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: 5 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 30 |
NetGPI | no | yes: 0, no: 30 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005829 | cytosol | 2 | 3 |
GO:0005930 | axoneme | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 31 |
GO:0006163 | purine nucleotide metabolic process | 5 | 31 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 31 |
GO:0006188 | IMP biosynthetic process | 8 | 31 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 31 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 31 |
GO:0006793 | phosphorus metabolic process | 3 | 31 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 31 |
GO:0006807 | nitrogen compound metabolic process | 2 | 31 |
GO:0008152 | metabolic process | 1 | 31 |
GO:0009058 | biosynthetic process | 2 | 31 |
GO:0009117 | nucleotide metabolic process | 5 | 31 |
GO:0009123 | nucleoside monophosphate metabolic process | 5 | 31 |
GO:0009124 | nucleoside monophosphate biosynthetic process | 6 | 31 |
GO:0009126 | purine nucleoside monophosphate metabolic process | 6 | 31 |
GO:0009127 | purine nucleoside monophosphate biosynthetic process | 7 | 31 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 31 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 31 |
GO:0009156 | ribonucleoside monophosphate biosynthetic process | 7 | 31 |
GO:0009161 | ribonucleoside monophosphate metabolic process | 6 | 31 |
GO:0009165 | nucleotide biosynthetic process | 6 | 31 |
GO:0009167 | purine ribonucleoside monophosphate metabolic process | 7 | 31 |
GO:0009168 | purine ribonucleoside monophosphate biosynthetic process | 8 | 31 |
GO:0009259 | ribonucleotide metabolic process | 5 | 31 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 31 |
GO:0009987 | cellular process | 1 | 31 |
GO:0018130 | heterocycle biosynthetic process | 4 | 31 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 31 |
GO:0019637 | organophosphate metabolic process | 3 | 31 |
GO:0019693 | ribose phosphate metabolic process | 4 | 31 |
GO:0032261 | purine nucleotide salvage | 5 | 31 |
GO:0032264 | IMP salvage | 7 | 31 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 31 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 31 |
GO:0043094 | cellular metabolic compound salvage | 3 | 31 |
GO:0043101 | purine-containing compound salvage | 4 | 31 |
GO:0043173 | nucleotide salvage | 4 | 31 |
GO:0044237 | cellular metabolic process | 2 | 31 |
GO:0044238 | primary metabolic process | 2 | 31 |
GO:0044249 | cellular biosynthetic process | 3 | 31 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 31 |
GO:0044281 | small molecule metabolic process | 2 | 31 |
GO:0046040 | IMP metabolic process | 7 | 31 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 31 |
GO:0046483 | heterocycle metabolic process | 3 | 31 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 31 |
GO:0071704 | organic substance metabolic process | 2 | 31 |
GO:0072521 | purine-containing compound metabolic process | 4 | 31 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 31 |
GO:0090407 | organophosphate biosynthetic process | 4 | 31 |
GO:0106380 | purine ribonucleotide salvage | 6 | 31 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 31 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 31 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 31 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 31 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 31 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 31 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 31 |
GO:1901576 | organic substance biosynthetic process | 3 | 31 |
GO:0046033 | AMP metabolic process | 7 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 31 |
GO:0003876 | AMP deaminase activity | 5 | 31 |
GO:0016787 | hydrolase activity | 2 | 31 |
GO:0016810 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds | 3 | 31 |
GO:0016814 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amidines | 4 | 31 |
GO:0019239 | deaminase activity | 3 | 31 |
GO:0047623 | adenosine-phosphate deaminase activity | 4 | 31 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1055 | 1059 | PF00656 | 0.363 |
CLV_C14_Caspase3-7 | 217 | 221 | PF00656 | 0.333 |
CLV_C14_Caspase3-7 | 389 | 393 | PF00656 | 0.366 |
CLV_C14_Caspase3-7 | 683 | 687 | PF00656 | 0.586 |
CLV_NRD_NRD_1 | 1348 | 1350 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 1364 | 1366 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 744 | 746 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.516 |
CLV_PCSK_KEX2_1 | 1239 | 1241 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 1348 | 1350 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 1364 | 1366 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 1421 | 1423 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 1461 | 1463 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 472 | 474 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 611 | 613 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 744 | 746 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 806 | 808 | PF00082 | 0.304 |
CLV_PCSK_PC1ET2_1 | 1239 | 1241 | PF00082 | 0.272 |
CLV_PCSK_PC1ET2_1 | 1421 | 1423 | PF00082 | 0.642 |
CLV_PCSK_PC1ET2_1 | 1461 | 1463 | PF00082 | 0.631 |
CLV_PCSK_PC1ET2_1 | 611 | 613 | PF00082 | 0.329 |
CLV_PCSK_PC1ET2_1 | 806 | 808 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 1246 | 1250 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 1266 | 1270 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 1352 | 1356 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 1376 | 1380 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 1421 | 1425 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 1435 | 1439 | PF00082 | 0.656 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 637 | 641 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 693 | 697 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 704 | 708 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 745 | 749 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 789 | 793 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 859 | 863 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 933 | 937 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.522 |
CLV_Separin_Metazoa | 1345 | 1349 | PF03568 | 0.316 |
CLV_Separin_Metazoa | 351 | 355 | PF03568 | 0.463 |
DEG_APCC_DBOX_1 | 1258 | 1266 | PF00400 | 0.294 |
DEG_APCC_DBOX_1 | 1351 | 1359 | PF00400 | 0.543 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.384 |
DEG_SCF_FBW7_1 | 896 | 901 | PF00400 | 0.404 |
DOC_CDC14_PxL_1 | 511 | 519 | PF14671 | 0.366 |
DOC_CYCLIN_RxL_1 | 1348 | 1359 | PF00134 | 0.578 |
DOC_CYCLIN_RxL_1 | 248 | 256 | PF00134 | 0.277 |
DOC_MAPK_gen_1 | 207 | 215 | PF00069 | 0.374 |
DOC_MAPK_gen_1 | 472 | 480 | PF00069 | 0.340 |
DOC_MAPK_gen_1 | 814 | 821 | PF00069 | 0.274 |
DOC_MAPK_gen_1 | 879 | 887 | PF00069 | 0.370 |
DOC_MAPK_gen_1 | 996 | 1004 | PF00069 | 0.349 |
DOC_MAPK_HePTP_8 | 890 | 902 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 363 | 372 | PF00069 | 0.341 |
DOC_MAPK_MEF2A_6 | 814 | 821 | PF00069 | 0.298 |
DOC_MAPK_MEF2A_6 | 893 | 902 | PF00069 | 0.440 |
DOC_MAPK_NFAT4_5 | 814 | 822 | PF00069 | 0.290 |
DOC_MAPK_RevD_3 | 66 | 81 | PF00069 | 0.505 |
DOC_MAPK_RevD_3 | 864 | 880 | PF00069 | 0.341 |
DOC_PP1_RVXF_1 | 1264 | 1270 | PF00149 | 0.306 |
DOC_PP1_RVXF_1 | 1420 | 1427 | PF00149 | 0.554 |
DOC_PP1_RVXF_1 | 635 | 641 | PF00149 | 0.311 |
DOC_PP1_RVXF_1 | 686 | 692 | PF00149 | 0.388 |
DOC_PP2B_LxvP_1 | 139 | 142 | PF13499 | 0.445 |
DOC_PP2B_LxvP_1 | 657 | 660 | PF13499 | 0.405 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 1225 | 1229 | PF00917 | 0.325 |
DOC_USP7_MATH_1 | 1401 | 1405 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 597 | 601 | PF00917 | 0.239 |
DOC_USP7_MATH_1 | 665 | 669 | PF00917 | 0.474 |
DOC_USP7_MATH_2 | 377 | 383 | PF00917 | 0.256 |
DOC_USP7_UBL2_3 | 859 | 863 | PF12436 | 0.256 |
DOC_USP7_UBL2_3 | 979 | 983 | PF12436 | 0.407 |
DOC_WW_Pin1_4 | 1068 | 1073 | PF00397 | 0.349 |
DOC_WW_Pin1_4 | 1157 | 1162 | PF00397 | 0.342 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 1406 | 1411 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.324 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.407 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 528 | 533 | PF00397 | 0.298 |
DOC_WW_Pin1_4 | 561 | 566 | PF00397 | 0.354 |
DOC_WW_Pin1_4 | 604 | 609 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 655 | 660 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 854 | 859 | PF00397 | 0.397 |
DOC_WW_Pin1_4 | 894 | 899 | PF00397 | 0.314 |
LIG_14-3-3_CanoR_1 | 1104 | 1110 | PF00244 | 0.347 |
LIG_14-3-3_CanoR_1 | 1226 | 1230 | PF00244 | 0.294 |
LIG_14-3-3_CanoR_1 | 1259 | 1269 | PF00244 | 0.275 |
LIG_14-3-3_CanoR_1 | 1349 | 1355 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 1403 | 1408 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 1435 | 1442 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 155 | 161 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 300 | 310 | PF00244 | 0.338 |
LIG_14-3-3_CanoR_1 | 525 | 531 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 587 | 592 | PF00244 | 0.315 |
LIG_14-3-3_CanoR_1 | 690 | 696 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 744 | 750 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 833 | 841 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 91 | 96 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 963 | 967 | PF00244 | 0.299 |
LIG_14-3-3_CanoR_1 | 970 | 974 | PF00244 | 0.299 |
LIG_Actin_WH2_2 | 303 | 318 | PF00022 | 0.335 |
LIG_Actin_WH2_2 | 849 | 865 | PF00022 | 0.256 |
LIG_AP2alpha_1 | 1176 | 1180 | PF02296 | 0.397 |
LIG_BRCT_BRCA1_1 | 1102 | 1106 | PF00533 | 0.306 |
LIG_BRCT_BRCA1_1 | 1172 | 1176 | PF00533 | 0.328 |
LIG_BRCT_BRCA1_1 | 179 | 183 | PF00533 | 0.293 |
LIG_BRCT_BRCA1_1 | 374 | 378 | PF00533 | 0.240 |
LIG_BRCT_BRCA1_1 | 62 | 66 | PF00533 | 0.535 |
LIG_deltaCOP1_diTrp_1 | 980 | 988 | PF00928 | 0.324 |
LIG_EH_1 | 1173 | 1177 | PF12763 | 0.294 |
LIG_EVH1_1 | 1450 | 1454 | PF00568 | 0.691 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.643 |
LIG_FHA_1 | 1060 | 1066 | PF00498 | 0.354 |
LIG_FHA_1 | 1106 | 1112 | PF00498 | 0.363 |
LIG_FHA_1 | 1454 | 1460 | PF00498 | 0.572 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.417 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.542 |
LIG_FHA_1 | 895 | 901 | PF00498 | 0.303 |
LIG_FHA_2 | 1074 | 1080 | PF00498 | 0.326 |
LIG_FHA_2 | 1094 | 1100 | PF00498 | 0.150 |
LIG_FHA_2 | 1293 | 1299 | PF00498 | 0.417 |
LIG_FHA_2 | 1340 | 1346 | PF00498 | 0.380 |
LIG_FHA_2 | 247 | 253 | PF00498 | 0.286 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.441 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.319 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.481 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.319 |
LIG_FHA_2 | 488 | 494 | PF00498 | 0.364 |
LIG_FHA_2 | 681 | 687 | PF00498 | 0.417 |
LIG_FHA_2 | 746 | 752 | PF00498 | 0.322 |
LIG_FHA_2 | 778 | 784 | PF00498 | 0.415 |
LIG_FHA_2 | 827 | 833 | PF00498 | 0.335 |
LIG_FHA_2 | 842 | 848 | PF00498 | 0.323 |
LIG_FHA_2 | 910 | 916 | PF00498 | 0.298 |
LIG_FHA_2 | 963 | 969 | PF00498 | 0.319 |
LIG_IBAR_NPY_1 | 110 | 112 | PF08397 | 0.651 |
LIG_Integrin_isoDGR_2 | 944 | 946 | PF01839 | 0.412 |
LIG_IRF3_LxIS_1 | 364 | 371 | PF10401 | 0.174 |
LIG_LIR_Gen_1 | 1052 | 1061 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 1064 | 1074 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 1103 | 1113 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 1312 | 1320 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 302 | 310 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 392 | 403 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 63 | 70 | PF02991 | 0.604 |
LIG_LIR_Gen_1 | 668 | 676 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 678 | 689 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 912 | 920 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 980 | 989 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 1019 | 1023 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 1025 | 1031 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 1052 | 1057 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 1064 | 1070 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 1103 | 1109 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 1173 | 1179 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 1312 | 1316 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 302 | 306 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 375 | 381 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 453 | 459 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 512 | 517 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 63 | 69 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 668 | 673 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 678 | 684 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 760 | 766 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 782 | 788 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 912 | 917 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 94 | 99 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 954 | 959 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 980 | 984 | PF02991 | 0.323 |
LIG_LYPXL_yS_3 | 514 | 517 | PF13949 | 0.341 |
LIG_MAD2 | 317 | 325 | PF02301 | 0.256 |
LIG_MYND_1 | 17 | 21 | PF01753 | 0.622 |
LIG_MYND_1 | 325 | 329 | PF01753 | 0.256 |
LIG_NRBOX | 249 | 255 | PF00104 | 0.440 |
LIG_NRBOX | 931 | 937 | PF00104 | 0.290 |
LIG_PCNA_yPIPBox_3 | 923 | 936 | PF02747 | 0.334 |
LIG_Pex14_2 | 1028 | 1032 | PF04695 | 0.325 |
LIG_Pex14_2 | 1176 | 1180 | PF04695 | 0.294 |
LIG_Pex14_2 | 1234 | 1238 | PF04695 | 0.294 |
LIG_Pex14_2 | 395 | 399 | PF04695 | 0.338 |
LIG_PTB_Apo_2 | 1077 | 1084 | PF02174 | 0.346 |
LIG_PTB_Apo_2 | 366 | 373 | PF02174 | 0.253 |
LIG_PTB_Apo_2 | 941 | 948 | PF02174 | 0.397 |
LIG_PTB_Phospho_1 | 1077 | 1083 | PF10480 | 0.311 |
LIG_PTB_Phospho_1 | 941 | 947 | PF10480 | 0.397 |
LIG_REV1ctd_RIR_1 | 1177 | 1186 | PF16727 | 0.294 |
LIG_RPA_C_Fungi | 1336 | 1348 | PF08784 | 0.434 |
LIG_SH2_CRK | 1091 | 1095 | PF00017 | 0.331 |
LIG_SH2_CRK | 1381 | 1385 | PF00017 | 0.641 |
LIG_SH2_CRK | 462 | 466 | PF00017 | 0.366 |
LIG_SH2_CRK | 681 | 685 | PF00017 | 0.409 |
LIG_SH2_CRK | 96 | 100 | PF00017 | 0.392 |
LIG_SH2_GRB2like | 1091 | 1094 | PF00017 | 0.324 |
LIG_SH2_GRB2like | 462 | 465 | PF00017 | 0.341 |
LIG_SH2_NCK_1 | 1207 | 1211 | PF00017 | 0.294 |
LIG_SH2_NCK_1 | 579 | 583 | PF00017 | 0.449 |
LIG_SH2_PTP2 | 1313 | 1316 | PF00017 | 0.353 |
LIG_SH2_SRC | 1086 | 1089 | PF00017 | 0.330 |
LIG_SH2_SRC | 1091 | 1094 | PF00017 | 0.319 |
LIG_SH2_SRC | 460 | 463 | PF00017 | 0.366 |
LIG_SH2_STAP1 | 1207 | 1211 | PF00017 | 0.311 |
LIG_SH2_STAP1 | 149 | 153 | PF00017 | 0.369 |
LIG_SH2_STAP1 | 334 | 338 | PF00017 | 0.320 |
LIG_SH2_STAP1 | 462 | 466 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 681 | 685 | PF00017 | 0.510 |
LIG_SH2_STAT3 | 1151 | 1154 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 1023 | 1026 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 1086 | 1089 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 1148 | 1151 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 1170 | 1173 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 1313 | 1316 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 1386 | 1389 | PF00017 | 0.617 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 499 | 502 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 672 | 675 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 722 | 725 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 947 | 950 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 964 | 967 | PF00017 | 0.325 |
LIG_SH3_1 | 1425 | 1431 | PF00018 | 0.600 |
LIG_SH3_1 | 1446 | 1452 | PF00018 | 0.634 |
LIG_SH3_1 | 233 | 239 | PF00018 | 0.447 |
LIG_SH3_2 | 236 | 241 | PF14604 | 0.227 |
LIG_SH3_3 | 1075 | 1081 | PF00018 | 0.374 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.652 |
LIG_SH3_3 | 1404 | 1410 | PF00018 | 0.675 |
LIG_SH3_3 | 1425 | 1431 | PF00018 | 0.582 |
LIG_SH3_3 | 1446 | 1452 | PF00018 | 0.634 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.715 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.307 |
LIG_SH3_3 | 686 | 692 | PF00018 | 0.461 |
LIG_SH3_3 | 723 | 729 | PF00018 | 0.508 |
LIG_SUMO_SIM_anti_2 | 1342 | 1348 | PF11976 | 0.567 |
LIG_TRAF2_1 | 1296 | 1299 | PF00917 | 0.448 |
LIG_TRAF2_1 | 1372 | 1375 | PF00917 | 0.608 |
LIG_TRAF2_1 | 659 | 662 | PF00917 | 0.600 |
LIG_TRFH_1 | 1109 | 1113 | PF08558 | 0.350 |
LIG_TYR_ITIM | 679 | 684 | PF00017 | 0.403 |
LIG_UBA3_1 | 1326 | 1334 | PF00899 | 0.612 |
LIG_UBA3_1 | 139 | 145 | PF00899 | 0.485 |
LIG_UBA3_1 | 394 | 400 | PF00899 | 0.322 |
LIG_WRC_WIRS_1 | 1017 | 1022 | PF05994 | 0.329 |
LIG_WRC_WIRS_1 | 1106 | 1111 | PF05994 | 0.330 |
LIG_WRC_WIRS_1 | 603 | 608 | PF05994 | 0.360 |
LIG_WW_2 | 1451 | 1454 | PF00397 | 0.689 |
MOD_CDC14_SPxK_1 | 564 | 567 | PF00782 | 0.440 |
MOD_CDK_SPK_2 | 854 | 859 | PF00069 | 0.397 |
MOD_CDK_SPxK_1 | 561 | 567 | PF00069 | 0.440 |
MOD_CDK_SPxxK_3 | 604 | 611 | PF00069 | 0.256 |
MOD_CK1_1 | 1160 | 1166 | PF00069 | 0.323 |
MOD_CK1_1 | 1187 | 1193 | PF00069 | 0.294 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.328 |
MOD_CK1_1 | 1257 | 1263 | PF00069 | 0.321 |
MOD_CK1_1 | 1391 | 1397 | PF00069 | 0.697 |
MOD_CK1_1 | 1406 | 1412 | PF00069 | 0.667 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.354 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.261 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.573 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.475 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.474 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.371 |
MOD_CK1_1 | 604 | 610 | PF00069 | 0.337 |
MOD_CK1_1 | 631 | 637 | PF00069 | 0.352 |
MOD_CK1_1 | 777 | 783 | PF00069 | 0.441 |
MOD_CK2_1 | 1073 | 1079 | PF00069 | 0.290 |
MOD_CK2_1 | 1093 | 1099 | PF00069 | 0.336 |
MOD_CK2_1 | 1115 | 1121 | PF00069 | 0.352 |
MOD_CK2_1 | 1292 | 1298 | PF00069 | 0.406 |
MOD_CK2_1 | 1339 | 1345 | PF00069 | 0.444 |
MOD_CK2_1 | 1350 | 1356 | PF00069 | 0.506 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.321 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.305 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.478 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.402 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.419 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.355 |
MOD_CK2_1 | 745 | 751 | PF00069 | 0.249 |
MOD_CK2_1 | 909 | 915 | PF00069 | 0.309 |
MOD_CK2_1 | 962 | 968 | PF00069 | 0.318 |
MOD_GlcNHglycan | 1051 | 1054 | PF01048 | 0.318 |
MOD_GlcNHglycan | 1117 | 1120 | PF01048 | 0.384 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.619 |
MOD_GlcNHglycan | 1216 | 1219 | PF01048 | 0.403 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.425 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.433 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.348 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.464 |
MOD_GlcNHglycan | 768 | 771 | PF01048 | 0.436 |
MOD_GlcNHglycan | 796 | 799 | PF01048 | 0.469 |
MOD_GlcNHglycan | 871 | 874 | PF01048 | 0.306 |
MOD_GSK3_1 | 1032 | 1039 | PF00069 | 0.273 |
MOD_GSK3_1 | 1049 | 1056 | PF00069 | 0.387 |
MOD_GSK3_1 | 1100 | 1107 | PF00069 | 0.321 |
MOD_GSK3_1 | 1384 | 1391 | PF00069 | 0.618 |
MOD_GSK3_1 | 1402 | 1409 | PF00069 | 0.505 |
MOD_GSK3_1 | 1438 | 1445 | PF00069 | 0.651 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.588 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.453 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.418 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.457 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.358 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.383 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.348 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.287 |
MOD_GSK3_1 | 698 | 705 | PF00069 | 0.576 |
MOD_GSK3_1 | 752 | 759 | PF00069 | 0.361 |
MOD_GSK3_1 | 841 | 848 | PF00069 | 0.341 |
MOD_GSK3_1 | 894 | 901 | PF00069 | 0.301 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.491 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.602 |
MOD_N-GLC_1 | 1184 | 1189 | PF02516 | 0.297 |
MOD_N-GLC_1 | 1254 | 1259 | PF02516 | 0.352 |
MOD_N-GLC_1 | 135 | 140 | PF02516 | 0.313 |
MOD_N-GLC_1 | 1356 | 1361 | PF02516 | 0.503 |
MOD_N-GLC_1 | 31 | 36 | PF02516 | 0.554 |
MOD_N-GLC_1 | 368 | 373 | PF02516 | 0.174 |
MOD_N-GLC_1 | 382 | 387 | PF02516 | 0.174 |
MOD_N-GLC_1 | 436 | 441 | PF02516 | 0.456 |
MOD_N-GLC_1 | 486 | 491 | PF02516 | 0.227 |
MOD_N-GLC_1 | 655 | 660 | PF02516 | 0.531 |
MOD_N-GLC_1 | 898 | 903 | PF02516 | 0.304 |
MOD_N-GLC_2 | 167 | 169 | PF02516 | 0.256 |
MOD_NEK2_1 | 1100 | 1105 | PF00069 | 0.311 |
MOD_NEK2_1 | 1184 | 1189 | PF00069 | 0.300 |
MOD_NEK2_1 | 1248 | 1253 | PF00069 | 0.318 |
MOD_NEK2_1 | 1292 | 1297 | PF00069 | 0.436 |
MOD_NEK2_1 | 1433 | 1438 | PF00069 | 0.606 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.447 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.358 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.476 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.278 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.174 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.341 |
MOD_NEK2_1 | 556 | 561 | PF00069 | 0.337 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.322 |
MOD_NEK2_1 | 602 | 607 | PF00069 | 0.379 |
MOD_NEK2_1 | 628 | 633 | PF00069 | 0.324 |
MOD_NEK2_2 | 1032 | 1037 | PF00069 | 0.325 |
MOD_NEK2_2 | 1254 | 1259 | PF00069 | 0.397 |
MOD_NEK2_2 | 334 | 339 | PF00069 | 0.174 |
MOD_NEK2_2 | 909 | 914 | PF00069 | 0.361 |
MOD_PIKK_1 | 102 | 108 | PF00454 | 0.377 |
MOD_PIKK_1 | 1150 | 1156 | PF00454 | 0.284 |
MOD_PIKK_1 | 1196 | 1202 | PF00454 | 0.290 |
MOD_PIKK_1 | 1339 | 1345 | PF00454 | 0.525 |
MOD_PIKK_1 | 1388 | 1394 | PF00454 | 0.476 |
MOD_PIKK_1 | 1411 | 1417 | PF00454 | 0.634 |
MOD_PIKK_1 | 1435 | 1441 | PF00454 | 0.651 |
MOD_PIKK_1 | 27 | 33 | PF00454 | 0.651 |
MOD_PK_1 | 1403 | 1409 | PF00069 | 0.458 |
MOD_PKA_2 | 1100 | 1106 | PF00069 | 0.306 |
MOD_PKA_2 | 1225 | 1231 | PF00069 | 0.320 |
MOD_PKA_2 | 1402 | 1408 | PF00069 | 0.636 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.384 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.324 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.378 |
MOD_PKA_2 | 482 | 488 | PF00069 | 0.300 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.306 |
MOD_PKA_2 | 586 | 592 | PF00069 | 0.321 |
MOD_PKA_2 | 743 | 749 | PF00069 | 0.306 |
MOD_PKA_2 | 832 | 838 | PF00069 | 0.344 |
MOD_PKA_2 | 962 | 968 | PF00069 | 0.344 |
MOD_PKA_2 | 969 | 975 | PF00069 | 0.367 |
MOD_PKB_1 | 241 | 249 | PF00069 | 0.227 |
MOD_Plk_1 | 1032 | 1038 | PF00069 | 0.311 |
MOD_Plk_1 | 1059 | 1065 | PF00069 | 0.343 |
MOD_Plk_1 | 1184 | 1190 | PF00069 | 0.297 |
MOD_Plk_1 | 1205 | 1211 | PF00069 | 0.294 |
MOD_Plk_1 | 1254 | 1260 | PF00069 | 0.334 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.376 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.298 |
MOD_Plk_1 | 263 | 269 | PF00069 | 0.364 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.403 |
MOD_Plk_1 | 332 | 338 | PF00069 | 0.389 |
MOD_Plk_1 | 368 | 374 | PF00069 | 0.174 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.174 |
MOD_Plk_1 | 628 | 634 | PF00069 | 0.323 |
MOD_Plk_1 | 752 | 758 | PF00069 | 0.275 |
MOD_Plk_1 | 898 | 904 | PF00069 | 0.284 |
MOD_Plk_1 | 909 | 915 | PF00069 | 0.250 |
MOD_Plk_2-3 | 680 | 686 | PF00069 | 0.408 |
MOD_Plk_2-3 | 962 | 968 | PF00069 | 0.325 |
MOD_Plk_4 | 1225 | 1231 | PF00069 | 0.308 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.332 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.258 |
MOD_Plk_4 | 597 | 603 | PF00069 | 0.338 |
MOD_Plk_4 | 680 | 686 | PF00069 | 0.405 |
MOD_Plk_4 | 909 | 915 | PF00069 | 0.306 |
MOD_Plk_4 | 969 | 975 | PF00069 | 0.363 |
MOD_ProDKin_1 | 1068 | 1074 | PF00069 | 0.349 |
MOD_ProDKin_1 | 1157 | 1163 | PF00069 | 0.342 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.572 |
MOD_ProDKin_1 | 1406 | 1412 | PF00069 | 0.698 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.324 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.407 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.440 |
MOD_ProDKin_1 | 528 | 534 | PF00069 | 0.298 |
MOD_ProDKin_1 | 561 | 567 | PF00069 | 0.354 |
MOD_ProDKin_1 | 604 | 610 | PF00069 | 0.487 |
MOD_ProDKin_1 | 655 | 661 | PF00069 | 0.574 |
MOD_ProDKin_1 | 854 | 860 | PF00069 | 0.397 |
MOD_ProDKin_1 | 894 | 900 | PF00069 | 0.314 |
MOD_SUMO_rev_2 | 1272 | 1281 | PF00179 | 0.393 |
MOD_SUMO_rev_2 | 1298 | 1307 | PF00179 | 0.460 |
MOD_SUMO_rev_2 | 285 | 292 | PF00179 | 0.412 |
MOD_SUMO_rev_2 | 809 | 815 | PF00179 | 0.311 |
TRG_DiLeu_BaLyEn_6 | 1199 | 1204 | PF01217 | 0.277 |
TRG_DiLeu_BaLyEn_6 | 1419 | 1424 | PF01217 | 0.561 |
TRG_ENDOCYTIC_2 | 1008 | 1011 | PF00928 | 0.294 |
TRG_ENDOCYTIC_2 | 1091 | 1094 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 1125 | 1128 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 1313 | 1316 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 462 | 465 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 514 | 517 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 681 | 684 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 785 | 788 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 924 | 927 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.437 |
TRG_ER_diArg_1 | 1347 | 1349 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 1363 | 1365 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 1446 | 1449 | PF00400 | 0.680 |
TRG_ER_diArg_1 | 155 | 158 | PF00400 | 0.352 |
TRG_ER_diArg_1 | 179 | 182 | PF00400 | 0.308 |
TRG_ER_diArg_1 | 232 | 234 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 240 | 243 | PF00400 | 0.339 |
TRG_ER_diArg_1 | 315 | 317 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 353 | 356 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 471 | 474 | PF00400 | 0.300 |
TRG_ER_diArg_1 | 688 | 691 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 90 | 93 | PF00400 | 0.380 |
TRG_NES_CRM1_1 | 583 | 595 | PF08389 | 0.397 |
TRG_NES_CRM1_1 | 646 | 661 | PF08389 | 0.460 |
TRG_NES_CRM1_1 | 809 | 824 | PF08389 | 0.440 |
TRG_Pf-PMV_PEXEL_1 | 1095 | 1099 | PF00026 | 0.306 |
TRG_Pf-PMV_PEXEL_1 | 1352 | 1356 | PF00026 | 0.382 |
TRG_Pf-PMV_PEXEL_1 | 573 | 577 | PF00026 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 786 | 790 | PF00026 | 0.385 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8L9 | Leptomonas seymouri | 35% | 94% |
A0A0N1IMV2 | Leptomonas seymouri | 78% | 100% |
A0A0S4J2U9 | Bodo saltans | 40% | 93% |
A0A0S4J7B1 | Bodo saltans | 56% | 100% |
A0A1X0NL73 | Trypanosomatidae | 39% | 87% |
A0A1X0NS01 | Trypanosomatidae | 35% | 100% |
A0A1X0P524 | Trypanosomatidae | 63% | 100% |
A0A3Q8IIT0 | Leishmania donovani | 89% | 100% |
A0A3Q8ITG5 | Leishmania donovani | 37% | 91% |
A0A3R7NE24 | Trypanosoma rangeli | 34% | 100% |
A0A3S7WSH4 | Leishmania donovani | 33% | 78% |
A0A422NN44 | Trypanosoma rangeli | 38% | 88% |
A0A422P172 | Trypanosoma rangeli | 61% | 100% |
A4H3U8 | Leishmania braziliensis | 39% | 75% |
A4HKP5 | Leishmania braziliensis | 34% | 91% |
A4HVM6 | Leishmania infantum | 33% | 89% |
A4I876 | Leishmania infantum | 37% | 91% |
A4IC17 | Leishmania infantum | 89% | 100% |
C9ZY16 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 87% |
C9ZYI5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 100% |
D0AAE6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AFV5 | Leishmania major | 88% | 100% |
E9APC2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 88% |
E9B334 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 91% |
E9B708 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 99% |
Q4Q520 | Leishmania major | 37% | 100% |
Q4QG56 | Leishmania major | 33% | 89% |
V5ARK9 | Trypanosoma cruzi | 62% | 100% |
V5BJ89 | Trypanosoma cruzi | 37% | 100% |