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: A0A3S7WUZ3
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 | 230 | 234 | PF00656 | 0.428 |
CLV_C14_Caspase3-7 | 736 | 740 | PF00656 | 0.464 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.421 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.384 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 751 | 753 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 787 | 789 | PF00082 | 0.321 |
CLV_PCSK_PC1ET2_1 | 100 | 102 | PF00082 | 0.384 |
CLV_PCSK_PC1ET2_1 | 336 | 338 | PF00082 | 0.321 |
CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.486 |
CLV_PCSK_PC1ET2_1 | 502 | 504 | PF00082 | 0.421 |
CLV_PCSK_PC1ET2_1 | 751 | 753 | PF00082 | 0.421 |
CLV_PCSK_PC1ET2_1 | 787 | 789 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 682 | 686 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 697 | 701 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 709 | 713 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 735 | 739 | PF00082 | 0.397 |
DEG_APCC_DBOX_1 | 258 | 266 | PF00400 | 0.462 |
DEG_ODPH_VHL_1 | 267 | 278 | PF01847 | 0.384 |
DEG_SPOP_SBC_1 | 623 | 627 | PF00917 | 0.599 |
DOC_CYCLIN_RxL_1 | 69 | 81 | PF00134 | 0.365 |
DOC_MAPK_DCC_7 | 367 | 377 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 100 | 108 | PF00069 | 0.468 |
DOC_MAPK_gen_1 | 362 | 372 | PF00069 | 0.450 |
DOC_PP1_RVXF_1 | 151 | 158 | PF00149 | 0.377 |
DOC_PP2B_LxvP_1 | 134 | 137 | PF13499 | 0.462 |
DOC_PP2B_LxvP_1 | 76 | 79 | PF13499 | 0.370 |
DOC_PP4_FxxP_1 | 700 | 703 | PF00568 | 0.421 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.231 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.353 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.379 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.327 |
DOC_USP7_MATH_1 | 609 | 613 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 820 | 824 | PF00917 | 0.621 |
DOC_USP7_UBL2_3 | 444 | 448 | PF12436 | 0.524 |
DOC_USP7_UBL2_3 | 799 | 803 | PF12436 | 0.321 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.302 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 617 | 622 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 628 | 633 | PF00397 | 0.628 |
LIG_14-3-3_CanoR_1 | 101 | 110 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 178 | 184 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 346 | 352 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 395 | 399 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 430 | 434 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 454 | 461 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 622 | 632 | PF00244 | 0.690 |
LIG_14-3-3_CanoR_1 | 689 | 693 | PF00244 | 0.429 |
LIG_Actin_WH2_2 | 401 | 419 | PF00022 | 0.420 |
LIG_Actin_WH2_2 | 487 | 504 | PF00022 | 0.421 |
LIG_BIR_III_2 | 181 | 185 | PF00653 | 0.287 |
LIG_BRCT_BRCA1_1 | 114 | 118 | PF00533 | 0.462 |
LIG_BRCT_BRCA1_1 | 260 | 264 | PF00533 | 0.323 |
LIG_BRCT_BRCA1_1 | 353 | 357 | PF00533 | 0.437 |
LIG_BRCT_BRCA1_1 | 776 | 780 | PF00533 | 0.462 |
LIG_Clathr_ClatBox_1 | 226 | 230 | PF01394 | 0.346 |
LIG_Clathr_ClatBox_1 | 91 | 95 | PF01394 | 0.462 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.214 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.346 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.341 |
LIG_FHA_1 | 743 | 749 | PF00498 | 0.423 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.462 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.421 |
LIG_FHA_2 | 40 | 46 | PF00498 | 0.421 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.439 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.365 |
LIG_FHA_2 | 734 | 740 | PF00498 | 0.421 |
LIG_FHA_2 | 766 | 772 | PF00498 | 0.462 |
LIG_GBD_Chelix_1 | 408 | 416 | PF00786 | 0.421 |
LIG_GBD_Chelix_1 | 442 | 450 | PF00786 | 0.494 |
LIG_LIR_Apic_2 | 749 | 753 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 129 | 138 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 16 | 24 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 169 | 177 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 261 | 272 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 289 | 299 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 347 | 353 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 354 | 364 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 45 | 55 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 456 | 465 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 511 | 521 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 592 | 600 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 646 | 657 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 718 | 727 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 813 | 822 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 104 | 110 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 129 | 134 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 16 | 21 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 261 | 267 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 289 | 294 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 347 | 351 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 456 | 461 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 592 | 598 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 627 | 633 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 646 | 652 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 666 | 670 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 718 | 724 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 771 | 775 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 826 | 830 | PF02991 | 0.654 |
LIG_LRP6_Inhibitor_1 | 516 | 522 | PF00058 | 0.248 |
LIG_MAD2 | 142 | 150 | PF02301 | 0.462 |
LIG_MLH1_MIPbox_1 | 260 | 264 | PF16413 | 0.406 |
LIG_PCNA_PIPBox_1 | 553 | 562 | PF02747 | 0.406 |
LIG_PCNA_yPIPBox_3 | 553 | 565 | PF02747 | 0.406 |
LIG_Pex14_2 | 344 | 348 | PF04695 | 0.321 |
LIG_Pex14_2 | 827 | 831 | PF04695 | 0.625 |
LIG_PTB_Apo_2 | 12 | 19 | PF02174 | 0.474 |
LIG_SH2_CRK | 670 | 674 | PF00017 | 0.462 |
LIG_SH2_CRK | 750 | 754 | PF00017 | 0.387 |
LIG_SH2_GRB2like | 559 | 562 | PF00017 | 0.400 |
LIG_SH2_PTP2 | 545 | 548 | PF00017 | 0.377 |
LIG_SH2_STAP1 | 220 | 224 | PF00017 | 0.384 |
LIG_SH2_STAP1 | 291 | 295 | PF00017 | 0.377 |
LIG_SH2_STAT3 | 263 | 266 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 545 | 548 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 559 | 562 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 569 | 572 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 715 | 718 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 759 | 762 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 773 | 776 | PF00017 | 0.321 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.377 |
LIG_Sin3_3 | 48 | 55 | PF02671 | 0.462 |
LIG_SUMO_SIM_anti_2 | 172 | 178 | PF11976 | 0.395 |
LIG_SUMO_SIM_anti_2 | 8 | 14 | PF11976 | 0.343 |
LIG_SUMO_SIM_anti_2 | 88 | 93 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 417 | 422 | PF11976 | 0.507 |
LIG_SUMO_SIM_par_1 | 474 | 479 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 490 | 496 | PF11976 | 0.379 |
LIG_SUMO_SIM_par_1 | 8 | 14 | PF11976 | 0.346 |
LIG_SUMO_SIM_par_1 | 90 | 97 | PF11976 | 0.462 |
LIG_SxIP_EBH_1 | 756 | 765 | PF03271 | 0.462 |
LIG_TYR_ITIM | 543 | 548 | PF00017 | 0.346 |
LIG_UBA3_1 | 794 | 803 | PF00899 | 0.321 |
MOD_CDK_SPK_2 | 617 | 622 | PF00069 | 0.613 |
MOD_CDK_SPxxK_3 | 146 | 153 | PF00069 | 0.377 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.441 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.325 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.390 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.395 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.299 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.435 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.498 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.397 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.618 |
MOD_CK1_1 | 625 | 631 | PF00069 | 0.604 |
MOD_CK1_1 | 728 | 734 | PF00069 | 0.389 |
MOD_CK1_1 | 823 | 829 | PF00069 | 0.646 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.462 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.373 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.421 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.479 |
MOD_CK2_1 | 490 | 496 | PF00069 | 0.411 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.439 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.462 |
MOD_CK2_1 | 765 | 771 | PF00069 | 0.431 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.474 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.408 |
MOD_GlcNHglycan | 298 | 302 | PF01048 | 0.365 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.342 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.406 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.647 |
MOD_GlcNHglycan | 675 | 678 | PF01048 | 0.421 |
MOD_GlcNHglycan | 712 | 715 | PF01048 | 0.377 |
MOD_GlcNHglycan | 725 | 730 | PF01048 | 0.349 |
MOD_GlcNHglycan | 822 | 825 | PF01048 | 0.570 |
MOD_GlcNHglycan | 95 | 99 | PF01048 | 0.347 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.383 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.365 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.341 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.384 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.365 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.393 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.346 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.345 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.593 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.314 |
MOD_GSK3_1 | 725 | 732 | PF00069 | 0.436 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.451 |
MOD_GSK3_1 | 742 | 749 | PF00069 | 0.269 |
MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.436 |
MOD_N-GLC_2 | 23 | 25 | PF02516 | 0.478 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.462 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.393 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.313 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.400 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.354 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.407 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.383 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.471 |
MOD_NEK2_1 | 512 | 517 | PF00069 | 0.321 |
MOD_NEK2_1 | 520 | 525 | PF00069 | 0.321 |
MOD_NEK2_1 | 652 | 657 | PF00069 | 0.384 |
MOD_NEK2_1 | 673 | 678 | PF00069 | 0.303 |
MOD_NEK2_1 | 716 | 721 | PF00069 | 0.384 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.418 |
MOD_NEK2_2 | 220 | 225 | PF00069 | 0.384 |
MOD_NEK2_2 | 429 | 434 | PF00069 | 0.599 |
MOD_NEK2_2 | 677 | 682 | PF00069 | 0.421 |
MOD_PIKK_1 | 482 | 488 | PF00454 | 0.414 |
MOD_PIKK_1 | 584 | 590 | PF00454 | 0.625 |
MOD_PIKK_1 | 658 | 664 | PF00454 | 0.421 |
MOD_PIKK_1 | 716 | 722 | PF00454 | 0.397 |
MOD_PIKK_1 | 793 | 799 | PF00454 | 0.351 |
MOD_PKA_1 | 100 | 106 | PF00069 | 0.384 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.418 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.421 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.384 |
MOD_PKA_2 | 394 | 400 | PF00069 | 0.541 |
MOD_PKA_2 | 429 | 435 | PF00069 | 0.593 |
MOD_PKA_2 | 453 | 459 | PF00069 | 0.543 |
MOD_PKA_2 | 523 | 529 | PF00069 | 0.377 |
MOD_PKA_2 | 688 | 694 | PF00069 | 0.418 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.436 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.321 |
MOD_Plk_1 | 297 | 303 | PF00069 | 0.370 |
MOD_Plk_1 | 352 | 358 | PF00069 | 0.551 |
MOD_Plk_1 | 577 | 583 | PF00069 | 0.498 |
MOD_Plk_1 | 658 | 664 | PF00069 | 0.421 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.462 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.350 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.334 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.346 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.346 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.281 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.354 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.361 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.442 |
MOD_Plk_4 | 640 | 646 | PF00069 | 0.558 |
MOD_Plk_4 | 652 | 658 | PF00069 | 0.459 |
MOD_Plk_4 | 733 | 739 | PF00069 | 0.377 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.467 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.302 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.384 |
MOD_ProDKin_1 | 617 | 623 | PF00069 | 0.624 |
MOD_ProDKin_1 | 628 | 634 | PF00069 | 0.622 |
MOD_SUMO_for_1 | 764 | 767 | PF00179 | 0.462 |
MOD_SUMO_rev_2 | 410 | 419 | PF00179 | 0.504 |
MOD_SUMO_rev_2 | 53 | 61 | PF00179 | 0.471 |
MOD_SUMO_rev_2 | 596 | 604 | PF00179 | 0.472 |
TRG_DiLeu_BaEn_1 | 659 | 664 | PF01217 | 0.316 |
TRG_DiLeu_BaEn_2 | 259 | 265 | PF01217 | 0.462 |
TRG_DiLeu_BaLyEn_6 | 334 | 339 | PF01217 | 0.421 |
TRG_DiLeu_BaLyEn_6 | 388 | 393 | PF01217 | 0.502 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 545 | 548 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 569 | 572 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 670 | 673 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 772 | 775 | PF00928 | 0.346 |
TRG_ER_diArg_1 | 177 | 179 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 363 | 366 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 521 | 524 | PF00400 | 0.421 |
TRG_NES_CRM1_1 | 84 | 96 | PF08389 | 0.462 |
TRG_Pf-PMV_PEXEL_1 | 648 | 653 | PF00026 | 0.395 |
TRG_Pf-PMV_PEXEL_1 | 810 | 814 | PF00026 | 0.568 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I839 | Leptomonas seymouri | 69% | 100% |
A0A1X0P6Z7 | Trypanosomatidae | 39% | 90% |
A0A422P0I7 | Trypanosoma rangeli | 38% | 91% |
A4H9L7 | Leishmania braziliensis | 88% | 100% |
A4HXY1 | Leishmania infantum | 100% | 100% |
D0A5C7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 91% |
E9ARP4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4QDT5 | Leishmania major | 96% | 100% |
Q55C58 | Dictyostelium discoideum | 26% | 100% |
Q93VQ0 | Arabidopsis thaliana | 26% | 97% |
Q9H269 | Homo sapiens | 27% | 99% |
Q9UT38 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 100% |
V5BGG7 | Trypanosoma cruzi | 22% | 83% |