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 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0042555 | MCM complex | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H477
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: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 |
GO:0003697 | single-stranded DNA binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 450 | 454 | PF00656 | 0.510 |
CLV_C14_Caspase3-7 | 512 | 516 | PF00656 | 0.425 |
CLV_C14_Caspase3-7 | 751 | 755 | PF00656 | 0.517 |
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 744 | 746 | PF00675 | 0.579 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 744 | 746 | PF00082 | 0.579 |
CLV_PCSK_PC1ET2_1 | 4 | 6 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.199 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 601 | 605 | PF00082 | 0.244 |
CLV_PCSK_SKI1_1 | 656 | 660 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 779 | 783 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 925 | 929 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 968 | 972 | PF00082 | 0.385 |
DEG_APCC_DBOX_1 | 937 | 945 | PF00400 | 0.468 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.541 |
DEG_SPOP_SBC_1 | 190 | 194 | PF00917 | 0.493 |
DEG_SPOP_SBC_1 | 607 | 611 | PF00917 | 0.508 |
DOC_CKS1_1 | 846 | 851 | PF01111 | 0.478 |
DOC_CYCLIN_RxL_1 | 776 | 786 | PF00134 | 0.355 |
DOC_CYCLIN_yCln2_LP_2 | 102 | 108 | PF00134 | 0.498 |
DOC_MAPK_DCC_7 | 68 | 76 | PF00069 | 0.432 |
DOC_MAPK_gen_1 | 422 | 429 | PF00069 | 0.510 |
DOC_MAPK_gen_1 | 924 | 931 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 553 | 560 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 573 | 580 | PF00069 | 0.358 |
DOC_MAPK_NFAT4_5 | 553 | 561 | PF00069 | 0.508 |
DOC_PP1_RVXF_1 | 777 | 784 | PF00149 | 0.346 |
DOC_PP2B_LxvP_1 | 355 | 358 | PF13499 | 0.358 |
DOC_PP2B_LxvP_1 | 74 | 77 | PF13499 | 0.461 |
DOC_PP2B_LxvP_1 | 772 | 775 | PF13499 | 0.472 |
DOC_PP2B_LxvP_1 | 903 | 906 | PF13499 | 0.445 |
DOC_PP4_FxxP_1 | 676 | 679 | PF00568 | 0.451 |
DOC_PP4_FxxP_1 | 846 | 849 | PF00568 | 0.477 |
DOC_SPAK_OSR1_1 | 714 | 718 | PF12202 | 0.429 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.391 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 607 | 611 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 914 | 918 | PF00917 | 0.571 |
DOC_USP7_UBL2_3 | 924 | 928 | PF12436 | 0.460 |
DOC_USP7_UBL2_3 | 986 | 990 | PF12436 | 0.453 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 705 | 710 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 845 | 850 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 855 | 860 | PF00397 | 0.444 |
LIG_14-3-3_CanoR_1 | 180 | 190 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 208 | 214 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 248 | 256 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 394 | 399 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 49 | 55 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 506 | 514 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 537 | 543 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 835 | 842 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 968 | 977 | PF00244 | 0.370 |
LIG_APCC_ABBA_1 | 950 | 955 | PF00400 | 0.359 |
LIG_BRCT_BRCA1_1 | 842 | 846 | PF00533 | 0.479 |
LIG_CtBP_PxDLS_1 | 548 | 553 | PF00389 | 0.451 |
LIG_deltaCOP1_diTrp_1 | 56 | 62 | PF00928 | 0.415 |
LIG_EH1_1 | 96 | 104 | PF00400 | 0.481 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.491 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.501 |
LIG_FHA_1 | 493 | 499 | PF00498 | 0.514 |
LIG_FHA_1 | 537 | 543 | PF00498 | 0.465 |
LIG_FHA_1 | 614 | 620 | PF00498 | 0.465 |
LIG_FHA_1 | 664 | 670 | PF00498 | 0.545 |
LIG_FHA_1 | 680 | 686 | PF00498 | 0.391 |
LIG_FHA_1 | 734 | 740 | PF00498 | 0.451 |
LIG_FHA_1 | 817 | 823 | PF00498 | 0.634 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.499 |
LIG_FHA_1 | 969 | 975 | PF00498 | 0.360 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.532 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.406 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.441 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.631 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.359 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.498 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.616 |
LIG_FHA_2 | 626 | 632 | PF00498 | 0.451 |
LIG_FHA_2 | 641 | 647 | PF00498 | 0.451 |
LIG_FHA_2 | 880 | 886 | PF00498 | 0.451 |
LIG_LIR_Apic_2 | 275 | 279 | PF02991 | 0.508 |
LIG_LIR_Apic_2 | 843 | 849 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 155 | 163 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 221 | 231 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 56 | 66 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 713 | 721 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 95 | 105 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 221 | 226 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 311 | 316 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 56 | 62 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 713 | 718 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 899 | 903 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 95 | 100 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 979 | 983 | PF02991 | 0.301 |
LIG_PALB2_WD40_1 | 530 | 538 | PF16756 | 0.451 |
LIG_Pex14_2 | 157 | 161 | PF04695 | 0.362 |
LIG_SH2_CRK | 210 | 214 | PF00017 | 0.408 |
LIG_SH2_CRK | 980 | 984 | PF00017 | 0.292 |
LIG_SH2_NCK_1 | 210 | 214 | PF00017 | 0.408 |
LIG_SH2_STAP1 | 50 | 54 | PF00017 | 0.582 |
LIG_SH2_STAP1 | 888 | 892 | PF00017 | 0.451 |
LIG_SH2_STAT3 | 804 | 807 | PF00017 | 0.385 |
LIG_SH2_STAT3 | 888 | 891 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 804 | 807 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 861 | 864 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 991 | 994 | PF00017 | 0.351 |
LIG_SH3_1 | 436 | 442 | PF00018 | 0.512 |
LIG_SH3_2 | 105 | 110 | PF14604 | 0.638 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.616 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.428 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.520 |
LIG_SH3_3 | 436 | 442 | PF00018 | 0.512 |
LIG_SH3_3 | 578 | 584 | PF00018 | 0.470 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.429 |
LIG_SUMO_SIM_par_1 | 149 | 155 | PF11976 | 0.360 |
LIG_SUMO_SIM_par_1 | 349 | 354 | PF11976 | 0.388 |
LIG_SUMO_SIM_par_1 | 577 | 583 | PF11976 | 0.451 |
LIG_SUMO_SIM_par_1 | 657 | 663 | PF11976 | 0.451 |
LIG_SUMO_SIM_par_1 | 72 | 78 | PF11976 | 0.712 |
LIG_SUMO_SIM_par_1 | 90 | 96 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 957 | 964 | PF11976 | 0.442 |
LIG_TRAF2_1 | 518 | 521 | PF00917 | 0.435 |
LIG_UBA3_1 | 546 | 553 | PF00899 | 0.451 |
LIG_WRC_WIRS_1 | 897 | 902 | PF05994 | 0.416 |
MOD_CDC14_SPxK_1 | 245 | 248 | PF00782 | 0.451 |
MOD_CDK_SPK_2 | 855 | 860 | PF00069 | 0.451 |
MOD_CDK_SPxK_1 | 242 | 248 | PF00069 | 0.451 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.630 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.625 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.599 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.462 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.489 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.545 |
MOD_CK1_1 | 625 | 631 | PF00069 | 0.451 |
MOD_CK1_1 | 724 | 730 | PF00069 | 0.391 |
MOD_CK1_1 | 845 | 851 | PF00069 | 0.497 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.536 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.519 |
MOD_CK2_1 | 515 | 521 | PF00069 | 0.449 |
MOD_CK2_1 | 625 | 631 | PF00069 | 0.451 |
MOD_CK2_1 | 927 | 933 | PF00069 | 0.364 |
MOD_Cter_Amidation | 108 | 111 | PF01082 | 0.502 |
MOD_Cter_Amidation | 2 | 5 | PF01082 | 0.630 |
MOD_Cter_Amidation | 922 | 925 | PF01082 | 0.633 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.616 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.337 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.308 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.630 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.463 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.739 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.610 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.554 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.489 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.446 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.244 |
MOD_GlcNHglycan | 624 | 627 | PF01048 | 0.251 |
MOD_GlcNHglycan | 765 | 768 | PF01048 | 0.479 |
MOD_GlcNHglycan | 8 | 12 | PF01048 | 0.622 |
MOD_GlcNHglycan | 842 | 845 | PF01048 | 0.548 |
MOD_GlcNHglycan | 907 | 910 | PF01048 | 0.543 |
MOD_GlcNHglycan | 916 | 919 | PF01048 | 0.558 |
MOD_GlcNHglycan | 968 | 971 | PF01048 | 0.402 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.536 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.451 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.578 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.579 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.571 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.417 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.592 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.451 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.469 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.527 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.647 |
MOD_GSK3_1 | 816 | 823 | PF00069 | 0.555 |
MOD_GSK3_1 | 834 | 841 | PF00069 | 0.567 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.570 |
MOD_GSK3_1 | 892 | 899 | PF00069 | 0.451 |
MOD_N-GLC_1 | 336 | 341 | PF02516 | 0.519 |
MOD_N-GLC_1 | 705 | 710 | PF02516 | 0.251 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.547 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.572 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.446 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.684 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.462 |
MOD_NEK2_1 | 556 | 561 | PF00069 | 0.451 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.451 |
MOD_NEK2_1 | 615 | 620 | PF00069 | 0.500 |
MOD_NEK2_1 | 674 | 679 | PF00069 | 0.451 |
MOD_NEK2_1 | 695 | 700 | PF00069 | 0.441 |
MOD_NEK2_1 | 721 | 726 | PF00069 | 0.399 |
MOD_NEK2_1 | 763 | 768 | PF00069 | 0.466 |
MOD_NEK2_1 | 783 | 788 | PF00069 | 0.360 |
MOD_NEK2_1 | 853 | 858 | PF00069 | 0.288 |
MOD_NEK2_1 | 892 | 897 | PF00069 | 0.451 |
MOD_NEK2_2 | 927 | 932 | PF00069 | 0.375 |
MOD_OFUCOSY | 606 | 613 | PF10250 | 0.251 |
MOD_PIKK_1 | 327 | 333 | PF00454 | 0.660 |
MOD_PIKK_1 | 336 | 342 | PF00454 | 0.475 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.554 |
MOD_PIKK_1 | 586 | 592 | PF00454 | 0.472 |
MOD_PIKK_1 | 783 | 789 | PF00454 | 0.360 |
MOD_PK_1 | 394 | 400 | PF00069 | 0.307 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.605 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.441 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.513 |
MOD_PKA_2 | 484 | 490 | PF00069 | 0.557 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.671 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.456 |
MOD_PKA_2 | 572 | 578 | PF00069 | 0.456 |
MOD_PKA_2 | 680 | 686 | PF00069 | 0.534 |
MOD_PKA_2 | 721 | 727 | PF00069 | 0.391 |
MOD_PKA_2 | 834 | 840 | PF00069 | 0.488 |
MOD_Plk_1 | 308 | 314 | PF00069 | 0.451 |
MOD_Plk_1 | 626 | 632 | PF00069 | 0.451 |
MOD_Plk_1 | 853 | 859 | PF00069 | 0.368 |
MOD_Plk_2-3 | 266 | 272 | PF00069 | 0.387 |
MOD_Plk_2-3 | 309 | 315 | PF00069 | 0.623 |
MOD_Plk_2-3 | 361 | 367 | PF00069 | 0.369 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.451 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.623 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.496 |
MOD_Plk_4 | 497 | 503 | PF00069 | 0.455 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.538 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.451 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.451 |
MOD_Plk_4 | 680 | 686 | PF00069 | 0.456 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.524 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.586 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.451 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.570 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.532 |
MOD_ProDKin_1 | 705 | 711 | PF00069 | 0.451 |
MOD_ProDKin_1 | 845 | 851 | PF00069 | 0.580 |
MOD_ProDKin_1 | 855 | 861 | PF00069 | 0.444 |
MOD_SUMO_for_1 | 873 | 876 | PF00179 | 0.451 |
MOD_SUMO_rev_2 | 376 | 385 | PF00179 | 0.382 |
MOD_SUMO_rev_2 | 649 | 658 | PF00179 | 0.451 |
TRG_DiLeu_BaEn_1 | 300 | 305 | PF01217 | 0.508 |
TRG_DiLeu_BaEn_1 | 654 | 659 | PF01217 | 0.451 |
TRG_DiLeu_BaEn_1 | 979 | 984 | PF01217 | 0.385 |
TRG_DiLeu_BaEn_4 | 300 | 306 | PF01217 | 0.508 |
TRG_DiLeu_BaLyEn_6 | 61 | 66 | PF01217 | 0.432 |
TRG_DiLeu_BaLyEn_6 | 98 | 103 | PF01217 | 0.541 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 980 | 983 | PF00928 | 0.295 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 393 | 396 | PF00400 | 0.373 |
TRG_ER_diArg_1 | 483 | 486 | PF00400 | 0.496 |
TRG_Pf-PMV_PEXEL_1 | 399 | 404 | PF00026 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 656 | 660 | PF00026 | 0.251 |
TRG_Pf-PMV_PEXEL_1 | 975 | 979 | PF00026 | 0.387 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAM6 | Leptomonas seymouri | 64% | 99% |
A0A3S5H5H2 | Leishmania donovani | 80% | 100% |
A4HSF2 | Leishmania infantum | 79% | 100% |
E9AKD9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 99% |
F4KAB8 | Arabidopsis thaliana | 26% | 100% |
Q4QJG9 | Leishmania major | 80% | 99% |
Q86B14 | Dictyostelium discoideum | 25% | 100% |