1 | 341 | 345 | PF01393 | 0.487 |
LIG_LIR_Gen_1 | 219 | 229 | PF02991 | 0.665 |
LIG_LIR_Gen_1 | 465 | 474 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 479 | 486 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 691 | 699 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 106 | 111 | PF02991 | 0.698 |
LIG_LIR_Nem_3 | 219 | 224 | PF02991 | 0.661 |
LIG_LIR_Nem_3 | 465 | 469 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 470 | 475 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 479 | 484 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 610 | 616 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 687 | 693 | PF02991 | 0.510 |
LIG_NRBOX | 181 | 187 | PF00104 | 0.627 |
LIG_NRBOX | 393 | 399 | PF00104 | 0.476 |
LIG_PCNA_yPIPBox_3 | 339 | 347 | PF02747 | 0.504 |
LIG_PDZ_Class_2 | 740 | 745 | PF00595 | 0.643 |
LIG_PTAP_UEV_1 | 412 | 417 | PF05743 | 0.362 |
LIG_PTB_Apo_2 | 660 | 667 | PF02174 | 0.548 |
LIG_Rb_LxCxE_1 | 470 | 492 | PF01857 | 0.465 |
LIG_SH2_CRK | 108 | 112 | PF00017 | 0.698 |
LIG_SH2_CRK | 481 | 485 | PF00017 | 0.435 |
LIG_SH2_CRK | 625 | 629 | PF00017 | 0.390 |
LIG_SH2_NCK_1 | 625 | 629 | PF00017 | 0.390 |
LIG_SH2_NCK_1 | 650 | 654 | PF00017 | 0.501 |
LIG_SH2_PTP2 | 693 | 696 | PF00017 | 0.420 |
LIG_SH2_SRC | 446 | 449 | PF00017 | 0.544 |
LIG_SH2_STAP1 | 481 | 485 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 481 | 484 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 546 | 549 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 560 | 563 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 567 | 570 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 693 | 696 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 714 | 717 | PF00017 | 0.466 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.526 |
LIG_SH3_3 | 501 | 507 | PF00018 | 0.602 |
LIG_SH3_3 | 559 | 565 | PF00018 | 0.505 |
LIG_SH3_CIN85_PxpxPR_1 | 500 | 505 | PF14604 | 0.433 |
LIG_SUMO_SIM_anti_2 | 268 | 274 | PF11976 | 0.532 |
LIG_SUMO_SIM_anti_2 | 604 | 610 | PF11976 | 0.675 |
LIG_TRAF2_1 | 153 | 156 | PF00917 | 0.597 |
LIG_TRAF2_2 | 54 | 59 | PF00917 | 0.445 |
LIG_TYR_ITSM | 689 | 696 | PF00017 | 0.557 |
LIG_UBA3_1 | 394 | 401 | PF00899 | 0.482 |
LIG_UBA3_1 | 608 | 614 | PF00899 | 0.600 |
LIG_WRC_WIRS_1 | 354 | 359 | PF05994 | 0.476 |
MOD_CDC14_SPxK_1 | 121 | 124 | PF00782 | 0.590 |
MOD_CDK_SPK_2 | 118 | 123 | PF00069 | 0.708 |
MOD_CDK_SPK_2 | 198 | 203 | PF00069 | 0.718 |
MOD_CDK_SPK_2 | 259 | 264 | PF00069 | 0.748 |
MOD_CDK_SPxK_1 | 118 | 124 | PF00069 | 0.594 |
MOD_CDK_SPxxK_3 | 118 | 125 | PF00069 | 0.712 |
MOD_CDK_SPxxK_3 | 498 | 505 | PF00069 | 0.507 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.783 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.646 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.624 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.715 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.691 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.566 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.503 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.655 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.482 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.634 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.736 |
MOD_CK1_1 | 517 | 523 | PF00069 | 0.605 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.639 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.765 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.502 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.705 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.637 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.560 |
MOD_CK2_1 | 442 | 448 | PF00069 | 0.479 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.656 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.699 |
MOD_CMANNOS | 570 | 573 | PF00535 | 0.594 |
MOD_Cter_Amidation | 294 | 297 | PF01082 | 0.664 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.626 |
MOD_GlcNHglycan | 196 | 200 | PF01048 | 0.672 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.615 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.409 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.530 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.512 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.365 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.619 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.653 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.709 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.739 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.573 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.727 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.745 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.503 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.641 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.609 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.673 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.517 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.362 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.622 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.634 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.509 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.639 |
MOD_GSK3_1 | 638 | 645 | PF00069 | 0.581 |
MOD_N-GLC_1 | 118 | 123 | PF02516 | 0.629 |
MOD_N-GLC_1 | 656 | 661 | PF02516 | 0.301 |
MOD_N-GLC_2 | 663 | 665 | PF02516 | 0.239 |
MOD_N-GLC_2 | 77 | 79 | PF02516 | 0.660 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.757 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.595 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.692 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.675 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.480 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.479 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.575 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.269 |
MOD_NEK2_1 | 615 | 620 | PF00069 | 0.619 |
MOD_NEK2_1 | 642 | 647 | PF00069 | 0.590 |
MOD_NEK2_1 | 656 | 661 | PF00069 | 0.521 |
MOD_NEK2_1 | 689 | 694 | PF00069 | 0.583 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.470 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.575 |
MOD_NEK2_2 | 246 | 251 | PF00069 | 0.501 |
MOD_NEK2_2 | 377 | 382 | PF00069 | 0.543 |
MOD_PIKK_1 | 20 | 26 | PF00454 | 0.477 |
MOD_PIKK_1 | 210 | 216 | PF00454 | 0.596 |
MOD_PIKK_1 | 520 | 526 | PF00454 | 0.322 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.729 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.731 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.679 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.498 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.471 |
MOD_PKA_2 | 462 | 468 | PF00069 | 0.382 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.502 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.590 |
MOD_Plk_1 | 427 | 433 | PF00069 | 0.437 |
MOD_Plk_1 | 479 | 485 | PF00069 | 0.435 |
MOD_Plk_1 | 656 | 662 | PF00069 | 0.476 |
MOD_Plk_2-3 | 190 | 196 | PF00069 | 0.685 |
MOD_Plk_2-3 | 287 | 293 | PF00069 | 0.637 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.658 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.465 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.450 |
MOD_Plk_4 | 565 | 571 | PF00069 | 0.524 |
MOD_Plk_4 | 602 | 608 | PF00069 | 0.686 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.532 |
MOD_Plk_4 | 673 | 679 | PF00069 | 0.544 |
MOD_Plk_4 | 689 | 695 | PF00069 | 0.426 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.711 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.779 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.573 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.541 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.747 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.633 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.649 |
MOD_ProDKin_1 | 496 | 502 | PF00069 | 0.673 |
MOD_ProDKin_1 | 510 | 516 | PF00069 | 0.635 |
MOD_ProDKin_1 | 561 | 567 | PF00069 | 0.534 |
MOD_ProDKin_1 | 632 | 638 | PF00069 | 0.544 |
MOD_SUMO_for_1 | 153 | 156 | PF00179 | 0.476 |
MOD_SUMO_rev_2 | 290 | 298 | PF00179 | 0.627 |
TRG_DiLeu_BaEn_1 | 287 | 292 | PF01217 | 0.611 |
TRG_DiLeu_BaEn_1 | 390 | 395 | PF01217 | 0.436 |
TRG_DiLeu_BaEn_1 | 457 | 462 | PF01217 | 0.547 |
TRG_DiLeu_BaEn_3 | 293 | 299 | PF01217 | 0.703 |
TRG_DiLeu_BaEn_4 | 177 | 183 | PF01217 | 0.556 |
TRG_DiLeu_BaLyEn_6 | 167 | 172 | PF01217 | 0.689 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.696 |
TRG_ENDOCYTIC_2 | 481 | 484 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 546 | 549 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 613 | 616 | PF00928 | 0.570 |
TRG_ENDOCYTIC_2 | 625 | 628 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 693 | 696 | PF00928 | 0.454 |
TRG_ER_diArg_1 | 122 | 124 | PF00400 | 0.589 |
TRG_ER_diArg_1 | 435 | 438 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 711 | 713 | PF00400 | 0.499 |
TRG_Pf-PMV_PEXEL_1 | 60 | 64 | PF00026 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 713 | 717 | PF00026 | 0.527 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I099 | Leptomonas seymouri | 42% | 100% |
A0A3S7WYH5 | Leishmania donovani | 86% | 100% |
A4HDN5 | Leishmania braziliensis | 75% | 100% |
C9ZWC8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AH82 | Leishmania infantum | 86% | 100% |
Q4QAF6 | Leishmania major | 86% | 99% |
V5CZP8 | Trypanosoma cruzi | 30% | 100% |