Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0008023 | transcription elongation factor complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 12 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009889 | regulation of biosynthetic process | 4 | 12 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 12 |
GO:0009893 | positive regulation of metabolic process | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0010468 | regulation of gene expression | 5 | 12 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 12 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 12 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 12 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 12 |
GO:0019222 | regulation of metabolic process | 3 | 12 |
GO:0031323 | regulation of cellular metabolic process | 4 | 12 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 12 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 12 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 12 |
GO:0032784 | regulation of DNA-templated transcription elongation | 7 | 12 |
GO:0032786 | positive regulation of DNA-templated transcription, elongation | 8 | 12 |
GO:0032968 | positive regulation of transcription elongation by RNA polymerase II | 9 | 12 |
GO:0034243 | regulation of transcription elongation by RNA polymerase II | 8 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0045893 | positive regulation of DNA-templated transcription | 7 | 12 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 12 |
GO:0045944 | positive regulation of transcription by RNA polymerase II | 8 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0048518 | positive regulation of biological process | 3 | 12 |
GO:0048522 | positive regulation of cellular process | 4 | 12 |
GO:0050789 | regulation of biological process | 2 | 12 |
GO:0050794 | regulation of cellular process | 3 | 12 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 12 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 12 |
GO:0051252 | regulation of RNA metabolic process | 5 | 12 |
GO:0051254 | positive regulation of RNA metabolic process | 6 | 12 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 12 |
GO:0065007 | biological regulation | 1 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0080090 | regulation of primary metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1902680 | positive regulation of RNA biosynthetic process | 7 | 12 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 12 |
GO:1903508 | positive regulation of nucleic acid-templated transcription | 8 | 12 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 12 |
GO:0006325 | chromatin organization | 4 | 1 |
GO:0006338 | chromatin remodeling | 5 | 1 |
GO:0006351 | DNA-templated transcription | 7 | 1 |
GO:0006354 | DNA-templated transcription elongation | 6 | 1 |
GO:0006366 | transcription by RNA polymerase II | 8 | 1 |
GO:0006368 | transcription elongation by RNA polymerase II | 7 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009299 | mRNA transcription | 7 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0032774 | RNA biosynthetic process | 5 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0034728 | nucleosome organization | 6 | 1 |
GO:0042789 | mRNA transcription by RNA polymerase II | 8 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0071824 | protein-DNA complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:0097659 | nucleic acid-templated transcription | 6 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003682 | chromatin binding | 2 | 1 |
GO:0005488 | binding | 1 | 4 |
GO:0005515 | protein binding | 2 | 1 |
GO:0031491 | nucleosome binding | 3 | 1 |
GO:0042393 | histone binding | 3 | 1 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
GO:0003676 | nucleic acid binding | 3 | 3 |
GO:0003746 | translation elongation factor activity | 4 | 2 |
GO:0008135 | translation factor activity, RNA binding | 3 | 2 |
GO:0045182 | translation regulator activity | 1 | 2 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 3 |
GO:1901363 | heterocyclic compound binding | 2 | 3 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1150 | 1154 | PF00656 | 0.731 |
CLV_C14_Caspase3-7 | 34 | 38 | PF00656 | 0.525 |
CLV_C14_Caspase3-7 | 387 | 391 | PF00656 | 0.591 |
CLV_C14_Caspase3-7 | 416 | 420 | PF00656 | 0.495 |
CLV_NRD_NRD_1 | 1020 | 1022 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 1039 | 1041 | PF00675 | 0.274 |
CLV_NRD_NRD_1 | 1043 | 1045 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 1138 | 1140 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 1167 | 1169 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 1177 | 1179 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 1302 | 1304 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 1348 | 1350 | PF00675 | 0.329 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.241 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 587 | 589 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 733 | 735 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 910 | 912 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 992 | 994 | PF00675 | 0.467 |
CLV_PCSK_FUR_1 | 83 | 87 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 1020 | 1022 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 1039 | 1041 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 1043 | 1045 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 1138 | 1140 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 1167 | 1169 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 1177 | 1179 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 1302 | 1304 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 1339 | 1341 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 1348 | 1350 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 1381 | 1383 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 1445 | 1447 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 530 | 532 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 587 | 589 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 910 | 912 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 992 | 994 | PF00082 | 0.417 |
CLV_PCSK_PC1ET2_1 | 1339 | 1341 | PF00082 | 0.376 |
CLV_PCSK_PC1ET2_1 | 1381 | 1383 | PF00082 | 0.546 |
CLV_PCSK_PC1ET2_1 | 1445 | 1447 | PF00082 | 0.616 |
CLV_PCSK_PC1ET2_1 | 530 | 532 | PF00082 | 0.457 |
CLV_PCSK_PC7_1 | 1035 | 1041 | PF00082 | 0.445 |
CLV_PCSK_PC7_1 | 1441 | 1447 | PF00082 | 0.610 |
CLV_PCSK_PC7_1 | 88 | 94 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 1043 | 1047 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 1108 | 1112 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 1113 | 1117 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 1168 | 1172 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 725 | 729 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 734 | 738 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 993 | 997 | PF00082 | 0.519 |
CLV_Separin_Metazoa | 785 | 789 | PF03568 | 0.475 |
DEG_APCC_DBOX_1 | 396 | 404 | PF00400 | 0.432 |
DEG_APCC_DBOX_1 | 724 | 732 | PF00400 | 0.223 |
DEG_APCC_DBOX_1 | 91 | 99 | PF00400 | 0.508 |
DEG_APCC_DBOX_1 | 992 | 1000 | PF00400 | 0.533 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.497 |
DEG_SPOP_SBC_1 | 970 | 974 | PF00917 | 0.552 |
DOC_ANK_TNKS_1 | 194 | 201 | PF00023 | 0.589 |
DOC_CDC14_PxL_1 | 505 | 513 | PF14671 | 0.353 |
DOC_CDC14_PxL_1 | 883 | 891 | PF14671 | 0.523 |
DOC_CYCLIN_RxL_1 | 431 | 440 | PF00134 | 0.389 |
DOC_CYCLIN_RxL_1 | 731 | 738 | PF00134 | 0.475 |
DOC_MAPK_gen_1 | 1039 | 1050 | PF00069 | 0.438 |
DOC_MAPK_gen_1 | 350 | 357 | PF00069 | 0.367 |
DOC_MAPK_gen_1 | 595 | 603 | PF00069 | 0.372 |
DOC_MAPK_HePTP_8 | 851 | 863 | PF00069 | 0.379 |
DOC_MAPK_MEF2A_6 | 1125 | 1133 | PF00069 | 0.521 |
DOC_MAPK_MEF2A_6 | 854 | 863 | PF00069 | 0.372 |
DOC_MAPK_RevD_3 | 362 | 378 | PF00069 | 0.471 |
DOC_PP1_MyPhoNE_1 | 1139 | 1146 | PF00149 | 0.458 |
DOC_PP1_RVXF_1 | 1019 | 1026 | PF00149 | 0.371 |
DOC_PP1_RVXF_1 | 563 | 569 | PF00149 | 0.455 |
DOC_PP1_RVXF_1 | 852 | 858 | PF00149 | 0.366 |
DOC_PP2B_LxvP_1 | 798 | 801 | PF13499 | 0.376 |
DOC_PP4_FxxP_1 | 1333 | 1336 | PF00568 | 0.344 |
DOC_USP7_MATH_1 | 1198 | 1202 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 1210 | 1214 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 1221 | 1225 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 1425 | 1429 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 500 | 504 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 641 | 645 | PF00917 | 0.332 |
DOC_USP7_MATH_1 | 896 | 900 | PF00917 | 0.324 |
DOC_USP7_UBL2_3 | 1418 | 1422 | PF12436 | 0.527 |
DOC_USP7_UBL2_3 | 1427 | 1431 | PF12436 | 0.576 |
DOC_WW_Pin1_4 | 1101 | 1106 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 1189 | 1194 | PF00397 | 0.299 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.379 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 841 | 846 | PF00397 | 0.330 |
DOC_WW_Pin1_4 | 933 | 938 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 953 | 958 | PF00397 | 0.486 |
LIG_14-3-3_CanoR_1 | 1108 | 1115 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 1138 | 1146 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 1219 | 1228 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 1273 | 1282 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 150 | 158 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 237 | 246 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 380 | 386 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 397 | 405 | PF00244 | 0.255 |
LIG_14-3-3_CanoR_1 | 457 | 466 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 617 | 627 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 635 | 640 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 734 | 744 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 788 | 793 | PF00244 | 0.363 |
LIG_APCC_ABBAyCdc20_2 | 1246 | 1252 | PF00400 | 0.344 |
LIG_BRCT_BRCA1_1 | 1367 | 1371 | PF00533 | 0.415 |
LIG_BRCT_BRCA1_1 | 142 | 146 | PF00533 | 0.565 |
LIG_BRCT_BRCA1_1 | 401 | 405 | PF00533 | 0.427 |
LIG_Clathr_ClatBox_1 | 126 | 130 | PF01394 | 0.339 |
LIG_Clathr_ClatBox_1 | 555 | 559 | PF01394 | 0.462 |
LIG_CSL_BTD_1 | 945 | 948 | PF09270 | 0.573 |
LIG_deltaCOP1_diTrp_1 | 1318 | 1323 | PF00928 | 0.449 |
LIG_deltaCOP1_diTrp_1 | 412 | 417 | PF00928 | 0.346 |
LIG_EH1_1 | 1024 | 1032 | PF00400 | 0.323 |
LIG_EH1_1 | 602 | 610 | PF00400 | 0.460 |
LIG_EH1_1 | 958 | 966 | PF00400 | 0.514 |
LIG_eIF4E_1 | 263 | 269 | PF01652 | 0.575 |
LIG_FHA_1 | 1081 | 1087 | PF00498 | 0.557 |
LIG_FHA_1 | 1091 | 1097 | PF00498 | 0.517 |
LIG_FHA_1 | 1102 | 1108 | PF00498 | 0.555 |
LIG_FHA_1 | 1114 | 1120 | PF00498 | 0.430 |
LIG_FHA_1 | 1138 | 1144 | PF00498 | 0.337 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.573 |
LIG_FHA_1 | 1228 | 1234 | PF00498 | 0.572 |
LIG_FHA_1 | 1274 | 1280 | PF00498 | 0.475 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.376 |
LIG_FHA_1 | 496 | 502 | PF00498 | 0.445 |
LIG_FHA_1 | 708 | 714 | PF00498 | 0.404 |
LIG_FHA_1 | 750 | 756 | PF00498 | 0.358 |
LIG_FHA_1 | 838 | 844 | PF00498 | 0.497 |
LIG_FHA_2 | 1044 | 1050 | PF00498 | 0.484 |
LIG_FHA_2 | 1229 | 1235 | PF00498 | 0.223 |
LIG_FHA_2 | 1322 | 1328 | PF00498 | 0.404 |
LIG_FHA_2 | 1374 | 1380 | PF00498 | 0.223 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.460 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.395 |
LIG_FHA_2 | 414 | 420 | PF00498 | 0.449 |
LIG_FHA_2 | 696 | 702 | PF00498 | 0.349 |
LIG_FHA_2 | 71 | 77 | PF00498 | 0.504 |
LIG_FHA_2 | 771 | 777 | PF00498 | 0.470 |
LIG_FXI_DFP_1 | 652 | 656 | PF00024 | 0.494 |
LIG_GBD_Chelix_1 | 247 | 255 | PF00786 | 0.456 |
LIG_GBD_Chelix_1 | 604 | 612 | PF00786 | 0.461 |
LIG_Integrin_isoDGR_2 | 1033 | 1035 | PF01839 | 0.530 |
LIG_LIR_Apic_2 | 1394 | 1399 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 1322 | 1330 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 1368 | 1375 | PF02991 | 0.223 |
LIG_LIR_Gen_1 | 1403 | 1414 | PF02991 | 0.366 |
LIG_LIR_Gen_1 | 412 | 421 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 427 | 438 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 439 | 450 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 602 | 611 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 663 | 674 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 695 | 702 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 772 | 782 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 793 | 803 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 1322 | 1326 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 1368 | 1374 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 1403 | 1409 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 210 | 215 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 318 | 323 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 412 | 417 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 427 | 433 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 439 | 445 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 602 | 606 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 663 | 669 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 695 | 700 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 772 | 777 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 793 | 798 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 943 | 949 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 956 | 961 | PF02991 | 0.366 |
LIG_MYND_1 | 887 | 891 | PF01753 | 0.519 |
LIG_NRBOX | 279 | 285 | PF00104 | 0.392 |
LIG_NRBOX | 356 | 362 | PF00104 | 0.356 |
LIG_NRBOX | 980 | 986 | PF00104 | 0.539 |
LIG_Pex14_2 | 1329 | 1333 | PF04695 | 0.344 |
LIG_Pex14_2 | 1371 | 1375 | PF04695 | 0.376 |
LIG_PTB_Apo_2 | 1044 | 1051 | PF02174 | 0.528 |
LIG_SH2_CRK | 1042 | 1046 | PF00017 | 0.413 |
LIG_SH2_CRK | 1396 | 1400 | PF00017 | 0.497 |
LIG_SH2_CRK | 576 | 580 | PF00017 | 0.461 |
LIG_SH2_CRK | 852 | 856 | PF00017 | 0.389 |
LIG_SH2_PTP2 | 1408 | 1411 | PF00017 | 0.378 |
LIG_SH2_SRC | 263 | 266 | PF00017 | 0.556 |
LIG_SH2_STAP1 | 1439 | 1443 | PF00017 | 0.594 |
LIG_SH2_STAP1 | 302 | 306 | PF00017 | 0.500 |
LIG_SH2_STAT3 | 253 | 256 | PF00017 | 0.522 |
LIG_SH2_STAT3 | 376 | 379 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 1059 | 1062 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 1091 | 1094 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 1136 | 1139 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 1356 | 1359 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 1373 | 1376 | PF00017 | 0.244 |
LIG_SH2_STAT5 | 1408 | 1411 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 551 | 554 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 567 | 570 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 626 | 629 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 816 | 819 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 959 | 962 | PF00017 | 0.431 |
LIG_SH3_3 | 1157 | 1163 | PF00018 | 0.542 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.508 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.485 |
LIG_SH3_3 | 658 | 664 | PF00018 | 0.363 |
LIG_SH3_3 | 772 | 778 | PF00018 | 0.332 |
LIG_SH3_3 | 781 | 787 | PF00018 | 0.322 |
LIG_SH3_3 | 814 | 820 | PF00018 | 0.344 |
LIG_SH3_3 | 871 | 877 | PF00018 | 0.372 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.482 |
LIG_SH3_3 | 931 | 937 | PF00018 | 0.532 |
LIG_SH3_3 | 942 | 948 | PF00018 | 0.542 |
LIG_SH3_3 | 996 | 1002 | PF00018 | 0.561 |
LIG_SH3_4 | 1418 | 1425 | PF00018 | 0.323 |
LIG_SUMO_SIM_par_1 | 122 | 131 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 491 | 498 | PF11976 | 0.465 |
LIG_TRAF2_1 | 1193 | 1196 | PF00917 | 0.594 |
LIG_TRAF2_1 | 153 | 156 | PF00917 | 0.381 |
LIG_TRAF2_1 | 441 | 444 | PF00917 | 0.387 |
LIG_TRAF2_1 | 988 | 991 | PF00917 | 0.498 |
LIG_TYR_ITIM | 574 | 579 | PF00017 | 0.455 |
LIG_UBA3_1 | 381 | 386 | PF00899 | 0.508 |
LIG_UBA3_1 | 493 | 499 | PF00899 | 0.490 |
LIG_UBA3_1 | 757 | 763 | PF00899 | 0.317 |
LIG_WRC_WIRS_1 | 636 | 641 | PF05994 | 0.460 |
MOD_CDK_SPK_2 | 1189 | 1194 | PF00069 | 0.299 |
MOD_CDK_SPxxK_3 | 1101 | 1108 | PF00069 | 0.638 |
MOD_CK1_1 | 1052 | 1058 | PF00069 | 0.434 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.618 |
MOD_CK1_1 | 1080 | 1086 | PF00069 | 0.594 |
MOD_CK1_1 | 1224 | 1230 | PF00069 | 0.548 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.645 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.415 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.462 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.457 |
MOD_CK1_1 | 540 | 546 | PF00069 | 0.343 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.486 |
MOD_CK1_1 | 692 | 698 | PF00069 | 0.403 |
MOD_CK1_1 | 718 | 724 | PF00069 | 0.378 |
MOD_CK1_1 | 791 | 797 | PF00069 | 0.334 |
MOD_CK1_1 | 830 | 836 | PF00069 | 0.381 |
MOD_CK2_1 | 1043 | 1049 | PF00069 | 0.400 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.657 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.419 |
MOD_CK2_1 | 1189 | 1195 | PF00069 | 0.398 |
MOD_CK2_1 | 1228 | 1234 | PF00069 | 0.387 |
MOD_CK2_1 | 1373 | 1379 | PF00069 | 0.223 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.574 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.384 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.476 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.447 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.393 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.615 |
MOD_CK2_1 | 718 | 724 | PF00069 | 0.409 |
MOD_CK2_1 | 823 | 829 | PF00069 | 0.507 |
MOD_Cter_Amidation | 1018 | 1021 | PF01082 | 0.553 |
MOD_DYRK1A_RPxSP_1 | 933 | 937 | PF00069 | 0.600 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.621 |
MOD_GlcNHglycan | 1061 | 1064 | PF01048 | 0.459 |
MOD_GlcNHglycan | 1075 | 1078 | PF01048 | 0.465 |
MOD_GlcNHglycan | 1079 | 1082 | PF01048 | 0.584 |
MOD_GlcNHglycan | 1351 | 1355 | PF01048 | 0.317 |
MOD_GlcNHglycan | 1366 | 1370 | PF01048 | 0.335 |
MOD_GlcNHglycan | 1389 | 1392 | PF01048 | 0.535 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.376 |
MOD_GlcNHglycan | 1427 | 1430 | PF01048 | 0.533 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.625 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.341 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.482 |
MOD_GlcNHglycan | 691 | 694 | PF01048 | 0.385 |
MOD_GlcNHglycan | 720 | 723 | PF01048 | 0.413 |
MOD_GSK3_1 | 1055 | 1062 | PF00069 | 0.488 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.678 |
MOD_GSK3_1 | 1073 | 1080 | PF00069 | 0.605 |
MOD_GSK3_1 | 1090 | 1097 | PF00069 | 0.398 |
MOD_GSK3_1 | 1109 | 1116 | PF00069 | 0.576 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.685 |
MOD_GSK3_1 | 1206 | 1213 | PF00069 | 0.659 |
MOD_GSK3_1 | 1220 | 1227 | PF00069 | 0.462 |
MOD_GSK3_1 | 1373 | 1380 | PF00069 | 0.410 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.581 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.473 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.531 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.213 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.529 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.438 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.439 |
MOD_GSK3_1 | 641 | 648 | PF00069 | 0.379 |
MOD_GSK3_1 | 702 | 709 | PF00069 | 0.364 |
MOD_GSK3_1 | 823 | 830 | PF00069 | 0.416 |
MOD_GSK3_1 | 837 | 844 | PF00069 | 0.461 |
MOD_GSK3_1 | 897 | 904 | PF00069 | 0.518 |
MOD_GSK3_1 | 949 | 956 | PF00069 | 0.513 |
MOD_GSK3_1 | 966 | 973 | PF00069 | 0.449 |
MOD_N-GLC_1 | 1228 | 1233 | PF02516 | 0.543 |
MOD_N-GLC_1 | 1290 | 1295 | PF02516 | 0.480 |
MOD_N-GLC_1 | 1392 | 1397 | PF02516 | 0.427 |
MOD_N-GLC_1 | 16 | 21 | PF02516 | 0.603 |
MOD_N-GLC_1 | 304 | 309 | PF02516 | 0.619 |
MOD_NEK2_1 | 1109 | 1114 | PF00069 | 0.497 |
MOD_NEK2_1 | 1172 | 1177 | PF00069 | 0.484 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.401 |
MOD_NEK2_1 | 1228 | 1233 | PF00069 | 0.583 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.600 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.601 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.468 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.586 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.384 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.462 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.370 |
MOD_NEK2_1 | 707 | 712 | PF00069 | 0.329 |
MOD_NEK2_1 | 837 | 842 | PF00069 | 0.449 |
MOD_NEK2_1 | 897 | 902 | PF00069 | 0.441 |
MOD_NEK2_1 | 949 | 954 | PF00069 | 0.381 |
MOD_NEK2_2 | 469 | 474 | PF00069 | 0.281 |
MOD_PIKK_1 | 1228 | 1234 | PF00454 | 0.387 |
MOD_PIKK_1 | 500 | 506 | PF00454 | 0.427 |
MOD_PIKK_1 | 611 | 617 | PF00454 | 0.435 |
MOD_PIKK_1 | 735 | 741 | PF00454 | 0.475 |
MOD_PK_1 | 1275 | 1281 | PF00069 | 0.449 |
MOD_PK_1 | 1340 | 1346 | PF00069 | 0.358 |
MOD_PK_1 | 788 | 794 | PF00069 | 0.475 |
MOD_PKA_1 | 1043 | 1049 | PF00069 | 0.403 |
MOD_PKA_2 | 1043 | 1049 | PF00069 | 0.403 |
MOD_PKA_2 | 1137 | 1143 | PF00069 | 0.523 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.592 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.441 |
MOD_PKA_2 | 634 | 640 | PF00069 | 0.487 |
MOD_PKA_2 | 740 | 746 | PF00069 | 0.449 |
MOD_PKB_1 | 1273 | 1281 | PF00069 | 0.449 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.542 |
MOD_Plk_1 | 1228 | 1234 | PF00069 | 0.540 |
MOD_Plk_1 | 1392 | 1398 | PF00069 | 0.411 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.504 |
MOD_Plk_1 | 443 | 449 | PF00069 | 0.405 |
MOD_Plk_1 | 679 | 685 | PF00069 | 0.547 |
MOD_Plk_1 | 830 | 836 | PF00069 | 0.386 |
MOD_Plk_1 | 857 | 863 | PF00069 | 0.334 |
MOD_Plk_1 | 949 | 955 | PF00069 | 0.376 |
MOD_Plk_2-3 | 110 | 116 | PF00069 | 0.481 |
MOD_Plk_2-3 | 117 | 123 | PF00069 | 0.559 |
MOD_Plk_4 | 1080 | 1086 | PF00069 | 0.531 |
MOD_Plk_4 | 1267 | 1273 | PF00069 | 0.413 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.449 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.530 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.493 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.413 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.343 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.411 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.337 |
MOD_Plk_4 | 599 | 605 | PF00069 | 0.452 |
MOD_Plk_4 | 702 | 708 | PF00069 | 0.399 |
MOD_Plk_4 | 740 | 746 | PF00069 | 0.344 |
MOD_Plk_4 | 770 | 776 | PF00069 | 0.429 |
MOD_Plk_4 | 823 | 829 | PF00069 | 0.425 |
MOD_Plk_4 | 857 | 863 | PF00069 | 0.350 |
MOD_Plk_4 | 897 | 903 | PF00069 | 0.555 |
MOD_Plk_4 | 949 | 955 | PF00069 | 0.376 |
MOD_ProDKin_1 | 1101 | 1107 | PF00069 | 0.640 |
MOD_ProDKin_1 | 1189 | 1195 | PF00069 | 0.306 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.376 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.444 |
MOD_ProDKin_1 | 841 | 847 | PF00069 | 0.327 |
MOD_ProDKin_1 | 933 | 939 | PF00069 | 0.601 |
MOD_ProDKin_1 | 953 | 959 | PF00069 | 0.487 |
MOD_SUMO_for_1 | 164 | 167 | PF00179 | 0.640 |
MOD_SUMO_rev_2 | 160 | 166 | PF00179 | 0.585 |
TRG_DiLeu_BaEn_1 | 264 | 269 | PF01217 | 0.441 |
TRG_DiLeu_BaEn_1 | 356 | 361 | PF01217 | 0.356 |
TRG_DiLeu_BaEn_1 | 559 | 564 | PF01217 | 0.454 |
TRG_DiLeu_BaEn_2 | 129 | 135 | PF01217 | 0.532 |
TRG_DiLeu_BaEn_2 | 598 | 604 | PF01217 | 0.461 |
TRG_DiLeu_BaEn_4 | 116 | 122 | PF01217 | 0.448 |
TRG_DiLeu_BaLyEn_6 | 275 | 280 | PF01217 | 0.358 |
TRG_DiLeu_BaLyEn_6 | 604 | 609 | PF01217 | 0.398 |
TRG_DiLeu_BaLyEn_6 | 753 | 758 | PF01217 | 0.449 |
TRG_DiLeu_LyEn_5 | 356 | 361 | PF01217 | 0.356 |
TRG_ENDOCYTIC_2 | 1042 | 1045 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 1214 | 1217 | PF00928 | 0.683 |
TRG_ENDOCYTIC_2 | 1309 | 1312 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 1408 | 1411 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 212 | 215 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 567 | 570 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 576 | 579 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 789 | 792 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 795 | 798 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 852 | 855 | PF00928 | 0.374 |
TRG_ER_diArg_1 | 1038 | 1040 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 1042 | 1044 | PF00400 | 0.403 |
TRG_ER_diArg_1 | 1137 | 1139 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 1166 | 1168 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 1176 | 1178 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 1272 | 1275 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 1348 | 1350 | PF00400 | 0.337 |
TRG_ER_diArg_1 | 376 | 378 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 431 | 434 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 594 | 597 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 83 | 86 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 932 | 935 | PF00400 | 0.593 |
TRG_NES_CRM1_1 | 599 | 615 | PF08389 | 0.461 |
TRG_NES_CRM1_1 | 858 | 872 | PF08389 | 0.471 |
TRG_Pf-PMV_PEXEL_1 | 195 | 199 | PF00026 | 0.590 |
TRG_Pf-PMV_PEXEL_1 | 237 | 241 | PF00026 | 0.465 |
TRG_Pf-PMV_PEXEL_1 | 33 | 37 | PF00026 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 434 | 439 | PF00026 | 0.485 |
TRG_Pf-PMV_PEXEL_1 | 486 | 491 | PF00026 | 0.503 |
TRG_Pf-PMV_PEXEL_1 | 734 | 739 | PF00026 | 0.449 |
TRG_Pf-PMV_PEXEL_1 | 849 | 853 | PF00026 | 0.504 |
TRG_Pf-PMV_PEXEL_1 | 85 | 89 | PF00026 | 0.561 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5K4 | Leptomonas seymouri | 74% | 99% |
A0A0S4JMH7 | Bodo saltans | 32% | 95% |
A0A1X0NS21 | Trypanosomatidae | 44% | 98% |
A0A3Q8IE14 | Leishmania donovani | 89% | 100% |
A0A3R7KQD9 | Trypanosoma rangeli | 44% | 98% |
A4I9F1 | Leishmania infantum | 89% | 100% |
C9ZJS2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 94% |
E9B4E9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q3M7 | Leishmania major | 89% | 100% |
V5B3D2 | Trypanosoma cruzi | 45% | 98% |