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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0031298 | replication fork protection complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
Related structures:
AlphaFold database: Q4QEL3
Term | Name | Level | Count |
---|---|---|---|
GO:0000075 | cell cycle checkpoint signaling | 4 | 2 |
GO:0000076 | DNA replication checkpoint signaling | 6 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006259 | DNA metabolic process | 4 | 2 |
GO:0006275 | regulation of DNA replication | 6 | 2 |
GO:0006281 | DNA repair | 5 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006950 | response to stress | 2 | 2 |
GO:0006974 | DNA damage response | 4 | 2 |
GO:0007165 | signal transduction | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0008156 | negative regulation of DNA replication | 7 | 2 |
GO:0009892 | negative regulation of metabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010564 | regulation of cell cycle process | 5 | 2 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 2 |
GO:0010948 | negative regulation of cell cycle process | 6 | 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:0031570 | DNA integrity checkpoint signaling | 5 | 2 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0035556 | intracellular signal transduction | 3 | 2 |
GO:0043111 | replication fork arrest | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0045005 | DNA-templated DNA replication maintenance of fidelity | 5 | 2 |
GO:0045786 | negative regulation of cell cycle | 5 | 2 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0048478 | obsolete replication fork protection | 6 | 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:0050896 | response to stimulus | 1 | 2 |
GO:0051052 | regulation of DNA metabolic process | 5 | 2 |
GO:0051053 | negative regulation of DNA metabolic process | 6 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0051726 | regulation of cell cycle | 4 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 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:0090329 | regulation of DNA-templated DNA replication | 7 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 2 |
GO:1901988 | negative regulation of cell cycle phase transition | 7 | 2 |
GO:2000104 | negative regulation of DNA-templated DNA replication | 8 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003677 | DNA binding | 4 | 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 | 1037 | 1041 | PF00656 | 0.760 |
CLV_C14_Caspase3-7 | 1091 | 1095 | PF00656 | 0.668 |
CLV_C14_Caspase3-7 | 1104 | 1108 | PF00656 | 0.653 |
CLV_C14_Caspase3-7 | 728 | 732 | PF00656 | 0.700 |
CLV_C14_Caspase3-7 | 75 | 79 | PF00656 | 0.606 |
CLV_C14_Caspase3-7 | 797 | 801 | PF00656 | 0.639 |
CLV_C14_Caspase3-7 | 997 | 1001 | PF00656 | 0.645 |
CLV_NRD_NRD_1 | 1088 | 1090 | PF00675 | 0.798 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 604 | 606 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 775 | 777 | PF00675 | 0.634 |
CLV_PCSK_KEX2_1 | 1002 | 1004 | PF00082 | 0.792 |
CLV_PCSK_KEX2_1 | 1069 | 1071 | PF00082 | 0.706 |
CLV_PCSK_KEX2_1 | 1086 | 1088 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.693 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 603 | 605 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 701 | 703 | PF00082 | 0.592 |
CLV_PCSK_PC1ET2_1 | 1002 | 1004 | PF00082 | 0.792 |
CLV_PCSK_PC1ET2_1 | 1069 | 1071 | PF00082 | 0.738 |
CLV_PCSK_PC1ET2_1 | 1086 | 1088 | PF00082 | 0.806 |
CLV_PCSK_PC1ET2_1 | 176 | 178 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 444 | 446 | PF00082 | 0.589 |
CLV_PCSK_PC1ET2_1 | 7 | 9 | PF00082 | 0.510 |
CLV_PCSK_PC1ET2_1 | 701 | 703 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 1028 | 1032 | PF00082 | 0.795 |
CLV_PCSK_SKI1_1 | 1054 | 1058 | PF00082 | 0.768 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 486 | 490 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 546 | 550 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 655 | 659 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 824 | 828 | PF00082 | 0.683 |
CLV_PCSK_SKI1_1 | 898 | 902 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 965 | 969 | PF00082 | 0.503 |
CLV_Separin_Metazoa | 483 | 487 | PF03568 | 0.317 |
CLV_Separin_Metazoa | 741 | 745 | PF03568 | 0.690 |
DEG_APCC_DBOX_1 | 1002 | 1010 | PF00400 | 0.606 |
DEG_APCC_DBOX_1 | 332 | 340 | PF00400 | 0.292 |
DEG_APCC_DBOX_1 | 545 | 553 | PF00400 | 0.474 |
DEG_APCC_DBOX_1 | 7 | 15 | PF00400 | 0.488 |
DEG_APCC_DBOX_1 | 823 | 831 | PF00400 | 0.713 |
DEG_SPOP_SBC_1 | 24 | 28 | PF00917 | 0.507 |
DOC_AGCK_PIF_1 | 677 | 682 | PF00069 | 0.468 |
DOC_CYCLIN_RxL_1 | 962 | 972 | PF00134 | 0.517 |
DOC_CYCLIN_yCln2_LP_2 | 105 | 111 | PF00134 | 0.485 |
DOC_MAPK_gen_1 | 176 | 184 | PF00069 | 0.530 |
DOC_MAPK_gen_1 | 502 | 512 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 603 | 612 | PF00069 | 0.452 |
DOC_MAPK_gen_1 | 7 | 14 | PF00069 | 0.568 |
DOC_MAPK_MEF2A_6 | 104 | 111 | PF00069 | 0.534 |
DOC_MAPK_MEF2A_6 | 127 | 136 | PF00069 | 0.403 |
DOC_MAPK_MEF2A_6 | 183 | 192 | PF00069 | 0.409 |
DOC_MAPK_MEF2A_6 | 217 | 225 | PF00069 | 0.399 |
DOC_MAPK_MEF2A_6 | 264 | 273 | PF00069 | 0.763 |
DOC_MAPK_MEF2A_6 | 603 | 612 | PF00069 | 0.503 |
DOC_MAPK_MEF2A_6 | 650 | 658 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 7 | 14 | PF00069 | 0.568 |
DOC_MAPK_NFAT4_5 | 7 | 15 | PF00069 | 0.572 |
DOC_MAPK_RevD_3 | 163 | 177 | PF00069 | 0.403 |
DOC_PP1_RVXF_1 | 548 | 555 | PF00149 | 0.296 |
DOC_PP1_RVXF_1 | 653 | 659 | PF00149 | 0.466 |
DOC_PP2B_LxvP_1 | 105 | 108 | PF13499 | 0.481 |
DOC_PP2B_LxvP_1 | 134 | 137 | PF13499 | 0.455 |
DOC_PP2B_LxvP_1 | 697 | 700 | PF13499 | 0.562 |
DOC_PP4_FxxP_1 | 922 | 925 | PF00568 | 0.425 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 526 | 530 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 642 | 646 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 700 | 704 | PF00917 | 0.651 |
DOC_USP7_UBL2_3 | 383 | 387 | PF12436 | 0.630 |
DOC_USP7_UBL2_3 | 690 | 694 | PF12436 | 0.516 |
DOC_USP7_UBL2_3 | 704 | 708 | PF12436 | 0.729 |
DOC_WW_Pin1_4 | 1015 | 1020 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 522 | 527 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 844 | 849 | PF00397 | 0.539 |
LIG_14-3-3_CanoR_1 | 138 | 145 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 23 | 31 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 367 | 373 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 486 | 491 | PF00244 | 0.321 |
LIG_14-3-3_CanoR_1 | 934 | 939 | PF00244 | 0.626 |
LIG_Actin_WH2_2 | 535 | 552 | PF00022 | 0.375 |
LIG_APCC_ABBAyCdc20_2 | 277 | 283 | PF00400 | 0.699 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.497 |
LIG_BRCT_BRCA1_1 | 1017 | 1021 | PF00533 | 0.579 |
LIG_BRCT_BRCA1_1 | 27 | 31 | PF00533 | 0.524 |
LIG_BRCT_BRCA1_1 | 478 | 482 | PF00533 | 0.499 |
LIG_BRCT_BRCA1_1 | 838 | 842 | PF00533 | 0.537 |
LIG_BRCT_BRCA1_1 | 885 | 889 | PF00533 | 0.538 |
LIG_Clathr_ClatBox_1 | 11 | 15 | PF01394 | 0.567 |
LIG_deltaCOP1_diTrp_1 | 1071 | 1076 | PF00928 | 0.576 |
LIG_deltaCOP1_diTrp_1 | 325 | 331 | PF00928 | 0.452 |
LIG_deltaCOP1_diTrp_1 | 386 | 390 | PF00928 | 0.684 |
LIG_deltaCOP1_diTrp_1 | 756 | 764 | PF00928 | 0.685 |
LIG_EH1_1 | 218 | 226 | PF00400 | 0.498 |
LIG_EH1_1 | 574 | 582 | PF00400 | 0.322 |
LIG_EH1_1 | 873 | 881 | PF00400 | 0.489 |
LIG_eIF4E_1 | 614 | 620 | PF01652 | 0.464 |
LIG_eIF4E_1 | 693 | 699 | PF01652 | 0.523 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.403 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.537 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.746 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.582 |
LIG_FHA_1 | 518 | 524 | PF00498 | 0.625 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.462 |
LIG_FHA_1 | 679 | 685 | PF00498 | 0.457 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.478 |
LIG_FHA_1 | 962 | 968 | PF00498 | 0.600 |
LIG_FHA_2 | 1113 | 1119 | PF00498 | 0.755 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.535 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.613 |
LIG_FHA_2 | 974 | 980 | PF00498 | 0.636 |
LIG_GBD_Chelix_1 | 611 | 619 | PF00786 | 0.382 |
LIG_IRF3_LxIS_1 | 14 | 20 | PF10401 | 0.572 |
LIG_KLC1_Yacidic_2 | 974 | 979 | PF13176 | 0.631 |
LIG_LIR_Apic_2 | 341 | 347 | PF02991 | 0.549 |
LIG_LIR_Apic_2 | 921 | 925 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 160 | 171 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 270 | 280 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 421 | 428 | PF02991 | 0.690 |
LIG_LIR_Gen_1 | 475 | 485 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 489 | 498 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 529 | 539 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 587 | 597 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 681 | 688 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 839 | 848 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 852 | 863 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 91 | 101 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 972 | 983 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 988 | 994 | PF02991 | 0.601 |
LIG_LIR_LC3C_4 | 103 | 107 | PF02991 | 0.493 |
LIG_LIR_LC3C_4 | 222 | 227 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 385 | 391 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 421 | 426 | PF02991 | 0.755 |
LIG_LIR_Nem_3 | 475 | 480 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 489 | 493 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 529 | 535 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 565 | 569 | PF02991 | 0.649 |
LIG_LIR_Nem_3 | 587 | 593 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 681 | 685 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 787 | 793 | PF02991 | 0.737 |
LIG_LIR_Nem_3 | 839 | 845 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 852 | 858 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 885 | 891 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 953 | 957 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 972 | 978 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 988 | 992 | PF02991 | 0.594 |
LIG_MAD2 | 917 | 925 | PF02301 | 0.519 |
LIG_MLH1_MIPbox_1 | 838 | 842 | PF16413 | 0.537 |
LIG_MLH1_MIPbox_1 | 885 | 889 | PF16413 | 0.560 |
LIG_NRBOX | 124 | 130 | PF00104 | 0.399 |
LIG_NRBOX | 368 | 374 | PF00104 | 0.662 |
LIG_NRBOX | 621 | 627 | PF00104 | 0.496 |
LIG_PCNA_yPIPBox_3 | 308 | 322 | PF02747 | 0.473 |
LIG_PDZ_Class_1 | 1140 | 1145 | PF00595 | 0.551 |
LIG_Pex14_1 | 760 | 764 | PF04695 | 0.686 |
LIG_Pex14_2 | 566 | 570 | PF04695 | 0.494 |
LIG_Pex14_2 | 889 | 893 | PF04695 | 0.431 |
LIG_Pex14_2 | 923 | 927 | PF04695 | 0.479 |
LIG_PTB_Apo_2 | 226 | 233 | PF02174 | 0.406 |
LIG_PTB_Apo_2 | 887 | 894 | PF02174 | 0.428 |
LIG_PTB_Apo_2 | 921 | 928 | PF02174 | 0.445 |
LIG_PTB_Phospho_1 | 226 | 232 | PF10480 | 0.400 |
LIG_REV1ctd_RIR_1 | 839 | 847 | PF16727 | 0.574 |
LIG_SH2_CRK | 232 | 236 | PF00017 | 0.587 |
LIG_SH2_CRK | 532 | 536 | PF00017 | 0.515 |
LIG_SH2_CRK | 541 | 545 | PF00017 | 0.463 |
LIG_SH2_CRK | 855 | 859 | PF00017 | 0.528 |
LIG_SH2_CRK | 989 | 993 | PF00017 | 0.695 |
LIG_SH2_GRB2like | 532 | 535 | PF00017 | 0.536 |
LIG_SH2_GRB2like | 74 | 77 | PF00017 | 0.718 |
LIG_SH2_NCK_1 | 64 | 68 | PF00017 | 0.585 |
LIG_SH2_NCK_1 | 989 | 993 | PF00017 | 0.695 |
LIG_SH2_SRC | 74 | 77 | PF00017 | 0.631 |
LIG_SH2_STAP1 | 664 | 668 | PF00017 | 0.610 |
LIG_SH2_STAT3 | 314 | 317 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 551 | 554 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 614 | 617 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 954 | 957 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 975 | 978 | PF00017 | 0.594 |
LIG_SH2_STAT5 | 989 | 992 | PF00017 | 0.698 |
LIG_SH3_3 | 1128 | 1134 | PF00018 | 0.761 |
LIG_SH3_3 | 520 | 526 | PF00018 | 0.558 |
LIG_SH3_3 | 565 | 571 | PF00018 | 0.608 |
LIG_SUMO_SIM_anti_2 | 222 | 228 | PF11976 | 0.491 |
LIG_SUMO_SIM_anti_2 | 606 | 613 | PF11976 | 0.438 |
LIG_SUMO_SIM_anti_2 | 617 | 624 | PF11976 | 0.422 |
LIG_SUMO_SIM_par_1 | 10 | 16 | PF11976 | 0.561 |
LIG_SUMO_SIM_par_1 | 191 | 198 | PF11976 | 0.404 |
LIG_SUMO_SIM_par_1 | 519 | 525 | PF11976 | 0.598 |
LIG_SUMO_SIM_par_1 | 578 | 584 | PF11976 | 0.409 |
LIG_SUMO_SIM_par_1 | 617 | 624 | PF11976 | 0.464 |
LIG_TRAF2_1 | 347 | 350 | PF00917 | 0.534 |
LIG_TYR_ITIM | 539 | 544 | PF00017 | 0.405 |
LIG_TYR_ITIM | 853 | 858 | PF00017 | 0.511 |
LIG_TYR_ITIM | 973 | 978 | PF00017 | 0.638 |
LIG_UBA3_1 | 121 | 127 | PF00899 | 0.404 |
LIG_UBA3_1 | 149 | 154 | PF00899 | 0.546 |
LIG_WRC_WIRS_1 | 477 | 482 | PF05994 | 0.493 |
LIG_WRC_WIRS_1 | 487 | 492 | PF05994 | 0.447 |
LIG_WRC_WIRS_1 | 593 | 598 | PF05994 | 0.488 |
LIG_WRC_WIRS_1 | 679 | 684 | PF05994 | 0.469 |
MOD_CDC14_SPxK_1 | 364 | 367 | PF00782 | 0.651 |
MOD_CDK_SPK_2 | 844 | 849 | PF00069 | 0.539 |
MOD_CDK_SPxK_1 | 361 | 367 | PF00069 | 0.652 |
MOD_CDK_SPxxK_3 | 1015 | 1022 | PF00069 | 0.642 |
MOD_CK1_1 | 1015 | 1021 | PF00069 | 0.723 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.413 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.521 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.630 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.711 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.732 |
MOD_CK1_1 | 517 | 523 | PF00069 | 0.596 |
MOD_CK1_1 | 591 | 597 | PF00069 | 0.342 |
MOD_CK1_1 | 662 | 668 | PF00069 | 0.482 |
MOD_CK1_1 | 729 | 735 | PF00069 | 0.744 |
MOD_CK1_1 | 767 | 773 | PF00069 | 0.716 |
MOD_CK1_1 | 818 | 824 | PF00069 | 0.631 |
MOD_CK1_1 | 828 | 834 | PF00069 | 0.560 |
MOD_CK2_1 | 1043 | 1049 | PF00069 | 0.740 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.585 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.496 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.597 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.588 |
MOD_CK2_1 | 829 | 835 | PF00069 | 0.548 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.589 |
MOD_CK2_1 | 973 | 979 | PF00069 | 0.509 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.632 |
MOD_GlcNHglycan | 1031 | 1034 | PF01048 | 0.796 |
MOD_GlcNHglycan | 1100 | 1106 | PF01048 | 0.796 |
MOD_GlcNHglycan | 1109 | 1112 | PF01048 | 0.746 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.528 |
MOD_GlcNHglycan | 265 | 269 | PF01048 | 0.748 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.648 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.709 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.441 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.499 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.494 |
MOD_GlcNHglycan | 577 | 580 | PF01048 | 0.520 |
MOD_GlcNHglycan | 731 | 734 | PF01048 | 0.743 |
MOD_GlcNHglycan | 770 | 773 | PF01048 | 0.654 |
MOD_GlcNHglycan | 779 | 782 | PF01048 | 0.753 |
MOD_GlcNHglycan | 838 | 841 | PF01048 | 0.559 |
MOD_GlcNHglycan | 948 | 951 | PF01048 | 0.541 |
MOD_GSK3_1 | 1029 | 1036 | PF00069 | 0.751 |
MOD_GSK3_1 | 1039 | 1046 | PF00069 | 0.671 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.492 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.640 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.649 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.753 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.574 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.560 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.561 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.320 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.366 |
MOD_GSK3_1 | 764 | 771 | PF00069 | 0.718 |
MOD_GSK3_1 | 804 | 811 | PF00069 | 0.699 |
MOD_GSK3_1 | 815 | 822 | PF00069 | 0.577 |
MOD_GSK3_1 | 825 | 832 | PF00069 | 0.586 |
MOD_GSK3_1 | 849 | 856 | PF00069 | 0.485 |
MOD_GSK3_1 | 946 | 953 | PF00069 | 0.602 |
MOD_GSK3_1 | 957 | 964 | PF00069 | 0.530 |
MOD_GSK3_1 | 969 | 976 | PF00069 | 0.521 |
MOD_GSK3_1 | 981 | 988 | PF00069 | 0.629 |
MOD_GSK3_1 | 992 | 999 | PF00069 | 0.547 |
MOD_LATS_1 | 262 | 268 | PF00433 | 0.706 |
MOD_N-GLC_1 | 1107 | 1112 | PF02516 | 0.692 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.461 |
MOD_N-GLC_1 | 230 | 235 | PF02516 | 0.492 |
MOD_N-GLC_1 | 258 | 263 | PF02516 | 0.649 |
MOD_N-GLC_1 | 726 | 731 | PF02516 | 0.737 |
MOD_N-GLC_1 | 822 | 827 | PF02516 | 0.596 |
MOD_N-GLC_1 | 849 | 854 | PF02516 | 0.513 |
MOD_NEK2_1 | 1057 | 1062 | PF00069 | 0.662 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.448 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.423 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.611 |
MOD_NEK2_1 | 488 | 493 | PF00069 | 0.418 |
MOD_NEK2_1 | 588 | 593 | PF00069 | 0.439 |
MOD_NEK2_1 | 621 | 626 | PF00069 | 0.407 |
MOD_NEK2_1 | 643 | 648 | PF00069 | 0.385 |
MOD_NEK2_1 | 680 | 685 | PF00069 | 0.369 |
MOD_NEK2_1 | 764 | 769 | PF00069 | 0.730 |
MOD_NEK2_1 | 853 | 858 | PF00069 | 0.417 |
MOD_NEK2_1 | 957 | 962 | PF00069 | 0.462 |
MOD_NEK2_1 | 973 | 978 | PF00069 | 0.503 |
MOD_NEK2_1 | 987 | 992 | PF00069 | 0.538 |
MOD_NEK2_2 | 418 | 423 | PF00069 | 0.750 |
MOD_PIKK_1 | 1034 | 1040 | PF00454 | 0.802 |
MOD_PIKK_1 | 1055 | 1061 | PF00454 | 0.581 |
MOD_PIKK_1 | 809 | 815 | PF00454 | 0.748 |
MOD_PK_1 | 815 | 821 | PF00069 | 0.742 |
MOD_PK_1 | 934 | 940 | PF00069 | 0.608 |
MOD_PKA_1 | 382 | 388 | PF00069 | 0.628 |
MOD_PKA_2 | 1038 | 1044 | PF00069 | 0.740 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.585 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.593 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.593 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.666 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.638 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.525 |
MOD_PKA_2 | 808 | 814 | PF00069 | 0.726 |
MOD_PKA_2 | 961 | 967 | PF00069 | 0.618 |
MOD_Plk_1 | 1004 | 1010 | PF00069 | 0.741 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.527 |
MOD_Plk_1 | 293 | 299 | PF00069 | 0.711 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.553 |
MOD_Plk_1 | 606 | 612 | PF00069 | 0.530 |
MOD_Plk_1 | 662 | 668 | PF00069 | 0.477 |
MOD_Plk_1 | 726 | 732 | PF00069 | 0.700 |
MOD_Plk_1 | 764 | 770 | PF00069 | 0.670 |
MOD_Plk_1 | 786 | 792 | PF00069 | 0.692 |
MOD_Plk_1 | 822 | 828 | PF00069 | 0.701 |
MOD_Plk_1 | 849 | 855 | PF00069 | 0.495 |
MOD_Plk_1 | 957 | 963 | PF00069 | 0.472 |
MOD_Plk_1 | 973 | 979 | PF00069 | 0.428 |
MOD_Plk_2-3 | 284 | 290 | PF00069 | 0.647 |
MOD_Plk_2-3 | 726 | 732 | PF00069 | 0.752 |
MOD_Plk_2-3 | 736 | 742 | PF00069 | 0.720 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.437 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.407 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.526 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.490 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.579 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.651 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.646 |
MOD_Plk_4 | 592 | 598 | PF00069 | 0.440 |
MOD_Plk_4 | 606 | 612 | PF00069 | 0.365 |
MOD_Plk_4 | 621 | 627 | PF00069 | 0.383 |
MOD_Plk_4 | 643 | 649 | PF00069 | 0.390 |
MOD_Plk_4 | 870 | 876 | PF00069 | 0.478 |
MOD_Plk_4 | 883 | 889 | PF00069 | 0.428 |
MOD_Plk_4 | 934 | 940 | PF00069 | 0.670 |
MOD_Plk_4 | 950 | 956 | PF00069 | 0.477 |
MOD_Plk_4 | 973 | 979 | PF00069 | 0.525 |
MOD_ProDKin_1 | 1015 | 1021 | PF00069 | 0.650 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.721 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.665 |
MOD_ProDKin_1 | 522 | 528 | PF00069 | 0.597 |
MOD_ProDKin_1 | 844 | 850 | PF00069 | 0.532 |
MOD_SUMO_for_1 | 1001 | 1004 | PF00179 | 0.762 |
MOD_SUMO_for_1 | 257 | 260 | PF00179 | 0.538 |
MOD_SUMO_for_1 | 559 | 562 | PF00179 | 0.537 |
MOD_SUMO_rev_2 | 265 | 273 | PF00179 | 0.700 |
MOD_SUMO_rev_2 | 501 | 510 | PF00179 | 0.568 |
MOD_SUMO_rev_2 | 770 | 779 | PF00179 | 0.742 |
MOD_SUMO_rev_2 | 974 | 983 | PF00179 | 0.495 |
TRG_DiLeu_BaEn_1 | 161 | 166 | PF01217 | 0.412 |
TRG_DiLeu_BaEn_1 | 617 | 622 | PF01217 | 0.448 |
TRG_DiLeu_BaEn_4 | 349 | 355 | PF01217 | 0.545 |
TRG_DiLeu_BaLyEn_6 | 105 | 110 | PF01217 | 0.404 |
TRG_DiLeu_BaLyEn_6 | 40 | 45 | PF01217 | 0.540 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.686 |
TRG_ENDOCYTIC_2 | 532 | 535 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 541 | 544 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.256 |
TRG_ENDOCYTIC_2 | 855 | 858 | PF00928 | 0.519 |
TRG_ENDOCYTIC_2 | 920 | 923 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 954 | 957 | PF00928 | 0.558 |
TRG_ENDOCYTIC_2 | 975 | 978 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 989 | 992 | PF00928 | 0.614 |
TRG_ER_diArg_1 | 1076 | 1079 | PF00400 | 0.763 |
TRG_ER_diArg_1 | 1087 | 1089 | PF00400 | 0.795 |
TRG_ER_diArg_1 | 40 | 43 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 428 | 430 | PF00400 | 0.707 |
TRG_ER_diArg_1 | 442 | 445 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 48 | 51 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 602 | 605 | PF00400 | 0.423 |
TRG_NLS_Bipartite_1 | 1069 | 1090 | PF00514 | 0.762 |
TRG_NLS_Bipartite_1 | 429 | 448 | PF00514 | 0.663 |
TRG_NLS_MonoCore_2 | 1085 | 1090 | PF00514 | 0.780 |
TRG_NLS_MonoExtC_3 | 1085 | 1091 | PF00514 | 0.825 |
TRG_NLS_MonoExtC_3 | 442 | 447 | PF00514 | 0.568 |
TRG_NLS_MonoExtN_4 | 1085 | 1090 | PF00514 | 0.835 |
TRG_NLS_MonoExtN_4 | 443 | 448 | PF00514 | 0.568 |
TRG_NLS_MonoExtN_4 | 700 | 705 | PF00514 | 0.606 |
TRG_Pf-PMV_PEXEL_1 | 308 | 312 | PF00026 | 0.675 |
TRG_Pf-PMV_PEXEL_1 | 43 | 47 | PF00026 | 0.438 |
TRG_Pf-PMV_PEXEL_1 | 553 | 557 | PF00026 | 0.506 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC20 | Leptomonas seymouri | 63% | 100% |
A0A3S7WU73 | Leishmania donovani | 90% | 100% |
A0A422N424 | Trypanosoma rangeli | 41% | 100% |
A4H8T1 | Leishmania braziliensis | 75% | 100% |
A4HX50 | Leishmania infantum | 90% | 100% |
C9ZVU2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AQW5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5BS96 | Trypanosoma cruzi | 40% | 100% |