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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0042555 | MCM complex | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QJG9
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016043 | cellular component organization | 3 | 7 |
GO:0032392 | DNA geometric change | 7 | 7 |
GO:0032508 | DNA duplex unwinding | 8 | 7 |
GO:0051276 | chromosome organization | 5 | 7 |
GO:0071103 | DNA conformation change | 6 | 7 |
GO:0071840 | cellular component organization or biogenesis | 2 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003677 | DNA binding | 4 | 7 |
GO:0003697 | single-stranded DNA binding | 5 | 2 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 445 | 449 | PF00656 | 0.533 |
CLV_C14_Caspase3-7 | 467 | 471 | PF00656 | 0.575 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 698 | 700 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 745 | 747 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 921 | 923 | PF00675 | 0.701 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 745 | 747 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 921 | 923 | PF00082 | 0.701 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.198 |
CLV_PCSK_SKI1_1 | 554 | 558 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 602 | 606 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 657 | 661 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 778 | 782 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 965 | 969 | PF00082 | 0.386 |
DEG_APCC_DBOX_1 | 934 | 942 | PF00400 | 0.473 |
DEG_SCF_TRCP1_1 | 835 | 840 | PF00400 | 0.588 |
DEG_SPOP_SBC_1 | 608 | 612 | PF00917 | 0.507 |
DOC_ANK_TNKS_1 | 3 | 10 | PF00023 | 0.628 |
DOC_ANK_TNKS_1 | 472 | 479 | PF00023 | 0.649 |
DOC_CKS1_1 | 105 | 110 | PF01111 | 0.592 |
DOC_CKS1_1 | 363 | 368 | PF01111 | 0.315 |
DOC_CYCLIN_RxL_1 | 775 | 785 | PF00134 | 0.351 |
DOC_MAPK_MEF2A_6 | 554 | 561 | PF00069 | 0.450 |
DOC_MAPK_MEF2A_6 | 574 | 581 | PF00069 | 0.357 |
DOC_MAPK_NFAT4_5 | 554 | 562 | PF00069 | 0.507 |
DOC_PP1_RVXF_1 | 506 | 512 | PF00149 | 0.594 |
DOC_PP1_RVXF_1 | 776 | 783 | PF00149 | 0.343 |
DOC_PP2B_LxvP_1 | 771 | 774 | PF13499 | 0.482 |
DOC_PP4_FxxP_1 | 677 | 680 | PF00568 | 0.450 |
DOC_SPAK_OSR1_1 | 695 | 699 | PF12202 | 0.407 |
DOC_SPAK_OSR1_1 | 715 | 719 | PF12202 | 0.428 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 502 | 506 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 608 | 612 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 725 | 729 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 821 | 825 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 902 | 906 | PF00917 | 0.697 |
DOC_USP7_UBL2_3 | 983 | 987 | PF12436 | 0.461 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.450 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.314 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 706 | 711 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 852 | 857 | PF00397 | 0.471 |
LIG_14-3-3_CanoR_1 | 248 | 256 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 404 | 410 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 49 | 55 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 508 | 518 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 538 | 544 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 699 | 703 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 921 | 927 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 965 | 974 | PF00244 | 0.372 |
LIG_APCC_ABBA_1 | 947 | 952 | PF00400 | 0.360 |
LIG_BRCT_BRCA1_1 | 511 | 515 | PF00533 | 0.527 |
LIG_CtBP_PxDLS_1 | 549 | 554 | PF00389 | 0.450 |
LIG_deltaCOP1_diTrp_1 | 29 | 36 | PF00928 | 0.427 |
LIG_deltaCOP1_diTrp_1 | 56 | 62 | PF00928 | 0.366 |
LIG_EH1_1 | 96 | 104 | PF00400 | 0.406 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.641 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.467 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.321 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.551 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.412 |
LIG_FHA_1 | 538 | 544 | PF00498 | 0.450 |
LIG_FHA_1 | 615 | 621 | PF00498 | 0.450 |
LIG_FHA_1 | 665 | 671 | PF00498 | 0.544 |
LIG_FHA_1 | 681 | 687 | PF00498 | 0.407 |
LIG_FHA_1 | 735 | 741 | PF00498 | 0.454 |
LIG_FHA_1 | 799 | 805 | PF00498 | 0.310 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.403 |
LIG_FHA_1 | 966 | 972 | PF00498 | 0.363 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.411 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.507 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.367 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.451 |
LIG_FHA_2 | 627 | 633 | PF00498 | 0.450 |
LIG_FHA_2 | 642 | 648 | PF00498 | 0.457 |
LIG_FHA_2 | 877 | 883 | PF00498 | 0.466 |
LIG_Integrin_RGD_1 | 473 | 475 | PF01839 | 0.655 |
LIG_LIR_Apic_2 | 275 | 279 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 155 | 165 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 221 | 231 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 56 | 66 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 714 | 722 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 91 | 102 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 221 | 226 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 523 | 529 | PF02991 | 0.250 |
LIG_LIR_Nem_3 | 56 | 62 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 714 | 719 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 896 | 900 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.416 |
LIG_PALB2_WD40_1 | 531 | 539 | PF16756 | 0.450 |
LIG_Pex14_1 | 161 | 165 | PF04695 | 0.345 |
LIG_Pex14_2 | 157 | 161 | PF04695 | 0.329 |
LIG_Pex14_2 | 511 | 515 | PF04695 | 0.527 |
LIG_SH2_CRK | 210 | 214 | PF00017 | 0.380 |
LIG_SH2_NCK_1 | 210 | 214 | PF00017 | 0.380 |
LIG_SH2_STAP1 | 50 | 54 | PF00017 | 0.497 |
LIG_SH2_STAP1 | 885 | 889 | PF00017 | 0.450 |
LIG_SH2_STAT3 | 803 | 806 | PF00017 | 0.389 |
LIG_SH2_STAT3 | 885 | 888 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 803 | 806 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 858 | 861 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 988 | 991 | PF00017 | 0.344 |
LIG_SH3_2 | 105 | 110 | PF14604 | 0.639 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.584 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.541 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.457 |
LIG_SH3_3 | 579 | 585 | PF00018 | 0.443 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.427 |
LIG_SH3_3 | 836 | 842 | PF00018 | 0.585 |
LIG_SUMO_SIM_par_1 | 149 | 155 | PF11976 | 0.334 |
LIG_SUMO_SIM_par_1 | 357 | 362 | PF11976 | 0.393 |
LIG_SUMO_SIM_par_1 | 578 | 584 | PF11976 | 0.450 |
LIG_SUMO_SIM_par_1 | 658 | 664 | PF11976 | 0.450 |
LIG_SUMO_SIM_par_1 | 72 | 78 | PF11976 | 0.624 |
LIG_SUMO_SIM_par_1 | 954 | 961 | PF11976 | 0.440 |
LIG_TRAF2_1 | 519 | 522 | PF00917 | 0.441 |
LIG_UBA3_1 | 547 | 554 | PF00899 | 0.450 |
LIG_WRC_WIRS_1 | 894 | 899 | PF05994 | 0.436 |
MOD_CDC14_SPxK_1 | 245 | 248 | PF00782 | 0.450 |
MOD_CDK_SPK_2 | 319 | 324 | PF00069 | 0.627 |
MOD_CDK_SPK_2 | 852 | 857 | PF00069 | 0.450 |
MOD_CDK_SPxK_1 | 104 | 110 | PF00069 | 0.583 |
MOD_CDK_SPxK_1 | 242 | 248 | PF00069 | 0.450 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.553 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.430 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.732 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.786 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.538 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.516 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.494 |
MOD_CK1_1 | 626 | 632 | PF00069 | 0.450 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.449 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.442 |
MOD_CK2_1 | 626 | 632 | PF00069 | 0.450 |
MOD_Cter_Amidation | 2 | 5 | PF01082 | 0.605 |
MOD_Cter_Amidation | 919 | 922 | PF01082 | 0.670 |
MOD_DYRK1A_RPxSP_1 | 190 | 194 | PF00069 | 0.599 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.561 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.685 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.332 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.524 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.307 |
MOD_GlcNHglycan | 325 | 329 | PF01048 | 0.677 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.598 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.538 |
MOD_GlcNHglycan | 413 | 417 | PF01048 | 0.585 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.585 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.650 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.597 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.432 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.372 |
MOD_GlcNHglycan | 602 | 605 | PF01048 | 0.243 |
MOD_GlcNHglycan | 625 | 628 | PF01048 | 0.250 |
MOD_GlcNHglycan | 728 | 731 | PF01048 | 0.250 |
MOD_GlcNHglycan | 827 | 830 | PF01048 | 0.575 |
MOD_GlcNHglycan | 835 | 838 | PF01048 | 0.681 |
MOD_GlcNHglycan | 839 | 842 | PF01048 | 0.561 |
MOD_GlcNHglycan | 902 | 905 | PF01048 | 0.563 |
MOD_GlcNHglycan | 913 | 916 | PF01048 | 0.627 |
MOD_GlcNHglycan | 942 | 947 | PF01048 | 0.440 |
MOD_GlcNHglycan | 965 | 968 | PF01048 | 0.401 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.528 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.452 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.505 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.592 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.569 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.685 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.450 |
MOD_GSK3_1 | 610 | 617 | PF00069 | 0.468 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.526 |
MOD_GSK3_1 | 821 | 828 | PF00069 | 0.581 |
MOD_GSK3_1 | 831 | 838 | PF00069 | 0.572 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.443 |
MOD_GSK3_1 | 889 | 896 | PF00069 | 0.451 |
MOD_N-GLC_1 | 706 | 711 | PF02516 | 0.250 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.564 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.507 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.655 |
MOD_NEK2_1 | 485 | 490 | PF00069 | 0.557 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.450 |
MOD_NEK2_1 | 557 | 562 | PF00069 | 0.450 |
MOD_NEK2_1 | 587 | 592 | PF00069 | 0.453 |
MOD_NEK2_1 | 616 | 621 | PF00069 | 0.499 |
MOD_NEK2_1 | 675 | 680 | PF00069 | 0.450 |
MOD_NEK2_1 | 782 | 787 | PF00069 | 0.350 |
MOD_NEK2_1 | 833 | 838 | PF00069 | 0.610 |
MOD_NEK2_1 | 850 | 855 | PF00069 | 0.325 |
MOD_NEK2_1 | 889 | 894 | PF00069 | 0.450 |
MOD_NEK2_1 | 900 | 905 | PF00069 | 0.538 |
MOD_NEK2_2 | 405 | 410 | PF00069 | 0.456 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.618 |
MOD_OFUCOSY | 607 | 614 | PF10250 | 0.250 |
MOD_PIKK_1 | 170 | 176 | PF00454 | 0.526 |
MOD_PIKK_1 | 327 | 333 | PF00454 | 0.695 |
MOD_PIKK_1 | 344 | 350 | PF00454 | 0.504 |
MOD_PIKK_1 | 408 | 414 | PF00454 | 0.590 |
MOD_PIKK_1 | 587 | 593 | PF00454 | 0.450 |
MOD_PIKK_1 | 782 | 788 | PF00454 | 0.352 |
MOD_PKA_1 | 168 | 174 | PF00069 | 0.515 |
MOD_PKA_1 | 921 | 927 | PF00069 | 0.499 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.457 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.440 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.645 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.422 |
MOD_PKA_2 | 507 | 513 | PF00069 | 0.633 |
MOD_PKA_2 | 537 | 543 | PF00069 | 0.450 |
MOD_PKA_2 | 573 | 579 | PF00069 | 0.450 |
MOD_PKA_2 | 681 | 687 | PF00069 | 0.533 |
MOD_PKA_2 | 698 | 704 | PF00069 | 0.379 |
MOD_PKA_2 | 921 | 927 | PF00069 | 0.566 |
MOD_Plk_1 | 308 | 314 | PF00069 | 0.450 |
MOD_Plk_1 | 627 | 633 | PF00069 | 0.450 |
MOD_Plk_1 | 850 | 856 | PF00069 | 0.367 |
MOD_Plk_2-3 | 309 | 315 | PF00069 | 0.507 |
MOD_Plk_2-3 | 369 | 375 | PF00069 | 0.375 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.452 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.552 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.465 |
MOD_Plk_4 | 543 | 549 | PF00069 | 0.450 |
MOD_Plk_4 | 557 | 563 | PF00069 | 0.450 |
MOD_Plk_4 | 681 | 687 | PF00069 | 0.458 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.583 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.599 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.592 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.450 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.473 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.447 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.313 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.504 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.578 |
MOD_ProDKin_1 | 706 | 712 | PF00069 | 0.468 |
MOD_ProDKin_1 | 852 | 858 | PF00069 | 0.471 |
MOD_SUMO_for_1 | 870 | 873 | PF00179 | 0.450 |
MOD_SUMO_rev_2 | 650 | 659 | PF00179 | 0.452 |
TRG_DiLeu_BaEn_1 | 300 | 305 | PF01217 | 0.507 |
TRG_DiLeu_BaEn_1 | 655 | 660 | PF01217 | 0.450 |
TRG_DiLeu_BaEn_1 | 976 | 981 | PF01217 | 0.387 |
TRG_DiLeu_BaEn_4 | 300 | 306 | PF01217 | 0.507 |
TRG_DiLeu_BaLyEn_6 | 61 | 66 | PF01217 | 0.395 |
TRG_DiLeu_BaLyEn_6 | 98 | 103 | PF01217 | 0.576 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.370 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.380 |
TRG_ER_diArg_1 | 401 | 404 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 429 | 432 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 921 | 923 | PF00400 | 0.637 |
TRG_Pf-PMV_PEXEL_1 | 407 | 412 | PF00026 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 657 | 661 | PF00026 | 0.250 |
TRG_Pf-PMV_PEXEL_1 | 972 | 976 | PF00026 | 0.392 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAM6 | Leptomonas seymouri | 64% | 98% |
A0A3S5H5H2 | Leishmania donovani | 92% | 100% |
A4H477 | Leishmania braziliensis | 80% | 100% |
A4HSF2 | Leishmania infantum | 91% | 100% |
E9AKD9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 99% |
E9AMM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
F4KAB8 | Arabidopsis thaliana | 26% | 100% |