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 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7WU73
Term | Name | Level | Count |
---|---|---|---|
GO:0000075 | cell cycle checkpoint signaling | 4 | 1 |
GO:0000076 | DNA replication checkpoint signaling | 6 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006275 | regulation of DNA replication | 6 | 1 |
GO:0006281 | DNA repair | 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:0007165 | signal transduction | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008156 | negative regulation of DNA replication | 7 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010564 | regulation of cell cycle process | 5 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0010948 | negative regulation of cell cycle process | 6 | 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:0031570 | DNA integrity checkpoint signaling | 5 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0043111 | replication fork arrest | 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:0045005 | DNA-templated DNA replication maintenance of fidelity | 5 | 1 |
GO:0045786 | negative regulation of cell cycle | 5 | 1 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0048478 | obsolete replication fork protection | 6 | 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:0050896 | response to stimulus | 1 | 1 |
GO:0051052 | regulation of DNA metabolic process | 5 | 1 |
GO:0051053 | negative regulation of DNA metabolic process | 6 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0051726 | regulation of cell cycle | 4 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 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:0090329 | regulation of DNA-templated DNA replication | 7 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 1 |
GO:1901988 | negative regulation of cell cycle phase transition | 7 | 1 |
GO:2000104 | negative regulation of DNA-templated DNA replication | 8 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 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 | 1038 | 1042 | PF00656 | 0.715 |
CLV_C14_Caspase3-7 | 1105 | 1109 | PF00656 | 0.579 |
CLV_C14_Caspase3-7 | 728 | 732 | PF00656 | 0.630 |
CLV_NRD_NRD_1 | 1025 | 1027 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 1028 | 1030 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 1077 | 1079 | PF00675 | 0.736 |
CLV_NRD_NRD_1 | 1089 | 1091 | PF00675 | 0.824 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 604 | 606 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 666 | 668 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 671 | 673 | PF00675 | 0.338 |
CLV_PCSK_FUR_1 | 1023 | 1027 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 1003 | 1005 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 1025 | 1027 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 1028 | 1030 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 1076 | 1078 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 1087 | 1089 | PF00082 | 0.758 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 603 | 605 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 666 | 668 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 701 | 703 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 808 | 810 | PF00082 | 0.552 |
CLV_PCSK_PC1ET2_1 | 1003 | 1005 | PF00082 | 0.620 |
CLV_PCSK_PC1ET2_1 | 1076 | 1078 | PF00082 | 0.725 |
CLV_PCSK_PC1ET2_1 | 1087 | 1089 | PF00082 | 0.758 |
CLV_PCSK_PC1ET2_1 | 176 | 178 | PF00082 | 0.410 |
CLV_PCSK_PC1ET2_1 | 444 | 446 | PF00082 | 0.527 |
CLV_PCSK_PC1ET2_1 | 7 | 9 | PF00082 | 0.435 |
CLV_PCSK_PC1ET2_1 | 701 | 703 | PF00082 | 0.551 |
CLV_PCSK_PC1ET2_1 | 808 | 810 | PF00082 | 0.552 |
CLV_PCSK_PC7_1 | 1073 | 1079 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 1029 | 1033 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 1055 | 1059 | PF00082 | 0.771 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 546 | 550 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 655 | 659 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 808 | 812 | PF00082 | 0.771 |
CLV_PCSK_SKI1_1 | 824 | 828 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 898 | 902 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 965 | 969 | PF00082 | 0.399 |
CLV_Separin_Metazoa | 741 | 745 | PF03568 | 0.575 |
DEG_APCC_DBOX_1 | 545 | 553 | PF00400 | 0.417 |
DEG_APCC_DBOX_1 | 7 | 15 | PF00400 | 0.413 |
DEG_APCC_DBOX_1 | 823 | 831 | PF00400 | 0.659 |
DOC_AGCK_PIF_1 | 677 | 682 | PF00069 | 0.411 |
DOC_CDC14_PxL_1 | 21 | 29 | PF14671 | 0.336 |
DOC_CYCLIN_RxL_1 | 962 | 972 | PF00134 | 0.419 |
DOC_CYCLIN_yCln2_LP_2 | 105 | 111 | PF00134 | 0.429 |
DOC_MAPK_gen_1 | 560 | 570 | PF00069 | 0.386 |
DOC_MAPK_gen_1 | 600 | 610 | PF00069 | 0.412 |
DOC_MAPK_gen_1 | 7 | 14 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 104 | 111 | PF00069 | 0.397 |
DOC_MAPK_MEF2A_6 | 127 | 136 | PF00069 | 0.329 |
DOC_MAPK_MEF2A_6 | 184 | 192 | PF00069 | 0.336 |
DOC_MAPK_MEF2A_6 | 217 | 225 | PF00069 | 0.325 |
DOC_MAPK_MEF2A_6 | 264 | 273 | PF00069 | 0.747 |
DOC_MAPK_MEF2A_6 | 603 | 612 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 7 | 14 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 934 | 943 | PF00069 | 0.483 |
DOC_MAPK_NFAT4_5 | 7 | 15 | PF00069 | 0.417 |
DOC_MAPK_RevD_3 | 163 | 177 | PF00069 | 0.337 |
DOC_PP2B_LxvP_1 | 105 | 108 | PF13499 | 0.426 |
DOC_PP2B_LxvP_1 | 134 | 137 | PF13499 | 0.387 |
DOC_PP2B_LxvP_1 | 697 | 700 | PF13499 | 0.496 |
DOC_PP4_FxxP_1 | 922 | 925 | PF00568 | 0.348 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.312 |
DOC_USP7_MATH_1 | 642 | 646 | PF00917 | 0.342 |
DOC_USP7_MATH_1 | 700 | 704 | PF00917 | 0.527 |
DOC_USP7_UBL2_3 | 383 | 387 | PF12436 | 0.576 |
DOC_USP7_UBL2_3 | 690 | 694 | PF12436 | 0.427 |
DOC_USP7_UBL2_3 | 704 | 708 | PF12436 | 0.522 |
DOC_WW_Pin1_4 | 1016 | 1021 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 1056 | 1061 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 522 | 527 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 844 | 849 | PF00397 | 0.480 |
LIG_14-3-3_CanoR_1 | 138 | 145 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 367 | 373 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 407 | 413 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 809 | 816 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 934 | 939 | PF00244 | 0.546 |
LIG_Actin_WH2_2 | 535 | 552 | PF00022 | 0.301 |
LIG_APCC_ABBAyCdc20_2 | 277 | 283 | PF00400 | 0.584 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.480 |
LIG_BIR_III_4 | 1103 | 1107 | PF00653 | 0.548 |
LIG_BRCT_BRCA1_1 | 27 | 31 | PF00533 | 0.510 |
LIG_BRCT_BRCA1_1 | 478 | 482 | PF00533 | 0.444 |
LIG_BRCT_BRCA1_1 | 838 | 842 | PF00533 | 0.478 |
LIG_BRCT_BRCA1_1 | 885 | 889 | PF00533 | 0.473 |
LIG_Clathr_ClatBox_1 | 11 | 15 | PF01394 | 0.412 |
LIG_deltaCOP1_diTrp_1 | 325 | 331 | PF00928 | 0.371 |
LIG_deltaCOP1_diTrp_1 | 386 | 390 | PF00928 | 0.545 |
LIG_deltaCOP1_diTrp_1 | 756 | 764 | PF00928 | 0.574 |
LIG_EH1_1 | 218 | 226 | PF00400 | 0.442 |
LIG_EH1_1 | 873 | 881 | PF00400 | 0.433 |
LIG_eIF4E_1 | 614 | 620 | PF01652 | 0.406 |
LIG_eIF4E_1 | 693 | 699 | PF01652 | 0.442 |
LIG_FHA_1 | 1116 | 1122 | PF00498 | 0.600 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.528 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.331 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.488 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.714 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.426 |
LIG_FHA_1 | 518 | 524 | PF00498 | 0.568 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.378 |
LIG_FHA_1 | 679 | 685 | PF00498 | 0.394 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.503 |
LIG_FHA_1 | 962 | 968 | PF00498 | 0.443 |
LIG_FHA_2 | 1114 | 1120 | PF00498 | 0.630 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.486 |
LIG_FHA_2 | 204 | 210 | PF00498 | 0.332 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.475 |
LIG_FHA_2 | 974 | 980 | PF00498 | 0.481 |
LIG_IRF3_LxIS_1 | 14 | 20 | PF10401 | 0.413 |
LIG_KLC1_Yacidic_2 | 974 | 979 | PF13176 | 0.476 |
LIG_LIR_Apic_2 | 341 | 347 | PF02991 | 0.394 |
LIG_LIR_Apic_2 | 921 | 925 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 1005 | 1015 | PF02991 | 0.716 |
LIG_LIR_Gen_1 | 1092 | 1099 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 160 | 171 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 421 | 428 | PF02991 | 0.567 |
LIG_LIR_Gen_1 | 475 | 485 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 489 | 498 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 529 | 539 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 565 | 571 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 582 | 593 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 681 | 688 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 839 | 848 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 852 | 863 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 91 | 101 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 972 | 983 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 988 | 994 | PF02991 | 0.524 |
LIG_LIR_LC3C_4 | 103 | 107 | PF02991 | 0.438 |
LIG_LIR_LC3C_4 | 222 | 227 | PF02991 | 0.380 |
LIG_LIR_LC3C_4 | 565 | 569 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 1005 | 1010 | PF02991 | 0.697 |
LIG_LIR_Nem_3 | 1092 | 1097 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 385 | 391 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 421 | 426 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 475 | 480 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 489 | 493 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 529 | 535 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 565 | 569 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 582 | 588 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 681 | 685 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 787 | 793 | PF02991 | 0.687 |
LIG_LIR_Nem_3 | 839 | 845 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 852 | 858 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 885 | 891 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 953 | 957 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 972 | 978 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 988 | 992 | PF02991 | 0.518 |
LIG_MAD2 | 917 | 925 | PF02301 | 0.462 |
LIG_MLH1_MIPbox_1 | 838 | 842 | PF16413 | 0.478 |
LIG_MLH1_MIPbox_1 | 885 | 889 | PF16413 | 0.402 |
LIG_NRBOX | 124 | 130 | PF00104 | 0.322 |
LIG_NRBOX | 368 | 374 | PF00104 | 0.615 |
LIG_NRBOX | 621 | 627 | PF00104 | 0.434 |
LIG_Pex14_1 | 760 | 764 | PF04695 | 0.574 |
LIG_Pex14_2 | 566 | 570 | PF04695 | 0.372 |
LIG_Pex14_2 | 889 | 893 | PF04695 | 0.342 |
LIG_Pex14_2 | 923 | 927 | PF04695 | 0.438 |
LIG_PTB_Apo_2 | 226 | 233 | PF02174 | 0.334 |
LIG_PTB_Apo_2 | 887 | 894 | PF02174 | 0.367 |
LIG_PTB_Apo_2 | 921 | 928 | PF02174 | 0.386 |
LIG_PTB_Phospho_1 | 226 | 232 | PF10480 | 0.326 |
LIG_REV1ctd_RIR_1 | 839 | 847 | PF16727 | 0.421 |
LIG_SH2_CRK | 1094 | 1098 | PF00017 | 0.544 |
LIG_SH2_CRK | 232 | 236 | PF00017 | 0.440 |
LIG_SH2_CRK | 532 | 536 | PF00017 | 0.458 |
LIG_SH2_CRK | 541 | 545 | PF00017 | 0.407 |
LIG_SH2_CRK | 855 | 859 | PF00017 | 0.469 |
LIG_SH2_CRK | 989 | 993 | PF00017 | 0.564 |
LIG_SH2_GRB2like | 532 | 535 | PF00017 | 0.490 |
LIG_SH2_GRB2like | 74 | 77 | PF00017 | 0.673 |
LIG_SH2_NCK_1 | 1094 | 1098 | PF00017 | 0.544 |
LIG_SH2_NCK_1 | 989 | 993 | PF00017 | 0.564 |
LIG_SH2_PTP2 | 551 | 554 | PF00017 | 0.358 |
LIG_SH2_PTP2 | 585 | 588 | PF00017 | 0.253 |
LIG_SH2_STAP1 | 1094 | 1098 | PF00017 | 0.544 |
LIG_SH2_STAP1 | 664 | 668 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 551 | 554 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 585 | 588 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 614 | 617 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 954 | 957 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 975 | 978 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 989 | 992 | PF00017 | 0.627 |
LIG_SH3_3 | 1054 | 1060 | PF00018 | 0.639 |
LIG_SH3_3 | 1129 | 1135 | PF00018 | 0.634 |
LIG_SH3_3 | 520 | 526 | PF00018 | 0.483 |
LIG_SH3_3 | 565 | 571 | PF00018 | 0.417 |
LIG_SUMO_SIM_anti_2 | 185 | 191 | PF11976 | 0.324 |
LIG_SUMO_SIM_anti_2 | 222 | 228 | PF11976 | 0.435 |
LIG_SUMO_SIM_anti_2 | 483 | 489 | PF11976 | 0.349 |
LIG_SUMO_SIM_anti_2 | 617 | 624 | PF11976 | 0.347 |
LIG_SUMO_SIM_par_1 | 10 | 15 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 185 | 191 | PF11976 | 0.348 |
LIG_SUMO_SIM_par_1 | 192 | 198 | PF11976 | 0.328 |
LIG_SUMO_SIM_par_1 | 483 | 489 | PF11976 | 0.409 |
LIG_SUMO_SIM_par_1 | 519 | 525 | PF11976 | 0.532 |
LIG_SUMO_SIM_par_1 | 578 | 584 | PF11976 | 0.339 |
LIG_SUMO_SIM_par_1 | 617 | 624 | PF11976 | 0.324 |
LIG_TRAF2_1 | 347 | 350 | PF00917 | 0.477 |
LIG_TYR_ITIM | 539 | 544 | PF00017 | 0.331 |
LIG_TYR_ITIM | 549 | 554 | PF00017 | 0.349 |
LIG_TYR_ITIM | 583 | 588 | PF00017 | 0.377 |
LIG_TYR_ITIM | 853 | 858 | PF00017 | 0.454 |
LIG_TYR_ITIM | 973 | 978 | PF00017 | 0.484 |
LIG_UBA3_1 | 121 | 127 | PF00899 | 0.327 |
LIG_UBA3_1 | 149 | 154 | PF00899 | 0.401 |
LIG_WRC_WIRS_1 | 487 | 492 | PF05994 | 0.373 |
LIG_WRC_WIRS_1 | 593 | 598 | PF05994 | 0.429 |
LIG_WRC_WIRS_1 | 679 | 684 | PF05994 | 0.412 |
MOD_CDC14_SPxK_1 | 364 | 367 | PF00782 | 0.525 |
MOD_CDK_SPK_2 | 844 | 849 | PF00069 | 0.480 |
MOD_CDK_SPxK_1 | 361 | 367 | PF00069 | 0.531 |
MOD_CDK_SPxxK_3 | 1016 | 1023 | PF00069 | 0.608 |
MOD_CK1_1 | 1016 | 1022 | PF00069 | 0.707 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.601 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.518 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.518 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.563 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.564 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.692 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.435 |
MOD_CK1_1 | 517 | 523 | PF00069 | 0.527 |
MOD_CK1_1 | 662 | 668 | PF00069 | 0.410 |
MOD_CK1_1 | 729 | 735 | PF00069 | 0.679 |
MOD_CK1_1 | 767 | 773 | PF00069 | 0.675 |
MOD_CK1_1 | 818 | 824 | PF00069 | 0.581 |
MOD_CK1_1 | 828 | 834 | PF00069 | 0.510 |
MOD_CK2_1 | 1044 | 1050 | PF00069 | 0.681 |
MOD_CK2_1 | 1113 | 1119 | PF00069 | 0.688 |
MOD_CK2_1 | 1141 | 1147 | PF00069 | 0.562 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.433 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.436 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.412 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.549 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.430 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.518 |
MOD_CK2_1 | 829 | 835 | PF00069 | 0.496 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.435 |
MOD_CK2_1 | 973 | 979 | PF00069 | 0.450 |
MOD_Cter_Amidation | 255 | 258 | PF01082 | 0.539 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.595 |
MOD_GlcNHglycan | 1032 | 1035 | PF01048 | 0.796 |
MOD_GlcNHglycan | 1101 | 1107 | PF01048 | 0.769 |
MOD_GlcNHglycan | 1110 | 1113 | PF01048 | 0.680 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.404 |
MOD_GlcNHglycan | 265 | 269 | PF01048 | 0.717 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.652 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.339 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.384 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.435 |
MOD_GlcNHglycan | 577 | 580 | PF01048 | 0.483 |
MOD_GlcNHglycan | 731 | 734 | PF01048 | 0.694 |
MOD_GlcNHglycan | 779 | 782 | PF01048 | 0.702 |
MOD_GlcNHglycan | 795 | 798 | PF01048 | 0.526 |
MOD_GlcNHglycan | 838 | 841 | PF01048 | 0.578 |
MOD_GlcNHglycan | 948 | 951 | PF01048 | 0.512 |
MOD_GSK3_1 | 1030 | 1037 | PF00069 | 0.818 |
MOD_GSK3_1 | 1040 | 1047 | PF00069 | 0.657 |
MOD_GSK3_1 | 1102 | 1109 | PF00069 | 0.690 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.303 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.557 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.629 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.571 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.593 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.731 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.564 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.487 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.470 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.267 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.295 |
MOD_GSK3_1 | 764 | 771 | PF00069 | 0.677 |
MOD_GSK3_1 | 804 | 811 | PF00069 | 0.644 |
MOD_GSK3_1 | 814 | 821 | PF00069 | 0.550 |
MOD_GSK3_1 | 822 | 829 | PF00069 | 0.460 |
MOD_GSK3_1 | 849 | 856 | PF00069 | 0.459 |
MOD_GSK3_1 | 946 | 953 | PF00069 | 0.560 |
MOD_GSK3_1 | 957 | 964 | PF00069 | 0.420 |
MOD_GSK3_1 | 969 | 976 | PF00069 | 0.474 |
MOD_LATS_1 | 262 | 268 | PF00433 | 0.600 |
MOD_N-GLC_1 | 230 | 235 | PF02516 | 0.430 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.457 |
MOD_N-GLC_1 | 726 | 731 | PF02516 | 0.673 |
MOD_N-GLC_1 | 849 | 854 | PF02516 | 0.453 |
MOD_N-GLC_1 | 968 | 973 | PF02516 | 0.458 |
MOD_N-GLC_1 | 997 | 1002 | PF02516 | 0.625 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.372 |
MOD_NEK2_1 | 488 | 493 | PF00069 | 0.341 |
MOD_NEK2_1 | 588 | 593 | PF00069 | 0.408 |
MOD_NEK2_1 | 621 | 626 | PF00069 | 0.326 |
MOD_NEK2_1 | 643 | 648 | PF00069 | 0.313 |
MOD_NEK2_1 | 680 | 685 | PF00069 | 0.295 |
MOD_NEK2_1 | 764 | 769 | PF00069 | 0.782 |
MOD_NEK2_1 | 853 | 858 | PF00069 | 0.398 |
MOD_NEK2_1 | 875 | 880 | PF00069 | 0.318 |
MOD_NEK2_1 | 957 | 962 | PF00069 | 0.408 |
MOD_NEK2_1 | 968 | 973 | PF00069 | 0.451 |
MOD_NEK2_1 | 987 | 992 | PF00069 | 0.473 |
MOD_NEK2_2 | 418 | 423 | PF00069 | 0.603 |
MOD_PIKK_1 | 1035 | 1041 | PF00454 | 0.659 |
MOD_PIKK_1 | 809 | 815 | PF00454 | 0.629 |
MOD_PK_1 | 1141 | 1147 | PF00069 | 0.513 |
MOD_PK_1 | 815 | 821 | PF00069 | 0.683 |
MOD_PK_1 | 934 | 940 | PF00069 | 0.460 |
MOD_PKA_1 | 176 | 182 | PF00069 | 0.412 |
MOD_PKA_1 | 382 | 388 | PF00069 | 0.575 |
MOD_PKA_1 | 808 | 814 | PF00069 | 0.550 |
MOD_PKA_2 | 1027 | 1033 | PF00069 | 0.659 |
MOD_PKA_2 | 1106 | 1112 | PF00069 | 0.553 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.433 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.412 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.612 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.565 |
MOD_PKA_2 | 808 | 814 | PF00069 | 0.707 |
MOD_PKA_2 | 961 | 967 | PF00069 | 0.431 |
MOD_Plk_1 | 1005 | 1011 | PF00069 | 0.731 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.476 |
MOD_Plk_1 | 293 | 299 | PF00069 | 0.585 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.501 |
MOD_Plk_1 | 606 | 612 | PF00069 | 0.380 |
MOD_Plk_1 | 726 | 732 | PF00069 | 0.671 |
MOD_Plk_1 | 756 | 762 | PF00069 | 0.564 |
MOD_Plk_1 | 764 | 770 | PF00069 | 0.571 |
MOD_Plk_1 | 822 | 828 | PF00069 | 0.637 |
MOD_Plk_1 | 849 | 855 | PF00069 | 0.425 |
MOD_Plk_1 | 957 | 963 | PF00069 | 0.378 |
MOD_Plk_1 | 968 | 974 | PF00069 | 0.417 |
MOD_Plk_2-3 | 726 | 732 | PF00069 | 0.693 |
MOD_Plk_2-3 | 736 | 742 | PF00069 | 0.673 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.361 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.334 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.543 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.462 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.581 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.599 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.576 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.328 |
MOD_Plk_4 | 562 | 568 | PF00069 | 0.456 |
MOD_Plk_4 | 621 | 627 | PF00069 | 0.294 |
MOD_Plk_4 | 643 | 649 | PF00069 | 0.316 |
MOD_Plk_4 | 870 | 876 | PF00069 | 0.417 |
MOD_Plk_4 | 883 | 889 | PF00069 | 0.351 |
MOD_Plk_4 | 934 | 940 | PF00069 | 0.565 |
MOD_Plk_4 | 950 | 956 | PF00069 | 0.313 |
MOD_Plk_4 | 973 | 979 | PF00069 | 0.455 |
MOD_ProDKin_1 | 1016 | 1022 | PF00069 | 0.616 |
MOD_ProDKin_1 | 1056 | 1062 | PF00069 | 0.566 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.706 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.516 |
MOD_ProDKin_1 | 522 | 528 | PF00069 | 0.537 |
MOD_ProDKin_1 | 844 | 850 | PF00069 | 0.474 |
MOD_SUMO_for_1 | 1002 | 1005 | PF00179 | 0.699 |
MOD_SUMO_for_1 | 559 | 562 | PF00179 | 0.446 |
MOD_SUMO_rev_2 | 1065 | 1071 | PF00179 | 0.578 |
MOD_SUMO_rev_2 | 501 | 510 | PF00179 | 0.508 |
MOD_SUMO_rev_2 | 595 | 602 | PF00179 | 0.416 |
MOD_SUMO_rev_2 | 770 | 779 | PF00179 | 0.681 |
MOD_SUMO_rev_2 | 974 | 983 | PF00179 | 0.418 |
TRG_DiLeu_BaEn_1 | 161 | 166 | PF01217 | 0.341 |
TRG_DiLeu_BaEn_1 | 617 | 622 | PF01217 | 0.321 |
TRG_DiLeu_BaEn_2 | 561 | 567 | PF01217 | 0.479 |
TRG_DiLeu_BaEn_4 | 349 | 355 | PF01217 | 0.487 |
TRG_DiLeu_BaLyEn_6 | 105 | 110 | PF01217 | 0.330 |
TRG_DiLeu_BaLyEn_6 | 40 | 45 | PF01217 | 0.392 |
TRG_DiLeu_BaLyEn_6 | 550 | 555 | PF01217 | 0.257 |
TRG_ENDOCYTIC_2 | 1094 | 1097 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.547 |
TRG_ENDOCYTIC_2 | 532 | 535 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 541 | 544 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.217 |
TRG_ENDOCYTIC_2 | 585 | 588 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 855 | 858 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 920 | 923 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 954 | 957 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 975 | 978 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 989 | 992 | PF00928 | 0.533 |
TRG_ER_diArg_1 | 1023 | 1026 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 1088 | 1090 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 40 | 43 | PF00400 | 0.355 |
TRG_ER_diArg_1 | 428 | 430 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 442 | 445 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 48 | 51 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 602 | 605 | PF00400 | 0.347 |
TRG_ER_diArg_1 | 666 | 668 | PF00400 | 0.403 |
TRG_NES_CRM1_1 | 9 | 22 | PF08389 | 0.306 |
TRG_NLS_Bipartite_1 | 1076 | 1091 | PF00514 | 0.731 |
TRG_NLS_Bipartite_1 | 429 | 448 | PF00514 | 0.610 |
TRG_NLS_MonoCore_2 | 1086 | 1091 | PF00514 | 0.718 |
TRG_NLS_MonoExtC_3 | 1086 | 1092 | PF00514 | 0.800 |
TRG_NLS_MonoExtC_3 | 442 | 447 | PF00514 | 0.505 |
TRG_NLS_MonoExtN_4 | 1073 | 1080 | PF00514 | 0.726 |
TRG_NLS_MonoExtN_4 | 1086 | 1091 | PF00514 | 0.818 |
TRG_NLS_MonoExtN_4 | 443 | 448 | PF00514 | 0.506 |
TRG_NLS_MonoExtN_4 | 700 | 705 | PF00514 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 308 | 312 | PF00026 | 0.531 |
TRG_Pf-PMV_PEXEL_1 | 43 | 47 | PF00026 | 0.361 |
TRG_Pf-PMV_PEXEL_1 | 553 | 557 | PF00026 | 0.443 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC20 | Leptomonas seymouri | 64% | 100% |
A0A422N424 | Trypanosoma rangeli | 41% | 100% |
A4H8T1 | Leishmania braziliensis | 75% | 100% |
A4HX50 | Leishmania infantum | 99% | 100% |
C9ZVU2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AQW5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4QEL3 | Leishmania major | 90% | 100% |
V5BS96 | Trypanosoma cruzi | 41% | 100% |