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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 11 |
GO:0016020 | membrane | 2 | 7 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: Q4Q8A5
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 2 |
GO:0006281 | DNA repair | 5 | 2 |
GO:0006289 | nucleotide-excision repair | 6 | 2 |
GO:0006302 | double-strand break repair | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006950 | response to stress | 2 | 2 |
GO:0006974 | DNA damage response | 4 | 2 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0022414 | reproductive process | 1 | 2 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1903046 | meiotic cell cycle process | 2 | 2 |
GO:1990918 | double-strand break repair involved in meiotic recombination | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003678 | DNA helicase activity | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 12 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016887 | ATP hydrolysis activity | 7 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1036 | 1040 | PF00656 | 0.738 |
CLV_C14_Caspase3-7 | 164 | 168 | PF00656 | 0.720 |
CLV_C14_Caspase3-7 | 629 | 633 | PF00656 | 0.591 |
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.265 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.246 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 511 | 513 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 814 | 816 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 960 | 962 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.476 |
CLV_PCSK_FUR_1 | 109 | 113 | PF00082 | 0.413 |
CLV_PCSK_FUR_1 | 472 | 476 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 474 | 476 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 511 | 513 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 572 | 574 | PF00082 | 0.260 |
CLV_PCSK_KEX2_1 | 960 | 962 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.425 |
CLV_PCSK_PC1ET2_1 | 124 | 126 | PF00082 | 0.565 |
CLV_PCSK_PC1ET2_1 | 478 | 480 | PF00082 | 0.747 |
CLV_PCSK_PC1ET2_1 | 572 | 574 | PF00082 | 0.260 |
CLV_PCSK_PC1ET2_1 | 97 | 99 | PF00082 | 0.423 |
CLV_PCSK_PC7_1 | 474 | 480 | PF00082 | 0.700 |
CLV_PCSK_SKI1_1 | 1096 | 1100 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 1108 | 1112 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 579 | 583 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 610 | 614 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 626 | 630 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 667 | 671 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 787 | 791 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 861 | 865 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 907 | 911 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 960 | 964 | PF00082 | 0.415 |
DEG_APCC_DBOX_1 | 388 | 396 | PF00400 | 0.512 |
DEG_SCF_TRCP1_1 | 632 | 638 | PF00400 | 0.662 |
DEG_SPOP_SBC_1 | 416 | 420 | PF00917 | 0.699 |
DEG_SPOP_SBC_1 | 715 | 719 | PF00917 | 0.605 |
DOC_CDC14_PxL_1 | 340 | 348 | PF14671 | 0.544 |
DOC_CKS1_1 | 42 | 47 | PF01111 | 0.624 |
DOC_CKS1_1 | 973 | 978 | PF01111 | 0.685 |
DOC_CYCLIN_RxL_1 | 432 | 443 | PF00134 | 0.595 |
DOC_CYCLIN_yCln2_LP_2 | 39 | 45 | PF00134 | 0.631 |
DOC_CYCLIN_yCln2_LP_2 | 741 | 747 | PF00134 | 0.554 |
DOC_CYCLIN_yCln2_LP_2 | 866 | 872 | PF00134 | 0.544 |
DOC_MAPK_gen_1 | 185 | 193 | PF00069 | 0.671 |
DOC_MAPK_gen_1 | 572 | 580 | PF00069 | 0.468 |
DOC_MAPK_gen_1 | 784 | 792 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 846 | 855 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 907 | 917 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 389 | 396 | PF00069 | 0.578 |
DOC_MAPK_MEF2A_6 | 572 | 580 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 861 | 870 | PF00069 | 0.444 |
DOC_MAPK_NFAT4_5 | 389 | 397 | PF00069 | 0.580 |
DOC_MAPK_NFAT4_5 | 573 | 581 | PF00069 | 0.557 |
DOC_MAPK_NFAT4_5 | 861 | 869 | PF00069 | 0.508 |
DOC_MAPK_RevD_3 | 802 | 816 | PF00069 | 0.393 |
DOC_PP1_RVXF_1 | 328 | 335 | PF00149 | 0.455 |
DOC_PP2B_LxvP_1 | 1016 | 1019 | PF13499 | 0.684 |
DOC_PP2B_LxvP_1 | 204 | 207 | PF13499 | 0.585 |
DOC_PP2B_LxvP_1 | 39 | 42 | PF13499 | 0.615 |
DOC_PP2B_LxvP_1 | 771 | 774 | PF13499 | 0.470 |
DOC_PP2B_LxvP_1 | 866 | 869 | PF13499 | 0.544 |
DOC_PP4_FxxP_1 | 203 | 206 | PF00568 | 0.618 |
DOC_PP4_FxxP_1 | 531 | 534 | PF00568 | 0.416 |
DOC_PP4_FxxP_1 | 811 | 814 | PF00568 | 0.469 |
DOC_USP7_MATH_1 | 1035 | 1039 | PF00917 | 0.824 |
DOC_USP7_MATH_1 | 1042 | 1046 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 1061 | 1065 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 1102 | 1106 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 594 | 598 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 601 | 605 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 715 | 719 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 872 | 876 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 974 | 978 | PF00917 | 0.771 |
DOC_USP7_UBL2_3 | 126 | 130 | PF12436 | 0.715 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 1038 | 1043 | PF00397 | 0.787 |
DOC_WW_Pin1_4 | 1071 | 1076 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 673 | 678 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 966 | 971 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 972 | 977 | PF00397 | 0.652 |
LIG_14-3-3_CanoR_1 | 1024 | 1030 | PF00244 | 0.760 |
LIG_14-3-3_CanoR_1 | 1049 | 1055 | PF00244 | 0.731 |
LIG_14-3-3_CanoR_1 | 1062 | 1072 | PF00244 | 0.654 |
LIG_14-3-3_CanoR_1 | 180 | 187 | PF00244 | 0.712 |
LIG_14-3-3_CanoR_1 | 522 | 531 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 735 | 739 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 846 | 855 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 936 | 940 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 953 | 963 | PF00244 | 0.608 |
LIG_Actin_WH2_2 | 206 | 223 | PF00022 | 0.508 |
LIG_Actin_WH2_2 | 649 | 665 | PF00022 | 0.520 |
LIG_Actin_WH2_2 | 747 | 764 | PF00022 | 0.583 |
LIG_Actin_WH2_2 | 891 | 909 | PF00022 | 0.503 |
LIG_APCC_ABBA_1 | 366 | 371 | PF00400 | 0.455 |
LIG_APCC_ABBA_1 | 458 | 463 | PF00400 | 0.337 |
LIG_BRCT_BRCA1_1 | 458 | 462 | PF00533 | 0.295 |
LIG_BRCT_BRCA1_1 | 654 | 658 | PF00533 | 0.470 |
LIG_deltaCOP1_diTrp_1 | 167 | 176 | PF00928 | 0.546 |
LIG_EH_1 | 558 | 562 | PF12763 | 0.283 |
LIG_eIF4E_1 | 327 | 333 | PF01652 | 0.436 |
LIG_eIF4E_1 | 345 | 351 | PF01652 | 0.455 |
LIG_eIF4E_1 | 912 | 918 | PF01652 | 0.452 |
LIG_EVH1_2 | 172 | 176 | PF00568 | 0.599 |
LIG_FHA_1 | 1005 | 1011 | PF00498 | 0.730 |
LIG_FHA_1 | 1089 | 1095 | PF00498 | 0.699 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.551 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.456 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.654 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.731 |
LIG_FHA_1 | 636 | 642 | PF00498 | 0.703 |
LIG_FHA_1 | 644 | 650 | PF00498 | 0.524 |
LIG_FHA_1 | 756 | 762 | PF00498 | 0.512 |
LIG_FHA_1 | 784 | 790 | PF00498 | 0.511 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.494 |
LIG_FHA_1 | 819 | 825 | PF00498 | 0.513 |
LIG_FHA_1 | 836 | 842 | PF00498 | 0.414 |
LIG_FHA_1 | 890 | 896 | PF00498 | 0.510 |
LIG_FHA_2 | 1034 | 1040 | PF00498 | 0.766 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.751 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.555 |
LIG_FHA_2 | 441 | 447 | PF00498 | 0.299 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.406 |
LIG_FHA_2 | 627 | 633 | PF00498 | 0.591 |
LIG_FHA_2 | 758 | 764 | PF00498 | 0.552 |
LIG_Integrin_isoDGR_2 | 492 | 494 | PF01839 | 0.663 |
LIG_Integrin_RGD_1 | 481 | 483 | PF01839 | 0.665 |
LIG_LIR_Apic_2 | 167 | 172 | PF02991 | 0.572 |
LIG_LIR_Apic_2 | 597 | 601 | PF02991 | 0.615 |
LIG_LIR_Apic_2 | 808 | 814 | PF02991 | 0.535 |
LIG_LIR_Apic_2 | 919 | 925 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 287 | 297 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 427 | 434 | PF02991 | 0.658 |
LIG_LIR_Gen_1 | 446 | 455 | PF02991 | 0.225 |
LIG_LIR_Gen_1 | 655 | 665 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 737 | 746 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 287 | 292 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 337 | 343 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 446 | 451 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 459 | 464 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 557 | 561 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 655 | 661 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 676 | 681 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 690 | 695 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 737 | 741 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 875 | 879 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 911 | 915 | PF02991 | 0.452 |
LIG_LYPXL_yS_3 | 343 | 346 | PF13949 | 0.544 |
LIG_MLH1_MIPbox_1 | 458 | 462 | PF16413 | 0.295 |
LIG_MYND_1 | 729 | 733 | PF01753 | 0.573 |
LIG_NRBOX | 577 | 583 | PF00104 | 0.543 |
LIG_Pex14_1 | 959 | 963 | PF04695 | 0.585 |
LIG_Pex14_2 | 175 | 179 | PF04695 | 0.548 |
LIG_PTB_Apo_2 | 740 | 747 | PF02174 | 0.589 |
LIG_REV1ctd_RIR_1 | 173 | 181 | PF16727 | 0.579 |
LIG_SH2_CRK | 548 | 552 | PF00017 | 0.244 |
LIG_SH2_CRK | 738 | 742 | PF00017 | 0.539 |
LIG_SH2_CRK | 776 | 780 | PF00017 | 0.533 |
LIG_SH2_CRK | 912 | 916 | PF00017 | 0.470 |
LIG_SH2_NCK_1 | 1085 | 1089 | PF00017 | 0.650 |
LIG_SH2_NCK_1 | 335 | 339 | PF00017 | 0.495 |
LIG_SH2_NCK_1 | 922 | 926 | PF00017 | 0.510 |
LIG_SH2_SRC | 335 | 338 | PF00017 | 0.532 |
LIG_SH2_STAP1 | 1085 | 1089 | PF00017 | 0.709 |
LIG_SH2_STAP1 | 706 | 710 | PF00017 | 0.539 |
LIG_SH2_STAP1 | 890 | 894 | PF00017 | 0.510 |
LIG_SH2_STAT3 | 107 | 110 | PF00017 | 0.569 |
LIG_SH2_STAT3 | 46 | 49 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.643 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 890 | 893 | PF00017 | 0.455 |
LIG_SH3_2 | 869 | 874 | PF14604 | 0.452 |
LIG_SH3_3 | 1019 | 1025 | PF00018 | 0.681 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.747 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.572 |
LIG_SH3_3 | 697 | 703 | PF00018 | 0.573 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.569 |
LIG_SH3_3 | 801 | 807 | PF00018 | 0.519 |
LIG_SH3_3 | 866 | 872 | PF00018 | 0.452 |
LIG_SUMO_SIM_anti_2 | 390 | 398 | PF11976 | 0.458 |
LIG_SUMO_SIM_anti_2 | 788 | 793 | PF11976 | 0.489 |
LIG_SUMO_SIM_par_1 | 443 | 449 | PF11976 | 0.341 |
LIG_SUMO_SIM_par_1 | 914 | 920 | PF11976 | 0.444 |
LIG_TRAF2_1 | 1116 | 1119 | PF00917 | 0.757 |
LIG_TRFH_1 | 345 | 349 | PF08558 | 0.444 |
LIG_TYR_ITIM | 333 | 338 | PF00017 | 0.485 |
LIG_UBA3_1 | 577 | 584 | PF00899 | 0.522 |
LIG_WRC_WIRS_1 | 447 | 452 | PF05994 | 0.402 |
MOD_CDC14_SPxK_1 | 1041 | 1044 | PF00782 | 0.663 |
MOD_CDK_SPK_2 | 97 | 102 | PF00069 | 0.649 |
MOD_CDK_SPxK_1 | 1038 | 1044 | PF00069 | 0.670 |
MOD_CK1_1 | 1033 | 1039 | PF00069 | 0.810 |
MOD_CK1_1 | 1113 | 1119 | PF00069 | 0.716 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.730 |
MOD_CK1_1 | 717 | 723 | PF00069 | 0.709 |
MOD_CK2_1 | 1113 | 1119 | PF00069 | 0.732 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.747 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.556 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.299 |
MOD_CK2_1 | 501 | 507 | PF00069 | 0.396 |
MOD_CK2_1 | 603 | 609 | PF00069 | 0.713 |
MOD_CK2_1 | 757 | 763 | PF00069 | 0.596 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.550 |
MOD_Cter_Amidation | 472 | 475 | PF01082 | 0.600 |
MOD_GlcNHglycan | 1019 | 1022 | PF01048 | 0.505 |
MOD_GlcNHglycan | 1044 | 1047 | PF01048 | 0.505 |
MOD_GlcNHglycan | 1063 | 1066 | PF01048 | 0.494 |
MOD_GlcNHglycan | 1067 | 1070 | PF01048 | 0.530 |
MOD_GlcNHglycan | 1112 | 1116 | PF01048 | 0.506 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.529 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.552 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.318 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.390 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.525 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.571 |
MOD_GlcNHglycan | 603 | 606 | PF01048 | 0.507 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.403 |
MOD_GlcNHglycan | 616 | 619 | PF01048 | 0.542 |
MOD_GlcNHglycan | 632 | 635 | PF01048 | 0.520 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.273 |
MOD_GlcNHglycan | 763 | 767 | PF01048 | 0.331 |
MOD_GlcNHglycan | 884 | 887 | PF01048 | 0.244 |
MOD_GlcNHglycan | 976 | 979 | PF01048 | 0.526 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.734 |
MOD_GSK3_1 | 1033 | 1040 | PF00069 | 0.769 |
MOD_GSK3_1 | 1061 | 1068 | PF00069 | 0.698 |
MOD_GSK3_1 | 1084 | 1091 | PF00069 | 0.661 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.676 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.725 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.728 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.702 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.710 |
MOD_GSK3_1 | 652 | 659 | PF00069 | 0.550 |
MOD_GSK3_1 | 669 | 676 | PF00069 | 0.451 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.569 |
MOD_GSK3_1 | 714 | 721 | PF00069 | 0.636 |
MOD_GSK3_1 | 723 | 730 | PF00069 | 0.667 |
MOD_GSK3_1 | 757 | 764 | PF00069 | 0.534 |
MOD_GSK3_1 | 968 | 975 | PF00069 | 0.711 |
MOD_LATS_1 | 116 | 122 | PF00433 | 0.793 |
MOD_LATS_1 | 178 | 184 | PF00433 | 0.656 |
MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.306 |
MOD_N-GLC_1 | 722 | 727 | PF02516 | 0.478 |
MOD_N-GLC_1 | 828 | 833 | PF02516 | 0.350 |
MOD_N-GLC_1 | 853 | 858 | PF02516 | 0.375 |
MOD_N-GLC_2 | 339 | 341 | PF02516 | 0.310 |
MOD_NEK2_1 | 1050 | 1055 | PF00069 | 0.717 |
MOD_NEK2_1 | 1076 | 1081 | PF00069 | 0.640 |
MOD_NEK2_1 | 1084 | 1089 | PF00069 | 0.649 |
MOD_NEK2_1 | 1110 | 1115 | PF00069 | 0.737 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.777 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.510 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.544 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.640 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.418 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.389 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.437 |
MOD_NEK2_1 | 554 | 559 | PF00069 | 0.283 |
MOD_NEK2_1 | 561 | 566 | PF00069 | 0.283 |
MOD_NEK2_1 | 652 | 657 | PF00069 | 0.475 |
MOD_NEK2_1 | 661 | 666 | PF00069 | 0.492 |
MOD_NEK2_1 | 734 | 739 | PF00069 | 0.570 |
MOD_NEK2_1 | 746 | 751 | PF00069 | 0.537 |
MOD_NEK2_1 | 757 | 762 | PF00069 | 0.521 |
MOD_NEK2_1 | 840 | 845 | PF00069 | 0.529 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.513 |
MOD_NEK2_1 | 952 | 957 | PF00069 | 0.542 |
MOD_NEK2_2 | 233 | 238 | PF00069 | 0.393 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.633 |
MOD_PIKK_1 | 501 | 507 | PF00454 | 0.452 |
MOD_PIKK_1 | 701 | 707 | PF00454 | 0.632 |
MOD_PIKK_1 | 724 | 730 | PF00454 | 0.727 |
MOD_PIKK_1 | 755 | 761 | PF00454 | 0.564 |
MOD_PIKK_1 | 805 | 811 | PF00454 | 0.503 |
MOD_PIKK_1 | 828 | 834 | PF00454 | 0.552 |
MOD_PIKK_1 | 954 | 960 | PF00454 | 0.494 |
MOD_PKA_1 | 118 | 124 | PF00069 | 0.752 |
MOD_PKA_2 | 1061 | 1067 | PF00069 | 0.728 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.773 |
MOD_PKA_2 | 734 | 740 | PF00069 | 0.598 |
MOD_PKA_2 | 761 | 767 | PF00069 | 0.524 |
MOD_PKA_2 | 929 | 935 | PF00069 | 0.486 |
MOD_PKA_2 | 952 | 958 | PF00069 | 0.625 |
MOD_PKB_1 | 1002 | 1010 | PF00069 | 0.736 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.494 |
MOD_Plk_1 | 608 | 614 | PF00069 | 0.758 |
MOD_Plk_1 | 687 | 693 | PF00069 | 0.579 |
MOD_Plk_1 | 941 | 947 | PF00069 | 0.588 |
MOD_Plk_2-3 | 158 | 164 | PF00069 | 0.658 |
MOD_Plk_2-3 | 381 | 387 | PF00069 | 0.455 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.601 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.482 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.384 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.603 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.238 |
MOD_Plk_4 | 687 | 693 | PF00069 | 0.560 |
MOD_Plk_4 | 727 | 733 | PF00069 | 0.600 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.532 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.718 |
MOD_ProDKin_1 | 1038 | 1044 | PF00069 | 0.788 |
MOD_ProDKin_1 | 1071 | 1077 | PF00069 | 0.695 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.678 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.550 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.475 |
MOD_ProDKin_1 | 673 | 679 | PF00069 | 0.563 |
MOD_ProDKin_1 | 966 | 972 | PF00069 | 0.654 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.575 |
MOD_SUMO_rev_2 | 348 | 357 | PF00179 | 0.436 |
TRG_DiLeu_BaEn_2 | 445 | 451 | PF01217 | 0.367 |
TRG_DiLeu_BaLyEn_6 | 346 | 351 | PF01217 | 0.455 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 548 | 551 | PF00928 | 0.244 |
TRG_ENDOCYTIC_2 | 738 | 741 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 776 | 779 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 912 | 915 | PF00928 | 0.452 |
TRG_ER_diArg_1 | 1002 | 1005 | PF00400 | 0.747 |
TRG_ER_diArg_1 | 108 | 111 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 118 | 120 | PF00400 | 0.706 |
TRG_ER_diArg_1 | 199 | 202 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 227 | 229 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 472 | 475 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 510 | 512 | PF00400 | 0.401 |
TRG_ER_diArg_1 | 521 | 524 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 959 | 961 | PF00400 | 0.542 |
TRG_NES_CRM1_1 | 307 | 317 | PF08389 | 0.515 |
TRG_NES_CRM1_1 | 398 | 412 | PF08389 | 0.620 |
TRG_NES_CRM1_1 | 456 | 467 | PF08389 | 0.310 |
TRG_NES_CRM1_1 | 857 | 871 | PF08389 | 0.452 |
TRG_NLS_Bipartite_1 | 111 | 128 | PF00514 | 0.714 |
TRG_NLS_MonoExtC_3 | 123 | 128 | PF00514 | 0.743 |
TRG_NLS_MonoExtC_3 | 184 | 190 | PF00514 | 0.619 |
TRG_NLS_MonoExtC_3 | 96 | 101 | PF00514 | 0.679 |
TRG_Pf-PMV_PEXEL_1 | 1082 | 1086 | PF00026 | 0.405 |
TRG_Pf-PMV_PEXEL_1 | 112 | 117 | PF00026 | 0.357 |
TRG_Pf-PMV_PEXEL_1 | 579 | 583 | PF00026 | 0.314 |
TRG_Pf-PMV_PEXEL_1 | 683 | 688 | PF00026 | 0.407 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8F0 | Leptomonas seymouri | 56% | 89% |
A0A0S4IQT3 | Bodo saltans | 38% | 100% |
A0A1X0NRE3 | Trypanosomatidae | 43% | 100% |
A0A3R7P0G4 | Trypanosoma rangeli | 43% | 100% |
A0A3S5H7J4 | Leishmania donovani | 92% | 100% |
A4HGL3 | Leishmania braziliensis | 79% | 100% |
A4I3N9 | Leishmania infantum | 91% | 88% |
D0A8C5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AZY0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5BAP9 | Trypanosoma cruzi | 43% | 100% |