Intracellular protein trafficking, adaptor gamma-1 chain
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: 5 |
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030119 | AP-type membrane coat adaptor complex | 3 | 12 |
GO:0030121 | AP-1 adaptor complex | 5 | 12 |
GO:0030131 | clathrin adaptor complex | 4 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0098796 | membrane protein complex | 2 | 12 |
Related structures:
AlphaFold database: A4IAG8
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0006886 | intracellular protein transport | 4 | 12 |
GO:0008104 | protein localization | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0015031 | protein transport | 4 | 12 |
GO:0016192 | vesicle-mediated transport | 4 | 12 |
GO:0033036 | macromolecule localization | 2 | 12 |
GO:0045184 | establishment of protein localization | 3 | 12 |
GO:0046907 | intracellular transport | 3 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051641 | cellular localization | 2 | 12 |
GO:0051649 | establishment of localization in cell | 3 | 12 |
GO:0070727 | cellular macromolecule localization | 3 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0071705 | nitrogen compound transport | 4 | 12 |
GO:0006892 | post-Golgi vesicle-mediated transport | 6 | 1 |
GO:0006896 | Golgi to vacuole transport | 5 | 1 |
GO:0006897 | endocytosis | 5 | 1 |
GO:0006898 | receptor-mediated endocytosis | 6 | 1 |
GO:0007034 | vacuolar transport | 4 | 1 |
GO:0048193 | Golgi vesicle transport | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0030276 | clathrin binding | 3 | 1 |
GO:0030674 | protein-macromolecule adaptor activity | 2 | 1 |
GO:0035615 | clathrin adaptor activity | 4 | 1 |
GO:0060090 | molecular adaptor activity | 1 | 1 |
GO:0140312 | cargo adaptor activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 148 | 152 | PF00656 | 0.426 |
CLV_C14_Caspase3-7 | 2 | 6 | PF00656 | 0.588 |
CLV_C14_Caspase3-7 | 288 | 292 | PF00656 | 0.253 |
CLV_C14_Caspase3-7 | 331 | 335 | PF00656 | 0.271 |
CLV_C14_Caspase3-7 | 687 | 691 | PF00656 | 0.481 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.268 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 437 | 441 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.334 |
DEG_APCC_DBOX_1 | 146 | 154 | PF00400 | 0.268 |
DEG_APCC_DBOX_1 | 49 | 57 | PF00400 | 0.268 |
DEG_ODPH_VHL_1 | 782 | 794 | PF01847 | 0.281 |
DEG_SPOP_SBC_1 | 674 | 678 | PF00917 | 0.511 |
DOC_CYCLIN_RxL_1 | 233 | 242 | PF00134 | 0.253 |
DOC_CYCLIN_RxL_1 | 374 | 384 | PF00134 | 0.287 |
DOC_CYCLIN_yClb1_LxF_4 | 334 | 340 | PF00134 | 0.313 |
DOC_MAPK_gen_1 | 375 | 383 | PF00069 | 0.253 |
DOC_MAPK_gen_1 | 440 | 450 | PF00069 | 0.268 |
DOC_MAPK_gen_1 | 48 | 56 | PF00069 | 0.308 |
DOC_MAPK_gen_1 | 488 | 496 | PF00069 | 0.396 |
DOC_MAPK_MEF2A_6 | 375 | 383 | PF00069 | 0.253 |
DOC_MAPK_MEF2A_6 | 488 | 496 | PF00069 | 0.396 |
DOC_MAPK_MEF2A_6 | 50 | 58 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 85 | 93 | PF00069 | 0.257 |
DOC_MAPK_NFAT4_5 | 376 | 384 | PF00069 | 0.268 |
DOC_MAPK_RevD_3 | 362 | 376 | PF00069 | 0.313 |
DOC_PP1_RVXF_1 | 258 | 265 | PF00149 | 0.253 |
DOC_PP2B_LxvP_1 | 393 | 396 | PF13499 | 0.268 |
DOC_PP2B_PxIxI_1 | 44 | 50 | PF00149 | 0.329 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.306 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.329 |
DOC_USP7_MATH_1 | 668 | 672 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 694 | 698 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 703 | 707 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 724 | 728 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 749 | 753 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 777 | 781 | PF00917 | 0.307 |
DOC_USP7_MATH_2 | 608 | 614 | PF00917 | 0.530 |
DOC_USP7_UBL2_3 | 544 | 548 | PF12436 | 0.347 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.404 |
DOC_WW_Pin1_4 | 638 | 643 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 659 | 664 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 710 | 715 | PF00397 | 0.629 |
LIG_14-3-3_CanoR_1 | 119 | 125 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 243 | 249 | PF00244 | 0.268 |
LIG_14-3-3_CanoR_1 | 327 | 333 | PF00244 | 0.313 |
LIG_14-3-3_CanoR_1 | 415 | 421 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 673 | 681 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 769 | 774 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 809 | 815 | PF00244 | 0.323 |
LIG_Actin_WH2_2 | 322 | 340 | PF00022 | 0.313 |
LIG_Actin_WH2_2 | 425 | 442 | PF00022 | 0.365 |
LIG_AP2alpha_2 | 254 | 256 | PF02296 | 0.268 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.526 |
LIG_BIR_III_2 | 42 | 46 | PF00653 | 0.305 |
LIG_BIR_III_2 | 551 | 555 | PF00653 | 0.305 |
LIG_BRCT_BRCA1_1 | 349 | 353 | PF00533 | 0.269 |
LIG_BRCT_BRCA1_1 | 434 | 438 | PF00533 | 0.455 |
LIG_BRCT_BRCA1_1 | 477 | 481 | PF00533 | 0.287 |
LIG_BRCT_BRCA1_1 | 741 | 745 | PF00533 | 0.416 |
LIG_BRCT_BRCA1_2 | 434 | 440 | PF00533 | 0.329 |
LIG_Clathr_ClatBox_1 | 630 | 634 | PF01394 | 0.632 |
LIG_deltaCOP1_diTrp_1 | 471 | 481 | PF00928 | 0.329 |
LIG_DLG_GKlike_1 | 120 | 127 | PF00625 | 0.281 |
LIG_eIF4E_1 | 124 | 130 | PF01652 | 0.396 |
LIG_eIF4E_1 | 537 | 543 | PF01652 | 0.253 |
LIG_eIF4E_1 | 88 | 94 | PF01652 | 0.396 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.374 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.364 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.370 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.325 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.327 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.275 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.347 |
LIG_FHA_1 | 577 | 583 | PF00498 | 0.268 |
LIG_FHA_1 | 622 | 628 | PF00498 | 0.642 |
LIG_FHA_1 | 644 | 650 | PF00498 | 0.693 |
LIG_FHA_1 | 770 | 776 | PF00498 | 0.267 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.253 |
LIG_FHA_2 | 19 | 25 | PF00498 | 0.368 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.253 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.298 |
LIG_FHA_2 | 512 | 518 | PF00498 | 0.329 |
LIG_FHA_2 | 563 | 569 | PF00498 | 0.287 |
LIG_FHA_2 | 624 | 630 | PF00498 | 0.630 |
LIG_FXI_DFP_1 | 582 | 586 | PF00024 | 0.477 |
LIG_LIR_Gen_1 | 123 | 132 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 253 | 264 | PF02991 | 0.233 |
LIG_LIR_Gen_1 | 350 | 361 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 435 | 446 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 501 | 510 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 529 | 539 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 577 | 586 | PF02991 | 0.254 |
LIG_LIR_Gen_1 | 592 | 601 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 65 | 75 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 730 | 739 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 742 | 750 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 123 | 127 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 253 | 259 | PF02991 | 0.233 |
LIG_LIR_Nem_3 | 350 | 356 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 435 | 441 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 501 | 505 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 529 | 534 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 577 | 581 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 664 | 670 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 678 | 684 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 730 | 734 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 742 | 748 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 79 | 84 | PF02991 | 0.338 |
LIG_LYPXL_SIV_4 | 45 | 53 | PF13949 | 0.396 |
LIG_LYPXL_SIV_4 | 784 | 792 | PF13949 | 0.305 |
LIG_NRBOX | 341 | 347 | PF00104 | 0.293 |
LIG_PCNA_yPIPBox_3 | 258 | 266 | PF02747 | 0.253 |
LIG_PCNA_yPIPBox_3 | 280 | 294 | PF02747 | 0.265 |
LIG_PCNA_yPIPBox_3 | 535 | 543 | PF02747 | 0.350 |
LIG_Pex14_1 | 430 | 434 | PF04695 | 0.313 |
LIG_Pex14_2 | 681 | 685 | PF04695 | 0.560 |
LIG_PTB_Apo_2 | 525 | 532 | PF02174 | 0.318 |
LIG_SH2_CRK | 401 | 405 | PF00017 | 0.396 |
LIG_SH2_CRK | 578 | 582 | PF00017 | 0.287 |
LIG_SH2_PTP2 | 46 | 49 | PF00017 | 0.329 |
LIG_SH2_PTP2 | 502 | 505 | PF00017 | 0.313 |
LIG_SH2_STAP1 | 434 | 438 | PF00017 | 0.347 |
LIG_SH2_STAP1 | 578 | 582 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.203 |
LIG_SH2_STAT5 | 578 | 581 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 814 | 817 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.253 |
LIG_SH3_3 | 580 | 586 | PF00018 | 0.409 |
LIG_SH3_3 | 595 | 601 | PF00018 | 0.564 |
LIG_SH3_3 | 636 | 642 | PF00018 | 0.702 |
LIG_SUMO_SIM_anti_2 | 382 | 387 | PF11976 | 0.253 |
LIG_SUMO_SIM_anti_2 | 501 | 507 | PF11976 | 0.313 |
LIG_SUMO_SIM_anti_2 | 764 | 769 | PF11976 | 0.439 |
LIG_SUMO_SIM_anti_2 | 96 | 106 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 205 | 210 | PF11976 | 0.329 |
LIG_SUMO_SIM_par_1 | 318 | 324 | PF11976 | 0.329 |
LIG_SUMO_SIM_par_1 | 380 | 387 | PF11976 | 0.287 |
LIG_SUMO_SIM_par_1 | 453 | 460 | PF11976 | 0.338 |
LIG_SUMO_SIM_par_1 | 579 | 584 | PF11976 | 0.461 |
LIG_SUMO_SIM_par_1 | 607 | 613 | PF11976 | 0.638 |
LIG_SUMO_SIM_par_1 | 96 | 106 | PF11976 | 0.263 |
LIG_TRAF2_1 | 21 | 24 | PF00917 | 0.377 |
LIG_TYR_ITIM | 122 | 127 | PF00017 | 0.379 |
LIG_TYR_ITIM | 300 | 305 | PF00017 | 0.253 |
LIG_TYR_ITIM | 399 | 404 | PF00017 | 0.268 |
LIG_TYR_ITIM | 86 | 91 | PF00017 | 0.268 |
LIG_UBA3_1 | 149 | 158 | PF00899 | 0.379 |
LIG_UBA3_1 | 454 | 463 | PF00899 | 0.385 |
LIG_UBA3_1 | 744 | 753 | PF00899 | 0.281 |
LIG_WRC_WIRS_1 | 557 | 562 | PF05994 | 0.389 |
LIG_WRC_WIRS_1 | 590 | 595 | PF05994 | 0.437 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.253 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.287 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.537 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.327 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.289 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.355 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.303 |
MOD_CK1_1 | 640 | 646 | PF00069 | 0.668 |
MOD_CK1_1 | 659 | 665 | PF00069 | 0.554 |
MOD_CK1_1 | 697 | 703 | PF00069 | 0.578 |
MOD_CK1_1 | 706 | 712 | PF00069 | 0.642 |
MOD_CK1_1 | 752 | 758 | PF00069 | 0.343 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.253 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.376 |
MOD_CK2_1 | 416 | 422 | PF00069 | 0.410 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.334 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.379 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.336 |
MOD_GlcNHglycan | 664 | 667 | PF01048 | 0.643 |
MOD_GlcNHglycan | 687 | 690 | PF01048 | 0.683 |
MOD_GlcNHglycan | 696 | 699 | PF01048 | 0.658 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.640 |
MOD_GlcNHglycan | 735 | 738 | PF01048 | 0.282 |
MOD_GlcNHglycan | 80 | 84 | PF01048 | 0.396 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.396 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.253 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.256 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.337 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.392 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.362 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.366 |
MOD_GSK3_1 | 634 | 641 | PF00069 | 0.643 |
MOD_GSK3_1 | 652 | 659 | PF00069 | 0.634 |
MOD_GSK3_1 | 662 | 669 | PF00069 | 0.558 |
MOD_GSK3_1 | 706 | 713 | PF00069 | 0.720 |
MOD_N-GLC_1 | 527 | 532 | PF02516 | 0.318 |
MOD_N-GLC_1 | 562 | 567 | PF02516 | 0.317 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.358 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.280 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.331 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.403 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.268 |
MOD_NEK2_1 | 591 | 596 | PF00069 | 0.497 |
MOD_NEK2_1 | 739 | 744 | PF00069 | 0.302 |
MOD_NEK2_1 | 761 | 766 | PF00069 | 0.369 |
MOD_NEK2_1 | 825 | 830 | PF00069 | 0.329 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.441 |
MOD_NEK2_2 | 370 | 375 | PF00069 | 0.248 |
MOD_NEK2_2 | 703 | 708 | PF00069 | 0.773 |
MOD_PIKK_1 | 457 | 463 | PF00454 | 0.360 |
MOD_PIKK_1 | 591 | 597 | PF00454 | 0.498 |
MOD_PIKK_1 | 612 | 618 | PF00454 | 0.611 |
MOD_PIKK_1 | 652 | 658 | PF00454 | 0.757 |
MOD_PIKK_1 | 668 | 674 | PF00454 | 0.726 |
MOD_PIKK_1 | 74 | 80 | PF00454 | 0.396 |
MOD_PIKK_1 | 794 | 800 | PF00454 | 0.433 |
MOD_PIKK_1 | 825 | 831 | PF00454 | 0.396 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.308 |
MOD_PKA_2 | 810 | 816 | PF00069 | 0.329 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.253 |
MOD_Plk_1 | 379 | 385 | PF00069 | 0.253 |
MOD_Plk_1 | 432 | 438 | PF00069 | 0.253 |
MOD_Plk_1 | 475 | 481 | PF00069 | 0.243 |
MOD_Plk_1 | 527 | 533 | PF00069 | 0.352 |
MOD_Plk_1 | 562 | 568 | PF00069 | 0.329 |
MOD_Plk_1 | 576 | 582 | PF00069 | 0.268 |
MOD_Plk_1 | 703 | 709 | PF00069 | 0.729 |
MOD_Plk_2-3 | 100 | 106 | PF00069 | 0.253 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.430 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.388 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.305 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.298 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.398 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.369 |
MOD_Plk_4 | 521 | 527 | PF00069 | 0.353 |
MOD_Plk_4 | 577 | 583 | PF00069 | 0.253 |
MOD_Plk_4 | 645 | 651 | PF00069 | 0.731 |
MOD_Plk_4 | 656 | 662 | PF00069 | 0.716 |
MOD_Plk_4 | 697 | 703 | PF00069 | 0.578 |
MOD_Plk_4 | 739 | 745 | PF00069 | 0.381 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.404 |
MOD_ProDKin_1 | 638 | 644 | PF00069 | 0.639 |
MOD_ProDKin_1 | 659 | 665 | PF00069 | 0.652 |
MOD_ProDKin_1 | 710 | 716 | PF00069 | 0.627 |
MOD_SUMO_for_1 | 707 | 710 | PF00179 | 0.585 |
TRG_DiLeu_BaEn_1 | 100 | 105 | PF01217 | 0.442 |
TRG_DiLeu_BaEn_1 | 125 | 130 | PF01217 | 0.396 |
TRG_DiLeu_BaEn_1 | 501 | 506 | PF01217 | 0.268 |
TRG_DiLeu_BaEn_1 | 577 | 582 | PF01217 | 0.313 |
TRG_DiLeu_BaEn_1 | 71 | 76 | PF01217 | 0.253 |
TRG_DiLeu_BaLyEn_6 | 11 | 16 | PF01217 | 0.418 |
TRG_DiLeu_BaLyEn_6 | 389 | 394 | PF01217 | 0.268 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.253 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 502 | 505 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.258 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.203 |
TRG_ENDOCYTIC_2 | 578 | 581 | PF00928 | 0.253 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.253 |
TRG_ER_diArg_1 | 374 | 377 | PF00400 | 0.253 |
TRG_ER_diArg_1 | 47 | 50 | PF00400 | 0.268 |
TRG_ER_diArg_1 | 808 | 811 | PF00400 | 0.329 |
TRG_NES_CRM1_1 | 199 | 210 | PF08389 | 0.389 |
TRG_NES_CRM1_1 | 759 | 774 | PF08389 | 0.396 |
TRG_Pf-PMV_PEXEL_1 | 14 | 18 | PF00026 | 0.556 |
TRG_Pf-PMV_PEXEL_1 | 147 | 151 | PF00026 | 0.396 |
TRG_Pf-PMV_PEXEL_1 | 392 | 397 | PF00026 | 0.253 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P707 | Leptomonas seymouri | 72% | 100% |
A0A0N1I3J7 | Leptomonas seymouri | 20% | 76% |
A0A0N1PA13 | Leptomonas seymouri | 26% | 86% |
A0A0S4JAH1 | Bodo saltans | 25% | 79% |
A0A0S4JIE7 | Bodo saltans | 40% | 95% |
A0A1X0NLY4 | Trypanosomatidae | 26% | 86% |
A0A1X0P1U8 | Trypanosomatidae | 26% | 81% |
A0A1X0PA59 | Trypanosomatidae | 51% | 100% |
A0A3Q8IHK1 | Leishmania donovani | 100% | 100% |
A0A3S7WPR4 | Leishmania donovani | 26% | 86% |
A0A422NSY3 | Trypanosoma rangeli | 48% | 100% |
A0A422NT90 | Trypanosoma rangeli | 25% | 86% |
A0A422P3I9 | Trypanosoma rangeli | 25% | 83% |
A4H4U8 | Leishmania braziliensis | 26% | 100% |
A4HBC0 | Leishmania braziliensis | 83% | 100% |
A4HT27 | Leishmania infantum | 26% | 100% |
C9ZLS4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AL15 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B5J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
O43747 | Homo sapiens | 30% | 100% |
O75843 | Homo sapiens | 35% | 100% |
O88512 | Mus musculus | 35% | 100% |
O94973 | Homo sapiens | 23% | 88% |
O95782 | Homo sapiens | 23% | 85% |
P17426 | Mus musculus | 23% | 85% |
P17427 | Mus musculus | 23% | 89% |
P18484 | Rattus norvegicus | 23% | 89% |
P22892 | Mus musculus | 30% | 100% |
P38065 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 21% | 81% |
P91926 | Drosophila melanogaster | 24% | 88% |
Q0VCK5 | Bos taurus | 24% | 89% |
Q12028 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 100% |
Q29N38 | Drosophila pseudoobscura pseudoobscura | 24% | 88% |
Q4Q2E4 | Leishmania major | 93% | 98% |
Q4QIT9 | Leishmania major | 26% | 100% |
Q5R5M2 | Pongo abelii | 30% | 100% |
Q7QG73 | Anopheles gambiae | 24% | 89% |
Q84K16 | Arabidopsis thaliana | 35% | 95% |
Q86KI1 | Dictyostelium discoideum | 28% | 84% |
Q8I8U2 | Dictyostelium discoideum | 38% | 93% |
Q8L7A9 | Arabidopsis thaliana | 27% | 89% |
Q8LPK4 | Arabidopsis thaliana | 26% | 82% |
Q8LPL6 | Arabidopsis thaliana | 26% | 82% |
Q99128 | Ustilago maydis (strain 521 / FGSC 9021) | 36% | 95% |
Q9C0W7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 95% |
Q9UTL8 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 21% | 100% |
Q9UU81 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 96% |
Q9ZUI6 | Arabidopsis thaliana | 30% | 96% |
V5B8U2 | Trypanosoma cruzi | 26% | 100% |
V5BPJ4 | Trypanosoma cruzi | 26% | 82% |
V5BW37 | Trypanosoma cruzi | 49% | 100% |