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: A0A3S5H5H2
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 | 119 | 123 | PF00656 | 0.548 |
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.433 |
CLV_C14_Caspase3-7 | 928 | 932 | PF00656 | 0.337 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 707 | 709 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 754 | 756 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 922 | 924 | PF00675 | 0.630 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 754 | 756 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 922 | 924 | PF00082 | 0.630 |
CLV_PCSK_PC1ET2_1 | 180 | 182 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.224 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 611 | 615 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 666 | 670 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 787 | 791 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 923 | 927 | PF00082 | 0.536 |
DEG_APCC_DBOX_1 | 935 | 943 | PF00400 | 0.510 |
DEG_SCF_TRCP1_1 | 844 | 849 | PF00400 | 0.613 |
DEG_SPOP_SBC_1 | 617 | 621 | PF00917 | 0.533 |
DOC_ANK_TNKS_1 | 180 | 187 | PF00023 | 0.595 |
DOC_ANK_TNKS_1 | 3 | 10 | PF00023 | 0.650 |
DOC_ANK_TNKS_1 | 472 | 479 | PF00023 | 0.668 |
DOC_CKS1_1 | 105 | 110 | PF01111 | 0.630 |
DOC_CYCLIN_RxL_1 | 784 | 794 | PF00134 | 0.374 |
DOC_CYCLIN_yCln2_LP_2 | 102 | 108 | PF00134 | 0.523 |
DOC_CYCLIN_yCln2_LP_2 | 144 | 150 | PF00134 | 0.360 |
DOC_MAPK_MEF2A_6 | 563 | 570 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 583 | 590 | PF00069 | 0.383 |
DOC_MAPK_NFAT4_5 | 563 | 571 | PF00069 | 0.533 |
DOC_PP1_RVXF_1 | 515 | 521 | PF00149 | 0.609 |
DOC_PP1_RVXF_1 | 785 | 792 | PF00149 | 0.368 |
DOC_PP2B_LxvP_1 | 363 | 366 | PF13499 | 0.386 |
DOC_PP2B_LxvP_1 | 780 | 783 | PF13499 | 0.504 |
DOC_PP4_FxxP_1 | 686 | 689 | PF00568 | 0.476 |
DOC_SPAK_OSR1_1 | 724 | 728 | PF12202 | 0.454 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 511 | 515 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 617 | 621 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 707 | 711 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 734 | 738 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 830 | 834 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 911 | 915 | PF00917 | 0.702 |
DOC_USP7_UBL2_3 | 984 | 988 | PF12436 | 0.489 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 715 | 720 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 861 | 866 | PF00397 | 0.470 |
LIG_14-3-3_CanoR_1 | 168 | 177 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 248 | 256 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 404 | 410 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 49 | 55 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 517 | 527 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 547 | 553 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 708 | 712 | PF00244 | 0.483 |
LIG_BRCT_BRCA1_1 | 520 | 524 | PF00533 | 0.548 |
LIG_CtBP_PxDLS_1 | 558 | 563 | PF00389 | 0.476 |
LIG_deltaCOP1_diTrp_1 | 29 | 36 | PF00928 | 0.512 |
LIG_EH1_1 | 147 | 155 | PF00400 | 0.329 |
LIG_EH1_1 | 96 | 104 | PF00400 | 0.501 |
LIG_eIF4E_1 | 148 | 154 | PF01652 | 0.333 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.592 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.511 |
LIG_FHA_1 | 547 | 553 | PF00498 | 0.476 |
LIG_FHA_1 | 624 | 630 | PF00498 | 0.476 |
LIG_FHA_1 | 674 | 680 | PF00498 | 0.570 |
LIG_FHA_1 | 690 | 696 | PF00498 | 0.410 |
LIG_FHA_1 | 744 | 750 | PF00498 | 0.476 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.528 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.435 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.466 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.533 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.391 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.630 |
LIG_FHA_2 | 636 | 642 | PF00498 | 0.476 |
LIG_FHA_2 | 651 | 657 | PF00498 | 0.476 |
LIG_FHA_2 | 721 | 727 | PF00498 | 0.433 |
LIG_FHA_2 | 886 | 892 | PF00498 | 0.476 |
LIG_Integrin_RGD_1 | 473 | 475 | PF01839 | 0.676 |
LIG_LIR_Apic_2 | 275 | 279 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 145 | 156 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 221 | 231 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 57 | 66 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 723 | 731 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 91 | 102 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 221 | 226 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 57 | 62 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 723 | 728 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 905 | 909 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.549 |
LIG_PALB2_WD40_1 | 540 | 548 | PF16756 | 0.476 |
LIG_Pex14_1 | 161 | 165 | PF04695 | 0.411 |
LIG_Pex14_2 | 157 | 161 | PF04695 | 0.398 |
LIG_Pex14_2 | 520 | 524 | PF04695 | 0.548 |
LIG_SH2_CRK | 210 | 214 | PF00017 | 0.442 |
LIG_SH2_NCK_1 | 210 | 214 | PF00017 | 0.442 |
LIG_SH2_PTP2 | 148 | 151 | PF00017 | 0.340 |
LIG_SH2_STAP1 | 50 | 54 | PF00017 | 0.590 |
LIG_SH2_STAP1 | 894 | 898 | PF00017 | 0.476 |
LIG_SH2_STAT3 | 812 | 815 | PF00017 | 0.413 |
LIG_SH2_STAT3 | 894 | 897 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 812 | 815 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 867 | 870 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 989 | 992 | PF00017 | 0.381 |
LIG_SH3_2 | 105 | 110 | PF14604 | 0.677 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.633 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.483 |
LIG_SH3_3 | 588 | 594 | PF00018 | 0.470 |
LIG_SH3_3 | 845 | 851 | PF00018 | 0.610 |
LIG_SUMO_SIM_par_1 | 149 | 155 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 357 | 362 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 587 | 593 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 667 | 673 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 72 | 78 | PF11976 | 0.725 |
LIG_SUMO_SIM_par_1 | 955 | 962 | PF11976 | 0.468 |
LIG_TRAF2_1 | 528 | 531 | PF00917 | 0.455 |
LIG_UBA3_1 | 556 | 563 | PF00899 | 0.476 |
LIG_WRC_WIRS_1 | 903 | 908 | PF05994 | 0.468 |
MOD_CDC14_SPxK_1 | 245 | 248 | PF00782 | 0.476 |
MOD_CDK_SPK_2 | 861 | 866 | PF00069 | 0.476 |
MOD_CDK_SPxK_1 | 104 | 110 | PF00069 | 0.621 |
MOD_CDK_SPxK_1 | 242 | 248 | PF00069 | 0.476 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.673 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.744 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.807 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.548 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.558 |
MOD_CK1_1 | 507 | 513 | PF00069 | 0.616 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.516 |
MOD_CK1_1 | 635 | 641 | PF00069 | 0.476 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.514 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.328 |
MOD_CK2_1 | 525 | 531 | PF00069 | 0.466 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.630 |
MOD_CK2_1 | 635 | 641 | PF00069 | 0.476 |
MOD_Cter_Amidation | 178 | 181 | PF01082 | 0.563 |
MOD_Cter_Amidation | 920 | 923 | PF01082 | 0.681 |
MOD_DYRK1A_RPxSP_1 | 190 | 194 | PF00069 | 0.644 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.585 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.724 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.361 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.511 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.337 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.671 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.564 |
MOD_GlcNHglycan | 413 | 417 | PF01048 | 0.582 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.614 |
MOD_GlcNHglycan | 506 | 509 | PF01048 | 0.731 |
MOD_GlcNHglycan | 513 | 516 | PF01048 | 0.607 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.453 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.387 |
MOD_GlcNHglycan | 611 | 614 | PF01048 | 0.270 |
MOD_GlcNHglycan | 634 | 637 | PF01048 | 0.276 |
MOD_GlcNHglycan | 737 | 740 | PF01048 | 0.254 |
MOD_GlcNHglycan | 844 | 847 | PF01048 | 0.705 |
MOD_GlcNHglycan | 848 | 851 | PF01048 | 0.585 |
MOD_GlcNHglycan | 911 | 914 | PF01048 | 0.580 |
MOD_GlcNHglycan | 943 | 948 | PF01048 | 0.494 |
MOD_GlcNHglycan | 966 | 969 | PF01048 | 0.424 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.476 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.531 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.600 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.589 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.707 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.476 |
MOD_GSK3_1 | 619 | 626 | PF00069 | 0.494 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.552 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.633 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.577 |
MOD_GSK3_1 | 840 | 847 | PF00069 | 0.598 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.581 |
MOD_GSK3_1 | 898 | 905 | PF00069 | 0.476 |
MOD_N-GLC_1 | 715 | 720 | PF02516 | 0.276 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.661 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.533 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.682 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.476 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.477 |
MOD_NEK2_1 | 596 | 601 | PF00069 | 0.476 |
MOD_NEK2_1 | 625 | 630 | PF00069 | 0.526 |
MOD_NEK2_1 | 684 | 689 | PF00069 | 0.476 |
MOD_NEK2_1 | 791 | 796 | PF00069 | 0.373 |
MOD_NEK2_1 | 842 | 847 | PF00069 | 0.636 |
MOD_NEK2_1 | 859 | 864 | PF00069 | 0.314 |
MOD_NEK2_1 | 898 | 903 | PF00069 | 0.476 |
MOD_NEK2_1 | 909 | 914 | PF00069 | 0.568 |
MOD_NEK2_2 | 405 | 410 | PF00069 | 0.485 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.644 |
MOD_OFUCOSY | 616 | 623 | PF10250 | 0.276 |
MOD_PIKK_1 | 170 | 176 | PF00454 | 0.559 |
MOD_PIKK_1 | 266 | 272 | PF00454 | 0.449 |
MOD_PIKK_1 | 327 | 333 | PF00454 | 0.716 |
MOD_PIKK_1 | 344 | 350 | PF00454 | 0.528 |
MOD_PIKK_1 | 408 | 414 | PF00454 | 0.599 |
MOD_PIKK_1 | 596 | 602 | PF00454 | 0.476 |
MOD_PIKK_1 | 791 | 797 | PF00454 | 0.373 |
MOD_PIKK_1 | 925 | 931 | PF00454 | 0.386 |
MOD_PKA_1 | 168 | 174 | PF00069 | 0.549 |
MOD_PKA_1 | 265 | 271 | PF00069 | 0.433 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.466 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.518 |
MOD_PKA_2 | 516 | 522 | PF00069 | 0.649 |
MOD_PKA_2 | 546 | 552 | PF00069 | 0.476 |
MOD_PKA_2 | 582 | 588 | PF00069 | 0.476 |
MOD_PKA_2 | 690 | 696 | PF00069 | 0.559 |
MOD_PKA_2 | 707 | 713 | PF00069 | 0.405 |
MOD_PKB_1 | 190 | 198 | PF00069 | 0.552 |
MOD_Plk_1 | 308 | 314 | PF00069 | 0.476 |
MOD_Plk_1 | 636 | 642 | PF00069 | 0.476 |
MOD_Plk_1 | 859 | 865 | PF00069 | 0.393 |
MOD_Plk_2-3 | 309 | 315 | PF00069 | 0.533 |
MOD_Plk_2-3 | 369 | 375 | PF00069 | 0.400 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.324 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.476 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.533 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.538 |
MOD_Plk_4 | 552 | 558 | PF00069 | 0.476 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.476 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.476 |
MOD_Plk_4 | 690 | 696 | PF00069 | 0.476 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.621 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.664 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.614 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.476 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.509 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.474 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.562 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.623 |
MOD_ProDKin_1 | 715 | 721 | PF00069 | 0.503 |
MOD_ProDKin_1 | 861 | 867 | PF00069 | 0.470 |
MOD_SUMO_for_1 | 879 | 882 | PF00179 | 0.476 |
MOD_SUMO_rev_2 | 659 | 668 | PF00179 | 0.476 |
TRG_DiLeu_BaEn_1 | 300 | 305 | PF01217 | 0.533 |
TRG_DiLeu_BaEn_1 | 664 | 669 | PF01217 | 0.476 |
TRG_DiLeu_BaEn_1 | 977 | 982 | PF01217 | 0.411 |
TRG_DiLeu_BaEn_4 | 300 | 306 | PF01217 | 0.533 |
TRG_DiLeu_BaLyEn_6 | 98 | 103 | PF01217 | 0.553 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.436 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 401 | 404 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 429 | 432 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 922 | 924 | PF00400 | 0.630 |
TRG_NLS_Bipartite_1 | 168 | 184 | PF00514 | 0.516 |
TRG_NLS_MonoExtC_3 | 179 | 185 | PF00514 | 0.570 |
TRG_NLS_MonoExtN_4 | 177 | 184 | PF00514 | 0.565 |
TRG_Pf-PMV_PEXEL_1 | 407 | 412 | PF00026 | 0.576 |
TRG_Pf-PMV_PEXEL_1 | 666 | 670 | PF00026 | 0.276 |
TRG_Pf-PMV_PEXEL_1 | 973 | 977 | PF00026 | 0.412 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAM6 | Leptomonas seymouri | 63% | 99% |
A4H477 | Leishmania braziliensis | 80% | 99% |
A4HSF2 | Leishmania infantum | 99% | 100% |
E9AKD9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QJG9 | Leishmania major | 92% | 99% |