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 | 2 |
GO:0008023 | transcription elongation factor complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006325 | chromatin organization | 4 | 2 |
GO:0006338 | chromatin remodeling | 5 | 2 |
GO:0006351 | DNA-templated transcription | 7 | 2 |
GO:0006354 | DNA-templated transcription elongation | 6 | 2 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 12 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 12 |
GO:0006366 | transcription by RNA polymerase II | 8 | 2 |
GO:0006368 | transcription elongation by RNA polymerase II | 7 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009059 | macromolecule biosynthetic process | 4 | 2 |
GO:0009299 | mRNA transcription | 7 | 2 |
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:0016043 | cellular component organization | 3 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016071 | mRNA metabolic process | 6 | 2 |
GO:0018130 | heterocycle biosynthetic process | 4 | 2 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 12 |
GO:0019222 | regulation of metabolic process | 3 | 12 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 2 |
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:0032774 | RNA biosynthetic process | 5 | 2 |
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:0034654 | nucleobase-containing compound biosynthetic process | 4 | 2 |
GO:0034728 | nucleosome organization | 6 | 2 |
GO:0042789 | mRNA transcription by RNA polymerase II | 8 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 2 |
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:0071824 | protein-DNA complex subunit organization | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:0097659 | nucleic acid-templated transcription | 6 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003682 | chromatin binding | 2 | 2 |
GO:0005488 | binding | 1 | 5 |
GO:0005515 | protein binding | 2 | 2 |
GO:0031491 | nucleosome binding | 3 | 2 |
GO:0042393 | histone binding | 3 | 2 |
GO:0044877 | protein-containing complex binding | 2 | 2 |
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 | 1103 | 1107 | PF00656 | 0.597 |
CLV_C14_Caspase3-7 | 340 | 344 | PF00656 | 0.554 |
CLV_C14_Caspase3-7 | 369 | 373 | PF00656 | 0.470 |
CLV_C14_Caspase3-7 | 58 | 62 | PF00656 | 0.641 |
CLV_NRD_NRD_1 | 1091 | 1093 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 1120 | 1122 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 1302 | 1304 | PF00675 | 0.267 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.220 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 540 | 542 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 686 | 688 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 863 | 865 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 945 | 947 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 973 | 975 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 992 | 994 | PF00675 | 0.243 |
CLV_NRD_NRD_1 | 996 | 998 | PF00675 | 0.320 |
CLV_PCSK_FUR_1 | 36 | 40 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 1091 | 1093 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 1120 | 1122 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 1302 | 1304 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 1335 | 1337 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 1399 | 1401 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 483 | 485 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 540 | 542 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 863 | 865 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 945 | 947 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 973 | 975 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 992 | 994 | PF00082 | 0.243 |
CLV_PCSK_KEX2_1 | 996 | 998 | PF00082 | 0.320 |
CLV_PCSK_PC1ET2_1 | 1335 | 1337 | PF00082 | 0.331 |
CLV_PCSK_PC1ET2_1 | 1399 | 1401 | PF00082 | 0.443 |
CLV_PCSK_PC1ET2_1 | 483 | 485 | PF00082 | 0.416 |
CLV_PCSK_PC7_1 | 1395 | 1401 | PF00082 | 0.519 |
CLV_PCSK_PC7_1 | 41 | 47 | PF00082 | 0.630 |
CLV_PCSK_PC7_1 | 988 | 994 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 1061 | 1065 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 1066 | 1070 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 1121 | 1125 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 678 | 682 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 687 | 691 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 946 | 950 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 996 | 1000 | PF00082 | 0.424 |
CLV_Separin_Metazoa | 738 | 742 | PF03568 | 0.331 |
DEG_APCC_DBOX_1 | 349 | 357 | PF00400 | 0.375 |
DEG_APCC_DBOX_1 | 44 | 52 | PF00400 | 0.508 |
DEG_APCC_DBOX_1 | 512 | 520 | PF00400 | 0.295 |
DEG_APCC_DBOX_1 | 945 | 953 | PF00400 | 0.489 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.290 |
DEG_SCF_TRCP1_1 | 61 | 66 | PF00400 | 0.602 |
DEG_SPOP_SBC_1 | 1027 | 1031 | PF00917 | 0.346 |
DEG_SPOP_SBC_1 | 923 | 927 | PF00917 | 0.515 |
DOC_ANK_TNKS_1 | 147 | 154 | PF00023 | 0.424 |
DOC_CDC14_PxL_1 | 458 | 466 | PF14671 | 0.290 |
DOC_CDC14_PxL_1 | 705 | 713 | PF14671 | 0.200 |
DOC_CDC14_PxL_1 | 836 | 844 | PF14671 | 0.385 |
DOC_CYCLIN_RxL_1 | 384 | 393 | PF00134 | 0.325 |
DOC_CYCLIN_RxL_1 | 684 | 691 | PF00134 | 0.331 |
DOC_CYCLIN_yCln2_LP_2 | 869 | 875 | PF00134 | 0.349 |
DOC_CYCLIN_yCln2_LP_2 | 898 | 904 | PF00134 | 0.247 |
DOC_MAPK_gen_1 | 109 | 117 | PF00069 | 0.362 |
DOC_MAPK_gen_1 | 303 | 310 | PF00069 | 0.302 |
DOC_MAPK_gen_1 | 548 | 556 | PF00069 | 0.308 |
DOC_MAPK_gen_1 | 973 | 980 | PF00069 | 0.550 |
DOC_MAPK_gen_1 | 992 | 1003 | PF00069 | 0.364 |
DOC_MAPK_HePTP_8 | 804 | 816 | PF00069 | 0.311 |
DOC_MAPK_MEF2A_6 | 513 | 521 | PF00069 | 0.343 |
DOC_MAPK_MEF2A_6 | 807 | 816 | PF00069 | 0.307 |
DOC_MAPK_MEF2A_6 | 973 | 980 | PF00069 | 0.455 |
DOC_MAPK_RevD_3 | 315 | 331 | PF00069 | 0.424 |
DOC_PP1_MyPhoNE_1 | 1092 | 1099 | PF00149 | 0.387 |
DOC_PP1_RVXF_1 | 160 | 167 | PF00149 | 0.424 |
DOC_PP1_RVXF_1 | 516 | 522 | PF00149 | 0.418 |
DOC_PP1_RVXF_1 | 805 | 811 | PF00149 | 0.296 |
DOC_PP2B_LxvP_1 | 751 | 754 | PF13499 | 0.314 |
DOC_PP4_FxxP_1 | 1287 | 1290 | PF00568 | 0.281 |
DOC_PP4_FxxP_1 | 99 | 102 | PF00568 | 0.465 |
DOC_USP7_MATH_1 | 1027 | 1031 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 1163 | 1167 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 1175 | 1179 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 1379 | 1383 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 921 | 925 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.453 |
DOC_USP7_UBL2_3 | 1372 | 1376 | PF12436 | 0.464 |
DOC_USP7_UBL2_3 | 1381 | 1385 | PF12436 | 0.519 |
DOC_WW_Pin1_4 | 1054 | 1059 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 886 | 891 | PF00397 | 0.406 |
LIG_14-3-3_CanoR_1 | 1061 | 1068 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 1091 | 1099 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 1172 | 1182 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 1227 | 1236 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 333 | 339 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 410 | 419 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 570 | 580 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 588 | 593 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 687 | 697 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 741 | 746 | PF00244 | 0.300 |
LIG_14-3-3_CanoR_1 | 795 | 805 | PF00244 | 0.312 |
LIG_14-3-3_CanoR_1 | 829 | 838 | PF00244 | 0.248 |
LIG_Actin_WH2_2 | 157 | 174 | PF00022 | 0.439 |
LIG_APCC_ABBAyCdc20_2 | 1200 | 1206 | PF00400 | 0.281 |
LIG_BIR_III_2 | 1106 | 1110 | PF00653 | 0.536 |
LIG_BRCT_BRCA1_1 | 1321 | 1325 | PF00533 | 0.362 |
LIG_BRCT_BRCA1_1 | 188 | 192 | PF00533 | 0.249 |
LIG_BRCT_BRCA1_1 | 354 | 358 | PF00533 | 0.371 |
LIG_BRCT_BRCA1_1 | 95 | 99 | PF00533 | 0.461 |
LIG_Clathr_ClatBox_1 | 508 | 512 | PF01394 | 0.425 |
LIG_CSL_BTD_1 | 898 | 901 | PF09270 | 0.475 |
LIG_deltaCOP1_diTrp_1 | 1272 | 1277 | PF00928 | 0.411 |
LIG_deltaCOP1_diTrp_1 | 365 | 370 | PF00928 | 0.283 |
LIG_EH1_1 | 555 | 563 | PF00400 | 0.423 |
LIG_EH1_1 | 911 | 919 | PF00400 | 0.351 |
LIG_eIF4E_1 | 216 | 222 | PF01652 | 0.545 |
LIG_FHA_1 | 1034 | 1040 | PF00498 | 0.498 |
LIG_FHA_1 | 1044 | 1050 | PF00498 | 0.458 |
LIG_FHA_1 | 1055 | 1061 | PF00498 | 0.491 |
LIG_FHA_1 | 1067 | 1073 | PF00498 | 0.335 |
LIG_FHA_1 | 1182 | 1188 | PF00498 | 0.512 |
LIG_FHA_1 | 1228 | 1234 | PF00498 | 0.331 |
LIG_FHA_1 | 1306 | 1312 | PF00498 | 0.337 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.426 |
LIG_FHA_1 | 626 | 632 | PF00498 | 0.260 |
LIG_FHA_1 | 661 | 667 | PF00498 | 0.393 |
LIG_FHA_1 | 754 | 760 | PF00498 | 0.393 |
LIG_FHA_1 | 791 | 797 | PF00498 | 0.409 |
LIG_FHA_2 | 1276 | 1282 | PF00498 | 0.348 |
LIG_FHA_2 | 133 | 139 | PF00498 | 0.561 |
LIG_FHA_2 | 24 | 30 | PF00498 | 0.523 |
LIG_FHA_2 | 367 | 373 | PF00498 | 0.399 |
LIG_FHA_2 | 997 | 1003 | PF00498 | 0.427 |
LIG_FXI_DFP_1 | 605 | 609 | PF00024 | 0.457 |
LIG_GBD_Chelix_1 | 200 | 208 | PF00786 | 0.385 |
LIG_GBD_Chelix_1 | 557 | 565 | PF00786 | 0.424 |
LIG_Integrin_isoDGR_2 | 986 | 988 | PF01839 | 0.477 |
LIG_LIR_Apic_2 | 1348 | 1353 | PF02991 | 0.413 |
LIG_LIR_Apic_2 | 96 | 102 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 1276 | 1284 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 1357 | 1368 | PF02991 | 0.292 |
LIG_LIR_Gen_1 | 189 | 200 | PF02991 | 0.235 |
LIG_LIR_Gen_1 | 365 | 374 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 380 | 391 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 392 | 403 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 555 | 564 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 616 | 627 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 648 | 655 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 746 | 754 | PF02991 | 0.302 |
LIG_LIR_LC3C_4 | 975 | 980 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 1276 | 1280 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 1357 | 1363 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 163 | 168 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 189 | 195 | PF02991 | 0.240 |
LIG_LIR_Nem_3 | 271 | 276 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 365 | 370 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 380 | 386 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 555 | 559 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 616 | 622 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 648 | 653 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 746 | 751 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 896 | 902 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 909 | 914 | PF02991 | 0.292 |
LIG_MYND_1 | 840 | 844 | PF01753 | 0.376 |
LIG_NRBOX | 232 | 238 | PF00104 | 0.316 |
LIG_NRBOX | 309 | 315 | PF00104 | 0.292 |
LIG_NRBOX | 933 | 939 | PF00104 | 0.466 |
LIG_Pex14_2 | 1283 | 1287 | PF04695 | 0.290 |
LIG_Pex14_2 | 1325 | 1329 | PF04695 | 0.314 |
LIG_PTB_Apo_2 | 997 | 1004 | PF02174 | 0.374 |
LIG_SH2_CRK | 1350 | 1354 | PF00017 | 0.391 |
LIG_SH2_CRK | 529 | 533 | PF00017 | 0.424 |
LIG_SH2_CRK | 805 | 809 | PF00017 | 0.316 |
LIG_SH2_CRK | 995 | 999 | PF00017 | 0.339 |
LIG_SH2_PTP2 | 1362 | 1365 | PF00017 | 0.301 |
LIG_SH2_SRC | 216 | 219 | PF00017 | 0.516 |
LIG_SH2_SRC | 912 | 915 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 1393 | 1397 | PF00017 | 0.503 |
LIG_SH2_STAP1 | 255 | 259 | PF00017 | 0.447 |
LIG_SH2_STAT3 | 206 | 209 | PF00017 | 0.479 |
LIG_SH2_STAT3 | 329 | 332 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 1012 | 1015 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 1044 | 1047 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 1089 | 1092 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 1310 | 1313 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 1362 | 1365 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 520 | 523 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 579 | 582 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 769 | 772 | PF00017 | 0.274 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.451 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.445 |
LIG_SH3_3 | 725 | 731 | PF00018 | 0.270 |
LIG_SH3_3 | 734 | 740 | PF00018 | 0.260 |
LIG_SH3_3 | 767 | 773 | PF00018 | 0.281 |
LIG_SH3_3 | 824 | 830 | PF00018 | 0.311 |
LIG_SH3_3 | 884 | 890 | PF00018 | 0.438 |
LIG_SH3_3 | 949 | 955 | PF00018 | 0.410 |
LIG_SUMO_SIM_anti_2 | 931 | 936 | PF11976 | 0.437 |
LIG_SUMO_SIM_anti_2 | 975 | 982 | PF11976 | 0.461 |
LIG_SUMO_SIM_par_1 | 444 | 451 | PF11976 | 0.432 |
LIG_SUMO_SIM_par_1 | 578 | 585 | PF11976 | 0.335 |
LIG_TRAF2_1 | 1146 | 1149 | PF00917 | 0.479 |
LIG_TRAF2_1 | 394 | 397 | PF00917 | 0.324 |
LIG_TRAF2_1 | 941 | 944 | PF00917 | 0.441 |
LIG_TYR_ITIM | 527 | 532 | PF00017 | 0.418 |
LIG_UBA3_1 | 334 | 339 | PF00899 | 0.436 |
LIG_UBA3_1 | 446 | 452 | PF00899 | 0.349 |
LIG_WRC_WIRS_1 | 4 | 9 | PF05994 | 0.470 |
LIG_WRC_WIRS_1 | 589 | 594 | PF05994 | 0.461 |
LIG_WRC_WIRS_1 | 714 | 719 | PF05994 | 0.365 |
MOD_CDK_SPxxK_3 | 1054 | 1061 | PF00069 | 0.490 |
MOD_CK1_1 | 1005 | 1011 | PF00069 | 0.363 |
MOD_CK1_1 | 1030 | 1036 | PF00069 | 0.563 |
MOD_CK1_1 | 1178 | 1184 | PF00069 | 0.483 |
MOD_CK1_1 | 1244 | 1250 | PF00069 | 0.373 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.423 |
MOD_CK1_1 | 1398 | 1404 | PF00069 | 0.489 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.382 |
MOD_CK1_1 | 456 | 462 | PF00069 | 0.405 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.437 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.286 |
MOD_CK1_1 | 582 | 588 | PF00069 | 0.447 |
MOD_CK1_1 | 645 | 651 | PF00069 | 0.354 |
MOD_CK1_1 | 671 | 677 | PF00069 | 0.329 |
MOD_CK1_1 | 744 | 750 | PF00069 | 0.272 |
MOD_CK1_1 | 924 | 930 | PF00069 | 0.489 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.568 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.662 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.333 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.645 |
MOD_CK2_1 | 671 | 677 | PF00069 | 0.385 |
MOD_CK2_1 | 776 | 782 | PF00069 | 0.504 |
MOD_CK2_1 | 996 | 1002 | PF00069 | 0.327 |
MOD_Cter_Amidation | 971 | 974 | PF01082 | 0.414 |
MOD_DYRK1A_RPxSP_1 | 886 | 890 | PF00069 | 0.407 |
MOD_GlcNHglycan | 1014 | 1017 | PF01048 | 0.381 |
MOD_GlcNHglycan | 1030 | 1033 | PF01048 | 0.550 |
MOD_GlcNHglycan | 1152 | 1155 | PF01048 | 0.653 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.600 |
MOD_GlcNHglycan | 1320 | 1324 | PF01048 | 0.272 |
MOD_GlcNHglycan | 1343 | 1346 | PF01048 | 0.411 |
MOD_GlcNHglycan | 1381 | 1384 | PF01048 | 0.454 |
MOD_GlcNHglycan | 15 | 21 | PF01048 | 0.719 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.281 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.496 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.649 |
MOD_GlcNHglycan | 644 | 647 | PF01048 | 0.325 |
MOD_GlcNHglycan | 673 | 676 | PF01048 | 0.354 |
MOD_GlcNHglycan | 724 | 727 | PF01048 | 0.381 |
MOD_GlcNHglycan | 796 | 799 | PF01048 | 0.409 |
MOD_GlcNHglycan | 851 | 854 | PF01048 | 0.484 |
MOD_GlcNHglycan | 963 | 966 | PF01048 | 0.467 |
MOD_GSK3_1 | 1008 | 1015 | PF00069 | 0.431 |
MOD_GSK3_1 | 1026 | 1033 | PF00069 | 0.549 |
MOD_GSK3_1 | 1043 | 1050 | PF00069 | 0.347 |
MOD_GSK3_1 | 1062 | 1069 | PF00069 | 0.539 |
MOD_GSK3_1 | 1159 | 1166 | PF00069 | 0.631 |
MOD_GSK3_1 | 1174 | 1181 | PF00069 | 0.404 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.499 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.191 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.487 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.399 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.344 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.399 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.685 |
MOD_GSK3_1 | 655 | 662 | PF00069 | 0.311 |
MOD_GSK3_1 | 790 | 797 | PF00069 | 0.365 |
MOD_GSK3_1 | 902 | 909 | PF00069 | 0.458 |
MOD_GSK3_1 | 919 | 926 | PF00069 | 0.359 |
MOD_N-GLC_1 | 1244 | 1249 | PF02516 | 0.465 |
MOD_N-GLC_1 | 1346 | 1351 | PF02516 | 0.265 |
MOD_N-GLC_1 | 257 | 262 | PF02516 | 0.486 |
MOD_N-GLC_2 | 425 | 427 | PF02516 | 0.245 |
MOD_NEK2_1 | 1062 | 1067 | PF00069 | 0.428 |
MOD_NEK2_1 | 1125 | 1130 | PF00069 | 0.440 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.570 |
MOD_NEK2_1 | 1294 | 1299 | PF00069 | 0.302 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.453 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.546 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.320 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.408 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.312 |
MOD_NEK2_1 | 660 | 665 | PF00069 | 0.280 |
MOD_NEK2_1 | 790 | 795 | PF00069 | 0.351 |
MOD_NEK2_1 | 902 | 907 | PF00069 | 0.328 |
MOD_PIKK_1 | 453 | 459 | PF00454 | 0.376 |
MOD_PIKK_1 | 564 | 570 | PF00454 | 0.344 |
MOD_PIKK_1 | 591 | 597 | PF00454 | 0.437 |
MOD_PIKK_1 | 688 | 694 | PF00454 | 0.331 |
MOD_PIKK_1 | 906 | 912 | PF00454 | 0.296 |
MOD_PK_1 | 1229 | 1235 | PF00069 | 0.411 |
MOD_PK_1 | 741 | 747 | PF00069 | 0.331 |
MOD_PKA_1 | 996 | 1002 | PF00069 | 0.329 |
MOD_PKA_2 | 1033 | 1039 | PF00069 | 0.552 |
MOD_PKA_2 | 1090 | 1096 | PF00069 | 0.479 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.418 |
MOD_PKA_2 | 587 | 593 | PF00069 | 0.484 |
MOD_PKA_2 | 693 | 699 | PF00069 | 0.411 |
MOD_PKA_2 | 794 | 800 | PF00069 | 0.318 |
MOD_PKA_2 | 996 | 1002 | PF00069 | 0.329 |
MOD_PKB_1 | 1227 | 1235 | PF00069 | 0.411 |
MOD_Plk_1 | 1346 | 1352 | PF00069 | 0.281 |
MOD_Plk_1 | 396 | 402 | PF00069 | 0.341 |
MOD_Plk_1 | 632 | 638 | PF00069 | 0.398 |
MOD_Plk_1 | 783 | 789 | PF00069 | 0.316 |
MOD_Plk_1 | 810 | 816 | PF00069 | 0.271 |
MOD_Plk_1 | 902 | 908 | PF00069 | 0.294 |
MOD_Plk_2-3 | 71 | 77 | PF00069 | 0.559 |
MOD_Plk_4 | 1033 | 1039 | PF00069 | 0.465 |
MOD_Plk_4 | 1221 | 1227 | PF00069 | 0.360 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.370 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.431 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.355 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.281 |
MOD_Plk_4 | 445 | 451 | PF00069 | 0.349 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.300 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.292 |
MOD_Plk_4 | 552 | 558 | PF00069 | 0.410 |
MOD_Plk_4 | 655 | 661 | PF00069 | 0.341 |
MOD_Plk_4 | 693 | 699 | PF00069 | 0.281 |
MOD_Plk_4 | 713 | 719 | PF00069 | 0.145 |
MOD_Plk_4 | 776 | 782 | PF00069 | 0.371 |
MOD_Plk_4 | 810 | 816 | PF00069 | 0.286 |
MOD_Plk_4 | 902 | 908 | PF00069 | 0.281 |
MOD_Plk_4 | 953 | 959 | PF00069 | 0.437 |
MOD_ProDKin_1 | 1054 | 1060 | PF00069 | 0.491 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.384 |
MOD_ProDKin_1 | 886 | 892 | PF00069 | 0.404 |
MOD_SUMO_for_1 | 117 | 120 | PF00179 | 0.500 |
MOD_SUMO_rev_2 | 105 | 111 | PF00179 | 0.582 |
MOD_SUMO_rev_2 | 113 | 119 | PF00179 | 0.528 |
TRG_DiLeu_BaEn_1 | 217 | 222 | PF01217 | 0.376 |
TRG_DiLeu_BaEn_1 | 309 | 314 | PF01217 | 0.293 |
TRG_DiLeu_BaEn_1 | 512 | 517 | PF01217 | 0.417 |
TRG_DiLeu_BaEn_2 | 551 | 557 | PF01217 | 0.423 |
TRG_DiLeu_BaEn_2 | 82 | 88 | PF01217 | 0.517 |
TRG_DiLeu_BaLyEn_6 | 228 | 233 | PF01217 | 0.291 |
TRG_DiLeu_BaLyEn_6 | 557 | 562 | PF01217 | 0.338 |
TRG_DiLeu_BaLyEn_6 | 706 | 711 | PF01217 | 0.411 |
TRG_DiLeu_LyEn_5 | 309 | 314 | PF01217 | 0.293 |
TRG_ENDOCYTIC_2 | 1167 | 1170 | PF00928 | 0.653 |
TRG_ENDOCYTIC_2 | 1263 | 1266 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 1362 | 1365 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 520 | 523 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 529 | 532 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 742 | 745 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 748 | 751 | PF00928 | 0.294 |
TRG_ENDOCYTIC_2 | 805 | 808 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 995 | 998 | PF00928 | 0.326 |
TRG_ER_diArg_1 | 1090 | 1092 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 1119 | 1121 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 1226 | 1229 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 1302 | 1304 | PF00400 | 0.274 |
TRG_ER_diArg_1 | 329 | 331 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 38 | 41 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 384 | 387 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 547 | 550 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 885 | 888 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 992 | 994 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 995 | 997 | PF00400 | 0.330 |
TRG_NES_CRM1_1 | 552 | 568 | PF08389 | 0.425 |
TRG_NES_CRM1_1 | 811 | 825 | PF08389 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 1336 | 1340 | PF00026 | 0.393 |
TRG_Pf-PMV_PEXEL_1 | 148 | 152 | PF00026 | 0.424 |
TRG_Pf-PMV_PEXEL_1 | 38 | 42 | PF00026 | 0.548 |
TRG_Pf-PMV_PEXEL_1 | 387 | 392 | PF00026 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 439 | 444 | PF00026 | 0.366 |
TRG_Pf-PMV_PEXEL_1 | 687 | 692 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 802 | 806 | PF00026 | 0.449 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5K4 | Leptomonas seymouri | 76% | 96% |
A0A0S4JMH7 | Bodo saltans | 32% | 92% |
A0A1X0NS21 | Trypanosomatidae | 44% | 95% |
A0A3Q8IE14 | Leishmania donovani | 95% | 97% |
A0A3R7KQD9 | Trypanosoma rangeli | 45% | 95% |
A4I9F1 | Leishmania infantum | 96% | 97% |
C9ZJS2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 91% |
E9AIV7 | Leishmania braziliensis | 89% | 97% |
E9B4E9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
V5B3D2 | Trypanosoma cruzi | 45% | 95% |