Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 2 |
Pissara et al. | yes | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 3 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0010494 | cytoplasmic stress granule | 5 | 1 |
GO:0034399 | nuclear periphery | 2 | 1 |
GO:0035770 | ribonucleoprotein granule | 3 | 1 |
GO:0036464 | cytoplasmic ribonucleoprotein granule | 4 | 1 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0097165 | nuclear stress granule | 4 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A4HMX7
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 13 |
GO:0003676 | nucleic acid binding | 3 | 13 |
GO:0003724 | RNA helicase activity | 3 | 13 |
GO:0003743 | translation initiation factor activity | 4 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004386 | helicase activity | 2 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0008135 | translation factor activity, RNA binding | 3 | 13 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 13 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0030554 | adenyl nucleotide binding | 5 | 13 |
GO:0032553 | ribonucleotide binding | 3 | 13 |
GO:0032555 | purine ribonucleotide binding | 4 | 13 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
GO:0036094 | small molecule binding | 2 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043168 | anion binding | 3 | 13 |
GO:0045182 | translation regulator activity | 1 | 13 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 13 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 13 |
GO:0140657 | ATP-dependent activity | 1 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
GO:0003723 | RNA binding | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 836 | 840 | PF00656 | 0.677 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.718 |
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.716 |
CLV_NRD_NRD_1 | 477 | 479 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 610 | 612 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 672 | 674 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 688 | 690 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 763 | 765 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 807 | 809 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 850 | 852 | PF00675 | 0.667 |
CLV_PCSK_FUR_1 | 40 | 44 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.655 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.716 |
CLV_PCSK_KEX2_1 | 606 | 608 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 610 | 612 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 672 | 674 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 688 | 690 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 763 | 765 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 806 | 808 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 850 | 852 | PF00082 | 0.667 |
CLV_PCSK_PC1ET2_1 | 606 | 608 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 538 | 542 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 626 | 630 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 764 | 768 | PF00082 | 0.501 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.704 |
DEG_SPOP_SBC_1 | 621 | 625 | PF00917 | 0.547 |
DOC_CYCLIN_RxL_1 | 549 | 560 | PF00134 | 0.496 |
DOC_CYCLIN_yCln2_LP_2 | 411 | 417 | PF00134 | 0.488 |
DOC_MAPK_DCC_7 | 701 | 709 | PF00069 | 0.550 |
DOC_MAPK_gen_1 | 378 | 386 | PF00069 | 0.538 |
DOC_MAPK_gen_1 | 476 | 485 | PF00069 | 0.498 |
DOC_MAPK_gen_1 | 610 | 618 | PF00069 | 0.403 |
DOC_MAPK_gen_1 | 701 | 709 | PF00069 | 0.526 |
DOC_MAPK_gen_1 | 760 | 769 | PF00069 | 0.534 |
DOC_MAPK_MEF2A_6 | 433 | 440 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 478 | 487 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 760 | 769 | PF00069 | 0.513 |
DOC_PP1_RVXF_1 | 500 | 507 | PF00149 | 0.539 |
DOC_PP2B_LxvP_1 | 316 | 319 | PF13499 | 0.551 |
DOC_PP2B_LxvP_1 | 718 | 721 | PF13499 | 0.533 |
DOC_PP4_FxxP_1 | 459 | 462 | PF00568 | 0.509 |
DOC_PP4_FxxP_1 | 729 | 732 | PF00568 | 0.539 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.712 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.778 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 470 | 475 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 702 | 707 | PF00397 | 0.496 |
LIG_14-3-3_CanoR_1 | 260 | 265 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 476 | 482 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 502 | 507 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 578 | 585 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 588 | 592 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 620 | 628 | PF00244 | 0.547 |
LIG_APCC_ABBA_1 | 495 | 500 | PF00400 | 0.533 |
LIG_APCC_ABBA_1 | 657 | 662 | PF00400 | 0.523 |
LIG_BRCT_BRCA1_1 | 593 | 597 | PF00533 | 0.533 |
LIG_Clathr_ClatBox_1 | 658 | 662 | PF01394 | 0.533 |
LIG_CtBP_PxDLS_1 | 393 | 397 | PF00389 | 0.524 |
LIG_deltaCOP1_diTrp_1 | 50 | 54 | PF00928 | 0.607 |
LIG_EH1_1 | 650 | 658 | PF00400 | 0.539 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.543 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.554 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.541 |
LIG_FHA_1 | 623 | 629 | PF00498 | 0.501 |
LIG_FHA_1 | 703 | 709 | PF00498 | 0.496 |
LIG_FHA_1 | 737 | 743 | PF00498 | 0.473 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.698 |
LIG_FHA_2 | 582 | 588 | PF00498 | 0.539 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.676 |
LIG_LIR_Apic_2 | 274 | 280 | PF02991 | 0.670 |
LIG_LIR_Apic_2 | 456 | 462 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 310 | 319 | PF02991 | 0.717 |
LIG_LIR_Gen_1 | 387 | 397 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 405 | 415 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 509 | 516 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 543 | 553 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 577 | 585 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 11 | 17 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 291 | 295 | PF02991 | 0.724 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.662 |
LIG_LIR_Nem_3 | 387 | 392 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 405 | 410 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 508 | 514 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 543 | 548 | PF02991 | 0.561 |
LIG_Pex14_2 | 593 | 597 | PF04695 | 0.509 |
LIG_PTAP_UEV_1 | 841 | 846 | PF05743 | 0.669 |
LIG_PTB_Apo_2 | 539 | 546 | PF02174 | 0.498 |
LIG_PTB_Phospho_1 | 539 | 545 | PF10480 | 0.539 |
LIG_SH2_CRK | 277 | 281 | PF00017 | 0.679 |
LIG_SH2_CRK | 389 | 393 | PF00017 | 0.578 |
LIG_SH2_CRK | 425 | 429 | PF00017 | 0.493 |
LIG_SH2_CRK | 434 | 438 | PF00017 | 0.508 |
LIG_SH2_CRK | 466 | 470 | PF00017 | 0.509 |
LIG_SH2_CRK | 512 | 516 | PF00017 | 0.539 |
LIG_SH2_NCK_1 | 389 | 393 | PF00017 | 0.518 |
LIG_SH2_NCK_1 | 512 | 516 | PF00017 | 0.539 |
LIG_SH2_SRC | 234 | 237 | PF00017 | 0.534 |
LIG_SH2_STAP1 | 201 | 205 | PF00017 | 0.651 |
LIG_SH2_STAP1 | 512 | 516 | PF00017 | 0.539 |
LIG_SH2_STAP1 | 738 | 742 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.649 |
LIG_SH2_STAT5 | 545 | 548 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 579 | 582 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 608 | 611 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 614 | 617 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 738 | 741 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 772 | 775 | PF00017 | 0.452 |
LIG_SH3_1 | 327 | 333 | PF00018 | 0.568 |
LIG_SH3_2 | 330 | 335 | PF14604 | 0.568 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.565 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.594 |
LIG_SH3_3 | 327 | 333 | PF00018 | 0.590 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.701 |
LIG_SH3_3 | 483 | 489 | PF00018 | 0.546 |
LIG_SH3_3 | 528 | 534 | PF00018 | 0.535 |
LIG_SH3_3 | 839 | 845 | PF00018 | 0.690 |
LIG_Sin3_3 | 408 | 415 | PF02671 | 0.503 |
LIG_SUMO_SIM_par_1 | 705 | 712 | PF11976 | 0.488 |
LIG_TRAF2_1 | 139 | 142 | PF00917 | 0.528 |
LIG_TRAF2_1 | 192 | 195 | PF00917 | 0.650 |
LIG_TRAF2_1 | 301 | 304 | PF00917 | 0.712 |
LIG_TYR_ITIM | 464 | 469 | PF00017 | 0.509 |
LIG_TYR_ITIM | 510 | 515 | PF00017 | 0.539 |
LIG_UBA3_1 | 601 | 606 | PF00899 | 0.451 |
LIG_WRC_WIRS_1 | 25 | 30 | PF05994 | 0.697 |
LIG_WRC_WIRS_1 | 292 | 297 | PF05994 | 0.722 |
LIG_WRC_WIRS_1 | 545 | 550 | PF05994 | 0.539 |
MOD_CDC14_SPxK_1 | 473 | 476 | PF00782 | 0.539 |
MOD_CDK_SPxK_1 | 470 | 476 | PF00069 | 0.539 |
MOD_CDK_SPxxK_3 | 426 | 433 | PF00069 | 0.389 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.528 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.536 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.541 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.496 |
MOD_CK1_1 | 680 | 686 | PF00069 | 0.509 |
MOD_CK1_1 | 822 | 828 | PF00069 | 0.555 |
MOD_CK1_1 | 840 | 846 | PF00069 | 0.740 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.550 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.654 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.677 |
MOD_Cter_Amidation | 185 | 188 | PF01082 | 0.718 |
MOD_Cter_Amidation | 223 | 226 | PF01082 | 0.695 |
MOD_Cter_Amidation | 287 | 290 | PF01082 | 0.715 |
MOD_Cter_Amidation | 40 | 43 | PF01082 | 0.686 |
MOD_Cter_Amidation | 804 | 807 | PF01082 | 0.695 |
MOD_Cter_Amidation | 848 | 851 | PF01082 | 0.687 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.604 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.606 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.655 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.676 |
MOD_GlcNHglycan | 303 | 307 | PF01048 | 0.680 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.666 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.325 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.339 |
MOD_GlcNHglycan | 55 | 59 | PF01048 | 0.776 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.341 |
MOD_GlcNHglycan | 64 | 68 | PF01048 | 0.624 |
MOD_GlcNHglycan | 821 | 824 | PF01048 | 0.717 |
MOD_GlcNHglycan | 842 | 845 | PF01048 | 0.829 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.634 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.582 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.651 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.543 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.534 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.538 |
MOD_GSK3_1 | 708 | 715 | PF00069 | 0.533 |
MOD_GSK3_1 | 833 | 840 | PF00069 | 0.679 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.665 |
MOD_N-GLC_1 | 626 | 631 | PF02516 | 0.519 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.545 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.660 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.505 |
MOD_NEK2_1 | 574 | 579 | PF00069 | 0.488 |
MOD_NEK2_1 | 591 | 596 | PF00069 | 0.606 |
MOD_NEK2_1 | 660 | 665 | PF00069 | 0.520 |
MOD_PIKK_1 | 199 | 205 | PF00454 | 0.546 |
MOD_PIKK_1 | 345 | 351 | PF00454 | 0.637 |
MOD_PIKK_1 | 626 | 632 | PF00454 | 0.519 |
MOD_PKA_1 | 260 | 266 | PF00069 | 0.541 |
MOD_PKA_1 | 353 | 359 | PF00069 | 0.603 |
MOD_PKA_1 | 502 | 508 | PF00069 | 0.573 |
MOD_PKA_1 | 7 | 13 | PF00069 | 0.695 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.543 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.645 |
MOD_PKA_2 | 379 | 385 | PF00069 | 0.760 |
MOD_PKA_2 | 477 | 483 | PF00069 | 0.473 |
MOD_PKA_2 | 577 | 583 | PF00069 | 0.534 |
MOD_PKA_2 | 587 | 593 | PF00069 | 0.541 |
MOD_PKA_2 | 840 | 846 | PF00069 | 0.669 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.723 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.700 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.532 |
MOD_Plk_2-3 | 24 | 30 | PF00069 | 0.654 |
MOD_Plk_2-3 | 581 | 587 | PF00069 | 0.539 |
MOD_Plk_4 | 587 | 593 | PF00069 | 0.541 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.610 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.777 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.669 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.393 |
MOD_ProDKin_1 | 470 | 476 | PF00069 | 0.496 |
MOD_ProDKin_1 | 702 | 708 | PF00069 | 0.496 |
MOD_SUMO_for_1 | 334 | 337 | PF00179 | 0.577 |
MOD_SUMO_rev_2 | 2 | 10 | PF00179 | 0.694 |
MOD_SUMO_rev_2 | 367 | 372 | PF00179 | 0.558 |
MOD_SUMO_rev_2 | 395 | 404 | PF00179 | 0.494 |
TRG_DiLeu_BaEn_1 | 526 | 531 | PF01217 | 0.496 |
TRG_DiLeu_BaEn_1 | 792 | 797 | PF01217 | 0.551 |
TRG_DiLeu_BaLyEn_6 | 640 | 645 | PF01217 | 0.539 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.542 |
TRG_ENDOCYTIC_2 | 389 | 392 | PF00928 | 0.572 |
TRG_ENDOCYTIC_2 | 466 | 469 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 512 | 515 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 545 | 548 | PF00928 | 0.561 |
TRG_ENDOCYTIC_2 | 579 | 582 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 613 | 616 | PF00928 | 0.381 |
TRG_ER_diArg_1 | 187 | 189 | PF00400 | 0.725 |
TRG_ER_diArg_1 | 214 | 216 | PF00400 | 0.708 |
TRG_ER_diArg_1 | 225 | 227 | PF00400 | 0.690 |
TRG_ER_diArg_1 | 259 | 261 | PF00400 | 0.686 |
TRG_ER_diArg_1 | 266 | 268 | PF00400 | 0.648 |
TRG_ER_diArg_1 | 280 | 283 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 352 | 354 | PF00400 | 0.726 |
TRG_ER_diArg_1 | 361 | 363 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 40 | 43 | PF00400 | 0.699 |
TRG_ER_diArg_1 | 609 | 611 | PF00400 | 0.403 |
TRG_ER_diArg_1 | 672 | 674 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 763 | 765 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 806 | 808 | PF00400 | 0.728 |
TRG_Pf-PMV_PEXEL_1 | 491 | 496 | PF00026 | 0.333 |
TRG_Pf-PMV_PEXEL_1 | 672 | 677 | PF00026 | 0.378 |
TRG_Pf-PMV_PEXEL_1 | 763 | 768 | PF00026 | 0.504 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCW9 | Leptomonas seymouri | 68% | 97% |
A0A0S4JDN6 | Bodo saltans | 49% | 100% |
A0A3Q8IJ79 | Leishmania donovani | 80% | 94% |
A0A3Q8IQY6 | Leishmania donovani | 36% | 100% |
A4H4Y0 | Leishmania braziliensis | 39% | 100% |
A4HK20 | Leishmania braziliensis | 50% | 100% |
A4HP82 | Leishmania braziliensis | 36% | 100% |
A4IBK1 | Leishmania infantum | 79% | 93% |
A4IDI7 | Leishmania infantum | 36% | 100% |
E9AFD4 | Leishmania major | 91% | 100% |
E9ASZ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9B2G1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9B6I9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 93% |
P24346 | Xenopus laevis | 39% | 100% |
Q4Q1K8 | Leishmania major | 36% | 100% |
Q4Q5M6 | Leishmania major | 27% | 100% |
Q4Q5P5 | Leishmania major | 49% | 100% |
Q4QIQ9 | Leishmania major | 40% | 100% |