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 | 11 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0042555 | MCM complex | 2 | 12 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: A4H5K0
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006270 | DNA replication initiation | 5 | 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:0009987 | cellular process | 1 | 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: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:0000724 | double-strand break repair via homologous recombination | 7 | 1 |
GO:0000725 | recombinational repair | 6 | 1 |
GO:0000727 | double-strand break repair via break-induced replication | 8 | 1 |
GO:0006268 | DNA unwinding involved in DNA replication | 9 | 1 |
GO:0006271 | DNA strand elongation involved in DNA replication | 6 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022616 | DNA strand elongation | 5 | 1 |
GO:0032392 | DNA geometric change | 7 | 1 |
GO:0032508 | DNA duplex unwinding | 8 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0071103 | DNA conformation change | 6 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1902292 | cell cycle DNA replication initiation | 3 | 1 |
GO:1902315 | nuclear cell cycle DNA replication initiation | 4 | 1 |
GO:1902975 | mitotic DNA replication initiation | 4 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 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:0003678 | DNA helicase activity | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 12 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 12 |
GO:0016887 | ATP hydrolysis activity | 7 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 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:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003697 | single-stranded DNA binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 328 | 332 | PF00656 | 0.300 |
CLV_C14_Caspase3-7 | 372 | 376 | PF00656 | 0.633 |
CLV_C14_Caspase3-7 | 684 | 688 | PF00656 | 0.626 |
CLV_C14_Caspase3-7 | 694 | 698 | PF00656 | 0.582 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 618 | 620 | PF00675 | 0.223 |
CLV_NRD_NRD_1 | 638 | 640 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 844 | 846 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 852 | 854 | PF00675 | 0.383 |
CLV_NRD_NRD_1 | 859 | 861 | PF00675 | 0.367 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.227 |
CLV_PCSK_KEX2_1 | 618 | 620 | PF00082 | 0.223 |
CLV_PCSK_KEX2_1 | 638 | 640 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 751 | 753 | PF00082 | 0.172 |
CLV_PCSK_KEX2_1 | 805 | 807 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 844 | 846 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 851 | 853 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 859 | 861 | PF00082 | 0.367 |
CLV_PCSK_PC1ET2_1 | 422 | 424 | PF00082 | 0.227 |
CLV_PCSK_PC1ET2_1 | 751 | 753 | PF00082 | 0.148 |
CLV_PCSK_PC1ET2_1 | 805 | 807 | PF00082 | 0.279 |
CLV_PCSK_PC1ET2_1 | 851 | 853 | PF00082 | 0.476 |
CLV_PCSK_PC7_1 | 29 | 35 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.212 |
CLV_PCSK_SKI1_1 | 542 | 546 | PF00082 | 0.212 |
CLV_PCSK_SKI1_1 | 619 | 623 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 639 | 643 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 814 | 818 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 868 | 872 | PF00082 | 0.360 |
CLV_Separin_Metazoa | 336 | 340 | PF03568 | 0.544 |
DEG_APCC_DBOX_1 | 422 | 430 | PF00400 | 0.412 |
DEG_APCC_DBOX_1 | 458 | 466 | PF00400 | 0.515 |
DEG_APCC_DBOX_1 | 541 | 549 | PF00400 | 0.412 |
DEG_APCC_DBOX_1 | 600 | 608 | PF00400 | 0.412 |
DEG_Kelch_Keap1_1 | 508 | 513 | PF01344 | 0.412 |
DOC_MAPK_DCC_7 | 204 | 214 | PF00069 | 0.412 |
DOC_MAPK_gen_1 | 204 | 214 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 751 | 760 | PF00069 | 0.348 |
DOC_MAPK_gen_1 | 789 | 798 | PF00069 | 0.412 |
DOC_MAPK_gen_1 | 805 | 812 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 113 | 120 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 125 | 132 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 207 | 214 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 459 | 466 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 601 | 609 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 805 | 812 | PF00069 | 0.501 |
DOC_MAPK_RevD_3 | 605 | 619 | PF00069 | 0.479 |
DOC_PP2B_PxIxI_1 | 209 | 215 | PF00149 | 0.423 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 540 | 544 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 577 | 581 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 763 | 767 | PF00917 | 0.437 |
DOC_USP7_UBL2_3 | 263 | 267 | PF12436 | 0.515 |
DOC_USP7_UBL2_3 | 99 | 103 | PF12436 | 0.515 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.350 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.514 |
LIG_14-3-3_CanoR_1 | 113 | 117 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 618 | 628 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 673 | 679 | PF00244 | 0.699 |
LIG_14-3-3_CanoR_1 | 782 | 790 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 791 | 798 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 806 | 811 | PF00244 | 0.408 |
LIG_Actin_WH2_2 | 145 | 162 | PF00022 | 0.464 |
LIG_AP2alpha_1 | 28 | 32 | PF02296 | 0.392 |
LIG_APCC_ABBA_1 | 25 | 30 | PF00400 | 0.458 |
LIG_APCC_ABBA_1 | 257 | 262 | PF00400 | 0.430 |
LIG_APCC_ABBA_1 | 625 | 630 | PF00400 | 0.412 |
LIG_APCC_ABBAyCdc20_2 | 435 | 441 | PF00400 | 0.515 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.431 |
LIG_BIR_III_4 | 687 | 691 | PF00653 | 0.754 |
LIG_BRCT_BRCA1_1 | 454 | 458 | PF00533 | 0.515 |
LIG_CaM_IQ_9 | 219 | 235 | PF13499 | 0.437 |
LIG_Clathr_ClatBox_1 | 823 | 827 | PF01394 | 0.488 |
LIG_eIF4E_1 | 153 | 159 | PF01652 | 0.464 |
LIG_eIF4E_1 | 260 | 266 | PF01652 | 0.515 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.528 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.520 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.372 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.470 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.671 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.547 |
LIG_FHA_1 | 500 | 506 | PF00498 | 0.412 |
LIG_FHA_1 | 509 | 515 | PF00498 | 0.412 |
LIG_FHA_1 | 539 | 545 | PF00498 | 0.412 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.412 |
LIG_FHA_1 | 567 | 573 | PF00498 | 0.412 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.348 |
LIG_FHA_1 | 673 | 679 | PF00498 | 0.569 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.348 |
LIG_FHA_1 | 818 | 824 | PF00498 | 0.462 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.331 |
LIG_FHA_1 | 905 | 911 | PF00498 | 0.437 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.310 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.552 |
LIG_FHA_2 | 692 | 698 | PF00498 | 0.607 |
LIG_Integrin_isoDGR_2 | 56 | 58 | PF01839 | 0.168 |
LIG_LIR_Gen_1 | 104 | 110 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 117 | 128 | PF02991 | 0.545 |
LIG_LIR_Gen_1 | 12 | 23 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 392 | 401 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 402 | 411 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 532 | 540 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 600 | 609 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 731 | 741 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 117 | 123 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 30 | 35 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 392 | 397 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 402 | 407 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 600 | 605 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 731 | 736 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 739 | 745 | PF02991 | 0.415 |
LIG_NRBOX | 461 | 467 | PF00104 | 0.515 |
LIG_NRBOX | 603 | 609 | PF00104 | 0.412 |
LIG_NRBOX | 845 | 851 | PF00104 | 0.442 |
LIG_NRBOX | 889 | 895 | PF00104 | 0.367 |
LIG_Pex14_1 | 220 | 224 | PF04695 | 0.515 |
LIG_Pex14_2 | 28 | 32 | PF04695 | 0.248 |
LIG_Pex14_2 | 602 | 606 | PF04695 | 0.412 |
LIG_RPA_C_Fungi | 848 | 860 | PF08784 | 0.394 |
LIG_SH2_PTP2 | 733 | 736 | PF00017 | 0.283 |
LIG_SH2_PTP2 | 757 | 760 | PF00017 | 0.342 |
LIG_SH2_STAP1 | 15 | 19 | PF00017 | 0.521 |
LIG_SH2_STAP1 | 249 | 253 | PF00017 | 0.248 |
LIG_SH2_STAP1 | 404 | 408 | PF00017 | 0.283 |
LIG_SH2_STAP1 | 792 | 796 | PF00017 | 0.184 |
LIG_SH2_STAT3 | 854 | 857 | PF00017 | 0.430 |
LIG_SH2_STAT3 | 94 | 97 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 490 | 493 | PF00017 | 0.248 |
LIG_SH2_STAT5 | 733 | 736 | PF00017 | 0.262 |
LIG_SH2_STAT5 | 757 | 760 | PF00017 | 0.248 |
LIG_SH2_STAT5 | 854 | 857 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.286 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.342 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.430 |
LIG_SH3_3 | 512 | 518 | PF00018 | 0.248 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.373 |
LIG_SH3_3 | 717 | 723 | PF00018 | 0.408 |
LIG_SH3_3 | 878 | 884 | PF00018 | 0.526 |
LIG_SUMO_SIM_anti_2 | 155 | 160 | PF11976 | 0.433 |
LIG_SUMO_SIM_anti_2 | 889 | 895 | PF11976 | 0.357 |
LIG_SUMO_SIM_anti_2 | 906 | 913 | PF11976 | 0.381 |
LIG_SUMO_SIM_par_1 | 114 | 119 | PF11976 | 0.285 |
LIG_SUMO_SIM_par_1 | 889 | 895 | PF11976 | 0.475 |
LIG_UBA3_1 | 195 | 199 | PF00899 | 0.392 |
LIG_WRC_WIRS_1 | 36 | 41 | PF05994 | 0.340 |
LIG_WRC_WIRS_1 | 408 | 413 | PF05994 | 0.248 |
LIG_WRC_WIRS_1 | 900 | 905 | PF05994 | 0.383 |
MOD_CDK_SPK_2 | 49 | 54 | PF00069 | 0.159 |
MOD_CDK_SPxK_1 | 308 | 314 | PF00069 | 0.392 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.459 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.475 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.295 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.358 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.423 |
MOD_CK1_1 | 634 | 640 | PF00069 | 0.587 |
MOD_CK1_1 | 674 | 680 | PF00069 | 0.672 |
MOD_CK1_1 | 681 | 687 | PF00069 | 0.670 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.389 |
MOD_CK1_1 | 766 | 772 | PF00069 | 0.283 |
MOD_CK1_1 | 794 | 800 | PF00069 | 0.392 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.283 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.283 |
MOD_Cter_Amidation | 857 | 860 | PF01082 | 0.373 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.632 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.410 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.412 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.392 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.248 |
MOD_GlcNHglycan | 633 | 636 | PF01048 | 0.553 |
MOD_GlcNHglycan | 643 | 647 | PF01048 | 0.681 |
MOD_GlcNHglycan | 684 | 687 | PF01048 | 0.722 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.419 |
MOD_GlcNHglycan | 770 | 773 | PF01048 | 0.264 |
MOD_GlcNHglycan | 814 | 817 | PF01048 | 0.411 |
MOD_GlcNHglycan | 875 | 878 | PF01048 | 0.577 |
MOD_GlcNHglycan | 894 | 897 | PF01048 | 0.290 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.368 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.614 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.248 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.392 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.248 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.248 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.631 |
MOD_GSK3_1 | 619 | 626 | PF00069 | 0.170 |
MOD_GSK3_1 | 667 | 674 | PF00069 | 0.693 |
MOD_GSK3_1 | 678 | 685 | PF00069 | 0.735 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.350 |
MOD_GSK3_1 | 764 | 771 | PF00069 | 0.251 |
MOD_GSK3_1 | 790 | 797 | PF00069 | 0.184 |
MOD_GSK3_1 | 814 | 821 | PF00069 | 0.428 |
MOD_GSK3_1 | 899 | 906 | PF00069 | 0.380 |
MOD_N-GLC_1 | 255 | 260 | PF02516 | 0.271 |
MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.159 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.243 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.696 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.554 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.303 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.174 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.263 |
MOD_NEK2_1 | 629 | 634 | PF00069 | 0.592 |
MOD_NEK2_1 | 812 | 817 | PF00069 | 0.419 |
MOD_NEK2_1 | 903 | 908 | PF00069 | 0.381 |
MOD_NEK2_1 | 910 | 915 | PF00069 | 0.427 |
MOD_NEK2_2 | 131 | 136 | PF00069 | 0.392 |
MOD_NEK2_2 | 61 | 66 | PF00069 | 0.159 |
MOD_NEK2_2 | 737 | 742 | PF00069 | 0.263 |
MOD_PIKK_1 | 472 | 478 | PF00454 | 0.248 |
MOD_PIKK_1 | 5 | 11 | PF00454 | 0.406 |
MOD_PIKK_1 | 577 | 583 | PF00454 | 0.248 |
MOD_PIKK_1 | 667 | 673 | PF00454 | 0.623 |
MOD_PK_1 | 806 | 812 | PF00069 | 0.159 |
MOD_PKA_1 | 349 | 355 | PF00069 | 0.484 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.351 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.248 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.549 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.406 |
MOD_PKA_2 | 567 | 573 | PF00069 | 0.248 |
MOD_PKA_2 | 672 | 678 | PF00069 | 0.681 |
MOD_PKA_2 | 737 | 743 | PF00069 | 0.269 |
MOD_PKA_2 | 763 | 769 | PF00069 | 0.308 |
MOD_PKA_2 | 781 | 787 | PF00069 | 0.283 |
MOD_PKA_2 | 790 | 796 | PF00069 | 0.392 |
MOD_PKA_2 | 858 | 864 | PF00069 | 0.404 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.331 |
MOD_Plk_1 | 13 | 19 | PF00069 | 0.415 |
MOD_Plk_1 | 225 | 231 | PF00069 | 0.342 |
MOD_Plk_1 | 255 | 261 | PF00069 | 0.271 |
MOD_Plk_1 | 667 | 673 | PF00069 | 0.623 |
MOD_Plk_1 | 794 | 800 | PF00069 | 0.308 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.415 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.533 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.263 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.383 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.525 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.392 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.248 |
MOD_Plk_4 | 594 | 600 | PF00069 | 0.248 |
MOD_Plk_4 | 623 | 629 | PF00069 | 0.248 |
MOD_Plk_4 | 737 | 743 | PF00069 | 0.322 |
MOD_Plk_4 | 776 | 782 | PF00069 | 0.248 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.289 |
MOD_Plk_4 | 906 | 912 | PF00069 | 0.336 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.348 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.342 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.162 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.392 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.651 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.391 |
MOD_SUMO_rev_2 | 258 | 265 | PF00179 | 0.263 |
MOD_SUMO_rev_2 | 797 | 807 | PF00179 | 0.251 |
TRG_DiLeu_BaEn_1 | 261 | 266 | PF01217 | 0.283 |
TRG_DiLeu_BaEn_1 | 461 | 466 | PF01217 | 0.342 |
TRG_DiLeu_BaEn_1 | 517 | 522 | PF01217 | 0.271 |
TRG_DiLeu_BaEn_1 | 889 | 894 | PF01217 | 0.352 |
TRG_DiLeu_BaEn_3 | 802 | 808 | PF01217 | 0.159 |
TRG_DiLeu_BaLyEn_6 | 67 | 72 | PF01217 | 0.159 |
TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.263 |
TRG_ENDOCYTIC_2 | 733 | 736 | PF00928 | 0.248 |
TRG_ENDOCYTIC_2 | 757 | 760 | PF00928 | 0.248 |
TRG_ER_diArg_1 | 32 | 34 | PF00400 | 0.403 |
TRG_ER_diArg_1 | 618 | 620 | PF00400 | 0.263 |
TRG_ER_diArg_1 | 843 | 845 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 852 | 854 | PF00400 | 0.377 |
TRG_NES_CRM1_1 | 585 | 595 | PF08389 | 0.392 |
TRG_Pf-PMV_PEXEL_1 | 844 | 848 | PF00026 | 0.535 |
TRG_Pf-PMV_PEXEL_1 | 853 | 857 | PF00026 | 0.531 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P860 | Leptomonas seymouri | 30% | 93% |
A0A0N1I383 | Leptomonas seymouri | 76% | 90% |
A0A0S4IK09 | Bodo saltans | 30% | 94% |
A0A0S4IW18 | Bodo saltans | 55% | 100% |
A0A0S4JM41 | Bodo saltans | 29% | 100% |
A0A1X0NNF6 | Trypanosomatidae | 57% | 100% |
A0A1X0NZT6 | Trypanosomatidae | 31% | 98% |
A0A3Q8IAX4 | Leishmania donovani | 31% | 95% |
A0A3R7K9K0 | Trypanosoma rangeli | 30% | 100% |
A0A3R7NBN0 | Trypanosoma rangeli | 31% | 97% |
A0A3S7WQI8 | Leishmania donovani | 88% | 100% |
A0A3S7WY81 | Leishmania donovani | 31% | 100% |
A0A422NDD9 | Trypanosoma rangeli | 56% | 100% |
A4FUD9 | Bos taurus | 32% | 100% |
A4HGC9 | Leishmania braziliensis | 32% | 95% |
A4HLY1 | Leishmania braziliensis | 30% | 100% |
A4HTX2 | Leishmania infantum | 88% | 100% |
A4I0T0 | Leishmania infantum | 31% | 100% |
A4I3G2 | Leishmania infantum | 31% | 95% |
B8AZ14 | Oryza sativa subsp. indica | 29% | 100% |
B8AZ99 | Oryza sativa subsp. indica | 30% | 100% |
B9FKM7 | Oryza sativa subsp. japonica | 29% | 100% |
D0A7X6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 97% |
D0A999 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
D3ZVK1 | Rattus norvegicus | 30% | 100% |
E1BPX4 | Bos taurus | 29% | 100% |
E9AMM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
E9AWT2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AZQ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 95% |
I0IUP3 | Gallus gallus | 29% | 100% |
P24279 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 95% |
P25205 | Homo sapiens | 32% | 100% |
P25206 | Mus musculus | 32% | 100% |
P29469 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
P30664 | Xenopus laevis | 42% | 100% |
P30666 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
P33991 | Homo sapiens | 41% | 100% |
P49739 | Xenopus laevis | 32% | 100% |
P55861 | Xenopus laevis | 30% | 100% |
Q0DHC4 | Oryza sativa subsp. japonica | 30% | 100% |
Q0V9Q6 | Xenopus tropicalis | 30% | 100% |
Q21902 | Caenorhabditis elegans | 28% | 100% |
Q26454 | Drosophila melanogaster | 40% | 100% |
Q43704 | Zea mays | 30% | 100% |
Q4Q8I2 | Leishmania major | 32% | 95% |
Q4QAP2 | Leishmania major | 30% | 100% |
Q4QI01 | Leishmania major | 87% | 98% |
Q5F310 | Xenopus laevis | 29% | 100% |
Q5R8G6 | Pongo abelii | 32% | 100% |
Q5XK83 | Xenopus laevis | 41% | 100% |
Q6DIH3 | Xenopus tropicalis | 30% | 100% |
Q6GL41 | Xenopus tropicalis | 42% | 100% |
Q7ZXZ0 | Xenopus laevis | 32% | 100% |
Q95XQ8 | Caenorhabditis elegans | 40% | 100% |
Q9CWV1 | Mus musculus | 30% | 100% |
Q9FL33 | Arabidopsis thaliana | 30% | 100% |
Q9SF37 | Arabidopsis thaliana | 29% | 100% |
Q9SX03 | Zea mays | 30% | 100% |
Q9SX04 | Zea mays | 30% | 100% |
Q9UJA3 | Homo sapiens | 28% | 100% |
Q9VF30 | Drosophila melanogaster | 24% | 100% |
Q9XYU1 | Drosophila melanogaster | 32% | 100% |
V5BAH7 | Trypanosoma cruzi | 30% | 100% |
V5BQA9 | Trypanosoma cruzi | 31% | 100% |
V5BSG2 | Trypanosoma cruzi | 57% | 100% |