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 |
Related structures:
AlphaFold database: A4H8K8
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 | 145 | 149 | PF00656 | 0.350 |
CLV_C14_Caspase3-7 | 244 | 248 | PF00656 | 0.686 |
CLV_C14_Caspase3-7 | 770 | 774 | PF00656 | 0.580 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 447 | 449 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 565 | 567 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.445 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 565 | 567 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 548 | 552 | PF00082 | 0.438 |
CLV_Separin_Metazoa | 624 | 628 | PF03568 | 0.299 |
DEG_APCC_DBOX_1 | 504 | 512 | PF00400 | 0.390 |
DEG_APCC_DBOX_1 | 547 | 555 | PF00400 | 0.493 |
DEG_APCC_DBOX_1 | 598 | 606 | PF00400 | 0.497 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.447 |
DEG_SCF_FBW7_1 | 613 | 620 | PF00400 | 0.566 |
DEG_SPOP_SBC_1 | 727 | 731 | PF00917 | 0.319 |
DOC_CKS1_1 | 698 | 703 | PF01111 | 0.623 |
DOC_CYCLIN_RxL_1 | 762 | 773 | PF00134 | 0.443 |
DOC_MAPK_FxFP_2 | 385 | 388 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 455 | 463 | PF00069 | 0.661 |
DOC_MAPK_gen_1 | 522 | 528 | PF00069 | 0.638 |
DOC_MAPK_JIP1_4 | 505 | 511 | PF00069 | 0.389 |
DOC_PP1_RVXF_1 | 716 | 723 | PF00149 | 0.325 |
DOC_PP2B_LxvP_1 | 509 | 512 | PF13499 | 0.572 |
DOC_PP4_FxxP_1 | 385 | 388 | PF00568 | 0.519 |
DOC_PP4_FxxP_1 | 698 | 701 | PF00568 | 0.575 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 536 | 540 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.377 |
DOC_USP7_MATH_1 | 608 | 612 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 693 | 697 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 768 | 772 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.683 |
DOC_USP7_MATH_2 | 191 | 197 | PF00917 | 0.481 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 600 | 605 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 613 | 618 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 629 | 634 | PF00397 | 0.393 |
DOC_WW_Pin1_4 | 697 | 702 | PF00397 | 0.455 |
LIG_14-3-3_CanoR_1 | 166 | 174 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 284 | 290 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 291 | 297 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 560 | 564 | PF00244 | 0.316 |
LIG_14-3-3_CanoR_1 | 57 | 63 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 754 | 759 | PF00244 | 0.550 |
LIG_Actin_WH2_2 | 120 | 135 | PF00022 | 0.449 |
LIG_Actin_WH2_2 | 490 | 507 | PF00022 | 0.526 |
LIG_Actin_WH2_2 | 96 | 111 | PF00022 | 0.405 |
LIG_AP2alpha_1 | 397 | 401 | PF02296 | 0.463 |
LIG_APCC_ABBA_1 | 394 | 399 | PF00400 | 0.456 |
LIG_BIR_III_2 | 641 | 645 | PF00653 | 0.378 |
LIG_BIR_III_4 | 535 | 539 | PF00653 | 0.582 |
LIG_BRCT_BRCA1_1 | 381 | 385 | PF00533 | 0.375 |
LIG_CSL_BTD_1 | 698 | 701 | PF09270 | 0.575 |
LIG_deltaCOP1_diTrp_1 | 207 | 214 | PF00928 | 0.395 |
LIG_deltaCOP1_diTrp_1 | 389 | 397 | PF00928 | 0.345 |
LIG_deltaCOP1_diTrp_1 | 653 | 659 | PF00928 | 0.469 |
LIG_deltaCOP1_diTrp_1 | 662 | 667 | PF00928 | 0.511 |
LIG_deltaCOP1_diTrp_1 | 759 | 766 | PF00928 | 0.509 |
LIG_eIF4E_1 | 491 | 497 | PF01652 | 0.382 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.424 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.439 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.603 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.554 |
LIG_FHA_1 | 630 | 636 | PF00498 | 0.512 |
LIG_FHA_1 | 753 | 759 | PF00498 | 0.562 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.743 |
LIG_FHA_2 | 477 | 483 | PF00498 | 0.403 |
LIG_FHA_2 | 488 | 494 | PF00498 | 0.302 |
LIG_FHA_2 | 618 | 624 | PF00498 | 0.606 |
LIG_LIR_Apic_2 | 382 | 388 | PF02991 | 0.500 |
LIG_LIR_Apic_2 | 696 | 701 | PF02991 | 0.586 |
LIG_LIR_Gen_1 | 207 | 218 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 285 | 294 | PF02991 | 0.578 |
LIG_LIR_Gen_1 | 389 | 400 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 490 | 498 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 759 | 769 | PF02991 | 0.500 |
LIG_LIR_LC3C_4 | 712 | 717 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 285 | 289 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 399 | 403 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 468 | 474 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 490 | 494 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 661 | 667 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 670 | 675 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 759 | 764 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 777 | 782 | PF02991 | 0.510 |
LIG_MYND_1 | 506 | 510 | PF01753 | 0.470 |
LIG_NRBOX | 621 | 627 | PF00104 | 0.462 |
LIG_NRBOX | 9 | 15 | PF00104 | 0.376 |
LIG_PCNA_PIPBox_1 | 760 | 769 | PF02747 | 0.496 |
LIG_PCNA_yPIPBox_3 | 754 | 767 | PF02747 | 0.536 |
LIG_Pex14_1 | 282 | 286 | PF04695 | 0.580 |
LIG_Pex14_1 | 722 | 726 | PF04695 | 0.384 |
LIG_Pex14_2 | 373 | 377 | PF04695 | 0.435 |
LIG_Pex14_2 | 397 | 401 | PF04695 | 0.419 |
LIG_SH2_CRK | 222 | 226 | PF00017 | 0.382 |
LIG_SH2_CRK | 598 | 602 | PF00017 | 0.572 |
LIG_SH2_GRB2like | 222 | 225 | PF00017 | 0.399 |
LIG_SH2_GRB2like | 400 | 403 | PF00017 | 0.333 |
LIG_SH2_GRB2like | 726 | 729 | PF00017 | 0.508 |
LIG_SH2_NCK_1 | 491 | 495 | PF00017 | 0.528 |
LIG_SH2_PTP2 | 156 | 159 | PF00017 | 0.373 |
LIG_SH2_PTP2 | 286 | 289 | PF00017 | 0.574 |
LIG_SH2_STAP1 | 222 | 226 | PF00017 | 0.396 |
LIG_SH2_STAP1 | 469 | 473 | PF00017 | 0.414 |
LIG_SH2_STAT3 | 469 | 472 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 726 | 729 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 779 | 782 | PF00017 | 0.447 |
LIG_SH3_1 | 598 | 604 | PF00018 | 0.575 |
LIG_SH3_3 | 260 | 266 | PF00018 | 0.684 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.594 |
LIG_SH3_3 | 524 | 530 | PF00018 | 0.640 |
LIG_SH3_3 | 552 | 558 | PF00018 | 0.492 |
LIG_SH3_3 | 598 | 604 | PF00018 | 0.554 |
LIG_SH3_5 | 396 | 400 | PF00018 | 0.333 |
LIG_SUMO_SIM_anti_2 | 492 | 498 | PF11976 | 0.448 |
LIG_SUMO_SIM_anti_2 | 712 | 718 | PF11976 | 0.479 |
LIG_SUMO_SIM_par_1 | 754 | 759 | PF11976 | 0.402 |
LIG_TRAF2_1 | 178 | 181 | PF00917 | 0.581 |
LIG_TRAF2_1 | 230 | 233 | PF00917 | 0.578 |
LIG_TRAF2_1 | 581 | 584 | PF00917 | 0.564 |
LIG_TRAF2_1 | 709 | 712 | PF00917 | 0.540 |
LIG_TRAF2_1 | 775 | 778 | PF00917 | 0.457 |
LIG_TRFH_1 | 502 | 506 | PF08558 | 0.437 |
LIG_TYR_ITIM | 154 | 159 | PF00017 | 0.337 |
MOD_CDK_SPK_2 | 476 | 481 | PF00069 | 0.352 |
MOD_CDK_SPxxK_3 | 697 | 704 | PF00069 | 0.438 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.423 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.666 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.721 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.413 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.626 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.345 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.500 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.488 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.496 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.323 |
MOD_CK1_1 | 697 | 703 | PF00069 | 0.521 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.578 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.608 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.488 |
MOD_CK2_1 | 476 | 482 | PF00069 | 0.457 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.392 |
MOD_CK2_1 | 578 | 584 | PF00069 | 0.561 |
MOD_CK2_1 | 608 | 614 | PF00069 | 0.452 |
MOD_CK2_1 | 706 | 712 | PF00069 | 0.524 |
MOD_CMANNOS | 655 | 658 | PF00535 | 0.257 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.538 |
MOD_GlcNHglycan | 179 | 185 | PF01048 | 0.652 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.472 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.656 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.741 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.754 |
MOD_GlcNHglycan | 358 | 362 | PF01048 | 0.496 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.478 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.479 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.564 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.513 |
MOD_GlcNHglycan | 669 | 672 | PF01048 | 0.518 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.475 |
MOD_GlcNHglycan | 741 | 744 | PF01048 | 0.613 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.479 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.521 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.488 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.689 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.720 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.490 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.575 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.611 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.686 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.727 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.659 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.694 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.489 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.540 |
MOD_GSK3_1 | 693 | 700 | PF00069 | 0.474 |
MOD_GSK3_1 | 739 | 746 | PF00069 | 0.608 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.515 |
MOD_N-GLC_1 | 407 | 412 | PF02516 | 0.395 |
MOD_N-GLC_1 | 432 | 437 | PF02516 | 0.468 |
MOD_N-GLC_1 | 727 | 732 | PF02516 | 0.482 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.428 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.539 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.682 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.513 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.427 |
MOD_NEK2_1 | 667 | 672 | PF00069 | 0.535 |
MOD_NEK2_1 | 684 | 689 | PF00069 | 0.538 |
MOD_NEK2_1 | 694 | 699 | PF00069 | 0.315 |
MOD_NEK2_1 | 738 | 743 | PF00069 | 0.745 |
MOD_NEK2_1 | 752 | 757 | PF00069 | 0.519 |
MOD_NEK2_2 | 500 | 505 | PF00069 | 0.523 |
MOD_PIKK_1 | 126 | 132 | PF00454 | 0.382 |
MOD_PIKK_1 | 352 | 358 | PF00454 | 0.639 |
MOD_PIKK_1 | 78 | 84 | PF00454 | 0.469 |
MOD_PK_1 | 754 | 760 | PF00069 | 0.544 |
MOD_PKA_1 | 446 | 452 | PF00069 | 0.488 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.449 |
MOD_PKA_2 | 271 | 277 | PF00069 | 0.733 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.585 |
MOD_PKA_2 | 454 | 460 | PF00069 | 0.501 |
MOD_PKA_2 | 504 | 510 | PF00069 | 0.548 |
MOD_PKA_2 | 559 | 565 | PF00069 | 0.582 |
MOD_Plk_1 | 180 | 186 | PF00069 | 0.644 |
MOD_Plk_1 | 388 | 394 | PF00069 | 0.462 |
MOD_Plk_1 | 780 | 786 | PF00069 | 0.369 |
MOD_Plk_2-3 | 325 | 331 | PF00069 | 0.420 |
MOD_Plk_2-3 | 578 | 584 | PF00069 | 0.388 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.305 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.308 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.584 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.495 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.307 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.553 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.323 |
MOD_Plk_4 | 504 | 510 | PF00069 | 0.500 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.684 |
MOD_Plk_4 | 559 | 565 | PF00069 | 0.325 |
MOD_Plk_4 | 617 | 623 | PF00069 | 0.452 |
MOD_Plk_4 | 685 | 691 | PF00069 | 0.379 |
MOD_Plk_4 | 694 | 700 | PF00069 | 0.450 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.633 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.683 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.345 |
MOD_ProDKin_1 | 600 | 606 | PF00069 | 0.445 |
MOD_ProDKin_1 | 613 | 619 | PF00069 | 0.500 |
MOD_ProDKin_1 | 629 | 635 | PF00069 | 0.389 |
MOD_ProDKin_1 | 697 | 703 | PF00069 | 0.463 |
MOD_SUMO_for_1 | 138 | 141 | PF00179 | 0.508 |
TRG_DiLeu_BaEn_3 | 389 | 395 | PF01217 | 0.289 |
TRG_DiLeu_BaEn_4 | 180 | 186 | PF01217 | 0.503 |
TRG_DiLeu_BaLyEn_6 | 710 | 715 | PF01217 | 0.458 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 491 | 494 | PF00928 | 0.402 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 305 | 307 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 446 | 448 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 564 | 566 | PF00400 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 765 | 770 | PF00026 | 0.432 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I059 | Leptomonas seymouri | 50% | 97% |
A0A1X0NQD9 | Trypanosomatidae | 26% | 100% |
A0A3R7NAY7 | Trypanosoma rangeli | 28% | 100% |
A0A3S7WTX8 | Leishmania donovani | 74% | 98% |
C9ZPM1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
E9AGN5 | Leishmania infantum | 74% | 98% |
E9AQP3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 98% |
Q4QET5 | Leishmania major | 74% | 100% |
V5BLP9 | Trypanosoma cruzi | 26% | 100% |