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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q8A3
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 10 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009451 | RNA modification | 5 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016070 | RNA metabolic process | 5 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0009982 | pseudouridine synthase activity | 4 | 12 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0016866 | intramolecular transferase activity | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0004730 | pseudouridylate synthase activity | 5 | 2 |
GO:0016829 | lyase activity | 2 | 2 |
GO:0016835 | carbon-oxygen lyase activity | 3 | 2 |
GO:0016836 | hydro-lyase activity | 4 | 2 |
GO:0106029 | tRNA pseudouridine synthase activity | 5 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 107 | 111 | PF00656 | 0.746 |
CLV_C14_Caspase3-7 | 439 | 443 | PF00656 | 0.174 |
CLV_C14_Caspase3-7 | 457 | 461 | PF00656 | 0.302 |
CLV_NRD_NRD_1 | 104 | 106 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.268 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 612 | 614 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 730 | 732 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 747 | 749 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 798 | 800 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 801 | 803 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 814 | 816 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.539 |
CLV_PCSK_FUR_1 | 799 | 803 | PF00082 | 0.512 |
CLV_PCSK_FUR_1 | 812 | 816 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.268 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 747 | 749 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 756 | 758 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 790 | 792 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 800 | 802 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 814 | 816 | PF00082 | 0.736 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.691 |
CLV_PCSK_PC1ET2_1 | 756 | 758 | PF00082 | 0.600 |
CLV_PCSK_PC1ET2_1 | 790 | 792 | PF00082 | 0.449 |
CLV_PCSK_PC1ET2_1 | 800 | 802 | PF00082 | 0.472 |
CLV_PCSK_PC7_1 | 152 | 158 | PF00082 | 0.455 |
CLV_PCSK_PC7_1 | 425 | 431 | PF00082 | 0.268 |
CLV_PCSK_PC7_1 | 743 | 749 | PF00082 | 0.489 |
CLV_PCSK_PC7_1 | 94 | 100 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.716 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 487 | 491 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 756 | 760 | PF00082 | 0.528 |
CLV_Separin_Metazoa | 606 | 610 | PF03568 | 0.268 |
DEG_APCC_DBOX_1 | 287 | 295 | PF00400 | 0.283 |
DEG_APCC_DBOX_1 | 335 | 343 | PF00400 | 0.304 |
DOC_CDC14_PxL_1 | 441 | 449 | PF14671 | 0.279 |
DOC_CKS1_1 | 4 | 9 | PF01111 | 0.443 |
DOC_CKS1_1 | 73 | 78 | PF01111 | 0.494 |
DOC_CYCLIN_RxL_1 | 609 | 621 | PF00134 | 0.362 |
DOC_CYCLIN_RxL_1 | 754 | 763 | PF00134 | 0.547 |
DOC_MAPK_DCC_7 | 72 | 81 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 307 | 315 | PF00069 | 0.272 |
DOC_MAPK_gen_1 | 424 | 436 | PF00069 | 0.351 |
DOC_MAPK_MEF2A_6 | 72 | 81 | PF00069 | 0.455 |
DOC_PP1_RVXF_1 | 754 | 761 | PF00149 | 0.515 |
DOC_PP2B_LxvP_1 | 663 | 666 | PF13499 | 0.424 |
DOC_PP2B_LxvP_1 | 721 | 724 | PF13499 | 0.516 |
DOC_PP4_FxxP_1 | 4 | 7 | PF00568 | 0.407 |
DOC_PP4_FxxP_1 | 604 | 607 | PF00568 | 0.268 |
DOC_PP4_FxxP_1 | 73 | 76 | PF00568 | 0.581 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 594 | 598 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 707 | 711 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 785 | 789 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 829 | 833 | PF00917 | 0.517 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.274 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.414 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.398 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 803 | 808 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 815 | 820 | PF00397 | 0.592 |
LIG_14-3-3_CanoR_1 | 271 | 276 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 369 | 373 | PF00244 | 0.268 |
LIG_14-3-3_CanoR_1 | 487 | 494 | PF00244 | 0.264 |
LIG_14-3-3_CanoR_1 | 632 | 636 | PF00244 | 0.285 |
LIG_14-3-3_CanoR_1 | 814 | 819 | PF00244 | 0.676 |
LIG_Actin_WH2_2 | 460 | 478 | PF00022 | 0.412 |
LIG_AP2alpha_2 | 728 | 730 | PF02296 | 0.624 |
LIG_BIR_III_2 | 206 | 210 | PF00653 | 0.461 |
LIG_BIR_III_2 | 442 | 446 | PF00653 | 0.262 |
LIG_BRCT_BRCA1_1 | 67 | 71 | PF00533 | 0.703 |
LIG_BRCT_BRCA1_1 | 842 | 846 | PF00533 | 0.593 |
LIG_CaM_IQ_9 | 120 | 135 | PF13499 | 0.552 |
LIG_CtBP_PxDLS_1 | 615 | 619 | PF00389 | 0.283 |
LIG_deltaCOP1_diTrp_1 | 538 | 543 | PF00928 | 0.441 |
LIG_eIF4E_1 | 320 | 326 | PF01652 | 0.302 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.718 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.279 |
LIG_FHA_1 | 502 | 508 | PF00498 | 0.283 |
LIG_FHA_1 | 657 | 663 | PF00498 | 0.553 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.713 |
LIG_FHA_1 | 778 | 784 | PF00498 | 0.629 |
LIG_FHA_1 | 828 | 834 | PF00498 | 0.774 |
LIG_FHA_2 | 169 | 175 | PF00498 | 0.569 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.651 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.287 |
LIG_FHA_2 | 417 | 423 | PF00498 | 0.145 |
LIG_FHA_2 | 437 | 443 | PF00498 | 0.240 |
LIG_FHA_2 | 455 | 461 | PF00498 | 0.302 |
LIG_FHA_2 | 529 | 535 | PF00498 | 0.327 |
LIG_FHA_2 | 540 | 546 | PF00498 | 0.334 |
LIG_FHA_2 | 554 | 560 | PF00498 | 0.327 |
LIG_FHA_2 | 681 | 687 | PF00498 | 0.527 |
LIG_LIR_Apic_2 | 603 | 607 | PF02991 | 0.269 |
LIG_LIR_Apic_2 | 70 | 76 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 378 | 389 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 538 | 547 | PF02991 | 0.412 |
LIG_LIR_LC3C_4 | 41 | 46 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 119 | 125 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 378 | 384 | PF02991 | 0.247 |
LIG_LIR_Nem_3 | 477 | 482 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 538 | 543 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 566 | 570 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 667 | 673 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 686 | 691 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 835 | 839 | PF02991 | 0.632 |
LIG_MYND_1 | 160 | 164 | PF01753 | 0.484 |
LIG_NRBOX | 404 | 410 | PF00104 | 0.268 |
LIG_PCNA_PIPBox_1 | 574 | 583 | PF02747 | 0.302 |
LIG_PCNA_yPIPBox_3 | 574 | 587 | PF02747 | 0.422 |
LIG_PCNA_yPIPBox_3 | 637 | 649 | PF02747 | 0.268 |
LIG_Pex14_1 | 539 | 543 | PF04695 | 0.412 |
LIG_Pex14_2 | 12 | 16 | PF04695 | 0.366 |
LIG_Pex14_2 | 331 | 335 | PF04695 | 0.268 |
LIG_Pex14_2 | 391 | 395 | PF04695 | 0.283 |
LIG_SH2_CRK | 581 | 585 | PF00017 | 0.395 |
LIG_SH2_CRK | 640 | 644 | PF00017 | 0.268 |
LIG_SH2_CRK | 793 | 797 | PF00017 | 0.598 |
LIG_SH2_GRB2like | 640 | 643 | PF00017 | 0.268 |
LIG_SH2_NCK_1 | 640 | 644 | PF00017 | 0.283 |
LIG_SH2_SRC | 622 | 625 | PF00017 | 0.276 |
LIG_SH2_SRC | 640 | 643 | PF00017 | 0.268 |
LIG_SH2_SRC | 691 | 694 | PF00017 | 0.596 |
LIG_SH2_STAP1 | 622 | 626 | PF00017 | 0.395 |
LIG_SH2_STAP1 | 640 | 644 | PF00017 | 0.268 |
LIG_SH2_STAP1 | 793 | 797 | PF00017 | 0.598 |
LIG_SH2_STAT3 | 365 | 368 | PF00017 | 0.293 |
LIG_SH2_STAT3 | 580 | 583 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 398 | 401 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 680 | 683 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 803 | 806 | PF00017 | 0.446 |
LIG_SH3_1 | 157 | 163 | PF00018 | 0.525 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.525 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.309 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.347 |
LIG_SH3_3 | 557 | 563 | PF00018 | 0.269 |
LIG_SH3_3 | 604 | 610 | PF00018 | 0.298 |
LIG_SH3_3 | 778 | 784 | PF00018 | 0.541 |
LIG_SUMO_SIM_anti_2 | 658 | 664 | PF11976 | 0.488 |
LIG_SUMO_SIM_par_1 | 614 | 619 | PF11976 | 0.334 |
LIG_TRAF2_1 | 116 | 119 | PF00917 | 0.484 |
LIG_TRAF2_1 | 38 | 41 | PF00917 | 0.384 |
LIG_UBA3_1 | 78 | 84 | PF00899 | 0.463 |
LIG_WRC_WIRS_1 | 494 | 499 | PF05994 | 0.412 |
LIG_WRC_WIRS_1 | 540 | 545 | PF05994 | 0.402 |
LIG_WRC_WIRS_1 | 833 | 838 | PF05994 | 0.703 |
LIG_WW_3 | 606 | 610 | PF00397 | 0.268 |
MOD_CDK_SPK_2 | 32 | 37 | PF00069 | 0.398 |
MOD_CDK_SPK_2 | 803 | 808 | PF00069 | 0.627 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.675 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.674 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.300 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.622 |
MOD_CK1_1 | 763 | 769 | PF00069 | 0.461 |
MOD_CK1_1 | 821 | 827 | PF00069 | 0.756 |
MOD_CK1_1 | 832 | 838 | PF00069 | 0.635 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.678 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.568 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.627 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.292 |
MOD_CK2_1 | 416 | 422 | PF00069 | 0.327 |
MOD_CK2_1 | 528 | 534 | PF00069 | 0.395 |
MOD_DYRK1A_RPxSP_1 | 815 | 819 | PF00069 | 0.619 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.655 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.572 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.692 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.343 |
MOD_GlcNHglycan | 598 | 601 | PF01048 | 0.362 |
MOD_GlcNHglycan | 623 | 627 | PF01048 | 0.174 |
MOD_GlcNHglycan | 650 | 653 | PF01048 | 0.453 |
MOD_GlcNHglycan | 787 | 790 | PF01048 | 0.598 |
MOD_GlcNHglycan | 826 | 829 | PF01048 | 0.721 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.714 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.642 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.654 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.511 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.373 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.302 |
MOD_GSK3_1 | 627 | 634 | PF00069 | 0.377 |
MOD_GSK3_1 | 759 | 766 | PF00069 | 0.656 |
MOD_GSK3_1 | 813 | 820 | PF00069 | 0.763 |
MOD_GSK3_1 | 823 | 830 | PF00069 | 0.733 |
MOD_GSK3_1 | 840 | 847 | PF00069 | 0.483 |
MOD_LATS_1 | 269 | 275 | PF00433 | 0.412 |
MOD_N-GLC_1 | 292 | 297 | PF02516 | 0.289 |
MOD_N-GLC_1 | 396 | 401 | PF02516 | 0.362 |
MOD_N-GLC_1 | 707 | 712 | PF02516 | 0.701 |
MOD_N-GLC_1 | 785 | 790 | PF02516 | 0.589 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.440 |
MOD_NEK2_1 | 648 | 653 | PF00069 | 0.526 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.633 |
MOD_NEK2_1 | 759 | 764 | PF00069 | 0.498 |
MOD_NEK2_1 | 813 | 818 | PF00069 | 0.681 |
MOD_NEK2_2 | 627 | 632 | PF00069 | 0.334 |
MOD_PIKK_1 | 416 | 422 | PF00454 | 0.334 |
MOD_PIKK_1 | 735 | 741 | PF00454 | 0.635 |
MOD_PIKK_1 | 763 | 769 | PF00454 | 0.602 |
MOD_PK_1 | 271 | 277 | PF00069 | 0.412 |
MOD_PK_1 | 340 | 346 | PF00069 | 0.334 |
MOD_PKA_1 | 487 | 493 | PF00069 | 0.268 |
MOD_PKA_1 | 801 | 807 | PF00069 | 0.712 |
MOD_PKA_1 | 814 | 820 | PF00069 | 0.734 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.581 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.456 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.294 |
MOD_PKA_2 | 487 | 493 | PF00069 | 0.268 |
MOD_PKA_2 | 545 | 551 | PF00069 | 0.444 |
MOD_PKA_2 | 553 | 559 | PF00069 | 0.412 |
MOD_PKA_2 | 631 | 637 | PF00069 | 0.305 |
MOD_PKA_2 | 742 | 748 | PF00069 | 0.604 |
MOD_PKA_2 | 801 | 807 | PF00069 | 0.635 |
MOD_PKA_2 | 813 | 819 | PF00069 | 0.690 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.696 |
MOD_PKB_1 | 216 | 224 | PF00069 | 0.484 |
MOD_PKB_1 | 799 | 807 | PF00069 | 0.483 |
MOD_PKB_1 | 812 | 820 | PF00069 | 0.645 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.643 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.283 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.398 |
MOD_Plk_1 | 401 | 407 | PF00069 | 0.302 |
MOD_Plk_1 | 616 | 622 | PF00069 | 0.412 |
MOD_Plk_1 | 760 | 766 | PF00069 | 0.587 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.580 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.277 |
MOD_Plk_4 | 658 | 664 | PF00069 | 0.527 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.571 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.274 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.410 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.388 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.502 |
MOD_ProDKin_1 | 803 | 809 | PF00069 | 0.626 |
MOD_ProDKin_1 | 815 | 821 | PF00069 | 0.590 |
MOD_SUMO_for_1 | 225 | 228 | PF00179 | 0.558 |
MOD_SUMO_for_1 | 83 | 86 | PF00179 | 0.503 |
MOD_SUMO_rev_2 | 68 | 74 | PF00179 | 0.753 |
MOD_SUMO_rev_2 | 705 | 714 | PF00179 | 0.602 |
MOD_SUMO_rev_2 | 749 | 758 | PF00179 | 0.559 |
TRG_DiLeu_BaEn_1 | 40 | 45 | PF01217 | 0.386 |
TRG_DiLeu_BaLyEn_6 | 74 | 79 | PF01217 | 0.475 |
TRG_DiLeu_BaLyEn_6 | 754 | 759 | PF01217 | 0.515 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 581 | 584 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 640 | 643 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 793 | 796 | PF00928 | 0.599 |
TRG_ER_diArg_1 | 127 | 130 | PF00400 | 0.724 |
TRG_ER_diArg_1 | 151 | 153 | PF00400 | 0.634 |
TRG_ER_diArg_1 | 288 | 291 | PF00400 | 0.271 |
TRG_ER_diArg_1 | 306 | 308 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 423 | 426 | PF00400 | 0.312 |
TRG_ER_diArg_1 | 428 | 430 | PF00400 | 0.312 |
TRG_ER_diArg_1 | 487 | 489 | PF00400 | 0.268 |
TRG_ER_diArg_1 | 552 | 555 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 799 | 802 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 811 | 814 | PF00400 | 0.611 |
TRG_NES_CRM1_1 | 280 | 292 | PF08389 | 0.327 |
TRG_NLS_Bipartite_1 | 790 | 804 | PF00514 | 0.497 |
TRG_NLS_MonoCore_2 | 798 | 803 | PF00514 | 0.624 |
TRG_NLS_MonoExtN_4 | 799 | 804 | PF00514 | 0.592 |
TRG_Pf-PMV_PEXEL_1 | 403 | 407 | PF00026 | 0.279 |
TRG_Pf-PMV_PEXEL_1 | 429 | 433 | PF00026 | 0.368 |
TRG_Pf-PMV_PEXEL_1 | 487 | 492 | PF00026 | 0.315 |
TRG_Pf-PMV_PEXEL_1 | 514 | 519 | PF00026 | 0.334 |
TRG_Pf-PMV_PEXEL_1 | 65 | 70 | PF00026 | 0.576 |
TRG_Pf-PMV_PEXEL_1 | 653 | 658 | PF00026 | 0.454 |
TRG_Pf-PMV_PEXEL_1 | 757 | 761 | PF00026 | 0.531 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P820 | Leptomonas seymouri | 65% | 85% |
A0A0S4K0L8 | Bodo saltans | 45% | 84% |
A0A1X0NQX7 | Trypanosomatidae | 57% | 92% |
A0A3Q8II50 | Leishmania donovani | 93% | 100% |
A0A3S5ISD4 | Trypanosoma rangeli | 60% | 96% |
A4HGL5 | Leishmania braziliensis | 84% | 100% |
A4I3P1 | Leishmania infantum | 95% | 100% |
D0A8C3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 92% |
E9AZY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5BFB8 | Trypanosoma cruzi | 54% | 92% |