N-acetylglucosamine-1-phosphotransferase homologous protein. Assumed to be a type II TM protein like its distant relatives.. Signal-anchored glycan biogenesis protein essential for mannose 6-P generation (lysosomal signal for the Metazoan hosts). Family only expended in Leishmaniids.. Localization: Golgi (by homology)
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: 120 |
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. | yes | yes: 32 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 37 |
NetGPI | no | yes: 0, no: 37 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 20 |
GO:0110165 | cellular anatomical entity | 1 | 27 |
GO:0005794 | Golgi apparatus | 5 | 9 |
GO:0043226 | organelle | 2 | 9 |
GO:0043227 | membrane-bounded organelle | 3 | 9 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 9 |
Related structures:
AlphaFold database: A0A3Q8IAD3
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 36 |
GO:0016740 | transferase activity | 2 | 36 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 172 | 176 | PF00656 | 0.408 |
CLV_C14_Caspase3-7 | 308 | 312 | PF00656 | 0.479 |
CLV_C14_Caspase3-7 | 420 | 424 | PF00656 | 0.341 |
CLV_C14_Caspase3-7 | 507 | 511 | PF00656 | 0.347 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 264 | 266 | PF00675 | 0.669 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 835 | 837 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 845 | 847 | PF00675 | 0.690 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 835 | 837 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 845 | 847 | PF00082 | 0.693 |
CLV_PCSK_PC1ET2_1 | 77 | 79 | PF00082 | 0.420 |
CLV_PCSK_PC7_1 | 74 | 80 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.647 |
CLV_PCSK_SKI1_1 | 723 | 727 | PF00082 | 0.646 |
CLV_PCSK_SKI1_1 | 732 | 736 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 845 | 849 | PF00082 | 0.585 |
DEG_APCC_DBOX_1 | 280 | 288 | PF00400 | 0.474 |
DEG_APCC_DBOX_1 | 722 | 730 | PF00400 | 0.280 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.602 |
DOC_CYCLIN_yCln2_LP_2 | 568 | 574 | PF00134 | 0.322 |
DOC_MAPK_DCC_7 | 652 | 660 | PF00069 | 0.400 |
DOC_MAPK_gen_1 | 292 | 301 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 366 | 375 | PF00069 | 0.432 |
DOC_MAPK_gen_1 | 561 | 570 | PF00069 | 0.398 |
DOC_MAPK_MEF2A_6 | 368 | 377 | PF00069 | 0.432 |
DOC_MAPK_MEF2A_6 | 483 | 490 | PF00069 | 0.323 |
DOC_MAPK_MEF2A_6 | 563 | 572 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 642 | 649 | PF00069 | 0.567 |
DOC_MAPK_MEF2A_6 | 784 | 791 | PF00069 | 0.455 |
DOC_MIT_MIM_1 | 181 | 190 | PF04212 | 0.364 |
DOC_PP1_RVXF_1 | 221 | 228 | PF00149 | 0.294 |
DOC_PP1_RVXF_1 | 77 | 84 | PF00149 | 0.423 |
DOC_PP1_RVXF_1 | 932 | 939 | PF00149 | 0.377 |
DOC_PP1_RVXF_1 | 964 | 971 | PF00149 | 0.435 |
DOC_PP2B_LxvP_1 | 568 | 571 | PF13499 | 0.394 |
DOC_PP2B_LxvP_1 | 898 | 901 | PF13499 | 0.403 |
DOC_PP4_FxxP_1 | 730 | 733 | PF00568 | 0.414 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 645 | 649 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 675 | 679 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 813 | 817 | PF00917 | 0.295 |
DOC_USP7_MATH_1 | 942 | 946 | PF00917 | 0.449 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.349 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.319 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.396 |
DOC_WW_Pin1_4 | 583 | 588 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 607 | 612 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 880 | 885 | PF00397 | 0.295 |
LIG_14-3-3_CanoR_1 | 129 | 135 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 265 | 271 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 281 | 285 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 31 | 37 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 337 | 342 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 352 | 356 | PF00244 | 0.348 |
LIG_14-3-3_CanoR_1 | 38 | 44 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 51 | 59 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 527 | 537 | PF00244 | 0.326 |
LIG_14-3-3_CanoR_1 | 561 | 570 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 602 | 611 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 68 | 76 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 697 | 706 | PF00244 | 0.321 |
LIG_14-3-3_CanoR_1 | 788 | 792 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 892 | 901 | PF00244 | 0.398 |
LIG_14-3-3_CterR_2 | 973 | 978 | PF00244 | 0.407 |
LIG_Actin_WH2_2 | 21 | 36 | PF00022 | 0.579 |
LIG_Actin_WH2_2 | 322 | 339 | PF00022 | 0.525 |
LIG_Actin_WH2_2 | 592 | 607 | PF00022 | 0.302 |
LIG_Actin_WH2_2 | 796 | 813 | PF00022 | 0.334 |
LIG_BIR_III_4 | 622 | 626 | PF00653 | 0.427 |
LIG_BRCT_BRCA1_1 | 517 | 521 | PF00533 | 0.341 |
LIG_BRCT_BRCA1_1 | 568 | 572 | PF00533 | 0.359 |
LIG_BRCT_BRCA1_1 | 585 | 589 | PF00533 | 0.380 |
LIG_BRCT_BRCA1_1 | 746 | 750 | PF00533 | 0.436 |
LIG_deltaCOP1_diTrp_1 | 964 | 970 | PF00928 | 0.316 |
LIG_DLG_GKlike_1 | 836 | 843 | PF00625 | 0.312 |
LIG_eIF4E_1 | 210 | 216 | PF01652 | 0.278 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.427 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.323 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.373 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.381 |
LIG_FHA_1 | 537 | 543 | PF00498 | 0.232 |
LIG_FHA_1 | 604 | 610 | PF00498 | 0.361 |
LIG_FHA_1 | 668 | 674 | PF00498 | 0.391 |
LIG_FHA_1 | 862 | 868 | PF00498 | 0.348 |
LIG_FHA_1 | 902 | 908 | PF00498 | 0.387 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.307 |
LIG_FHA_1 | 948 | 954 | PF00498 | 0.372 |
LIG_FHA_2 | 252 | 258 | PF00498 | 0.405 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.487 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.480 |
LIG_FHA_2 | 418 | 424 | PF00498 | 0.387 |
LIG_FHA_2 | 458 | 464 | PF00498 | 0.432 |
LIG_FHA_2 | 712 | 718 | PF00498 | 0.291 |
LIG_FHA_2 | 800 | 806 | PF00498 | 0.440 |
LIG_GBD_Chelix_1 | 86 | 94 | PF00786 | 0.317 |
LIG_GBD_Chelix_1 | 99 | 107 | PF00786 | 0.313 |
LIG_Integrin_isoDGR_2 | 165 | 167 | PF01839 | 0.620 |
LIG_LIR_Apic_2 | 108 | 112 | PF02991 | 0.296 |
LIG_LIR_Apic_2 | 728 | 733 | PF02991 | 0.317 |
LIG_LIR_Apic_2 | 950 | 954 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 128 | 138 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 60 | 69 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 956 | 965 | PF02991 | 0.453 |
LIG_LIR_LC3C_4 | 921 | 926 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 128 | 133 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 390 | 396 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 518 | 524 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 586 | 592 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 60 | 65 | PF02991 | 0.640 |
LIG_LIR_Nem_3 | 679 | 685 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 747 | 753 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 908 | 913 | PF02991 | 0.412 |
LIG_MYND_1 | 611 | 615 | PF01753 | 0.411 |
LIG_NRBOX | 88 | 94 | PF00104 | 0.271 |
LIG_PCNA_yPIPBox_3 | 223 | 235 | PF02747 | 0.337 |
LIG_PCNA_yPIPBox_3 | 251 | 262 | PF02747 | 0.352 |
LIG_PTB_Apo_2 | 221 | 228 | PF02174 | 0.451 |
LIG_PTB_Apo_2 | 375 | 382 | PF02174 | 0.397 |
LIG_PTB_Apo_2 | 481 | 488 | PF02174 | 0.296 |
LIG_PTB_Phospho_1 | 375 | 381 | PF10480 | 0.403 |
LIG_RPA_C_Fungi | 923 | 935 | PF08784 | 0.458 |
LIG_SH2_CRK | 198 | 202 | PF00017 | 0.548 |
LIG_SH2_CRK | 210 | 214 | PF00017 | 0.480 |
LIG_SH2_GRB2like | 376 | 379 | PF00017 | 0.610 |
LIG_SH2_PTP2 | 592 | 595 | PF00017 | 0.314 |
LIG_SH2_SRC | 764 | 767 | PF00017 | 0.580 |
LIG_SH2_STAP1 | 529 | 533 | PF00017 | 0.476 |
LIG_SH2_STAP1 | 825 | 829 | PF00017 | 0.384 |
LIG_SH2_STAT3 | 812 | 815 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 537 | 540 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 544 | 547 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 592 | 595 | PF00017 | 0.455 |
LIG_SH3_2 | 140 | 145 | PF14604 | 0.403 |
LIG_SH3_2 | 884 | 889 | PF14604 | 0.374 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.633 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.546 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.378 |
LIG_SH3_3 | 584 | 590 | PF00018 | 0.453 |
LIG_SH3_3 | 612 | 618 | PF00018 | 0.585 |
LIG_SH3_3 | 633 | 639 | PF00018 | 0.553 |
LIG_SH3_3 | 856 | 862 | PF00018 | 0.530 |
LIG_SH3_3 | 881 | 887 | PF00018 | 0.351 |
LIG_SH3_3 | 946 | 952 | PF00018 | 0.526 |
LIG_SUMO_SIM_anti_2 | 921 | 927 | PF11976 | 0.532 |
LIG_SUMO_SIM_anti_2 | 98 | 103 | PF11976 | 0.327 |
LIG_SUMO_SIM_par_1 | 103 | 108 | PF11976 | 0.345 |
LIG_SUMO_SIM_par_1 | 193 | 199 | PF11976 | 0.362 |
LIG_SUMO_SIM_par_1 | 297 | 302 | PF11976 | 0.541 |
LIG_SUMO_SIM_par_1 | 90 | 96 | PF11976 | 0.307 |
LIG_SUMO_SIM_par_1 | 903 | 909 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 921 | 927 | PF11976 | 0.340 |
LIG_TRAF2_1 | 178 | 181 | PF00917 | 0.663 |
LIG_TRAF2_1 | 648 | 651 | PF00917 | 0.468 |
LIG_TRAF2_1 | 763 | 766 | PF00917 | 0.568 |
LIG_TYR_ITIM | 196 | 201 | PF00017 | 0.617 |
LIG_TYR_ITIM | 542 | 547 | PF00017 | 0.448 |
LIG_WRC_WIRS_1 | 197 | 202 | PF05994 | 0.544 |
LIG_WW_3 | 496 | 500 | PF00397 | 0.478 |
MOD_CDC14_SPxK_1 | 496 | 499 | PF00782 | 0.475 |
MOD_CDK_SPK_2 | 583 | 588 | PF00069 | 0.485 |
MOD_CDK_SPxK_1 | 493 | 499 | PF00069 | 0.462 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.395 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.492 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.611 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.502 |
MOD_CK1_1 | 517 | 523 | PF00069 | 0.413 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.211 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.325 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.506 |
MOD_CK2_1 | 645 | 651 | PF00069 | 0.503 |
MOD_CK2_1 | 711 | 717 | PF00069 | 0.586 |
MOD_CK2_1 | 760 | 766 | PF00069 | 0.454 |
MOD_CK2_1 | 799 | 805 | PF00069 | 0.597 |
MOD_CK2_1 | 854 | 860 | PF00069 | 0.429 |
MOD_CMANNOS | 967 | 970 | PF00535 | 0.375 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.385 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.602 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.604 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.643 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.392 |
MOD_GlcNHglycan | 815 | 818 | PF01048 | 0.532 |
MOD_GlcNHglycan | 856 | 859 | PF01048 | 0.380 |
MOD_GlcNHglycan | 868 | 871 | PF01048 | 0.365 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.620 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.519 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.468 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.576 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.487 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.623 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.393 |
MOD_GSK3_1 | 603 | 610 | PF00069 | 0.583 |
MOD_GSK3_1 | 827 | 834 | PF00069 | 0.379 |
MOD_LATS_1 | 335 | 341 | PF00433 | 0.490 |
MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.517 |
MOD_N-GLC_1 | 368 | 373 | PF02516 | 0.485 |
MOD_N-GLC_2 | 661 | 663 | PF02516 | 0.359 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.436 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.409 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.670 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.473 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.610 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.623 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.489 |
MOD_NEK2_1 | 528 | 533 | PF00069 | 0.347 |
MOD_NEK2_1 | 553 | 558 | PF00069 | 0.433 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.496 |
MOD_NEK2_1 | 771 | 776 | PF00069 | 0.402 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.355 |
MOD_NEK2_1 | 947 | 952 | PF00069 | 0.438 |
MOD_NEK2_2 | 147 | 152 | PF00069 | 0.405 |
MOD_NEK2_2 | 245 | 250 | PF00069 | 0.371 |
MOD_NEK2_2 | 46 | 51 | PF00069 | 0.485 |
MOD_NEK2_2 | 57 | 62 | PF00069 | 0.443 |
MOD_NEK2_2 | 591 | 596 | PF00069 | 0.330 |
MOD_NEK2_2 | 827 | 832 | PF00069 | 0.331 |
MOD_OFUCOSY | 55 | 61 | PF10250 | 0.442 |
MOD_PIKK_1 | 111 | 117 | PF00454 | 0.365 |
MOD_PIKK_1 | 634 | 640 | PF00454 | 0.553 |
MOD_PIKK_1 | 697 | 703 | PF00454 | 0.318 |
MOD_PK_1 | 32 | 38 | PF00069 | 0.459 |
MOD_PKA_1 | 264 | 270 | PF00069 | 0.585 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.588 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.718 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.610 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.542 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.567 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.450 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.427 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.645 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.483 |
MOD_PKA_2 | 787 | 793 | PF00069 | 0.510 |
MOD_PKB_1 | 32 | 40 | PF00069 | 0.696 |
MOD_PKB_1 | 561 | 569 | PF00069 | 0.334 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.456 |
MOD_Plk_1 | 566 | 572 | PF00069 | 0.211 |
MOD_Plk_1 | 799 | 805 | PF00069 | 0.497 |
MOD_Plk_2-3 | 274 | 280 | PF00069 | 0.631 |
MOD_Plk_2-3 | 457 | 463 | PF00069 | 0.378 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.476 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.517 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.576 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.469 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.414 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.249 |
MOD_Plk_4 | 609 | 615 | PF00069 | 0.626 |
MOD_Plk_4 | 667 | 673 | PF00069 | 0.393 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.672 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.511 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.405 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.368 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.480 |
MOD_ProDKin_1 | 583 | 589 | PF00069 | 0.501 |
MOD_ProDKin_1 | 607 | 613 | PF00069 | 0.590 |
MOD_ProDKin_1 | 880 | 886 | PF00069 | 0.338 |
MOD_SUMO_rev_2 | 463 | 473 | PF00179 | 0.613 |
MOD_SUMO_rev_2 | 612 | 621 | PF00179 | 0.520 |
MOD_SUMO_rev_2 | 648 | 653 | PF00179 | 0.429 |
MOD_SUMO_rev_2 | 927 | 936 | PF00179 | 0.485 |
TRG_DiLeu_BaEn_1 | 944 | 949 | PF01217 | 0.462 |
TRG_DiLeu_BaLyEn_6 | 183 | 188 | PF01217 | 0.439 |
TRG_DiLeu_BaLyEn_6 | 77 | 82 | PF01217 | 0.473 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.555 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.582 |
TRG_ENDOCYTIC_2 | 544 | 547 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 574 | 577 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 592 | 595 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 958 | 961 | PF00928 | 0.445 |
TRG_ER_diArg_1 | 210 | 212 | PF00400 | 0.354 |
TRG_ER_diArg_1 | 295 | 298 | PF00400 | 0.578 |
TRG_ER_diArg_1 | 31 | 34 | PF00400 | 0.774 |
TRG_ER_diArg_1 | 365 | 368 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 524 | 527 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 78 | 80 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 845 | 847 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 872 | 875 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 970 | 973 | PF00400 | 0.441 |
TRG_NES_CRM1_1 | 890 | 903 | PF08389 | 0.426 |
TRG_NLS_MonoCore_2 | 76 | 81 | PF00514 | 0.366 |
TRG_NLS_MonoExtC_3 | 831 | 836 | PF00514 | 0.352 |
TRG_NLS_MonoExtN_4 | 74 | 81 | PF00514 | 0.425 |
TRG_Pf-PMV_PEXEL_1 | 41 | 45 | PF00026 | 0.478 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4JNL6 | Bodo saltans | 28% | 90% |
A0A1X0NYY7 | Trypanosomatidae | 39% | 100% |
A0A3Q8IAF8 | Leishmania donovani | 57% | 100% |
A0A3Q8IAK8 | Leishmania donovani | 54% | 100% |
A0A3Q8IJ32 | Leishmania donovani | 53% | 100% |
A0A3S5H6Y1 | Leishmania donovani | 53% | 100% |
A0A3S7WTZ8 | Leishmania donovani | 52% | 95% |
A0A3S7WU13 | Leishmania donovani | 53% | 100% |
A0A422NAR5 | Trypanosoma rangeli | 38% | 100% |
A4H8M5 | Leishmania braziliensis | 49% | 100% |
A4H8M7 | Leishmania braziliensis | 54% | 100% |
A4H8N0 | Leishmania braziliensis | 44% | 100% |
A4H8N1 | Leishmania braziliensis | 77% | 100% |
A4HWZ5 | Leishmania infantum | 53% | 100% |
A4HWZ6 | Leishmania infantum | 49% | 100% |
A4HWZ8 | Leishmania infantum | 54% | 100% |
A4HX00 | Leishmania infantum | 52% | 100% |
A4HX01 | Leishmania infantum | 100% | 100% |
A4HX05 | Leishmania infantum | 57% | 100% |
E8NHI9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 100% |
E9AQQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 100% |
E9AQR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 100% |
E9AQR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 100% |
E9AQR2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 100% |
E9AQR3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 52% | 100% |
E9AQR4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QER2 | Leishmania major | 91% | 100% |
Q4QER3 | Leishmania major | 52% | 100% |
Q4QER4 | Leishmania major | 57% | 94% |
Q4QER5 | Leishmania major | 54% | 100% |
Q4QER6 | Leishmania major | 54% | 100% |
Q4QER7 | Leishmania major | 55% | 100% |
Q4QER8 | Leishmania major | 55% | 100% |
Q4QER9 | Leishmania major | 54% | 100% |
Q4QES0 | Leishmania major | 54% | 100% |
V5ANJ8 | Trypanosoma cruzi | 38% | 100% |