Topoisomerase, DNA topoisomerase 2 TOP2
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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0020023 | kinetoplast | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HWL4
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 6 |
GO:0006259 | DNA metabolic process | 4 | 6 |
GO:0006265 | DNA topological change | 5 | 6 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0006996 | organelle organization | 4 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016043 | cellular component organization | 3 | 6 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 6 |
GO:0046483 | heterocycle metabolic process | 3 | 6 |
GO:0051276 | chromosome organization | 5 | 6 |
GO:0071103 | DNA conformation change | 6 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:0071840 | cellular component organization or biogenesis | 2 | 6 |
GO:0090304 | nucleic acid metabolic process | 4 | 6 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 6 |
GO:0000712 | resolution of meiotic recombination intermediates | 4 | 1 |
GO:0000819 | sister chromatid segregation | 4 | 1 |
GO:0007059 | chromosome segregation | 2 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022414 | reproductive process | 1 | 1 |
GO:0061982 | meiosis I cell cycle process | 3 | 1 |
GO:0098813 | nuclear chromosome segregation | 3 | 1 |
GO:1903046 | meiotic cell cycle process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 6 |
GO:0003676 | nucleic acid binding | 3 | 6 |
GO:0003677 | DNA binding | 4 | 6 |
GO:0003824 | catalytic activity | 1 | 6 |
GO:0003916 | DNA topoisomerase activity | 3 | 6 |
GO:0003918 | DNA topoisomerase type II (double strand cut, ATP-hydrolyzing) activity | 3 | 6 |
GO:0005488 | binding | 1 | 6 |
GO:0005524 | ATP binding | 5 | 6 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 6 |
GO:0016853 | isomerase activity | 2 | 6 |
GO:0017076 | purine nucleotide binding | 4 | 6 |
GO:0030554 | adenyl nucleotide binding | 5 | 6 |
GO:0032553 | ribonucleotide binding | 3 | 6 |
GO:0032555 | purine ribonucleotide binding | 4 | 6 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 6 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 6 |
GO:0036094 | small molecule binding | 2 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043168 | anion binding | 3 | 6 |
GO:0043169 | cation binding | 3 | 6 |
GO:0046872 | metal ion binding | 4 | 6 |
GO:0097159 | organic cyclic compound binding | 2 | 6 |
GO:0097367 | carbohydrate derivative binding | 2 | 6 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 6 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 6 |
GO:0140657 | ATP-dependent activity | 1 | 6 |
GO:1901265 | nucleoside phosphate binding | 3 | 6 |
GO:1901363 | heterocyclic compound binding | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 309 | 313 | PF00656 | 0.573 |
CLV_C14_Caspase3-7 | 426 | 430 | PF00656 | 0.677 |
CLV_C14_Caspase3-7 | 439 | 443 | PF00656 | 0.458 |
CLV_C14_Caspase3-7 | 516 | 520 | PF00656 | 0.611 |
CLV_NRD_NRD_1 | 1017 | 1019 | PF00675 | 0.206 |
CLV_NRD_NRD_1 | 1169 | 1171 | PF00675 | 0.744 |
CLV_NRD_NRD_1 | 1206 | 1208 | PF00675 | 0.805 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.724 |
CLV_NRD_NRD_1 | 639 | 641 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 696 | 698 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 705 | 707 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 874 | 876 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 991 | 993 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 999 | 1001 | PF00675 | 0.473 |
CLV_PCSK_KEX2_1 | 1089 | 1091 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 1168 | 1170 | PF00082 | 0.717 |
CLV_PCSK_KEX2_1 | 1190 | 1192 | PF00082 | 0.764 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.724 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 705 | 707 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 874 | 876 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 991 | 993 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 997 | 999 | PF00082 | 0.407 |
CLV_PCSK_PC1ET2_1 | 1089 | 1091 | PF00082 | 0.506 |
CLV_PCSK_PC1ET2_1 | 1168 | 1170 | PF00082 | 0.717 |
CLV_PCSK_PC1ET2_1 | 1190 | 1192 | PF00082 | 0.764 |
CLV_PCSK_PC1ET2_1 | 214 | 216 | PF00082 | 0.562 |
CLV_PCSK_PC1ET2_1 | 219 | 221 | PF00082 | 0.449 |
CLV_PCSK_PC1ET2_1 | 286 | 288 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 478 | 480 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 997 | 999 | PF00082 | 0.506 |
CLV_PCSK_PC7_1 | 1186 | 1192 | PF00082 | 0.764 |
CLV_PCSK_PC7_1 | 215 | 221 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 1061 | 1065 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 1149 | 1153 | PF00082 | 0.686 |
CLV_PCSK_SKI1_1 | 1196 | 1200 | PF00082 | 0.805 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.640 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.211 |
CLV_PCSK_SKI1_1 | 475 | 479 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 661 | 665 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 697 | 701 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 774 | 778 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 785 | 789 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.569 |
DEG_APCC_DBOX_1 | 1137 | 1145 | PF00400 | 0.633 |
DEG_APCC_DBOX_1 | 465 | 473 | PF00400 | 0.611 |
DEG_APCC_DBOX_1 | 696 | 704 | PF00400 | 0.506 |
DOC_CDC14_PxL_1 | 251 | 259 | PF14671 | 0.482 |
DOC_CKS1_1 | 30 | 35 | PF01111 | 0.567 |
DOC_CKS1_1 | 551 | 556 | PF01111 | 0.611 |
DOC_CYCLIN_RxL_1 | 779 | 792 | PF00134 | 0.506 |
DOC_CYCLIN_yCln2_LP_2 | 1059 | 1065 | PF00134 | 0.506 |
DOC_CYCLIN_yCln2_LP_2 | 1137 | 1143 | PF00134 | 0.625 |
DOC_MAPK_FxFP_2 | 202 | 205 | PF00069 | 0.588 |
DOC_MAPK_gen_1 | 105 | 113 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 1207 | 1215 | PF00069 | 0.797 |
DOC_MAPK_gen_1 | 186 | 195 | PF00069 | 0.604 |
DOC_MAPK_gen_1 | 333 | 343 | PF00069 | 0.611 |
DOC_MAPK_gen_1 | 481 | 491 | PF00069 | 0.515 |
DOC_MAPK_gen_1 | 563 | 570 | PF00069 | 0.611 |
DOC_MAPK_gen_1 | 658 | 665 | PF00069 | 0.611 |
DOC_MAPK_gen_1 | 779 | 788 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 997 | 1006 | PF00069 | 0.506 |
DOC_MAPK_MEF2A_6 | 1041 | 1048 | PF00069 | 0.506 |
DOC_MAPK_MEF2A_6 | 1207 | 1215 | PF00069 | 0.723 |
DOC_MAPK_MEF2A_6 | 1229 | 1236 | PF00069 | 0.669 |
DOC_MAPK_MEF2A_6 | 336 | 344 | PF00069 | 0.611 |
DOC_MAPK_MEF2A_6 | 484 | 493 | PF00069 | 0.528 |
DOC_MAPK_MEF2A_6 | 613 | 620 | PF00069 | 0.611 |
DOC_MAPK_MEF2A_6 | 78 | 86 | PF00069 | 0.506 |
DOC_MAPK_NFAT4_5 | 613 | 621 | PF00069 | 0.611 |
DOC_MAPK_RevD_3 | 207 | 220 | PF00069 | 0.566 |
DOC_PIKK_1 | 391 | 398 | PF02985 | 0.516 |
DOC_PP1_RVXF_1 | 1059 | 1066 | PF00149 | 0.370 |
DOC_PP1_RVXF_1 | 190 | 196 | PF00149 | 0.572 |
DOC_PP1_RVXF_1 | 695 | 702 | PF00149 | 0.506 |
DOC_PP1_RVXF_1 | 783 | 789 | PF00149 | 0.506 |
DOC_PP2B_LxvP_1 | 663 | 666 | PF13499 | 0.611 |
DOC_PP2B_LxvP_1 | 753 | 756 | PF13499 | 0.506 |
DOC_PP4_FxxP_1 | 202 | 205 | PF00568 | 0.428 |
DOC_PP4_FxxP_1 | 551 | 554 | PF00568 | 0.611 |
DOC_PP4_FxxP_1 | 805 | 808 | PF00568 | 0.428 |
DOC_SPAK_OSR1_1 | 894 | 898 | PF12202 | 0.506 |
DOC_USP7_MATH_1 | 1171 | 1175 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 1178 | 1182 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 520 | 524 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 569 | 573 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 582 | 586 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 976 | 980 | PF00917 | 0.506 |
DOC_USP7_UBL2_3 | 1041 | 1045 | PF12436 | 0.506 |
DOC_USP7_UBL2_3 | 1208 | 1212 | PF12436 | 0.812 |
DOC_USP7_UBL2_3 | 320 | 324 | PF12436 | 0.603 |
DOC_USP7_UBL2_3 | 559 | 563 | PF12436 | 0.611 |
DOC_WW_Pin1_4 | 1089 | 1094 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 500 | 505 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 550 | 555 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 966 | 971 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 972 | 977 | PF00397 | 0.407 |
DOC_WW_Pin1_4 | 979 | 984 | PF00397 | 0.279 |
LIG_14-3-3_CanoR_1 | 1013 | 1021 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 1068 | 1074 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 1124 | 1132 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 173 | 178 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 243 | 252 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 336 | 341 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 358 | 364 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 406 | 414 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 431 | 437 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 479 | 486 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 587 | 593 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 658 | 664 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 705 | 714 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 78 | 82 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 894 | 903 | PF00244 | 0.506 |
LIG_Actin_WH2_2 | 42 | 59 | PF00022 | 0.569 |
LIG_BIR_III_4 | 519 | 523 | PF00653 | 0.611 |
LIG_BRCT_BRCA1_1 | 149 | 153 | PF00533 | 0.506 |
LIG_BRCT_BRCA1_1 | 318 | 322 | PF00533 | 0.591 |
LIG_BRCT_BRCA1_2 | 318 | 324 | PF00533 | 0.611 |
LIG_CaM_IQ_9 | 1011 | 1027 | PF13499 | 0.428 |
LIG_Clathr_ClatBox_1 | 1006 | 1010 | PF01394 | 0.506 |
LIG_Clathr_ClatBox_1 | 1048 | 1052 | PF01394 | 0.506 |
LIG_Clathr_ClatBox_1 | 1141 | 1145 | PF01394 | 0.658 |
LIG_CNOT1_NIM_1 | 242 | 251 | PF04054 | 0.562 |
LIG_CtBP_PxDLS_1 | 494 | 499 | PF00389 | 0.611 |
LIG_deltaCOP1_diTrp_1 | 636 | 643 | PF00928 | 0.611 |
LIG_deltaCOP1_diTrp_1 | 899 | 909 | PF00928 | 0.506 |
LIG_EVH1_2 | 262 | 266 | PF00568 | 0.595 |
LIG_FHA_1 | 1069 | 1075 | PF00498 | 0.506 |
LIG_FHA_1 | 1089 | 1095 | PF00498 | 0.175 |
LIG_FHA_1 | 1127 | 1133 | PF00498 | 0.659 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.421 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.573 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.492 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.613 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.225 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.582 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.497 |
LIG_FHA_1 | 660 | 666 | PF00498 | 0.501 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.506 |
LIG_FHA_1 | 969 | 975 | PF00498 | 0.409 |
LIG_FHA_1 | 999 | 1005 | PF00498 | 0.506 |
LIG_FHA_2 | 1067 | 1073 | PF00498 | 0.370 |
LIG_FHA_2 | 1097 | 1103 | PF00498 | 0.383 |
LIG_FHA_2 | 1105 | 1111 | PF00498 | 0.374 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.526 |
LIG_FHA_2 | 437 | 443 | PF00498 | 0.611 |
LIG_FHA_2 | 480 | 486 | PF00498 | 0.556 |
LIG_FHA_2 | 514 | 520 | PF00498 | 0.557 |
LIG_FHA_2 | 598 | 604 | PF00498 | 0.611 |
LIG_FHA_2 | 662 | 668 | PF00498 | 0.597 |
LIG_FHA_2 | 802 | 808 | PF00498 | 0.412 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.541 |
LIG_FHA_2 | 902 | 908 | PF00498 | 0.506 |
LIG_FHA_2 | 945 | 951 | PF00498 | 0.506 |
LIG_Integrin_isoDGR_2 | 892 | 894 | PF01839 | 0.506 |
LIG_IRF3_LxIS_1 | 909 | 914 | PF10401 | 0.506 |
LIG_LIR_Apic_2 | 500 | 504 | PF02991 | 0.584 |
LIG_LIR_Apic_2 | 549 | 554 | PF02991 | 0.506 |
LIG_LIR_Apic_2 | 802 | 808 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 1052 | 1063 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 1110 | 1119 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 150 | 160 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 198 | 207 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 246 | 255 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 488 | 497 | PF02991 | 0.611 |
LIG_LIR_Gen_1 | 506 | 515 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 606 | 616 | PF02991 | 0.611 |
LIG_LIR_Gen_1 | 781 | 789 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 80 | 86 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 878 | 889 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 1052 | 1058 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 1105 | 1111 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 115 | 121 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 198 | 202 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 244 | 248 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 488 | 493 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 5 | 10 | PF02991 | 0.664 |
LIG_LIR_Nem_3 | 506 | 512 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 534 | 540 | PF02991 | 0.611 |
LIG_LIR_Nem_3 | 572 | 576 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 781 | 786 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 80 | 84 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 836 | 840 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 878 | 884 | PF02991 | 0.506 |
LIG_MYND_3 | 380 | 384 | PF01753 | 0.601 |
LIG_PCNA_TLS_4 | 370 | 377 | PF02747 | 0.611 |
LIG_Pex14_1 | 865 | 869 | PF04695 | 0.506 |
LIG_Pex14_2 | 1020 | 1024 | PF04695 | 0.345 |
LIG_Pex14_2 | 1104 | 1108 | PF04695 | 0.557 |
LIG_Pex14_2 | 164 | 168 | PF04695 | 0.569 |
LIG_Pex14_2 | 533 | 537 | PF04695 | 0.611 |
LIG_PTB_Apo_2 | 234 | 241 | PF02174 | 0.591 |
LIG_PTB_Apo_2 | 541 | 548 | PF02174 | 0.556 |
LIG_PTB_Phospho_1 | 541 | 547 | PF10480 | 0.560 |
LIG_REV1ctd_RIR_1 | 1063 | 1072 | PF16727 | 0.506 |
LIG_SH2_CRK | 248 | 252 | PF00017 | 0.545 |
LIG_SH2_CRK | 268 | 272 | PF00017 | 0.506 |
LIG_SH2_CRK | 459 | 463 | PF00017 | 0.611 |
LIG_SH2_CRK | 501 | 505 | PF00017 | 0.589 |
LIG_SH2_CRK | 509 | 513 | PF00017 | 0.539 |
LIG_SH2_CRK | 593 | 597 | PF00017 | 0.611 |
LIG_SH2_CRK | 7 | 11 | PF00017 | 0.654 |
LIG_SH2_GRB2like | 962 | 965 | PF00017 | 0.428 |
LIG_SH2_NCK_1 | 1161 | 1165 | PF00017 | 0.603 |
LIG_SH2_NCK_1 | 252 | 256 | PF00017 | 0.535 |
LIG_SH2_NCK_1 | 268 | 272 | PF00017 | 0.336 |
LIG_SH2_PTP2 | 547 | 550 | PF00017 | 0.529 |
LIG_SH2_PTP2 | 81 | 84 | PF00017 | 0.506 |
LIG_SH2_PTP2 | 811 | 814 | PF00017 | 0.506 |
LIG_SH2_SRC | 811 | 814 | PF00017 | 0.506 |
LIG_SH2_SRC | 962 | 965 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 1111 | 1115 | PF00017 | 0.595 |
LIG_SH2_STAP1 | 248 | 252 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 588 | 592 | PF00017 | 0.611 |
LIG_SH2_STAP1 | 989 | 993 | PF00017 | 0.506 |
LIG_SH2_STAT3 | 277 | 280 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 1057 | 1060 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 588 | 591 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 720 | 723 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 775 | 778 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 811 | 814 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 887 | 890 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 962 | 965 | PF00017 | 0.428 |
LIG_SH3_3 | 1129 | 1135 | PF00018 | 0.648 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.611 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.507 |
LIG_SH3_3 | 810 | 816 | PF00018 | 0.367 |
LIG_SH3_3 | 964 | 970 | PF00018 | 0.506 |
LIG_SH3_5 | 794 | 798 | PF00018 | 0.506 |
LIG_SUMO_SIM_anti_2 | 935 | 940 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 1140 | 1145 | PF11976 | 0.644 |
LIG_SUMO_SIM_par_1 | 434 | 440 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 661 | 667 | PF11976 | 0.556 |
LIG_SUMO_SIM_par_1 | 838 | 843 | PF11976 | 0.506 |
LIG_SxIP_EBH_1 | 894 | 906 | PF03271 | 0.506 |
LIG_TRAF2_1 | 1107 | 1110 | PF00917 | 0.570 |
LIG_TRAF2_1 | 733 | 736 | PF00917 | 0.506 |
LIG_TYR_ITIM | 507 | 512 | PF00017 | 0.558 |
LIG_UBA3_1 | 1115 | 1121 | PF00899 | 0.540 |
LIG_UBA3_1 | 1141 | 1149 | PF00899 | 0.680 |
LIG_UBA3_1 | 413 | 419 | PF00899 | 0.623 |
LIG_WRC_WIRS_1 | 242 | 247 | PF05994 | 0.572 |
LIG_WRC_WIRS_1 | 570 | 575 | PF05994 | 0.556 |
LIG_WRC_WIRS_1 | 834 | 839 | PF05994 | 0.389 |
MOD_CDC14_SPxK_1 | 284 | 287 | PF00782 | 0.611 |
MOD_CDK_SPK_2 | 281 | 286 | PF00069 | 0.624 |
MOD_CDK_SPxK_1 | 1089 | 1095 | PF00069 | 0.506 |
MOD_CDK_SPxK_1 | 281 | 287 | PF00069 | 0.506 |
MOD_CDK_SPxxK_3 | 550 | 557 | PF00069 | 0.506 |
MOD_CK1_1 | 1126 | 1132 | PF00069 | 0.568 |
MOD_CK1_1 | 1214 | 1220 | PF00069 | 0.698 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.389 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.612 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.611 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.655 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.611 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.477 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.438 |
MOD_CK1_1 | 659 | 665 | PF00069 | 0.584 |
MOD_CK1_1 | 709 | 715 | PF00069 | 0.431 |
MOD_CK1_1 | 722 | 728 | PF00069 | 0.291 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.506 |
MOD_CK1_1 | 915 | 921 | PF00069 | 0.428 |
MOD_CK1_1 | 944 | 950 | PF00069 | 0.428 |
MOD_CK1_1 | 979 | 985 | PF00069 | 0.428 |
MOD_CK2_1 | 1066 | 1072 | PF00069 | 0.370 |
MOD_CK2_1 | 1104 | 1110 | PF00069 | 0.504 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.578 |
MOD_CK2_1 | 479 | 485 | PF00069 | 0.556 |
MOD_CK2_1 | 500 | 506 | PF00069 | 0.611 |
MOD_CK2_1 | 597 | 603 | PF00069 | 0.611 |
MOD_CK2_1 | 661 | 667 | PF00069 | 0.611 |
MOD_CK2_1 | 730 | 736 | PF00069 | 0.506 |
MOD_CK2_1 | 801 | 807 | PF00069 | 0.506 |
MOD_CK2_1 | 901 | 907 | PF00069 | 0.506 |
MOD_CK2_1 | 944 | 950 | PF00069 | 0.506 |
MOD_Cter_Amidation | 1188 | 1191 | PF01082 | 0.769 |
MOD_Cter_Amidation | 404 | 407 | PF01082 | 0.713 |
MOD_GlcNHglycan | 1145 | 1149 | PF01048 | 0.601 |
MOD_GlcNHglycan | 1182 | 1185 | PF01048 | 0.702 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.409 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.411 |
MOD_GlcNHglycan | 560 | 563 | PF01048 | 0.384 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.356 |
MOD_GlcNHglycan | 717 | 720 | PF01048 | 0.506 |
MOD_GlcNHglycan | 723 | 727 | PF01048 | 0.407 |
MOD_GlcNHglycan | 841 | 845 | PF01048 | 0.506 |
MOD_GlcNHglycan | 853 | 856 | PF01048 | 0.307 |
MOD_GlcNHglycan | 917 | 920 | PF01048 | 0.467 |
MOD_GlcNHglycan | 927 | 931 | PF01048 | 0.379 |
MOD_GSK3_1 | 1035 | 1042 | PF00069 | 0.355 |
MOD_GSK3_1 | 1064 | 1071 | PF00069 | 0.506 |
MOD_GSK3_1 | 1122 | 1129 | PF00069 | 0.651 |
MOD_GSK3_1 | 1180 | 1187 | PF00069 | 0.598 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.421 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.208 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.605 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.542 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.426 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.488 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.601 |
MOD_GSK3_1 | 715 | 722 | PF00069 | 0.447 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.396 |
MOD_GSK3_1 | 730 | 737 | PF00069 | 0.287 |
MOD_GSK3_1 | 829 | 836 | PF00069 | 0.389 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.291 |
MOD_GSK3_1 | 911 | 918 | PF00069 | 0.502 |
MOD_GSK3_1 | 966 | 973 | PF00069 | 0.506 |
MOD_LATS_1 | 171 | 177 | PF00433 | 0.622 |
MOD_N-GLC_1 | 1032 | 1037 | PF02516 | 0.506 |
MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.506 |
MOD_N-GLC_1 | 188 | 193 | PF02516 | 0.593 |
MOD_N-GLC_1 | 205 | 210 | PF02516 | 0.468 |
MOD_N-GLC_1 | 271 | 276 | PF02516 | 0.530 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.463 |
MOD_N-GLC_1 | 743 | 748 | PF02516 | 0.506 |
MOD_N-GLC_1 | 963 | 968 | PF02516 | 0.506 |
MOD_NEK2_1 | 1014 | 1019 | PF00069 | 0.508 |
MOD_NEK2_1 | 1039 | 1044 | PF00069 | 0.396 |
MOD_NEK2_1 | 1066 | 1071 | PF00069 | 0.506 |
MOD_NEK2_1 | 1088 | 1093 | PF00069 | 0.506 |
MOD_NEK2_1 | 1104 | 1109 | PF00069 | 0.368 |
MOD_NEK2_1 | 1115 | 1120 | PF00069 | 0.395 |
MOD_NEK2_1 | 1144 | 1149 | PF00069 | 0.692 |
MOD_NEK2_1 | 1192 | 1197 | PF00069 | 0.771 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.350 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.577 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.594 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.495 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.512 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.549 |
MOD_NEK2_1 | 489 | 494 | PF00069 | 0.556 |
MOD_NEK2_1 | 596 | 601 | PF00069 | 0.611 |
MOD_NEK2_1 | 627 | 632 | PF00069 | 0.497 |
MOD_NEK2_1 | 734 | 739 | PF00069 | 0.506 |
MOD_NEK2_1 | 830 | 835 | PF00069 | 0.506 |
MOD_NEK2_1 | 840 | 845 | PF00069 | 0.341 |
MOD_NEK2_1 | 869 | 874 | PF00069 | 0.506 |
MOD_NEK2_1 | 911 | 916 | PF00069 | 0.506 |
MOD_NEK2_2 | 1194 | 1199 | PF00069 | 0.584 |
MOD_NEK2_2 | 546 | 551 | PF00069 | 0.533 |
MOD_NEK2_2 | 569 | 574 | PF00069 | 0.611 |
MOD_PIKK_1 | 1078 | 1084 | PF00454 | 0.506 |
MOD_PIKK_1 | 26 | 32 | PF00454 | 0.612 |
MOD_PIKK_1 | 279 | 285 | PF00454 | 0.607 |
MOD_PIKK_1 | 344 | 350 | PF00454 | 0.505 |
MOD_PIKK_1 | 692 | 698 | PF00454 | 0.506 |
MOD_PK_1 | 1124 | 1130 | PF00069 | 0.657 |
MOD_PKA_1 | 406 | 412 | PF00069 | 0.699 |
MOD_PKA_1 | 998 | 1004 | PF00069 | 0.506 |
MOD_PKA_2 | 1067 | 1073 | PF00069 | 0.506 |
MOD_PKA_2 | 1123 | 1129 | PF00069 | 0.490 |
MOD_PKA_2 | 1178 | 1184 | PF00069 | 0.726 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.699 |
MOD_PKA_2 | 586 | 592 | PF00069 | 0.611 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.506 |
MOD_PKA_2 | 998 | 1004 | PF00069 | 0.506 |
MOD_Plk_1 | 1035 | 1041 | PF00069 | 0.506 |
MOD_Plk_1 | 1051 | 1057 | PF00069 | 0.506 |
MOD_Plk_1 | 1104 | 1110 | PF00069 | 0.569 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.593 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.471 |
MOD_Plk_1 | 722 | 728 | PF00069 | 0.506 |
MOD_Plk_1 | 730 | 736 | PF00069 | 0.374 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.365 |
MOD_Plk_2-3 | 801 | 807 | PF00069 | 0.428 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.655 |
MOD_Plk_4 | 532 | 538 | PF00069 | 0.611 |
MOD_Plk_4 | 627 | 633 | PF00069 | 0.497 |
MOD_Plk_4 | 734 | 740 | PF00069 | 0.506 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.506 |
MOD_Plk_4 | 801 | 807 | PF00069 | 0.353 |
MOD_Plk_4 | 963 | 969 | PF00069 | 0.506 |
MOD_ProDKin_1 | 1089 | 1095 | PF00069 | 0.506 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.435 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.356 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.565 |
MOD_ProDKin_1 | 500 | 506 | PF00069 | 0.584 |
MOD_ProDKin_1 | 550 | 556 | PF00069 | 0.506 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.630 |
MOD_ProDKin_1 | 966 | 972 | PF00069 | 0.506 |
MOD_ProDKin_1 | 979 | 985 | PF00069 | 0.279 |
MOD_SUMO_rev_2 | 106 | 111 | PF00179 | 0.506 |
MOD_SUMO_rev_2 | 1086 | 1091 | PF00179 | 0.506 |
MOD_SUMO_rev_2 | 208 | 216 | PF00179 | 0.420 |
TRG_DiLeu_BaEn_2 | 377 | 383 | PF01217 | 0.611 |
TRG_DiLeu_BaEn_2 | 800 | 806 | PF01217 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 1137 | 1142 | PF01217 | 0.616 |
TRG_DiLeu_BaLyEn_6 | 1226 | 1231 | PF01217 | 0.731 |
TRG_DiLeu_BaLyEn_6 | 508 | 513 | PF01217 | 0.611 |
TRG_DiLeu_BaLyEn_6 | 782 | 787 | PF01217 | 0.506 |
TRG_DiLeu_LyEn_5 | 791 | 796 | PF01217 | 0.506 |
TRG_ENDOCYTIC_2 | 1111 | 1114 | PF00928 | 0.598 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.565 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.547 |
TRG_ENDOCYTIC_2 | 459 | 462 | PF00928 | 0.611 |
TRG_ENDOCYTIC_2 | 509 | 512 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 547 | 550 | PF00928 | 0.529 |
TRG_ENDOCYTIC_2 | 593 | 596 | PF00928 | 0.611 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.661 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 811 | 814 | PF00928 | 0.506 |
TRG_ER_diArg_1 | 104 | 107 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 1169 | 1171 | PF00400 | 0.744 |
TRG_ER_diArg_1 | 406 | 408 | PF00400 | 0.724 |
TRG_ER_diArg_1 | 704 | 706 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 873 | 875 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 991 | 993 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 998 | 1000 | PF00400 | 0.390 |
TRG_NES_CRM1_1 | 485 | 496 | PF08389 | 0.611 |
TRG_NES_CRM1_1 | 610 | 624 | PF08389 | 0.611 |
TRG_NLS_MonoCore_2 | 996 | 1001 | PF00514 | 0.506 |
TRG_NLS_MonoExtC_3 | 1167 | 1173 | PF00514 | 0.745 |
TRG_NLS_MonoExtN_4 | 1165 | 1172 | PF00514 | 0.728 |
TRG_NLS_MonoExtN_4 | 475 | 482 | PF00514 | 0.611 |
TRG_Pf-PMV_PEXEL_1 | 785 | 790 | PF00026 | 0.506 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P778 | Leptomonas seymouri | 85% | 100% |
A0A0N1HUJ9 | Leptomonas seymouri | 36% | 82% |
A0A0S4IZ11 | Bodo saltans | 35% | 83% |
A0A0S4JGE3 | Bodo saltans | 51% | 99% |
A0A1X0NR68 | Trypanosomatidae | 36% | 82% |
A0A1X0NUH3 | Trypanosomatidae | 70% | 100% |
A0A3Q8II93 | Leishmania donovani | 35% | 83% |
A0A3R7MTQ1 | Trypanosoma rangeli | 70% | 100% |
A0A3S7WTK8 | Leishmania donovani | 100% | 100% |
A0A422N9B0 | Trypanosoma rangeli | 36% | 85% |
A4H891 | Leishmania braziliensis | 94% | 100% |
A4HGT2 | Leishmania braziliensis | 35% | 100% |
A4I3V9 | Leishmania infantum | 35% | 99% |
C9ZXS6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 70% | 100% |
D0A926 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 85% |
D0A927 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 84% |
E9AQC1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
E9B049 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
O16140 | Bombyx mori | 34% | 80% |
O24308 | Pisum sativum | 33% | 85% |
O42130 | Gallus gallus | 33% | 80% |
O42131 | Gallus gallus | 32% | 76% |
O46374 | Sus scrofa | 32% | 81% |
O61078 | Leishmania chagasi | 99% | 100% |
O93794 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 32% | 88% |
P06786 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 87% |
P08096 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 83% |
P0C9C0 | African swine fever virus (isolate Tick/South Africa/Pretoriuskop Pr4/1996) | 24% | 100% |
P0C9C1 | African swine fever virus (isolate Warthog/Namibia/Wart80/1980) | 24% | 100% |
P0C9C2 | African swine fever virus (isolate Pig/Kenya/KEN-50/1950) | 26% | 100% |
P11388 | Homo sapiens | 32% | 81% |
P12531 | Trypanosoma brucei brucei | 70% | 100% |
P15348 | Drosophila melanogaster | 36% | 85% |
P27570 | Crithidia fasciculata | 86% | 100% |
P30182 | Arabidopsis thaliana | 35% | 84% |
P30190 | Trypanosoma cruzi | 70% | 100% |
P34203 | African swine fever virus (isolate Tick/Malawi/Lil 20-1/1983) | 25% | 100% |
P34534 | Caenorhabditis elegans | 32% | 100% |
P41001 | Plasmodium falciparum (isolate K1 / Thailand) | 33% | 88% |
P41515 | Cricetulus griseus | 32% | 81% |
P41516 | Rattus norvegicus | 32% | 81% |
P87078 | Candida albicans | 34% | 85% |
P90520 | Dictyostelium discoideum | 33% | 96% |
Q00942 | African swine fever virus (strain Badajoz 1971 Vero-adapted) | 25% | 100% |
Q01320 | Mus musculus | 32% | 81% |
Q01879 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 33% | 88% |
Q02880 | Homo sapiens | 32% | 76% |
Q196X4 | Invertebrate iridescent virus 3 | 30% | 100% |
Q23670 | Caenorhabditis elegans | 34% | 81% |
Q4Q836 | Leishmania major | 33% | 100% |
Q4QF53 | Leishmania major | 98% | 100% |
Q55BP5 | Dictyostelium discoideum | 37% | 81% |
Q5UQE6 | Acanthamoeba polyphaga mimivirus | 31% | 98% |
Q64399 | Cricetulus longicaudatus | 33% | 77% |
Q64511 | Mus musculus | 33% | 77% |
Q9QSK1 | Invertebrate iridescent virus 6 | 29% | 100% |
Q9Y8G8 | Penicillium chrysogenum | 32% | 78% |
V5B5B2 | Trypanosoma cruzi | 33% | 85% |
V5BUD4 | Trypanosoma cruzi | 71% | 100% |