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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005739 | mitochondrion | 5 | 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: A4IDG7
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006259 | DNA metabolic process | 4 | 11 |
GO:0006281 | DNA repair | 5 | 11 |
GO:0006298 | mismatch repair | 6 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0006950 | response to stress | 2 | 11 |
GO:0006974 | DNA damage response | 4 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0033554 | cellular response to stress | 3 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0050896 | response to stimulus | 1 | 11 |
GO:0051716 | cellular response to stimulus | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:0032042 | mitochondrial DNA metabolic process | 5 | 1 |
GO:0043504 | mitochondrial DNA repair | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003677 | DNA binding | 4 | 11 |
GO:0003690 | double-stranded DNA binding | 5 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0030983 | mismatched DNA binding | 6 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 11 |
GO:0140299 | small molecule sensor activity | 1 | 11 |
GO:0140612 | DNA damage sensor activity | 2 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:0140664 | ATP-dependent DNA damage sensor activity | 3 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 229 | 233 | PF00656 | 0.460 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 264 | 266 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 608 | 610 | PF00675 | 0.342 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.261 |
CLV_PCSK_KEX2_1 | 459 | 461 | PF00082 | 0.261 |
CLV_PCSK_KEX2_1 | 563 | 565 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 608 | 610 | PF00082 | 0.342 |
CLV_PCSK_PC1ET2_1 | 221 | 223 | PF00082 | 0.645 |
CLV_PCSK_PC1ET2_1 | 459 | 461 | PF00082 | 0.261 |
CLV_PCSK_PC1ET2_1 | 563 | 565 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.685 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 527 | 531 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 628 | 632 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 653 | 657 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 673 | 677 | PF00082 | 0.128 |
CLV_PCSK_SKI1_1 | 771 | 775 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 815 | 819 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 903 | 907 | PF00082 | 0.364 |
DEG_ODPH_VHL_1 | 172 | 183 | PF01847 | 0.537 |
DEG_SCF_TRCP1_1 | 342 | 348 | PF00400 | 0.667 |
DEG_SPOP_SBC_1 | 584 | 588 | PF00917 | 0.541 |
DOC_ANK_TNKS_1 | 943 | 950 | PF00023 | 0.481 |
DOC_CKS1_1 | 149 | 154 | PF01111 | 0.461 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 438 | 447 | PF00134 | 0.564 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 506 | 513 | PF00134 | 0.541 |
DOC_CYCLIN_yCln2_LP_2 | 799 | 805 | PF00134 | 0.564 |
DOC_MAPK_FxFP_2 | 15 | 18 | PF00069 | 0.565 |
DOC_MAPK_gen_1 | 367 | 375 | PF00069 | 0.381 |
DOC_MAPK_gen_1 | 459 | 469 | PF00069 | 0.564 |
DOC_MAPK_gen_1 | 506 | 513 | PF00069 | 0.489 |
DOC_MAPK_gen_1 | 53 | 62 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 506 | 513 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 55 | 63 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 628 | 637 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 788 | 796 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 828 | 837 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 968 | 976 | PF00069 | 0.475 |
DOC_PP2B_LxvP_1 | 579 | 582 | PF13499 | 0.564 |
DOC_PP4_FxxP_1 | 15 | 18 | PF00568 | 0.565 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 558 | 562 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 574 | 578 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 781 | 785 | PF00917 | 0.461 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 580 | 585 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 641 | 646 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 808 | 813 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 905 | 910 | PF00397 | 0.554 |
LIG_14-3-3_CanoR_1 | 236 | 245 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 412 | 418 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 420 | 428 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 653 | 659 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 700 | 708 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 731 | 740 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 860 | 870 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 903 | 909 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 942 | 947 | PF00244 | 0.411 |
LIG_BRCT_BRCA1_1 | 11 | 15 | PF00533 | 0.503 |
LIG_BRCT_BRCA1_1 | 280 | 284 | PF00533 | 0.522 |
LIG_BRCT_BRCA1_1 | 471 | 475 | PF00533 | 0.499 |
LIG_BRCT_BRCA1_1 | 942 | 946 | PF00533 | 0.541 |
LIG_Clathr_ClatBox_1 | 630 | 634 | PF01394 | 0.513 |
LIG_CtBP_PxDLS_1 | 777 | 783 | PF00389 | 0.461 |
LIG_deltaCOP1_diTrp_1 | 109 | 114 | PF00928 | 0.461 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.501 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.400 |
LIG_FHA_1 | 592 | 598 | PF00498 | 0.479 |
LIG_FHA_1 | 787 | 793 | PF00498 | 0.461 |
LIG_FHA_1 | 830 | 836 | PF00498 | 0.460 |
LIG_FHA_1 | 838 | 844 | PF00498 | 0.461 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.411 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.461 |
LIG_FHA_2 | 277 | 283 | PF00498 | 0.547 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.469 |
LIG_FHA_2 | 554 | 560 | PF00498 | 0.564 |
LIG_FHA_2 | 669 | 675 | PF00498 | 0.537 |
LIG_FHA_2 | 732 | 738 | PF00498 | 0.603 |
LIG_FHA_2 | 804 | 810 | PF00498 | 0.541 |
LIG_LIR_Apic_2 | 12 | 18 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 1009 | 1014 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 109 | 116 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 311 | 319 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 468 | 478 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 54 | 63 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 73 | 79 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 814 | 825 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 831 | 841 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 891 | 902 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 1009 | 1014 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 109 | 113 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 14 | 20 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 311 | 316 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 46 | 52 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 468 | 473 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 477 | 481 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 54 | 60 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 696 | 701 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 726 | 732 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 73 | 77 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 814 | 820 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 831 | 837 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 891 | 897 | PF02991 | 0.461 |
LIG_LRP6_Inhibitor_1 | 1007 | 1013 | PF00058 | 0.358 |
LIG_LYPXL_SIV_4 | 589 | 597 | PF13949 | 0.495 |
LIG_LYPXL_yS_3 | 17 | 20 | PF13949 | 0.504 |
LIG_LYPXL_yS_3 | 729 | 732 | PF13949 | 0.447 |
LIG_NRBOX | 237 | 243 | PF00104 | 0.425 |
LIG_NRBOX | 547 | 553 | PF00104 | 0.541 |
LIG_PDZ_Class_2 | 1009 | 1014 | PF00595 | 0.583 |
LIG_Pex14_1 | 110 | 114 | PF04695 | 0.449 |
LIG_Pex14_1 | 525 | 529 | PF04695 | 0.541 |
LIG_Pex14_2 | 15 | 19 | PF04695 | 0.493 |
LIG_Pex14_2 | 698 | 702 | PF04695 | 0.541 |
LIG_Pex14_2 | 924 | 928 | PF04695 | 0.411 |
LIG_PTAP_UEV_1 | 24 | 29 | PF05743 | 0.561 |
LIG_PTB_Apo_2 | 77 | 84 | PF02174 | 0.533 |
LIG_PTB_Apo_2 | 951 | 958 | PF02174 | 0.509 |
LIG_Rb_pABgroove_1 | 563 | 571 | PF01858 | 0.513 |
LIG_REV1ctd_RIR_1 | 60 | 69 | PF16727 | 0.475 |
LIG_SH2_CRK | 227 | 231 | PF00017 | 0.411 |
LIG_SH2_CRK | 441 | 445 | PF00017 | 0.564 |
LIG_SH2_CRK | 57 | 61 | PF00017 | 0.489 |
LIG_SH2_CRK | 74 | 78 | PF00017 | 0.420 |
LIG_SH2_CRK | 894 | 898 | PF00017 | 0.461 |
LIG_SH2_CRK | 959 | 963 | PF00017 | 0.475 |
LIG_SH2_NCK_1 | 590 | 594 | PF00017 | 0.411 |
LIG_SH2_PTP2 | 498 | 501 | PF00017 | 0.541 |
LIG_SH2_PTP2 | 834 | 837 | PF00017 | 0.475 |
LIG_SH2_SRC | 38 | 41 | PF00017 | 0.566 |
LIG_SH2_SRC | 498 | 501 | PF00017 | 0.541 |
LIG_SH2_STAP1 | 331 | 335 | PF00017 | 0.451 |
LIG_SH2_STAP1 | 365 | 369 | PF00017 | 0.519 |
LIG_SH2_STAP1 | 72 | 76 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 660 | 663 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 710 | 713 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 834 | 837 | PF00017 | 0.475 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.476 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.460 |
LIG_SH3_3 | 724 | 730 | PF00018 | 0.485 |
LIG_SH3_3 | 880 | 886 | PF00018 | 0.491 |
LIG_SUMO_SIM_anti_2 | 145 | 151 | PF11976 | 0.475 |
LIG_SUMO_SIM_anti_2 | 381 | 387 | PF11976 | 0.461 |
LIG_SUMO_SIM_anti_2 | 739 | 744 | PF11976 | 0.435 |
LIG_SUMO_SIM_anti_2 | 973 | 978 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 145 | 151 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 771 | 776 | PF11976 | 0.374 |
LIG_SUMO_SIM_par_1 | 885 | 892 | PF11976 | 0.461 |
LIG_TRAF2_1 | 430 | 433 | PF00917 | 0.426 |
LIG_TRAF2_1 | 573 | 576 | PF00917 | 0.541 |
LIG_TRAF2_1 | 935 | 938 | PF00917 | 0.481 |
LIG_TYR_ITIM | 727 | 732 | PF00017 | 0.482 |
LIG_UBA3_1 | 241 | 248 | PF00899 | 0.415 |
LIG_UBA3_1 | 748 | 756 | PF00899 | 0.540 |
LIG_WRC_WIRS_1 | 312 | 317 | PF05994 | 0.499 |
MOD_CDK_SPxxK_3 | 808 | 815 | PF00069 | 0.541 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.564 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.621 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.503 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.497 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.523 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.478 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.499 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.489 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.456 |
MOD_CK1_1 | 583 | 589 | PF00069 | 0.512 |
MOD_CK1_1 | 689 | 695 | PF00069 | 0.572 |
MOD_CK1_1 | 848 | 854 | PF00069 | 0.558 |
MOD_CK1_1 | 950 | 956 | PF00069 | 0.516 |
MOD_CK1_1 | 996 | 1002 | PF00069 | 0.568 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.461 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.509 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.347 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.532 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.432 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.475 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.475 |
MOD_CK2_1 | 553 | 559 | PF00069 | 0.564 |
MOD_CK2_1 | 660 | 666 | PF00069 | 0.510 |
MOD_CK2_1 | 668 | 674 | PF00069 | 0.516 |
MOD_CK2_1 | 731 | 737 | PF00069 | 0.593 |
MOD_CK2_1 | 803 | 809 | PF00069 | 0.519 |
MOD_Cter_Amidation | 409 | 412 | PF01082 | 0.261 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.482 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.489 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.644 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.513 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.616 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.629 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.291 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.331 |
MOD_GlcNHglycan | 575 | 579 | PF01048 | 0.268 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.253 |
MOD_GlcNHglycan | 702 | 705 | PF01048 | 0.364 |
MOD_GlcNHglycan | 845 | 848 | PF01048 | 0.341 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.682 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.550 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.513 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.516 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.477 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.469 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.528 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.431 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.580 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.491 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.540 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.534 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.470 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.529 |
MOD_GSK3_1 | 702 | 709 | PF00069 | 0.328 |
MOD_GSK3_1 | 782 | 789 | PF00069 | 0.461 |
MOD_GSK3_1 | 885 | 892 | PF00069 | 0.533 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.574 |
MOD_GSK3_1 | 901 | 908 | PF00069 | 0.417 |
MOD_GSK3_1 | 989 | 996 | PF00069 | 0.524 |
MOD_N-GLC_1 | 490 | 495 | PF02516 | 0.295 |
MOD_N-GLC_1 | 761 | 766 | PF02516 | 0.340 |
MOD_N-GLC_2 | 399 | 401 | PF02516 | 0.275 |
MOD_N-GLC_2 | 403 | 405 | PF02516 | 0.247 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.391 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.558 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.613 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.475 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.522 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.531 |
MOD_NEK2_1 | 668 | 673 | PF00069 | 0.575 |
MOD_NEK2_1 | 702 | 707 | PF00069 | 0.537 |
MOD_NEK2_1 | 773 | 778 | PF00069 | 0.334 |
MOD_NEK2_1 | 786 | 791 | PF00069 | 0.441 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.515 |
MOD_NEK2_2 | 829 | 834 | PF00069 | 0.475 |
MOD_NEK2_2 | 871 | 876 | PF00069 | 0.513 |
MOD_PIKK_1 | 490 | 496 | PF00454 | 0.496 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.512 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.374 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.526 |
MOD_PKA_2 | 859 | 865 | PF00069 | 0.461 |
MOD_PKA_2 | 996 | 1002 | PF00069 | 0.568 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.461 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.597 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.397 |
MOD_Plk_1 | 673 | 679 | PF00069 | 0.564 |
MOD_Plk_1 | 761 | 767 | PF00069 | 0.446 |
MOD_Plk_2-3 | 282 | 288 | PF00069 | 0.486 |
MOD_Plk_2-3 | 394 | 400 | PF00069 | 0.541 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.595 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.468 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.622 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.435 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.518 |
MOD_Plk_4 | 682 | 688 | PF00069 | 0.529 |
MOD_Plk_4 | 706 | 712 | PF00069 | 0.475 |
MOD_Plk_4 | 782 | 788 | PF00069 | 0.461 |
MOD_Plk_4 | 829 | 835 | PF00069 | 0.461 |
MOD_Plk_4 | 885 | 891 | PF00069 | 0.531 |
MOD_Plk_4 | 980 | 986 | PF00069 | 0.513 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.486 |
MOD_ProDKin_1 | 580 | 586 | PF00069 | 0.518 |
MOD_ProDKin_1 | 641 | 647 | PF00069 | 0.541 |
MOD_ProDKin_1 | 808 | 814 | PF00069 | 0.541 |
MOD_ProDKin_1 | 905 | 911 | PF00069 | 0.554 |
MOD_SUMO_for_1 | 220 | 223 | PF00179 | 0.664 |
MOD_SUMO_for_1 | 926 | 929 | PF00179 | 0.541 |
MOD_SUMO_for_1 | 990 | 993 | PF00179 | 0.564 |
MOD_SUMO_rev_2 | 202 | 209 | PF00179 | 0.691 |
MOD_SUMO_rev_2 | 46 | 54 | PF00179 | 0.475 |
TRG_DiLeu_BaEn_1 | 575 | 580 | PF01217 | 0.542 |
TRG_DiLeu_BaEn_1 | 769 | 774 | PF01217 | 0.476 |
TRG_DiLeu_BaEn_2 | 432 | 438 | PF01217 | 0.428 |
TRG_DiLeu_BaLyEn_6 | 748 | 753 | PF01217 | 0.478 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 729 | 732 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 834 | 837 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 894 | 897 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 921 | 924 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 959 | 962 | PF00928 | 0.475 |
TRG_ER_diArg_1 | 192 | 194 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 367 | 369 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 411 | 413 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 607 | 609 | PF00400 | 0.542 |
TRG_NES_CRM1_1 | 307 | 321 | PF08389 | 0.503 |
TRG_NES_CRM1_1 | 465 | 479 | PF08389 | 0.564 |
TRG_Pf-PMV_PEXEL_1 | 144 | 148 | PF00026 | 0.261 |
TRG_Pf-PMV_PEXEL_1 | 609 | 613 | PF00026 | 0.322 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6K5 | Leptomonas seymouri | 66% | 98% |
A0A0S4IMQ7 | Bodo saltans | 40% | 100% |
A0A0S4J224 | Bodo saltans | 26% | 100% |
A0A3Q8IK49 | Leishmania donovani | 100% | 100% |
A0A3R7LRN7 | Trypanosoma rangeli | 47% | 100% |
A0L7L5 | Magnetococcus marinus (strain ATCC BAA-1437 / JCM 17883 / MC-1) | 28% | 100% |
A0LG76 | Syntrophobacter fumaroxidans (strain DSM 10017 / MPOB) | 26% | 100% |
A0Q809 | Francisella tularensis subsp. novicida (strain U112) | 22% | 100% |
A1DCB2 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 26% | 91% |
A1K764 | Azoarcus sp. (strain BH72) | 25% | 100% |
A1R0M2 | Borrelia turicatae (strain 91E135) | 25% | 100% |
A1U2E8 | Marinobacter nauticus (strain ATCC 700491 / DSM 11845 / VT8) | 25% | 100% |
A1UU95 | Bartonella bacilliformis (strain ATCC 35685 / NCTC 12138 / KC583) | 25% | 100% |
A3PNR5 | Cereibacter sphaeroides (strain ATCC 17029 / ATH 2.4.9) | 26% | 100% |
A4HL76 | Leishmania braziliensis | 26% | 100% |
A4HP61 | Leishmania braziliensis | 85% | 100% |
A4IXL2 | Francisella tularensis subsp. tularensis (strain WY96-3418) | 22% | 100% |
A4SFT1 | Chlorobium phaeovibrioides (strain DSM 265 / 1930) | 26% | 100% |
A5VN83 | Brucella ovis (strain ATCC 25840 / 63/290 / NCTC 10512) | 25% | 100% |
A6LLR1 | Thermosipho melanesiensis (strain DSM 12029 / CIP 104789 / BI429) | 26% | 100% |
A6TD24 | Klebsiella pneumoniae subsp. pneumoniae (strain ATCC 700721 / MGH 78578) | 27% | 100% |
A6ZTR3 | Saccharomyces cerevisiae (strain YJM789) | 23% | 100% |
A7N9Y6 | Francisella tularensis subsp. holarctica (strain FTNF002-00 / FTA) | 22% | 100% |
A8F753 | Pseudothermotoga lettingae (strain ATCC BAA-301 / DSM 14385 / NBRC 107922 / TMO) | 25% | 100% |
A8I275 | Azorhizobium caulinodans (strain ATCC 43989 / DSM 5975 / JCM 20966 / LMG 6465 / NBRC 14845 / NCIMB 13405 / ORS 571) | 27% | 100% |
A8ZXH5 | Desulfococcus oleovorans (strain DSM 6200 / JCM 39069 / Hxd3) | 25% | 100% |
A9ILT1 | Bartonella tribocorum (strain CIP 105476 / IBS 506) | 25% | 100% |
A9KG24 | Coxiella burnetii (strain Dugway 5J108-111) | 24% | 100% |
A9KL10 | Lachnoclostridium phytofermentans (strain ATCC 700394 / DSM 18823 / ISDg) | 24% | 100% |
A9M792 | Brucella canis (strain ATCC 23365 / NCTC 10854) | 25% | 100% |
A9MF43 | Salmonella arizonae (strain ATCC BAA-731 / CDC346-86 / RSK2980) | 26% | 100% |
A9N1F8 | Salmonella paratyphi B (strain ATCC BAA-1250 / SPB7) | 26% | 100% |
A9NCN3 | Coxiella burnetii (strain RSA 331 / Henzerling II) | 24% | 100% |
A9WFZ9 | Chloroflexus aurantiacus (strain ATCC 29366 / DSM 635 / J-10-fl) | 28% | 100% |
B0CIQ5 | Brucella suis (strain ATCC 23445 / NCTC 10510) | 26% | 100% |
B0TX99 | Francisella philomiragia subsp. philomiragia (strain ATCC 25017 / FSC 153 / O#319-036) | 21% | 100% |
B0YCF6 | Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) | 26% | 90% |
B1N025 | Leuconostoc citreum (strain KM20) | 26% | 100% |
B2SEQ6 | Francisella tularensis subsp. mediasiatica (strain FSC147) | 22% | 100% |
B3EEE1 | Chlorobium limicola (strain DSM 245 / NBRC 103803 / 6330) | 26% | 100% |
B3EP11 | Chlorobium phaeobacteroides (strain BS1) | 26% | 100% |
B3H2J9 | Actinobacillus pleuropneumoniae serotype 7 (strain AP76) | 25% | 100% |
B3QPY5 | Chlorobaculum parvum (strain DSM 263 / NCIMB 8327) | 27% | 100% |
B4T436 | Salmonella newport (strain SL254) | 26% | 100% |
B4TFU6 | Salmonella heidelberg (strain SL476) | 26% | 100% |
B4TTU0 | Salmonella schwarzengrund (strain CVM19633) | 26% | 100% |
B5EA63 | Citrifermentans bemidjiense (strain ATCC BAA-1014 / DSM 16622 / JCM 12645 / Bem) | 25% | 100% |
B5F3Y8 | Salmonella agona (strain SL483) | 26% | 100% |
B5RDN2 | Salmonella gallinarum (strain 287/91 / NCTC 13346) | 26% | 100% |
B5XV49 | Klebsiella pneumoniae (strain 342) | 27% | 100% |
B9K800 | Thermotoga neapolitana (strain ATCC 49049 / DSM 4359 / NBRC 107923 / NS-E) | 25% | 100% |
B9LB04 | Chloroflexus aurantiacus (strain ATCC 29364 / DSM 637 / Y-400-fl) | 28% | 100% |
C0R5H4 | Wolbachia sp. subsp. Drosophila simulans (strain wRi) | 24% | 100% |
C4K6P7 | Hamiltonella defensa subsp. Acyrthosiphon pisum (strain 5AT) | 25% | 100% |
C5BGI4 | Edwardsiella ictaluri (strain 93-146) | 26% | 100% |
C6DZZ3 | Geobacter sp. (strain M21) | 26% | 100% |
D0A350 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E1BYJ2 | Gallus gallus | 27% | 76% |
E9ASW9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
O04716 | Arabidopsis thaliana | 29% | 77% |
O65607 | Arabidopsis thaliana | 29% | 94% |
O74502 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 81% |
P0A1Y0 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 26% | 100% |
P0A1Y1 | Salmonella typhi | 26% | 100% |
P13705 | Mus musculus | 26% | 93% |
P20585 | Homo sapiens | 25% | 89% |
P25336 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 100% |
P26359 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 100% |
P43246 | Homo sapiens | 23% | 100% |
P43247 | Mus musculus | 23% | 100% |
P52701 | Homo sapiens | 28% | 75% |
P61669 | Leptospira interrogans serogroup Icterohaemorrhagiae serovar copenhageni (strain Fiocruz L1-130) | 25% | 100% |
P61670 | Rhodopseudomonas palustris (strain ATCC BAA-98 / CGA009) | 27% | 100% |
P61672 | Treponema denticola (strain ATCC 35405 / DSM 14222 / CIP 103919 / JCM 8153 / KCTC 15104) | 26% | 100% |
P61673 | Wolbachia pipientis wMel | 23% | 100% |
Q03834 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 82% |
Q0BNM7 | Francisella tularensis subsp. holarctica (strain OSU18) | 22% | 100% |
Q0BV38 | Granulibacter bethesdensis (strain ATCC BAA-1260 / CGDNIH1) | 26% | 100% |
Q0STR4 | Clostridium perfringens (strain SM101 / Type A) | 24% | 100% |
Q0TRD6 | Clostridium perfringens (strain ATCC 13124 / DSM 756 / JCM 1290 / NCIMB 6125 / NCTC 8237 / Type A) | 24% | 100% |
Q14GB1 | Francisella tularensis subsp. tularensis (strain FSC 198) | 22% | 100% |
Q1QE46 | Psychrobacter cryohalolentis (strain ATCC BAA-1226 / DSM 17306 / VKM B-2378 / K5) | 28% | 98% |
Q28VY6 | Jannaschia sp. (strain CCS1) | 27% | 100% |
Q2A5B5 | Francisella tularensis subsp. holarctica (strain LVS) | 22% | 100% |
Q2GG13 | Ehrlichia chaffeensis (strain ATCC CRL-10679 / Arkansas) | 24% | 100% |
Q2GJL7 | Anaplasma phagocytophilum (strain HZ) | 26% | 100% |
Q2JIA6 | Synechococcus sp. (strain JA-2-3B'a(2-13)) | 26% | 100% |
Q2KD76 | Rhizobium etli (strain CFN 42 / ATCC 51251) | 25% | 100% |
Q2RNG0 | Rhodospirillum rubrum (strain ATCC 11170 / ATH 1.1.1 / DSM 467 / LMG 4362 / NCIMB 8255 / S1) | 30% | 100% |
Q2YB94 | Nitrosospira multiformis (strain ATCC 25196 / NCIMB 11849 / C 71) | 26% | 100% |
Q2YNZ0 | Brucella abortus (strain 2308) | 26% | 100% |
Q3IDC8 | Pseudoalteromonas translucida (strain TAC 125) | 25% | 100% |
Q3IYI5 | Cereibacter sphaeroides (strain ATCC 17023 / DSM 158 / JCM 6121 / CCUG 31486 / LMG 2827 / NBRC 12203 / NCIMB 8253 / ATH 2.4.1.) | 26% | 100% |
Q3M892 | Trichormus variabilis (strain ATCC 29413 / PCC 7937) | 25% | 100% |
Q3MHE4 | Bos taurus | 23% | 100% |
Q3YSJ8 | Ehrlichia canis (strain Jake) | 24% | 100% |
Q46CE2 | Methanosarcina barkeri (strain Fusaro / DSM 804) | 25% | 100% |
Q47DJ8 | Dechloromonas aromatica (strain RCB) | 26% | 100% |
Q47WN0 | Colwellia psychrerythraea (strain 34H / ATCC BAA-681) | 25% | 100% |
Q4Q1M8 | Leishmania major | 93% | 100% |
Q4Q4J6 | Leishmania major | 26% | 100% |
Q4WGB7 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 26% | 90% |
Q57FM9 | Brucella abortus biovar 1 (strain 9-941) | 26% | 100% |
Q57KL5 | Salmonella choleraesuis (strain SC-B67) | 26% | 100% |
Q5L7B7 | Bacteroides fragilis (strain ATCC 25285 / DSM 2151 / CCUG 4856 / JCM 11019 / NCTC 9343 / Onslow) | 24% | 100% |
Q5NEV8 | Francisella tularensis subsp. tularensis (strain SCHU S4 / Schu 4) | 22% | 100% |
Q5PEE6 | Salmonella paratyphi A (strain ATCC 9150 / SARB42) | 26% | 100% |
Q5QUB6 | Idiomarina loihiensis (strain ATCC BAA-735 / DSM 15497 / L2-TR) | 24% | 100% |
Q60BA1 | Methylococcus capsulatus (strain ATCC 33009 / NCIMB 11132 / Bath) | 26% | 100% |
Q64MG7 | Bacteroides fragilis (strain YCH46) | 24% | 100% |
Q6G542 | Bartonella henselae (strain ATCC 49882 / DSM 28221 / Houston 1) | 25% | 100% |
Q7MXR7 | Porphyromonas gingivalis (strain ATCC BAA-308 / W83) | 25% | 100% |
Q7NRW7 | Chromobacterium violaceum (strain ATCC 12472 / DSM 30191 / JCM 1249 / NBRC 12614 / NCIMB 9131 / NCTC 9757) | 25% | 100% |
Q7W880 | Bordetella parapertussis (strain 12822 / ATCC BAA-587 / NCTC 13253) | 25% | 100% |
Q7WLT5 | Bordetella bronchiseptica (strain ATCC BAA-588 / NCTC 13252 / RB50) | 25% | 100% |
Q83CQ2 | Coxiella burnetii (strain RSA 493 / Nine Mile phase I) | 24% | 100% |
Q89VX1 | Bradyrhizobium diazoefficiens (strain JCM 10833 / BCRC 13528 / IAM 13628 / NBRC 14792 / USDA 110) | 26% | 100% |
Q8A334 | Bacteroides thetaiotaomicron (strain ATCC 29148 / DSM 2079 / JCM 5827 / CCUG 10774 / NCTC 10582 / VPI-5482 / E50) | 24% | 100% |
Q8F496 | Leptospira interrogans serogroup Icterohaemorrhagiae serovar Lai (strain 56601) | 25% | 100% |
Q8G310 | Brucella suis biovar 1 (strain 1330) | 25% | 100% |
Q8KCC0 | Chlorobaculum tepidum (strain ATCC 49652 / DSM 12025 / NBRC 103806 / TLS) | 27% | 100% |
Q8UIF2 | Agrobacterium fabrum (strain C58 / ATCC 33970) | 26% | 100% |
Q8XL87 | Clostridium perfringens (strain 13 / Type A) | 24% | 100% |
Q8YES6 | Brucella melitensis biotype 1 (strain 16M / ATCC 23456 / NCTC 10094) | 25% | 100% |
Q98C21 | Mesorhizobium japonicum (strain LMG 29417 / CECT 9101 / MAFF 303099) | 25% | 100% |
V5DCH4 | Trypanosoma cruzi | 49% | 100% |