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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005657 | replication fork | 2 | 1 |
GO:0043596 | nuclear replication fork | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0016020 | membrane | 2 | 2 |
Related structures:
AlphaFold database: A0A3Q8I7U7
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006275 | regulation of DNA replication | 6 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008156 | negative regulation of DNA replication | 7 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031297 | replication fork processing | 6 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0045005 | DNA-templated DNA replication maintenance of fidelity | 5 | 1 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0048478 | obsolete replication fork protection | 6 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051052 | regulation of DNA metabolic process | 5 | 1 |
GO:0051053 | negative regulation of DNA metabolic process | 6 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:0090329 | regulation of DNA-templated DNA replication | 7 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:2000104 | negative regulation of DNA-templated DNA replication | 8 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004386 | helicase activity | 2 | 8 |
GO:0004518 | nuclease activity | 4 | 11 |
GO:0004519 | endonuclease activity | 5 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 11 |
GO:0016491 | oxidoreductase activity | 2 | 10 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 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:0051213 | dioxygenase activity | 3 | 10 |
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:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:0140658 | ATP-dependent chromatin remodeler activity | 3 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0004520 | DNA endonuclease activity | 5 | 1 |
GO:0004536 | DNA nuclease activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 310 | 314 | PF00656 | 0.462 |
CLV_C14_Caspase3-7 | 473 | 477 | PF00656 | 0.461 |
CLV_MEL_PAP_1 | 83 | 89 | PF00089 | 0.350 |
CLV_NRD_NRD_1 | 155 | 157 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.324 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.181 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.262 |
CLV_NRD_NRD_1 | 692 | 694 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 720 | 722 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 739 | 741 | PF00675 | 0.326 |
CLV_NRD_NRD_1 | 809 | 811 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 816 | 818 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 847 | 849 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 955 | 957 | PF00675 | 0.497 |
CLV_PCSK_FUR_1 | 921 | 925 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.186 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 668 | 670 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 692 | 694 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 719 | 721 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 739 | 741 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 809 | 811 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 816 | 818 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 847 | 849 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 923 | 925 | PF00082 | 0.600 |
CLV_PCSK_PC1ET2_1 | 325 | 327 | PF00082 | 0.265 |
CLV_PCSK_PC1ET2_1 | 487 | 489 | PF00082 | 0.262 |
CLV_PCSK_PC1ET2_1 | 668 | 670 | PF00082 | 0.423 |
CLV_PCSK_PC1ET2_1 | 923 | 925 | PF00082 | 0.600 |
CLV_PCSK_PC7_1 | 483 | 489 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 464 | 468 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 723 | 727 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 923 | 927 | PF00082 | 0.576 |
CLV_Separin_Metazoa | 407 | 411 | PF03568 | 0.496 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.444 |
DOC_ANK_TNKS_1 | 513 | 520 | PF00023 | 0.418 |
DOC_ANK_TNKS_1 | 849 | 856 | PF00023 | 0.419 |
DOC_CDC14_PxL_1 | 172 | 180 | PF14671 | 0.445 |
DOC_CDC14_PxL_1 | 222 | 230 | PF14671 | 0.496 |
DOC_CYCLIN_yCln2_LP_2 | 121 | 127 | PF00134 | 0.472 |
DOC_MAPK_DCC_7 | 52 | 61 | PF00069 | 0.440 |
DOC_MAPK_gen_1 | 325 | 333 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 399 | 408 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 410 | 418 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 487 | 498 | PF00069 | 0.426 |
DOC_MAPK_gen_1 | 50 | 58 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 719 | 730 | PF00069 | 0.678 |
DOC_MAPK_gen_1 | 847 | 853 | PF00069 | 0.349 |
DOC_MAPK_gen_1 | 921 | 929 | PF00069 | 0.640 |
DOC_MAPK_HePTP_8 | 49 | 61 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 52 | 61 | PF00069 | 0.435 |
DOC_MAPK_MEF2A_6 | 74 | 82 | PF00069 | 0.283 |
DOC_PP1_RVXF_1 | 198 | 204 | PF00149 | 0.335 |
DOC_PP1_RVXF_1 | 234 | 240 | PF00149 | 0.496 |
DOC_PP1_RVXF_1 | 382 | 389 | PF00149 | 0.570 |
DOC_PP1_RVXF_1 | 737 | 744 | PF00149 | 0.465 |
DOC_PP1_RVXF_1 | 801 | 807 | PF00149 | 0.529 |
DOC_PP1_RVXF_1 | 950 | 956 | PF00149 | 0.492 |
DOC_PP2B_LxvP_1 | 406 | 409 | PF13499 | 0.484 |
DOC_PP4_FxxP_1 | 147 | 150 | PF00568 | 0.424 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 590 | 594 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 604 | 608 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 647 | 651 | PF00917 | 0.489 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.450 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 685 | 690 | PF00397 | 0.551 |
LIG_14-3-3_CanoR_1 | 439 | 445 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 50 | 59 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 582 | 588 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 594 | 599 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 646 | 654 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 723 | 729 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 803 | 807 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 816 | 820 | PF00244 | 0.318 |
LIG_14-3-3_CanoR_1 | 86 | 94 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 935 | 939 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 952 | 956 | PF00244 | 0.357 |
LIG_Actin_WH2_2 | 141 | 158 | PF00022 | 0.453 |
LIG_BRCT_BRCA1_1 | 649 | 653 | PF00533 | 0.684 |
LIG_BRCT_BRCA1_1 | 793 | 797 | PF00533 | 0.446 |
LIG_BRCT_BRCA1_1 | 87 | 91 | PF00533 | 0.498 |
LIG_Clathr_ClatBox_1 | 4 | 8 | PF01394 | 0.476 |
LIG_CSL_BTD_1 | 700 | 703 | PF09270 | 0.411 |
LIG_deltaCOP1_diTrp_1 | 671 | 680 | PF00928 | 0.476 |
LIG_DLG_GKlike_1 | 594 | 602 | PF00625 | 0.624 |
LIG_EH_1 | 340 | 344 | PF12763 | 0.461 |
LIG_eIF4E_1 | 462 | 468 | PF01652 | 0.322 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.433 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.442 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.476 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.546 |
LIG_FHA_1 | 638 | 644 | PF00498 | 0.411 |
LIG_FHA_1 | 725 | 731 | PF00498 | 0.582 |
LIG_FHA_1 | 901 | 907 | PF00498 | 0.279 |
LIG_FHA_1 | 935 | 941 | PF00498 | 0.586 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.533 |
LIG_FHA_2 | 677 | 683 | PF00498 | 0.446 |
LIG_FHA_2 | 911 | 917 | PF00498 | 0.279 |
LIG_FHA_2 | 934 | 940 | PF00498 | 0.624 |
LIG_GBD_Chelix_1 | 102 | 110 | PF00786 | 0.368 |
LIG_Integrin_RGD_1 | 501 | 503 | PF01839 | 0.296 |
LIG_LIR_Apic_2 | 745 | 751 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 313 | 323 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 340 | 349 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 374 | 381 | PF02991 | 0.571 |
LIG_LIR_Gen_1 | 387 | 392 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 460 | 469 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 578 | 587 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 651 | 662 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 671 | 681 | PF02991 | 0.265 |
LIG_LIR_Gen_1 | 939 | 947 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 22 | 27 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 223 | 228 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 293 | 297 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 313 | 319 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 372 | 376 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 387 | 391 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 460 | 465 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 578 | 583 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 651 | 657 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 671 | 677 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 88 | 94 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 939 | 945 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 954 | 958 | PF02991 | 0.448 |
LIG_LYPXL_yS_3 | 225 | 228 | PF13949 | 0.496 |
LIG_Pex14_2 | 24 | 28 | PF04695 | 0.370 |
LIG_Pex14_2 | 653 | 657 | PF04695 | 0.494 |
LIG_Rb_LxCxE_1 | 293 | 315 | PF01857 | 0.496 |
LIG_REV1ctd_RIR_1 | 804 | 814 | PF16727 | 0.521 |
LIG_SH2_CRK | 316 | 320 | PF00017 | 0.450 |
LIG_SH2_CRK | 368 | 372 | PF00017 | 0.496 |
LIG_SH2_CRK | 462 | 466 | PF00017 | 0.322 |
LIG_SH2_GRB2like | 440 | 443 | PF00017 | 0.443 |
LIG_SH2_PTP2 | 779 | 782 | PF00017 | 0.621 |
LIG_SH2_SRC | 440 | 443 | PF00017 | 0.443 |
LIG_SH2_STAP1 | 17 | 21 | PF00017 | 0.395 |
LIG_SH2_STAP1 | 316 | 320 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 440 | 444 | PF00017 | 0.362 |
LIG_SH2_STAP1 | 462 | 466 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 724 | 728 | PF00017 | 0.599 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 567 | 570 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 654 | 657 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 742 | 745 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 748 | 751 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 779 | 782 | PF00017 | 0.621 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.443 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.343 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.432 |
LIG_SH3_3 | 869 | 875 | PF00018 | 0.402 |
LIG_SH3_3 | 926 | 932 | PF00018 | 0.649 |
LIG_SUMO_SIM_anti_2 | 33 | 40 | PF11976 | 0.502 |
LIG_SUMO_SIM_anti_2 | 463 | 469 | PF11976 | 0.584 |
LIG_SUMO_SIM_anti_2 | 849 | 855 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 273 | 278 | PF11976 | 0.496 |
LIG_SUMO_SIM_par_1 | 59 | 64 | PF11976 | 0.320 |
LIG_SUMO_SIM_par_1 | 74 | 79 | PF11976 | 0.301 |
LIG_TRAF2_1 | 252 | 255 | PF00917 | 0.487 |
LIG_TRAF2_1 | 435 | 438 | PF00917 | 0.548 |
LIG_TYR_ITIM | 564 | 569 | PF00017 | 0.398 |
LIG_UBA3_1 | 397 | 402 | PF00899 | 0.442 |
LIG_UBA3_1 | 632 | 638 | PF00899 | 0.498 |
LIG_WRC_WIRS_1 | 677 | 682 | PF05994 | 0.517 |
MOD_CDK_SPxxK_3 | 685 | 692 | PF00069 | 0.548 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.543 |
MOD_CK1_1 | 637 | 643 | PF00069 | 0.459 |
MOD_CK1_1 | 648 | 654 | PF00069 | 0.467 |
MOD_CK1_1 | 825 | 831 | PF00069 | 0.380 |
MOD_CK1_1 | 948 | 954 | PF00069 | 0.605 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.531 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.498 |
MOD_CK2_1 | 583 | 589 | PF00069 | 0.480 |
MOD_CK2_1 | 676 | 682 | PF00069 | 0.420 |
MOD_CMANNOS | 732 | 735 | PF00535 | 0.541 |
MOD_Cter_Amidation | 323 | 326 | PF01082 | 0.235 |
MOD_Cter_Amidation | 845 | 848 | PF01082 | 0.423 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.511 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.442 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.335 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.352 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.255 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.665 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.662 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.434 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.626 |
MOD_GlcNHglycan | 715 | 718 | PF01048 | 0.724 |
MOD_GlcNHglycan | 798 | 801 | PF01048 | 0.442 |
MOD_GlcNHglycan | 810 | 813 | PF01048 | 0.393 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.429 |
MOD_GlcNHglycan | 948 | 951 | PF01048 | 0.560 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.497 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.252 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.570 |
MOD_GSK3_1 | 614 | 621 | PF00069 | 0.708 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.407 |
MOD_GSK3_1 | 648 | 655 | PF00069 | 0.580 |
MOD_GSK3_1 | 676 | 683 | PF00069 | 0.437 |
MOD_GSK3_1 | 833 | 840 | PF00069 | 0.522 |
MOD_N-GLC_1 | 307 | 312 | PF02516 | 0.336 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.506 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.477 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.504 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.425 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.525 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.442 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.502 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.326 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.447 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.558 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.450 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.641 |
MOD_NEK2_1 | 634 | 639 | PF00069 | 0.429 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.436 |
MOD_NEK2_1 | 680 | 685 | PF00069 | 0.467 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.449 |
MOD_NEK2_1 | 796 | 801 | PF00069 | 0.425 |
MOD_NEK2_1 | 837 | 842 | PF00069 | 0.385 |
MOD_NEK2_2 | 6 | 11 | PF00069 | 0.394 |
MOD_NEK2_2 | 802 | 807 | PF00069 | 0.491 |
MOD_PIKK_1 | 267 | 273 | PF00454 | 0.469 |
MOD_PIKK_1 | 570 | 576 | PF00454 | 0.449 |
MOD_PIKK_1 | 598 | 604 | PF00454 | 0.726 |
MOD_PK_1 | 74 | 80 | PF00069 | 0.457 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.445 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.573 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.457 |
MOD_PKA_2 | 645 | 651 | PF00069 | 0.549 |
MOD_PKA_2 | 802 | 808 | PF00069 | 0.452 |
MOD_PKA_2 | 815 | 821 | PF00069 | 0.329 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.416 |
MOD_PKA_2 | 934 | 940 | PF00069 | 0.599 |
MOD_PKA_2 | 951 | 957 | PF00069 | 0.358 |
MOD_Plk_1 | 299 | 305 | PF00069 | 0.484 |
MOD_Plk_1 | 312 | 318 | PF00069 | 0.547 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.475 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.366 |
MOD_Plk_1 | 822 | 828 | PF00069 | 0.480 |
MOD_Plk_1 | 894 | 900 | PF00069 | 0.342 |
MOD_Plk_2-3 | 129 | 135 | PF00069 | 0.435 |
MOD_Plk_2-3 | 249 | 255 | PF00069 | 0.496 |
MOD_Plk_2-3 | 264 | 270 | PF00069 | 0.386 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.442 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.464 |
MOD_Plk_4 | 676 | 682 | PF00069 | 0.498 |
MOD_Plk_4 | 802 | 808 | PF00069 | 0.464 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.450 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.473 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.479 |
MOD_ProDKin_1 | 685 | 691 | PF00069 | 0.548 |
TRG_DiLeu_BaEn_1 | 387 | 392 | PF01217 | 0.442 |
TRG_DiLeu_BaLyEn_6 | 628 | 633 | PF01217 | 0.495 |
TRG_DiLeu_LyEn_5 | 223 | 228 | PF01217 | 0.536 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.569 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 368 | 371 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 376 | 379 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 462 | 465 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 566 | 569 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 654 | 657 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 779 | 782 | PF00928 | 0.612 |
TRG_ER_diArg_1 | 179 | 181 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 384 | 386 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 398 | 400 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 49 | 52 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 718 | 721 | PF00400 | 0.669 |
TRG_ER_diArg_1 | 738 | 740 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 808 | 810 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 815 | 817 | PF00400 | 0.404 |
TRG_NES_CRM1_1 | 241 | 255 | PF08389 | 0.498 |
TRG_NES_CRM1_1 | 68 | 81 | PF08389 | 0.493 |
TRG_NLS_Bipartite_1 | 399 | 414 | PF00514 | 0.496 |
TRG_NLS_MonoExtN_4 | 409 | 414 | PF00514 | 0.496 |
TRG_Pf-PMV_PEXEL_1 | 200 | 205 | PF00026 | 0.305 |
TRG_Pf-PMV_PEXEL_1 | 399 | 403 | PF00026 | 0.242 |
TRG_Pf-PMV_PEXEL_1 | 585 | 589 | PF00026 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 918 | 922 | PF00026 | 0.580 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHR1 | Leptomonas seymouri | 58% | 99% |
A0A1X0NWY2 | Trypanosomatidae | 40% | 97% |
A0A3R7RKP1 | Trypanosoma rangeli | 41% | 97% |
A4H9V3 | Leishmania braziliensis | 83% | 100% |
A4HUR7 | Leishmania infantum | 100% | 100% |
D0A7P6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9ANF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4QH75 | Leishmania major | 93% | 100% |
V5BRH2 | Trypanosoma cruzi | 42% | 98% |