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:0000428 | DNA-directed RNA polymerase complex | 4 | 12 |
GO:0005666 | RNA polymerase III complex | 4 | 2 |
GO:0030880 | RNA polymerase complex | 3 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0055029 | nuclear DNA-directed RNA polymerase complex | 3 | 2 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 12 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 12 |
GO:1902494 | catalytic complex | 2 | 12 |
GO:1990234 | transferase complex | 3 | 12 |
Related structures:
AlphaFold database: Q4QD43
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006351 | DNA-templated transcription | 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:0009058 | biosynthetic process | 2 | 12 |
GO:0009059 | macromolecule biosynthetic process | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0018130 | heterocycle biosynthetic process | 4 | 12 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 12 |
GO:0032774 | RNA biosynthetic process | 5 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044249 | cellular biosynthetic process | 3 | 12 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:0097659 | nucleic acid-templated transcription | 6 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 12 |
GO:1901576 | organic substance biosynthetic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0001882 | nucleoside binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003899 | DNA-directed 5'-3' RNA polymerase activity | 6 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016779 | nucleotidyltransferase activity | 4 | 12 |
GO:0032549 | ribonucleoside binding | 4 | 12 |
GO:0034062 | 5'-3' RNA polymerase activity | 5 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0097747 | RNA polymerase activity | 4 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 278 | 282 | PF00656 | 0.524 |
CLV_C14_Caspase3-7 | 402 | 406 | PF00656 | 0.514 |
CLV_C14_Caspase3-7 | 517 | 521 | PF00656 | 0.544 |
CLV_C14_Caspase3-7 | 957 | 961 | PF00656 | 0.503 |
CLV_C14_Caspase3-7 | 967 | 971 | PF00656 | 0.478 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.243 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.200 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 573 | 575 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 782 | 784 | PF00675 | 0.253 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.243 |
CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 573 | 575 | PF00082 | 0.253 |
CLV_PCSK_PC1ET2_1 | 289 | 291 | PF00082 | 0.339 |
CLV_PCSK_PC1ET2_1 | 369 | 371 | PF00082 | 0.253 |
CLV_PCSK_PC1ET2_1 | 439 | 441 | PF00082 | 0.444 |
CLV_PCSK_PC7_1 | 435 | 441 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.221 |
CLV_PCSK_SKI1_1 | 1028 | 1032 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.122 |
CLV_PCSK_SKI1_1 | 701 | 705 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 823 | 827 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 882 | 886 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 986 | 990 | PF00082 | 0.249 |
DEG_APCC_DBOX_1 | 150 | 158 | PF00400 | 0.464 |
DEG_APCC_DBOX_1 | 16 | 24 | PF00400 | 0.524 |
DEG_SCF_FBW7_2 | 493 | 500 | PF00400 | 0.453 |
DOC_CDC14_PxL_1 | 20 | 28 | PF14671 | 0.409 |
DOC_CKS1_1 | 92 | 97 | PF01111 | 0.539 |
DOC_CYCLIN_RxL_1 | 237 | 247 | PF00134 | 0.514 |
DOC_CYCLIN_RxL_1 | 259 | 269 | PF00134 | 0.488 |
DOC_CYCLIN_RxL_1 | 47 | 56 | PF00134 | 0.464 |
DOC_CYCLIN_RxL_1 | 937 | 949 | PF00134 | 0.478 |
DOC_MAPK_gen_1 | 1039 | 1047 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 118 | 126 | PF00069 | 0.539 |
DOC_MAPK_gen_1 | 128 | 137 | PF00069 | 0.539 |
DOC_MAPK_gen_1 | 218 | 224 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 337 | 345 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 573 | 584 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 601 | 609 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 783 | 789 | PF00069 | 0.464 |
DOC_MAPK_MEF2A_6 | 106 | 113 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 131 | 139 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 577 | 584 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 601 | 609 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 904 | 911 | PF00069 | 0.557 |
DOC_PP1_RVXF_1 | 260 | 266 | PF00149 | 0.488 |
DOC_PP2B_PxIxI_1 | 233 | 239 | PF00149 | 0.539 |
DOC_PP4_FxxP_1 | 1003 | 1006 | PF00568 | 0.453 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.373 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 615 | 619 | PF00917 | 0.409 |
DOC_USP7_MATH_2 | 1035 | 1041 | PF00917 | 0.464 |
DOC_USP7_MATH_2 | 802 | 808 | PF00917 | 0.557 |
DOC_USP7_UBL2_3 | 171 | 175 | PF12436 | 0.453 |
DOC_WW_Pin1_4 | 1127 | 1132 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 536 | 541 | PF00397 | 0.424 |
DOC_WW_Pin1_4 | 835 | 840 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 863 | 868 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.453 |
LIG_14-3-3_CanoR_1 | 1067 | 1075 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 1091 | 1095 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 1125 | 1129 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 227 | 236 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 391 | 401 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 428 | 438 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 445 | 455 | PF00244 | 0.218 |
LIG_14-3-3_CanoR_1 | 466 | 472 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 589 | 594 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 627 | 635 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 692 | 696 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 937 | 941 | PF00244 | 0.453 |
LIG_Actin_WH2_2 | 1110 | 1127 | PF00022 | 0.537 |
LIG_Actin_WH2_2 | 939 | 957 | PF00022 | 0.539 |
LIG_BRCT_BRCA1_1 | 1071 | 1075 | PF00533 | 0.453 |
LIG_Clathr_ClatBox_1 | 43 | 47 | PF01394 | 0.443 |
LIG_deltaCOP1_diTrp_1 | 333 | 341 | PF00928 | 0.453 |
LIG_EH1_1 | 344 | 352 | PF00400 | 0.453 |
LIG_EH1_1 | 409 | 417 | PF00400 | 0.478 |
LIG_eIF4E_1 | 1058 | 1064 | PF01652 | 0.453 |
LIG_eIF4E_1 | 1108 | 1114 | PF01652 | 0.453 |
LIG_FHA_1 | 1074 | 1080 | PF00498 | 0.514 |
LIG_FHA_1 | 1099 | 1105 | PF00498 | 0.539 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.460 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.514 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.539 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.520 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.443 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.299 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.514 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.537 |
LIG_FHA_1 | 539 | 545 | PF00498 | 0.438 |
LIG_FHA_1 | 546 | 552 | PF00498 | 0.216 |
LIG_FHA_1 | 590 | 596 | PF00498 | 0.522 |
LIG_FHA_1 | 638 | 644 | PF00498 | 0.518 |
LIG_FHA_1 | 662 | 668 | PF00498 | 0.385 |
LIG_FHA_1 | 704 | 710 | PF00498 | 0.502 |
LIG_FHA_1 | 715 | 721 | PF00498 | 0.441 |
LIG_FHA_1 | 883 | 889 | PF00498 | 0.445 |
LIG_FHA_1 | 992 | 998 | PF00498 | 0.478 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.453 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.514 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.529 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.457 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.440 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.453 |
LIG_FHA_2 | 537 | 543 | PF00498 | 0.437 |
LIG_FHA_2 | 628 | 634 | PF00498 | 0.463 |
LIG_FHA_2 | 663 | 669 | PF00498 | 0.350 |
LIG_FHA_2 | 736 | 742 | PF00498 | 0.453 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.514 |
LIG_Integrin_RGD_1 | 106 | 108 | PF01839 | 0.253 |
LIG_IRF3_LxIS_1 | 1064 | 1071 | PF10401 | 0.539 |
LIG_LIR_Gen_1 | 259 | 268 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 39 | 48 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 640 | 647 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 738 | 747 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 796 | 803 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 259 | 263 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 39 | 43 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 486 | 491 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 541 | 546 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 640 | 645 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 738 | 743 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 755 | 759 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 796 | 800 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 809 | 815 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 987 | 993 | PF02991 | 0.453 |
LIG_MAD2 | 882 | 890 | PF02301 | 0.473 |
LIG_NRBOX | 376 | 382 | PF00104 | 0.453 |
LIG_PCNA_yPIPBox_3 | 896 | 910 | PF02747 | 0.453 |
LIG_Pex14_2 | 341 | 345 | PF04695 | 0.539 |
LIG_PTB_Apo_2 | 365 | 372 | PF02174 | 0.453 |
LIG_SH2_CRK | 1009 | 1013 | PF00017 | 0.453 |
LIG_SH2_CRK | 546 | 550 | PF00017 | 0.266 |
LIG_SH2_CRK | 72 | 76 | PF00017 | 0.453 |
LIG_SH2_CRK | 830 | 834 | PF00017 | 0.484 |
LIG_SH2_CRK | 852 | 856 | PF00017 | 0.514 |
LIG_SH2_CRK | 990 | 994 | PF00017 | 0.453 |
LIG_SH2_GRB2like | 72 | 75 | PF00017 | 0.464 |
LIG_SH2_PTP2 | 642 | 645 | PF00017 | 0.539 |
LIG_SH2_SRC | 642 | 645 | PF00017 | 0.539 |
LIG_SH2_SRC | 72 | 75 | PF00017 | 0.539 |
LIG_SH2_STAP1 | 1108 | 1112 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 663 | 667 | PF00017 | 0.384 |
LIG_SH2_STAP1 | 830 | 834 | PF00017 | 0.539 |
LIG_SH2_STAP1 | 871 | 875 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 1001 | 1004 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 1094 | 1097 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 457 | 460 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 522 | 525 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 546 | 549 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 642 | 645 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 663 | 666 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 712 | 715 | PF00017 | 0.464 |
LIG_SH3_1 | 158 | 164 | PF00018 | 0.464 |
LIG_SH3_3 | 1101 | 1107 | PF00018 | 0.453 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.453 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.539 |
LIG_SH3_3 | 722 | 728 | PF00018 | 0.453 |
LIG_SH3_3 | 796 | 802 | PF00018 | 0.495 |
LIG_SH3_3 | 885 | 891 | PF00018 | 0.453 |
LIG_SH3_3 | 911 | 917 | PF00018 | 0.464 |
LIG_SH3_5 | 867 | 871 | PF00018 | 0.539 |
LIG_SUMO_SIM_anti_2 | 670 | 676 | PF11976 | 0.359 |
LIG_SUMO_SIM_anti_2 | 716 | 722 | PF11976 | 0.514 |
LIG_SUMO_SIM_par_1 | 134 | 141 | PF11976 | 0.453 |
LIG_SUMO_SIM_par_1 | 41 | 47 | PF11976 | 0.539 |
LIG_SUMO_SIM_par_1 | 514 | 520 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 605 | 611 | PF11976 | 0.494 |
LIG_TRAF2_1 | 150 | 153 | PF00917 | 0.478 |
LIG_TRAF2_1 | 94 | 97 | PF00917 | 0.539 |
LIG_TYR_ITIM | 1007 | 1012 | PF00017 | 0.305 |
LIG_TYR_ITIM | 544 | 549 | PF00017 | 0.374 |
LIG_TYR_ITIM | 70 | 75 | PF00017 | 0.305 |
LIG_TYR_ITIM | 988 | 993 | PF00017 | 0.305 |
LIG_TYR_ITSM | 638 | 645 | PF00017 | 0.231 |
LIG_UBA3_1 | 235 | 240 | PF00899 | 0.426 |
LIG_UBA3_1 | 381 | 387 | PF00899 | 0.305 |
LIG_UBA3_1 | 605 | 613 | PF00899 | 0.426 |
LIG_UBA3_1 | 943 | 950 | PF00899 | 0.305 |
LIG_WRC_WIRS_1 | 37 | 42 | PF05994 | 0.305 |
LIG_WRC_WIRS_1 | 976 | 981 | PF05994 | 0.426 |
MOD_CK1_1 | 1029 | 1035 | PF00069 | 0.305 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.246 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.297 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.357 |
MOD_CK1_1 | 583 | 589 | PF00069 | 0.338 |
MOD_CK1_1 | 936 | 942 | PF00069 | 0.305 |
MOD_CK1_1 | 968 | 974 | PF00069 | 0.418 |
MOD_CK1_1 | 991 | 997 | PF00069 | 0.305 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.340 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.305 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.369 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.311 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.305 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.305 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.305 |
MOD_CK2_1 | 662 | 668 | PF00069 | 0.374 |
MOD_CK2_1 | 735 | 741 | PF00069 | 0.305 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.305 |
MOD_GlcNHglycan | 1041 | 1044 | PF01048 | 0.305 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.450 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.408 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.305 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.305 |
MOD_GlcNHglycan | 617 | 620 | PF01048 | 0.466 |
MOD_GlcNHglycan | 689 | 692 | PF01048 | 0.310 |
MOD_GlcNHglycan | 696 | 699 | PF01048 | 0.297 |
MOD_GlcNHglycan | 756 | 759 | PF01048 | 0.305 |
MOD_GlcNHglycan | 806 | 809 | PF01048 | 0.380 |
MOD_GlcNHglycan | 967 | 970 | PF01048 | 0.397 |
MOD_GlcNHglycan | 990 | 993 | PF01048 | 0.318 |
MOD_GSK3_1 | 1022 | 1029 | PF00069 | 0.310 |
MOD_GSK3_1 | 1033 | 1040 | PF00069 | 0.294 |
MOD_GSK3_1 | 1069 | 1076 | PF00069 | 0.318 |
MOD_GSK3_1 | 1090 | 1097 | PF00069 | 0.434 |
MOD_GSK3_1 | 1120 | 1127 | PF00069 | 0.315 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.377 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.426 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.305 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.308 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.381 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.305 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.305 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.300 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.492 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.330 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.321 |
MOD_GSK3_1 | 729 | 736 | PF00069 | 0.426 |
MOD_N-GLC_1 | 196 | 201 | PF02516 | 0.406 |
MOD_N-GLC_1 | 305 | 310 | PF02516 | 0.443 |
MOD_N-GLC_1 | 53 | 58 | PF02516 | 0.305 |
MOD_N-GLC_1 | 551 | 556 | PF02516 | 0.321 |
MOD_N-GLC_1 | 645 | 650 | PF02516 | 0.426 |
MOD_N-GLC_1 | 687 | 692 | PF02516 | 0.321 |
MOD_N-GLC_1 | 767 | 772 | PF02516 | 0.362 |
MOD_N-GLC_2 | 1090 | 1092 | PF02516 | 0.445 |
MOD_N-GLC_2 | 649 | 651 | PF02516 | 0.305 |
MOD_NEK2_1 | 1120 | 1125 | PF00069 | 0.305 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.305 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.397 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.206 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.305 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.377 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.305 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.320 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.321 |
MOD_NEK2_1 | 572 | 577 | PF00069 | 0.293 |
MOD_NEK2_1 | 729 | 734 | PF00069 | 0.305 |
MOD_NEK2_1 | 735 | 740 | PF00069 | 0.305 |
MOD_NEK2_1 | 754 | 759 | PF00069 | 0.305 |
MOD_NEK2_1 | 946 | 951 | PF00069 | 0.321 |
MOD_NEK2_1 | 954 | 959 | PF00069 | 0.321 |
MOD_NEK2_2 | 213 | 218 | PF00069 | 0.321 |
MOD_NEK2_2 | 568 | 573 | PF00069 | 0.352 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.426 |
MOD_PIKK_1 | 275 | 281 | PF00454 | 0.321 |
MOD_PIKK_1 | 297 | 303 | PF00454 | 0.386 |
MOD_PIKK_1 | 446 | 452 | PF00454 | 0.381 |
MOD_PIKK_1 | 483 | 489 | PF00454 | 0.305 |
MOD_PIKK_1 | 509 | 515 | PF00454 | 0.305 |
MOD_PIKK_1 | 583 | 589 | PF00454 | 0.369 |
MOD_PIKK_1 | 970 | 976 | PF00454 | 0.363 |
MOD_PK_1 | 218 | 224 | PF00069 | 0.426 |
MOD_PKA_1 | 218 | 224 | PF00069 | 0.426 |
MOD_PKA_1 | 290 | 296 | PF00069 | 0.321 |
MOD_PKA_1 | 403 | 409 | PF00069 | 0.321 |
MOD_PKA_1 | 475 | 481 | PF00069 | 0.305 |
MOD_PKA_2 | 1022 | 1028 | PF00069 | 0.321 |
MOD_PKA_2 | 1090 | 1096 | PF00069 | 0.402 |
MOD_PKA_2 | 1124 | 1130 | PF00069 | 0.315 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.426 |
MOD_PKA_2 | 453 | 459 | PF00069 | 0.305 |
MOD_PKA_2 | 572 | 578 | PF00069 | 0.312 |
MOD_PKA_2 | 691 | 697 | PF00069 | 0.305 |
MOD_PKA_2 | 936 | 942 | PF00069 | 0.305 |
MOD_PKA_2 | 954 | 960 | PF00069 | 0.305 |
MOD_PKB_1 | 625 | 633 | PF00069 | 0.536 |
MOD_PKB_1 | 99 | 107 | PF00069 | 0.305 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.305 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.308 |
MOD_Plk_1 | 767 | 773 | PF00069 | 0.362 |
MOD_Plk_1 | 871 | 877 | PF00069 | 0.306 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.402 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.390 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.305 |
MOD_Plk_4 | 373 | 379 | PF00069 | 0.305 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.294 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.350 |
MOD_Plk_4 | 670 | 676 | PF00069 | 0.343 |
MOD_Plk_4 | 714 | 720 | PF00069 | 0.305 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.291 |
MOD_ProDKin_1 | 536 | 542 | PF00069 | 0.422 |
MOD_ProDKin_1 | 835 | 841 | PF00069 | 0.313 |
MOD_ProDKin_1 | 863 | 869 | PF00069 | 0.338 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.305 |
MOD_SUMO_rev_2 | 127 | 132 | PF00179 | 0.324 |
MOD_SUMO_rev_2 | 432 | 441 | PF00179 | 0.407 |
MOD_SUMO_rev_2 | 55 | 63 | PF00179 | 0.335 |
MOD_SUMO_rev_2 | 872 | 881 | PF00179 | 0.305 |
TRG_DiLeu_BaEn_1 | 174 | 179 | PF01217 | 0.305 |
TRG_DiLeu_BaEn_1 | 269 | 274 | PF01217 | 0.468 |
TRG_DiLeu_BaEn_1 | 500 | 505 | PF01217 | 0.305 |
TRG_DiLeu_BaEn_1 | 670 | 675 | PF01217 | 0.361 |
TRG_DiLeu_BaEn_4 | 269 | 275 | PF01217 | 0.426 |
TRG_DiLeu_BaLyEn_6 | 1064 | 1069 | PF01217 | 0.305 |
TRG_DiLeu_BaLyEn_6 | 601 | 606 | PF01217 | 0.426 |
TRG_DiLeu_LyEn_5 | 269 | 274 | PF01217 | 0.363 |
TRG_ENDOCYTIC_2 | 1001 | 1004 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 1009 | 1012 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 342 | 345 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 546 | 549 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 642 | 645 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 740 | 743 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 830 | 833 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 990 | 993 | PF00928 | 0.305 |
TRG_ER_diArg_1 | 572 | 574 | PF00400 | 0.305 |
TRG_ER_diArg_1 | 588 | 591 | PF00400 | 0.426 |
TRG_NES_CRM1_1 | 1115 | 1129 | PF08389 | 0.426 |
TRG_NES_CRM1_1 | 633 | 647 | PF08389 | 0.402 |
TRG_Pf-PMV_PEXEL_1 | 187 | 191 | PF00026 | 0.305 |
TRG_Pf-PMV_PEXEL_1 | 413 | 417 | PF00026 | 0.305 |
TRG_Pf-PMV_PEXEL_1 | 50 | 55 | PF00026 | 0.321 |
TRG_Pf-PMV_PEXEL_1 | 873 | 878 | PF00026 | 0.426 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4S3 | Leptomonas seymouri | 94% | 100% |
A0A0N1PFE3 | Leptomonas seymouri | 35% | 95% |
A0A0S4IQ42 | Bodo saltans | 75% | 100% |
A0A0S4J556 | Bodo saltans | 34% | 97% |
A0A1X0NKP7 | Trypanosomatidae | 34% | 94% |
A0A1X0NXA3 | Trypanosomatidae | 79% | 100% |
A0A3R7N5U9 | Trypanosoma rangeli | 34% | 95% |
A0A3S7WVP1 | Leishmania donovani | 99% | 100% |
A0A3S7X436 | Leishmania donovani | 35% | 96% |
A0A422N812 | Trypanosoma rangeli | 79% | 100% |
A2RML9 | Lactococcus lactis subsp. cremoris (strain MG1363) | 26% | 95% |
A4HBG9 | Leishmania braziliensis | 96% | 100% |
A4HIZ1 | Leishmania braziliensis | 35% | 96% |
A4I6A8 | Leishmania infantum | 35% | 96% |
A5DHT2 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 33% | 92% |
A6MMT6 | Illicium oligandrum | 24% | 100% |
A8F4G0 | Pseudothermotoga lettingae (strain ATCC BAA-301 / DSM 14385 / NBRC 107922 / TMO) | 25% | 97% |
A8F976 | Bacillus pumilus (strain SAFR-032) | 25% | 95% |
A8YXJ8 | Lactobacillus helveticus (strain DPC 4571) | 26% | 93% |
B1HMZ6 | Lysinibacillus sphaericus (strain C3-41) | 26% | 95% |
B8JKD7 | Danio rerio | 28% | 100% |
B8YB55 | Saccharolobus shibatae | 34% | 100% |
C9ZHX4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 78% | 100% |
C9ZN35 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 95% |
E9AGT7 | Leishmania infantum | 99% | 100% |
E9AUE0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
E9B1G4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 96% |
F4I366 | Arabidopsis thaliana | 26% | 96% |
F4KD38 | Arabidopsis thaliana | 46% | 98% |
O57230 | Vaccinia virus (strain Ankara) | 24% | 98% |
O74633 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 27% | 92% |
P08266 | Drosophila melanogaster | 34% | 96% |
P08518 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 92% |
P0C8K2 | African swine fever virus (isolate Pig/Kenya/KEN-50/1950) | 24% | 91% |
P0C8K3 | African swine fever virus (isolate Tick/Malawi/Lil 20-1/1983) | 24% | 91% |
P0C8K4 | African swine fever virus (isolate Tick/South Africa/Pretoriuskop Pr4/1996) | 24% | 91% |
P0C8K5 | African swine fever virus (isolate Warthog/Namibia/Wart80/1980) | 24% | 91% |
P0DST3 | Variola virus (isolate Human/India/Ind3/1967) | 24% | 97% |
P0DST4 | Variola virus | 24% | 97% |
P11513 | Sulfolobus acidocaldarius (strain ATCC 33909 / DSM 639 / JCM 8929 / NBRC 15157 / NCIMB 11770) | 34% | 100% |
P16716 | Sheeppox virus (strain KS-1) | 25% | 100% |
P17474 | Cowpox virus (strain Brighton Red) | 24% | 97% |
P20028 | Drosophila melanogaster | 26% | 100% |
P22138 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 94% |
P22276 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 48% | 99% |
P22703 | Nostoc sp. (strain PCC 7120 / SAG 25.82 / UTEX 2576) | 26% | 100% |
P25167 | Drosophila melanogaster | 46% | 100% |
P28365 | Euplotoides octocarinatus | 28% | 97% |
P30876 | Homo sapiens | 34% | 96% |
P31814 | Thermococcus celer | 36% | 100% |
P38420 | Arabidopsis thaliana | 35% | 95% |
P42487 | African swine fever virus (strain Badajoz 1971 Vero-adapted) | 24% | 91% |
P59470 | Mus musculus | 49% | 100% |
P59642 | Tropheryma whipplei (strain TW08/27) | 23% | 98% |
P59643 | Tropheryma whipplei | 23% | 98% |
P68694 | Vaccinia virus (strain Copenhagen) | 24% | 97% |
P70700 | Mus musculus | 29% | 100% |
Q02061 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 94% |
Q02X59 | Lactococcus lactis subsp. cremoris (strain SK11) | 26% | 95% |
Q03587 | Thermoplasma acidophilum (strain ATCC 25905 / DSM 1728 / JCM 9062 / NBRC 15155 / AMRC-C165) | 33% | 95% |
Q04C22 | Lactobacillus delbrueckii subsp. bulgaricus (strain ATCC BAA-365 / Lb-18) | 27% | 93% |
Q0P3M6 | Ostreococcus tauri | 24% | 100% |
Q10233 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 49% | 97% |
Q10578 | Caenorhabditis elegans | 34% | 95% |
Q197F1 | Invertebrate iridescent virus 3 | 30% | 99% |
Q1GBM5 | Lactobacillus delbrueckii subsp. bulgaricus (strain ATCC 11842 / DSM 20081 / BCRC 10696 / JCM 1002 / NBRC 13953 / NCIMB 11778 / NCTC 12712 / WDCM 00102 / Lb 14) | 27% | 93% |
Q3M5D0 | Trichormus variabilis (strain ATCC 29413 / PCC 7937) | 26% | 100% |
Q42877 | Solanum lycopersicum | 35% | 95% |
Q4Q6P8 | Leishmania major | 34% | 100% |
Q54BM1 | Dictyostelium discoideum | 27% | 100% |
Q54J75 | Dictyostelium discoideum | 34% | 97% |
Q5FM97 | Lactobacillus acidophilus (strain ATCC 700396 / NCK56 / N2 / NCFM) | 26% | 93% |
Q5REE8 | Pongo abelii | 30% | 100% |
Q5WLS0 | Alkalihalobacillus clausii (strain KSM-K16) | 25% | 96% |
Q6FLD5 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 34% | 93% |
Q6GZR3 | Frog virus 3 (isolate Goorha) | 29% | 93% |
Q6RZF8 | Rabbitpox virus (strain Utrecht) | 24% | 97% |
Q753Q4 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 33% | 93% |
Q75DS1 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 28% | 95% |
Q76ZP7 | Vaccinia virus (strain Western Reserve) | 24% | 97% |
Q775Q3 | Camelpox virus (strain CMS) | 24% | 97% |
Q7T6X7 | Acanthamoeba polyphaga mimivirus | 30% | 95% |
Q80DV1 | Cowpox virus (strain GRI-90 / Grishak) | 24% | 97% |
Q8CFI7 | Mus musculus | 34% | 96% |
Q8JL90 | Ectromelia virus (strain Moscow) | 24% | 97% |
Q8SR75 | Encephalitozoon cuniculi (strain GB-M1) | 35% | 99% |
Q8V2N1 | Camelpox virus (strain M-96) | 24% | 97% |
Q8V4V3 | Monkeypox virus (strain Zaire-96-I-16) | 24% | 97% |
Q91F97 | Invertebrate iridescent virus 6 | 29% | 95% |
Q93GF2 | Tropheryma whipplei (strain Twist) | 23% | 98% |
Q980R1 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 34% | 100% |
Q9CEN6 | Lactococcus lactis subsp. lactis (strain IL1403) | 26% | 95% |
Q9H9Y6 | Homo sapiens | 29% | 100% |
Q9J544 | Fowlpox virus (strain NVSL) | 23% | 98% |
Q9JF79 | Vaccinia virus (strain Tian Tan) | 24% | 97% |
Q9LK40 | Arabidopsis thaliana | 30% | 97% |
Q9LV32 | Arabidopsis thaliana | 31% | 100% |
Q9NW08 | Homo sapiens | 49% | 100% |
Q9P7X8 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 96% |
V5AYL6 | Trypanosoma cruzi | 33% | 95% |
V5BAG3 | Trypanosoma cruzi | 79% | 100% |