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 | 2 |
GO:0042995 | cell projection | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 2 |
Related structures:
AlphaFold database: Q4QJJ8
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 | 81 | 85 | PF00656 | 0.628 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.746 |
CLV_NRD_NRD_1 | 600 | 602 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 791 | 793 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 805 | 807 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 823 | 825 | PF00675 | 0.481 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 600 | 602 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 791 | 793 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 804 | 806 | PF00082 | 0.540 |
CLV_PCSK_PC1ET2_1 | 266 | 268 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.647 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.687 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 646 | 650 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 710 | 714 | PF00082 | 0.514 |
CLV_Separin_Metazoa | 457 | 461 | PF03568 | 0.500 |
CLV_Separin_Metazoa | 66 | 70 | PF03568 | 0.506 |
CLV_Separin_Metazoa | 788 | 792 | PF03568 | 0.407 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.742 |
DOC_CDC14_PxL_1 | 305 | 313 | PF14671 | 0.534 |
DOC_CDC14_PxL_1 | 320 | 328 | PF14671 | 0.388 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 415 | 424 | PF00134 | 0.624 |
DOC_CYCLIN_yCln2_LP_2 | 513 | 519 | PF00134 | 0.428 |
DOC_CYCLIN_yCln2_LP_2 | 718 | 721 | PF00134 | 0.531 |
DOC_MAPK_DCC_7 | 611 | 621 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 266 | 274 | PF00069 | 0.647 |
DOC_MAPK_gen_1 | 538 | 546 | PF00069 | 0.344 |
DOC_MAPK_gen_1 | 681 | 690 | PF00069 | 0.545 |
DOC_MAPK_MEF2A_6 | 267 | 276 | PF00069 | 0.568 |
DOC_MAPK_MEF2A_6 | 436 | 445 | PF00069 | 0.410 |
DOC_MAPK_RevD_3 | 588 | 601 | PF00069 | 0.278 |
DOC_PP1_RVXF_1 | 175 | 182 | PF00149 | 0.591 |
DOC_PP1_RVXF_1 | 410 | 416 | PF00149 | 0.485 |
DOC_PP1_RVXF_1 | 434 | 441 | PF00149 | 0.425 |
DOC_PP1_RVXF_1 | 447 | 453 | PF00149 | 0.383 |
DOC_PP2B_LxvP_1 | 326 | 329 | PF13499 | 0.481 |
DOC_PP2B_LxvP_1 | 443 | 446 | PF13499 | 0.466 |
DOC_PP2B_LxvP_1 | 520 | 523 | PF13499 | 0.521 |
DOC_PP2B_LxvP_1 | 718 | 721 | PF13499 | 0.507 |
DOC_PP4_FxxP_1 | 36 | 39 | PF00568 | 0.557 |
DOC_PP4_FxxP_1 | 648 | 651 | PF00568 | 0.547 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 617 | 621 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 658 | 662 | PF00917 | 0.591 |
DOC_USP7_UBL2_3 | 162 | 166 | PF12436 | 0.639 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 646 | 651 | PF00397 | 0.473 |
LIG_14-3-3_CanoR_1 | 232 | 237 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 267 | 275 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 407 | 416 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 460 | 464 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 501 | 510 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 541 | 545 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 6 | 13 | PF00244 | 0.717 |
LIG_14-3-3_CanoR_1 | 791 | 795 | PF00244 | 0.655 |
LIG_Actin_WH2_2 | 183 | 200 | PF00022 | 0.602 |
LIG_Actin_WH2_2 | 459 | 475 | PF00022 | 0.504 |
LIG_BRCT_BRCA1_1 | 142 | 146 | PF00533 | 0.432 |
LIG_deltaCOP1_diTrp_1 | 508 | 515 | PF00928 | 0.418 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.528 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.457 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.514 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.619 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.545 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.553 |
LIG_FHA_1 | 613 | 619 | PF00498 | 0.507 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.679 |
LIG_FHA_1 | 785 | 791 | PF00498 | 0.619 |
LIG_FHA_1 | 795 | 801 | PF00498 | 0.568 |
LIG_FHA_1 | 807 | 813 | PF00498 | 0.505 |
LIG_FHA_2 | 783 | 789 | PF00498 | 0.556 |
LIG_FHA_2 | 79 | 85 | PF00498 | 0.622 |
LIG_Integrin_isoDGR_2 | 447 | 449 | PF01839 | 0.428 |
LIG_LIR_Apic_2 | 33 | 39 | PF02991 | 0.560 |
LIG_LIR_Apic_2 | 550 | 555 | PF02991 | 0.419 |
LIG_LIR_Apic_2 | 647 | 651 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 298 | 309 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 437 | 446 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 730 | 740 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 743 | 753 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 208 | 214 | PF02991 | 0.613 |
LIG_LIR_Nem_3 | 298 | 304 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 386 | 392 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 437 | 443 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 476 | 480 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 743 | 749 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 84 | 90 | PF02991 | 0.480 |
LIG_LYPXL_SIV_4 | 346 | 354 | PF13949 | 0.494 |
LIG_PCNA_yPIPBox_3 | 600 | 609 | PF02747 | 0.425 |
LIG_PCNA_yPIPBox_3 | 699 | 710 | PF02747 | 0.559 |
LIG_Pex14_2 | 300 | 304 | PF04695 | 0.412 |
LIG_PTB_Apo_2 | 563 | 570 | PF02174 | 0.510 |
LIG_PTB_Phospho_1 | 563 | 569 | PF10480 | 0.517 |
LIG_SH2_CRK | 467 | 471 | PF00017 | 0.500 |
LIG_SH2_CRK | 537 | 541 | PF00017 | 0.433 |
LIG_SH2_PTP2 | 552 | 555 | PF00017 | 0.540 |
LIG_SH2_SRC | 552 | 555 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 247 | 251 | PF00017 | 0.591 |
LIG_SH2_STAP1 | 483 | 487 | PF00017 | 0.501 |
LIG_SH2_STAT3 | 247 | 250 | PF00017 | 0.588 |
LIG_SH2_STAT3 | 769 | 772 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 552 | 555 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 746 | 749 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 769 | 772 | PF00017 | 0.494 |
LIG_SH3_3 | 427 | 433 | PF00018 | 0.468 |
LIG_SH3_3 | 652 | 658 | PF00018 | 0.633 |
LIG_SUMO_SIM_anti_2 | 268 | 276 | PF11976 | 0.593 |
LIG_SUMO_SIM_anti_2 | 632 | 637 | PF11976 | 0.413 |
LIG_SUMO_SIM_anti_2 | 686 | 694 | PF11976 | 0.561 |
LIG_SUMO_SIM_par_1 | 55 | 61 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 639 | 644 | PF11976 | 0.431 |
LIG_TRAF2_1 | 206 | 209 | PF00917 | 0.533 |
LIG_TRAF2_1 | 525 | 528 | PF00917 | 0.525 |
LIG_TRAF2_1 | 755 | 758 | PF00917 | 0.580 |
LIG_TRFH_1 | 716 | 720 | PF08558 | 0.503 |
LIG_TYR_ITIM | 465 | 470 | PF00017 | 0.485 |
LIG_TYR_ITIM | 535 | 540 | PF00017 | 0.439 |
LIG_WRC_WIRS_1 | 161 | 166 | PF05994 | 0.442 |
LIG_WRC_WIRS_1 | 297 | 302 | PF05994 | 0.536 |
LIG_WRC_WIRS_1 | 618 | 623 | PF05994 | 0.460 |
MOD_CDK_SPK_2 | 1 | 6 | PF00069 | 0.631 |
MOD_CDK_SPxxK_3 | 1 | 8 | PF00069 | 0.631 |
MOD_CDK_SPxxK_3 | 646 | 653 | PF00069 | 0.469 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.591 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.615 |
MOD_CK1_1 | 612 | 618 | PF00069 | 0.522 |
MOD_CK1_1 | 620 | 626 | PF00069 | 0.564 |
MOD_CK1_1 | 660 | 666 | PF00069 | 0.458 |
MOD_CK1_1 | 697 | 703 | PF00069 | 0.578 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.468 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.592 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.585 |
MOD_CK2_1 | 730 | 736 | PF00069 | 0.514 |
MOD_CK2_1 | 782 | 788 | PF00069 | 0.537 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.526 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.511 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.575 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.514 |
MOD_GlcNHglycan | 554 | 558 | PF01048 | 0.515 |
MOD_GlcNHglycan | 624 | 627 | PF01048 | 0.610 |
MOD_GlcNHglycan | 774 | 778 | PF01048 | 0.608 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.564 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.589 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.538 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.453 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.414 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.451 |
MOD_GSK3_1 | 694 | 701 | PF00069 | 0.564 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.447 |
MOD_GSK3_1 | 790 | 797 | PF00069 | 0.501 |
MOD_N-GLC_1 | 140 | 145 | PF02516 | 0.558 |
MOD_N-GLC_1 | 407 | 412 | PF02516 | 0.594 |
MOD_N-GLC_1 | 794 | 799 | PF02516 | 0.526 |
MOD_N-GLC_2 | 596 | 598 | PF02516 | 0.492 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.472 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.562 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.508 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.378 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.574 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.537 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.421 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.361 |
MOD_NEK2_1 | 540 | 545 | PF00069 | 0.400 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.602 |
MOD_NEK2_1 | 794 | 799 | PF00069 | 0.558 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.514 |
MOD_PIKK_1 | 127 | 133 | PF00454 | 0.486 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.437 |
MOD_PIKK_1 | 381 | 387 | PF00454 | 0.561 |
MOD_PIKK_1 | 503 | 509 | PF00454 | 0.346 |
MOD_PIKK_1 | 571 | 577 | PF00454 | 0.375 |
MOD_PIKK_1 | 580 | 586 | PF00454 | 0.382 |
MOD_PIKK_1 | 620 | 626 | PF00454 | 0.546 |
MOD_PIKK_1 | 827 | 833 | PF00454 | 0.580 |
MOD_PKA_1 | 266 | 272 | PF00069 | 0.549 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.588 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.626 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.429 |
MOD_PKA_2 | 540 | 546 | PF00069 | 0.390 |
MOD_PKA_2 | 790 | 796 | PF00069 | 0.615 |
MOD_PKB_1 | 804 | 812 | PF00069 | 0.511 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.530 |
MOD_Plk_1 | 402 | 408 | PF00069 | 0.515 |
MOD_Plk_1 | 420 | 426 | PF00069 | 0.490 |
MOD_Plk_1 | 485 | 491 | PF00069 | 0.475 |
MOD_Plk_1 | 794 | 800 | PF00069 | 0.598 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.560 |
MOD_Plk_2-3 | 196 | 202 | PF00069 | 0.560 |
MOD_Plk_2-3 | 397 | 403 | PF00069 | 0.596 |
MOD_Plk_2-3 | 481 | 487 | PF00069 | 0.494 |
MOD_Plk_2-3 | 629 | 635 | PF00069 | 0.392 |
MOD_Plk_2-3 | 730 | 736 | PF00069 | 0.552 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.486 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.484 |
MOD_Plk_4 | 485 | 491 | PF00069 | 0.340 |
MOD_Plk_4 | 665 | 671 | PF00069 | 0.513 |
MOD_Plk_4 | 701 | 707 | PF00069 | 0.560 |
MOD_Plk_4 | 730 | 736 | PF00069 | 0.510 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.499 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.645 |
MOD_ProDKin_1 | 646 | 652 | PF00069 | 0.487 |
MOD_SUMO_for_1 | 146 | 149 | PF00179 | 0.545 |
MOD_SUMO_rev_2 | 115 | 124 | PF00179 | 0.485 |
MOD_SUMO_rev_2 | 169 | 174 | PF00179 | 0.460 |
MOD_SUMO_rev_2 | 192 | 200 | PF00179 | 0.564 |
MOD_SUMO_rev_2 | 259 | 268 | PF00179 | 0.609 |
MOD_SUMO_rev_2 | 334 | 340 | PF00179 | 0.533 |
TRG_DiLeu_BaEn_1 | 531 | 536 | PF01217 | 0.350 |
TRG_DiLeu_BaEn_1 | 63 | 68 | PF01217 | 0.459 |
TRG_DiLeu_BaEn_4 | 65 | 71 | PF01217 | 0.582 |
TRG_DiLeu_BaLyEn_6 | 130 | 135 | PF01217 | 0.487 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.611 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 537 | 540 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 732 | 735 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 746 | 749 | PF00928 | 0.444 |
TRG_ER_diArg_1 | 112 | 114 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 599 | 601 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 790 | 792 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 804 | 806 | PF00400 | 0.486 |
TRG_NES_CRM1_1 | 631 | 644 | PF08389 | 0.505 |
TRG_NES_CRM1_1 | 730 | 744 | PF08389 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 133 | 138 | PF00026 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 205 | 209 | PF00026 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 234 | 238 | PF00026 | 0.580 |
TRG_Pf-PMV_PEXEL_1 | 390 | 394 | PF00026 | 0.549 |
TRG_Pf-PMV_PEXEL_1 | 824 | 828 | PF00026 | 0.573 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC98 | Leptomonas seymouri | 66% | 100% |
A0A0S4JP59 | Bodo saltans | 30% | 88% |
A0A1X0P3L6 | Trypanosomatidae | 46% | 99% |
A0A3S5H5F6 | Leishmania donovani | 94% | 100% |
A0A422NYC2 | Trypanosoma rangeli | 46% | 98% |
A4H451 | Leishmania braziliensis | 85% | 99% |
A4HSC8 | Leishmania infantum | 94% | 100% |
C9ZPY3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 99% |
E9AKA9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 99% |
V5BAC3 | Trypanosoma cruzi | 45% | 98% |