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 | 2 |
GO:0005739 | mitochondrion | 5 | 2 |
GO:0016020 | membrane | 2 | 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: Q4Q6K0
Term | Name | Level | Count |
---|---|---|---|
GO:0000959 | mitochondrial RNA metabolic process | 6 | 2 |
GO:0000963 | mitochondrial RNA processing | 6 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009451 | RNA modification | 5 | 2 |
GO:0009892 | negative regulation of metabolic process | 4 | 2 |
GO:0009893 | positive regulation of metabolic process | 4 | 2 |
GO:0009894 | regulation of catabolic process | 4 | 2 |
GO:0009895 | negative regulation of catabolic process | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010467 | gene expression | 4 | 2 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 2 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 2 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 2 |
GO:0010628 | positive regulation of gene expression | 6 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016553 | base conversion or substitution editing | 6 | 2 |
GO:0016554 | cytidine to uridine editing | 7 | 2 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 2 |
GO:0031329 | regulation of cellular catabolic process | 5 | 2 |
GO:0031330 | negative regulation of cellular catabolic process | 6 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043487 | regulation of RNA stability | 3 | 2 |
GO:0043488 | regulation of mRNA stability | 4 | 2 |
GO:0043489 | RNA stabilization | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0048255 | mRNA stabilization | 5 | 2 |
GO:0048518 | positive regulation of biological process | 3 | 2 |
GO:0048519 | negative regulation of biological process | 3 | 2 |
GO:0048523 | negative regulation of cellular process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 2 |
GO:0051252 | regulation of RNA metabolic process | 5 | 2 |
GO:0051253 | negative regulation of RNA metabolic process | 6 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0061013 | regulation of mRNA catabolic process | 6 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065008 | regulation of biological quality | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:0140053 | mitochondrial gene expression | 5 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1902369 | negative regulation of RNA catabolic process | 7 | 2 |
GO:1902373 | negative regulation of mRNA catabolic process | 7 | 2 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 2 |
GO:1903312 | negative regulation of mRNA metabolic process | 7 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0003729 | mRNA binding | 5 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 210 | 214 | PF00656 | 0.759 |
CLV_C14_Caspase3-7 | 287 | 291 | PF00656 | 0.371 |
CLV_C14_Caspase3-7 | 543 | 547 | PF00656 | 0.731 |
CLV_C14_Caspase3-7 | 780 | 784 | PF00656 | 0.334 |
CLV_C14_Caspase3-7 | 824 | 828 | PF00656 | 0.522 |
CLV_NRD_NRD_1 | 1006 | 1008 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 578 | 580 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 805 | 807 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 808 | 810 | PF00675 | 0.397 |
CLV_PCSK_FUR_1 | 174 | 178 | PF00082 | 0.546 |
CLV_PCSK_FUR_1 | 576 | 580 | PF00082 | 0.360 |
CLV_PCSK_FUR_1 | 806 | 810 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 1006 | 1008 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 472 | 474 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 578 | 580 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 745 | 747 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 766 | 768 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 807 | 809 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 816 | 818 | PF00082 | 0.492 |
CLV_PCSK_PC1ET2_1 | 101 | 103 | PF00082 | 0.532 |
CLV_PCSK_PC1ET2_1 | 173 | 175 | PF00082 | 0.626 |
CLV_PCSK_PC1ET2_1 | 327 | 329 | PF00082 | 0.479 |
CLV_PCSK_PC1ET2_1 | 422 | 424 | PF00082 | 0.382 |
CLV_PCSK_PC1ET2_1 | 479 | 481 | PF00082 | 0.432 |
CLV_PCSK_PC1ET2_1 | 745 | 747 | PF00082 | 0.446 |
CLV_PCSK_PC1ET2_1 | 766 | 768 | PF00082 | 0.381 |
CLV_PCSK_PC1ET2_1 | 807 | 809 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 816 | 818 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 526 | 530 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 634 | 638 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 856 | 860 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 912 | 916 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 917 | 921 | PF00082 | 0.367 |
CLV_Separin_Metazoa | 447 | 451 | PF03568 | 0.328 |
CLV_Separin_Metazoa | 668 | 672 | PF03568 | 0.380 |
DEG_APCC_DBOX_1 | 11 | 19 | PF00400 | 0.434 |
DEG_APCC_DBOX_1 | 479 | 487 | PF00400 | 0.367 |
DEG_APCC_DBOX_1 | 880 | 888 | PF00400 | 0.483 |
DEG_APCC_DBOX_1 | 916 | 924 | PF00400 | 0.381 |
DEG_APCC_DBOX_1 | 961 | 969 | PF00400 | 0.394 |
DEG_APCC_DBOX_1 | 983 | 991 | PF00400 | 0.387 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.433 |
DEG_ODPH_VHL_1 | 655 | 666 | PF01847 | 0.327 |
DEG_SCF_FBW7_2 | 754 | 759 | PF00400 | 0.412 |
DEG_SPOP_SBC_1 | 341 | 345 | PF00917 | 0.528 |
DOC_CDC14_PxL_1 | 69 | 77 | PF14671 | 0.576 |
DOC_CDC14_PxL_1 | 907 | 915 | PF14671 | 0.414 |
DOC_CYCLIN_RxL_1 | 851 | 862 | PF00134 | 0.403 |
DOC_CYCLIN_RxL_1 | 912 | 921 | PF00134 | 0.476 |
DOC_CYCLIN_yClb1_LxF_4 | 432 | 438 | PF00134 | 0.355 |
DOC_CYCLIN_yCln2_LP_2 | 609 | 615 | PF00134 | 0.448 |
DOC_CYCLIN_yCln2_LP_2 | 872 | 878 | PF00134 | 0.530 |
DOC_MAPK_DCC_7 | 607 | 615 | PF00069 | 0.365 |
DOC_MAPK_DCC_7 | 868 | 878 | PF00069 | 0.555 |
DOC_MAPK_gen_1 | 12 | 21 | PF00069 | 0.433 |
DOC_MAPK_gen_1 | 421 | 427 | PF00069 | 0.376 |
DOC_MAPK_gen_1 | 634 | 644 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 660 | 669 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 719 | 726 | PF00069 | 0.561 |
DOC_MAPK_gen_1 | 745 | 751 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 766 | 774 | PF00069 | 0.406 |
DOC_MAPK_gen_1 | 806 | 813 | PF00069 | 0.522 |
DOC_MAPK_gen_1 | 922 | 931 | PF00069 | 0.522 |
DOC_MAPK_gen_1 | 979 | 987 | PF00069 | 0.422 |
DOC_MAPK_JIP1_4 | 611 | 617 | PF00069 | 0.454 |
DOC_MAPK_MEF2A_6 | 767 | 776 | PF00069 | 0.320 |
DOC_MAPK_MEF2A_6 | 969 | 978 | PF00069 | 0.452 |
DOC_MAPK_RevD_3 | 465 | 480 | PF00069 | 0.390 |
DOC_PP1_RVXF_1 | 12 | 18 | PF00149 | 0.421 |
DOC_PP1_RVXF_1 | 421 | 428 | PF00149 | 0.364 |
DOC_PP4_FxxP_1 | 598 | 601 | PF00568 | 0.366 |
DOC_PP4_FxxP_1 | 621 | 624 | PF00568 | 0.368 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 708 | 712 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 750 | 754 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 795 | 799 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 934 | 938 | PF00917 | 0.486 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 675 | 680 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 752 | 757 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 815 | 820 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 960 | 965 | PF00397 | 0.349 |
DOC_WW_Pin1_4 | 968 | 973 | PF00397 | 0.349 |
LIG_14-3-3_CanoR_1 | 102 | 111 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 253 | 261 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 295 | 299 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 497 | 506 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 566 | 572 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 628 | 636 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 67 | 72 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 671 | 680 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 7 | 11 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 721 | 727 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 997 | 1004 | PF00244 | 0.582 |
LIG_Actin_WH2_2 | 237 | 255 | PF00022 | 0.362 |
LIG_Actin_WH2_2 | 657 | 673 | PF00022 | 0.365 |
LIG_BIR_III_4 | 216 | 220 | PF00653 | 0.685 |
LIG_BRCT_BRCA1_1 | 462 | 466 | PF00533 | 0.493 |
LIG_BRCT_BRCA1_1 | 58 | 62 | PF00533 | 0.458 |
LIG_CaM_IQ_9 | 319 | 334 | PF13499 | 0.458 |
LIG_EVH1_2 | 622 | 626 | PF00568 | 0.342 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.533 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.411 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.450 |
LIG_FHA_1 | 587 | 593 | PF00498 | 0.306 |
LIG_FHA_1 | 625 | 631 | PF00498 | 0.408 |
LIG_FHA_1 | 637 | 643 | PF00498 | 0.315 |
LIG_FHA_1 | 721 | 727 | PF00498 | 0.620 |
LIG_FHA_1 | 753 | 759 | PF00498 | 0.413 |
LIG_FHA_1 | 933 | 939 | PF00498 | 0.522 |
LIG_FHA_1 | 955 | 961 | PF00498 | 0.404 |
LIG_FHA_1 | 968 | 974 | PF00498 | 0.394 |
LIG_FHA_1 | 993 | 999 | PF00498 | 0.452 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.663 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.702 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.305 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.594 |
LIG_FHA_2 | 394 | 400 | PF00498 | 0.524 |
LIG_FHA_2 | 660 | 666 | PF00498 | 0.493 |
LIG_FHA_2 | 680 | 686 | PF00498 | 0.476 |
LIG_FHA_2 | 701 | 707 | PF00498 | 0.660 |
LIG_FHA_2 | 778 | 784 | PF00498 | 0.348 |
LIG_FHA_2 | 831 | 837 | PF00498 | 0.601 |
LIG_FHA_2 | 947 | 953 | PF00498 | 0.378 |
LIG_FHA_2 | 961 | 967 | PF00498 | 0.358 |
LIG_Integrin_RGD_1 | 223 | 225 | PF01839 | 0.503 |
LIG_LIR_Apic_2 | 441 | 445 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 463 | 474 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 493 | 503 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 511 | 521 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 589 | 598 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 625 | 630 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 783 | 790 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 852 | 859 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 20 | 26 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 37 | 42 | PF02991 | 0.666 |
LIG_LIR_Nem_3 | 406 | 411 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 424 | 430 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 505 | 509 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 511 | 517 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 589 | 594 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 625 | 629 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 783 | 788 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 840 | 846 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 852 | 857 | PF02991 | 0.386 |
LIG_NRBOX | 281 | 287 | PF00104 | 0.293 |
LIG_Pex14_2 | 17 | 21 | PF04695 | 0.418 |
LIG_Pex14_2 | 41 | 45 | PF04695 | 0.463 |
LIG_SH2_CRK | 156 | 160 | PF00017 | 0.567 |
LIG_SH2_CRK | 408 | 412 | PF00017 | 0.461 |
LIG_SH2_CRK | 489 | 493 | PF00017 | 0.456 |
LIG_SH2_CRK | 869 | 873 | PF00017 | 0.552 |
LIG_SH2_STAP1 | 52 | 56 | PF00017 | 0.460 |
LIG_SH2_STAT3 | 228 | 231 | PF00017 | 0.575 |
LIG_SH2_STAT3 | 301 | 304 | PF00017 | 0.438 |
LIG_SH2_STAT3 | 52 | 55 | PF00017 | 0.459 |
LIG_SH2_STAT3 | 842 | 845 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 434 | 437 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 605 | 608 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 620 | 623 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 694 | 697 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 702 | 705 | PF00017 | 0.654 |
LIG_SH2_STAT5 | 770 | 773 | PF00017 | 0.388 |
LIG_SH3_1 | 479 | 485 | PF00018 | 0.509 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.623 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.651 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.372 |
LIG_SH3_3 | 458 | 464 | PF00018 | 0.493 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.509 |
LIG_SH3_3 | 610 | 616 | PF00018 | 0.465 |
LIG_SH3_3 | 651 | 657 | PF00018 | 0.477 |
LIG_SH3_3 | 724 | 730 | PF00018 | 0.464 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.625 |
LIG_SUMO_SIM_anti_2 | 254 | 262 | PF11976 | 0.515 |
LIG_SUMO_SIM_anti_2 | 662 | 668 | PF11976 | 0.328 |
LIG_SUMO_SIM_anti_2 | 723 | 728 | PF11976 | 0.471 |
LIG_SUMO_SIM_anti_2 | 888 | 894 | PF11976 | 0.377 |
LIG_SUMO_SIM_par_1 | 254 | 262 | PF11976 | 0.601 |
LIG_SUMO_SIM_par_1 | 283 | 291 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 755 | 763 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 775 | 780 | PF11976 | 0.336 |
LIG_TRAF2_1 | 125 | 128 | PF00917 | 0.581 |
LIG_TRAF2_1 | 262 | 265 | PF00917 | 0.413 |
LIG_TRAF2_1 | 367 | 370 | PF00917 | 0.670 |
LIG_TRAF2_1 | 541 | 544 | PF00917 | 0.573 |
LIG_TRAF2_1 | 703 | 706 | PF00917 | 0.667 |
LIG_UBA3_1 | 919 | 925 | PF00899 | 0.411 |
LIG_WRC_WIRS_1 | 18 | 23 | PF05994 | 0.421 |
LIG_WRC_WIRS_1 | 434 | 439 | PF05994 | 0.348 |
LIG_WRC_WIRS_1 | 503 | 508 | PF05994 | 0.351 |
LIG_WRC_WIRS_1 | 740 | 745 | PF05994 | 0.315 |
LIG_WW_2 | 80 | 83 | PF00397 | 0.438 |
MOD_CDK_SPxxK_3 | 166 | 173 | PF00069 | 0.514 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.596 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.651 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.564 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.653 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.571 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.447 |
MOD_CK1_1 | 586 | 592 | PF00069 | 0.305 |
MOD_CK1_1 | 697 | 703 | PF00069 | 0.564 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.545 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.422 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.512 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.636 |
MOD_CK2_1 | 393 | 399 | PF00069 | 0.373 |
MOD_CK2_1 | 700 | 706 | PF00069 | 0.619 |
MOD_CK2_1 | 830 | 836 | PF00069 | 0.633 |
MOD_CK2_1 | 885 | 891 | PF00069 | 0.465 |
MOD_CK2_1 | 915 | 921 | PF00069 | 0.472 |
MOD_CK2_1 | 960 | 966 | PF00069 | 0.477 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.588 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.560 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.546 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.619 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.597 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.698 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.734 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.402 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.393 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.324 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.587 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.675 |
MOD_GlcNHglycan | 714 | 717 | PF01048 | 0.765 |
MOD_GlcNHglycan | 796 | 800 | PF01048 | 0.387 |
MOD_GlcNHglycan | 830 | 833 | PF01048 | 0.748 |
MOD_GlcNHglycan | 887 | 890 | PF01048 | 0.339 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.591 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.566 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.496 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.542 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.665 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.662 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.515 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.563 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.422 |
MOD_GSK3_1 | 671 | 678 | PF00069 | 0.457 |
MOD_GSK3_1 | 694 | 701 | PF00069 | 0.488 |
MOD_GSK3_1 | 708 | 715 | PF00069 | 0.680 |
MOD_GSK3_1 | 986 | 993 | PF00069 | 0.420 |
MOD_N-GLC_1 | 185 | 190 | PF02516 | 0.568 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.438 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.742 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.385 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.590 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.370 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.508 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.454 |
MOD_NEK2_1 | 629 | 634 | PF00069 | 0.404 |
MOD_NEK2_1 | 695 | 700 | PF00069 | 0.466 |
MOD_NEK2_1 | 739 | 744 | PF00069 | 0.305 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.651 |
MOD_NEK2_1 | 913 | 918 | PF00069 | 0.403 |
MOD_OFUCOSY | 88 | 93 | PF10250 | 0.538 |
MOD_PIKK_1 | 103 | 109 | PF00454 | 0.597 |
MOD_PIKK_1 | 280 | 286 | PF00454 | 0.417 |
MOD_PIKK_1 | 300 | 306 | PF00454 | 0.428 |
MOD_PIKK_1 | 319 | 325 | PF00454 | 0.325 |
MOD_PIKK_1 | 565 | 571 | PF00454 | 0.475 |
MOD_PIKK_1 | 671 | 677 | PF00454 | 0.412 |
MOD_PIKK_1 | 679 | 685 | PF00454 | 0.341 |
MOD_PIKK_1 | 777 | 783 | PF00454 | 0.383 |
MOD_PKA_1 | 101 | 107 | PF00069 | 0.512 |
MOD_PKA_1 | 67 | 73 | PF00069 | 0.636 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.550 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.554 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.407 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.409 |
MOD_PKA_2 | 565 | 571 | PF00069 | 0.500 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.414 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.601 |
MOD_PKA_2 | 720 | 726 | PF00069 | 0.641 |
MOD_PKA_2 | 828 | 834 | PF00069 | 0.583 |
MOD_PKA_2 | 850 | 856 | PF00069 | 0.334 |
MOD_PKA_2 | 996 | 1002 | PF00069 | 0.443 |
MOD_Plk_1 | 114 | 120 | PF00069 | 0.544 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.601 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.433 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.656 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.433 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.388 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.449 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.327 |
MOD_Plk_4 | 722 | 728 | PF00069 | 0.611 |
MOD_Plk_4 | 934 | 940 | PF00069 | 0.532 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.636 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.443 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.493 |
MOD_ProDKin_1 | 675 | 681 | PF00069 | 0.412 |
MOD_ProDKin_1 | 752 | 758 | PF00069 | 0.496 |
MOD_ProDKin_1 | 815 | 821 | PF00069 | 0.520 |
MOD_ProDKin_1 | 960 | 966 | PF00069 | 0.351 |
MOD_ProDKin_1 | 968 | 974 | PF00069 | 0.343 |
MOD_SUMO_rev_2 | 163 | 169 | PF00179 | 0.528 |
MOD_SUMO_rev_2 | 518 | 528 | PF00179 | 0.457 |
MOD_SUMO_rev_2 | 543 | 550 | PF00179 | 0.698 |
TRG_DiLeu_BaEn_1 | 256 | 261 | PF01217 | 0.516 |
TRG_DiLeu_BaEn_1 | 668 | 673 | PF01217 | 0.494 |
TRG_DiLeu_BaEn_4 | 523 | 529 | PF01217 | 0.546 |
TRG_DiLeu_BaLyEn_6 | 753 | 758 | PF01217 | 0.409 |
TRG_DiLeu_LyEn_5 | 668 | 673 | PF01217 | 0.343 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.699 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 408 | 411 | PF00928 | 0.458 |
TRG_ENDOCYTIC_2 | 434 | 437 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 489 | 492 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 843 | 846 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 869 | 872 | PF00928 | 0.560 |
TRG_ER_diArg_1 | 108 | 110 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 12 | 15 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 174 | 177 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 328 | 330 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 472 | 474 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 576 | 579 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 66 | 68 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 718 | 721 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 728 | 731 | PF00400 | 0.361 |
TRG_ER_diArg_1 | 805 | 808 | PF00400 | 0.459 |
TRG_NES_CRM1_1 | 883 | 894 | PF08389 | 0.333 |
TRG_NLS_Bipartite_1 | 157 | 177 | PF00514 | 0.587 |
TRG_NLS_MonoCore_2 | 172 | 177 | PF00514 | 0.596 |
TRG_NLS_MonoCore_2 | 326 | 331 | PF00514 | 0.479 |
TRG_NLS_MonoExtC_3 | 172 | 177 | PF00514 | 0.583 |
TRG_NLS_MonoExtN_4 | 170 | 177 | PF00514 | 0.575 |
TRG_Pf-PMV_PEXEL_1 | 507 | 511 | PF00026 | 0.363 |
TRG_Pf-PMV_PEXEL_1 | 641 | 645 | PF00026 | 0.349 |
TRG_Pf-PMV_PEXEL_1 | 671 | 675 | PF00026 | 0.354 |
TRG_Pf-PMV_PEXEL_1 | 917 | 921 | PF00026 | 0.497 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDG9 | Leptomonas seymouri | 56% | 100% |
A0A1X0NJ60 | Trypanosomatidae | 42% | 100% |
A0A3Q8IF71 | Leishmania donovani | 94% | 100% |
A0A3S5IRN6 | Trypanosoma rangeli | 43% | 100% |
A4HJ42 | Leishmania braziliensis | 80% | 100% |
A4I6F7 | Leishmania infantum | 93% | 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% | 100% |