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: A4H451
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 | 105 | 109 | PF00656 | 0.523 |
CLV_C14_Caspase3-7 | 81 | 85 | PF00656 | 0.636 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 600 | 602 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 790 | 792 | PF00675 | 0.626 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 599 | 601 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 790 | 792 | PF00082 | 0.628 |
CLV_PCSK_PC1ET2_1 | 266 | 268 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 763 | 767 | PF00082 | 0.418 |
CLV_Separin_Metazoa | 456 | 460 | PF03568 | 0.562 |
CLV_Separin_Metazoa | 66 | 70 | PF03568 | 0.567 |
DEG_APCC_DBOX_1 | 600 | 608 | PF00400 | 0.358 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.783 |
DOC_CDC14_PxL_1 | 305 | 313 | PF14671 | 0.581 |
DOC_CDC14_PxL_1 | 320 | 328 | PF14671 | 0.588 |
DOC_CDC14_PxL_1 | 354 | 362 | PF14671 | 0.429 |
DOC_CKS1_1 | 326 | 331 | PF01111 | 0.416 |
DOC_CYCLIN_RxL_1 | 348 | 359 | PF00134 | 0.509 |
DOC_CYCLIN_RxL_1 | 445 | 456 | PF00134 | 0.327 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 414 | 423 | PF00134 | 0.652 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 739 | 748 | PF00134 | 0.356 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 790 | 797 | PF00134 | 0.395 |
DOC_CYCLIN_yCln2_LP_2 | 512 | 518 | PF00134 | 0.464 |
DOC_CYCLIN_yCln2_LP_2 | 717 | 720 | PF00134 | 0.573 |
DOC_MAPK_DCC_7 | 610 | 620 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 266 | 274 | PF00069 | 0.611 |
DOC_MAPK_gen_1 | 50 | 59 | PF00069 | 0.644 |
DOC_MAPK_gen_1 | 537 | 545 | PF00069 | 0.375 |
DOC_MAPK_gen_1 | 680 | 689 | PF00069 | 0.561 |
DOC_MAPK_gen_1 | 805 | 815 | PF00069 | 0.380 |
DOC_MAPK_MEF2A_6 | 267 | 276 | PF00069 | 0.584 |
DOC_MAPK_MEF2A_6 | 435 | 444 | PF00069 | 0.439 |
DOC_MAPK_MEF2A_6 | 808 | 815 | PF00069 | 0.382 |
DOC_MAPK_NFAT4_5 | 808 | 816 | PF00069 | 0.379 |
DOC_PP1_RVXF_1 | 175 | 182 | PF00149 | 0.592 |
DOC_PP1_RVXF_1 | 409 | 415 | PF00149 | 0.526 |
DOC_PP1_RVXF_1 | 433 | 440 | PF00149 | 0.452 |
DOC_PP1_RVXF_1 | 446 | 452 | PF00149 | 0.431 |
DOC_PP2B_LxvP_1 | 355 | 358 | PF13499 | 0.383 |
DOC_PP2B_LxvP_1 | 442 | 445 | PF13499 | 0.492 |
DOC_PP2B_LxvP_1 | 519 | 522 | PF13499 | 0.543 |
DOC_PP2B_LxvP_1 | 717 | 720 | PF13499 | 0.551 |
DOC_PP4_FxxP_1 | 36 | 39 | PF00568 | 0.587 |
DOC_PP4_FxxP_1 | 647 | 650 | PF00568 | 0.621 |
DOC_SPAK_OSR1_1 | 500 | 504 | PF12202 | 0.300 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 608 | 612 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 616 | 620 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 657 | 661 | PF00917 | 0.699 |
DOC_USP7_UBL2_3 | 162 | 166 | PF12436 | 0.622 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 653 | 658 | PF00397 | 0.712 |
LIG_14-3-3_CanoR_1 | 151 | 160 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 232 | 237 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 267 | 275 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 459 | 463 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 540 | 544 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 7 | 13 | PF00244 | 0.762 |
LIG_14-3-3_CanoR_1 | 707 | 713 | PF00244 | 0.392 |
LIG_Actin_WH2_2 | 183 | 200 | PF00022 | 0.591 |
LIG_Actin_WH2_2 | 458 | 474 | PF00022 | 0.524 |
LIG_BIR_III_4 | 314 | 318 | PF00653 | 0.420 |
LIG_deltaCOP1_diTrp_1 | 507 | 514 | PF00928 | 0.452 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.522 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.530 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.470 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.535 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.637 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.561 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.601 |
LIG_FHA_1 | 612 | 618 | PF00498 | 0.524 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.701 |
LIG_FHA_1 | 784 | 790 | PF00498 | 0.628 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.437 |
LIG_FHA_2 | 782 | 788 | PF00498 | 0.577 |
LIG_FHA_2 | 834 | 840 | PF00498 | 0.515 |
LIG_LIR_Apic_2 | 33 | 39 | PF02991 | 0.585 |
LIG_LIR_Apic_2 | 549 | 554 | PF02991 | 0.476 |
LIG_LIR_Apic_2 | 646 | 650 | PF02991 | 0.613 |
LIG_LIR_Gen_1 | 729 | 739 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 208 | 214 | PF02991 | 0.648 |
LIG_LIR_Nem_3 | 298 | 304 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 742 | 748 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 767 | 771 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 84 | 90 | PF02991 | 0.528 |
LIG_LYPXL_SIV_4 | 346 | 354 | PF13949 | 0.549 |
LIG_PTB_Apo_2 | 433 | 440 | PF02174 | 0.491 |
LIG_PTB_Apo_2 | 562 | 569 | PF02174 | 0.600 |
LIG_PTB_Phospho_1 | 562 | 568 | PF10480 | 0.605 |
LIG_SH2_CRK | 301 | 305 | PF00017 | 0.327 |
LIG_SH2_CRK | 466 | 470 | PF00017 | 0.521 |
LIG_SH2_CRK | 536 | 540 | PF00017 | 0.458 |
LIG_SH2_PTP2 | 551 | 554 | PF00017 | 0.588 |
LIG_SH2_SRC | 551 | 554 | PF00017 | 0.588 |
LIG_SH2_STAP1 | 247 | 251 | PF00017 | 0.617 |
LIG_SH2_STAP1 | 482 | 486 | PF00017 | 0.547 |
LIG_SH2_STAT3 | 247 | 250 | PF00017 | 0.616 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.583 |
LIG_SH2_STAT5 | 551 | 554 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 768 | 771 | PF00017 | 0.539 |
LIG_SH3_3 | 426 | 432 | PF00018 | 0.506 |
LIG_SUMO_SIM_anti_2 | 268 | 276 | PF11976 | 0.644 |
LIG_SUMO_SIM_anti_2 | 631 | 636 | PF11976 | 0.450 |
LIG_SUMO_SIM_anti_2 | 685 | 693 | PF11976 | 0.579 |
LIG_SUMO_SIM_par_1 | 353 | 359 | PF11976 | 0.382 |
LIG_SUMO_SIM_par_1 | 55 | 61 | PF11976 | 0.584 |
LIG_SUMO_SIM_par_1 | 685 | 693 | PF11976 | 0.511 |
LIG_TRAF2_1 | 524 | 527 | PF00917 | 0.514 |
LIG_TRAF2_1 | 754 | 757 | PF00917 | 0.597 |
LIG_TRFH_1 | 715 | 719 | PF08558 | 0.547 |
LIG_TYR_ITIM | 464 | 469 | PF00017 | 0.508 |
LIG_TYR_ITIM | 534 | 539 | PF00017 | 0.465 |
LIG_TYR_ITSM | 297 | 304 | PF00017 | 0.321 |
LIG_UBA3_1 | 354 | 362 | PF00899 | 0.406 |
LIG_WRC_WIRS_1 | 161 | 166 | PF05994 | 0.455 |
LIG_WRC_WIRS_1 | 297 | 302 | PF05994 | 0.553 |
LIG_WRC_WIRS_1 | 405 | 410 | PF05994 | 0.437 |
LIG_WRC_WIRS_1 | 617 | 622 | PF05994 | 0.511 |
MOD_CDK_SPK_2 | 325 | 330 | PF00069 | 0.416 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.609 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.498 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.653 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.596 |
MOD_CK1_1 | 611 | 617 | PF00069 | 0.538 |
MOD_CK1_1 | 619 | 625 | PF00069 | 0.614 |
MOD_CK1_1 | 656 | 662 | PF00069 | 0.538 |
MOD_CK1_1 | 696 | 702 | PF00069 | 0.593 |
MOD_CK1_1 | 831 | 837 | PF00069 | 0.512 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.518 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.479 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.582 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.480 |
MOD_CK2_1 | 729 | 735 | PF00069 | 0.553 |
MOD_CK2_1 | 781 | 787 | PF00069 | 0.567 |
MOD_CK2_1 | 833 | 839 | PF00069 | 0.501 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.566 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.524 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.604 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.565 |
MOD_GlcNHglycan | 526 | 531 | PF01048 | 0.473 |
MOD_GlcNHglycan | 553 | 557 | PF01048 | 0.570 |
MOD_GlcNHglycan | 623 | 626 | PF01048 | 0.659 |
MOD_GlcNHglycan | 773 | 777 | PF01048 | 0.634 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.576 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.595 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.554 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.610 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.518 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.461 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.413 |
MOD_GSK3_1 | 653 | 660 | PF00069 | 0.554 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.508 |
MOD_GSK3_1 | 693 | 700 | PF00069 | 0.578 |
MOD_GSK3_1 | 718 | 725 | PF00069 | 0.535 |
MOD_GSK3_1 | 829 | 836 | PF00069 | 0.517 |
MOD_N-GLC_2 | 595 | 597 | PF02516 | 0.516 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.485 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.568 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.594 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.530 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.584 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.685 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.452 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.398 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.413 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.619 |
MOD_NEK2_1 | 829 | 834 | PF00069 | 0.560 |
MOD_PIKK_1 | 127 | 133 | PF00454 | 0.505 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.449 |
MOD_PIKK_1 | 380 | 386 | PF00454 | 0.581 |
MOD_PIKK_1 | 502 | 508 | PF00454 | 0.377 |
MOD_PIKK_1 | 570 | 576 | PF00454 | 0.423 |
MOD_PIKK_1 | 619 | 625 | PF00454 | 0.641 |
MOD_PIKK_1 | 722 | 728 | PF00454 | 0.511 |
MOD_PKA_1 | 266 | 272 | PF00069 | 0.567 |
MOD_PKA_1 | 7 | 13 | PF00069 | 0.691 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.581 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.631 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.518 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.453 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.383 |
MOD_PKA_2 | 708 | 714 | PF00069 | 0.530 |
MOD_Plk_1 | 191 | 197 | PF00069 | 0.566 |
MOD_Plk_1 | 401 | 407 | PF00069 | 0.532 |
MOD_Plk_1 | 419 | 425 | PF00069 | 0.703 |
MOD_Plk_1 | 484 | 490 | PF00069 | 0.490 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.566 |
MOD_Plk_2-3 | 102 | 108 | PF00069 | 0.360 |
MOD_Plk_2-3 | 191 | 197 | PF00069 | 0.526 |
MOD_Plk_2-3 | 242 | 248 | PF00069 | 0.521 |
MOD_Plk_2-3 | 480 | 486 | PF00069 | 0.503 |
MOD_Plk_2-3 | 628 | 634 | PF00069 | 0.430 |
MOD_Plk_2-3 | 643 | 649 | PF00069 | 0.441 |
MOD_Plk_2-3 | 729 | 735 | PF00069 | 0.585 |
MOD_Plk_2-3 | 781 | 787 | PF00069 | 0.416 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.483 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.481 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.393 |
MOD_Plk_4 | 664 | 670 | PF00069 | 0.626 |
MOD_Plk_4 | 729 | 735 | PF00069 | 0.550 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.580 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.509 |
MOD_ProDKin_1 | 653 | 659 | PF00069 | 0.709 |
MOD_SUMO_for_1 | 146 | 149 | PF00179 | 0.554 |
MOD_SUMO_rev_2 | 115 | 124 | PF00179 | 0.511 |
MOD_SUMO_rev_2 | 169 | 174 | PF00179 | 0.469 |
MOD_SUMO_rev_2 | 191 | 200 | PF00179 | 0.561 |
MOD_SUMO_rev_2 | 259 | 268 | PF00179 | 0.603 |
MOD_SUMO_rev_2 | 334 | 340 | PF00179 | 0.567 |
TRG_DiLeu_BaEn_1 | 63 | 68 | PF01217 | 0.523 |
TRG_DiLeu_BaEn_4 | 65 | 71 | PF01217 | 0.629 |
TRG_DiLeu_BaLyEn_6 | 130 | 135 | PF01217 | 0.504 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.652 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 466 | 469 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 536 | 539 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 731 | 734 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 745 | 748 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 768 | 771 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 826 | 829 | PF00928 | 0.490 |
TRG_ER_diArg_1 | 112 | 114 | PF00400 | 0.627 |
TRG_ER_diArg_1 | 423 | 425 | PF00400 | 0.619 |
TRG_ER_diArg_1 | 598 | 601 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 789 | 791 | PF00400 | 0.602 |
TRG_NES_CRM1_1 | 630 | 643 | PF08389 | 0.531 |
TRG_NES_CRM1_1 | 729 | 742 | PF08389 | 0.585 |
TRG_Pf-PMV_PEXEL_1 | 133 | 138 | PF00026 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 234 | 238 | PF00026 | 0.611 |
TRG_Pf-PMV_PEXEL_1 | 389 | 393 | PF00026 | 0.583 |
TRG_Pf-PMV_PEXEL_1 | 763 | 767 | PF00026 | 0.405 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC98 | Leptomonas seymouri | 68% | 100% |
A0A0S4JP59 | Bodo saltans | 30% | 89% |
A0A1X0P3L6 | Trypanosomatidae | 45% | 100% |
A0A3S5H5F6 | Leishmania donovani | 84% | 100% |
A0A422NYC2 | Trypanosoma rangeli | 46% | 99% |
A4HSC8 | Leishmania infantum | 85% | 100% |
C9ZPY3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 99% |
E9AKA9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4QJJ8 | Leishmania major | 85% | 100% |
V5BAC3 | Trypanosoma cruzi | 45% | 99% |