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:0005634 | nucleus | 5 | 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: E9AWR6
Term | Name | Level | Count |
---|---|---|---|
GO:0000724 | double-strand break repair via homologous recombination | 7 | 1 |
GO:0000725 | recombinational repair | 6 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0007131 | reciprocal meiotic recombination | 3 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022414 | reproductive process | 1 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0035825 | homologous recombination | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0045003 | double-strand break repair via synthesis-dependent strand annealing | 8 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:0140527 | reciprocal homologous recombination | 7 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1903046 | meiotic cell cycle process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 11 |
GO:0016491 | oxidoreductase activity | 2 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0051213 | dioxygenase activity | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:0140658 | ATP-dependent chromatin remodeler activity | 3 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0015616 | DNA translocase activity | 3 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1033 | 1037 | PF00656 | 0.286 |
CLV_C14_Caspase3-7 | 1061 | 1065 | PF00656 | 0.420 |
CLV_C14_Caspase3-7 | 1109 | 1113 | PF00656 | 0.461 |
CLV_C14_Caspase3-7 | 278 | 282 | PF00656 | 0.531 |
CLV_NRD_NRD_1 | 1 | 3 | PF00675 | 0.660 |
CLV_NRD_NRD_1 | 1009 | 1011 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.200 |
CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.200 |
CLV_NRD_NRD_1 | 671 | 673 | PF00675 | 0.200 |
CLV_NRD_NRD_1 | 722 | 724 | PF00675 | 0.200 |
CLV_NRD_NRD_1 | 765 | 767 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.635 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 414 | 416 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 671 | 673 | PF00082 | 0.200 |
CLV_PCSK_KEX2_1 | 764 | 766 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 811 | 813 | PF00082 | 0.223 |
CLV_PCSK_KEX2_1 | 854 | 856 | PF00082 | 0.226 |
CLV_PCSK_KEX2_1 | 917 | 919 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.597 |
CLV_PCSK_PC1ET2_1 | 414 | 416 | PF00082 | 0.395 |
CLV_PCSK_PC1ET2_1 | 811 | 813 | PF00082 | 0.223 |
CLV_PCSK_PC1ET2_1 | 854 | 856 | PF00082 | 0.226 |
CLV_PCSK_PC1ET2_1 | 917 | 919 | PF00082 | 0.280 |
CLV_PCSK_PC7_1 | 410 | 416 | PF00082 | 0.394 |
CLV_PCSK_PC7_1 | 667 | 673 | PF00082 | 0.200 |
CLV_PCSK_SKI1_1 | 1081 | 1085 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 597 | 601 | PF00082 | 0.200 |
CLV_PCSK_SKI1_1 | 627 | 631 | PF00082 | 0.200 |
CLV_PCSK_SKI1_1 | 667 | 671 | PF00082 | 0.200 |
CLV_PCSK_SKI1_1 | 785 | 789 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 890 | 894 | PF00082 | 0.200 |
CLV_PCSK_SKI1_1 | 917 | 921 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 965 | 969 | PF00082 | 0.333 |
DEG_MDM2_SWIB_1 | 48 | 55 | PF02201 | 0.580 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.586 |
DEG_SPOP_SBC_1 | 17 | 21 | PF00917 | 0.548 |
DOC_ANK_TNKS_1 | 538 | 545 | PF00023 | 0.400 |
DOC_CKS1_1 | 498 | 503 | PF01111 | 0.400 |
DOC_MAPK_gen_1 | 340 | 348 | PF00069 | 0.539 |
DOC_MAPK_gen_1 | 402 | 409 | PF00069 | 0.471 |
DOC_MAPK_gen_1 | 420 | 427 | PF00069 | 0.300 |
DOC_MAPK_gen_1 | 434 | 443 | PF00069 | 0.265 |
DOC_MAPK_gen_1 | 723 | 731 | PF00069 | 0.400 |
DOC_MAPK_JIP1_4 | 788 | 794 | PF00069 | 0.531 |
DOC_MAPK_MEF2A_6 | 239 | 247 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 420 | 427 | PF00069 | 0.325 |
DOC_MAPK_MEF2A_6 | 436 | 445 | PF00069 | 0.293 |
DOC_MAPK_MEF2A_6 | 684 | 693 | PF00069 | 0.400 |
DOC_MAPK_MEF2A_6 | 799 | 807 | PF00069 | 0.294 |
DOC_MAPK_MEF2A_6 | 877 | 885 | PF00069 | 0.400 |
DOC_PP1_RVXF_1 | 225 | 231 | PF00149 | 0.476 |
DOC_PP1_RVXF_1 | 888 | 895 | PF00149 | 0.400 |
DOC_PP4_FxxP_1 | 15 | 18 | PF00568 | 0.568 |
DOC_PP4_FxxP_1 | 374 | 377 | PF00568 | 0.590 |
DOC_PP4_FxxP_1 | 60 | 63 | PF00568 | 0.647 |
DOC_PP4_FxxP_1 | 618 | 621 | PF00568 | 0.400 |
DOC_PP4_FxxP_1 | 634 | 637 | PF00568 | 0.400 |
DOC_PP4_FxxP_1 | 862 | 865 | PF00568 | 0.400 |
DOC_USP7_MATH_1 | 1034 | 1038 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 1071 | 1075 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 746 | 750 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 772 | 776 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 989 | 993 | PF00917 | 0.534 |
DOC_USP7_UBL2_3 | 290 | 294 | PF12436 | 0.361 |
DOC_USP7_UBL2_3 | 326 | 330 | PF12436 | 0.407 |
DOC_USP7_UBL2_3 | 965 | 969 | PF12436 | 0.456 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 497 | 502 | PF00397 | 0.400 |
DOC_WW_Pin1_4 | 527 | 532 | PF00397 | 0.400 |
DOC_WW_Pin1_4 | 600 | 605 | PF00397 | 0.400 |
DOC_WW_Pin1_4 | 711 | 716 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 847 | 852 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.609 |
LIG_14-3-3_CanoR_1 | 1030 | 1038 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 120 | 126 | PF00244 | 0.709 |
LIG_14-3-3_CanoR_1 | 16 | 26 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 2 | 10 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 29 | 35 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 420 | 426 | PF00244 | 0.329 |
LIG_14-3-3_CanoR_1 | 923 | 930 | PF00244 | 0.316 |
LIG_Actin_WH2_2 | 469 | 486 | PF00022 | 0.414 |
LIG_Actin_WH2_2 | 551 | 567 | PF00022 | 0.400 |
LIG_APCC_ABBA_1 | 729 | 734 | PF00400 | 0.450 |
LIG_BIR_III_2 | 209 | 213 | PF00653 | 0.654 |
LIG_BRCT_BRCA1_1 | 1055 | 1059 | PF00533 | 0.300 |
LIG_BRCT_BRCA1_1 | 308 | 312 | PF00533 | 0.336 |
LIG_BRCT_BRCA1_1 | 354 | 358 | PF00533 | 0.567 |
LIG_BRCT_BRCA1_1 | 359 | 363 | PF00533 | 0.578 |
LIG_Clathr_ClatBox_1 | 891 | 895 | PF01394 | 0.400 |
LIG_CtBP_PxDLS_1 | 637 | 641 | PF00389 | 0.495 |
LIG_FHA_1 | 1042 | 1048 | PF00498 | 0.418 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.654 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.398 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.362 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.551 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.497 |
LIG_FHA_1 | 584 | 590 | PF00498 | 0.400 |
LIG_FHA_1 | 671 | 677 | PF00498 | 0.400 |
LIG_FHA_1 | 686 | 692 | PF00498 | 0.400 |
LIG_FHA_1 | 712 | 718 | PF00498 | 0.431 |
LIG_FHA_1 | 824 | 830 | PF00498 | 0.423 |
LIG_FHA_1 | 925 | 931 | PF00498 | 0.286 |
LIG_FHA_1 | 976 | 982 | PF00498 | 0.307 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.651 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.603 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.475 |
LIG_FHA_2 | 927 | 933 | PF00498 | 0.410 |
LIG_FHA_2 | 958 | 964 | PF00498 | 0.446 |
LIG_FHA_2 | 972 | 978 | PF00498 | 0.375 |
LIG_FHA_2 | 983 | 989 | PF00498 | 0.446 |
LIG_LIR_Apic_2 | 125 | 129 | PF02991 | 0.537 |
LIG_LIR_Apic_2 | 14 | 18 | PF02991 | 0.608 |
LIG_LIR_Apic_2 | 371 | 377 | PF02991 | 0.515 |
LIG_LIR_Apic_2 | 59 | 63 | PF02991 | 0.652 |
LIG_LIR_Apic_2 | 678 | 683 | PF02991 | 0.400 |
LIG_LIR_Apic_2 | 860 | 865 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 355 | 363 | PF02991 | 0.626 |
LIG_LIR_Gen_1 | 550 | 558 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 610 | 619 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 628 | 638 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 688 | 695 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 698 | 708 | PF02991 | 0.400 |
LIG_LIR_LC3C_4 | 566 | 571 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 223 | 228 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 355 | 361 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 478 | 483 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 50 | 55 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 550 | 554 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 628 | 633 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 688 | 693 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 698 | 704 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 860 | 864 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.612 |
LIG_LYPXL_S_1 | 96 | 100 | PF13949 | 0.615 |
LIG_LYPXL_yS_3 | 97 | 100 | PF13949 | 0.615 |
LIG_Pex14_1 | 508 | 512 | PF04695 | 0.400 |
LIG_Pex14_2 | 1053 | 1057 | PF04695 | 0.222 |
LIG_Pex14_2 | 48 | 52 | PF04695 | 0.577 |
LIG_Pex14_2 | 630 | 634 | PF04695 | 0.400 |
LIG_Pex14_2 | 894 | 898 | PF04695 | 0.400 |
LIG_PTB_Apo_2 | 54 | 61 | PF02174 | 0.480 |
LIG_PTB_Apo_2 | 9 | 16 | PF02174 | 0.620 |
LIG_Rb_pABgroove_1 | 441 | 449 | PF01858 | 0.274 |
LIG_REV1ctd_RIR_1 | 310 | 319 | PF16727 | 0.376 |
LIG_SH2_CRK | 225 | 229 | PF00017 | 0.477 |
LIG_SH2_CRK | 258 | 262 | PF00017 | 0.498 |
LIG_SH2_CRK | 480 | 484 | PF00017 | 0.400 |
LIG_SH2_CRK | 551 | 555 | PF00017 | 0.400 |
LIG_SH2_CRK | 701 | 705 | PF00017 | 0.447 |
LIG_SH2_CRK | 922 | 926 | PF00017 | 0.268 |
LIG_SH2_GRB2like | 861 | 864 | PF00017 | 0.495 |
LIG_SH2_NCK_1 | 258 | 262 | PF00017 | 0.365 |
LIG_SH2_SRC | 680 | 683 | PF00017 | 0.400 |
LIG_SH2_STAT3 | 935 | 938 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 480 | 483 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 557 | 560 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 660 | 663 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 680 | 683 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 843 | 846 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 861 | 864 | PF00017 | 0.495 |
LIG_SH3_1 | 268 | 274 | PF00018 | 0.424 |
LIG_SH3_2 | 271 | 276 | PF14604 | 0.423 |
LIG_SH3_3 | 1009 | 1015 | PF00018 | 0.631 |
LIG_SH3_3 | 1076 | 1082 | PF00018 | 0.577 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.436 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.424 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.656 |
LIG_SH3_3 | 423 | 429 | PF00018 | 0.306 |
LIG_SH3_3 | 495 | 501 | PF00018 | 0.414 |
LIG_SH3_3 | 641 | 647 | PF00018 | 0.400 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.650 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.491 |
LIG_SUMO_SIM_anti_2 | 1107 | 1117 | PF11976 | 0.693 |
LIG_SUMO_SIM_anti_2 | 545 | 550 | PF11976 | 0.400 |
LIG_SUMO_SIM_anti_2 | 566 | 571 | PF11976 | 0.386 |
LIG_SUMO_SIM_anti_2 | 714 | 720 | PF11976 | 0.423 |
LIG_SUMO_SIM_anti_2 | 817 | 823 | PF11976 | 0.435 |
LIG_SUMO_SIM_anti_2 | 828 | 833 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 244 | 251 | PF11976 | 0.370 |
LIG_SUMO_SIM_par_1 | 295 | 300 | PF11976 | 0.335 |
LIG_SUMO_SIM_par_1 | 545 | 550 | PF11976 | 0.400 |
LIG_SUMO_SIM_par_1 | 714 | 720 | PF11976 | 0.400 |
LIG_SUMO_SIM_par_1 | 817 | 823 | PF11976 | 0.432 |
LIG_TRAF2_1 | 1083 | 1086 | PF00917 | 0.689 |
LIG_TRAF2_1 | 1124 | 1127 | PF00917 | 0.704 |
LIG_TRAF2_1 | 335 | 338 | PF00917 | 0.508 |
LIG_TRAF2_1 | 929 | 932 | PF00917 | 0.290 |
LIG_TRAF2_1 | 960 | 963 | PF00917 | 0.396 |
LIG_TYR_ITIM | 549 | 554 | PF00017 | 0.235 |
LIG_TYR_ITIM | 699 | 704 | PF00017 | 0.290 |
LIG_TYR_ITIM | 841 | 846 | PF00017 | 0.368 |
LIG_TYR_ITIM | 859 | 864 | PF00017 | 0.368 |
LIG_TYR_ITIM | 95 | 100 | PF00017 | 0.612 |
LIG_UBA3_1 | 718 | 724 | PF00899 | 0.235 |
LIG_UBA3_1 | 831 | 839 | PF00899 | 0.368 |
LIG_WRC_WIRS_1 | 1035 | 1040 | PF05994 | 0.455 |
LIG_WRC_WIRS_1 | 1054 | 1059 | PF05994 | 0.301 |
MOD_CDK_SPK_2 | 527 | 532 | PF00069 | 0.235 |
MOD_CDK_SPxK_1 | 847 | 853 | PF00069 | 0.368 |
MOD_CDK_SPxxK_3 | 220 | 227 | PF00069 | 0.517 |
MOD_CDK_SPxxK_3 | 847 | 854 | PF00069 | 0.368 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.561 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.717 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.514 |
MOD_CK1_1 | 527 | 533 | PF00069 | 0.235 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.678 |
MOD_CK1_1 | 662 | 668 | PF00069 | 0.244 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.684 |
MOD_CK1_1 | 823 | 829 | PF00069 | 0.235 |
MOD_CK1_1 | 926 | 932 | PF00069 | 0.289 |
MOD_CK2_1 | 1101 | 1107 | PF00069 | 0.587 |
MOD_CK2_1 | 1121 | 1127 | PF00069 | 0.451 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.595 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.518 |
MOD_CK2_1 | 672 | 678 | PF00069 | 0.235 |
MOD_CK2_1 | 926 | 932 | PF00069 | 0.289 |
MOD_CK2_1 | 957 | 963 | PF00069 | 0.415 |
MOD_CK2_1 | 982 | 988 | PF00069 | 0.416 |
MOD_Cter_Amidation | 418 | 421 | PF01082 | 0.515 |
MOD_Cter_Amidation | 762 | 765 | PF01082 | 0.694 |
MOD_GlcNHglycan | 1018 | 1021 | PF01048 | 0.480 |
MOD_GlcNHglycan | 1032 | 1035 | PF01048 | 0.470 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.661 |
MOD_GlcNHglycan | 156 | 160 | PF01048 | 0.717 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.548 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.531 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.550 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.336 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.542 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.348 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.235 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.706 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.573 |
MOD_GlcNHglycan | 709 | 712 | PF01048 | 0.286 |
MOD_GlcNHglycan | 719 | 722 | PF01048 | 0.197 |
MOD_GlcNHglycan | 744 | 747 | PF01048 | 0.530 |
MOD_GlcNHglycan | 748 | 751 | PF01048 | 0.582 |
MOD_GlcNHglycan | 769 | 772 | PF01048 | 0.761 |
MOD_GlcNHglycan | 944 | 947 | PF01048 | 0.423 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.664 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.468 |
MOD_GSK3_1 | 1030 | 1037 | PF00069 | 0.497 |
MOD_GSK3_1 | 1122 | 1129 | PF00069 | 0.629 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.695 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.438 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.556 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.537 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.219 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.662 |
MOD_GSK3_1 | 672 | 679 | PF00069 | 0.235 |
MOD_GSK3_1 | 707 | 714 | PF00069 | 0.303 |
MOD_GSK3_1 | 742 | 749 | PF00069 | 0.511 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.607 |
MOD_GSK3_1 | 971 | 978 | PF00069 | 0.321 |
MOD_GSK3_1 | 989 | 996 | PF00069 | 0.521 |
MOD_N-GLC_1 | 11 | 16 | PF02516 | 0.628 |
MOD_N-GLC_1 | 353 | 358 | PF02516 | 0.624 |
MOD_N-GLC_1 | 56 | 61 | PF02516 | 0.482 |
MOD_N-GLC_1 | 676 | 681 | PF02516 | 0.281 |
MOD_N-GLC_1 | 823 | 828 | PF02516 | 0.235 |
MOD_N-GLC_2 | 507 | 509 | PF02516 | 0.235 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.540 |
MOD_NEK2_1 | 1053 | 1058 | PF00069 | 0.225 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.335 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.529 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.235 |
MOD_NEK2_1 | 670 | 675 | PF00069 | 0.235 |
MOD_NEK2_1 | 835 | 840 | PF00069 | 0.269 |
MOD_NEK2_1 | 846 | 851 | PF00069 | 0.206 |
MOD_NEK2_1 | 872 | 877 | PF00069 | 0.235 |
MOD_NEK2_1 | 924 | 929 | PF00069 | 0.285 |
MOD_NEK2_1 | 982 | 987 | PF00069 | 0.414 |
MOD_NEK2_1 | 993 | 998 | PF00069 | 0.524 |
MOD_NEK2_2 | 11 | 16 | PF00069 | 0.691 |
MOD_PIKK_1 | 1092 | 1098 | PF00454 | 0.539 |
MOD_PIKK_1 | 119 | 125 | PF00454 | 0.659 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.591 |
MOD_PIKK_1 | 662 | 668 | PF00454 | 0.235 |
MOD_PIKK_1 | 670 | 676 | PF00454 | 0.235 |
MOD_PIKK_1 | 823 | 829 | PF00454 | 0.235 |
MOD_PIKK_1 | 864 | 870 | PF00454 | 0.235 |
MOD_PK_1 | 239 | 245 | PF00069 | 0.467 |
MOD_PK_1 | 284 | 290 | PF00069 | 0.396 |
MOD_PK_1 | 421 | 427 | PF00069 | 0.450 |
MOD_PK_1 | 672 | 678 | PF00069 | 0.219 |
MOD_PKA_1 | 1016 | 1022 | PF00069 | 0.513 |
MOD_PKA_1 | 29 | 35 | PF00069 | 0.479 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.544 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.699 |
MOD_PKA_2 | 559 | 565 | PF00069 | 0.235 |
MOD_PKA_2 | 670 | 676 | PF00069 | 0.235 |
MOD_PKA_2 | 767 | 773 | PF00069 | 0.605 |
MOD_PKB_1 | 764 | 772 | PF00069 | 0.616 |
MOD_Plk_1 | 1087 | 1093 | PF00069 | 0.742 |
MOD_Plk_1 | 353 | 359 | PF00069 | 0.618 |
MOD_Plk_1 | 56 | 62 | PF00069 | 0.436 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.505 |
MOD_Plk_1 | 676 | 682 | PF00069 | 0.235 |
MOD_Plk_1 | 685 | 691 | PF00069 | 0.235 |
MOD_Plk_4 | 1053 | 1059 | PF00069 | 0.306 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.395 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.562 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.332 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.235 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.235 |
MOD_Plk_4 | 659 | 665 | PF00069 | 0.386 |
MOD_Plk_4 | 676 | 682 | PF00069 | 0.139 |
MOD_Plk_4 | 685 | 691 | PF00069 | 0.235 |
MOD_Plk_4 | 778 | 784 | PF00069 | 0.349 |
MOD_Plk_4 | 801 | 807 | PF00069 | 0.299 |
MOD_Plk_4 | 963 | 969 | PF00069 | 0.474 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.410 |
MOD_ProDKin_1 | 497 | 503 | PF00069 | 0.235 |
MOD_ProDKin_1 | 527 | 533 | PF00069 | 0.235 |
MOD_ProDKin_1 | 600 | 606 | PF00069 | 0.235 |
MOD_ProDKin_1 | 711 | 717 | PF00069 | 0.278 |
MOD_ProDKin_1 | 847 | 853 | PF00069 | 0.368 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.607 |
MOD_SUMO_for_1 | 169 | 172 | PF00179 | 0.645 |
MOD_SUMO_for_1 | 275 | 278 | PF00179 | 0.427 |
MOD_SUMO_for_1 | 329 | 332 | PF00179 | 0.454 |
MOD_SUMO_rev_2 | 1003 | 1007 | PF00179 | 0.508 |
MOD_SUMO_rev_2 | 1019 | 1028 | PF00179 | 0.573 |
MOD_SUMO_rev_2 | 21 | 27 | PF00179 | 0.614 |
MOD_SUMO_rev_2 | 319 | 327 | PF00179 | 0.479 |
MOD_SUMO_rev_2 | 332 | 341 | PF00179 | 0.489 |
MOD_SUMO_rev_2 | 769 | 778 | PF00179 | 0.378 |
MOD_SUMO_rev_2 | 926 | 934 | PF00179 | 0.277 |
MOD_SUMO_rev_2 | 962 | 967 | PF00179 | 0.494 |
TRG_DiLeu_BaEn_1 | 815 | 820 | PF01217 | 0.300 |
TRG_DiLeu_BaEn_1 | 869 | 874 | PF01217 | 0.235 |
TRG_DiLeu_BaEn_4 | 1117 | 1123 | PF01217 | 0.589 |
TRG_DiLeu_BaEn_4 | 635 | 641 | PF01217 | 0.313 |
TRG_DiLeu_BaLyEn_6 | 32 | 37 | PF01217 | 0.662 |
TRG_DiLeu_BaLyEn_6 | 887 | 892 | PF01217 | 0.235 |
TRG_DiLeu_BaLyEn_6 | 920 | 925 | PF01217 | 0.292 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 480 | 483 | PF00928 | 0.235 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.235 |
TRG_ENDOCYTIC_2 | 660 | 663 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 701 | 704 | PF00928 | 0.235 |
TRG_ENDOCYTIC_2 | 843 | 846 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 861 | 864 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 922 | 925 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.615 |
TRG_ER_diArg_1 | 363 | 366 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 595 | 598 | PF00400 | 0.235 |
TRG_ER_diArg_1 | 670 | 672 | PF00400 | 0.219 |
TRG_ER_diArg_1 | 764 | 766 | PF00400 | 0.701 |
TRG_NES_CRM1_1 | 559 | 573 | PF08389 | 0.300 |
TRG_NLS_MonoExtN_4 | 1015 | 1020 | PF00514 | 0.621 |
TRG_NLS_MonoExtN_4 | 851 | 857 | PF00514 | 0.368 |
TRG_Pf-PMV_PEXEL_1 | 514 | 518 | PF00026 | 0.313 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5G3 | Leptomonas seymouri | 80% | 99% |
A0A1X0NIN9 | Trypanosomatidae | 65% | 100% |
A0A3S7WY74 | Leishmania donovani | 94% | 100% |
A0A422MV13 | Trypanosoma rangeli | 67% | 100% |
A4HDD3 | Leishmania braziliensis | 89% | 100% |
A4HRE5 | Leishmania infantum | 25% | 100% |
A4I0R4 | Leishmania infantum | 94% | 100% |
D0A743 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 65% | 100% |
Q4QAQ7 | Leishmania major | 94% | 100% |
Q6PFE3 | Mus musculus | 38% | 100% |
Q9DG67 | Gallus gallus | 36% | 100% |
V5BVU6 | Trypanosoma cruzi | 73% | 100% |