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:0005634 | nucleus | 5 | 1 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0042555 | MCM complex | 2 | 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: A4HNF5
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016043 | cellular component organization | 3 | 11 |
GO:0032392 | DNA geometric change | 7 | 11 |
GO:0032508 | DNA duplex unwinding | 8 | 11 |
GO:0051276 | chromosome organization | 5 | 11 |
GO:0071103 | DNA conformation change | 6 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
GO:0000724 | double-strand break repair via homologous recombination | 7 | 1 |
GO:0000725 | recombinational repair | 6 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006310 | DNA recombination | 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: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 | 11 |
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003677 | DNA binding | 4 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 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:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0003697 | single-stranded DNA binding | 5 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 2 | 6 | PF00656 | 0.431 |
CLV_C14_Caspase3-7 | 26 | 30 | PF00656 | 0.462 |
CLV_C14_Caspase3-7 | 80 | 84 | PF00656 | 0.285 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.272 |
CLV_NRD_NRD_1 | 733 | 735 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 900 | 902 | PF00675 | 0.618 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.227 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 472 | 474 | PF00082 | 0.246 |
CLV_PCSK_KEX2_1 | 843 | 845 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 902 | 904 | PF00082 | 0.562 |
CLV_PCSK_PC1ET2_1 | 143 | 145 | PF00082 | 0.227 |
CLV_PCSK_PC1ET2_1 | 309 | 311 | PF00082 | 0.486 |
CLV_PCSK_PC1ET2_1 | 843 | 845 | PF00082 | 0.577 |
CLV_PCSK_PC1ET2_1 | 902 | 904 | PF00082 | 0.620 |
CLV_PCSK_PC7_1 | 139 | 145 | PF00082 | 0.227 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.214 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 734 | 738 | PF00082 | 0.414 |
DEG_APCC_DBOX_1 | 126 | 134 | PF00400 | 0.211 |
DEG_APCC_DBOX_1 | 214 | 222 | PF00400 | 0.414 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.594 |
DEG_SCF_FBW7_2 | 495 | 502 | PF00400 | 0.445 |
DEG_SPOP_SBC_1 | 274 | 278 | PF00917 | 0.653 |
DEG_SPOP_SBC_1 | 380 | 384 | PF00917 | 0.414 |
DEG_SPOP_SBC_1 | 635 | 639 | PF00917 | 0.389 |
DEG_SPOP_SBC_1 | 886 | 890 | PF00917 | 0.492 |
DOC_CKS1_1 | 496 | 501 | PF01111 | 0.445 |
DOC_CYCLIN_yCln2_LP_2 | 624 | 630 | PF00134 | 0.490 |
DOC_CYCLIN_yCln2_LP_2 | 869 | 875 | PF00134 | 0.649 |
DOC_MAPK_gen_1 | 156 | 163 | PF00069 | 0.375 |
DOC_MAPK_gen_1 | 212 | 221 | PF00069 | 0.352 |
DOC_MAPK_gen_1 | 307 | 316 | PF00069 | 0.486 |
DOC_MAPK_gen_1 | 472 | 481 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 109 | 117 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 212 | 221 | PF00069 | 0.352 |
DOC_MAPK_MEF2A_6 | 876 | 885 | PF00069 | 0.560 |
DOC_PP1_RVXF_1 | 532 | 539 | PF00149 | 0.316 |
DOC_PP1_RVXF_1 | 908 | 915 | PF00149 | 0.578 |
DOC_PP2B_LxvP_1 | 327 | 330 | PF13499 | 0.427 |
DOC_PP2B_LxvP_1 | 883 | 886 | PF13499 | 0.679 |
DOC_PP4_FxxP_1 | 164 | 167 | PF00568 | 0.451 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 518 | 522 | PF00917 | 0.409 |
DOC_USP7_MATH_1 | 571 | 575 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 726 | 730 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 748 | 752 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 773 | 777 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 818 | 822 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 879 | 883 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 886 | 890 | PF00917 | 0.491 |
DOC_USP7_UBL2_3 | 307 | 311 | PF12436 | 0.517 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 495 | 500 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 569 | 574 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 781 | 786 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 877 | 882 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 887 | 892 | PF00397 | 0.552 |
LIG_14-3-3_CanoR_1 | 109 | 117 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 139 | 147 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 212 | 218 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 272 | 282 | PF00244 | 0.683 |
LIG_14-3-3_CanoR_1 | 287 | 296 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 312 | 317 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 381 | 388 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 434 | 438 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 458 | 464 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 473 | 481 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 619 | 625 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 702 | 709 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 710 | 715 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 798 | 804 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 901 | 909 | PF00244 | 0.635 |
LIG_BIR_III_2 | 577 | 581 | PF00653 | 0.470 |
LIG_BRCT_BRCA1_1 | 324 | 328 | PF00533 | 0.445 |
LIG_BRCT_BRCA1_1 | 910 | 914 | PF00533 | 0.581 |
LIG_Clathr_ClatBox_1 | 218 | 222 | PF01394 | 0.414 |
LIG_EH_1 | 165 | 169 | PF12763 | 0.462 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.464 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.351 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.508 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.425 |
LIG_FHA_1 | 714 | 720 | PF00498 | 0.566 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.364 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.330 |
LIG_FHA_2 | 218 | 224 | PF00498 | 0.427 |
LIG_FHA_2 | 518 | 524 | PF00498 | 0.614 |
LIG_FHA_2 | 526 | 532 | PF00498 | 0.509 |
LIG_FHA_2 | 604 | 610 | PF00498 | 0.414 |
LIG_FHA_2 | 682 | 688 | PF00498 | 0.674 |
LIG_FHA_2 | 78 | 84 | PF00498 | 0.416 |
LIG_FHA_2 | 854 | 860 | PF00498 | 0.738 |
LIG_LIR_Apic_2 | 162 | 167 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 487 | 495 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 299 | 305 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 487 | 492 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 835 | 839 | PF02991 | 0.564 |
LIG_NRBOX | 331 | 337 | PF00104 | 0.386 |
LIG_Pex14_1 | 245 | 249 | PF04695 | 0.429 |
LIG_Pex14_2 | 164 | 168 | PF04695 | 0.468 |
LIG_Pex14_2 | 301 | 305 | PF04695 | 0.438 |
LIG_Pex14_2 | 489 | 493 | PF04695 | 0.414 |
LIG_SH2_CRK | 671 | 675 | PF00017 | 0.565 |
LIG_SH2_NCK_1 | 543 | 547 | PF00017 | 0.374 |
LIG_SH2_STAP1 | 148 | 152 | PF00017 | 0.508 |
LIG_SH2_STAP1 | 836 | 840 | PF00017 | 0.508 |
LIG_SH2_STAT3 | 563 | 566 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 13 | 16 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 535 | 538 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 836 | 839 | PF00017 | 0.566 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.470 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.556 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.427 |
LIG_SH3_3 | 404 | 410 | PF00018 | 0.414 |
LIG_SH3_3 | 478 | 484 | PF00018 | 0.416 |
LIG_SH3_3 | 804 | 810 | PF00018 | 0.604 |
LIG_SH3_3 | 871 | 877 | PF00018 | 0.731 |
LIG_SH3_3 | 878 | 884 | PF00018 | 0.627 |
LIG_SUMO_SIM_anti_2 | 800 | 805 | PF11976 | 0.465 |
LIG_SUMO_SIM_par_1 | 159 | 165 | PF11976 | 0.368 |
LIG_SUMO_SIM_par_1 | 216 | 224 | PF11976 | 0.416 |
LIG_SUMO_SIM_par_1 | 745 | 751 | PF11976 | 0.549 |
LIG_TRAF2_1 | 521 | 524 | PF00917 | 0.420 |
LIG_TRAF2_1 | 528 | 531 | PF00917 | 0.273 |
LIG_TRAF2_1 | 845 | 848 | PF00917 | 0.582 |
LIG_TRFH_1 | 893 | 897 | PF08558 | 0.655 |
LIG_TYR_ITIM | 11 | 16 | PF00017 | 0.503 |
LIG_UBA3_1 | 137 | 143 | PF00899 | 0.382 |
LIG_WRC_WIRS_1 | 302 | 307 | PF05994 | 0.451 |
MOD_CDK_SPxxK_3 | 427 | 434 | PF00069 | 0.382 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.427 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.295 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.570 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.490 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.257 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.603 |
MOD_CK1_1 | 675 | 681 | PF00069 | 0.450 |
MOD_CK1_1 | 713 | 719 | PF00069 | 0.637 |
MOD_CK1_1 | 729 | 735 | PF00069 | 0.499 |
MOD_CK1_1 | 783 | 789 | PF00069 | 0.688 |
MOD_CK1_1 | 862 | 868 | PF00069 | 0.704 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.251 |
MOD_CK2_1 | 517 | 523 | PF00069 | 0.606 |
MOD_CK2_1 | 525 | 531 | PF00069 | 0.534 |
MOD_CK2_1 | 635 | 641 | PF00069 | 0.578 |
MOD_CK2_1 | 681 | 687 | PF00069 | 0.495 |
MOD_CK2_1 | 747 | 753 | PF00069 | 0.528 |
MOD_CK2_1 | 772 | 778 | PF00069 | 0.732 |
MOD_Cter_Amidation | 841 | 844 | PF01082 | 0.589 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.269 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.594 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.559 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.592 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.282 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.295 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.571 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.260 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.251 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.170 |
MOD_GlcNHglycan | 661 | 664 | PF01048 | 0.415 |
MOD_GlcNHglycan | 674 | 677 | PF01048 | 0.506 |
MOD_GlcNHglycan | 737 | 740 | PF01048 | 0.554 |
MOD_GlcNHglycan | 750 | 753 | PF01048 | 0.521 |
MOD_GlcNHglycan | 762 | 765 | PF01048 | 0.597 |
MOD_GlcNHglycan | 813 | 816 | PF01048 | 0.654 |
MOD_GlcNHglycan | 865 | 868 | PF01048 | 0.608 |
MOD_GlcNHglycan | 903 | 906 | PF01048 | 0.735 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.342 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.390 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.320 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.260 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.236 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.505 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.274 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.542 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.251 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.276 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.310 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.314 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.251 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.517 |
MOD_GSK3_1 | 709 | 716 | PF00069 | 0.642 |
MOD_GSK3_1 | 773 | 780 | PF00069 | 0.598 |
MOD_GSK3_1 | 834 | 841 | PF00069 | 0.541 |
MOD_GSK3_1 | 855 | 862 | PF00069 | 0.697 |
MOD_GSK3_1 | 863 | 870 | PF00069 | 0.709 |
MOD_GSK3_1 | 887 | 894 | PF00069 | 0.638 |
MOD_GSK3_1 | 897 | 904 | PF00069 | 0.614 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.418 |
MOD_LATS_1 | 670 | 676 | PF00433 | 0.354 |
MOD_N-GLC_1 | 207 | 212 | PF02516 | 0.382 |
MOD_N-GLC_1 | 710 | 715 | PF02516 | 0.607 |
MOD_N-GLC_1 | 726 | 731 | PF02516 | 0.451 |
MOD_N-GLC_1 | 897 | 902 | PF02516 | 0.732 |
MOD_N-GLC_2 | 65 | 67 | PF02516 | 0.256 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.518 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.319 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.330 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.430 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.219 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.330 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.211 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.243 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.251 |
MOD_NEK2_1 | 617 | 622 | PF00069 | 0.331 |
MOD_NEK2_1 | 737 | 742 | PF00069 | 0.492 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.384 |
MOD_NEK2_1 | 791 | 796 | PF00069 | 0.616 |
MOD_NEK2_1 | 797 | 802 | PF00069 | 0.634 |
MOD_NEK2_2 | 346 | 351 | PF00069 | 0.327 |
MOD_NEK2_2 | 49 | 54 | PF00069 | 0.405 |
MOD_PIKK_1 | 173 | 179 | PF00454 | 0.374 |
MOD_PIKK_1 | 366 | 372 | PF00454 | 0.251 |
MOD_PIKK_1 | 538 | 544 | PF00454 | 0.371 |
MOD_PIKK_1 | 704 | 710 | PF00454 | 0.604 |
MOD_PIKK_1 | 729 | 735 | PF00454 | 0.505 |
MOD_PIKK_1 | 791 | 797 | PF00454 | 0.623 |
MOD_PIKK_1 | 816 | 822 | PF00454 | 0.697 |
MOD_PIKK_1 | 867 | 873 | PF00454 | 0.702 |
MOD_PKA_1 | 285 | 291 | PF00069 | 0.570 |
MOD_PKA_1 | 901 | 907 | PF00069 | 0.627 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.344 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.365 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.160 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.267 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.457 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.570 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.251 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.475 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.281 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.251 |
MOD_PKA_2 | 457 | 463 | PF00069 | 0.211 |
MOD_PKA_2 | 701 | 707 | PF00069 | 0.660 |
MOD_PKA_2 | 709 | 715 | PF00069 | 0.596 |
MOD_PKA_2 | 760 | 766 | PF00069 | 0.648 |
MOD_PKA_2 | 797 | 803 | PF00069 | 0.673 |
MOD_PKB_1 | 310 | 318 | PF00069 | 0.332 |
MOD_Plk_1 | 223 | 229 | PF00069 | 0.330 |
MOD_Plk_1 | 525 | 531 | PF00069 | 0.493 |
MOD_Plk_1 | 617 | 623 | PF00069 | 0.387 |
MOD_Plk_1 | 704 | 710 | PF00069 | 0.447 |
MOD_Plk_2-3 | 433 | 439 | PF00069 | 0.251 |
MOD_Plk_2-3 | 525 | 531 | PF00069 | 0.526 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.251 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.567 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.251 |
MOD_Plk_4 | 726 | 732 | PF00069 | 0.571 |
MOD_Plk_4 | 742 | 748 | PF00069 | 0.520 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.383 |
MOD_Plk_4 | 799 | 805 | PF00069 | 0.537 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.382 |
MOD_ProDKin_1 | 495 | 501 | PF00069 | 0.295 |
MOD_ProDKin_1 | 569 | 575 | PF00069 | 0.295 |
MOD_ProDKin_1 | 781 | 787 | PF00069 | 0.582 |
MOD_ProDKin_1 | 877 | 883 | PF00069 | 0.706 |
MOD_ProDKin_1 | 887 | 893 | PF00069 | 0.555 |
MOD_SUMO_rev_2 | 169 | 176 | PF00179 | 0.382 |
TRG_DiLeu_BaEn_1 | 409 | 414 | PF01217 | 0.251 |
TRG_DiLeu_BaEn_1 | 850 | 855 | PF01217 | 0.690 |
TRG_DiLeu_BaLyEn_6 | 481 | 486 | PF01217 | 0.251 |
TRG_DiLeu_BaLyEn_6 | 546 | 551 | PF01217 | 0.167 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.511 |
TRG_ENDOCYTIC_2 | 562 | 565 | PF00928 | 0.269 |
TRG_ENDOCYTIC_2 | 836 | 839 | PF00928 | 0.566 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 155 | 158 | PF00400 | 0.330 |
TRG_ER_diArg_1 | 284 | 287 | PF00400 | 0.614 |
TRG_NES_CRM1_1 | 186 | 200 | PF08389 | 0.270 |
TRG_NES_CRM1_1 | 5 | 20 | PF08389 | 0.346 |
TRG_NES_CRM1_1 | 694 | 705 | PF08389 | 0.414 |
TRG_NLS_MonoCore_2 | 308 | 313 | PF00514 | 0.431 |
TRG_NLS_MonoExtC_3 | 900 | 906 | PF00514 | 0.679 |
TRG_NLS_MonoExtN_4 | 307 | 314 | PF00514 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 640 | 644 | PF00026 | 0.382 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P860 | Leptomonas seymouri | 28% | 92% |
A0A0N0P9H0 | Leptomonas seymouri | 74% | 99% |
A0A0S4J4D4 | Bodo saltans | 44% | 98% |
A0A1X0P4W1 | Trypanosomatidae | 60% | 100% |
A0A3Q8IQ79 | Leishmania donovani | 85% | 100% |
A0A3R7MUG3 | Trypanosoma rangeli | 57% | 100% |
A0A3S7WY81 | Leishmania donovani | 27% | 100% |
A4HDE7 | Leishmania braziliensis | 26% | 100% |
A4HGC9 | Leishmania braziliensis | 28% | 94% |
A4I0T0 | Leishmania infantum | 27% | 100% |
A4IC27 | Leishmania infantum | 85% | 100% |
B8B406 | Oryza sativa subsp. indica | 33% | 100% |
C9ZYH2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
E9AFW6 | Leishmania major | 85% | 99% |
E9AWT2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AZQ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 94% |
E9B719 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4QAP2 | Leishmania major | 27% | 100% |
Q69QA6 | Oryza sativa subsp. japonica | 33% | 100% |
Q9SF37 | Arabidopsis thaliana | 28% | 100% |