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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 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: E9B002
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 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:0009987 | cellular process | 1 | 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:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 8 |
GO:0016491 | oxidoreductase activity | 2 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0043169 | cation binding | 3 | 8 |
GO:0046872 | metal ion binding | 4 | 8 |
GO:0051213 | dioxygenase activity | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 8 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 8 |
GO:0140657 | ATP-dependent activity | 1 | 8 |
GO:0140658 | ATP-dependent chromatin remodeler activity | 3 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 433 | 437 | PF00656 | 0.518 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.293 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.383 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.293 |
CLV_NRD_NRD_1 | 517 | 519 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 577 | 579 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 637 | 639 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 848 | 850 | PF00675 | 0.544 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 517 | 519 | PF00082 | 0.697 |
CLV_PCSK_KEX2_1 | 577 | 579 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 637 | 639 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 643 | 645 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 850 | 852 | PF00082 | 0.548 |
CLV_PCSK_PC1ET2_1 | 255 | 257 | PF00082 | 0.318 |
CLV_PCSK_PC1ET2_1 | 446 | 448 | PF00082 | 0.332 |
CLV_PCSK_PC1ET2_1 | 643 | 645 | PF00082 | 0.590 |
CLV_PCSK_PC1ET2_1 | 850 | 852 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.689 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.175 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.175 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 580 | 584 | PF00082 | 0.708 |
CLV_PCSK_SKI1_1 | 630 | 634 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 779 | 783 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.684 |
CLV_PCSK_SKI1_1 | 826 | 830 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 850 | 854 | PF00082 | 0.565 |
CLV_Separin_Metazoa | 11 | 15 | PF03568 | 0.624 |
CLV_Separin_Metazoa | 400 | 404 | PF03568 | 0.532 |
DEG_APCC_DBOX_1 | 761 | 769 | PF00400 | 0.397 |
DEG_APCC_DBOX_1 | 778 | 786 | PF00400 | 0.504 |
DEG_MDM2_SWIB_1 | 330 | 338 | PF02201 | 0.532 |
DEG_SCF_TRCP1_1 | 85 | 90 | PF00400 | 0.695 |
DEG_SPOP_SBC_1 | 137 | 141 | PF00917 | 0.593 |
DOC_CYCLIN_yCln2_LP_2 | 652 | 658 | PF00134 | 0.625 |
DOC_MAPK_gen_1 | 188 | 195 | PF00069 | 0.493 |
DOC_MAPK_gen_1 | 254 | 260 | PF00069 | 0.518 |
DOC_MAPK_gen_1 | 643 | 654 | PF00069 | 0.536 |
DOC_MAPK_gen_1 | 760 | 768 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 875 | 884 | PF00069 | 0.574 |
DOC_MAPK_MEF2A_6 | 413 | 422 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 647 | 656 | PF00069 | 0.596 |
DOC_MAPK_MEF2A_6 | 774 | 782 | PF00069 | 0.526 |
DOC_PP1_RVXF_1 | 723 | 730 | PF00149 | 0.493 |
DOC_PP1_RVXF_1 | 824 | 831 | PF00149 | 0.476 |
DOC_PP2B_LxvP_1 | 142 | 145 | PF13499 | 0.575 |
DOC_PP2B_LxvP_1 | 386 | 389 | PF13499 | 0.493 |
DOC_PP2B_LxvP_1 | 441 | 444 | PF13499 | 0.493 |
DOC_PP2B_LxvP_1 | 652 | 655 | PF13499 | 0.611 |
DOC_PP2B_LxvP_1 | 884 | 887 | PF13499 | 0.566 |
DOC_PP2B_PxIxI_1 | 508 | 514 | PF00149 | 0.493 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 666 | 670 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 746 | 750 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 887 | 891 | PF00917 | 0.752 |
DOC_USP7_UBL2_3 | 469 | 473 | PF12436 | 0.532 |
DOC_USP7_UBL2_3 | 643 | 647 | PF12436 | 0.494 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 484 | 489 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 774 | 779 | PF00397 | 0.532 |
LIG_14-3-3_CanoR_1 | 136 | 145 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 256 | 261 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 320 | 330 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 364 | 373 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 384 | 389 | PF00244 | 0.347 |
LIG_14-3-3_CanoR_1 | 413 | 422 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 447 | 452 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 501 | 511 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 762 | 766 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 875 | 884 | PF00244 | 0.574 |
LIG_Actin_WH2_2 | 414 | 430 | PF00022 | 0.532 |
LIG_Actin_WH2_2 | 564 | 582 | PF00022 | 0.628 |
LIG_APCC_ABBA_1 | 690 | 695 | PF00400 | 0.647 |
LIG_APCC_ABBA_1 | 766 | 771 | PF00400 | 0.583 |
LIG_APCC_ABBAyCdc20_2 | 176 | 182 | PF00400 | 0.532 |
LIG_BRCT_BRCA1_1 | 20 | 24 | PF00533 | 0.597 |
LIG_BRCT_BRCA1_1 | 418 | 422 | PF00533 | 0.532 |
LIG_Clathr_ClatBox_1 | 653 | 657 | PF01394 | 0.622 |
LIG_Clathr_ClatBox_1 | 691 | 695 | PF01394 | 0.426 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.600 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.564 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.444 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.493 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.440 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.454 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.398 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.532 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.532 |
LIG_FHA_1 | 571 | 577 | PF00498 | 0.616 |
LIG_FHA_1 | 708 | 714 | PF00498 | 0.406 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.696 |
LIG_FHA_1 | 823 | 829 | PF00498 | 0.456 |
LIG_FHA_1 | 876 | 882 | PF00498 | 0.543 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.583 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.499 |
LIG_FHA_2 | 492 | 498 | PF00498 | 0.493 |
LIG_HP1_1 | 778 | 782 | PF01393 | 0.532 |
LIG_LIR_Gen_1 | 21 | 32 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 266 | 274 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 309 | 318 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 493 | 500 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 829 | 835 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 182 | 186 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 21 | 27 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 266 | 270 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 272 | 277 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 309 | 313 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 378 | 383 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 419 | 425 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 493 | 499 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 730 | 735 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 829 | 833 | PF02991 | 0.458 |
LIG_LYPXL_S_1 | 379 | 383 | PF13949 | 0.332 |
LIG_LYPXL_yS_3 | 380 | 383 | PF13949 | 0.532 |
LIG_NRBOX | 49 | 55 | PF00104 | 0.565 |
LIG_PCNA_PIPBox_1 | 323 | 332 | PF02747 | 0.532 |
LIG_PCNA_yPIPBox_3 | 320 | 330 | PF02747 | 0.532 |
LIG_Pex14_2 | 330 | 334 | PF04695 | 0.532 |
LIG_Pex14_2 | 492 | 496 | PF04695 | 0.532 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.532 |
LIG_SH2_CRK | 267 | 271 | PF00017 | 0.532 |
LIG_SH2_CRK | 274 | 278 | PF00017 | 0.532 |
LIG_SH2_CRK | 463 | 467 | PF00017 | 0.493 |
LIG_SH2_GRB2like | 404 | 407 | PF00017 | 0.532 |
LIG_SH2_PTP2 | 510 | 513 | PF00017 | 0.624 |
LIG_SH2_SRC | 267 | 270 | PF00017 | 0.532 |
LIG_SH2_STAP1 | 267 | 271 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 510 | 513 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 712 | 715 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 735 | 738 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 856 | 859 | PF00017 | 0.556 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.493 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.532 |
LIG_SH3_3 | 609 | 615 | PF00018 | 0.406 |
LIG_SH3_3 | 772 | 778 | PF00018 | 0.532 |
LIG_SUMO_SIM_anti_2 | 416 | 422 | PF11976 | 0.532 |
LIG_SUMO_SIM_anti_2 | 649 | 655 | PF11976 | 0.547 |
LIG_SUMO_SIM_par_1 | 191 | 199 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 654 | 660 | PF11976 | 0.595 |
LIG_TRAF2_1 | 456 | 459 | PF00917 | 0.532 |
LIG_TRAF2_1 | 899 | 902 | PF00917 | 0.794 |
LIG_TYR_ITIM | 402 | 407 | PF00017 | 0.583 |
LIG_UBA3_1 | 440 | 446 | PF00899 | 0.493 |
LIG_UBA3_1 | 591 | 599 | PF00899 | 0.406 |
LIG_UBA3_1 | 881 | 889 | PF00899 | 0.579 |
LIG_WRC_WIRS_1 | 489 | 494 | PF05994 | 0.525 |
LIG_WRC_WIRS_1 | 729 | 734 | PF05994 | 0.498 |
MOD_CDK_SPK_2 | 774 | 779 | PF00069 | 0.532 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.694 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.493 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.493 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.642 |
MOD_CK1_1 | 646 | 652 | PF00069 | 0.644 |
MOD_CK1_1 | 707 | 713 | PF00069 | 0.394 |
MOD_CK1_1 | 861 | 867 | PF00069 | 0.619 |
MOD_CK1_1 | 890 | 896 | PF00069 | 0.726 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.566 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.491 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.532 |
MOD_CK2_1 | 491 | 497 | PF00069 | 0.493 |
MOD_CK2_1 | 587 | 593 | PF00069 | 0.700 |
MOD_CK2_1 | 761 | 767 | PF00069 | 0.583 |
MOD_CK2_1 | 896 | 902 | PF00069 | 0.737 |
MOD_DYRK1A_RPxSP_1 | 774 | 778 | PF00069 | 0.527 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.565 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.754 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.756 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.297 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.307 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.766 |
MOD_GlcNHglycan | 668 | 671 | PF01048 | 0.691 |
MOD_GlcNHglycan | 681 | 684 | PF01048 | 0.690 |
MOD_GlcNHglycan | 753 | 756 | PF01048 | 0.311 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.732 |
MOD_GlcNHglycan | 853 | 856 | PF01048 | 0.566 |
MOD_GlcNHglycan | 863 | 866 | PF01048 | 0.565 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.674 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.522 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.532 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.493 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.566 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.532 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.501 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.715 |
MOD_GSK3_1 | 700 | 707 | PF00069 | 0.575 |
MOD_GSK3_1 | 727 | 734 | PF00069 | 0.493 |
MOD_GSK3_1 | 751 | 758 | PF00069 | 0.490 |
MOD_GSK3_1 | 822 | 829 | PF00069 | 0.601 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.654 |
MOD_GSK3_1 | 857 | 864 | PF00069 | 0.537 |
MOD_GSK3_1 | 887 | 894 | PF00069 | 0.702 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.596 |
MOD_LATS_1 | 411 | 417 | PF00433 | 0.532 |
MOD_LATS_1 | 597 | 603 | PF00433 | 0.595 |
MOD_N-GLC_1 | 666 | 671 | PF02516 | 0.705 |
MOD_N-GLC_1 | 700 | 705 | PF02516 | 0.600 |
MOD_N-GLC_1 | 792 | 797 | PF02516 | 0.293 |
MOD_N-GLC_1 | 841 | 846 | PF02516 | 0.498 |
MOD_N-GLC_2 | 798 | 800 | PF02516 | 0.332 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.684 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.559 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.412 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.493 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.466 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.532 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.495 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.542 |
MOD_NEK2_1 | 570 | 575 | PF00069 | 0.631 |
MOD_NEK2_1 | 587 | 592 | PF00069 | 0.502 |
MOD_NEK2_1 | 633 | 638 | PF00069 | 0.406 |
MOD_NEK2_1 | 659 | 664 | PF00069 | 0.657 |
MOD_NEK2_1 | 704 | 709 | PF00069 | 0.550 |
MOD_NEK2_1 | 713 | 718 | PF00069 | 0.589 |
MOD_NEK2_1 | 781 | 786 | PF00069 | 0.493 |
MOD_NEK2_1 | 792 | 797 | PF00069 | 0.493 |
MOD_NEK2_1 | 858 | 863 | PF00069 | 0.642 |
MOD_NEK2_2 | 18 | 23 | PF00069 | 0.591 |
MOD_NEK2_2 | 755 | 760 | PF00069 | 0.532 |
MOD_PIKK_1 | 224 | 230 | PF00454 | 0.493 |
MOD_PIKK_1 | 707 | 713 | PF00454 | 0.477 |
MOD_PIKK_1 | 841 | 847 | PF00454 | 0.497 |
MOD_PKA_1 | 643 | 649 | PF00069 | 0.576 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.532 |
MOD_PKA_2 | 502 | 508 | PF00069 | 0.532 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.784 |
MOD_PKA_2 | 643 | 649 | PF00069 | 0.576 |
MOD_PKA_2 | 761 | 767 | PF00069 | 0.427 |
MOD_PKB_1 | 254 | 262 | PF00069 | 0.532 |
MOD_PKB_1 | 849 | 857 | PF00069 | 0.578 |
MOD_Plk_1 | 160 | 166 | PF00069 | 0.778 |
MOD_Plk_1 | 700 | 706 | PF00069 | 0.614 |
MOD_Plk_1 | 841 | 847 | PF00069 | 0.497 |
MOD_Plk_2-3 | 897 | 903 | PF00069 | 0.751 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.505 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.479 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.465 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.493 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.527 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.501 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.472 |
MOD_Plk_4 | 570 | 576 | PF00069 | 0.689 |
MOD_Plk_4 | 587 | 593 | PF00069 | 0.543 |
MOD_Plk_4 | 728 | 734 | PF00069 | 0.539 |
MOD_Plk_4 | 761 | 767 | PF00069 | 0.583 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.756 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.583 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.493 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.532 |
MOD_ProDKin_1 | 484 | 490 | PF00069 | 0.539 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.481 |
MOD_ProDKin_1 | 774 | 780 | PF00069 | 0.532 |
MOD_SUMO_rev_2 | 432 | 440 | PF00179 | 0.494 |
MOD_SUMO_rev_2 | 719 | 727 | PF00179 | 0.539 |
MOD_SUMO_rev_2 | 844 | 852 | PF00179 | 0.528 |
TRG_DiLeu_BaEn_2 | 10 | 16 | PF01217 | 0.625 |
TRG_DiLeu_BaLyEn_6 | 378 | 383 | PF01217 | 0.493 |
TRG_DiLeu_LyEn_5 | 57 | 62 | PF01217 | 0.653 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 380 | 383 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.583 |
TRG_ENDOCYTIC_2 | 463 | 466 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.570 |
TRG_ENDOCYTIC_2 | 510 | 513 | PF00928 | 0.624 |
TRG_ER_diArg_1 | 320 | 322 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 427 | 429 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 500 | 503 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 516 | 518 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 576 | 578 | PF00400 | 0.630 |
TRG_NES_CRM1_1 | 46 | 57 | PF08389 | 0.398 |
TRG_NES_CRM1_1 | 711 | 724 | PF08389 | 0.375 |
TRG_Pf-PMV_PEXEL_1 | 320 | 325 | PF00026 | 0.322 |
TRG_Pf-PMV_PEXEL_1 | 336 | 340 | PF00026 | 0.227 |
TRG_Pf-PMV_PEXEL_1 | 565 | 569 | PF00026 | 0.695 |
TRG_Pf-PMV_PEXEL_1 | 718 | 723 | PF00026 | 0.383 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFY0 | Leptomonas seymouri | 69% | 73% |
A0A0S4IS76 | Bodo saltans | 38% | 82% |
A0A3S7X1L6 | Leishmania donovani | 89% | 72% |
A4HGN6 | Leishmania braziliensis | 79% | 100% |
A4I3Q9 | Leishmania infantum | 89% | 72% |
D0A899 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 100% |
O13762 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% |
O60177 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 87% |
P0CQ66 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 26% | 76% |
P0CQ67 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 26% | 76% |
P32849 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 78% |
P36607 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 80% |
Q10332 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% |
Q14527 | Homo sapiens | 29% | 90% |
Q4IJ84 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 27% | 79% |
Q4Q883 | Leishmania major | 88% | 100% |
Q4WVM1 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 28% | 73% |
Q5ACX1 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 27% | 84% |
Q5BHD6 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 26% | 76% |
Q6BIP2 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 24% | 76% |
Q6C2R8 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 28% | 89% |
Q6CJM4 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 26% | 82% |
Q6FY76 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 27% | 79% |
Q6PCN7 | Mus musculus | 28% | 91% |
Q753V5 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 27% | 84% |
Q7S1P9 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 27% | 74% |
Q94BR5 | Arabidopsis thaliana | 25% | 93% |
Q95216 | Oryctolagus cuniculus | 27% | 90% |
Q9FIY7 | Arabidopsis thaliana | 27% | 71% |
Q9FNI6 | Arabidopsis thaliana | 28% | 88% |
Q9LHE4 | Arabidopsis thaliana | 27% | 87% |