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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
Related structures:
AlphaFold database: A0A3S5H5F6
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006163 | purine nucleotide metabolic process | 5 | 11 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 11 |
GO:0006171 | cAMP biosynthetic process | 8 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 11 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009117 | nucleotide metabolic process | 5 | 11 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 11 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 11 |
GO:0009165 | nucleotide biosynthetic process | 6 | 11 |
GO:0009187 | cyclic nucleotide metabolic process | 6 | 11 |
GO:0009190 | cyclic nucleotide biosynthetic process | 7 | 11 |
GO:0009259 | ribonucleotide metabolic process | 5 | 11 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0018130 | heterocycle biosynthetic process | 4 | 11 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 11 |
GO:0019637 | organophosphate metabolic process | 3 | 11 |
GO:0019693 | ribose phosphate metabolic process | 4 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044249 | cellular biosynthetic process | 3 | 11 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 11 |
GO:0044281 | small molecule metabolic process | 2 | 11 |
GO:0046058 | cAMP metabolic process | 7 | 11 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0052652 | cyclic purine nucleotide metabolic process | 6 | 11 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0072521 | purine-containing compound metabolic process | 4 | 11 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 11 |
GO:0090407 | organophosphate biosynthetic process | 4 | 11 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 11 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 11 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 11 |
GO:1901576 | organic substance biosynthetic process | 3 | 11 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 528 | 532 | PF00656 | 0.427 |
CLV_C14_Caspase3-7 | 81 | 85 | PF00656 | 0.630 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.745 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 600 | 602 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 791 | 793 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 823 | 825 | PF00675 | 0.500 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 600 | 602 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 791 | 793 | PF00082 | 0.648 |
CLV_PCSK_PC1ET2_1 | 266 | 268 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.699 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 646 | 650 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 710 | 714 | PF00082 | 0.534 |
CLV_Separin_Metazoa | 457 | 461 | PF03568 | 0.568 |
CLV_Separin_Metazoa | 66 | 70 | PF03568 | 0.561 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.790 |
DEG_SPOP_SBC_1 | 216 | 220 | PF00917 | 0.423 |
DOC_CDC14_PxL_1 | 305 | 313 | PF14671 | 0.600 |
DOC_CDC14_PxL_1 | 320 | 328 | PF14671 | 0.575 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 415 | 424 | PF00134 | 0.659 |
DOC_CYCLIN_yCln2_LP_2 | 718 | 721 | PF00134 | 0.559 |
DOC_MAPK_gen_1 | 266 | 274 | PF00069 | 0.606 |
DOC_MAPK_gen_1 | 50 | 59 | PF00069 | 0.652 |
DOC_MAPK_gen_1 | 538 | 546 | PF00069 | 0.374 |
DOC_MAPK_gen_1 | 681 | 690 | PF00069 | 0.559 |
DOC_MAPK_MEF2A_6 | 267 | 276 | PF00069 | 0.582 |
DOC_MAPK_MEF2A_6 | 436 | 445 | PF00069 | 0.431 |
DOC_PP1_RVXF_1 | 175 | 182 | PF00149 | 0.580 |
DOC_PP1_RVXF_1 | 410 | 416 | PF00149 | 0.534 |
DOC_PP1_RVXF_1 | 434 | 441 | PF00149 | 0.446 |
DOC_PP1_RVXF_1 | 447 | 453 | PF00149 | 0.410 |
DOC_PP2B_LxvP_1 | 326 | 329 | PF13499 | 0.517 |
DOC_PP2B_LxvP_1 | 443 | 446 | PF13499 | 0.481 |
DOC_PP2B_LxvP_1 | 520 | 523 | PF13499 | 0.549 |
DOC_PP2B_LxvP_1 | 718 | 721 | PF13499 | 0.536 |
DOC_PP4_FxxP_1 | 36 | 39 | PF00568 | 0.585 |
DOC_PP4_FxxP_1 | 648 | 651 | PF00568 | 0.600 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 514 | 518 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 617 | 621 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 658 | 662 | PF00917 | 0.605 |
DOC_USP7_UBL2_3 | 162 | 166 | PF12436 | 0.627 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 646 | 651 | PF00397 | 0.559 |
LIG_14-3-3_CanoR_1 | 151 | 160 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 232 | 237 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 267 | 275 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 407 | 416 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 460 | 464 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 501 | 510 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 541 | 545 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 6 | 13 | PF00244 | 0.777 |
LIG_14-3-3_CanoR_1 | 791 | 795 | PF00244 | 0.680 |
LIG_Actin_WH2_2 | 183 | 200 | PF00022 | 0.584 |
LIG_Actin_WH2_2 | 459 | 475 | PF00022 | 0.522 |
LIG_BRCT_BRCA1_1 | 142 | 146 | PF00533 | 0.463 |
LIG_deltaCOP1_diTrp_1 | 508 | 515 | PF00928 | 0.448 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.518 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.479 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.531 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.650 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.557 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.603 |
LIG_FHA_1 | 613 | 619 | PF00498 | 0.519 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.705 |
LIG_FHA_1 | 785 | 791 | PF00498 | 0.645 |
LIG_FHA_1 | 795 | 801 | PF00498 | 0.601 |
LIG_FHA_1 | 807 | 813 | PF00498 | 0.531 |
LIG_FHA_2 | 783 | 789 | PF00498 | 0.582 |
LIG_FHA_2 | 79 | 85 | PF00498 | 0.552 |
LIG_Integrin_isoDGR_2 | 447 | 449 | PF01839 | 0.470 |
LIG_LIR_Apic_2 | 33 | 39 | PF02991 | 0.584 |
LIG_LIR_Apic_2 | 550 | 555 | PF02991 | 0.453 |
LIG_LIR_Apic_2 | 645 | 651 | PF02991 | 0.568 |
LIG_LIR_Gen_1 | 298 | 309 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 437 | 446 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 730 | 740 | PF02991 | 0.559 |
LIG_LIR_Gen_1 | 743 | 753 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 208 | 214 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 298 | 304 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 386 | 392 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 437 | 443 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 476 | 480 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 743 | 749 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 84 | 90 | PF02991 | 0.523 |
LIG_LYPXL_SIV_4 | 346 | 354 | PF13949 | 0.547 |
LIG_PCNA_yPIPBox_3 | 600 | 609 | PF02747 | 0.454 |
LIG_PCNA_yPIPBox_3 | 699 | 710 | PF02747 | 0.574 |
LIG_Pex14_2 | 300 | 304 | PF04695 | 0.454 |
LIG_PTB_Apo_2 | 563 | 570 | PF02174 | 0.569 |
LIG_PTB_Phospho_1 | 563 | 569 | PF10480 | 0.577 |
LIG_SH2_CRK | 467 | 471 | PF00017 | 0.516 |
LIG_SH2_CRK | 537 | 541 | PF00017 | 0.457 |
LIG_SH2_PTP2 | 552 | 555 | PF00017 | 0.561 |
LIG_SH2_SRC | 552 | 555 | PF00017 | 0.561 |
LIG_SH2_STAP1 | 247 | 251 | PF00017 | 0.618 |
LIG_SH2_STAP1 | 483 | 487 | PF00017 | 0.516 |
LIG_SH2_STAT3 | 247 | 250 | PF00017 | 0.615 |
LIG_SH2_STAT3 | 769 | 772 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.589 |
LIG_SH2_STAT5 | 552 | 555 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 746 | 749 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 769 | 772 | PF00017 | 0.503 |
LIG_SH3_3 | 427 | 433 | PF00018 | 0.502 |
LIG_SH3_3 | 652 | 658 | PF00018 | 0.646 |
LIG_SUMO_SIM_anti_2 | 268 | 276 | PF11976 | 0.643 |
LIG_SUMO_SIM_anti_2 | 686 | 694 | PF11976 | 0.578 |
LIG_SUMO_SIM_par_1 | 272 | 278 | PF11976 | 0.558 |
LIG_SUMO_SIM_par_1 | 55 | 61 | PF11976 | 0.583 |
LIG_SUMO_SIM_par_1 | 639 | 645 | PF11976 | 0.475 |
LIG_TRAF2_1 | 206 | 209 | PF00917 | 0.490 |
LIG_TRAF2_1 | 525 | 528 | PF00917 | 0.516 |
LIG_TRAF2_1 | 755 | 758 | PF00917 | 0.591 |
LIG_TRFH_1 | 716 | 720 | PF08558 | 0.530 |
LIG_TYR_ITIM | 465 | 470 | PF00017 | 0.507 |
LIG_TYR_ITIM | 535 | 540 | PF00017 | 0.463 |
LIG_WRC_WIRS_1 | 297 | 302 | PF05994 | 0.566 |
LIG_WRC_WIRS_1 | 618 | 623 | PF05994 | 0.482 |
MOD_CDK_SPK_2 | 1 | 6 | PF00069 | 0.658 |
MOD_CDK_SPxxK_3 | 1 | 8 | PF00069 | 0.661 |
MOD_CDK_SPxxK_3 | 646 | 653 | PF00069 | 0.500 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.618 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.658 |
MOD_CK1_1 | 612 | 618 | PF00069 | 0.536 |
MOD_CK1_1 | 620 | 626 | PF00069 | 0.584 |
MOD_CK1_1 | 660 | 666 | PF00069 | 0.472 |
MOD_CK1_1 | 697 | 703 | PF00069 | 0.589 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.497 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.574 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.570 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.593 |
MOD_CK2_1 | 730 | 736 | PF00069 | 0.547 |
MOD_CK2_1 | 782 | 788 | PF00069 | 0.563 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.567 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.622 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.451 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.576 |
MOD_GlcNHglycan | 554 | 558 | PF01048 | 0.542 |
MOD_GlcNHglycan | 624 | 627 | PF01048 | 0.644 |
MOD_GlcNHglycan | 774 | 778 | PF01048 | 0.612 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.549 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.539 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.477 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.385 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.506 |
MOD_GSK3_1 | 694 | 701 | PF00069 | 0.578 |
MOD_GSK3_1 | 719 | 726 | PF00069 | 0.524 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.490 |
MOD_GSK3_1 | 790 | 797 | PF00069 | 0.557 |
MOD_N-GLC_1 | 140 | 145 | PF02516 | 0.576 |
MOD_N-GLC_1 | 407 | 412 | PF02516 | 0.632 |
MOD_N-GLC_1 | 794 | 799 | PF02516 | 0.585 |
MOD_N-GLC_2 | 596 | 598 | PF02516 | 0.506 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.502 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.551 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.419 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.614 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.690 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.456 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.396 |
MOD_NEK2_1 | 540 | 545 | PF00069 | 0.412 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.612 |
MOD_NEK2_1 | 794 | 799 | PF00069 | 0.596 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.566 |
MOD_PIKK_1 | 127 | 133 | PF00454 | 0.505 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.467 |
MOD_PIKK_1 | 381 | 387 | PF00454 | 0.594 |
MOD_PIKK_1 | 503 | 509 | PF00454 | 0.375 |
MOD_PIKK_1 | 571 | 577 | PF00454 | 0.402 |
MOD_PIKK_1 | 580 | 586 | PF00454 | 0.410 |
MOD_PIKK_1 | 620 | 626 | PF00454 | 0.611 |
MOD_PIKK_1 | 723 | 729 | PF00454 | 0.504 |
MOD_PIKK_1 | 95 | 101 | PF00454 | 0.550 |
MOD_PKA_1 | 266 | 272 | PF00069 | 0.561 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.568 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.625 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.457 |
MOD_PKA_2 | 540 | 546 | PF00069 | 0.381 |
MOD_PKA_2 | 790 | 796 | PF00069 | 0.650 |
MOD_PKB_1 | 804 | 812 | PF00069 | 0.552 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.533 |
MOD_Plk_1 | 402 | 408 | PF00069 | 0.562 |
MOD_Plk_1 | 420 | 426 | PF00069 | 0.706 |
MOD_Plk_1 | 485 | 491 | PF00069 | 0.465 |
MOD_Plk_1 | 644 | 650 | PF00069 | 0.450 |
MOD_Plk_1 | 794 | 800 | PF00069 | 0.628 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.567 |
MOD_Plk_2-3 | 196 | 202 | PF00069 | 0.569 |
MOD_Plk_2-3 | 397 | 403 | PF00069 | 0.629 |
MOD_Plk_2-3 | 481 | 487 | PF00069 | 0.477 |
MOD_Plk_2-3 | 730 | 736 | PF00069 | 0.578 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.504 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.497 |
MOD_Plk_4 | 485 | 491 | PF00069 | 0.368 |
MOD_Plk_4 | 665 | 671 | PF00069 | 0.524 |
MOD_Plk_4 | 701 | 707 | PF00069 | 0.569 |
MOD_Plk_4 | 730 | 736 | PF00069 | 0.544 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.630 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.664 |
MOD_ProDKin_1 | 646 | 652 | PF00069 | 0.572 |
MOD_SUMO_for_1 | 146 | 149 | PF00179 | 0.571 |
MOD_SUMO_rev_2 | 115 | 124 | PF00179 | 0.508 |
MOD_SUMO_rev_2 | 169 | 174 | PF00179 | 0.461 |
MOD_SUMO_rev_2 | 191 | 200 | PF00179 | 0.551 |
MOD_SUMO_rev_2 | 259 | 268 | PF00179 | 0.596 |
MOD_SUMO_rev_2 | 334 | 340 | PF00179 | 0.568 |
TRG_DiLeu_BaEn_1 | 63 | 68 | PF01217 | 0.515 |
TRG_DiLeu_BaEn_4 | 65 | 71 | PF01217 | 0.623 |
TRG_DiLeu_BaLyEn_6 | 130 | 135 | PF01217 | 0.511 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.638 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 537 | 540 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 732 | 735 | PF00928 | 0.527 |
TRG_ENDOCYTIC_2 | 746 | 749 | PF00928 | 0.470 |
TRG_ER_diArg_1 | 112 | 114 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 366 | 368 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 424 | 426 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 599 | 601 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 790 | 792 | PF00400 | 0.627 |
TRG_NES_CRM1_1 | 631 | 645 | PF08389 | 0.521 |
TRG_NES_CRM1_1 | 730 | 744 | PF08389 | 0.580 |
TRG_Pf-PMV_PEXEL_1 | 133 | 138 | PF00026 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 205 | 209 | PF00026 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 234 | 238 | PF00026 | 0.609 |
TRG_Pf-PMV_PEXEL_1 | 390 | 394 | PF00026 | 0.580 |
TRG_Pf-PMV_PEXEL_1 | 824 | 828 | PF00026 | 0.582 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC98 | Leptomonas seymouri | 68% | 100% |
A0A0S4JP59 | Bodo saltans | 30% | 88% |
A0A1X0P3L6 | Trypanosomatidae | 45% | 99% |
A0A422NYC2 | Trypanosoma rangeli | 45% | 98% |
A4H451 | Leishmania braziliensis | 84% | 100% |
A4HSC8 | Leishmania infantum | 100% | 100% |
C9ZPY3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 99% |
E9AKA9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4QJJ8 | Leishmania major | 94% | 100% |
V5BAC3 | Trypanosoma cruzi | 43% | 98% |