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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 10 |
GO:0012505 | endomembrane system | 2 | 9 |
GO:0032991 | protein-containing complex | 1 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005768 | endosome | 7 | 1 |
GO:0030897 | HOPS complex | 3 | 1 |
GO:0031410 | cytoplasmic vesicle | 6 | 1 |
GO:0031982 | vesicle | 4 | 1 |
GO:0097708 | intracellular vesicle | 5 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
GO:0099023 | vesicle tethering complex | 2 | 1 |
Related structures:
AlphaFold database: A4H9L7
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 10 |
GO:0006886 | intracellular protein transport | 4 | 10 |
GO:0006996 | organelle organization | 4 | 10 |
GO:0007033 | vacuole organization | 5 | 10 |
GO:0008104 | protein localization | 4 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0015031 | protein transport | 4 | 10 |
GO:0016043 | cellular component organization | 3 | 10 |
GO:0033036 | macromolecule localization | 2 | 10 |
GO:0045184 | establishment of protein localization | 3 | 10 |
GO:0046907 | intracellular transport | 3 | 10 |
GO:0051179 | localization | 1 | 10 |
GO:0051234 | establishment of localization | 2 | 10 |
GO:0051641 | cellular localization | 2 | 10 |
GO:0051649 | establishment of localization in cell | 3 | 10 |
GO:0070727 | cellular macromolecule localization | 3 | 10 |
GO:0071702 | organic substance transport | 4 | 10 |
GO:0071705 | nitrogen compound transport | 4 | 10 |
GO:0071840 | cellular component organization or biogenesis | 2 | 10 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0016197 | endosomal transport | 4 | 1 |
GO:0042144 | vacuole fusion, non-autophagic | 7 | 1 |
GO:0048284 | organelle fusion | 5 | 1 |
GO:0097576 | vacuole fusion | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003779 | actin binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0008092 | cytoskeletal protein binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 323 | 327 | PF00656 | 0.480 |
CLV_C14_Caspase3-7 | 829 | 833 | PF00656 | 0.463 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.560 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 595 | 597 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 707 | 709 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 844 | 846 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 880 | 882 | PF00082 | 0.314 |
CLV_PCSK_PC1ET2_1 | 429 | 431 | PF00082 | 0.323 |
CLV_PCSK_PC1ET2_1 | 455 | 457 | PF00082 | 0.487 |
CLV_PCSK_PC1ET2_1 | 595 | 597 | PF00082 | 0.422 |
CLV_PCSK_PC1ET2_1 | 707 | 709 | PF00082 | 0.395 |
CLV_PCSK_PC1ET2_1 | 84 | 86 | PF00082 | 0.192 |
CLV_PCSK_PC1ET2_1 | 844 | 846 | PF00082 | 0.422 |
CLV_PCSK_PC1ET2_1 | 880 | 882 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 775 | 779 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 790 | 794 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 802 | 806 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 828 | 832 | PF00082 | 0.399 |
DEG_APCC_DBOX_1 | 351 | 359 | PF00400 | 0.464 |
DEG_APCC_DBOX_1 | 86 | 94 | PF00400 | 0.211 |
DEG_SCF_FBW7_1 | 205 | 212 | PF00400 | 0.211 |
DOC_CYCLIN_RxL_1 | 167 | 179 | PF00134 | 0.367 |
DOC_CYCLIN_RxL_1 | 215 | 224 | PF00134 | 0.211 |
DOC_MAPK_DCC_7 | 460 | 470 | PF00069 | 0.556 |
DOC_MAPK_gen_1 | 275 | 281 | PF00069 | 0.211 |
DOC_MAPK_gen_1 | 352 | 360 | PF00069 | 0.211 |
DOC_MAPK_gen_1 | 455 | 465 | PF00069 | 0.497 |
DOC_MAPK_gen_1 | 84 | 90 | PF00069 | 0.192 |
DOC_MAPK_gen_1 | 9 | 19 | PF00069 | 0.330 |
DOC_MAPK_MEF2A_6 | 103 | 112 | PF00069 | 0.404 |
DOC_PP1_RVXF_1 | 248 | 255 | PF00149 | 0.379 |
DOC_PP1_RVXF_1 | 352 | 358 | PF00149 | 0.211 |
DOC_PP2B_LxvP_1 | 174 | 177 | PF13499 | 0.379 |
DOC_PP2B_LxvP_1 | 231 | 234 | PF13499 | 0.464 |
DOC_PP4_FxxP_1 | 793 | 796 | PF00568 | 0.422 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.383 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.224 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.390 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.233 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.334 |
DOC_USP7_MATH_1 | 621 | 625 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 702 | 706 | PF00917 | 0.514 |
DOC_USP7_UBL2_3 | 197 | 201 | PF12436 | 0.211 |
DOC_USP7_UBL2_3 | 537 | 541 | PF12436 | 0.534 |
DOC_USP7_UBL2_3 | 892 | 896 | PF12436 | 0.323 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.323 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.342 |
DOC_WW_Pin1_4 | 710 | 715 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 721 | 726 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.318 |
LIG_14-3-3_CanoR_1 | 181 | 190 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 275 | 281 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 367 | 372 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 439 | 445 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 488 | 492 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 523 | 527 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 617 | 625 | PF00244 | 0.211 |
LIG_14-3-3_CanoR_1 | 782 | 786 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 788 | 796 | PF00244 | 0.381 |
LIG_Actin_WH2_2 | 580 | 597 | PF00022 | 0.422 |
LIG_BRCT_BRCA1_1 | 211 | 215 | PF00533 | 0.464 |
LIG_BRCT_BRCA1_1 | 264 | 268 | PF00533 | 0.238 |
LIG_BRCT_BRCA1_1 | 446 | 450 | PF00533 | 0.440 |
LIG_BRCT_BRCA1_1 | 869 | 873 | PF00533 | 0.464 |
LIG_Clathr_ClatBox_1 | 189 | 193 | PF01394 | 0.466 |
LIG_Clathr_ClatBox_1 | 319 | 323 | PF01394 | 0.347 |
LIG_Clathr_ClatBox_1 | 511 | 515 | PF01394 | 0.274 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.379 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.464 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.285 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.216 |
LIG_FHA_1 | 563 | 569 | PF00498 | 0.298 |
LIG_FHA_1 | 580 | 586 | PF00498 | 0.181 |
LIG_FHA_1 | 606 | 612 | PF00498 | 0.327 |
LIG_FHA_1 | 629 | 635 | PF00498 | 0.478 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.430 |
LIG_FHA_1 | 836 | 842 | PF00498 | 0.453 |
LIG_FHA_1 | 913 | 919 | PF00498 | 0.567 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.420 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.358 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.313 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.421 |
LIG_FHA_2 | 628 | 634 | PF00498 | 0.440 |
LIG_FHA_2 | 827 | 833 | PF00498 | 0.422 |
LIG_FHA_2 | 859 | 865 | PF00498 | 0.464 |
LIG_GBD_Chelix_1 | 535 | 543 | PF00786 | 0.504 |
LIG_LIR_Apic_2 | 791 | 796 | PF02991 | 0.351 |
LIG_LIR_Apic_2 | 842 | 846 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 114 | 122 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 143 | 153 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 15 | 24 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 226 | 235 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 265 | 274 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 383 | 392 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 440 | 449 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 547 | 555 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 604 | 614 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 685 | 693 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 739 | 750 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 811 | 820 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 114 | 119 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 143 | 149 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 15 | 19 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 202 | 207 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 226 | 231 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 383 | 387 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 440 | 444 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 49 | 54 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 547 | 551 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 685 | 691 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 720 | 726 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 739 | 745 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 759 | 763 | PF02991 | 0.134 |
LIG_LIR_Nem_3 | 811 | 817 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 864 | 868 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 906 | 912 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 919 | 923 | PF02991 | 0.573 |
LIG_MAD2 | 239 | 247 | PF02301 | 0.464 |
LIG_Pex14_2 | 437 | 441 | PF04695 | 0.323 |
LIG_Pex14_2 | 920 | 924 | PF04695 | 0.601 |
LIG_PTB_Apo_2 | 110 | 117 | PF02174 | 0.476 |
LIG_SH2_CRK | 51 | 55 | PF00017 | 0.447 |
LIG_SH2_CRK | 763 | 767 | PF00017 | 0.464 |
LIG_SH2_CRK | 843 | 847 | PF00017 | 0.422 |
LIG_SH2_GRB2like | 33 | 36 | PF00017 | 0.211 |
LIG_SH2_PTP2 | 638 | 641 | PF00017 | 0.492 |
LIG_SH2_STAP1 | 33 | 37 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 384 | 388 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 638 | 641 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 662 | 665 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 668 | 671 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 808 | 811 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 852 | 855 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 866 | 869 | PF00017 | 0.323 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.312 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.379 |
LIG_Sin3_3 | 146 | 153 | PF02671 | 0.464 |
LIG_SUMO_SIM_anti_2 | 106 | 112 | PF11976 | 0.347 |
LIG_SUMO_SIM_anti_2 | 185 | 191 | PF11976 | 0.453 |
LIG_SUMO_SIM_anti_2 | 269 | 275 | PF11976 | 0.397 |
LIG_SUMO_SIM_par_1 | 108 | 114 | PF11976 | 0.347 |
LIG_SUMO_SIM_par_1 | 188 | 194 | PF11976 | 0.464 |
LIG_SUMO_SIM_par_1 | 510 | 515 | PF11976 | 0.504 |
LIG_SUMO_SIM_par_1 | 53 | 59 | PF11976 | 0.256 |
LIG_SUMO_SIM_par_1 | 567 | 572 | PF11976 | 0.412 |
LIG_SUMO_SIM_par_1 | 582 | 589 | PF11976 | 0.307 |
LIG_SxIP_EBH_1 | 849 | 858 | PF03271 | 0.464 |
LIG_TYR_ITIM | 636 | 641 | PF00017 | 0.492 |
LIG_UBA3_1 | 887 | 896 | PF00899 | 0.323 |
LIG_WRC_WIRS_1 | 281 | 286 | PF05994 | 0.211 |
LIG_WRC_WIRS_1 | 548 | 553 | PF05994 | 0.211 |
MOD_CDK_SPK_2 | 56 | 61 | PF00069 | 0.211 |
MOD_CDK_SPK_2 | 710 | 715 | PF00069 | 0.632 |
MOD_CDK_SPxxK_3 | 243 | 250 | PF00069 | 0.379 |
MOD_CDK_SPxxK_3 | 77 | 84 | PF00069 | 0.211 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.211 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.456 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.211 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.328 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.399 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.386 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.436 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.211 |
MOD_CK1_1 | 682 | 688 | PF00069 | 0.616 |
MOD_CK1_1 | 713 | 719 | PF00069 | 0.617 |
MOD_CK1_1 | 821 | 827 | PF00069 | 0.367 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.420 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.313 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.444 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.422 |
MOD_CK2_1 | 547 | 553 | PF00069 | 0.318 |
MOD_CK2_1 | 583 | 589 | PF00069 | 0.399 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.332 |
MOD_CK2_1 | 733 | 739 | PF00069 | 0.438 |
MOD_CK2_1 | 858 | 864 | PF00069 | 0.433 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.476 |
MOD_GlcNHglycan | 391 | 395 | PF01048 | 0.391 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.415 |
MOD_GlcNHglycan | 446 | 450 | PF01048 | 0.512 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.234 |
MOD_GlcNHglycan | 684 | 687 | PF01048 | 0.642 |
MOD_GlcNHglycan | 728 | 731 | PF01048 | 0.534 |
MOD_GlcNHglycan | 768 | 771 | PF01048 | 0.422 |
MOD_GlcNHglycan | 805 | 808 | PF01048 | 0.357 |
MOD_GlcNHglycan | 818 | 823 | PF01048 | 0.410 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.464 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.385 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.381 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.395 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.379 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.413 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.317 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.337 |
MOD_GSK3_1 | 713 | 720 | PF00069 | 0.611 |
MOD_GSK3_1 | 766 | 773 | PF00069 | 0.323 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.367 |
MOD_GSK3_1 | 818 | 825 | PF00069 | 0.405 |
MOD_GSK3_1 | 835 | 842 | PF00069 | 0.283 |
MOD_GSK3_1 | 908 | 915 | PF00069 | 0.434 |
MOD_N-GLC_1 | 224 | 229 | PF02516 | 0.438 |
MOD_N-GLC_1 | 63 | 68 | PF02516 | 0.332 |
MOD_N-GLC_2 | 121 | 123 | PF02516 | 0.476 |
MOD_N-GLC_2 | 328 | 330 | PF02516 | 0.442 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.427 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.385 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.464 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.389 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.391 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.211 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.391 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.427 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.422 |
MOD_NEK2_1 | 605 | 610 | PF00069 | 0.323 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.402 |
MOD_NEK2_1 | 766 | 771 | PF00069 | 0.323 |
MOD_NEK2_1 | 912 | 917 | PF00069 | 0.506 |
MOD_NEK2_2 | 522 | 527 | PF00069 | 0.606 |
MOD_NEK2_2 | 770 | 775 | PF00069 | 0.422 |
MOD_PIKK_1 | 575 | 581 | PF00454 | 0.471 |
MOD_PIKK_1 | 642 | 648 | PF00454 | 0.372 |
MOD_PIKK_1 | 677 | 683 | PF00454 | 0.624 |
MOD_PIKK_1 | 713 | 719 | PF00454 | 0.465 |
MOD_PIKK_1 | 751 | 757 | PF00454 | 0.417 |
MOD_PIKK_1 | 886 | 892 | PF00454 | 0.352 |
MOD_PIKK_1 | 910 | 916 | PF00454 | 0.576 |
MOD_PK_1 | 367 | 373 | PF00069 | 0.268 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.395 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.211 |
MOD_PKA_2 | 487 | 493 | PF00069 | 0.542 |
MOD_PKA_2 | 522 | 528 | PF00069 | 0.604 |
MOD_PKA_2 | 562 | 568 | PF00069 | 0.360 |
MOD_PKA_2 | 616 | 622 | PF00069 | 0.379 |
MOD_PKA_2 | 781 | 787 | PF00069 | 0.420 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.400 |
MOD_PKB_1 | 615 | 623 | PF00069 | 0.211 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.464 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.438 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.323 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.323 |
MOD_Plk_1 | 390 | 396 | PF00069 | 0.379 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.211 |
MOD_Plk_1 | 445 | 451 | PF00069 | 0.552 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.211 |
MOD_Plk_1 | 751 | 757 | PF00069 | 0.389 |
MOD_Plk_2-3 | 684 | 690 | PF00069 | 0.523 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.509 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.327 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.311 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.347 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.328 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.383 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.356 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.430 |
MOD_Plk_4 | 579 | 585 | PF00069 | 0.318 |
MOD_Plk_4 | 664 | 670 | PF00069 | 0.311 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.285 |
MOD_Plk_4 | 733 | 739 | PF00069 | 0.565 |
MOD_Plk_4 | 826 | 832 | PF00069 | 0.362 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.459 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.323 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.342 |
MOD_ProDKin_1 | 710 | 716 | PF00069 | 0.642 |
MOD_ProDKin_1 | 721 | 727 | PF00069 | 0.624 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.318 |
MOD_SUMO_for_1 | 857 | 860 | PF00179 | 0.464 |
MOD_SUMO_rev_2 | 151 | 159 | PF00179 | 0.453 |
MOD_SUMO_rev_2 | 193 | 203 | PF00179 | 0.211 |
MOD_SUMO_rev_2 | 503 | 512 | PF00179 | 0.503 |
MOD_SUMO_rev_2 | 687 | 697 | PF00179 | 0.467 |
TRG_DiLeu_BaEn_1 | 752 | 757 | PF01217 | 0.323 |
TRG_DiLeu_BaEn_2 | 352 | 358 | PF01217 | 0.464 |
TRG_DiLeu_BaEn_2 | 68 | 74 | PF01217 | 0.211 |
TRG_DiLeu_BaLyEn_6 | 427 | 432 | PF01217 | 0.422 |
TRG_DiLeu_BaLyEn_6 | 481 | 486 | PF01217 | 0.508 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 638 | 641 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 662 | 665 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 763 | 766 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 865 | 868 | PF00928 | 0.347 |
TRG_ER_diArg_1 | 274 | 276 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 456 | 459 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 614 | 617 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 85 | 88 | PF00400 | 0.192 |
TRG_NES_CRM1_1 | 182 | 196 | PF08389 | 0.464 |
TRG_NES_CRM1_1 | 503 | 515 | PF08389 | 0.286 |
TRG_NLS_MonoCore_2 | 83 | 88 | PF00514 | 0.192 |
TRG_NLS_MonoExtN_4 | 81 | 88 | PF00514 | 0.192 |
TRG_Pf-PMV_PEXEL_1 | 741 | 746 | PF00026 | 0.393 |
TRG_Pf-PMV_PEXEL_1 | 903 | 907 | PF00026 | 0.538 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I839 | Leptomonas seymouri | 70% | 100% |
A0A1X0P477 | Trypanosomatidae | 23% | 92% |
A0A1X0P6Z7 | Trypanosomatidae | 39% | 100% |
A0A3S7WUZ3 | Leishmania donovani | 88% | 100% |
A0A422P0I7 | Trypanosoma rangeli | 38% | 100% |
A4HXY1 | Leishmania infantum | 88% | 100% |
D0A5C7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9ARP4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q11182 | Caenorhabditis elegans | 22% | 100% |
Q4QDT5 | Leishmania major | 88% | 100% |
Q55C58 | Dictyostelium discoideum | 25% | 100% |
Q5E9L7 | Bos taurus | 26% | 100% |
Q920Q4 | Mus musculus | 25% | 100% |
Q93VQ0 | Arabidopsis thaliana | 26% | 100% |
Q9H269 | Homo sapiens | 26% | 100% |
Q9UT38 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
V5BGG7 | Trypanosoma cruzi | 23% | 92% |