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:0005634 | nucleus | 5 | 12 |
GO:0032300 | mismatch repair complex | 2 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032301 | MutSalpha complex | 3 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A4HL76
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006281 | DNA repair | 5 | 12 |
GO:0006298 | mismatch repair | 6 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006950 | response to stress | 2 | 12 |
GO:0006974 | DNA damage response | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0033554 | cellular response to stress | 3 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0050896 | response to stimulus | 1 | 12 |
GO:0051716 | cellular response to stimulus | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006312 | mitotic recombination | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003690 | double-stranded DNA binding | 5 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0030983 | mismatched DNA binding | 6 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 12 |
GO:0140299 | small molecule sensor activity | 1 | 12 |
GO:0140612 | DNA damage sensor activity | 2 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:0140664 | ATP-dependent DNA damage sensor activity | 3 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 177 | 181 | PF00656 | 0.380 |
CLV_C14_Caspase3-7 | 283 | 287 | PF00656 | 0.417 |
CLV_C14_Caspase3-7 | 3 | 7 | PF00656 | 0.498 |
CLV_C14_Caspase3-7 | 546 | 550 | PF00656 | 0.410 |
CLV_MEL_PAP_1 | 726 | 732 | PF00089 | 0.210 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.255 |
CLV_NRD_NRD_1 | 401 | 403 | PF00675 | 0.277 |
CLV_NRD_NRD_1 | 528 | 530 | PF00675 | 0.210 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.240 |
CLV_NRD_NRD_1 | 580 | 582 | PF00675 | 0.221 |
CLV_NRD_NRD_1 | 893 | 895 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.407 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.228 |
CLV_PCSK_KEX2_1 | 401 | 403 | PF00082 | 0.257 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 580 | 582 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 901 | 903 | PF00082 | 0.450 |
CLV_PCSK_PC1ET2_1 | 387 | 389 | PF00082 | 0.313 |
CLV_PCSK_PC1ET2_1 | 580 | 582 | PF00082 | 0.265 |
CLV_PCSK_PC1ET2_1 | 901 | 903 | PF00082 | 0.450 |
CLV_PCSK_PC7_1 | 397 | 403 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 536 | 540 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 623 | 627 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 917 | 921 | PF00082 | 0.518 |
CLV_Separin_Metazoa | 254 | 258 | PF03568 | 0.486 |
DEG_APCC_DBOX_1 | 657 | 665 | PF00400 | 0.317 |
DEG_APCC_DBOX_1 | 932 | 940 | PF00400 | 0.549 |
DOC_CYCLIN_RxL_1 | 160 | 171 | PF00134 | 0.400 |
DOC_CYCLIN_RxL_1 | 397 | 409 | PF00134 | 0.515 |
DOC_CYCLIN_RxL_1 | 915 | 925 | PF00134 | 0.418 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 183 | 192 | PF00134 | 0.363 |
DOC_MAPK_DCC_7 | 627 | 635 | PF00069 | 0.384 |
DOC_MAPK_gen_1 | 397 | 406 | PF00069 | 0.410 |
DOC_MAPK_gen_1 | 536 | 544 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 655 | 664 | PF00069 | 0.376 |
DOC_MAPK_gen_1 | 791 | 798 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 917 | 926 | PF00069 | 0.379 |
DOC_MAPK_HePTP_8 | 652 | 664 | PF00069 | 0.373 |
DOC_MAPK_MEF2A_6 | 146 | 155 | PF00069 | 0.401 |
DOC_MAPK_MEF2A_6 | 223 | 230 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 364 | 372 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 655 | 664 | PF00069 | 0.376 |
DOC_MAPK_MEF2A_6 | 698 | 706 | PF00069 | 0.410 |
DOC_MAPK_MEF2A_6 | 917 | 926 | PF00069 | 0.379 |
DOC_PP1_RVXF_1 | 150 | 156 | PF00149 | 0.338 |
DOC_PP1_RVXF_1 | 161 | 168 | PF00149 | 0.430 |
DOC_PP2B_LxvP_1 | 256 | 259 | PF13499 | 0.344 |
DOC_PP2B_LxvP_1 | 664 | 667 | PF13499 | 0.291 |
DOC_PP4_FxxP_1 | 441 | 444 | PF00568 | 0.431 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.354 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 880 | 884 | PF00917 | 0.693 |
DOC_USP7_UBL2_3 | 47 | 51 | PF12436 | 0.444 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.379 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 884 | 889 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.429 |
LIG_14-3-3_CanoR_1 | 163 | 168 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 213 | 220 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 364 | 368 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 401 | 405 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 472 | 478 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 533 | 542 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 552 | 561 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 770 | 776 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 791 | 797 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 832 | 838 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 894 | 903 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 90 | 96 | PF00244 | 0.350 |
LIG_Actin_WH2_2 | 392 | 409 | PF00022 | 0.477 |
LIG_Actin_WH2_2 | 520 | 538 | PF00022 | 0.513 |
LIG_Actin_WH2_2 | 76 | 92 | PF00022 | 0.341 |
LIG_Actin_WH2_2 | 817 | 834 | PF00022 | 0.421 |
LIG_APCC_ABBA_1 | 368 | 373 | PF00400 | 0.513 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.464 |
LIG_BRCT_BRCA1_1 | 139 | 143 | PF00533 | 0.377 |
LIG_BRCT_BRCA1_1 | 20 | 24 | PF00533 | 0.411 |
LIG_BRCT_BRCA1_1 | 798 | 802 | PF00533 | 0.405 |
LIG_Clathr_ClatBox_1 | 125 | 129 | PF01394 | 0.412 |
LIG_CtBP_PxDLS_1 | 687 | 693 | PF00389 | 0.410 |
LIG_deltaCOP1_diTrp_1 | 870 | 874 | PF00928 | 0.543 |
LIG_EH1_1 | 272 | 280 | PF00400 | 0.375 |
LIG_eIF4E_1 | 607 | 613 | PF01652 | 0.413 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.352 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.485 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.363 |
LIG_FHA_1 | 601 | 607 | PF00498 | 0.513 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.330 |
LIG_FHA_1 | 678 | 684 | PF00498 | 0.376 |
LIG_FHA_1 | 731 | 737 | PF00498 | 0.410 |
LIG_FHA_1 | 740 | 746 | PF00498 | 0.410 |
LIG_FHA_1 | 759 | 765 | PF00498 | 0.410 |
LIG_FHA_2 | 117 | 123 | PF00498 | 0.432 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.374 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.399 |
LIG_FHA_2 | 364 | 370 | PF00498 | 0.477 |
LIG_FHA_2 | 455 | 461 | PF00498 | 0.462 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.477 |
LIG_FHA_2 | 544 | 550 | PF00498 | 0.447 |
LIG_FHA_2 | 885 | 891 | PF00498 | 0.444 |
LIG_GBD_Chelix_1 | 583 | 591 | PF00786 | 0.265 |
LIG_LIR_Apic_2 | 427 | 432 | PF02991 | 0.495 |
LIG_LIR_Apic_2 | 439 | 444 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 301 | 311 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 409 | 420 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 496 | 506 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 799 | 809 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 870 | 879 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 166 | 170 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 21 | 27 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 301 | 306 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 329 | 335 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 409 | 415 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 496 | 502 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 520 | 524 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 562 | 568 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 589 | 593 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 653 | 657 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 772 | 778 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 799 | 805 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 845 | 849 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 870 | 874 | PF02991 | 0.543 |
LIG_NRBOX | 187 | 193 | PF00104 | 0.360 |
LIG_PCNA_yPIPBox_3 | 374 | 388 | PF02747 | 0.513 |
LIG_Pex14_1 | 40 | 44 | PF04695 | 0.409 |
LIG_Pex14_2 | 778 | 782 | PF04695 | 0.410 |
LIG_Pex14_2 | 798 | 802 | PF04695 | 0.318 |
LIG_PTB_Apo_2 | 814 | 821 | PF02174 | 0.410 |
LIG_SH2_CRK | 429 | 433 | PF00017 | 0.465 |
LIG_SH2_CRK | 521 | 525 | PF00017 | 0.410 |
LIG_SH2_CRK | 565 | 569 | PF00017 | 0.435 |
LIG_SH2_PTP2 | 303 | 306 | PF00017 | 0.270 |
LIG_SH2_SRC | 515 | 518 | PF00017 | 0.519 |
LIG_SH2_SRC | 590 | 593 | PF00017 | 0.435 |
LIG_SH2_STAP1 | 899 | 903 | PF00017 | 0.393 |
LIG_SH2_STAT3 | 835 | 838 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 523 | 526 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 590 | 593 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 835 | 838 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 849 | 852 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 935 | 938 | PF00017 | 0.577 |
LIG_SH3_1 | 100 | 106 | PF00018 | 0.329 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.329 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.505 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.421 |
LIG_Sin3_3 | 415 | 422 | PF02671 | 0.352 |
LIG_SUMO_SIM_anti_2 | 280 | 288 | PF11976 | 0.292 |
LIG_SUMO_SIM_anti_2 | 414 | 420 | PF11976 | 0.352 |
LIG_SUMO_SIM_anti_2 | 631 | 637 | PF11976 | 0.580 |
LIG_SUMO_SIM_anti_2 | 69 | 74 | PF11976 | 0.366 |
LIG_SUMO_SIM_anti_2 | 758 | 767 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 540 | 547 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 71 | 77 | PF11976 | 0.369 |
LIG_SUMO_SIM_par_1 | 758 | 767 | PF11976 | 0.456 |
LIG_TRFH_1 | 835 | 839 | PF08558 | 0.410 |
LIG_UBA3_1 | 541 | 548 | PF00899 | 0.352 |
LIG_Vh1_VBS_1 | 747 | 765 | PF01044 | 0.477 |
LIG_WRC_WIRS_1 | 651 | 656 | PF05994 | 0.445 |
LIG_WRC_WIRS_1 | 740 | 745 | PF05994 | 0.410 |
MOD_CAAXbox | 937 | 940 | PF01239 | 0.394 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.533 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.435 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.411 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.418 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.582 |
MOD_CK1_1 | 645 | 651 | PF00069 | 0.363 |
MOD_CK1_1 | 755 | 761 | PF00069 | 0.470 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.420 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.330 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.433 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.421 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.490 |
MOD_CK2_1 | 525 | 531 | PF00069 | 0.427 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.412 |
MOD_CK2_1 | 856 | 862 | PF00069 | 0.431 |
MOD_CK2_1 | 884 | 890 | PF00069 | 0.531 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.416 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.567 |
MOD_GlcNHglycan | 243 | 247 | PF01048 | 0.404 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.452 |
MOD_GlcNHglycan | 536 | 539 | PF01048 | 0.341 |
MOD_GlcNHglycan | 568 | 571 | PF01048 | 0.245 |
MOD_GlcNHglycan | 644 | 647 | PF01048 | 0.588 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.531 |
MOD_GlcNHglycan | 749 | 752 | PF01048 | 0.210 |
MOD_GlcNHglycan | 754 | 757 | PF01048 | 0.210 |
MOD_GlcNHglycan | 882 | 885 | PF01048 | 0.592 |
MOD_GlcNHglycan | 896 | 899 | PF01048 | 0.399 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.455 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.528 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.493 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.421 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.511 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.435 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.419 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.568 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.246 |
MOD_GSK3_1 | 692 | 699 | PF00069 | 0.410 |
MOD_GSK3_1 | 752 | 759 | PF00069 | 0.352 |
MOD_GSK3_1 | 792 | 799 | PF00069 | 0.483 |
MOD_GSK3_1 | 827 | 834 | PF00069 | 0.434 |
MOD_GSK3_1 | 880 | 887 | PF00069 | 0.455 |
MOD_LATS_1 | 23 | 29 | PF00433 | 0.235 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.407 |
MOD_N-GLC_1 | 158 | 163 | PF02516 | 0.333 |
MOD_N-GLC_1 | 473 | 478 | PF02516 | 0.250 |
MOD_N-GLC_2 | 336 | 338 | PF02516 | 0.210 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.383 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.322 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.374 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.376 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.439 |
MOD_NEK2_1 | 488 | 493 | PF00069 | 0.513 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.421 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.412 |
MOD_NEK2_1 | 674 | 679 | PF00069 | 0.402 |
MOD_NEK2_1 | 683 | 688 | PF00069 | 0.388 |
MOD_NEK2_1 | 747 | 752 | PF00069 | 0.410 |
MOD_NEK2_1 | 796 | 801 | PF00069 | 0.412 |
MOD_NEK2_1 | 831 | 836 | PF00069 | 0.417 |
MOD_NEK2_2 | 650 | 655 | PF00069 | 0.384 |
MOD_NEK2_2 | 827 | 832 | PF00069 | 0.391 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.382 |
MOD_PIKK_1 | 406 | 412 | PF00454 | 0.513 |
MOD_PIKK_1 | 488 | 494 | PF00454 | 0.465 |
MOD_PIKK_1 | 803 | 809 | PF00454 | 0.421 |
MOD_PK_1 | 5 | 11 | PF00069 | 0.336 |
MOD_PK_1 | 91 | 97 | PF00069 | 0.341 |
MOD_PKA_1 | 566 | 572 | PF00069 | 0.465 |
MOD_PKA_1 | 894 | 900 | PF00069 | 0.578 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.430 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.475 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.421 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.410 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.443 |
MOD_PKA_2 | 525 | 531 | PF00069 | 0.416 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.513 |
MOD_PKA_2 | 769 | 775 | PF00069 | 0.422 |
MOD_PKA_2 | 792 | 798 | PF00069 | 0.508 |
MOD_PKA_2 | 831 | 837 | PF00069 | 0.421 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.411 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.320 |
MOD_Plk_1 | 459 | 465 | PF00069 | 0.427 |
MOD_Plk_1 | 473 | 479 | PF00069 | 0.406 |
MOD_Plk_1 | 803 | 809 | PF00069 | 0.421 |
MOD_Plk_2-3 | 870 | 876 | PF00069 | 0.503 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.408 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.263 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.332 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.410 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.410 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.395 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.484 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.357 |
MOD_Plk_4 | 586 | 592 | PF00069 | 0.419 |
MOD_Plk_4 | 631 | 637 | PF00069 | 0.634 |
MOD_Plk_4 | 692 | 698 | PF00069 | 0.410 |
MOD_Plk_4 | 739 | 745 | PF00069 | 0.410 |
MOD_Plk_4 | 792 | 798 | PF00069 | 0.477 |
MOD_Plk_4 | 856 | 862 | PF00069 | 0.506 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.377 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.428 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.573 |
MOD_ProDKin_1 | 884 | 890 | PF00069 | 0.435 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.424 |
MOD_SUMO_for_1 | 437 | 440 | PF00179 | 0.513 |
MOD_SUMO_for_1 | 513 | 516 | PF00179 | 0.410 |
MOD_SUMO_for_1 | 636 | 639 | PF00179 | 0.670 |
MOD_SUMO_rev_2 | 595 | 600 | PF00179 | 0.410 |
TRG_DiLeu_BaEn_1 | 312 | 317 | PF01217 | 0.513 |
TRG_DiLeu_BaEn_1 | 631 | 636 | PF01217 | 0.428 |
TRG_DiLeu_BaEn_2 | 407 | 413 | PF01217 | 0.352 |
TRG_DiLeu_BaEn_4 | 260 | 266 | PF01217 | 0.453 |
TRG_DiLeu_BaLyEn_6 | 647 | 652 | PF01217 | 0.415 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 499 | 502 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 521 | 524 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 565 | 568 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 590 | 593 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 775 | 778 | PF00928 | 0.410 |
TRG_ER_diArg_1 | 217 | 219 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 295 | 297 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 565 | 567 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 89 | 91 | PF00400 | 0.392 |
TRG_NES_CRM1_1 | 359 | 373 | PF08389 | 0.421 |
TRG_NES_CRM1_1 | 734 | 749 | PF08389 | 0.410 |
TRG_NLS_Bipartite_1 | 566 | 584 | PF00514 | 0.513 |
TRG_NLS_MonoExtC_3 | 579 | 585 | PF00514 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 218 | 222 | PF00026 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 231 | 235 | PF00026 | 0.417 |
TRG_Pf-PMV_PEXEL_1 | 456 | 460 | PF00026 | 0.253 |
TRG_Pf-PMV_PEXEL_1 | 581 | 585 | PF00026 | 0.332 |
TRG_Pf-PMV_PEXEL_1 | 904 | 908 | PF00026 | 0.526 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6K5 | Leptomonas seymouri | 24% | 91% |
A0A0N1I6N3 | Leptomonas seymouri | 79% | 99% |
A0A0S4J224 | Bodo saltans | 49% | 100% |
A0A0S4JK96 | Bodo saltans | 24% | 99% |
A0A1X0P1A3 | Trypanosomatidae | 58% | 98% |
A0A3Q8IGP6 | Leishmania donovani | 88% | 100% |
A0A3Q8IK49 | Leishmania donovani | 26% | 93% |
A0A3R7KEP9 | Trypanosoma rangeli | 58% | 98% |
A3CR17 | Streptococcus sanguinis (strain SK36) | 28% | 100% |
A4HP61 | Leishmania braziliensis | 26% | 93% |
A4I8Q5 | Leishmania infantum | 88% | 100% |
A4IDG7 | Leishmania infantum | 26% | 93% |
A4JFW7 | Burkholderia vietnamiensis (strain G4 / LMG 22486) | 28% | 100% |
A5G447 | Geotalea uraniireducens (strain Rf4) | 30% | 100% |
A6GWN3 | Flavobacterium psychrophilum (strain ATCC 49511 / DSM 21280 / CIP 103535 / JIP02/86) | 28% | 100% |
A6LWJ5 | Clostridium beijerinckii (strain ATCC 51743 / NCIMB 8052) | 27% | 100% |
A8EZG1 | Rickettsia canadensis (strain McKiel) | 29% | 100% |
A8F164 | Rickettsia massiliae (strain Mtu5) | 29% | 100% |
A8H1T4 | Shewanella pealeana (strain ATCC 700345 / ANG-SQ1) | 31% | 100% |
B0CF30 | Acaryochloris marina (strain MBIC 11017) | 27% | 100% |
B1KSA3 | Clostridium botulinum (strain Loch Maree / Type A3) | 29% | 100% |
B1N025 | Leuconostoc citreum (strain KM20) | 32% | 100% |
B4F220 | Proteus mirabilis (strain HI4320) | 29% | 100% |
B8CX98 | Halothermothrix orenii (strain H 168 / OCM 544 / DSM 9562) | 30% | 100% |
B8DFS4 | Listeria monocytogenes serotype 4a (strain HCC23) | 28% | 100% |
D0A4P2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 99% |
E9B3L9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
O13396 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 31% | 100% |
O24617 | Arabidopsis thaliana | 33% | 100% |
O74773 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 96% |
P25847 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 98% |
P43246 | Homo sapiens | 33% | 100% |
P43247 | Mus musculus | 33% | 100% |
P43248 | Drosophila melanogaster | 31% | 100% |
P54275 | Rattus norvegicus | 33% | 100% |
P61672 | Treponema denticola (strain ATCC 35405 / DSM 14222 / CIP 103919 / JCM 8153 / KCTC 15104) | 28% | 100% |
Q10YG4 | Trichodesmium erythraeum (strain IMS101) | 28% | 100% |
Q12PY3 | Shewanella denitrificans (strain OS217 / ATCC BAA-1090 / DSM 15013) | 29% | 100% |
Q1MRT4 | Lawsonia intracellularis (strain PHE/MN1-00) | 29% | 100% |
Q2S254 | Salinibacter ruber (strain DSM 13855 / M31) | 31% | 100% |
Q3ACA5 | Carboxydothermus hydrogenoformans (strain ATCC BAA-161 / DSM 6008 / Z-2901) | 30% | 100% |
Q3JYM3 | Streptococcus agalactiae serotype Ia (strain ATCC 27591 / A909 / CDC SS700) | 28% | 100% |
Q3M892 | Trichormus variabilis (strain ATCC 29413 / PCC 7937) | 28% | 100% |
Q3MHE4 | Bos taurus | 33% | 100% |
Q4Q1M8 | Leishmania major | 26% | 93% |
Q4Q4J6 | Leishmania major | 89% | 100% |
Q553L4 | Dictyostelium discoideum | 31% | 100% |
Q5HPP5 | Staphylococcus epidermidis (strain ATCC 35984 / RP62A) | 31% | 100% |
Q5QUB6 | Idiomarina loihiensis (strain ATCC BAA-735 / DSM 15497 / L2-TR) | 30% | 100% |
Q5WFY3 | Alkalihalobacillus clausii (strain KSM-K16) | 30% | 100% |
Q5XXB5 | Chlorocebus aethiops | 33% | 100% |
Q60BA1 | Methylococcus capsulatus (strain ATCC 33009 / NCIMB 11132 / Bath) | 30% | 100% |
Q65ZX6 | Borrelia garinii subsp. bavariensis (strain ATCC BAA-2496 / DSM 23469 / PBi) | 28% | 100% |
Q68X73 | Rickettsia typhi (strain ATCC VR-144 / Wilmington) | 28% | 100% |
Q6LMU0 | Photobacterium profundum (strain SS9) | 30% | 100% |
Q7MXR7 | Porphyromonas gingivalis (strain ATCC BAA-308 / W83) | 28% | 100% |
Q8CPF0 | Staphylococcus epidermidis (strain ATCC 12228 / FDA PCI 1200) | 31% | 100% |
Q8DWW1 | Streptococcus agalactiae serotype V (strain ATCC BAA-611 / 2603 V/R) | 28% | 100% |
Q8E2R3 | Streptococcus agalactiae serotype III (strain NEM316) | 28% | 100% |
Q8PWA7 | Methanosarcina mazei (strain ATCC BAA-159 / DSM 3647 / Goe1 / Go1 / JCM 11833 / OCM 88) | 28% | 100% |
Q8RA71 | Caldanaerobacter subterraneus subsp. tengcongensis (strain DSM 15242 / JCM 11007 / NBRC 100824 / MB4) | 30% | 100% |
Q8Y789 | Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) | 27% | 100% |
Q92BV3 | Listeria innocua serovar 6a (strain ATCC BAA-680 / CLIP 11262) | 27% | 100% |
Q9XGC9 | Zea mays | 32% | 100% |
Q9ZDM9 | Rickettsia prowazekii (strain Madrid E) | 28% | 100% |
V5BB82 | Trypanosoma cruzi | 58% | 98% |
V5BK71 | Trypanosoma cruzi | 26% | 100% |