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: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: A4HDD3
Term | Name | Level | Count |
---|---|---|---|
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:0007131 | reciprocal meiotic recombination | 3 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022414 | reproductive process | 1 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0035825 | homologous recombination | 6 | 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:0045003 | double-strand break repair via synthesis-dependent strand annealing | 8 | 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:0140527 | reciprocal homologous recombination | 7 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1903046 | meiotic cell cycle process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 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: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:0015616 | DNA translocase activity | 3 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1058 | 1062 | PF00656 | 0.424 |
CLV_C14_Caspase3-7 | 186 | 190 | PF00656 | 0.476 |
CLV_C14_Caspase3-7 | 279 | 283 | PF00656 | 0.554 |
CLV_NRD_NRD_1 | 1 | 3 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 1006 | 1008 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.199 |
CLV_NRD_NRD_1 | 555 | 557 | PF00675 | 0.199 |
CLV_NRD_NRD_1 | 672 | 674 | PF00675 | 0.199 |
CLV_NRD_NRD_1 | 723 | 725 | PF00675 | 0.199 |
CLV_NRD_NRD_1 | 759 | 761 | PF00675 | 0.698 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.627 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 672 | 674 | PF00082 | 0.199 |
CLV_PCSK_KEX2_1 | 758 | 760 | PF00082 | 0.696 |
CLV_PCSK_KEX2_1 | 833 | 835 | PF00082 | 0.173 |
CLV_PCSK_KEX2_1 | 848 | 850 | PF00082 | 0.224 |
CLV_PCSK_KEX2_1 | 911 | 913 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.588 |
CLV_PCSK_PC1ET2_1 | 415 | 417 | PF00082 | 0.397 |
CLV_PCSK_PC1ET2_1 | 833 | 835 | PF00082 | 0.173 |
CLV_PCSK_PC1ET2_1 | 848 | 850 | PF00082 | 0.224 |
CLV_PCSK_PC1ET2_1 | 911 | 913 | PF00082 | 0.279 |
CLV_PCSK_PC7_1 | 411 | 417 | PF00082 | 0.398 |
CLV_PCSK_PC7_1 | 668 | 674 | PF00082 | 0.199 |
CLV_PCSK_SKI1_1 | 1078 | 1082 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 445 | 449 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 598 | 602 | PF00082 | 0.199 |
CLV_PCSK_SKI1_1 | 628 | 632 | PF00082 | 0.199 |
CLV_PCSK_SKI1_1 | 668 | 672 | PF00082 | 0.199 |
CLV_PCSK_SKI1_1 | 779 | 783 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 884 | 888 | PF00082 | 0.199 |
CLV_PCSK_SKI1_1 | 911 | 915 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 959 | 963 | PF00082 | 0.335 |
DEG_MDM2_SWIB_1 | 48 | 55 | PF02201 | 0.583 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.615 |
DEG_SPOP_SBC_1 | 17 | 21 | PF00917 | 0.548 |
DOC_ANK_TNKS_1 | 539 | 546 | PF00023 | 0.399 |
DOC_CKS1_1 | 499 | 504 | PF01111 | 0.399 |
DOC_MAPK_gen_1 | 341 | 349 | PF00069 | 0.526 |
DOC_MAPK_gen_1 | 403 | 410 | PF00069 | 0.475 |
DOC_MAPK_gen_1 | 421 | 428 | PF00069 | 0.300 |
DOC_MAPK_gen_1 | 435 | 444 | PF00069 | 0.263 |
DOC_MAPK_gen_1 | 561 | 570 | PF00069 | 0.344 |
DOC_MAPK_gen_1 | 724 | 732 | PF00069 | 0.399 |
DOC_MAPK_JIP1_4 | 782 | 788 | PF00069 | 0.521 |
DOC_MAPK_MEF2A_6 | 240 | 248 | PF00069 | 0.465 |
DOC_MAPK_MEF2A_6 | 421 | 428 | PF00069 | 0.325 |
DOC_MAPK_MEF2A_6 | 437 | 446 | PF00069 | 0.290 |
DOC_MAPK_MEF2A_6 | 564 | 572 | PF00069 | 0.344 |
DOC_MAPK_MEF2A_6 | 685 | 694 | PF00069 | 0.399 |
DOC_MAPK_MEF2A_6 | 793 | 801 | PF00069 | 0.293 |
DOC_MAPK_MEF2A_6 | 871 | 879 | PF00069 | 0.399 |
DOC_PP1_RVXF_1 | 226 | 232 | PF00149 | 0.492 |
DOC_PP1_RVXF_1 | 562 | 568 | PF00149 | 0.344 |
DOC_PP1_RVXF_1 | 882 | 889 | PF00149 | 0.399 |
DOC_PP4_FxxP_1 | 15 | 18 | PF00568 | 0.568 |
DOC_PP4_FxxP_1 | 375 | 378 | PF00568 | 0.616 |
DOC_PP4_FxxP_1 | 619 | 622 | PF00568 | 0.399 |
DOC_PP4_FxxP_1 | 635 | 638 | PF00568 | 0.399 |
DOC_PP4_FxxP_1 | 856 | 859 | PF00568 | 0.399 |
DOC_USP7_MATH_1 | 1068 | 1072 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.408 |
DOC_USP7_UBL2_3 | 291 | 295 | PF12436 | 0.390 |
DOC_USP7_UBL2_3 | 327 | 331 | PF12436 | 0.409 |
DOC_USP7_UBL2_3 | 959 | 963 | PF12436 | 0.458 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 498 | 503 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 528 | 533 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 601 | 606 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 712 | 717 | PF00397 | 0.430 |
DOC_WW_Pin1_4 | 841 | 846 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.615 |
LIG_14-3-3_CanoR_1 | 1027 | 1033 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 1067 | 1076 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 120 | 126 | PF00244 | 0.749 |
LIG_14-3-3_CanoR_1 | 16 | 26 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 2 | 10 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 421 | 427 | PF00244 | 0.329 |
LIG_14-3-3_CanoR_1 | 759 | 769 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 917 | 924 | PF00244 | 0.318 |
LIG_Actin_WH2_1 | 564 | 582 | PF00022 | 0.344 |
LIG_Actin_WH2_2 | 470 | 487 | PF00022 | 0.412 |
LIG_Actin_WH2_2 | 552 | 568 | PF00022 | 0.399 |
LIG_APCC_ABBA_1 | 730 | 735 | PF00400 | 0.449 |
LIG_BIR_III_2 | 210 | 214 | PF00653 | 0.646 |
LIG_BRCT_BRCA1_1 | 1052 | 1056 | PF00533 | 0.315 |
LIG_BRCT_BRCA1_1 | 309 | 313 | PF00533 | 0.334 |
LIG_BRCT_BRCA1_1 | 360 | 364 | PF00533 | 0.582 |
LIG_Clathr_ClatBox_1 | 168 | 172 | PF01394 | 0.648 |
LIG_Clathr_ClatBox_1 | 885 | 889 | PF01394 | 0.399 |
LIG_CtBP_PxDLS_1 | 638 | 642 | PF00389 | 0.494 |
LIG_FHA_1 | 1039 | 1045 | PF00498 | 0.428 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.689 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.416 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.375 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.520 |
LIG_FHA_1 | 585 | 591 | PF00498 | 0.399 |
LIG_FHA_1 | 672 | 678 | PF00498 | 0.399 |
LIG_FHA_1 | 687 | 693 | PF00498 | 0.399 |
LIG_FHA_1 | 713 | 719 | PF00498 | 0.430 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.632 |
LIG_FHA_1 | 818 | 824 | PF00498 | 0.421 |
LIG_FHA_1 | 919 | 925 | PF00498 | 0.289 |
LIG_FHA_1 | 970 | 976 | PF00498 | 0.312 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.654 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.606 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.502 |
LIG_FHA_2 | 921 | 927 | PF00498 | 0.413 |
LIG_FHA_2 | 952 | 958 | PF00498 | 0.443 |
LIG_FHA_2 | 966 | 972 | PF00498 | 0.381 |
LIG_FHA_2 | 977 | 983 | PF00498 | 0.490 |
LIG_LIR_Apic_2 | 125 | 129 | PF02991 | 0.548 |
LIG_LIR_Apic_2 | 14 | 18 | PF02991 | 0.608 |
LIG_LIR_Apic_2 | 372 | 378 | PF02991 | 0.539 |
LIG_LIR_Apic_2 | 632 | 638 | PF02991 | 0.344 |
LIG_LIR_Apic_2 | 679 | 684 | PF02991 | 0.399 |
LIG_LIR_Apic_2 | 854 | 859 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 357 | 364 | PF02991 | 0.624 |
LIG_LIR_Gen_1 | 551 | 559 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 611 | 620 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 629 | 639 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 689 | 696 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 699 | 709 | PF02991 | 0.399 |
LIG_LIR_LC3C_4 | 569 | 572 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 357 | 362 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 479 | 484 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 50 | 55 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 551 | 555 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 629 | 634 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 689 | 694 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 699 | 705 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 854 | 858 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.621 |
LIG_LYPXL_S_1 | 96 | 100 | PF13949 | 0.626 |
LIG_LYPXL_yS_3 | 97 | 100 | PF13949 | 0.626 |
LIG_Pex14_1 | 509 | 513 | PF04695 | 0.399 |
LIG_Pex14_2 | 48 | 52 | PF04695 | 0.583 |
LIG_Pex14_2 | 631 | 635 | PF04695 | 0.399 |
LIG_Pex14_2 | 888 | 892 | PF04695 | 0.399 |
LIG_PTAP_UEV_1 | 181 | 186 | PF05743 | 0.461 |
LIG_PTB_Apo_2 | 9 | 16 | PF02174 | 0.626 |
LIG_Rb_pABgroove_1 | 442 | 450 | PF01858 | 0.274 |
LIG_REV1ctd_RIR_1 | 311 | 320 | PF16727 | 0.370 |
LIG_SH2_CRK | 226 | 230 | PF00017 | 0.493 |
LIG_SH2_CRK | 259 | 263 | PF00017 | 0.500 |
LIG_SH2_CRK | 481 | 485 | PF00017 | 0.399 |
LIG_SH2_CRK | 552 | 556 | PF00017 | 0.399 |
LIG_SH2_CRK | 702 | 706 | PF00017 | 0.445 |
LIG_SH2_CRK | 916 | 920 | PF00017 | 0.268 |
LIG_SH2_GRB2like | 855 | 858 | PF00017 | 0.494 |
LIG_SH2_NCK_1 | 259 | 263 | PF00017 | 0.367 |
LIG_SH2_SRC | 681 | 684 | PF00017 | 0.399 |
LIG_SH2_STAT3 | 929 | 932 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 481 | 484 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 558 | 561 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 661 | 664 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 681 | 684 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 837 | 840 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 855 | 858 | PF00017 | 0.494 |
LIG_SH3_1 | 179 | 185 | PF00018 | 0.578 |
LIG_SH3_1 | 269 | 275 | PF00018 | 0.470 |
LIG_SH3_2 | 272 | 277 | PF14604 | 0.459 |
LIG_SH3_3 | 1006 | 1012 | PF00018 | 0.658 |
LIG_SH3_3 | 1073 | 1079 | PF00018 | 0.583 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.671 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.461 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.470 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.676 |
LIG_SH3_3 | 424 | 430 | PF00018 | 0.306 |
LIG_SH3_3 | 496 | 502 | PF00018 | 0.412 |
LIG_SH3_3 | 642 | 648 | PF00018 | 0.399 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.496 |
LIG_SUMO_SIM_anti_2 | 1104 | 1114 | PF11976 | 0.689 |
LIG_SUMO_SIM_anti_2 | 546 | 551 | PF11976 | 0.399 |
LIG_SUMO_SIM_anti_2 | 715 | 721 | PF11976 | 0.422 |
LIG_SUMO_SIM_anti_2 | 811 | 817 | PF11976 | 0.433 |
LIG_SUMO_SIM_anti_2 | 82 | 89 | PF11976 | 0.442 |
LIG_SUMO_SIM_anti_2 | 822 | 827 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 245 | 252 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 296 | 301 | PF11976 | 0.360 |
LIG_SUMO_SIM_par_1 | 546 | 551 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 715 | 721 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 81 | 89 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 811 | 817 | PF11976 | 0.430 |
LIG_TRAF2_1 | 1120 | 1123 | PF00917 | 0.701 |
LIG_TRAF2_1 | 336 | 339 | PF00917 | 0.511 |
LIG_TRAF2_1 | 696 | 699 | PF00917 | 0.344 |
LIG_TRAF2_1 | 923 | 926 | PF00917 | 0.292 |
LIG_TRAF2_1 | 954 | 957 | PF00917 | 0.395 |
LIG_TYR_ITIM | 550 | 555 | PF00017 | 0.234 |
LIG_TYR_ITIM | 835 | 840 | PF00017 | 0.367 |
LIG_TYR_ITIM | 853 | 858 | PF00017 | 0.367 |
LIG_TYR_ITIM | 95 | 100 | PF00017 | 0.624 |
LIG_UBA3_1 | 719 | 725 | PF00899 | 0.234 |
LIG_UBA3_1 | 825 | 833 | PF00899 | 0.367 |
LIG_WRC_WIRS_1 | 1032 | 1037 | PF05994 | 0.466 |
LIG_WRC_WIRS_1 | 1051 | 1056 | PF05994 | 0.315 |
MOD_CDK_SPK_2 | 528 | 533 | PF00069 | 0.234 |
MOD_CDK_SPxK_1 | 841 | 847 | PF00069 | 0.367 |
MOD_CDK_SPxxK_3 | 221 | 228 | PF00069 | 0.541 |
MOD_CDK_SPxxK_3 | 841 | 848 | PF00069 | 0.367 |
MOD_CK1_1 | 1031 | 1037 | PF00069 | 0.583 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.603 |
MOD_CK1_1 | 1050 | 1056 | PF00069 | 0.451 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.564 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.234 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.688 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.649 |
MOD_CK1_1 | 663 | 669 | PF00069 | 0.242 |
MOD_CK1_1 | 817 | 823 | PF00069 | 0.234 |
MOD_CK1_1 | 920 | 926 | PF00069 | 0.291 |
MOD_CK2_1 | 1098 | 1104 | PF00069 | 0.587 |
MOD_CK2_1 | 1117 | 1123 | PF00069 | 0.448 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.531 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.598 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.501 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.548 |
MOD_CK2_1 | 673 | 679 | PF00069 | 0.234 |
MOD_CK2_1 | 920 | 926 | PF00069 | 0.291 |
MOD_CK2_1 | 951 | 957 | PF00069 | 0.418 |
MOD_CK2_1 | 976 | 982 | PF00069 | 0.439 |
MOD_Cter_Amidation | 419 | 422 | PF01082 | 0.516 |
MOD_Cter_Amidation | 756 | 759 | PF01082 | 0.693 |
MOD_GlcNHglycan | 1015 | 1018 | PF01048 | 0.474 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.639 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.704 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.614 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.465 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.572 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.534 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.333 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.525 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.599 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.703 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.234 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.727 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.584 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.284 |
MOD_GlcNHglycan | 720 | 723 | PF01048 | 0.196 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.475 |
MOD_GlcNHglycan | 749 | 752 | PF01048 | 0.616 |
MOD_GlcNHglycan | 763 | 766 | PF01048 | 0.757 |
MOD_GlcNHglycan | 938 | 941 | PF01048 | 0.438 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.688 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.495 |
MOD_GSK3_1 | 1027 | 1034 | PF00069 | 0.520 |
MOD_GSK3_1 | 1118 | 1125 | PF00069 | 0.630 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.467 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.544 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.524 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.234 |
MOD_GSK3_1 | 708 | 715 | PF00069 | 0.302 |
MOD_GSK3_1 | 965 | 972 | PF00069 | 0.327 |
MOD_GSK3_1 | 987 | 994 | PF00069 | 0.600 |
MOD_N-GLC_1 | 11 | 16 | PF02516 | 0.633 |
MOD_N-GLC_1 | 354 | 359 | PF02516 | 0.609 |
MOD_N-GLC_1 | 677 | 682 | PF02516 | 0.280 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.498 |
MOD_N-GLC_1 | 817 | 822 | PF02516 | 0.234 |
MOD_N-GLC_2 | 508 | 510 | PF02516 | 0.234 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.568 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.352 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.517 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.234 |
MOD_NEK2_1 | 671 | 676 | PF00069 | 0.234 |
MOD_NEK2_1 | 829 | 834 | PF00069 | 0.268 |
MOD_NEK2_1 | 840 | 845 | PF00069 | 0.204 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.525 |
MOD_NEK2_1 | 866 | 871 | PF00069 | 0.234 |
MOD_NEK2_1 | 918 | 923 | PF00069 | 0.287 |
MOD_NEK2_1 | 976 | 981 | PF00069 | 0.427 |
MOD_NEK2_2 | 11 | 16 | PF00069 | 0.696 |
MOD_NEK2_2 | 286 | 291 | PF00069 | 0.318 |
MOD_PIKK_1 | 1089 | 1095 | PF00454 | 0.544 |
MOD_PIKK_1 | 119 | 125 | PF00454 | 0.709 |
MOD_PIKK_1 | 663 | 669 | PF00454 | 0.234 |
MOD_PIKK_1 | 671 | 677 | PF00454 | 0.234 |
MOD_PIKK_1 | 817 | 823 | PF00454 | 0.234 |
MOD_PIKK_1 | 858 | 864 | PF00454 | 0.234 |
MOD_PK_1 | 240 | 246 | PF00069 | 0.485 |
MOD_PK_1 | 29 | 35 | PF00069 | 0.473 |
MOD_PK_1 | 422 | 428 | PF00069 | 0.451 |
MOD_PK_1 | 673 | 679 | PF00069 | 0.217 |
MOD_PKA_1 | 1013 | 1019 | PF00069 | 0.514 |
MOD_PKA_1 | 2 | 8 | PF00069 | 0.472 |
MOD_PKA_1 | 29 | 35 | PF00069 | 0.495 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.569 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.748 |
MOD_PKA_2 | 560 | 566 | PF00069 | 0.234 |
MOD_PKA_2 | 671 | 677 | PF00069 | 0.234 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.620 |
MOD_PKA_2 | 761 | 767 | PF00069 | 0.605 |
MOD_PKA_2 | 991 | 997 | PF00069 | 0.587 |
MOD_PKB_1 | 758 | 766 | PF00069 | 0.614 |
MOD_Plk_1 | 1084 | 1090 | PF00069 | 0.747 |
MOD_Plk_1 | 345 | 351 | PF00069 | 0.646 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.604 |
MOD_Plk_1 | 677 | 683 | PF00069 | 0.234 |
MOD_Plk_1 | 686 | 692 | PF00069 | 0.234 |
MOD_Plk_4 | 1047 | 1053 | PF00069 | 0.362 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.559 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.333 |
MOD_Plk_4 | 476 | 482 | PF00069 | 0.234 |
MOD_Plk_4 | 501 | 507 | PF00069 | 0.234 |
MOD_Plk_4 | 660 | 666 | PF00069 | 0.385 |
MOD_Plk_4 | 677 | 683 | PF00069 | 0.138 |
MOD_Plk_4 | 686 | 692 | PF00069 | 0.234 |
MOD_Plk_4 | 795 | 801 | PF00069 | 0.300 |
MOD_Plk_4 | 957 | 963 | PF00069 | 0.474 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.434 |
MOD_ProDKin_1 | 498 | 504 | PF00069 | 0.234 |
MOD_ProDKin_1 | 528 | 534 | PF00069 | 0.234 |
MOD_ProDKin_1 | 601 | 607 | PF00069 | 0.234 |
MOD_ProDKin_1 | 712 | 718 | PF00069 | 0.277 |
MOD_ProDKin_1 | 841 | 847 | PF00069 | 0.367 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.613 |
MOD_SUMO_for_1 | 276 | 279 | PF00179 | 0.446 |
MOD_SUMO_for_1 | 696 | 699 | PF00179 | 0.156 |
MOD_SUMO_rev_2 | 1016 | 1025 | PF00179 | 0.577 |
MOD_SUMO_rev_2 | 21 | 27 | PF00179 | 0.622 |
MOD_SUMO_rev_2 | 320 | 328 | PF00179 | 0.478 |
MOD_SUMO_rev_2 | 333 | 342 | PF00179 | 0.495 |
MOD_SUMO_rev_2 | 920 | 928 | PF00179 | 0.280 |
MOD_SUMO_rev_2 | 956 | 961 | PF00179 | 0.492 |
MOD_SUMO_rev_2 | 996 | 1004 | PF00179 | 0.520 |
TRG_DiLeu_BaEn_1 | 809 | 814 | PF01217 | 0.298 |
TRG_DiLeu_BaEn_1 | 863 | 868 | PF01217 | 0.234 |
TRG_DiLeu_BaEn_4 | 636 | 642 | PF01217 | 0.312 |
TRG_DiLeu_BaLyEn_6 | 32 | 37 | PF01217 | 0.681 |
TRG_DiLeu_BaLyEn_6 | 881 | 886 | PF01217 | 0.234 |
TRG_DiLeu_BaLyEn_6 | 914 | 919 | PF01217 | 0.290 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 481 | 484 | PF00928 | 0.234 |
TRG_ENDOCYTIC_2 | 552 | 555 | PF00928 | 0.234 |
TRG_ENDOCYTIC_2 | 661 | 664 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 702 | 705 | PF00928 | 0.234 |
TRG_ENDOCYTIC_2 | 837 | 840 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 855 | 858 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 916 | 919 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.626 |
TRG_ER_diArg_1 | 321 | 324 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 364 | 367 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 564 | 567 | PF00400 | 0.156 |
TRG_ER_diArg_1 | 596 | 599 | PF00400 | 0.234 |
TRG_ER_diArg_1 | 671 | 673 | PF00400 | 0.217 |
TRG_ER_diArg_1 | 758 | 760 | PF00400 | 0.700 |
TRG_ER_diArg_1 | 91 | 93 | PF00400 | 0.558 |
TRG_NES_CRM1_1 | 560 | 574 | PF08389 | 0.298 |
TRG_NLS_Bipartite_1 | 833 | 851 | PF00514 | 0.156 |
TRG_NLS_MonoExtN_4 | 1012 | 1017 | PF00514 | 0.623 |
TRG_NLS_MonoExtN_4 | 845 | 851 | PF00514 | 0.367 |
TRG_Pf-PMV_PEXEL_1 | 396 | 400 | PF00026 | 0.392 |
TRG_Pf-PMV_PEXEL_1 | 515 | 519 | PF00026 | 0.312 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5G3 | Leptomonas seymouri | 80% | 99% |
A0A1X0NIN9 | Trypanosomatidae | 65% | 100% |
A0A3S7WY74 | Leishmania donovani | 90% | 100% |
A0A422MV13 | Trypanosoma rangeli | 65% | 100% |
A4HRE5 | Leishmania infantum | 26% | 100% |
A4I0R4 | Leishmania infantum | 90% | 100% |
B4KHL5 | Drosophila mojavensis | 37% | 100% |
D0A743 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 66% | 100% |
E9AWR6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QAQ7 | Leishmania major | 89% | 100% |
Q6PFE3 | Mus musculus | 40% | 100% |
Q9DG67 | Gallus gallus | 37% | 100% |
V5BVU6 | Trypanosoma cruzi | 74% | 100% |