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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030870 | Mre11 complex | 3 | 6 |
GO:0032991 | protein-containing complex | 1 | 6 |
GO:0140513 | nuclear protein-containing complex | 2 | 6 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AQI9
Term | Name | Level | Count |
---|---|---|---|
GO:0000075 | cell cycle checkpoint signaling | 4 | 6 |
GO:0000077 | DNA damage checkpoint signaling | 5 | 6 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 6 |
GO:0006259 | DNA metabolic process | 4 | 6 |
GO:0006281 | DNA repair | 5 | 6 |
GO:0006302 | double-strand break repair | 6 | 6 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0006950 | response to stress | 2 | 6 |
GO:0006974 | DNA damage response | 4 | 6 |
GO:0007093 | mitotic cell cycle checkpoint signaling | 4 | 6 |
GO:0007095 | mitotic G2 DNA damage checkpoint signaling | 6 | 6 |
GO:0007165 | signal transduction | 2 | 6 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0010389 | regulation of G2/M transition of mitotic cell cycle | 7 | 6 |
GO:0010564 | regulation of cell cycle process | 5 | 6 |
GO:0010948 | negative regulation of cell cycle process | 6 | 6 |
GO:0010972 | negative regulation of G2/M transition of mitotic cell cycle | 8 | 6 |
GO:0022402 | cell cycle process | 2 | 6 |
GO:0031570 | DNA integrity checkpoint signaling | 5 | 6 |
GO:0033554 | cellular response to stress | 3 | 6 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 6 |
GO:0035556 | intracellular signal transduction | 3 | 6 |
GO:0042770 | signal transduction in response to DNA damage | 4 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 6 |
GO:0044773 | mitotic DNA damage checkpoint signaling | 6 | 6 |
GO:0044774 | mitotic DNA integrity checkpoint signaling | 5 | 6 |
GO:0044818 | mitotic G2/M transition checkpoint | 5 | 6 |
GO:0045786 | negative regulation of cell cycle | 5 | 6 |
GO:0045930 | negative regulation of mitotic cell cycle | 6 | 6 |
GO:0046483 | heterocycle metabolic process | 3 | 6 |
GO:0048519 | negative regulation of biological process | 3 | 6 |
GO:0048523 | negative regulation of cellular process | 4 | 6 |
GO:0050789 | regulation of biological process | 2 | 6 |
GO:0050794 | regulation of cellular process | 3 | 6 |
GO:0050896 | response to stimulus | 1 | 6 |
GO:0051716 | cellular response to stimulus | 2 | 6 |
GO:0051726 | regulation of cell cycle | 4 | 6 |
GO:0065007 | biological regulation | 1 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:0090304 | nucleic acid metabolic process | 4 | 6 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 6 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 6 |
GO:1901988 | negative regulation of cell cycle phase transition | 7 | 6 |
GO:1901990 | regulation of mitotic cell cycle phase transition | 6 | 6 |
GO:1901991 | negative regulation of mitotic cell cycle phase transition | 7 | 6 |
GO:1902749 | regulation of cell cycle G2/M phase transition | 7 | 6 |
GO:1902750 | negative regulation of cell cycle G2/M phase transition | 8 | 6 |
GO:1903047 | mitotic cell cycle process | 3 | 6 |
GO:0000724 | double-strand break repair via homologous recombination | 7 | 1 |
GO:0000725 | recombinational repair | 6 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0032392 | DNA geometric change | 7 | 1 |
GO:0032508 | DNA duplex unwinding | 8 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0071103 | DNA conformation change | 6 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003684 | damaged DNA binding | 5 | 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 | 1117 | 1121 | PF00656 | 0.387 |
CLV_C14_Caspase3-7 | 1137 | 1141 | PF00656 | 0.383 |
CLV_C14_Caspase3-7 | 121 | 125 | PF00656 | 0.463 |
CLV_C14_Caspase3-7 | 286 | 290 | PF00656 | 0.358 |
CLV_C14_Caspase3-7 | 394 | 398 | PF00656 | 0.571 |
CLV_NRD_NRD_1 | 1044 | 1046 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 1051 | 1053 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 1228 | 1230 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 618 | 620 | PF00675 | 0.701 |
CLV_NRD_NRD_1 | 663 | 665 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 671 | 673 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 678 | 680 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 733 | 735 | PF00675 | 0.679 |
CLV_NRD_NRD_1 | 742 | 744 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 850 | 852 | PF00675 | 0.716 |
CLV_NRD_NRD_1 | 924 | 926 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 995 | 997 | PF00675 | 0.640 |
CLV_PCSK_KEX2_1 | 1044 | 1046 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 1051 | 1053 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 1228 | 1230 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 618 | 620 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 663 | 665 | PF00082 | 0.708 |
CLV_PCSK_KEX2_1 | 671 | 673 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 678 | 680 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 733 | 735 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 742 | 744 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 850 | 852 | PF00082 | 0.716 |
CLV_PCSK_KEX2_1 | 924 | 926 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 995 | 997 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 1220 | 1224 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 1228 | 1232 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.227 |
CLV_PCSK_SKI1_1 | 996 | 1000 | PF00082 | 0.698 |
CLV_Separin_Metazoa | 271 | 275 | PF03568 | 0.346 |
DEG_APCC_DBOX_1 | 364 | 372 | PF00400 | 0.432 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.413 |
DEG_ODPH_VHL_1 | 601 | 614 | PF01847 | 0.658 |
DEG_SCF_FBW7_1 | 997 | 1003 | PF00400 | 0.632 |
DEG_SPOP_SBC_1 | 528 | 532 | PF00917 | 0.652 |
DEG_SPOP_SBC_1 | 771 | 775 | PF00917 | 0.695 |
DOC_CDC14_PxL_1 | 438 | 446 | PF14671 | 0.627 |
DOC_CKS1_1 | 186 | 191 | PF01111 | 0.417 |
DOC_CKS1_1 | 991 | 996 | PF01111 | 0.685 |
DOC_CKS1_1 | 997 | 1002 | PF01111 | 0.656 |
DOC_CYCLIN_RxL_1 | 28 | 39 | PF00134 | 0.385 |
DOC_CYCLIN_yCln2_LP_2 | 34 | 40 | PF00134 | 0.276 |
DOC_MAPK_DCC_7 | 104 | 114 | PF00069 | 0.425 |
DOC_MAPK_FxFP_2 | 92 | 95 | PF00069 | 0.385 |
DOC_MAPK_gen_1 | 28 | 35 | PF00069 | 0.385 |
DOC_MAPK_gen_1 | 910 | 918 | PF00069 | 0.683 |
DOC_MAPK_gen_1 | 98 | 105 | PF00069 | 0.342 |
DOC_MAPK_MEF2A_6 | 108 | 116 | PF00069 | 0.365 |
DOC_MAPK_MEF2A_6 | 870 | 877 | PF00069 | 0.566 |
DOC_MAPK_MEF2A_6 | 98 | 105 | PF00069 | 0.393 |
DOC_MAPK_NFAT4_5 | 98 | 106 | PF00069 | 0.342 |
DOC_MAPK_RevD_3 | 434 | 447 | PF00069 | 0.506 |
DOC_PP1_RVXF_1 | 1151 | 1158 | PF00149 | 0.438 |
DOC_PP4_FxxP_1 | 17 | 20 | PF00568 | 0.416 |
DOC_PP4_FxxP_1 | 210 | 213 | PF00568 | 0.483 |
DOC_PP4_FxxP_1 | 92 | 95 | PF00568 | 0.385 |
DOC_USP7_MATH_1 | 1014 | 1018 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 1239 | 1243 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.292 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 519 | 523 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 714 | 718 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 735 | 739 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 771 | 775 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 782 | 786 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 820 | 824 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 899 | 903 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 976 | 980 | PF00917 | 0.631 |
DOC_USP7_UBL2_3 | 1196 | 1200 | PF12436 | 0.402 |
DOC_WW_Pin1_4 | 1051 | 1056 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 1138 | 1143 | PF00397 | 0.396 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.789 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.797 |
DOC_WW_Pin1_4 | 551 | 556 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 775 | 780 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 888 | 893 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 904 | 909 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 990 | 995 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 996 | 1001 | PF00397 | 0.656 |
LIG_14-3-3_CanoR_1 | 1001 | 1007 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 104 | 112 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 1045 | 1055 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 1089 | 1097 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 1135 | 1139 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 1144 | 1148 | PF00244 | 0.351 |
LIG_14-3-3_CanoR_1 | 230 | 236 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 292 | 302 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 315 | 322 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 422 | 430 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 56 | 60 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 618 | 623 | PF00244 | 0.697 |
LIG_14-3-3_CanoR_1 | 664 | 670 | PF00244 | 0.700 |
LIG_14-3-3_CanoR_1 | 671 | 677 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 855 | 860 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 888 | 892 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 924 | 929 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 934 | 942 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 974 | 983 | PF00244 | 0.670 |
LIG_Actin_WH2_2 | 281 | 296 | PF00022 | 0.309 |
LIG_AP2alpha_1 | 1118 | 1122 | PF02296 | 0.437 |
LIG_BIR_III_2 | 397 | 401 | PF00653 | 0.548 |
LIG_BRCT_BRCA1_1 | 297 | 301 | PF00533 | 0.494 |
LIG_BRCT_BRCA1_1 | 404 | 408 | PF00533 | 0.664 |
LIG_BRCT_BRCA1_1 | 620 | 624 | PF00533 | 0.697 |
LIG_BRCT_BRCA1_1 | 976 | 980 | PF00533 | 0.631 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.556 |
LIG_FHA_1 | 1090 | 1096 | PF00498 | 0.557 |
LIG_FHA_1 | 1217 | 1223 | PF00498 | 0.526 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.430 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.490 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.680 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.277 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.666 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.665 |
LIG_FHA_1 | 579 | 585 | PF00498 | 0.556 |
LIG_FHA_1 | 645 | 651 | PF00498 | 0.678 |
LIG_FHA_1 | 684 | 690 | PF00498 | 0.630 |
LIG_FHA_1 | 788 | 794 | PF00498 | 0.704 |
LIG_FHA_2 | 1135 | 1141 | PF00498 | 0.412 |
LIG_FHA_2 | 1144 | 1150 | PF00498 | 0.354 |
LIG_FHA_2 | 1162 | 1168 | PF00498 | 0.436 |
LIG_FHA_2 | 169 | 175 | PF00498 | 0.334 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.343 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.460 |
LIG_FHA_2 | 724 | 730 | PF00498 | 0.726 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.371 |
LIG_FHA_2 | 888 | 894 | PF00498 | 0.701 |
LIG_IRF3_LxIS_1 | 112 | 119 | PF10401 | 0.405 |
LIG_LIR_Apic_2 | 209 | 213 | PF02991 | 0.490 |
LIG_LIR_Apic_2 | 90 | 95 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 1021 | 1026 | PF02991 | 0.638 |
LIG_LIR_Gen_1 | 1098 | 1107 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 239 | 249 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 255 | 265 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 267 | 276 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 1021 | 1025 | PF02991 | 0.640 |
LIG_LIR_Nem_3 | 1164 | 1168 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 1197 | 1202 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 234 | 238 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 239 | 244 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 255 | 261 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 267 | 272 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 311 | 317 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 977 | 983 | PF02991 | 0.516 |
LIG_LYPXL_yS_3 | 1165 | 1168 | PF13949 | 0.421 |
LIG_MAD2 | 32 | 40 | PF02301 | 0.385 |
LIG_PCNA_yPIPBox_3 | 1089 | 1101 | PF02747 | 0.528 |
LIG_Pex14_2 | 1114 | 1118 | PF04695 | 0.451 |
LIG_PTB_Apo_2 | 1159 | 1166 | PF02174 | 0.407 |
LIG_PTB_Phospho_1 | 1159 | 1165 | PF10480 | 0.401 |
LIG_SH2_CRK | 1199 | 1203 | PF00017 | 0.458 |
LIG_SH2_CRK | 184 | 188 | PF00017 | 0.406 |
LIG_SH2_CRK | 228 | 232 | PF00017 | 0.483 |
LIG_SH2_GRB2like | 1160 | 1163 | PF00017 | 0.441 |
LIG_SH2_NCK_1 | 1172 | 1176 | PF00017 | 0.364 |
LIG_SH2_NCK_1 | 184 | 188 | PF00017 | 0.406 |
LIG_SH2_SRC | 1160 | 1163 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 153 | 157 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 269 | 273 | PF00017 | 0.329 |
LIG_SH2_STAT3 | 152 | 155 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 1100 | 1103 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 1160 | 1163 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 2 | 5 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.429 |
LIG_SH3_3 | 1070 | 1076 | PF00018 | 0.613 |
LIG_SH3_3 | 1163 | 1169 | PF00018 | 0.418 |
LIG_SH3_3 | 1219 | 1225 | PF00018 | 0.569 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.487 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.541 |
LIG_SH3_3 | 532 | 538 | PF00018 | 0.541 |
LIG_SH3_3 | 56 | 62 | PF00018 | 0.385 |
LIG_SH3_3 | 802 | 808 | PF00018 | 0.642 |
LIG_SH3_3 | 810 | 816 | PF00018 | 0.647 |
LIG_SH3_3 | 893 | 899 | PF00018 | 0.583 |
LIG_SH3_3 | 903 | 909 | PF00018 | 0.618 |
LIG_SUMO_SIM_anti_2 | 126 | 132 | PF11976 | 0.437 |
LIG_SUMO_SIM_anti_2 | 304 | 311 | PF11976 | 0.433 |
LIG_SUMO_SIM_anti_2 | 556 | 562 | PF11976 | 0.526 |
LIG_SUMO_SIM_anti_2 | 874 | 880 | PF11976 | 0.642 |
LIG_SUMO_SIM_par_1 | 114 | 119 | PF11976 | 0.403 |
LIG_SUMO_SIM_par_1 | 304 | 311 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 553 | 562 | PF11976 | 0.569 |
LIG_TRAF2_1 | 171 | 174 | PF00917 | 0.337 |
LIG_TRAF2_1 | 637 | 640 | PF00917 | 0.556 |
LIG_WRC_WIRS_1 | 1119 | 1124 | PF05994 | 0.324 |
LIG_WW_3 | 907 | 911 | PF00397 | 0.610 |
MOD_CDC14_SPxK_1 | 1141 | 1144 | PF00782 | 0.407 |
MOD_CDC14_SPxK_1 | 458 | 461 | PF00782 | 0.705 |
MOD_CDC14_SPxK_1 | 907 | 910 | PF00782 | 0.607 |
MOD_CDK_SPK_2 | 990 | 995 | PF00069 | 0.667 |
MOD_CDK_SPK_2 | 996 | 1001 | PF00069 | 0.672 |
MOD_CDK_SPxK_1 | 1138 | 1144 | PF00069 | 0.398 |
MOD_CDK_SPxK_1 | 455 | 461 | PF00069 | 0.707 |
MOD_CDK_SPxK_1 | 904 | 910 | PF00069 | 0.624 |
MOD_CDK_SPxK_1 | 990 | 996 | PF00069 | 0.655 |
MOD_CK1_1 | 1069 | 1075 | PF00069 | 0.641 |
MOD_CK1_1 | 1084 | 1090 | PF00069 | 0.553 |
MOD_CK1_1 | 1113 | 1119 | PF00069 | 0.282 |
MOD_CK1_1 | 1121 | 1127 | PF00069 | 0.274 |
MOD_CK1_1 | 1143 | 1149 | PF00069 | 0.323 |
MOD_CK1_1 | 1173 | 1179 | PF00069 | 0.436 |
MOD_CK1_1 | 1208 | 1214 | PF00069 | 0.429 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.447 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.662 |
MOD_CK1_1 | 513 | 519 | PF00069 | 0.632 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.724 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.603 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.608 |
MOD_CK1_1 | 592 | 598 | PF00069 | 0.676 |
MOD_CK1_1 | 774 | 780 | PF00069 | 0.663 |
MOD_CK2_1 | 1121 | 1127 | PF00069 | 0.447 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.443 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.273 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.451 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.381 |
MOD_CK2_1 | 543 | 549 | PF00069 | 0.553 |
MOD_CK2_1 | 634 | 640 | PF00069 | 0.657 |
MOD_CK2_1 | 723 | 729 | PF00069 | 0.690 |
MOD_CK2_1 | 735 | 741 | PF00069 | 0.644 |
MOD_CK2_1 | 752 | 758 | PF00069 | 0.552 |
MOD_CK2_1 | 887 | 893 | PF00069 | 0.702 |
MOD_Cter_Amidation | 1042 | 1045 | PF01082 | 0.532 |
MOD_Cter_Amidation | 26 | 29 | PF01082 | 0.385 |
MOD_GlcNHglycan | 1004 | 1007 | PF01048 | 0.562 |
MOD_GlcNHglycan | 1010 | 1013 | PF01048 | 0.586 |
MOD_GlcNHglycan | 1048 | 1051 | PF01048 | 0.683 |
MOD_GlcNHglycan | 1086 | 1089 | PF01048 | 0.634 |
MOD_GlcNHglycan | 1214 | 1217 | PF01048 | 0.305 |
MOD_GlcNHglycan | 1231 | 1234 | PF01048 | 0.575 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.586 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.590 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.541 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.665 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.675 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.702 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.595 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.703 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.715 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.708 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.619 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.636 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.565 |
MOD_GlcNHglycan | 61 | 65 | PF01048 | 0.385 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.678 |
MOD_GlcNHglycan | 673 | 676 | PF01048 | 0.637 |
MOD_GlcNHglycan | 704 | 707 | PF01048 | 0.691 |
MOD_GlcNHglycan | 716 | 719 | PF01048 | 0.603 |
MOD_GlcNHglycan | 723 | 726 | PF01048 | 0.549 |
MOD_GlcNHglycan | 738 | 741 | PF01048 | 0.644 |
MOD_GlcNHglycan | 745 | 748 | PF01048 | 0.701 |
MOD_GlcNHglycan | 761 | 765 | PF01048 | 0.563 |
MOD_GlcNHglycan | 857 | 860 | PF01048 | 0.680 |
MOD_GlcNHglycan | 861 | 864 | PF01048 | 0.658 |
MOD_GlcNHglycan | 879 | 882 | PF01048 | 0.522 |
MOD_GlcNHglycan | 919 | 922 | PF01048 | 0.684 |
MOD_GlcNHglycan | 948 | 951 | PF01048 | 0.561 |
MOD_GlcNHglycan | 971 | 974 | PF01048 | 0.632 |
MOD_GSK3_1 | 1014 | 1021 | PF00069 | 0.527 |
MOD_GSK3_1 | 1024 | 1031 | PF00069 | 0.598 |
MOD_GSK3_1 | 1059 | 1066 | PF00069 | 0.672 |
MOD_GSK3_1 | 1084 | 1091 | PF00069 | 0.656 |
MOD_GSK3_1 | 1106 | 1113 | PF00069 | 0.324 |
MOD_GSK3_1 | 1134 | 1141 | PF00069 | 0.414 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.432 |
MOD_GSK3_1 | 1170 | 1177 | PF00069 | 0.490 |
MOD_GSK3_1 | 1190 | 1197 | PF00069 | 0.253 |
MOD_GSK3_1 | 1208 | 1215 | PF00069 | 0.286 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.338 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.478 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.329 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.661 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.562 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.536 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.670 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.751 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.665 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.653 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.653 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.634 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.650 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.592 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.538 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.654 |
MOD_GSK3_1 | 618 | 625 | PF00069 | 0.700 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.694 |
MOD_GSK3_1 | 667 | 674 | PF00069 | 0.651 |
MOD_GSK3_1 | 678 | 685 | PF00069 | 0.630 |
MOD_GSK3_1 | 696 | 703 | PF00069 | 0.540 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.385 |
MOD_GSK3_1 | 770 | 777 | PF00069 | 0.691 |
MOD_GSK3_1 | 782 | 789 | PF00069 | 0.604 |
MOD_GSK3_1 | 855 | 862 | PF00069 | 0.691 |
MOD_GSK3_1 | 879 | 886 | PF00069 | 0.646 |
MOD_GSK3_1 | 996 | 1003 | PF00069 | 0.679 |
MOD_N-GLC_1 | 1069 | 1074 | PF02516 | 0.612 |
MOD_N-GLC_1 | 1081 | 1086 | PF02516 | 0.548 |
MOD_N-GLC_1 | 1093 | 1098 | PF02516 | 0.429 |
MOD_N-GLC_1 | 1161 | 1166 | PF02516 | 0.447 |
MOD_N-GLC_1 | 428 | 433 | PF02516 | 0.640 |
MOD_N-GLC_1 | 474 | 479 | PF02516 | 0.597 |
MOD_N-GLC_1 | 483 | 488 | PF02516 | 0.567 |
MOD_N-GLC_1 | 644 | 649 | PF02516 | 0.721 |
MOD_N-GLC_1 | 683 | 688 | PF02516 | 0.592 |
MOD_N-GLC_1 | 787 | 792 | PF02516 | 0.653 |
MOD_N-GLC_1 | 957 | 962 | PF02516 | 0.526 |
MOD_NEK2_1 | 1002 | 1007 | PF00069 | 0.590 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.442 |
MOD_NEK2_1 | 1118 | 1123 | PF00069 | 0.342 |
MOD_NEK2_1 | 1171 | 1176 | PF00069 | 0.450 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.469 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.453 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.368 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.656 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.621 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.265 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.662 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.585 |
MOD_NEK2_1 | 624 | 629 | PF00069 | 0.719 |
MOD_NEK2_1 | 677 | 682 | PF00069 | 0.667 |
MOD_NEK2_1 | 700 | 705 | PF00069 | 0.701 |
MOD_NEK2_1 | 772 | 777 | PF00069 | 0.615 |
MOD_NEK2_1 | 877 | 882 | PF00069 | 0.651 |
MOD_NEK2_1 | 932 | 937 | PF00069 | 0.630 |
MOD_NEK2_2 | 219 | 224 | PF00069 | 0.479 |
MOD_NEK2_2 | 231 | 236 | PF00069 | 0.379 |
MOD_NEK2_2 | 342 | 347 | PF00069 | 0.410 |
MOD_NEK2_2 | 493 | 498 | PF00069 | 0.596 |
MOD_OFUCOSY | 1058 | 1063 | PF10250 | 0.511 |
MOD_PIKK_1 | 1053 | 1059 | PF00454 | 0.680 |
MOD_PIKK_1 | 1185 | 1191 | PF00454 | 0.329 |
MOD_PIKK_1 | 1239 | 1245 | PF00454 | 0.625 |
MOD_PIKK_1 | 983 | 989 | PF00454 | 0.691 |
MOD_PK_1 | 1081 | 1087 | PF00069 | 0.569 |
MOD_PK_1 | 1205 | 1211 | PF00069 | 0.452 |
MOD_PK_1 | 678 | 684 | PF00069 | 0.664 |
MOD_PKA_1 | 1228 | 1234 | PF00069 | 0.680 |
MOD_PKA_1 | 201 | 207 | PF00069 | 0.482 |
MOD_PKA_1 | 618 | 624 | PF00069 | 0.699 |
MOD_PKA_1 | 671 | 677 | PF00069 | 0.659 |
MOD_PKA_1 | 678 | 684 | PF00069 | 0.646 |
MOD_PKA_1 | 924 | 930 | PF00069 | 0.533 |
MOD_PKA_2 | 1000 | 1006 | PF00069 | 0.668 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.436 |
MOD_PKA_2 | 1088 | 1094 | PF00069 | 0.604 |
MOD_PKA_2 | 1134 | 1140 | PF00069 | 0.441 |
MOD_PKA_2 | 1143 | 1149 | PF00069 | 0.358 |
MOD_PKA_2 | 1228 | 1234 | PF00069 | 0.680 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.536 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.613 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.612 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.728 |
MOD_PKA_2 | 509 | 515 | PF00069 | 0.537 |
MOD_PKA_2 | 522 | 528 | PF00069 | 0.518 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.385 |
MOD_PKA_2 | 588 | 594 | PF00069 | 0.531 |
MOD_PKA_2 | 618 | 624 | PF00069 | 0.699 |
MOD_PKA_2 | 670 | 676 | PF00069 | 0.678 |
MOD_PKA_2 | 677 | 683 | PF00069 | 0.628 |
MOD_PKA_2 | 887 | 893 | PF00069 | 0.702 |
MOD_PKA_2 | 924 | 930 | PF00069 | 0.564 |
MOD_PKB_1 | 292 | 300 | PF00069 | 0.485 |
MOD_PKB_1 | 415 | 423 | PF00069 | 0.537 |
MOD_PKB_1 | 447 | 455 | PF00069 | 0.623 |
MOD_PKB_1 | 611 | 619 | PF00069 | 0.664 |
MOD_Plk_1 | 1069 | 1075 | PF00069 | 0.613 |
MOD_Plk_1 | 1093 | 1099 | PF00069 | 0.508 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.459 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.287 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.445 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.433 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.386 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.348 |
MOD_Plk_1 | 683 | 689 | PF00069 | 0.577 |
MOD_Plk_1 | 932 | 938 | PF00069 | 0.631 |
MOD_Plk_1 | 983 | 989 | PF00069 | 0.647 |
MOD_Plk_2-3 | 168 | 174 | PF00069 | 0.294 |
MOD_Plk_2-3 | 313 | 319 | PF00069 | 0.393 |
MOD_Plk_4 | 1096 | 1102 | PF00069 | 0.515 |
MOD_Plk_4 | 1110 | 1116 | PF00069 | 0.321 |
MOD_Plk_4 | 1118 | 1124 | PF00069 | 0.325 |
MOD_Plk_4 | 1134 | 1140 | PF00069 | 0.396 |
MOD_Plk_4 | 1205 | 1211 | PF00069 | 0.452 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.443 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.470 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.350 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.482 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.463 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.284 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.478 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.440 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.299 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.385 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.590 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.292 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.644 |
MOD_Plk_4 | 684 | 690 | PF00069 | 0.602 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.506 |
MOD_ProDKin_1 | 1051 | 1057 | PF00069 | 0.632 |
MOD_ProDKin_1 | 1138 | 1144 | PF00069 | 0.398 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.427 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.415 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.497 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.532 |
MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.789 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.754 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.707 |
MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.795 |
MOD_ProDKin_1 | 551 | 557 | PF00069 | 0.559 |
MOD_ProDKin_1 | 775 | 781 | PF00069 | 0.593 |
MOD_ProDKin_1 | 888 | 894 | PF00069 | 0.611 |
MOD_ProDKin_1 | 904 | 910 | PF00069 | 0.604 |
MOD_ProDKin_1 | 990 | 996 | PF00069 | 0.685 |
MOD_SUMO_rev_2 | 198 | 204 | PF00179 | 0.578 |
TRG_DiLeu_BaEn_4 | 356 | 362 | PF01217 | 0.382 |
TRG_DiLeu_BaLyEn_6 | 397 | 402 | PF01217 | 0.591 |
TRG_ENDOCYTIC_2 | 1100 | 1103 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 1165 | 1168 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 1199 | 1202 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.552 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.414 |
TRG_ER_diArg_1 | 1007 | 1010 | PF00400 | 0.644 |
TRG_ER_diArg_1 | 1228 | 1230 | PF00400 | 0.641 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 291 | 294 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 402 | 404 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 446 | 449 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 611 | 614 | PF00400 | 0.668 |
TRG_ER_diArg_1 | 677 | 679 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 733 | 735 | PF00400 | 0.679 |
TRG_ER_diArg_1 | 849 | 851 | PF00400 | 0.677 |
TRG_ER_diArg_1 | 909 | 912 | PF00400 | 0.663 |
TRG_ER_diArg_1 | 924 | 926 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 98 | 101 | PF00400 | 0.342 |
TRG_ER_diArg_1 | 994 | 996 | PF00400 | 0.639 |
TRG_NES_CRM1_1 | 155 | 168 | PF08389 | 0.384 |
TRG_Pf-PMV_PEXEL_1 | 91 | 96 | PF00026 | 0.385 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WTU2 | Leishmania donovani | 82% | 98% |
A4H8F8 | Leishmania braziliensis | 60% | 98% |
A4HWT1 | Leishmania infantum | 82% | 98% |
Q4QEY8 | Leishmania major | 82% | 100% |