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: A0A3Q8IGP6
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 | 176 | 180 | PF00656 | 0.423 |
CLV_C14_Caspase3-7 | 3 | 7 | PF00656 | 0.536 |
CLV_C14_Caspase3-7 | 545 | 549 | PF00656 | 0.450 |
CLV_MEL_PAP_1 | 725 | 731 | PF00089 | 0.250 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.271 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.250 |
CLV_NRD_NRD_1 | 565 | 567 | PF00675 | 0.279 |
CLV_NRD_NRD_1 | 579 | 581 | PF00675 | 0.261 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 892 | 894 | PF00675 | 0.586 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.257 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.229 |
CLV_PCSK_KEX2_1 | 565 | 567 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 654 | 656 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 900 | 902 | PF00082 | 0.501 |
CLV_PCSK_PC1ET2_1 | 386 | 388 | PF00082 | 0.336 |
CLV_PCSK_PC1ET2_1 | 579 | 581 | PF00082 | 0.355 |
CLV_PCSK_PC1ET2_1 | 654 | 656 | PF00082 | 0.316 |
CLV_PCSK_PC1ET2_1 | 900 | 902 | PF00082 | 0.501 |
CLV_PCSK_PC7_1 | 396 | 402 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.274 |
CLV_Separin_Metazoa | 253 | 257 | PF03568 | 0.510 |
DEG_APCC_DBOX_1 | 656 | 664 | PF00400 | 0.382 |
DEG_APCC_DBOX_1 | 931 | 939 | PF00400 | 0.589 |
DOC_CYCLIN_RxL_1 | 159 | 170 | PF00134 | 0.522 |
DOC_CYCLIN_RxL_1 | 396 | 408 | PF00134 | 0.536 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 182 | 191 | PF00134 | 0.410 |
DOC_MAPK_gen_1 | 396 | 405 | PF00069 | 0.450 |
DOC_MAPK_gen_1 | 535 | 543 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 654 | 663 | PF00069 | 0.516 |
DOC_MAPK_gen_1 | 790 | 797 | PF00069 | 0.490 |
DOC_MAPK_HePTP_8 | 651 | 663 | PF00069 | 0.511 |
DOC_MAPK_MEF2A_6 | 222 | 229 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 363 | 371 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 654 | 663 | PF00069 | 0.516 |
DOC_MAPK_MEF2A_6 | 697 | 705 | PF00069 | 0.450 |
DOC_PP1_RVXF_1 | 160 | 167 | PF00149 | 0.468 |
DOC_PP2B_LxvP_1 | 255 | 258 | PF13499 | 0.391 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 878 | 882 | PF00917 | 0.688 |
DOC_USP7_MATH_2 | 258 | 264 | PF00917 | 0.472 |
DOC_USP7_UBL2_3 | 47 | 51 | PF12436 | 0.483 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.393 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.577 |
LIG_14-3-3_CanoR_1 | 162 | 167 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 212 | 219 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 261 | 265 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 295 | 299 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 363 | 367 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 400 | 404 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 532 | 541 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 551 | 560 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 769 | 775 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 790 | 796 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 831 | 837 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 89 | 95 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 893 | 902 | PF00244 | 0.512 |
LIG_Actin_WH2_2 | 391 | 408 | PF00022 | 0.510 |
LIG_Actin_WH2_2 | 519 | 537 | PF00022 | 0.536 |
LIG_Actin_WH2_2 | 75 | 91 | PF00022 | 0.393 |
LIG_Actin_WH2_2 | 816 | 833 | PF00022 | 0.461 |
LIG_APCC_ABBA_1 | 367 | 372 | PF00400 | 0.536 |
LIG_BIR_III_2 | 646 | 650 | PF00653 | 0.521 |
LIG_BRCT_BRCA1_1 | 138 | 142 | PF00533 | 0.491 |
LIG_BRCT_BRCA1_1 | 20 | 24 | PF00533 | 0.498 |
LIG_BRCT_BRCA1_1 | 797 | 801 | PF00533 | 0.444 |
LIG_CaM_IQ_9 | 232 | 248 | PF13499 | 0.547 |
LIG_CaM_IQ_9 | 379 | 395 | PF13499 | 0.453 |
LIG_Clathr_ClatBox_1 | 124 | 128 | PF01394 | 0.470 |
LIG_CtBP_PxDLS_1 | 686 | 692 | PF00389 | 0.450 |
LIG_deltaCOP1_diTrp_1 | 869 | 873 | PF00928 | 0.586 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.369 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.512 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.414 |
LIG_FHA_1 | 535 | 541 | PF00498 | 0.561 |
LIG_FHA_1 | 600 | 606 | PF00498 | 0.536 |
LIG_FHA_1 | 629 | 635 | PF00498 | 0.679 |
LIG_FHA_1 | 677 | 683 | PF00498 | 0.418 |
LIG_FHA_1 | 730 | 736 | PF00498 | 0.450 |
LIG_FHA_1 | 739 | 745 | PF00498 | 0.450 |
LIG_FHA_1 | 758 | 764 | PF00498 | 0.450 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.455 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.355 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.417 |
LIG_FHA_2 | 204 | 210 | PF00498 | 0.594 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.510 |
LIG_FHA_2 | 454 | 460 | PF00498 | 0.498 |
LIG_FHA_2 | 543 | 549 | PF00498 | 0.485 |
LIG_GBD_Chelix_1 | 582 | 590 | PF00786 | 0.355 |
LIG_LIR_Apic_2 | 427 | 431 | PF02991 | 0.519 |
LIG_LIR_Apic_2 | 438 | 443 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 300 | 310 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 408 | 419 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 798 | 808 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 869 | 878 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 165 | 169 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 21 | 27 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 300 | 305 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 328 | 334 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 408 | 414 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 495 | 501 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 519 | 523 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 561 | 567 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 588 | 592 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 652 | 656 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 771 | 777 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 798 | 804 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 844 | 848 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 869 | 873 | PF02991 | 0.572 |
LIG_NRBOX | 186 | 192 | PF00104 | 0.406 |
LIG_PCNA_yPIPBox_3 | 373 | 387 | PF02747 | 0.536 |
LIG_PDZ_Class_3 | 934 | 939 | PF00595 | 0.581 |
LIG_Pex14_2 | 777 | 781 | PF04695 | 0.450 |
LIG_Pex14_2 | 797 | 801 | PF04695 | 0.319 |
LIG_PTB_Apo_2 | 813 | 820 | PF02174 | 0.450 |
LIG_SH2_CRK | 428 | 432 | PF00017 | 0.555 |
LIG_SH2_CRK | 498 | 502 | PF00017 | 0.499 |
LIG_SH2_CRK | 520 | 524 | PF00017 | 0.450 |
LIG_SH2_CRK | 564 | 568 | PF00017 | 0.474 |
LIG_SH2_PTP2 | 440 | 443 | PF00017 | 0.458 |
LIG_SH2_SRC | 589 | 592 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 898 | 902 | PF00017 | 0.442 |
LIG_SH2_STAT3 | 834 | 837 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 522 | 525 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 589 | 592 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 834 | 837 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 848 | 851 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 934 | 937 | PF00017 | 0.612 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.529 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.551 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.461 |
LIG_SUMO_SIM_anti_2 | 631 | 636 | PF11976 | 0.727 |
LIG_SUMO_SIM_anti_2 | 70 | 76 | PF11976 | 0.400 |
LIG_SUMO_SIM_anti_2 | 759 | 766 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 539 | 546 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 70 | 76 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 759 | 766 | PF11976 | 0.490 |
LIG_TRFH_1 | 834 | 838 | PF08558 | 0.450 |
LIG_Vh1_VBS_1 | 746 | 764 | PF01044 | 0.510 |
LIG_WRC_WIRS_1 | 650 | 655 | PF05994 | 0.490 |
LIG_WRC_WIRS_1 | 739 | 744 | PF05994 | 0.450 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.552 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.442 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.471 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.598 |
MOD_CK1_1 | 751 | 757 | PF00069 | 0.516 |
MOD_CK1_1 | 826 | 832 | PF00069 | 0.499 |
MOD_CK1_1 | 879 | 885 | PF00069 | 0.561 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.441 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.382 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.476 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.461 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.520 |
MOD_CK2_1 | 524 | 530 | PF00069 | 0.467 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.451 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.446 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.613 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.467 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.511 |
MOD_GlcNHglycan | 640 | 643 | PF01048 | 0.673 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.555 |
MOD_GlcNHglycan | 748 | 751 | PF01048 | 0.250 |
MOD_GlcNHglycan | 811 | 814 | PF01048 | 0.344 |
MOD_GlcNHglycan | 824 | 828 | PF01048 | 0.281 |
MOD_GlcNHglycan | 881 | 884 | PF01048 | 0.683 |
MOD_GlcNHglycan | 895 | 898 | PF01048 | 0.375 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.479 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.563 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.421 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.461 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.504 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.452 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.459 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.541 |
MOD_GSK3_1 | 691 | 698 | PF00069 | 0.450 |
MOD_GSK3_1 | 791 | 798 | PF00069 | 0.515 |
MOD_GSK3_1 | 826 | 833 | PF00069 | 0.474 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.555 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.457 |
MOD_N-GLC_1 | 157 | 162 | PF02516 | 0.384 |
MOD_N-GLC_1 | 62 | 67 | PF02516 | 0.452 |
MOD_N-GLC_2 | 335 | 337 | PF02516 | 0.250 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.440 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.369 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.384 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.453 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.502 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.478 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.536 |
MOD_NEK2_1 | 524 | 529 | PF00069 | 0.461 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.452 |
MOD_NEK2_1 | 673 | 678 | PF00069 | 0.460 |
MOD_NEK2_1 | 682 | 687 | PF00069 | 0.424 |
MOD_NEK2_1 | 746 | 751 | PF00069 | 0.450 |
MOD_NEK2_1 | 795 | 800 | PF00069 | 0.452 |
MOD_NEK2_1 | 830 | 835 | PF00069 | 0.447 |
MOD_NEK2_2 | 649 | 654 | PF00069 | 0.520 |
MOD_PIKK_1 | 142 | 148 | PF00454 | 0.439 |
MOD_PIKK_1 | 18 | 24 | PF00454 | 0.434 |
MOD_PIKK_1 | 379 | 385 | PF00454 | 0.428 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.536 |
MOD_PIKK_1 | 487 | 493 | PF00454 | 0.555 |
MOD_PIKK_1 | 674 | 680 | PF00454 | 0.369 |
MOD_PIKK_1 | 754 | 760 | PF00454 | 0.498 |
MOD_PIKK_1 | 802 | 808 | PF00454 | 0.461 |
MOD_PK_1 | 90 | 96 | PF00069 | 0.389 |
MOD_PKA_1 | 565 | 571 | PF00069 | 0.555 |
MOD_PKA_1 | 57 | 63 | PF00069 | 0.496 |
MOD_PKA_1 | 893 | 899 | PF00069 | 0.574 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.548 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.474 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.480 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.466 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.461 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.450 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.461 |
MOD_PKA_2 | 524 | 530 | PF00069 | 0.455 |
MOD_PKA_2 | 534 | 540 | PF00069 | 0.440 |
MOD_PKA_2 | 565 | 571 | PF00069 | 0.536 |
MOD_PKA_2 | 768 | 774 | PF00069 | 0.462 |
MOD_PKA_2 | 791 | 797 | PF00069 | 0.533 |
MOD_PKA_2 | 830 | 836 | PF00069 | 0.461 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.501 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.449 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.370 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.650 |
MOD_Plk_1 | 458 | 464 | PF00069 | 0.467 |
MOD_Plk_1 | 802 | 808 | PF00069 | 0.461 |
MOD_Plk_2-3 | 260 | 266 | PF00069 | 0.474 |
MOD_Plk_2-3 | 869 | 875 | PF00069 | 0.561 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.590 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.340 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.300 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.396 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.450 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.450 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.427 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.555 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.458 |
MOD_Plk_4 | 691 | 697 | PF00069 | 0.450 |
MOD_Plk_4 | 738 | 744 | PF00069 | 0.450 |
MOD_Plk_4 | 748 | 754 | PF00069 | 0.450 |
MOD_Plk_4 | 791 | 797 | PF00069 | 0.510 |
MOD_Plk_4 | 855 | 861 | PF00069 | 0.524 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.393 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.470 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.591 |
MOD_SUMO_for_1 | 436 | 439 | PF00179 | 0.536 |
MOD_SUMO_for_1 | 512 | 515 | PF00179 | 0.450 |
MOD_SUMO_for_1 | 635 | 638 | PF00179 | 0.706 |
MOD_SUMO_for_1 | 921 | 924 | PF00179 | 0.538 |
MOD_SUMO_rev_2 | 594 | 599 | PF00179 | 0.450 |
TRG_DiLeu_BaEn_1 | 311 | 316 | PF01217 | 0.536 |
TRG_DiLeu_BaEn_4 | 259 | 265 | PF01217 | 0.490 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 498 | 501 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 520 | 523 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 564 | 567 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 589 | 592 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 774 | 777 | PF00928 | 0.450 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 294 | 296 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 564 | 566 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 789 | 792 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 88 | 90 | PF00400 | 0.447 |
TRG_NES_CRM1_1 | 358 | 372 | PF08389 | 0.461 |
TRG_NES_CRM1_1 | 733 | 748 | PF08389 | 0.450 |
TRG_NLS_Bipartite_1 | 565 | 583 | PF00514 | 0.536 |
TRG_NLS_MonoExtC_3 | 578 | 584 | PF00514 | 0.510 |
TRG_Pf-PMV_PEXEL_1 | 217 | 221 | PF00026 | 0.409 |
TRG_Pf-PMV_PEXEL_1 | 230 | 234 | PF00026 | 0.463 |
TRG_Pf-PMV_PEXEL_1 | 455 | 459 | PF00026 | 0.290 |
TRG_Pf-PMV_PEXEL_1 | 565 | 569 | PF00026 | 0.330 |
TRG_Pf-PMV_PEXEL_1 | 580 | 584 | PF00026 | 0.348 |
TRG_Pf-PMV_PEXEL_1 | 903 | 907 | PF00026 | 0.558 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6N3 | Leptomonas seymouri | 80% | 99% |
A0A0S4J224 | Bodo saltans | 50% | 100% |
A0A1X0P1A3 | Trypanosomatidae | 59% | 98% |
A0A3R7KEP9 | Trypanosoma rangeli | 59% | 98% |
A1R0M2 | Borrelia turicatae (strain 91E135) | 29% | 100% |
A4HL76 | Leishmania braziliensis | 88% | 100% |
A4I8Q5 | Leishmania infantum | 100% | 100% |
A6LLR1 | Thermosipho melanesiensis (strain DSM 12029 / CIP 104789 / BI429) | 26% | 100% |
A7HMG4 | Fervidobacterium nodosum (strain ATCC 35602 / DSM 5306 / Rt17-B1) | 28% | 100% |
A9NGL6 | Acholeplasma laidlawii (strain PG-8A) | 27% | 100% |
A9WFZ9 | Chloroflexus aurantiacus (strain ATCC 29366 / DSM 635 / J-10-fl) | 31% | 97% |
B0B918 | Chlamydia trachomatis serovar L2 (strain 434/Bu / ATCC VR-902B) | 27% | 100% |
B0BAP7 | Chlamydia trachomatis serovar L2b (strain UCH-1/proctitis) | 27% | 100% |
B0VAU7 | Acinetobacter baumannii (strain AYE) | 29% | 100% |
B2HX50 | Acinetobacter baumannii (strain ACICU) | 29% | 100% |
B3E6P2 | Trichlorobacter lovleyi (strain ATCC BAA-1151 / DSM 17278 / SZ) | 31% | 100% |
B3EEE1 | Chlorobium limicola (strain DSM 245 / NBRC 103803 / 6330) | 31% | 100% |
B7GW85 | Acinetobacter baumannii (strain AB307-0294) | 29% | 100% |
B7IBV9 | Acinetobacter baumannii (strain AB0057) | 29% | 100% |
B9LB04 | Chloroflexus aurantiacus (strain ATCC 29364 / DSM 637 / Y-400-fl) | 31% | 97% |
C5D9H5 | Geobacillus sp. (strain WCH70) | 31% | 100% |
D0A4P2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 99% |
E9B3L9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
O13396 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 31% | 100% |
O24617 | Arabidopsis thaliana | 33% | 100% |
O74502 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 75% |
O74773 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 96% |
P25847 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 97% |
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) | 29% | 100% |
Q03R33 | Levilactobacillus brevis (strain ATCC 367 / BCRC 12310 / CIP 105137 / JCM 1170 / LMG 11437 / NCIMB 947 / NCTC 947) | 30% | 100% |
Q07V29 | Rhodopseudomonas palustris (strain BisA53) | 30% | 100% |
Q1WT15 | Ligilactobacillus salivarius (strain UCC118) | 30% | 100% |
Q24X61 | Desulfitobacterium hafniense (strain Y51) | 31% | 100% |
Q2JT35 | Synechococcus sp. (strain JA-3-3Ab) | 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% |
Q49X88 | Staphylococcus saprophyticus subsp. saprophyticus (strain ATCC 15305 / DSM 20229 / NCIMB 8711 / NCTC 7292 / S-41) | 29% | 100% |
Q4Q4J6 | Leishmania major | 96% | 100% |
Q553L4 | Dictyostelium discoideum | 33% | 100% |
Q5NYP9 | Aromatoleum aromaticum (strain EbN1) | 31% | 100% |
Q5UZG9 | Haloarcula marismortui (strain ATCC 43049 / DSM 3752 / JCM 8966 / VKM B-1809) | 27% | 100% |
Q5XXB5 | Chlorocebus aethiops | 33% | 100% |
Q60BA1 | Methylococcus capsulatus (strain ATCC 33009 / NCIMB 11132 / Bath) | 30% | 100% |
Q65JE2 | Bacillus licheniformis (strain ATCC 14580 / DSM 13 / JCM 2505 / CCUG 7422 / NBRC 12200 / NCIMB 9375 / NCTC 10341 / NRRL NRS-1264 / Gibson 46) | 31% | 100% |
Q6G542 | Bartonella henselae (strain ATCC 49882 / DSM 28221 / Houston 1) | 28% | 100% |
Q8DWW1 | Streptococcus agalactiae serotype V (strain ATCC BAA-611 / 2603 V/R) | 28% | 100% |
Q8E2R3 | Streptococcus agalactiae serotype III (strain NEM316) | 28% | 100% |
Q9XGC9 | Zea mays | 31% | 100% |
V5BB82 | Trypanosoma cruzi | 58% | 98% |
V5BK71 | Trypanosoma cruzi | 28% | 100% |