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 | 1102 | 1106 | PF00656 | 0.615 |
CLV_C14_Caspase3-7 | 1155 | 1159 | PF00656 | 0.486 |
CLV_C14_Caspase3-7 | 339 | 343 | PF00656 | 0.582 |
CLV_C14_Caspase3-7 | 368 | 372 | PF00656 | 0.473 |
CLV_C14_Caspase3-7 | 57 | 61 | PF00656 | 0.656 |
CLV_NRD_NRD_1 | 1090 | 1092 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 1119 | 1121 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 1129 | 1131 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 1255 | 1257 | PF00675 | 0.311 |
CLV_NRD_NRD_1 | 1301 | 1303 | PF00675 | 0.278 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.242 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 539 | 541 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 685 | 687 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 862 | 864 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 944 | 946 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 972 | 974 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 991 | 993 | PF00675 | 0.256 |
CLV_NRD_NRD_1 | 995 | 997 | PF00675 | 0.340 |
CLV_PCSK_KEX2_1 | 1090 | 1092 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 1099 | 1101 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 1119 | 1121 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 1129 | 1131 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 1255 | 1257 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 1301 | 1303 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 1334 | 1336 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 539 | 541 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 862 | 864 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 944 | 946 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 972 | 974 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 991 | 993 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 995 | 997 | PF00082 | 0.353 |
CLV_PCSK_PC1ET2_1 | 1099 | 1101 | PF00082 | 0.491 |
CLV_PCSK_PC1ET2_1 | 1334 | 1336 | PF00082 | 0.357 |
CLV_PCSK_PC1ET2_1 | 482 | 484 | PF00082 | 0.426 |
CLV_PCSK_PC7_1 | 40 | 46 | PF00082 | 0.648 |
CLV_PCSK_PC7_1 | 987 | 993 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 1060 | 1064 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 1065 | 1069 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 1120 | 1124 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 677 | 681 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 686 | 690 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 945 | 949 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 995 | 999 | PF00082 | 0.443 |
CLV_Separin_Metazoa | 737 | 741 | PF03568 | 0.357 |
DEG_APCC_DBOX_1 | 348 | 356 | PF00400 | 0.384 |
DEG_APCC_DBOX_1 | 43 | 51 | PF00400 | 0.524 |
DEG_APCC_DBOX_1 | 511 | 519 | PF00400 | 0.306 |
DEG_APCC_DBOX_1 | 944 | 952 | PF00400 | 0.501 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.275 |
DEG_SCF_TRCP1_1 | 60 | 65 | PF00400 | 0.629 |
DEG_SPOP_SBC_1 | 922 | 926 | PF00917 | 0.532 |
DOC_ANK_TNKS_1 | 146 | 153 | PF00023 | 0.467 |
DOC_CDC14_PxL_1 | 457 | 465 | PF14671 | 0.302 |
DOC_CDC14_PxL_1 | 835 | 843 | PF14671 | 0.416 |
DOC_CYCLIN_RxL_1 | 383 | 392 | PF00134 | 0.335 |
DOC_CYCLIN_RxL_1 | 683 | 690 | PF00134 | 0.357 |
DOC_CYCLIN_yCln2_LP_2 | 868 | 874 | PF00134 | 0.389 |
DOC_MAPK_gen_1 | 302 | 309 | PF00069 | 0.310 |
DOC_MAPK_gen_1 | 547 | 555 | PF00069 | 0.320 |
DOC_MAPK_gen_1 | 972 | 979 | PF00069 | 0.560 |
DOC_MAPK_gen_1 | 991 | 1002 | PF00069 | 0.385 |
DOC_MAPK_HePTP_8 | 803 | 815 | PF00069 | 0.328 |
DOC_MAPK_MEF2A_6 | 1077 | 1085 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 512 | 520 | PF00069 | 0.355 |
DOC_MAPK_MEF2A_6 | 806 | 815 | PF00069 | 0.322 |
DOC_MAPK_MEF2A_6 | 972 | 979 | PF00069 | 0.474 |
DOC_MAPK_RevD_3 | 314 | 330 | PF00069 | 0.432 |
DOC_PP1_RVXF_1 | 159 | 166 | PF00149 | 0.441 |
DOC_PP1_RVXF_1 | 515 | 521 | PF00149 | 0.426 |
DOC_PP1_RVXF_1 | 804 | 810 | PF00149 | 0.352 |
DOC_PP2B_LxvP_1 | 750 | 753 | PF13499 | 0.326 |
DOC_PP4_FxxP_1 | 1286 | 1289 | PF00568 | 0.292 |
DOC_PP4_FxxP_1 | 98 | 101 | PF00568 | 0.502 |
DOC_USP7_MATH_1 | 1162 | 1166 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 1174 | 1178 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 1378 | 1382 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 1395 | 1399 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 848 | 852 | PF00917 | 0.304 |
DOC_USP7_MATH_1 | 920 | 924 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 960 | 964 | PF00917 | 0.249 |
DOC_USP7_UBL2_3 | 1371 | 1375 | PF12436 | 0.453 |
DOC_USP7_UBL2_3 | 1380 | 1384 | PF12436 | 0.441 |
DOC_WW_Pin1_4 | 1053 | 1058 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.403 |
DOC_WW_Pin1_4 | 793 | 798 | PF00397 | 0.275 |
DOC_WW_Pin1_4 | 885 | 890 | PF00397 | 0.465 |
LIG_14-3-3_CanoR_1 | 1060 | 1067 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 1090 | 1098 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 1226 | 1235 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 132 | 136 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 1394 | 1401 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 332 | 338 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 409 | 418 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 569 | 579 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 587 | 592 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 686 | 696 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 740 | 745 | PF00244 | 0.312 |
LIG_Actin_WH2_2 | 156 | 173 | PF00022 | 0.456 |
LIG_APCC_ABBAyCdc20_2 | 1199 | 1205 | PF00400 | 0.292 |
LIG_BIR_III_2 | 1105 | 1109 | PF00653 | 0.543 |
LIG_BRCT_BRCA1_1 | 1320 | 1324 | PF00533 | 0.373 |
LIG_BRCT_BRCA1_1 | 353 | 357 | PF00533 | 0.380 |
LIG_Clathr_ClatBox_1 | 507 | 511 | PF01394 | 0.444 |
LIG_CSL_BTD_1 | 897 | 900 | PF09270 | 0.526 |
LIG_deltaCOP1_diTrp_1 | 1271 | 1276 | PF00928 | 0.419 |
LIG_deltaCOP1_diTrp_1 | 364 | 369 | PF00928 | 0.292 |
LIG_EH1_1 | 554 | 562 | PF00400 | 0.431 |
LIG_EH1_1 | 910 | 918 | PF00400 | 0.386 |
LIG_eIF4E_1 | 215 | 221 | PF01652 | 0.587 |
LIG_FHA_1 | 1033 | 1039 | PF00498 | 0.548 |
LIG_FHA_1 | 1043 | 1049 | PF00498 | 0.479 |
LIG_FHA_1 | 1054 | 1060 | PF00498 | 0.511 |
LIG_FHA_1 | 1066 | 1072 | PF00498 | 0.460 |
LIG_FHA_1 | 1181 | 1187 | PF00498 | 0.531 |
LIG_FHA_1 | 1227 | 1233 | PF00498 | 0.401 |
LIG_FHA_1 | 1305 | 1311 | PF00498 | 0.384 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.435 |
LIG_FHA_1 | 660 | 666 | PF00498 | 0.411 |
LIG_FHA_1 | 702 | 708 | PF00498 | 0.341 |
LIG_FHA_1 | 753 | 759 | PF00498 | 0.402 |
LIG_FHA_1 | 790 | 796 | PF00498 | 0.482 |
LIG_FHA_2 | 1275 | 1281 | PF00498 | 0.359 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.572 |
LIG_FHA_2 | 23 | 29 | PF00498 | 0.523 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.407 |
LIG_FHA_2 | 648 | 654 | PF00498 | 0.326 |
LIG_FHA_2 | 723 | 729 | PF00498 | 0.453 |
LIG_FHA_2 | 996 | 1002 | PF00498 | 0.458 |
LIG_FXI_DFP_1 | 604 | 608 | PF00024 | 0.475 |
LIG_GBD_Chelix_1 | 199 | 207 | PF00786 | 0.418 |
LIG_GBD_Chelix_1 | 556 | 564 | PF00786 | 0.432 |
LIG_Integrin_isoDGR_2 | 985 | 987 | PF01839 | 0.495 |
LIG_LIR_Apic_2 | 1347 | 1352 | PF02991 | 0.435 |
LIG_LIR_Apic_2 | 96 | 101 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 1275 | 1283 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 1356 | 1367 | PF02991 | 0.302 |
LIG_LIR_Gen_1 | 364 | 373 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 379 | 390 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 391 | 402 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 554 | 563 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 615 | 626 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 647 | 654 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 724 | 734 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 745 | 753 | PF02991 | 0.323 |
LIG_LIR_LC3C_4 | 974 | 979 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 1275 | 1279 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 1356 | 1362 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 162 | 167 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 364 | 369 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 379 | 385 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 391 | 397 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 554 | 558 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 615 | 621 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 647 | 652 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 724 | 729 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 745 | 750 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 895 | 901 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 908 | 913 | PF02991 | 0.165 |
LIG_MYND_1 | 839 | 843 | PF01753 | 0.411 |
LIG_NRBOX | 231 | 237 | PF00104 | 0.337 |
LIG_NRBOX | 308 | 314 | PF00104 | 0.304 |
LIG_NRBOX | 932 | 938 | PF00104 | 0.491 |
LIG_PCNA_PIPBox_1 | 1 | 10 | PF02747 | 0.319 |
LIG_Pex14_2 | 1282 | 1286 | PF04695 | 0.292 |
LIG_Pex14_2 | 1324 | 1328 | PF04695 | 0.326 |
LIG_PTB_Apo_2 | 996 | 1003 | PF02174 | 0.407 |
LIG_SH2_CRK | 1349 | 1353 | PF00017 | 0.405 |
LIG_SH2_CRK | 528 | 532 | PF00017 | 0.433 |
LIG_SH2_CRK | 804 | 808 | PF00017 | 0.354 |
LIG_SH2_CRK | 994 | 998 | PF00017 | 0.359 |
LIG_SH2_PTP2 | 1361 | 1364 | PF00017 | 0.307 |
LIG_SH2_SRC | 215 | 218 | PF00017 | 0.553 |
LIG_SH2_STAP1 | 1392 | 1396 | PF00017 | 0.527 |
LIG_SH2_STAT3 | 205 | 208 | PF00017 | 0.515 |
LIG_SH2_STAT3 | 328 | 331 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 1011 | 1014 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 1043 | 1046 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 1088 | 1091 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 1309 | 1312 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 1361 | 1364 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 578 | 581 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 768 | 771 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 911 | 914 | PF00017 | 0.400 |
LIG_SH3_3 | 1109 | 1115 | PF00018 | 0.517 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.470 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.474 |
LIG_SH3_3 | 610 | 616 | PF00018 | 0.337 |
LIG_SH3_3 | 724 | 730 | PF00018 | 0.280 |
LIG_SH3_3 | 733 | 739 | PF00018 | 0.271 |
LIG_SH3_3 | 766 | 772 | PF00018 | 0.292 |
LIG_SH3_3 | 823 | 829 | PF00018 | 0.322 |
LIG_SH3_3 | 883 | 889 | PF00018 | 0.482 |
LIG_SH3_3 | 894 | 900 | PF00018 | 0.528 |
LIG_SH3_3 | 948 | 954 | PF00018 | 0.460 |
LIG_SUMO_SIM_anti_2 | 974 | 981 | PF11976 | 0.480 |
LIG_SUMO_SIM_par_1 | 443 | 450 | PF11976 | 0.441 |
LIG_SUMO_SIM_par_1 | 577 | 584 | PF11976 | 0.354 |
LIG_TRAF2_1 | 1145 | 1148 | PF00917 | 0.500 |
LIG_TRAF2_1 | 393 | 396 | PF00917 | 0.335 |
LIG_TRAF2_1 | 940 | 943 | PF00917 | 0.459 |
LIG_TYR_ITIM | 526 | 531 | PF00017 | 0.426 |
LIG_UBA3_1 | 333 | 338 | PF00899 | 0.467 |
LIG_UBA3_1 | 445 | 451 | PF00899 | 0.377 |
LIG_WRC_WIRS_1 | 4 | 9 | PF05994 | 0.480 |
LIG_WRC_WIRS_1 | 588 | 593 | PF05994 | 0.476 |
LIG_WW_3 | 1143 | 1147 | PF00397 | 0.287 |
MOD_CDK_SPxxK_3 | 1053 | 1060 | PF00069 | 0.525 |
MOD_CK1_1 | 1004 | 1010 | PF00069 | 0.379 |
MOD_CK1_1 | 1032 | 1038 | PF00069 | 0.623 |
MOD_CK1_1 | 1177 | 1183 | PF00069 | 0.514 |
MOD_CK1_1 | 1243 | 1249 | PF00069 | 0.414 |
MOD_CK1_1 | 1397 | 1403 | PF00069 | 0.495 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.377 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.442 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.459 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.446 |
MOD_CK1_1 | 492 | 498 | PF00069 | 0.297 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.468 |
MOD_CK1_1 | 644 | 650 | PF00069 | 0.373 |
MOD_CK1_1 | 670 | 676 | PF00069 | 0.365 |
MOD_CK1_1 | 743 | 749 | PF00069 | 0.283 |
MOD_CK1_1 | 923 | 929 | PF00069 | 0.520 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.578 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.452 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.658 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.378 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.344 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.684 |
MOD_CK2_1 | 670 | 676 | PF00069 | 0.416 |
MOD_CK2_1 | 775 | 781 | PF00069 | 0.379 |
MOD_CK2_1 | 995 | 1001 | PF00069 | 0.346 |
MOD_Cter_Amidation | 970 | 973 | PF01082 | 0.438 |
MOD_DYRK1A_RPxSP_1 | 885 | 889 | PF00069 | 0.464 |
MOD_GlcNHglycan | 1013 | 1016 | PF01048 | 0.398 |
MOD_GlcNHglycan | 1027 | 1030 | PF01048 | 0.582 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.621 |
MOD_GlcNHglycan | 1319 | 1323 | PF01048 | 0.283 |
MOD_GlcNHglycan | 1342 | 1345 | PF01048 | 0.419 |
MOD_GlcNHglycan | 1380 | 1383 | PF01048 | 0.455 |
MOD_GlcNHglycan | 14 | 20 | PF01048 | 0.679 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.402 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.291 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.509 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.691 |
MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.346 |
MOD_GlcNHglycan | 672 | 675 | PF01048 | 0.346 |
MOD_GlcNHglycan | 850 | 853 | PF01048 | 0.326 |
MOD_GlcNHglycan | 962 | 965 | PF01048 | 0.516 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.414 |
MOD_GSK3_1 | 1007 | 1014 | PF00069 | 0.445 |
MOD_GSK3_1 | 1025 | 1032 | PF00069 | 0.622 |
MOD_GSK3_1 | 1042 | 1049 | PF00069 | 0.521 |
MOD_GSK3_1 | 1061 | 1068 | PF00069 | 0.558 |
MOD_GSK3_1 | 1158 | 1165 | PF00069 | 0.616 |
MOD_GSK3_1 | 1173 | 1180 | PF00069 | 0.431 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.513 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.192 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.525 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.402 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.702 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.427 |
MOD_GSK3_1 | 654 | 661 | PF00069 | 0.354 |
MOD_GSK3_1 | 789 | 796 | PF00069 | 0.417 |
MOD_GSK3_1 | 901 | 908 | PF00069 | 0.492 |
MOD_GSK3_1 | 918 | 925 | PF00069 | 0.510 |
MOD_N-GLC_1 | 1243 | 1248 | PF02516 | 0.357 |
MOD_N-GLC_1 | 1345 | 1350 | PF02516 | 0.282 |
MOD_N-GLC_1 | 256 | 261 | PF02516 | 0.518 |
MOD_NEK2_1 | 1061 | 1066 | PF00069 | 0.453 |
MOD_NEK2_1 | 1124 | 1129 | PF00069 | 0.466 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.585 |
MOD_NEK2_1 | 1293 | 1298 | PF00069 | 0.327 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.481 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.559 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.329 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.435 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.324 |
MOD_NEK2_1 | 789 | 794 | PF00069 | 0.389 |
MOD_NEK2_1 | 901 | 906 | PF00069 | 0.318 |
MOD_PIKK_1 | 452 | 458 | PF00454 | 0.412 |
MOD_PIKK_1 | 563 | 569 | PF00454 | 0.407 |
MOD_PIKK_1 | 590 | 596 | PF00454 | 0.486 |
MOD_PIKK_1 | 687 | 693 | PF00454 | 0.357 |
MOD_PIKK_1 | 905 | 911 | PF00454 | 0.354 |
MOD_PK_1 | 1228 | 1234 | PF00069 | 0.419 |
MOD_PK_1 | 740 | 746 | PF00069 | 0.385 |
MOD_PKA_1 | 995 | 1001 | PF00069 | 0.349 |
MOD_PKA_2 | 1032 | 1038 | PF00069 | 0.599 |
MOD_PKA_2 | 1089 | 1095 | PF00069 | 0.491 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.489 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.457 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.337 |
MOD_PKA_2 | 586 | 592 | PF00069 | 0.474 |
MOD_PKA_2 | 692 | 698 | PF00069 | 0.432 |
MOD_PKA_2 | 995 | 1001 | PF00069 | 0.349 |
MOD_PKB_1 | 1226 | 1234 | PF00069 | 0.419 |
MOD_Plk_1 | 1345 | 1351 | PF00069 | 0.300 |
MOD_Plk_1 | 155 | 161 | PF00069 | 0.413 |
MOD_Plk_1 | 395 | 401 | PF00069 | 0.353 |
MOD_Plk_1 | 631 | 637 | PF00069 | 0.442 |
MOD_Plk_1 | 782 | 788 | PF00069 | 0.332 |
MOD_Plk_1 | 809 | 815 | PF00069 | 0.301 |
MOD_Plk_1 | 901 | 907 | PF00069 | 0.319 |
MOD_Plk_2-3 | 70 | 76 | PF00069 | 0.585 |
MOD_Plk_4 | 1032 | 1038 | PF00069 | 0.480 |
MOD_Plk_4 | 1220 | 1226 | PF00069 | 0.371 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.419 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.440 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.364 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.290 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.397 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.349 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.303 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.431 |
MOD_Plk_4 | 654 | 660 | PF00069 | 0.372 |
MOD_Plk_4 | 692 | 698 | PF00069 | 0.299 |
MOD_Plk_4 | 722 | 728 | PF00069 | 0.410 |
MOD_Plk_4 | 775 | 781 | PF00069 | 0.411 |
MOD_Plk_4 | 809 | 815 | PF00069 | 0.298 |
MOD_Plk_4 | 901 | 907 | PF00069 | 0.328 |
MOD_Plk_4 | 952 | 958 | PF00069 | 0.489 |
MOD_ProDKin_1 | 1053 | 1059 | PF00069 | 0.527 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.400 |
MOD_ProDKin_1 | 793 | 799 | PF00069 | 0.272 |
MOD_ProDKin_1 | 885 | 891 | PF00069 | 0.466 |
MOD_SUMO_for_1 | 116 | 119 | PF00179 | 0.538 |
MOD_SUMO_rev_2 | 112 | 118 | PF00179 | 0.552 |
TRG_DiLeu_BaEn_1 | 216 | 221 | PF01217 | 0.414 |
TRG_DiLeu_BaEn_1 | 308 | 313 | PF01217 | 0.304 |
TRG_DiLeu_BaEn_1 | 511 | 516 | PF01217 | 0.425 |
TRG_DiLeu_BaEn_2 | 550 | 556 | PF01217 | 0.432 |
TRG_DiLeu_BaEn_2 | 81 | 87 | PF01217 | 0.529 |
TRG_DiLeu_BaLyEn_6 | 227 | 232 | PF01217 | 0.304 |
TRG_DiLeu_BaLyEn_6 | 556 | 561 | PF01217 | 0.349 |
TRG_DiLeu_BaLyEn_6 | 705 | 710 | PF01217 | 0.429 |
TRG_DiLeu_LyEn_5 | 308 | 313 | PF01217 | 0.304 |
TRG_ENDOCYTIC_2 | 1166 | 1169 | PF00928 | 0.666 |
TRG_ENDOCYTIC_2 | 1262 | 1265 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 1361 | 1364 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 519 | 522 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 741 | 744 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 747 | 750 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 804 | 807 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 994 | 997 | PF00928 | 0.347 |
TRG_ER_diArg_1 | 1089 | 1091 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 1118 | 1120 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 1128 | 1130 | PF00400 | 0.313 |
TRG_ER_diArg_1 | 1225 | 1228 | PF00400 | 0.419 |
TRG_ER_diArg_1 | 1301 | 1303 | PF00400 | 0.285 |
TRG_ER_diArg_1 | 21 | 23 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 328 | 330 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 37 | 40 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 383 | 386 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 546 | 549 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 884 | 887 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 991 | 993 | PF00400 | 0.388 |
TRG_ER_diArg_1 | 994 | 996 | PF00400 | 0.350 |
TRG_NES_CRM1_1 | 551 | 567 | PF08389 | 0.433 |
TRG_NES_CRM1_1 | 810 | 824 | PF08389 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 1335 | 1339 | PF00026 | 0.402 |
TRG_Pf-PMV_PEXEL_1 | 147 | 151 | PF00026 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 189 | 193 | PF00026 | 0.412 |
TRG_Pf-PMV_PEXEL_1 | 37 | 41 | PF00026 | 0.574 |
TRG_Pf-PMV_PEXEL_1 | 386 | 391 | PF00026 | 0.454 |
TRG_Pf-PMV_PEXEL_1 | 438 | 443 | PF00026 | 0.394 |
TRG_Pf-PMV_PEXEL_1 | 686 | 691 | PF00026 | 0.419 |
TRG_Pf-PMV_PEXEL_1 | 801 | 805 | PF00026 | 0.489 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5K4 | Leptomonas seymouri | 76% | 96% |
A0A0S4JMH7 | Bodo saltans | 32% | 92% |
A0A1X0NS21 | Trypanosomatidae | 44% | 95% |
A0A3Q8IE14 | Leishmania donovani | 96% | 96% |
A0A3R7KQD9 | Trypanosoma rangeli | 45% | 95% |
A4I9F1 | Leishmania infantum | 96% | 96% |
C9ZJS2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 91% |
E9AIV7 | Leishmania braziliensis | 91% | 100% |
Q4Q3M7 | Leishmania major | 95% | 100% |
V5B3D2 | Trypanosoma cruzi | 45% | 95% |