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 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: A0A3S7WSQ7
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006304 | DNA modification | 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:0043412 | macromolecule modification | 4 | 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:0070580 | base J metabolic process | 6 | 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:0006281 | DNA repair | 5 | 1 |
GO:0006283 | transcription-coupled nucleotide-excision repair | 7 | 1 |
GO:0006289 | nucleotide-excision repair | 6 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 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:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 12 |
GO:0016491 | oxidoreductase activity | 2 | 12 |
GO:0016705 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen | 3 | 12 |
GO:0016706 | 2-oxoglutarate-dependent dioxygenase activity | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 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:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0050341 | thymine dioxygenase activity | 5 | 12 |
GO:0051213 | dioxygenase activity | 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:0140658 | ATP-dependent chromatin remodeler activity | 3 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003678 | DNA helicase activity | 3 | 3 |
GO:0004386 | helicase activity | 2 | 4 |
GO:0005506 | iron ion binding | 6 | 1 |
GO:0008198 | ferrous iron binding | 7 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 3 |
GO:0016787 | hydrolase activity | 2 | 4 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 3 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 3 |
GO:0016887 | ATP hydrolysis activity | 7 | 3 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 3 |
GO:0046914 | transition metal ion binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 176 | 180 | PF00656 | 0.612 |
CLV_C14_Caspase3-7 | 807 | 811 | PF00656 | 0.578 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 592 | 594 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 831 | 833 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 873 | 875 | PF00675 | 0.278 |
CLV_NRD_NRD_1 | 928 | 930 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 931 | 933 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 954 | 956 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 989 | 991 | PF00675 | 0.448 |
CLV_PCSK_FUR_1 | 593 | 597 | PF00082 | 0.381 |
CLV_PCSK_FUR_1 | 871 | 875 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 592 | 594 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 595 | 597 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 662 | 664 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 871 | 873 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 928 | 930 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 989 | 991 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 367 | 369 | PF00082 | 0.325 |
CLV_PCSK_PC1ET2_1 | 595 | 597 | PF00082 | 0.325 |
CLV_PCSK_PC1ET2_1 | 662 | 664 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 1006 | 1010 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 592 | 596 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 629 | 633 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 851 | 855 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 933 | 937 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 947 | 951 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 956 | 960 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 961 | 965 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 970 | 974 | PF00082 | 0.446 |
DEG_APCC_DBOX_1 | 345 | 353 | PF00400 | 0.487 |
DEG_APCC_DBOX_1 | 423 | 431 | PF00400 | 0.575 |
DEG_APCC_DBOX_1 | 624 | 632 | PF00400 | 0.572 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.479 |
DEG_ODPH_VHL_1 | 302 | 314 | PF01847 | 0.581 |
DEG_ODPH_VHL_1 | 467 | 479 | PF01847 | 0.505 |
DEG_SIAH_1 | 58 | 66 | PF03145 | 0.401 |
DOC_CKS1_1 | 520 | 525 | PF01111 | 0.537 |
DOC_CYCLIN_RxL_1 | 33 | 43 | PF00134 | 0.670 |
DOC_CYCLIN_RxL_1 | 44 | 53 | PF00134 | 0.369 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 625 | 632 | PF00134 | 0.581 |
DOC_CYCLIN_yCln2_LP_2 | 38 | 44 | PF00134 | 0.516 |
DOC_MAPK_DCC_7 | 462 | 472 | PF00069 | 0.523 |
DOC_MAPK_gen_1 | 367 | 377 | PF00069 | 0.564 |
DOC_MAPK_gen_1 | 423 | 432 | PF00069 | 0.579 |
DOC_MAPK_gen_1 | 573 | 581 | PF00069 | 0.538 |
DOC_MAPK_gen_1 | 592 | 603 | PF00069 | 0.399 |
DOC_MAPK_gen_1 | 623 | 632 | PF00069 | 0.563 |
DOC_MAPK_gen_1 | 818 | 827 | PF00069 | 0.533 |
DOC_MAPK_gen_1 | 832 | 839 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 928 | 937 | PF00069 | 0.607 |
DOC_MAPK_HePTP_8 | 815 | 827 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 498 | 507 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 595 | 603 | PF00069 | 0.518 |
DOC_MAPK_MEF2A_6 | 623 | 632 | PF00069 | 0.581 |
DOC_MAPK_MEF2A_6 | 818 | 827 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 883 | 890 | PF00069 | 0.508 |
DOC_MAPK_NFAT4_5 | 883 | 891 | PF00069 | 0.553 |
DOC_MAPK_RevD_3 | 819 | 833 | PF00069 | 0.517 |
DOC_PP1_RVXF_1 | 45 | 52 | PF00149 | 0.560 |
DOC_PP1_RVXF_1 | 644 | 651 | PF00149 | 0.487 |
DOC_PP1_RVXF_1 | 833 | 840 | PF00149 | 0.476 |
DOC_PP2B_LxvP_1 | 243 | 246 | PF13499 | 0.597 |
DOC_PP2B_LxvP_1 | 457 | 460 | PF13499 | 0.418 |
DOC_USP7_MATH_1 | 1002 | 1006 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 784 | 788 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.777 |
DOC_USP7_UBL2_3 | 293 | 297 | PF12436 | 0.581 |
DOC_USP7_UBL2_3 | 367 | 371 | PF12436 | 0.487 |
DOC_USP7_UBL2_3 | 79 | 83 | PF12436 | 0.398 |
DOC_WW_Pin1_4 | 519 | 524 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 595 | 600 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 632 | 637 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.635 |
LIG_14-3-3_CanoR_1 | 122 | 128 | PF00244 | 0.715 |
LIG_14-3-3_CanoR_1 | 17 | 21 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 4 | 11 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 403 | 407 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 441 | 446 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 462 | 470 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 783 | 792 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 851 | 858 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 932 | 938 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 939 | 948 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 989 | 993 | PF00244 | 0.252 |
LIG_Actin_WH2_2 | 362 | 378 | PF00022 | 0.614 |
LIG_Actin_WH2_2 | 614 | 631 | PF00022 | 0.581 |
LIG_Actin_WH2_2 | 728 | 744 | PF00022 | 0.539 |
LIG_APCC_ABBA_1 | 107 | 112 | PF00400 | 0.671 |
LIG_APCC_ABBAyCdc20_2 | 199 | 205 | PF00400 | 0.529 |
LIG_APCC_ABBAyCdc20_2 | 335 | 341 | PF00400 | 0.487 |
LIG_APCC_ABBAyCdc20_2 | 697 | 703 | PF00400 | 0.562 |
LIG_BRCT_BRCA1_1 | 149 | 153 | PF00533 | 0.708 |
LIG_BRCT_BRCA1_1 | 554 | 558 | PF00533 | 0.487 |
LIG_BRCT_BRCA1_2 | 149 | 155 | PF00533 | 0.717 |
LIG_Clathr_ClatBox_1 | 601 | 605 | PF01394 | 0.454 |
LIG_deltaCOP1_diTrp_1 | 694 | 701 | PF00928 | 0.476 |
LIG_eIF4E_1 | 409 | 415 | PF01652 | 0.395 |
LIG_EVH1_2 | 660 | 664 | PF00568 | 0.517 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.476 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.449 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.476 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.545 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.396 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.512 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.487 |
LIG_FHA_1 | 596 | 602 | PF00498 | 0.581 |
LIG_FHA_1 | 616 | 622 | PF00498 | 0.345 |
LIG_FHA_1 | 792 | 798 | PF00498 | 0.547 |
LIG_FHA_1 | 858 | 864 | PF00498 | 0.582 |
LIG_FHA_1 | 952 | 958 | PF00498 | 0.445 |
LIG_FHA_1 | 996 | 1002 | PF00498 | 0.461 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.672 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.426 |
LIG_GBD_Chelix_1 | 406 | 414 | PF00786 | 0.391 |
LIG_IRF3_LxIS_1 | 71 | 76 | PF10401 | 0.624 |
LIG_LIR_Apic_2 | 911 | 916 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 187 | 196 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 296 | 305 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 323 | 330 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 504 | 514 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 70 | 78 | PF02991 | 0.640 |
LIG_LIR_Gen_1 | 763 | 770 | PF02991 | 0.648 |
LIG_LIR_Gen_1 | 798 | 804 | PF02991 | 0.553 |
LIG_LIR_Gen_1 | 810 | 819 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 991 | 1001 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 142 | 147 | PF02991 | 0.717 |
LIG_LIR_Nem_3 | 187 | 191 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 192 | 197 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 24 | 28 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 323 | 328 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 504 | 510 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 642 | 648 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 70 | 75 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 713 | 717 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 798 | 803 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 810 | 815 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 936 | 941 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 991 | 996 | PF02991 | 0.413 |
LIG_NRBOX | 431 | 437 | PF00104 | 0.632 |
LIG_PCNA_yPIPBox_3 | 367 | 381 | PF02747 | 0.615 |
LIG_PCNA_yPIPBox_3 | 646 | 659 | PF02747 | 0.517 |
LIG_PCNA_yPIPBox_3 | 806 | 820 | PF02747 | 0.507 |
LIG_Pex14_1 | 695 | 699 | PF04695 | 0.476 |
LIG_Pex14_2 | 590 | 594 | PF04695 | 0.581 |
LIG_Pex14_2 | 910 | 914 | PF04695 | 0.537 |
LIG_PTB_Apo_2 | 15 | 22 | PF02174 | 0.569 |
LIG_PTB_Apo_2 | 353 | 360 | PF02174 | 0.562 |
LIG_PTB_Apo_2 | 580 | 587 | PF02174 | 0.487 |
LIG_PTB_Phospho_1 | 15 | 21 | PF10480 | 0.644 |
LIG_PTB_Phospho_1 | 580 | 586 | PF10480 | 0.487 |
LIG_SH2_CRK | 261 | 265 | PF00017 | 0.476 |
LIG_SH2_CRK | 299 | 303 | PF00017 | 0.566 |
LIG_SH2_CRK | 645 | 649 | PF00017 | 0.487 |
LIG_SH2_CRK | 683 | 687 | PF00017 | 0.581 |
LIG_SH2_CRK | 938 | 942 | PF00017 | 0.485 |
LIG_SH2_NCK_1 | 11 | 15 | PF00017 | 0.557 |
LIG_SH2_NCK_1 | 5 | 9 | PF00017 | 0.636 |
LIG_SH2_PTP2 | 800 | 803 | PF00017 | 0.503 |
LIG_SH2_SRC | 1014 | 1017 | PF00017 | 0.551 |
LIG_SH2_SRC | 217 | 220 | PF00017 | 0.516 |
LIG_SH2_STAP1 | 299 | 303 | PF00017 | 0.517 |
LIG_SH2_STAP1 | 727 | 731 | PF00017 | 0.556 |
LIG_SH2_STAT3 | 1012 | 1015 | PF00017 | 0.545 |
LIG_SH2_STAT3 | 54 | 57 | PF00017 | 0.549 |
LIG_SH2_STAT3 | 565 | 568 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 586 | 589 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 691 | 694 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 714 | 717 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 758 | 761 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 800 | 803 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 842 | 845 | PF00017 | 0.496 |
LIG_SH3_1 | 90 | 96 | PF00018 | 0.619 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.528 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.522 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.538 |
LIG_SH3_3 | 391 | 397 | PF00018 | 0.520 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.554 |
LIG_SH3_3 | 655 | 661 | PF00018 | 0.517 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.619 |
LIG_SH3_5 | 710 | 714 | PF00018 | 0.487 |
LIG_Sin3_3 | 230 | 237 | PF02671 | 0.545 |
LIG_SUMO_SIM_anti_2 | 517 | 522 | PF11976 | 0.476 |
LIG_SUMO_SIM_anti_2 | 884 | 892 | PF11976 | 0.550 |
LIG_SUMO_SIM_par_1 | 499 | 504 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 517 | 522 | PF11976 | 0.538 |
LIG_SUMO_SIM_par_1 | 598 | 606 | PF11976 | 0.505 |
LIG_SUMO_SIM_par_1 | 884 | 892 | PF11976 | 0.545 |
LIG_TRAF2_1 | 157 | 160 | PF00917 | 0.753 |
LIG_TRAF2_1 | 173 | 176 | PF00917 | 0.586 |
LIG_TRAF2_1 | 875 | 878 | PF00917 | 0.553 |
LIG_TYR_ITSM | 934 | 941 | PF00017 | 0.501 |
LIG_UBA3_1 | 291 | 297 | PF00899 | 0.415 |
LIG_UBA3_1 | 518 | 524 | PF00899 | 0.413 |
LIG_UBA3_1 | 885 | 893 | PF00899 | 0.398 |
LIG_WRC_WIRS_1 | 181 | 186 | PF05994 | 0.690 |
LIG_WRC_WIRS_1 | 858 | 863 | PF05994 | 0.396 |
MOD_CDC14_SPxK_1 | 76 | 79 | PF00782 | 0.607 |
MOD_CDK_SPK_2 | 519 | 524 | PF00069 | 0.413 |
MOD_CDK_SPxK_1 | 73 | 79 | PF00069 | 0.611 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.766 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.624 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.328 |
MOD_CK1_1 | 765 | 771 | PF00069 | 0.645 |
MOD_CK1_1 | 779 | 785 | PF00069 | 0.731 |
MOD_CK2_1 | 1014 | 1020 | PF00069 | 0.583 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.750 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.799 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.606 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.387 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.505 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.594 |
MOD_CK2_1 | 784 | 790 | PF00069 | 0.642 |
MOD_CK2_1 | 939 | 945 | PF00069 | 0.407 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.793 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.664 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.489 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.344 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.478 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.629 |
MOD_GlcNHglycan | 632 | 635 | PF01048 | 0.337 |
MOD_GlcNHglycan | 770 | 773 | PF01048 | 0.631 |
MOD_GlcNHglycan | 814 | 818 | PF01048 | 0.377 |
MOD_GlcNHglycan | 941 | 944 | PF01048 | 0.455 |
MOD_GSK3_1 | 1014 | 1021 | PF00069 | 0.567 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.755 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.709 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.672 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.328 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.328 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.548 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.495 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.483 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.387 |
MOD_N-GLC_1 | 441 | 446 | PF02516 | 0.598 |
MOD_N-GLC_1 | 779 | 784 | PF02516 | 0.751 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.585 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.641 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.328 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.371 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.592 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.327 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.338 |
MOD_NEK2_1 | 731 | 736 | PF00069 | 0.606 |
MOD_NEK2_1 | 888 | 893 | PF00069 | 0.328 |
MOD_NEK2_1 | 899 | 904 | PF00069 | 0.328 |
MOD_NEK2_1 | 909 | 914 | PF00069 | 0.315 |
MOD_NEK2_1 | 996 | 1001 | PF00069 | 0.411 |
MOD_NEK2_2 | 1014 | 1019 | PF00069 | 0.552 |
MOD_NEK2_2 | 223 | 228 | PF00069 | 0.585 |
MOD_NEK2_2 | 859 | 864 | PF00069 | 0.449 |
MOD_PIKK_1 | 265 | 271 | PF00454 | 0.350 |
MOD_PIKK_1 | 297 | 303 | PF00454 | 0.440 |
MOD_PIKK_1 | 313 | 319 | PF00454 | 0.449 |
MOD_PIKK_1 | 505 | 511 | PF00454 | 0.398 |
MOD_PIKK_1 | 784 | 790 | PF00454 | 0.667 |
MOD_PIKK_1 | 842 | 848 | PF00454 | 0.348 |
MOD_PIKK_1 | 865 | 871 | PF00454 | 0.449 |
MOD_PIKK_1 | 949 | 955 | PF00454 | 0.426 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.654 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.537 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.328 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.647 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.362 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.554 |
MOD_PKA_2 | 784 | 790 | PF00069 | 0.656 |
MOD_PKA_2 | 865 | 871 | PF00069 | 0.364 |
MOD_PKA_2 | 966 | 972 | PF00069 | 0.547 |
MOD_PKA_2 | 988 | 994 | PF00069 | 0.264 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.733 |
MOD_Plk_1 | 174 | 180 | PF00069 | 0.640 |
MOD_Plk_1 | 383 | 389 | PF00069 | 0.407 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.566 |
MOD_Plk_1 | 450 | 456 | PF00069 | 0.529 |
MOD_Plk_2-3 | 187 | 193 | PF00069 | 0.435 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.733 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.600 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.526 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.344 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.445 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.396 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.326 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.552 |
MOD_Plk_4 | 765 | 771 | PF00069 | 0.673 |
MOD_Plk_4 | 909 | 915 | PF00069 | 0.328 |
MOD_Plk_4 | 933 | 939 | PF00069 | 0.433 |
MOD_ProDKin_1 | 519 | 525 | PF00069 | 0.413 |
MOD_ProDKin_1 | 595 | 601 | PF00069 | 0.475 |
MOD_ProDKin_1 | 632 | 638 | PF00069 | 0.328 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.643 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.699 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.635 |
MOD_SUMO_rev_2 | 722 | 731 | PF00179 | 0.460 |
MOD_SUMO_rev_2 | 878 | 885 | PF00179 | 0.417 |
MOD_SUMO_rev_2 | 942 | 949 | PF00179 | 0.548 |
TRG_DiLeu_BaEn_1 | 643 | 648 | PF01217 | 0.328 |
TRG_DiLeu_BaEn_1 | 881 | 886 | PF01217 | 0.398 |
TRG_DiLeu_BaEn_4 | 728 | 734 | PF01217 | 0.568 |
TRG_DiLeu_BaLyEn_6 | 287 | 292 | PF01217 | 0.428 |
TRG_DiLeu_BaLyEn_6 | 426 | 431 | PF01217 | 0.571 |
TRG_DiLeu_BaLyEn_6 | 596 | 601 | PF01217 | 0.300 |
TRG_DiLeu_BaLyEn_6 | 83 | 88 | PF01217 | 0.620 |
TRG_DiLeu_BaLyEn_6 | 936 | 941 | PF01217 | 0.493 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.647 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 645 | 648 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 683 | 686 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 714 | 717 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 758 | 761 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 766 | 769 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 800 | 803 | PF00928 | 0.580 |
TRG_ENDOCYTIC_2 | 938 | 941 | PF00928 | 0.484 |
TRG_ER_diArg_1 | 591 | 593 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 783 | 786 | PF00400 | 0.676 |
TRG_ER_diArg_1 | 863 | 866 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 871 | 874 | PF00400 | 0.319 |
TRG_ER_diArg_1 | 927 | 929 | PF00400 | 0.344 |
TRG_NES_CRM1_1 | 788 | 798 | PF08389 | 0.620 |
TRG_NLS_MonoExtC_3 | 366 | 371 | PF00514 | 0.437 |
TRG_Pf-PMV_PEXEL_1 | 820 | 824 | PF00026 | 0.449 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5A7 | Leptomonas seymouri | 68% | 93% |
A0A0S4IUR7 | Bodo saltans | 41% | 97% |
A0A1X0NNS9 | Trypanosomatidae | 48% | 94% |
A0A3R7NZA3 | Trypanosoma rangeli | 48% | 94% |
A4H7G5 | Leishmania braziliensis | 90% | 100% |
A4HVU6 | Leishmania infantum | 100% | 100% |
B6EU02 | Leishmania tarentolae | 94% | 93% |
C9ZT80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 95% |
E9APJ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
Q4DCH3 | Trypanosoma cruzi (strain CL Brener) | 48% | 94% |
Q4QFY1 | Leishmania major | 97% | 100% |
Q57X81 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 45% | 95% |
V5BHQ6 | Trypanosoma cruzi | 49% | 94% |