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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B1L4
Term | Name | Level | Count |
---|---|---|---|
GO:0000959 | mitochondrial RNA metabolic process | 6 | 1 |
GO:0000963 | mitochondrial RNA processing | 6 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 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:0010467 | gene expression | 4 | 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:0140053 | mitochondrial gene expression | 5 | 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:0003729 | mRNA binding | 5 | 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 | 169 | 173 | PF00656 | 0.758 |
CLV_C14_Caspase3-7 | 246 | 250 | PF00656 | 0.571 |
CLV_C14_Caspase3-7 | 502 | 506 | PF00656 | 0.724 |
CLV_C14_Caspase3-7 | 783 | 787 | PF00656 | 0.608 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.679 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.642 |
CLV_NRD_NRD_1 | 431 | 433 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 767 | 769 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 964 | 966 | PF00675 | 0.635 |
CLV_PCSK_FUR_1 | 287 | 291 | PF00082 | 0.402 |
CLV_PCSK_FUR_1 | 535 | 539 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 704 | 706 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 725 | 727 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 766 | 768 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 775 | 777 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.632 |
CLV_PCSK_PC1ET2_1 | 286 | 288 | PF00082 | 0.542 |
CLV_PCSK_PC1ET2_1 | 381 | 383 | PF00082 | 0.442 |
CLV_PCSK_PC1ET2_1 | 438 | 440 | PF00082 | 0.474 |
CLV_PCSK_PC1ET2_1 | 704 | 706 | PF00082 | 0.595 |
CLV_PCSK_PC1ET2_1 | 725 | 727 | PF00082 | 0.539 |
CLV_PCSK_PC1ET2_1 | 766 | 768 | PF00082 | 0.552 |
CLV_PCSK_PC1ET2_1 | 775 | 777 | PF00082 | 0.679 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 815 | 819 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 871 | 875 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 876 | 880 | PF00082 | 0.435 |
CLV_Separin_Metazoa | 406 | 410 | PF03568 | 0.398 |
CLV_Separin_Metazoa | 627 | 631 | PF03568 | 0.446 |
DEG_APCC_DBOX_1 | 438 | 446 | PF00400 | 0.442 |
DEG_APCC_DBOX_1 | 839 | 847 | PF00400 | 0.529 |
DEG_APCC_DBOX_1 | 875 | 883 | PF00400 | 0.449 |
DEG_APCC_DBOX_1 | 920 | 928 | PF00400 | 0.465 |
DEG_APCC_DBOX_1 | 942 | 950 | PF00400 | 0.515 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.482 |
DEG_ODPH_VHL_1 | 614 | 625 | PF01847 | 0.400 |
DEG_SCF_FBW7_2 | 713 | 718 | PF00400 | 0.558 |
DEG_SPOP_SBC_1 | 117 | 121 | PF00917 | 0.575 |
DOC_CDC14_PxL_1 | 45 | 53 | PF14671 | 0.736 |
DOC_CDC14_PxL_1 | 866 | 874 | PF14671 | 0.571 |
DOC_CYCLIN_RxL_1 | 810 | 821 | PF00134 | 0.552 |
DOC_CYCLIN_RxL_1 | 871 | 880 | PF00134 | 0.525 |
DOC_CYCLIN_yClb1_LxF_4 | 391 | 397 | PF00134 | 0.479 |
DOC_CYCLIN_yCln2_LP_2 | 831 | 837 | PF00134 | 0.580 |
DOC_MAPK_DCC_7 | 827 | 837 | PF00069 | 0.608 |
DOC_MAPK_gen_1 | 380 | 386 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 593 | 603 | PF00069 | 0.500 |
DOC_MAPK_gen_1 | 619 | 628 | PF00069 | 0.504 |
DOC_MAPK_gen_1 | 678 | 685 | PF00069 | 0.720 |
DOC_MAPK_gen_1 | 704 | 710 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 725 | 733 | PF00069 | 0.472 |
DOC_MAPK_gen_1 | 766 | 772 | PF00069 | 0.564 |
DOC_MAPK_gen_1 | 881 | 890 | PF00069 | 0.567 |
DOC_MAPK_gen_1 | 938 | 946 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 726 | 735 | PF00069 | 0.392 |
DOC_MAPK_MEF2A_6 | 928 | 937 | PF00069 | 0.505 |
DOC_MAPK_RevD_3 | 424 | 439 | PF00069 | 0.456 |
DOC_PP1_RVXF_1 | 380 | 387 | PF00149 | 0.425 |
DOC_PP4_FxxP_1 | 557 | 560 | PF00568 | 0.432 |
DOC_PP4_FxxP_1 | 580 | 583 | PF00568 | 0.450 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 709 | 713 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 754 | 758 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 893 | 897 | PF00917 | 0.604 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.315 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 634 | 639 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 664 | 669 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 711 | 716 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 774 | 779 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 919 | 924 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 927 | 932 | PF00397 | 0.417 |
LIG_14-3-3_CanoR_1 | 212 | 220 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 254 | 258 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 456 | 465 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 587 | 595 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 596 | 603 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 630 | 639 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 680 | 686 | PF00244 | 0.673 |
LIG_14-3-3_CanoR_1 | 956 | 963 | PF00244 | 0.615 |
LIG_Actin_WH2_2 | 196 | 214 | PF00022 | 0.425 |
LIG_Actin_WH2_2 | 38 | 54 | PF00022 | 0.452 |
LIG_Actin_WH2_2 | 616 | 632 | PF00022 | 0.483 |
LIG_BRCT_BRCA1_1 | 34 | 38 | PF00533 | 0.530 |
LIG_BRCT_BRCA1_1 | 421 | 425 | PF00533 | 0.542 |
LIG_CaM_IQ_9 | 278 | 293 | PF13499 | 0.578 |
LIG_EH1_1 | 238 | 246 | PF00400 | 0.417 |
LIG_EVH1_2 | 581 | 585 | PF00568 | 0.420 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.473 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.482 |
LIG_FHA_1 | 546 | 552 | PF00498 | 0.367 |
LIG_FHA_1 | 584 | 590 | PF00498 | 0.413 |
LIG_FHA_1 | 596 | 602 | PF00498 | 0.360 |
LIG_FHA_1 | 680 | 686 | PF00498 | 0.665 |
LIG_FHA_1 | 712 | 718 | PF00498 | 0.559 |
LIG_FHA_1 | 892 | 898 | PF00498 | 0.588 |
LIG_FHA_1 | 914 | 920 | PF00498 | 0.553 |
LIG_FHA_1 | 927 | 933 | PF00498 | 0.457 |
LIG_FHA_1 | 952 | 958 | PF00498 | 0.526 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.618 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.541 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.314 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.445 |
LIG_FHA_2 | 619 | 625 | PF00498 | 0.484 |
LIG_FHA_2 | 639 | 645 | PF00498 | 0.526 |
LIG_FHA_2 | 660 | 666 | PF00498 | 0.711 |
LIG_FHA_2 | 737 | 743 | PF00498 | 0.419 |
LIG_FHA_2 | 906 | 912 | PF00498 | 0.447 |
LIG_FHA_2 | 920 | 926 | PF00498 | 0.428 |
LIG_FHA_2 | 945 | 951 | PF00498 | 0.453 |
LIG_Integrin_RGD_1 | 182 | 184 | PF01839 | 0.613 |
LIG_LIR_Apic_2 | 400 | 404 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 422 | 433 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 452 | 462 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 470 | 480 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 548 | 557 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 584 | 591 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 742 | 749 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 811 | 819 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 914 | 923 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 13 | 18 | PF02991 | 0.705 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 365 | 370 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 383 | 389 | PF02991 | 0.238 |
LIG_LIR_Nem_3 | 463 | 468 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 470 | 476 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 548 | 553 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 584 | 588 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 742 | 747 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 799 | 805 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 811 | 816 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 821 | 825 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 914 | 918 | PF02991 | 0.546 |
LIG_Pex14_2 | 17 | 21 | PF04695 | 0.643 |
LIG_SH2_CRK | 132 | 136 | PF00017 | 0.705 |
LIG_SH2_CRK | 367 | 371 | PF00017 | 0.509 |
LIG_SH2_CRK | 448 | 452 | PF00017 | 0.505 |
LIG_SH2_CRK | 828 | 832 | PF00017 | 0.603 |
LIG_SH2_STAP1 | 28 | 32 | PF00017 | 0.528 |
LIG_SH2_STAT3 | 187 | 190 | PF00017 | 0.579 |
LIG_SH2_STAT3 | 260 | 263 | PF00017 | 0.587 |
LIG_SH2_STAT3 | 28 | 31 | PF00017 | 0.530 |
LIG_SH2_STAT3 | 801 | 804 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 564 | 567 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 579 | 582 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 653 | 656 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 661 | 664 | PF00017 | 0.684 |
LIG_SH2_STAT5 | 729 | 732 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 825 | 828 | PF00017 | 0.401 |
LIG_SH3_1 | 438 | 444 | PF00018 | 0.564 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.470 |
LIG_SH3_3 | 417 | 423 | PF00018 | 0.542 |
LIG_SH3_3 | 438 | 444 | PF00018 | 0.564 |
LIG_SH3_3 | 51 | 57 | PF00018 | 0.692 |
LIG_SH3_3 | 569 | 575 | PF00018 | 0.508 |
LIG_SH3_3 | 610 | 616 | PF00018 | 0.519 |
LIG_SH3_3 | 683 | 689 | PF00018 | 0.539 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.688 |
LIG_SUMO_SIM_anti_2 | 213 | 221 | PF11976 | 0.567 |
LIG_SUMO_SIM_anti_2 | 621 | 627 | PF11976 | 0.392 |
LIG_SUMO_SIM_anti_2 | 682 | 687 | PF11976 | 0.595 |
LIG_SUMO_SIM_anti_2 | 847 | 853 | PF11976 | 0.526 |
LIG_SUMO_SIM_par_1 | 213 | 221 | PF11976 | 0.620 |
LIG_SUMO_SIM_par_1 | 242 | 250 | PF11976 | 0.401 |
LIG_SUMO_SIM_par_1 | 714 | 722 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 734 | 739 | PF11976 | 0.205 |
LIG_TRAF2_1 | 221 | 224 | PF00917 | 0.466 |
LIG_TRAF2_1 | 326 | 329 | PF00917 | 0.725 |
LIG_TRAF2_1 | 662 | 665 | PF00917 | 0.720 |
LIG_TRAF2_1 | 89 | 92 | PF00917 | 0.604 |
LIG_TRAF2_1 | 948 | 951 | PF00917 | 0.385 |
LIG_UBA3_1 | 878 | 884 | PF00899 | 0.563 |
LIG_WRC_WIRS_1 | 393 | 398 | PF05994 | 0.470 |
LIG_WRC_WIRS_1 | 462 | 467 | PF05994 | 0.418 |
LIG_WRC_WIRS_1 | 699 | 704 | PF05994 | 0.389 |
LIG_WRC_WIRS_1 | 741 | 746 | PF05994 | 0.262 |
LIG_WRC_WIRS_1 | 912 | 917 | PF05994 | 0.441 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.589 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.562 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.615 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.476 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.479 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.629 |
MOD_CK1_1 | 545 | 551 | PF00069 | 0.355 |
MOD_CK1_1 | 656 | 662 | PF00069 | 0.588 |
MOD_CK1_1 | 667 | 673 | PF00069 | 0.681 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.479 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.566 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.451 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.316 |
MOD_CK2_1 | 659 | 665 | PF00069 | 0.662 |
MOD_CK2_1 | 740 | 746 | PF00069 | 0.264 |
MOD_CK2_1 | 844 | 850 | PF00069 | 0.511 |
MOD_CK2_1 | 874 | 880 | PF00069 | 0.490 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.612 |
MOD_CK2_1 | 919 | 925 | PF00069 | 0.529 |
MOD_CK2_1 | 944 | 950 | PF00069 | 0.511 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.590 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.571 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.694 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.613 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.461 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.371 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.657 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.647 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.485 |
MOD_GlcNHglycan | 669 | 672 | PF01048 | 0.736 |
MOD_GlcNHglycan | 755 | 759 | PF01048 | 0.422 |
MOD_GlcNHglycan | 789 | 792 | PF01048 | 0.758 |
MOD_GlcNHglycan | 846 | 849 | PF01048 | 0.409 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.612 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.490 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.531 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.543 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.627 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.527 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.477 |
MOD_GSK3_1 | 630 | 637 | PF00069 | 0.511 |
MOD_GSK3_1 | 655 | 662 | PF00069 | 0.554 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.631 |
MOD_GSK3_1 | 736 | 743 | PF00069 | 0.507 |
MOD_GSK3_1 | 774 | 781 | PF00069 | 0.431 |
MOD_GSK3_1 | 945 | 952 | PF00069 | 0.573 |
MOD_N-GLC_1 | 111 | 116 | PF02516 | 0.451 |
MOD_N-GLC_1 | 144 | 149 | PF02516 | 0.666 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.762 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.448 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.710 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.707 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.438 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.522 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.382 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.694 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.588 |
MOD_NEK2_1 | 698 | 703 | PF00069 | 0.521 |
MOD_NEK2_1 | 872 | 877 | PF00069 | 0.464 |
MOD_NEK2_1 | 944 | 949 | PF00069 | 0.443 |
MOD_NEK2_2 | 127 | 132 | PF00069 | 0.518 |
MOD_OFUCOSY | 64 | 69 | PF10250 | 0.657 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.633 |
MOD_PIKK_1 | 239 | 245 | PF00454 | 0.476 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.252 |
MOD_PIKK_1 | 278 | 284 | PF00454 | 0.368 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.495 |
MOD_PIKK_1 | 630 | 636 | PF00454 | 0.534 |
MOD_PIKK_1 | 638 | 644 | PF00454 | 0.233 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.598 |
MOD_PIKK_1 | 736 | 742 | PF00454 | 0.535 |
MOD_PIKK_1 | 79 | 85 | PF00454 | 0.746 |
MOD_PKA_1 | 43 | 49 | PF00069 | 0.690 |
MOD_PKA_1 | 77 | 83 | PF00069 | 0.600 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.473 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.466 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.666 |
MOD_PKA_2 | 595 | 601 | PF00069 | 0.390 |
MOD_PKA_2 | 679 | 685 | PF00069 | 0.692 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.622 |
MOD_PKA_2 | 787 | 793 | PF00069 | 0.744 |
MOD_PKA_2 | 809 | 815 | PF00069 | 0.398 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.633 |
MOD_PKA_2 | 955 | 961 | PF00069 | 0.604 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.619 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.671 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.578 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.601 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.466 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.553 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.456 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.507 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.448 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.397 |
MOD_Plk_4 | 568 | 574 | PF00069 | 0.372 |
MOD_Plk_4 | 656 | 662 | PF00069 | 0.581 |
MOD_Plk_4 | 681 | 687 | PF00069 | 0.634 |
MOD_Plk_4 | 740 | 746 | PF00069 | 0.425 |
MOD_Plk_4 | 893 | 899 | PF00069 | 0.564 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.467 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.551 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.540 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.316 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.644 |
MOD_ProDKin_1 | 634 | 640 | PF00069 | 0.478 |
MOD_ProDKin_1 | 664 | 670 | PF00069 | 0.619 |
MOD_ProDKin_1 | 711 | 717 | PF00069 | 0.537 |
MOD_ProDKin_1 | 774 | 780 | PF00069 | 0.636 |
MOD_ProDKin_1 | 919 | 925 | PF00069 | 0.421 |
MOD_ProDKin_1 | 927 | 933 | PF00069 | 0.410 |
MOD_SUMO_rev_2 | 477 | 487 | PF00179 | 0.494 |
TRG_DiLeu_BaEn_1 | 215 | 220 | PF01217 | 0.566 |
TRG_DiLeu_BaEn_1 | 627 | 632 | PF01217 | 0.501 |
TRG_DiLeu_BaEn_4 | 482 | 488 | PF01217 | 0.583 |
TRG_DiLeu_BaLyEn_6 | 712 | 717 | PF01217 | 0.555 |
TRG_DiLeu_LyEn_5 | 627 | 632 | PF01217 | 0.461 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.708 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 393 | 396 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 448 | 451 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 802 | 805 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 828 | 831 | PF00928 | 0.616 |
TRG_ER_diArg_1 | 132 | 134 | PF00400 | 0.601 |
TRG_ER_diArg_1 | 287 | 290 | PF00400 | 0.699 |
TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 431 | 433 | PF00400 | 0.419 |
TRG_ER_diArg_1 | 535 | 538 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 677 | 680 | PF00400 | 0.774 |
TRG_ER_diArg_1 | 687 | 690 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 77 | 79 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 84 | 86 | PF00400 | 0.658 |
TRG_NES_CRM1_1 | 842 | 853 | PF08389 | 0.400 |
TRG_NLS_MonoCore_2 | 285 | 290 | PF00514 | 0.598 |
TRG_NLS_MonoExtC_3 | 285 | 290 | PF00514 | 0.458 |
TRG_Pf-PMV_PEXEL_1 | 466 | 470 | PF00026 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 600 | 604 | PF00026 | 0.464 |
TRG_Pf-PMV_PEXEL_1 | 630 | 634 | PF00026 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 876 | 880 | PF00026 | 0.521 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDG9 | Leptomonas seymouri | 57% | 100% |
A0A1X0NJ60 | Trypanosomatidae | 42% | 100% |
A0A3Q8IF71 | Leishmania donovani | 87% | 98% |
A0A3S5IRN6 | Trypanosoma rangeli | 41% | 100% |
A4HJ42 | Leishmania braziliensis | 79% | 100% |
A4I6F7 | Leishmania infantum | 87% | 96% |
C9ZN75 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
C9ZWW8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
Q4Q6K0 | Leishmania major | 87% | 100% |