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 |
Related structures:
AlphaFold database: A4HLN4
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0009895 | negative regulation of catabolic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0010628 | positive regulation of gene expression | 6 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016553 | base conversion or substitution editing | 6 | 1 |
GO:0016554 | cytidine to uridine editing | 7 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 1 |
GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0031330 | negative regulation of cellular catabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043487 | regulation of RNA stability | 3 | 1 |
GO:0043488 | regulation of mRNA stability | 4 | 1 |
GO:0043489 | RNA stabilization | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0048255 | mRNA stabilization | 5 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0051253 | negative regulation of RNA metabolic process | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0061013 | regulation of mRNA catabolic process | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1902369 | negative regulation of RNA catabolic process | 7 | 1 |
GO:1902373 | negative regulation of mRNA catabolic process | 7 | 1 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 1 |
GO:1903312 | negative regulation of mRNA metabolic process | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 323 | 327 | PF00656 | 0.399 |
CLV_C14_Caspase3-7 | 504 | 508 | PF00656 | 0.458 |
CLV_C14_Caspase3-7 | 646 | 650 | PF00656 | 0.483 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 517 | 519 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 766 | 768 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 814 | 816 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 865 | 867 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 879 | 881 | PF00675 | 0.420 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 558 | 560 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 728 | 730 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 766 | 768 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 814 | 816 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 865 | 867 | PF00082 | 0.384 |
CLV_PCSK_KEX2_1 | 879 | 881 | PF00082 | 0.417 |
CLV_PCSK_PC1ET2_1 | 395 | 397 | PF00082 | 0.407 |
CLV_PCSK_PC1ET2_1 | 558 | 560 | PF00082 | 0.507 |
CLV_PCSK_PC1ET2_1 | 728 | 730 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.214 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 600 | 604 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 671 | 675 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 680 | 684 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 686 | 690 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 777 | 781 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 804 | 808 | PF00082 | 0.390 |
CLV_Separin_Metazoa | 639 | 643 | PF03568 | 0.518 |
DEG_APCC_DBOX_1 | 305 | 313 | PF00400 | 0.530 |
DEG_APCC_DBOX_1 | 395 | 403 | PF00400 | 0.400 |
DEG_APCC_DBOX_1 | 43 | 51 | PF00400 | 0.496 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.416 |
DEG_SCF_FBW7_1 | 779 | 784 | PF00400 | 0.452 |
DEG_SCF_FBW7_2 | 623 | 628 | PF00400 | 0.546 |
DEG_SPOP_SBC_1 | 103 | 107 | PF00917 | 0.379 |
DOC_CDC14_PxL_1 | 342 | 350 | PF14671 | 0.522 |
DOC_CKS1_1 | 778 | 783 | PF01111 | 0.520 |
DOC_CKS1_1 | 825 | 830 | PF01111 | 0.428 |
DOC_CKS1_1 | 834 | 839 | PF01111 | 0.366 |
DOC_CYCLIN_RxL_1 | 416 | 426 | PF00134 | 0.337 |
DOC_CYCLIN_yCln2_LP_2 | 759 | 765 | PF00134 | 0.441 |
DOC_MAPK_DCC_7 | 444 | 454 | PF00069 | 0.386 |
DOC_MAPK_gen_1 | 41 | 50 | PF00069 | 0.536 |
DOC_MAPK_gen_1 | 503 | 512 | PF00069 | 0.505 |
DOC_PP2B_LxvP_1 | 387 | 390 | PF13499 | 0.394 |
DOC_PP2B_LxvP_1 | 759 | 762 | PF13499 | 0.259 |
DOC_PP4_FxxP_1 | 664 | 667 | PF00568 | 0.406 |
DOC_PP4_FxxP_1 | 778 | 781 | PF00568 | 0.309 |
DOC_PP4_FxxP_1 | 825 | 828 | PF00568 | 0.494 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.390 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.341 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.299 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 560 | 564 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.253 |
DOC_USP7_MATH_1 | 888 | 892 | PF00917 | 0.574 |
DOC_USP7_UBL2_3 | 686 | 690 | PF12436 | 0.398 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 621 | 626 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.360 |
DOC_WW_Pin1_4 | 777 | 782 | PF00397 | 0.249 |
DOC_WW_Pin1_4 | 824 | 829 | PF00397 | 0.423 |
DOC_WW_Pin1_4 | 833 | 838 | PF00397 | 0.367 |
DOC_WW_Pin1_4 | 850 | 855 | PF00397 | 0.314 |
LIG_14-3-3_CanoR_1 | 102 | 111 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 130 | 138 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 41 | 50 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 459 | 464 | PF00244 | 0.271 |
LIG_14-3-3_CanoR_1 | 518 | 527 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 642 | 651 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 703 | 709 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 771 | 779 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 832 | 837 | PF00244 | 0.475 |
LIG_14-3-3_CterR_2 | 894 | 898 | PF00244 | 0.618 |
LIG_Actin_WH2_2 | 108 | 124 | PF00022 | 0.452 |
LIG_Actin_WH2_2 | 750 | 768 | PF00022 | 0.466 |
LIG_APCC_ABBA_1 | 34 | 39 | PF00400 | 0.419 |
LIG_BIR_III_2 | 887 | 891 | PF00653 | 0.474 |
LIG_BIR_III_4 | 180 | 184 | PF00653 | 0.405 |
LIG_BIR_III_4 | 39 | 43 | PF00653 | 0.290 |
LIG_BIR_III_4 | 490 | 494 | PF00653 | 0.451 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.391 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.304 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.588 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.517 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.481 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.320 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.371 |
LIG_FHA_1 | 825 | 831 | PF00498 | 0.445 |
LIG_FHA_1 | 834 | 840 | PF00498 | 0.376 |
LIG_FHA_1 | 876 | 882 | PF00498 | 0.408 |
LIG_FHA_2 | 17 | 23 | PF00498 | 0.519 |
LIG_FHA_2 | 261 | 267 | PF00498 | 0.517 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.441 |
LIG_FHA_2 | 443 | 449 | PF00498 | 0.491 |
LIG_FHA_2 | 641 | 647 | PF00498 | 0.530 |
LIG_FHA_2 | 750 | 756 | PF00498 | 0.368 |
LIG_FHA_2 | 778 | 784 | PF00498 | 0.452 |
LIG_HCF-1_HBM_1 | 669 | 672 | PF13415 | 0.477 |
LIG_LIR_Gen_1 | 231 | 241 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 296 | 305 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 417 | 424 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 507 | 516 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 545 | 556 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 611 | 619 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 656 | 665 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 722 | 731 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 736 | 747 | PF02991 | 0.249 |
LIG_LIR_Gen_1 | 97 | 104 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 231 | 236 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 296 | 300 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 344 | 348 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 411 | 415 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 417 | 423 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 507 | 512 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 545 | 551 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 611 | 616 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 656 | 661 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 722 | 727 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.500 |
LIG_LYPXL_yS_3 | 345 | 348 | PF13949 | 0.532 |
LIG_PCNA_TLS_4 | 503 | 510 | PF02747 | 0.384 |
LIG_PCNA_yPIPBox_3 | 3 | 15 | PF02747 | 0.350 |
LIG_SH2_NCK_1 | 134 | 138 | PF00017 | 0.337 |
LIG_SH2_SRC | 37 | 40 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 134 | 138 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 658 | 662 | PF00017 | 0.255 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 554 | 557 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 672 | 675 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 723 | 726 | PF00017 | 0.480 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.495 |
LIG_SH3_3 | 277 | 283 | PF00018 | 0.479 |
LIG_SH3_3 | 836 | 842 | PF00018 | 0.379 |
LIG_SUMO_SIM_anti_2 | 337 | 342 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 160 | 167 | PF11976 | 0.397 |
LIG_SUMO_SIM_par_1 | 30 | 35 | PF11976 | 0.363 |
LIG_SUMO_SIM_par_1 | 333 | 339 | PF11976 | 0.455 |
LIG_SUMO_SIM_par_1 | 353 | 359 | PF11976 | 0.243 |
LIG_TRAF2_1 | 218 | 221 | PF00917 | 0.345 |
LIG_TRAF2_1 | 263 | 266 | PF00917 | 0.522 |
LIG_TRAF2_1 | 367 | 370 | PF00917 | 0.499 |
LIG_UBA3_1 | 750 | 756 | PF00899 | 0.448 |
LIG_WRC_WIRS_1 | 415 | 420 | PF05994 | 0.480 |
MOD_CDK_SPxxK_3 | 850 | 857 | PF00069 | 0.312 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.454 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.466 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.525 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.496 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.498 |
MOD_CK1_1 | 568 | 574 | PF00069 | 0.384 |
MOD_CK1_1 | 702 | 708 | PF00069 | 0.382 |
MOD_CK1_1 | 732 | 738 | PF00069 | 0.526 |
MOD_CK1_1 | 826 | 832 | PF00069 | 0.517 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.559 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.547 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.408 |
MOD_CK2_1 | 260 | 266 | PF00069 | 0.528 |
MOD_CK2_1 | 832 | 838 | PF00069 | 0.531 |
MOD_Cter_Amidation | 77 | 80 | PF01082 | 0.366 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.554 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.362 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.434 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.505 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.526 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.727 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.387 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.382 |
MOD_GlcNHglycan | 605 | 608 | PF01048 | 0.493 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.373 |
MOD_GlcNHglycan | 704 | 707 | PF01048 | 0.377 |
MOD_GlcNHglycan | 847 | 850 | PF01048 | 0.586 |
MOD_GlcNHglycan | 860 | 863 | PF01048 | 0.329 |
MOD_GlcNHglycan | 866 | 869 | PF01048 | 0.286 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.539 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.376 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.385 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.477 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.519 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.600 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.553 |
MOD_GSK3_1 | 708 | 715 | PF00069 | 0.398 |
MOD_GSK3_1 | 777 | 784 | PF00069 | 0.312 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.540 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.472 |
MOD_N-GLC_2 | 274 | 276 | PF02516 | 0.367 |
MOD_N-GLC_2 | 407 | 409 | PF02516 | 0.446 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.513 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.536 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.394 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.449 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.393 |
MOD_NEK2_1 | 640 | 645 | PF00069 | 0.400 |
MOD_NEK2_1 | 730 | 735 | PF00069 | 0.435 |
MOD_NEK2_1 | 845 | 850 | PF00069 | 0.512 |
MOD_NEK2_2 | 723 | 728 | PF00069 | 0.362 |
MOD_PIKK_1 | 519 | 525 | PF00454 | 0.396 |
MOD_PIKK_1 | 608 | 614 | PF00454 | 0.504 |
MOD_PK_1 | 459 | 465 | PF00069 | 0.318 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.418 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.503 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.462 |
MOD_PKA_2 | 542 | 548 | PF00069 | 0.547 |
MOD_PKA_2 | 702 | 708 | PF00069 | 0.480 |
MOD_PKA_2 | 770 | 776 | PF00069 | 0.472 |
MOD_PKA_2 | 864 | 870 | PF00069 | 0.391 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.413 |
MOD_Plk_1 | 336 | 342 | PF00069 | 0.419 |
MOD_Plk_1 | 817 | 823 | PF00069 | 0.369 |
MOD_Plk_2-3 | 268 | 274 | PF00069 | 0.473 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.292 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.525 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.480 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.369 |
MOD_Plk_4 | 708 | 714 | PF00069 | 0.427 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.479 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.512 |
MOD_ProDKin_1 | 621 | 627 | PF00069 | 0.499 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.360 |
MOD_ProDKin_1 | 777 | 783 | PF00069 | 0.246 |
MOD_ProDKin_1 | 824 | 830 | PF00069 | 0.421 |
MOD_ProDKin_1 | 833 | 839 | PF00069 | 0.360 |
MOD_ProDKin_1 | 850 | 856 | PF00069 | 0.313 |
MOD_SUMO_for_1 | 602 | 605 | PF00179 | 0.321 |
MOD_SUMO_rev_2 | 388 | 397 | PF00179 | 0.403 |
MOD_SUMO_rev_2 | 668 | 673 | PF00179 | 0.346 |
TRG_DiLeu_BaEn_1 | 737 | 742 | PF01217 | 0.403 |
TRG_DiLeu_BaEn_2 | 292 | 298 | PF01217 | 0.346 |
TRG_DiLeu_BaEn_2 | 588 | 594 | PF01217 | 0.465 |
TRG_DiLeu_BaEn_2 | 773 | 779 | PF01217 | 0.419 |
TRG_DiLeu_BaLyEn_6 | 174 | 179 | PF01217 | 0.438 |
TRG_DiLeu_BaLyEn_6 | 382 | 387 | PF01217 | 0.467 |
TRG_DiLeu_BaLyEn_6 | 839 | 844 | PF01217 | 0.378 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 658 | 661 | PF00928 | 0.338 |
TRG_ER_diArg_1 | 641 | 644 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 765 | 767 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 814 | 816 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 864 | 866 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 879 | 881 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 893 | 896 | PF00400 | 0.477 |
TRG_NES_CRM1_1 | 292 | 307 | PF08389 | 0.374 |
TRG_NES_CRM1_1 | 504 | 515 | PF08389 | 0.373 |
TRG_Pf-PMV_PEXEL_1 | 306 | 310 | PF00026 | 0.405 |
TRG_Pf-PMV_PEXEL_1 | 436 | 440 | PF00026 | 0.356 |
TRG_Pf-PMV_PEXEL_1 | 485 | 489 | PF00026 | 0.687 |
TRG_Pf-PMV_PEXEL_1 | 871 | 875 | PF00026 | 0.398 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAS6 | Leptomonas seymouri | 60% | 99% |
A0A0S4JFF4 | Bodo saltans | 34% | 86% |
A0A1X0P174 | Trypanosomatidae | 42% | 100% |
A0A3Q8IHV0 | Leishmania donovani | 89% | 100% |
A0A3R7M0F7 | Trypanosoma rangeli | 41% | 100% |
A4I969 | Leishmania infantum | 89% | 100% |
C9ZIW5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9B410 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q414 | Leishmania major | 90% | 99% |
V5AXB1 | Trypanosoma cruzi | 43% | 100% |