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 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4I9F1
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 | 108 | 112 | PF00656 | 0.629 |
CLV_C14_Caspase3-7 | 1153 | 1157 | PF00656 | 0.548 |
CLV_C14_Caspase3-7 | 34 | 38 | PF00656 | 0.536 |
CLV_C14_Caspase3-7 | 390 | 394 | PF00656 | 0.534 |
CLV_C14_Caspase3-7 | 419 | 423 | PF00656 | 0.451 |
CLV_NRD_NRD_1 | 1023 | 1025 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 1042 | 1044 | PF00675 | 0.196 |
CLV_NRD_NRD_1 | 1046 | 1048 | PF00675 | 0.329 |
CLV_NRD_NRD_1 | 1141 | 1143 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 1170 | 1172 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 1180 | 1182 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 1306 | 1308 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 1352 | 1354 | PF00675 | 0.224 |
CLV_NRD_NRD_1 | 345 | 347 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.194 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 590 | 592 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 736 | 738 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 913 | 915 | PF00675 | 0.401 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 995 | 997 | PF00675 | 0.372 |
CLV_PCSK_FUR_1 | 86 | 90 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 1023 | 1025 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 1042 | 1044 | PF00082 | 0.257 |
CLV_PCSK_KEX2_1 | 1046 | 1048 | PF00082 | 0.341 |
CLV_PCSK_KEX2_1 | 1141 | 1143 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 1150 | 1152 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 1170 | 1172 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 1180 | 1182 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 1306 | 1308 | PF00082 | 0.256 |
CLV_PCSK_KEX2_1 | 1352 | 1354 | PF00082 | 0.223 |
CLV_PCSK_KEX2_1 | 1385 | 1387 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 1449 | 1451 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 533 | 535 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 590 | 592 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 913 | 915 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 995 | 997 | PF00082 | 0.318 |
CLV_PCSK_PC1ET2_1 | 1150 | 1152 | PF00082 | 0.402 |
CLV_PCSK_PC1ET2_1 | 1385 | 1387 | PF00082 | 0.304 |
CLV_PCSK_PC1ET2_1 | 1449 | 1451 | PF00082 | 0.515 |
CLV_PCSK_PC1ET2_1 | 533 | 535 | PF00082 | 0.479 |
CLV_PCSK_PC7_1 | 1038 | 1044 | PF00082 | 0.337 |
CLV_PCSK_PC7_1 | 1445 | 1451 | PF00082 | 0.544 |
CLV_PCSK_PC7_1 | 91 | 97 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 1046 | 1050 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 1111 | 1115 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 1116 | 1120 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 1171 | 1175 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 728 | 732 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 73 | 77 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 737 | 741 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 996 | 1000 | PF00082 | 0.431 |
CLV_Separin_Metazoa | 788 | 792 | PF03568 | 0.304 |
DEG_APCC_DBOX_1 | 399 | 407 | PF00400 | 0.345 |
DEG_APCC_DBOX_1 | 562 | 570 | PF00400 | 0.317 |
DEG_APCC_DBOX_1 | 94 | 102 | PF00400 | 0.489 |
DEG_APCC_DBOX_1 | 995 | 1003 | PF00400 | 0.447 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.514 |
DEG_SCF_TRCP1_1 | 111 | 116 | PF00400 | 0.591 |
DEG_SPOP_SBC_1 | 12 | 16 | PF00917 | 0.523 |
DEG_SPOP_SBC_1 | 1278 | 1282 | PF00917 | 0.166 |
DEG_SPOP_SBC_1 | 973 | 977 | PF00917 | 0.540 |
DOC_ANK_TNKS_1 | 197 | 204 | PF00023 | 0.448 |
DOC_CDC14_PxL_1 | 508 | 516 | PF14671 | 0.269 |
DOC_CDC14_PxL_1 | 886 | 894 | PF14671 | 0.341 |
DOC_CYCLIN_RxL_1 | 434 | 443 | PF00134 | 0.328 |
DOC_CYCLIN_RxL_1 | 734 | 741 | PF00134 | 0.304 |
DOC_CYCLIN_yCln2_LP_2 | 919 | 925 | PF00134 | 0.347 |
DOC_MAPK_gen_1 | 1023 | 1030 | PF00069 | 0.475 |
DOC_MAPK_gen_1 | 1042 | 1053 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 353 | 360 | PF00069 | 0.263 |
DOC_MAPK_gen_1 | 598 | 606 | PF00069 | 0.304 |
DOC_MAPK_HePTP_8 | 854 | 866 | PF00069 | 0.282 |
DOC_MAPK_MEF2A_6 | 1023 | 1030 | PF00069 | 0.389 |
DOC_MAPK_MEF2A_6 | 1128 | 1136 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 460 | 469 | PF00069 | 0.266 |
DOC_MAPK_MEF2A_6 | 563 | 571 | PF00069 | 0.362 |
DOC_MAPK_MEF2A_6 | 857 | 866 | PF00069 | 0.274 |
DOC_MAPK_RevD_3 | 365 | 381 | PF00069 | 0.406 |
DOC_PP1_RVXF_1 | 210 | 217 | PF00149 | 0.400 |
DOC_PP1_RVXF_1 | 566 | 572 | PF00149 | 0.416 |
DOC_PP1_RVXF_1 | 855 | 861 | PF00149 | 0.308 |
DOC_PP2B_LxvP_1 | 801 | 804 | PF13499 | 0.272 |
DOC_PP4_FxxP_1 | 1337 | 1340 | PF00568 | 0.239 |
DOC_PP4_FxxP_1 | 149 | 152 | PF00568 | 0.555 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 1213 | 1217 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 1225 | 1229 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 1278 | 1282 | PF00917 | 0.166 |
DOC_USP7_MATH_1 | 1429 | 1433 | PF00917 | 0.422 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.422 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.379 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 971 | 975 | PF00917 | 0.433 |
DOC_USP7_UBL2_3 | 1422 | 1426 | PF12436 | 0.495 |
DOC_USP7_UBL2_3 | 1431 | 1435 | PF12436 | 0.408 |
DOC_WW_Pin1_4 | 1104 | 1109 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.341 |
DOC_WW_Pin1_4 | 936 | 941 | PF00397 | 0.410 |
LIG_14-3-3_CanoR_1 | 1111 | 1118 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 1141 | 1149 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 1222 | 1232 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 1277 | 1287 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 183 | 187 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 383 | 389 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 460 | 469 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 620 | 630 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 638 | 643 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 737 | 747 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 791 | 796 | PF00244 | 0.258 |
LIG_14-3-3_CanoR_1 | 845 | 855 | PF00244 | 0.465 |
LIG_Actin_WH2_2 | 1156 | 1172 | PF00022 | 0.336 |
LIG_Actin_WH2_2 | 207 | 224 | PF00022 | 0.418 |
LIG_APCC_ABBAyCdc20_2 | 1250 | 1256 | PF00400 | 0.239 |
LIG_BIR_III_2 | 1156 | 1160 | PF00653 | 0.486 |
LIG_BRCT_BRCA1_1 | 1308 | 1312 | PF00533 | 0.166 |
LIG_BRCT_BRCA1_1 | 1371 | 1375 | PF00533 | 0.319 |
LIG_BRCT_BRCA1_1 | 145 | 149 | PF00533 | 0.548 |
LIG_BRCT_BRCA1_1 | 404 | 408 | PF00533 | 0.367 |
LIG_BRCT_BRCA1_1 | 515 | 519 | PF00533 | 0.200 |
LIG_CaM_IQ_9 | 988 | 1003 | PF13499 | 0.253 |
LIG_Clathr_ClatBox_1 | 558 | 562 | PF01394 | 0.442 |
LIG_CSL_BTD_1 | 948 | 951 | PF09270 | 0.476 |
LIG_deltaCOP1_diTrp_1 | 1322 | 1327 | PF00928 | 0.366 |
LIG_deltaCOP1_diTrp_1 | 415 | 420 | PF00928 | 0.267 |
LIG_EH1_1 | 605 | 613 | PF00400 | 0.422 |
LIG_EH1_1 | 961 | 969 | PF00400 | 0.342 |
LIG_eIF4E_1 | 266 | 272 | PF01652 | 0.444 |
LIG_FHA_1 | 1084 | 1090 | PF00498 | 0.519 |
LIG_FHA_1 | 1094 | 1100 | PF00498 | 0.377 |
LIG_FHA_1 | 1105 | 1111 | PF00498 | 0.406 |
LIG_FHA_1 | 1117 | 1123 | PF00498 | 0.380 |
LIG_FHA_1 | 1232 | 1238 | PF00498 | 0.555 |
LIG_FHA_1 | 1278 | 1284 | PF00498 | 0.347 |
LIG_FHA_1 | 1356 | 1362 | PF00498 | 0.330 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.486 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.406 |
LIG_FHA_1 | 711 | 717 | PF00498 | 0.357 |
LIG_FHA_1 | 753 | 759 | PF00498 | 0.287 |
LIG_FHA_1 | 804 | 810 | PF00498 | 0.348 |
LIG_FHA_1 | 841 | 847 | PF00498 | 0.480 |
LIG_FHA_2 | 1047 | 1053 | PF00498 | 0.452 |
LIG_FHA_2 | 1326 | 1332 | PF00498 | 0.305 |
LIG_FHA_2 | 183 | 189 | PF00498 | 0.459 |
LIG_FHA_2 | 417 | 423 | PF00498 | 0.382 |
LIG_FHA_2 | 699 | 705 | PF00498 | 0.272 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.469 |
LIG_FHA_2 | 774 | 780 | PF00498 | 0.399 |
LIG_FHA_2 | 989 | 995 | PF00498 | 0.259 |
LIG_FXI_DFP_1 | 655 | 659 | PF00024 | 0.549 |
LIG_GBD_Chelix_1 | 250 | 258 | PF00786 | 0.330 |
LIG_GBD_Chelix_1 | 607 | 615 | PF00786 | 0.419 |
LIG_Integrin_isoDGR_2 | 1036 | 1038 | PF01839 | 0.456 |
LIG_LIR_Apic_2 | 1397 | 1403 | PF02991 | 0.480 |
LIG_LIR_Apic_2 | 146 | 152 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 1326 | 1334 | PF02991 | 0.289 |
LIG_LIR_Gen_1 | 1407 | 1418 | PF02991 | 0.289 |
LIG_LIR_Gen_1 | 415 | 424 | PF02991 | 0.286 |
LIG_LIR_Gen_1 | 430 | 441 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 442 | 453 | PF02991 | 0.386 |
LIG_LIR_Gen_1 | 516 | 524 | PF02991 | 0.273 |
LIG_LIR_Gen_1 | 605 | 614 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 666 | 677 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 698 | 705 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 775 | 785 | PF02991 | 0.309 |
LIG_LIR_Gen_1 | 796 | 804 | PF02991 | 0.270 |
LIG_LIR_LC3C_4 | 1025 | 1030 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 1326 | 1330 | PF02991 | 0.244 |
LIG_LIR_Nem_3 | 1407 | 1413 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 213 | 218 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 23 | 29 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 321 | 326 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 415 | 420 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 430 | 436 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 442 | 448 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 516 | 522 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 605 | 609 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 666 | 672 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 698 | 703 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 775 | 780 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 796 | 801 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 946 | 952 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 959 | 964 | PF02991 | 0.149 |
LIG_MYND_1 | 890 | 894 | PF01753 | 0.345 |
LIG_NRBOX | 282 | 288 | PF00104 | 0.278 |
LIG_NRBOX | 359 | 365 | PF00104 | 0.257 |
LIG_NRBOX | 983 | 989 | PF00104 | 0.443 |
LIG_Pex14_2 | 1333 | 1337 | PF04695 | 0.239 |
LIG_Pex14_2 | 1375 | 1379 | PF04695 | 0.272 |
LIG_PTB_Apo_2 | 1047 | 1054 | PF02174 | 0.397 |
LIG_SH2_CRK | 1045 | 1049 | PF00017 | 0.335 |
LIG_SH2_CRK | 1400 | 1404 | PF00017 | 0.417 |
LIG_SH2_CRK | 579 | 583 | PF00017 | 0.429 |
LIG_SH2_CRK | 855 | 859 | PF00017 | 0.312 |
LIG_SH2_PTP2 | 1412 | 1415 | PF00017 | 0.278 |
LIG_SH2_SRC | 266 | 269 | PF00017 | 0.414 |
LIG_SH2_STAP1 | 1443 | 1447 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 305 | 309 | PF00017 | 0.346 |
LIG_SH2_STAT3 | 256 | 259 | PF00017 | 0.418 |
LIG_SH2_STAT3 | 379 | 382 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 1062 | 1065 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 1094 | 1097 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 1139 | 1142 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 1360 | 1363 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 1412 | 1415 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 323 | 326 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 554 | 557 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 570 | 573 | PF00017 | 0.258 |
LIG_SH2_STAT5 | 629 | 632 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 819 | 822 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 962 | 965 | PF00017 | 0.365 |
LIG_SH3_3 | 1160 | 1166 | PF00018 | 0.437 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.450 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.420 |
LIG_SH3_3 | 775 | 781 | PF00018 | 0.227 |
LIG_SH3_3 | 784 | 790 | PF00018 | 0.217 |
LIG_SH3_3 | 817 | 823 | PF00018 | 0.239 |
LIG_SH3_3 | 874 | 880 | PF00018 | 0.312 |
LIG_SH3_3 | 934 | 940 | PF00018 | 0.401 |
LIG_SH3_3 | 945 | 951 | PF00018 | 0.514 |
LIG_SH3_3 | 999 | 1005 | PF00018 | 0.411 |
LIG_SUMO_SIM_anti_2 | 1025 | 1032 | PF11976 | 0.385 |
LIG_SUMO_SIM_anti_2 | 981 | 986 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 494 | 501 | PF11976 | 0.422 |
LIG_SUMO_SIM_par_1 | 628 | 635 | PF11976 | 0.317 |
LIG_TRAF2_1 | 1196 | 1199 | PF00917 | 0.508 |
LIG_TRAF2_1 | 444 | 447 | PF00917 | 0.320 |
LIG_TRAF2_1 | 991 | 994 | PF00917 | 0.463 |
LIG_TYR_ITIM | 577 | 582 | PF00017 | 0.417 |
LIG_UBA3_1 | 384 | 389 | PF00899 | 0.390 |
LIG_UBA3_1 | 496 | 502 | PF00899 | 0.353 |
LIG_WRC_WIRS_1 | 53 | 58 | PF05994 | 0.460 |
LIG_WRC_WIRS_1 | 639 | 644 | PF05994 | 0.418 |
MOD_CDK_SPxxK_3 | 1104 | 1111 | PF00069 | 0.421 |
MOD_CK1_1 | 1055 | 1061 | PF00069 | 0.373 |
MOD_CK1_1 | 1083 | 1089 | PF00069 | 0.601 |
MOD_CK1_1 | 1228 | 1234 | PF00069 | 0.520 |
MOD_CK1_1 | 1294 | 1300 | PF00069 | 0.360 |
MOD_CK1_1 | 1394 | 1400 | PF00069 | 0.351 |
MOD_CK1_1 | 1448 | 1454 | PF00069 | 0.562 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.379 |
MOD_CK1_1 | 498 | 504 | PF00069 | 0.416 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.430 |
MOD_CK1_1 | 535 | 541 | PF00069 | 0.496 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.284 |
MOD_CK1_1 | 632 | 638 | PF00069 | 0.439 |
MOD_CK1_1 | 695 | 701 | PF00069 | 0.319 |
MOD_CK1_1 | 721 | 727 | PF00069 | 0.312 |
MOD_CK1_1 | 794 | 800 | PF00069 | 0.229 |
MOD_CK1_1 | 974 | 980 | PF00069 | 0.522 |
MOD_CK2_1 | 1046 | 1052 | PF00069 | 0.342 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.647 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.419 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.465 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.442 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.393 |
MOD_CK2_1 | 407 | 413 | PF00069 | 0.330 |
MOD_CK2_1 | 721 | 727 | PF00069 | 0.362 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.607 |
MOD_CK2_1 | 826 | 832 | PF00069 | 0.325 |
MOD_CK2_1 | 988 | 994 | PF00069 | 0.428 |
MOD_Cter_Amidation | 1021 | 1024 | PF01082 | 0.369 |
MOD_DYRK1A_RPxSP_1 | 936 | 940 | PF00069 | 0.392 |
MOD_GlcNHglycan | 1005 | 1008 | PF01048 | 0.474 |
MOD_GlcNHglycan | 1013 | 1016 | PF01048 | 0.516 |
MOD_GlcNHglycan | 1064 | 1067 | PF01048 | 0.421 |
MOD_GlcNHglycan | 1078 | 1081 | PF01048 | 0.632 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.651 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.635 |
MOD_GlcNHglycan | 1202 | 1205 | PF01048 | 0.703 |
MOD_GlcNHglycan | 1308 | 1311 | PF01048 | 0.166 |
MOD_GlcNHglycan | 1370 | 1374 | PF01048 | 0.229 |
MOD_GlcNHglycan | 1393 | 1396 | PF01048 | 0.468 |
MOD_GlcNHglycan | 1431 | 1434 | PF01048 | 0.420 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.522 |
MOD_GlcNHglycan | 2 | 6 | PF01048 | 0.647 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.282 |
MOD_GlcNHglycan | 634 | 637 | PF01048 | 0.480 |
MOD_GlcNHglycan | 65 | 71 | PF01048 | 0.737 |
MOD_GlcNHglycan | 694 | 697 | PF01048 | 0.292 |
MOD_GlcNHglycan | 723 | 726 | PF01048 | 0.292 |
MOD_GlcNHglycan | 846 | 849 | PF01048 | 0.453 |
MOD_GSK3_1 | 1058 | 1065 | PF00069 | 0.439 |
MOD_GSK3_1 | 1076 | 1083 | PF00069 | 0.674 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.667 |
MOD_GSK3_1 | 1093 | 1100 | PF00069 | 0.423 |
MOD_GSK3_1 | 1112 | 1119 | PF00069 | 0.494 |
MOD_GSK3_1 | 1209 | 1216 | PF00069 | 0.624 |
MOD_GSK3_1 | 1224 | 1231 | PF00069 | 0.446 |
MOD_GSK3_1 | 1390 | 1397 | PF00069 | 0.303 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.469 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.166 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.470 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.394 |
MOD_GSK3_1 | 637 | 644 | PF00069 | 0.382 |
MOD_GSK3_1 | 705 | 712 | PF00069 | 0.300 |
MOD_GSK3_1 | 840 | 847 | PF00069 | 0.408 |
MOD_GSK3_1 | 952 | 959 | PF00069 | 0.437 |
MOD_GSK3_1 | 969 | 976 | PF00069 | 0.492 |
MOD_N-GLC_1 | 1097 | 1102 | PF02516 | 0.269 |
MOD_N-GLC_1 | 1294 | 1299 | PF02516 | 0.304 |
MOD_N-GLC_1 | 307 | 312 | PF02516 | 0.416 |
MOD_NEK2_1 | 1112 | 1117 | PF00069 | 0.385 |
MOD_NEK2_1 | 1175 | 1180 | PF00069 | 0.424 |
MOD_NEK2_1 | 1344 | 1349 | PF00069 | 0.274 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.559 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.472 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.482 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.310 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.372 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.279 |
MOD_NEK2_1 | 528 | 533 | PF00069 | 0.290 |
MOD_NEK2_1 | 710 | 715 | PF00069 | 0.238 |
MOD_NEK2_1 | 840 | 845 | PF00069 | 0.376 |
MOD_NEK2_1 | 952 | 957 | PF00069 | 0.252 |
MOD_PIKK_1 | 503 | 509 | PF00454 | 0.381 |
MOD_PIKK_1 | 614 | 620 | PF00454 | 0.387 |
MOD_PIKK_1 | 641 | 647 | PF00454 | 0.437 |
MOD_PIKK_1 | 738 | 744 | PF00454 | 0.304 |
MOD_PIKK_1 | 956 | 962 | PF00454 | 0.323 |
MOD_PIKK_1 | 988 | 994 | PF00454 | 0.260 |
MOD_PK_1 | 1279 | 1285 | PF00069 | 0.366 |
MOD_PK_1 | 791 | 797 | PF00069 | 0.332 |
MOD_PKA_1 | 1046 | 1052 | PF00069 | 0.345 |
MOD_PKA_1 | 1306 | 1312 | PF00069 | 0.288 |
MOD_PKA_2 | 1046 | 1052 | PF00069 | 0.345 |
MOD_PKA_2 | 1083 | 1089 | PF00069 | 0.578 |
MOD_PKA_2 | 1140 | 1146 | PF00069 | 0.434 |
MOD_PKA_2 | 1278 | 1284 | PF00069 | 0.361 |
MOD_PKA_2 | 1306 | 1312 | PF00069 | 0.199 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.376 |
MOD_PKA_2 | 296 | 302 | PF00069 | 0.457 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.353 |
MOD_PKA_2 | 637 | 643 | PF00069 | 0.432 |
MOD_PKA_2 | 743 | 749 | PF00069 | 0.379 |
MOD_PKA_2 | 844 | 850 | PF00069 | 0.484 |
MOD_PKB_1 | 1277 | 1285 | PF00069 | 0.366 |
MOD_PKB_1 | 381 | 389 | PF00069 | 0.374 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.409 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.499 |
MOD_Plk_1 | 446 | 452 | PF00069 | 0.310 |
MOD_Plk_1 | 682 | 688 | PF00069 | 0.417 |
MOD_Plk_1 | 833 | 839 | PF00069 | 0.328 |
MOD_Plk_1 | 860 | 866 | PF00069 | 0.253 |
MOD_Plk_1 | 952 | 958 | PF00069 | 0.255 |
MOD_Plk_2-3 | 121 | 127 | PF00069 | 0.571 |
MOD_Plk_4 | 1083 | 1089 | PF00069 | 0.459 |
MOD_Plk_4 | 1271 | 1277 | PF00069 | 0.317 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.411 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.373 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.333 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.263 |
MOD_Plk_4 | 495 | 501 | PF00069 | 0.372 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.317 |
MOD_Plk_4 | 543 | 549 | PF00069 | 0.290 |
MOD_Plk_4 | 602 | 608 | PF00069 | 0.411 |
MOD_Plk_4 | 705 | 711 | PF00069 | 0.318 |
MOD_Plk_4 | 743 | 749 | PF00069 | 0.245 |
MOD_Plk_4 | 773 | 779 | PF00069 | 0.356 |
MOD_Plk_4 | 826 | 832 | PF00069 | 0.358 |
MOD_Plk_4 | 860 | 866 | PF00069 | 0.250 |
MOD_Plk_4 | 952 | 958 | PF00069 | 0.263 |
MOD_ProDKin_1 | 1104 | 1110 | PF00069 | 0.422 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.338 |
MOD_ProDKin_1 | 936 | 942 | PF00069 | 0.423 |
MOD_SUMO_for_1 | 167 | 170 | PF00179 | 0.506 |
MOD_SUMO_rev_2 | 163 | 169 | PF00179 | 0.515 |
TRG_AP2beta_CARGO_1 | 23 | 33 | PF09066 | 0.375 |
TRG_DiLeu_BaEn_1 | 267 | 272 | PF01217 | 0.268 |
TRG_DiLeu_BaEn_1 | 359 | 364 | PF01217 | 0.259 |
TRG_DiLeu_BaEn_1 | 562 | 567 | PF01217 | 0.449 |
TRG_DiLeu_BaEn_2 | 132 | 138 | PF01217 | 0.565 |
TRG_DiLeu_BaEn_2 | 601 | 607 | PF01217 | 0.417 |
TRG_DiLeu_BaLyEn_6 | 278 | 283 | PF01217 | 0.251 |
TRG_DiLeu_BaLyEn_6 | 607 | 612 | PF01217 | 0.332 |
TRG_DiLeu_BaLyEn_6 | 756 | 761 | PF01217 | 0.375 |
TRG_DiLeu_LyEn_5 | 359 | 364 | PF01217 | 0.259 |
TRG_ENDOCYTIC_2 | 1045 | 1048 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 1217 | 1220 | PF00928 | 0.629 |
TRG_ENDOCYTIC_2 | 1313 | 1316 | PF00928 | 0.239 |
TRG_ENDOCYTIC_2 | 1412 | 1415 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 433 | 436 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 570 | 573 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 579 | 582 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 792 | 795 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 798 | 801 | PF00928 | 0.267 |
TRG_ENDOCYTIC_2 | 855 | 858 | PF00928 | 0.298 |
TRG_ER_diArg_1 | 1042 | 1044 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 1045 | 1047 | PF00400 | 0.325 |
TRG_ER_diArg_1 | 1140 | 1142 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 1169 | 1171 | PF00400 | 0.368 |
TRG_ER_diArg_1 | 1179 | 1181 | PF00400 | 0.291 |
TRG_ER_diArg_1 | 1276 | 1279 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 1352 | 1354 | PF00400 | 0.231 |
TRG_ER_diArg_1 | 379 | 381 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 434 | 437 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 597 | 600 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 72 | 74 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 88 | 91 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 935 | 938 | PF00400 | 0.404 |
TRG_NES_CRM1_1 | 602 | 618 | PF08389 | 0.421 |
TRG_NES_CRM1_1 | 861 | 875 | PF08389 | 0.413 |
TRG_Pf-PMV_PEXEL_1 | 1386 | 1390 | PF00026 | 0.446 |
TRG_Pf-PMV_PEXEL_1 | 198 | 202 | PF00026 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 240 | 244 | PF00026 | 0.400 |
TRG_Pf-PMV_PEXEL_1 | 33 | 37 | PF00026 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 437 | 442 | PF00026 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 489 | 494 | PF00026 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 737 | 742 | PF00026 | 0.366 |
TRG_Pf-PMV_PEXEL_1 | 852 | 856 | PF00026 | 0.465 |
TRG_Pf-PMV_PEXEL_1 | 88 | 92 | PF00026 | 0.509 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5K4 | Leptomonas seymouri | 76% | 100% |
A0A0S4JMH7 | Bodo saltans | 32% | 96% |
A0A1X0NS21 | Trypanosomatidae | 44% | 99% |
A0A3Q8IE14 | Leishmania donovani | 100% | 100% |
A0A3R7KQD9 | Trypanosoma rangeli | 44% | 98% |
C9ZJS2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 94% |
E9AIV7 | Leishmania braziliensis | 89% | 100% |
E9B4E9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
Q4Q3M7 | Leishmania major | 96% | 100% |
V5B3D2 | Trypanosoma cruzi | 44% | 98% |