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: A0A3Q8IF71
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 | 188 | 192 | PF00656 | 0.731 |
CLV_C14_Caspase3-7 | 265 | 269 | PF00656 | 0.567 |
CLV_C14_Caspase3-7 | 521 | 525 | PF00656 | 0.752 |
CLV_C14_Caspase3-7 | 640 | 644 | PF00656 | 0.306 |
CLV_C14_Caspase3-7 | 758 | 762 | PF00656 | 0.385 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 556 | 558 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 783 | 785 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 786 | 788 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 984 | 986 | PF00675 | 0.620 |
CLV_PCSK_FUR_1 | 554 | 558 | PF00082 | 0.399 |
CLV_PCSK_FUR_1 | 784 | 788 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 723 | 725 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 744 | 746 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 785 | 787 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 794 | 796 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 984 | 986 | PF00082 | 0.607 |
CLV_PCSK_PC1ET2_1 | 151 | 153 | PF00082 | 0.661 |
CLV_PCSK_PC1ET2_1 | 305 | 307 | PF00082 | 0.514 |
CLV_PCSK_PC1ET2_1 | 400 | 402 | PF00082 | 0.422 |
CLV_PCSK_PC1ET2_1 | 45 | 47 | PF00082 | 0.466 |
CLV_PCSK_PC1ET2_1 | 457 | 459 | PF00082 | 0.463 |
CLV_PCSK_PC1ET2_1 | 723 | 725 | PF00082 | 0.519 |
CLV_PCSK_PC1ET2_1 | 744 | 746 | PF00082 | 0.470 |
CLV_PCSK_PC1ET2_1 | 785 | 787 | PF00082 | 0.532 |
CLV_PCSK_PC1ET2_1 | 79 | 81 | PF00082 | 0.586 |
CLV_PCSK_PC1ET2_1 | 794 | 796 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 834 | 838 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 890 | 894 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 895 | 899 | PF00082 | 0.401 |
CLV_Separin_Metazoa | 425 | 429 | PF03568 | 0.358 |
CLV_Separin_Metazoa | 646 | 650 | PF03568 | 0.421 |
DEG_APCC_DBOX_1 | 457 | 465 | PF00400 | 0.401 |
DEG_APCC_DBOX_1 | 858 | 866 | PF00400 | 0.509 |
DEG_APCC_DBOX_1 | 894 | 902 | PF00400 | 0.414 |
DEG_APCC_DBOX_1 | 939 | 947 | PF00400 | 0.431 |
DEG_APCC_DBOX_1 | 961 | 969 | PF00400 | 0.457 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.445 |
DEG_SCF_FBW7_2 | 732 | 737 | PF00400 | 0.496 |
DEG_SPOP_SBC_1 | 319 | 323 | PF00917 | 0.577 |
DOC_CDC14_PxL_1 | 47 | 55 | PF14671 | 0.671 |
DOC_CDC14_PxL_1 | 885 | 893 | PF14671 | 0.505 |
DOC_CYCLIN_RxL_1 | 829 | 840 | PF00134 | 0.491 |
DOC_CYCLIN_RxL_1 | 890 | 899 | PF00134 | 0.505 |
DOC_CYCLIN_yClb1_LxF_4 | 410 | 416 | PF00134 | 0.422 |
DOC_CYCLIN_yCln2_LP_2 | 587 | 593 | PF00134 | 0.479 |
DOC_CYCLIN_yCln2_LP_2 | 850 | 856 | PF00134 | 0.578 |
DOC_MAPK_DCC_7 | 585 | 593 | PF00069 | 0.402 |
DOC_MAPK_DCC_7 | 846 | 856 | PF00069 | 0.613 |
DOC_MAPK_gen_1 | 399 | 405 | PF00069 | 0.416 |
DOC_MAPK_gen_1 | 638 | 647 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 697 | 704 | PF00069 | 0.657 |
DOC_MAPK_gen_1 | 723 | 729 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 744 | 752 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 784 | 791 | PF00069 | 0.544 |
DOC_MAPK_gen_1 | 900 | 909 | PF00069 | 0.545 |
DOC_MAPK_gen_1 | 957 | 965 | PF00069 | 0.457 |
DOC_MAPK_JIP1_4 | 589 | 595 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 745 | 754 | PF00069 | 0.357 |
DOC_MAPK_MEF2A_6 | 947 | 956 | PF00069 | 0.480 |
DOC_MAPK_RevD_3 | 443 | 458 | PF00069 | 0.420 |
DOC_PP1_RVXF_1 | 399 | 406 | PF00149 | 0.403 |
DOC_PP4_FxxP_1 | 118 | 121 | PF00568 | 0.487 |
DOC_PP4_FxxP_1 | 576 | 579 | PF00568 | 0.399 |
DOC_PP4_FxxP_1 | 599 | 602 | PF00568 | 0.438 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 690 | 694 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 728 | 732 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 773 | 777 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 912 | 916 | PF00917 | 0.550 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 653 | 658 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 730 | 735 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 793 | 798 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 938 | 943 | PF00397 | 0.382 |
DOC_WW_Pin1_4 | 946 | 951 | PF00397 | 0.381 |
LIG_14-3-3_CanoR_1 | 2 | 8 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 231 | 239 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 273 | 277 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 46 | 50 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 475 | 484 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 544 | 550 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 606 | 614 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 615 | 622 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 649 | 658 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 699 | 705 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 975 | 982 | PF00244 | 0.598 |
LIG_Actin_WH2_2 | 215 | 233 | PF00022 | 0.392 |
LIG_Actin_WH2_2 | 635 | 651 | PF00022 | 0.435 |
LIG_BIR_III_2 | 168 | 172 | PF00653 | 0.538 |
LIG_BRCT_BRCA1_1 | 36 | 40 | PF00533 | 0.466 |
LIG_BRCT_BRCA1_1 | 440 | 444 | PF00533 | 0.523 |
LIG_CaM_IQ_9 | 297 | 312 | PF13499 | 0.525 |
LIG_EH1_1 | 257 | 265 | PF00400 | 0.386 |
LIG_EVH1_2 | 600 | 604 | PF00568 | 0.406 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.494 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.527 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.443 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.480 |
LIG_FHA_1 | 565 | 571 | PF00498 | 0.341 |
LIG_FHA_1 | 603 | 609 | PF00498 | 0.414 |
LIG_FHA_1 | 699 | 705 | PF00498 | 0.644 |
LIG_FHA_1 | 731 | 737 | PF00498 | 0.495 |
LIG_FHA_1 | 911 | 917 | PF00498 | 0.556 |
LIG_FHA_1 | 933 | 939 | PF00498 | 0.484 |
LIG_FHA_1 | 946 | 952 | PF00498 | 0.423 |
LIG_FHA_1 | 971 | 977 | PF00498 | 0.490 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.728 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.609 |
LIG_FHA_2 | 638 | 644 | PF00498 | 0.524 |
LIG_FHA_2 | 658 | 664 | PF00498 | 0.246 |
LIG_FHA_2 | 679 | 685 | PF00498 | 0.712 |
LIG_FHA_2 | 756 | 762 | PF00498 | 0.381 |
LIG_FHA_2 | 809 | 815 | PF00498 | 0.621 |
LIG_FHA_2 | 925 | 931 | PF00498 | 0.411 |
LIG_FHA_2 | 939 | 945 | PF00498 | 0.393 |
LIG_FHA_2 | 964 | 970 | PF00498 | 0.409 |
LIG_Integrin_RGD_1 | 201 | 203 | PF01839 | 0.553 |
LIG_LIR_Apic_2 | 116 | 121 | PF02991 | 0.487 |
LIG_LIR_Apic_2 | 419 | 423 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 15 | 25 | PF02991 | 0.604 |
LIG_LIR_Gen_1 | 441 | 452 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 471 | 481 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 489 | 499 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 567 | 576 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 603 | 608 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 761 | 768 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 830 | 837 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 933 | 942 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 15 | 20 | PF02991 | 0.694 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 402 | 408 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 483 | 487 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 489 | 495 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 567 | 572 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 603 | 607 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 761 | 766 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 818 | 824 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 830 | 835 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 933 | 937 | PF02991 | 0.535 |
LIG_Pex14_2 | 19 | 23 | PF04695 | 0.505 |
LIG_SH2_CRK | 134 | 138 | PF00017 | 0.637 |
LIG_SH2_CRK | 386 | 390 | PF00017 | 0.484 |
LIG_SH2_CRK | 467 | 471 | PF00017 | 0.481 |
LIG_SH2_CRK | 847 | 851 | PF00017 | 0.618 |
LIG_SH2_STAP1 | 30 | 34 | PF00017 | 0.469 |
LIG_SH2_STAT3 | 206 | 209 | PF00017 | 0.563 |
LIG_SH2_STAT3 | 279 | 282 | PF00017 | 0.523 |
LIG_SH2_STAT3 | 30 | 33 | PF00017 | 0.470 |
LIG_SH2_STAT3 | 820 | 823 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 583 | 586 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 598 | 601 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 672 | 675 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 680 | 683 | PF00017 | 0.707 |
LIG_SH3_1 | 457 | 463 | PF00018 | 0.536 |
LIG_SH3_3 | 436 | 442 | PF00018 | 0.526 |
LIG_SH3_3 | 457 | 463 | PF00018 | 0.536 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.676 |
LIG_SH3_3 | 588 | 594 | PF00018 | 0.499 |
LIG_SH3_3 | 629 | 635 | PF00018 | 0.502 |
LIG_SH3_3 | 702 | 708 | PF00018 | 0.532 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.656 |
LIG_SUMO_SIM_anti_2 | 232 | 240 | PF11976 | 0.545 |
LIG_SUMO_SIM_anti_2 | 701 | 706 | PF11976 | 0.547 |
LIG_SUMO_SIM_anti_2 | 866 | 872 | PF11976 | 0.457 |
LIG_SUMO_SIM_par_1 | 111 | 117 | PF11976 | 0.752 |
LIG_SUMO_SIM_par_1 | 232 | 240 | PF11976 | 0.612 |
LIG_SUMO_SIM_par_1 | 261 | 269 | PF11976 | 0.369 |
LIG_SUMO_SIM_par_1 | 733 | 741 | PF11976 | 0.504 |
LIG_SUMO_SIM_par_1 | 753 | 758 | PF11976 | 0.207 |
LIG_TRAF2_1 | 103 | 106 | PF00917 | 0.608 |
LIG_TRAF2_1 | 240 | 243 | PF00917 | 0.445 |
LIG_TRAF2_1 | 345 | 348 | PF00917 | 0.692 |
LIG_TRAF2_1 | 519 | 522 | PF00917 | 0.672 |
LIG_TRAF2_1 | 681 | 684 | PF00917 | 0.716 |
LIG_TRAF2_1 | 91 | 94 | PF00917 | 0.569 |
LIG_UBA3_1 | 897 | 903 | PF00899 | 0.492 |
LIG_WRC_WIRS_1 | 115 | 120 | PF05994 | 0.488 |
LIG_WRC_WIRS_1 | 412 | 417 | PF05994 | 0.415 |
LIG_WRC_WIRS_1 | 481 | 486 | PF05994 | 0.384 |
LIG_WRC_WIRS_1 | 931 | 936 | PF05994 | 0.397 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.614 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.641 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.454 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.543 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.678 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.476 |
MOD_CK1_1 | 530 | 536 | PF00069 | 0.645 |
MOD_CK1_1 | 564 | 570 | PF00069 | 0.351 |
MOD_CK1_1 | 675 | 681 | PF00069 | 0.579 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.457 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.543 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.664 |
MOD_CK2_1 | 678 | 684 | PF00069 | 0.659 |
MOD_CK2_1 | 685 | 691 | PF00069 | 0.727 |
MOD_CK2_1 | 808 | 814 | PF00069 | 0.651 |
MOD_CK2_1 | 863 | 869 | PF00069 | 0.490 |
MOD_CK2_1 | 893 | 899 | PF00069 | 0.463 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.591 |
MOD_CK2_1 | 938 | 944 | PF00069 | 0.508 |
MOD_CK2_1 | 963 | 969 | PF00069 | 0.454 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.584 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.576 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.695 |
MOD_GlcNHglycan | 162 | 166 | PF01048 | 0.741 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.633 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.701 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.709 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.552 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.424 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.346 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.639 |
MOD_GlcNHglycan | 688 | 691 | PF01048 | 0.724 |
MOD_GlcNHglycan | 692 | 695 | PF01048 | 0.791 |
MOD_GlcNHglycan | 774 | 778 | PF01048 | 0.418 |
MOD_GlcNHglycan | 808 | 811 | PF01048 | 0.743 |
MOD_GlcNHglycan | 865 | 868 | PF01048 | 0.372 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.611 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.515 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.523 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.678 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.508 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.689 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.621 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.469 |
MOD_GSK3_1 | 649 | 656 | PF00069 | 0.490 |
MOD_GSK3_1 | 672 | 679 | PF00069 | 0.498 |
MOD_GSK3_1 | 686 | 693 | PF00069 | 0.656 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.477 |
MOD_GSK3_1 | 964 | 971 | PF00069 | 0.503 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.483 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.748 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.419 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.473 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.646 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.404 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.510 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.445 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.678 |
MOD_NEK2_1 | 673 | 678 | PF00069 | 0.570 |
MOD_NEK2_1 | 891 | 896 | PF00069 | 0.434 |
MOD_NEK2_1 | 963 | 968 | PF00069 | 0.401 |
MOD_OFUCOSY | 66 | 71 | PF10250 | 0.608 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.451 |
MOD_PIKK_1 | 278 | 284 | PF00454 | 0.257 |
MOD_PIKK_1 | 297 | 303 | PF00454 | 0.346 |
MOD_PIKK_1 | 543 | 549 | PF00454 | 0.534 |
MOD_PIKK_1 | 649 | 655 | PF00454 | 0.501 |
MOD_PIKK_1 | 657 | 663 | PF00454 | 0.393 |
MOD_PIKK_1 | 755 | 761 | PF00454 | 0.466 |
MOD_PIKK_1 | 81 | 87 | PF00454 | 0.684 |
MOD_PKA_1 | 152 | 158 | PF00069 | 0.534 |
MOD_PKA_1 | 45 | 51 | PF00069 | 0.668 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.459 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.733 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.440 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.437 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.637 |
MOD_PKA_2 | 543 | 549 | PF00069 | 0.545 |
MOD_PKA_2 | 614 | 620 | PF00069 | 0.391 |
MOD_PKA_2 | 698 | 704 | PF00069 | 0.676 |
MOD_PKA_2 | 806 | 812 | PF00069 | 0.658 |
MOD_PKA_2 | 828 | 834 | PF00069 | 0.368 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.594 |
MOD_PKA_2 | 974 | 980 | PF00069 | 0.529 |
MOD_Plk_1 | 202 | 208 | PF00069 | 0.612 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.627 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.587 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.437 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.420 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.481 |
MOD_Plk_4 | 561 | 567 | PF00069 | 0.364 |
MOD_Plk_4 | 700 | 706 | PF00069 | 0.626 |
MOD_Plk_4 | 912 | 918 | PF00069 | 0.530 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.511 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.524 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.621 |
MOD_ProDKin_1 | 653 | 659 | PF00069 | 0.470 |
MOD_ProDKin_1 | 730 | 736 | PF00069 | 0.519 |
MOD_ProDKin_1 | 793 | 799 | PF00069 | 0.560 |
MOD_ProDKin_1 | 938 | 944 | PF00069 | 0.386 |
MOD_ProDKin_1 | 946 | 952 | PF00069 | 0.375 |
MOD_SUMO_rev_2 | 496 | 506 | PF00179 | 0.467 |
MOD_SUMO_rev_2 | 521 | 528 | PF00179 | 0.749 |
TRG_DiLeu_BaEn_1 | 234 | 239 | PF01217 | 0.553 |
TRG_DiLeu_BaEn_1 | 646 | 651 | PF01217 | 0.489 |
TRG_DiLeu_BaEn_4 | 501 | 507 | PF01217 | 0.572 |
TRG_DiLeu_BaLyEn_6 | 583 | 588 | PF01217 | 0.299 |
TRG_DiLeu_BaLyEn_6 | 731 | 736 | PF01217 | 0.491 |
TRG_DiLeu_LyEn_5 | 646 | 651 | PF01217 | 0.416 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.702 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.524 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 412 | 415 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 821 | 824 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 847 | 850 | PF00928 | 0.624 |
TRG_ER_diArg_1 | 134 | 136 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 152 | 154 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 306 | 308 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 450 | 452 | PF00400 | 0.378 |
TRG_ER_diArg_1 | 554 | 557 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 696 | 699 | PF00400 | 0.707 |
TRG_ER_diArg_1 | 706 | 709 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 783 | 786 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 86 | 88 | PF00400 | 0.638 |
TRG_NES_CRM1_1 | 861 | 872 | PF08389 | 0.364 |
TRG_NLS_Bipartite_1 | 135 | 155 | PF00514 | 0.631 |
TRG_NLS_MonoCore_2 | 150 | 155 | PF00514 | 0.617 |
TRG_NLS_MonoCore_2 | 304 | 309 | PF00514 | 0.545 |
TRG_Pf-PMV_PEXEL_1 | 485 | 489 | PF00026 | 0.397 |
TRG_Pf-PMV_PEXEL_1 | 619 | 623 | PF00026 | 0.419 |
TRG_Pf-PMV_PEXEL_1 | 649 | 653 | PF00026 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 895 | 899 | PF00026 | 0.501 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDG9 | Leptomonas seymouri | 57% | 100% |
A0A1X0NJ60 | Trypanosomatidae | 42% | 100% |
A0A3S5IRN6 | Trypanosoma rangeli | 43% | 100% |
A4HJ42 | Leishmania braziliensis | 79% | 100% |
A4I6F7 | Leishmania infantum | 100% | 100% |
C9ZN75 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
C9ZWW8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9B1L4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 98% |
Q4Q6K0 | Leishmania major | 94% | 100% |