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: 15 |
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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032300 | mismatch repair complex | 2 | 7 |
GO:0032991 | protein-containing complex | 1 | 7 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032389 | MutLalpha complex | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
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 |
Related structures:
AlphaFold database: A4I0Y1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006259 | DNA metabolic process | 4 | 7 |
GO:0006281 | DNA repair | 5 | 7 |
GO:0006298 | mismatch repair | 6 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0006950 | response to stress | 2 | 7 |
GO:0006974 | DNA damage response | 4 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0033554 | cellular response to stress | 3 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0050896 | response to stimulus | 1 | 7 |
GO:0051716 | cellular response to stimulus | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003677 | DNA binding | 4 | 7 |
GO:0003690 | double-stranded DNA binding | 5 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 7 |
GO:0016462 | pyrophosphatase activity | 5 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 7 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 7 |
GO:0016887 | ATP hydrolysis activity | 7 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0030983 | mismatched DNA binding | 6 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 7 |
GO:0140299 | small molecule sensor activity | 1 | 7 |
GO:0140612 | DNA damage sensor activity | 2 | 7 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 7 |
GO:0140657 | ATP-dependent activity | 1 | 7 |
GO:0140664 | ATP-dependent DNA damage sensor activity | 3 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 418 | 422 | PF00656 | 0.709 |
CLV_C14_Caspase3-7 | 541 | 545 | PF00656 | 0.734 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.851 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 440 | 442 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.652 |
CLV_NRD_NRD_1 | 687 | 689 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 771 | 773 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 775 | 777 | PF00675 | 0.411 |
CLV_PCSK_FUR_1 | 4 | 8 | PF00082 | 0.699 |
CLV_PCSK_FUR_1 | 438 | 442 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.851 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 686 | 688 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 771 | 773 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 775 | 777 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 437 | 439 | PF00082 | 0.732 |
CLV_PCSK_PC1ET2_1 | 686 | 688 | PF00082 | 0.542 |
CLV_PCSK_PC7_1 | 771 | 777 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.775 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.723 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.732 |
CLV_PCSK_SKI1_1 | 604 | 608 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 630 | 634 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 724 | 728 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 781 | 785 | PF00082 | 0.515 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.496 |
DEG_SCF_FBW7_1 | 929 | 936 | PF00400 | 0.409 |
DEG_SPOP_SBC_1 | 182 | 186 | PF00917 | 0.712 |
DEG_SPOP_SBC_1 | 245 | 249 | PF00917 | 0.733 |
DEG_SPOP_SBC_1 | 250 | 254 | PF00917 | 0.652 |
DEG_SPOP_SBC_1 | 328 | 332 | PF00917 | 0.786 |
DEG_SPOP_SBC_1 | 834 | 838 | PF00917 | 0.824 |
DOC_CKS1_1 | 648 | 653 | PF01111 | 0.512 |
DOC_CKS1_1 | 869 | 874 | PF01111 | 0.598 |
DOC_CKS1_1 | 930 | 935 | PF01111 | 0.409 |
DOC_CYCLIN_RxL_1 | 775 | 786 | PF00134 | 0.411 |
DOC_MAPK_gen_1 | 127 | 136 | PF00069 | 0.548 |
DOC_MAPK_gen_1 | 34 | 42 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 812 | 820 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 34 | 42 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 653 | 662 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 69 | 78 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 812 | 820 | PF00069 | 0.419 |
DOC_PP1_RVXF_1 | 722 | 729 | PF00149 | 0.538 |
DOC_PP2B_LxvP_1 | 640 | 643 | PF13499 | 0.411 |
DOC_PP2B_LxvP_1 | 669 | 672 | PF13499 | 0.588 |
DOC_PP2B_LxvP_1 | 76 | 79 | PF13499 | 0.411 |
DOC_PP2B_LxvP_1 | 925 | 928 | PF13499 | 0.411 |
DOC_PP4_FxxP_1 | 346 | 349 | PF00568 | 0.754 |
DOC_PP4_FxxP_1 | 648 | 651 | PF00568 | 0.411 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.814 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 519 | 523 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 543 | 547 | PF00917 | 0.820 |
DOC_USP7_MATH_1 | 703 | 707 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 754 | 758 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 828 | 832 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 833 | 837 | PF00917 | 0.783 |
DOC_USP7_MATH_1 | 853 | 857 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 875 | 879 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 933 | 937 | PF00917 | 0.352 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 582 | 587 | PF00397 | 0.407 |
DOC_WW_Pin1_4 | 647 | 652 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 735 | 740 | PF00397 | 0.743 |
DOC_WW_Pin1_4 | 868 | 873 | PF00397 | 0.804 |
DOC_WW_Pin1_4 | 884 | 889 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 929 | 934 | PF00397 | 0.422 |
LIG_14-3-3_CanoR_1 | 129 | 136 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 69 | 74 | PF00244 | 0.411 |
LIG_Actin_WH2_2 | 974 | 989 | PF00022 | 0.394 |
LIG_BIR_III_2 | 583 | 587 | PF00653 | 0.409 |
LIG_BRCT_BRCA1_1 | 340 | 344 | PF00533 | 0.780 |
LIG_BRCT_BRCA1_1 | 602 | 606 | PF00533 | 0.512 |
LIG_Clathr_ClatBox_1 | 994 | 998 | PF01394 | 0.512 |
LIG_EVH1_1 | 640 | 644 | PF00568 | 0.411 |
LIG_EVH1_1 | 925 | 929 | PF00568 | 0.512 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.585 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.740 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.749 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.710 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.662 |
LIG_FHA_1 | 610 | 616 | PF00498 | 0.512 |
LIG_FHA_1 | 617 | 623 | PF00498 | 0.411 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.448 |
LIG_FHA_1 | 702 | 708 | PF00498 | 0.660 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.368 |
LIG_FHA_1 | 942 | 948 | PF00498 | 0.512 |
LIG_FHA_1 | 952 | 958 | PF00498 | 0.314 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.772 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.694 |
LIG_FHA_2 | 367 | 373 | PF00498 | 0.721 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.411 |
LIG_FHA_2 | 880 | 886 | PF00498 | 0.808 |
LIG_FHA_2 | 933 | 939 | PF00498 | 0.450 |
LIG_GBD_Chelix_1 | 654 | 662 | PF00786 | 0.512 |
LIG_GBD_Chelix_1 | 914 | 922 | PF00786 | 0.411 |
LIG_KLC1_Yacidic_2 | 786 | 791 | PF13176 | 0.512 |
LIG_LIR_Apic_2 | 307 | 313 | PF02991 | 0.740 |
LIG_LIR_Apic_2 | 920 | 926 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 17 | 25 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 314 | 322 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 471 | 480 | PF02991 | 0.598 |
LIG_LIR_Gen_1 | 786 | 797 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 314 | 318 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 471 | 477 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 57 | 63 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 786 | 792 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 998 | 1004 | PF02991 | 0.411 |
LIG_MYND_1 | 667 | 671 | PF01753 | 0.697 |
LIG_NRBOX | 653 | 659 | PF00104 | 0.512 |
LIG_PCNA_TLS_4 | 222 | 229 | PF02747 | 0.664 |
LIG_PDZ_Class_3 | 1002 | 1007 | PF00595 | 0.411 |
LIG_Pex14_2 | 628 | 632 | PF04695 | 0.383 |
LIG_RPA_C_Fungi | 435 | 447 | PF08784 | 0.606 |
LIG_RPA_C_Fungi | 619 | 631 | PF08784 | 0.347 |
LIG_SH2_CRK | 526 | 530 | PF00017 | 0.684 |
LIG_SH2_CRK | 60 | 64 | PF00017 | 0.411 |
LIG_SH2_CRK | 664 | 668 | PF00017 | 0.684 |
LIG_SH2_CRK | 923 | 927 | PF00017 | 0.512 |
LIG_SH2_NCK_1 | 310 | 314 | PF00017 | 0.604 |
LIG_SH2_NCK_1 | 526 | 530 | PF00017 | 0.684 |
LIG_SH2_PTP2 | 789 | 792 | PF00017 | 0.512 |
LIG_SH2_SRC | 789 | 792 | PF00017 | 0.512 |
LIG_SH2_STAT3 | 228 | 231 | PF00017 | 0.637 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.637 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 526 | 529 | PF00017 | 0.681 |
LIG_SH2_STAT5 | 769 | 772 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 787 | 790 | PF00017 | 0.411 |
LIG_SH3_1 | 923 | 929 | PF00018 | 0.512 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.650 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.714 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.616 |
LIG_SH3_3 | 481 | 487 | PF00018 | 0.709 |
LIG_SH3_3 | 561 | 567 | PF00018 | 0.628 |
LIG_SH3_3 | 635 | 641 | PF00018 | 0.411 |
LIG_SH3_3 | 796 | 802 | PF00018 | 0.411 |
LIG_SH3_3 | 824 | 830 | PF00018 | 0.411 |
LIG_SH3_3 | 866 | 872 | PF00018 | 0.604 |
LIG_SH3_3 | 923 | 929 | PF00018 | 0.419 |
LIG_SUMO_SIM_anti_2 | 656 | 661 | PF11976 | 0.438 |
LIG_SUMO_SIM_anti_2 | 675 | 682 | PF11976 | 0.324 |
LIG_SUMO_SIM_anti_2 | 72 | 77 | PF11976 | 0.512 |
LIG_SUMO_SIM_par_1 | 557 | 563 | PF11976 | 0.700 |
LIG_SUMO_SIM_par_1 | 675 | 682 | PF11976 | 0.536 |
LIG_SUMO_SIM_par_1 | 71 | 77 | PF11976 | 0.512 |
LIG_SUMO_SIM_par_1 | 993 | 999 | PF11976 | 0.411 |
LIG_TRAF2_1 | 258 | 261 | PF00917 | 0.750 |
LIG_TRFH_1 | 923 | 927 | PF08558 | 0.512 |
LIG_UBA3_1 | 676 | 685 | PF00899 | 0.423 |
LIG_UBA3_1 | 969 | 974 | PF00899 | 0.411 |
LIG_WW_3 | 809 | 813 | PF00397 | 0.512 |
MOD_CDC14_SPxK_1 | 348 | 351 | PF00782 | 0.733 |
MOD_CDK_SPxK_1 | 345 | 351 | PF00069 | 0.733 |
MOD_CDK_SPxK_1 | 647 | 653 | PF00069 | 0.512 |
MOD_CDK_SPxxK_3 | 345 | 352 | PF00069 | 0.733 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.666 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.688 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.712 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.571 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.453 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.756 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.784 |
MOD_CK1_1 | 571 | 577 | PF00069 | 0.364 |
MOD_CK1_1 | 705 | 711 | PF00069 | 0.623 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.512 |
MOD_CK1_1 | 836 | 842 | PF00069 | 0.830 |
MOD_CK1_1 | 874 | 880 | PF00069 | 0.812 |
MOD_CK1_1 | 931 | 937 | PF00069 | 0.442 |
MOD_CK1_1 | 993 | 999 | PF00069 | 0.411 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.567 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.771 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.670 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.666 |
MOD_CK2_1 | 485 | 491 | PF00069 | 0.794 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.411 |
MOD_CK2_1 | 879 | 885 | PF00069 | 0.807 |
MOD_CK2_1 | 932 | 938 | PF00069 | 0.450 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.618 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.678 |
MOD_GlcNHglycan | 150 | 154 | PF01048 | 0.683 |
MOD_GlcNHglycan | 156 | 160 | PF01048 | 0.650 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.754 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.672 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.841 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.727 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.411 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.658 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.411 |
MOD_GlcNHglycan | 672 | 675 | PF01048 | 0.515 |
MOD_GlcNHglycan | 745 | 748 | PF01048 | 0.756 |
MOD_GlcNHglycan | 763 | 766 | PF01048 | 0.261 |
MOD_GlcNHglycan | 830 | 833 | PF01048 | 0.621 |
MOD_GlcNHglycan | 840 | 843 | PF01048 | 0.770 |
MOD_GlcNHglycan | 935 | 938 | PF01048 | 0.512 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.720 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.665 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.411 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.770 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.629 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.775 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.717 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.646 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.394 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.412 |
MOD_GSK3_1 | 701 | 708 | PF00069 | 0.660 |
MOD_GSK3_1 | 731 | 738 | PF00069 | 0.635 |
MOD_GSK3_1 | 834 | 841 | PF00069 | 0.816 |
MOD_GSK3_1 | 870 | 877 | PF00069 | 0.796 |
MOD_GSK3_1 | 928 | 935 | PF00069 | 0.419 |
MOD_GSK3_1 | 949 | 956 | PF00069 | 0.522 |
MOD_LATS_1 | 483 | 489 | PF00433 | 0.747 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.450 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.591 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.776 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.692 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.400 |
MOD_NEK2_1 | 524 | 529 | PF00069 | 0.688 |
MOD_NEK2_1 | 569 | 574 | PF00069 | 0.465 |
MOD_NEK2_1 | 702 | 707 | PF00069 | 0.599 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.355 |
MOD_PIKK_1 | 227 | 233 | PF00454 | 0.646 |
MOD_PIKK_1 | 267 | 273 | PF00454 | 0.657 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.686 |
MOD_PIKK_1 | 301 | 307 | PF00454 | 0.695 |
MOD_PIKK_1 | 538 | 544 | PF00454 | 0.776 |
MOD_PIKK_1 | 879 | 885 | PF00454 | 0.795 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.588 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.755 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.711 |
MOD_PKB_1 | 7 | 15 | PF00069 | 0.607 |
MOD_Plk_1 | 394 | 400 | PF00069 | 0.659 |
MOD_Plk_1 | 470 | 476 | PF00069 | 0.665 |
MOD_Plk_1 | 519 | 525 | PF00069 | 0.727 |
MOD_Plk_2-3 | 311 | 317 | PF00069 | 0.584 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.647 |
MOD_Plk_4 | 524 | 530 | PF00069 | 0.690 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.727 |
MOD_Plk_4 | 571 | 577 | PF00069 | 0.260 |
MOD_Plk_4 | 593 | 599 | PF00069 | 0.411 |
MOD_Plk_4 | 610 | 616 | PF00069 | 0.411 |
MOD_Plk_4 | 672 | 678 | PF00069 | 0.571 |
MOD_Plk_4 | 754 | 760 | PF00069 | 0.698 |
MOD_Plk_4 | 918 | 924 | PF00069 | 0.394 |
MOD_Plk_4 | 990 | 996 | PF00069 | 0.411 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.667 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.716 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.743 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.707 |
MOD_ProDKin_1 | 582 | 588 | PF00069 | 0.407 |
MOD_ProDKin_1 | 647 | 653 | PF00069 | 0.443 |
MOD_ProDKin_1 | 735 | 741 | PF00069 | 0.743 |
MOD_ProDKin_1 | 868 | 874 | PF00069 | 0.804 |
MOD_ProDKin_1 | 884 | 890 | PF00069 | 0.671 |
MOD_ProDKin_1 | 929 | 935 | PF00069 | 0.422 |
MOD_SUMO_rev_2 | 532 | 541 | PF00179 | 0.687 |
MOD_SUMO_rev_2 | 731 | 737 | PF00179 | 0.686 |
TRG_DiLeu_BaEn_1 | 445 | 450 | PF01217 | 0.732 |
TRG_DiLeu_BaLyEn_6 | 576 | 581 | PF01217 | 0.450 |
TRG_ENDOCYTIC_2 | 1001 | 1004 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 526 | 529 | PF00928 | 0.681 |
TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 787 | 790 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 4 | 7 | PF00400 | 0.706 |
TRG_ER_diArg_1 | 438 | 441 | PF00400 | 0.617 |
TRG_ER_diArg_1 | 770 | 772 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 774 | 776 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 811 | 814 | PF00400 | 0.512 |
TRG_NLS_MonoCore_2 | 684 | 689 | PF00514 | 0.441 |
TRG_NLS_MonoExtC_3 | 436 | 441 | PF00514 | 0.721 |
TRG_NLS_MonoExtN_4 | 434 | 441 | PF00514 | 0.726 |
TRG_NLS_MonoExtN_4 | 685 | 690 | PF00514 | 0.455 |
TRG_Pf-PMV_PEXEL_1 | 579 | 583 | PF00026 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 781 | 786 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 916 | 920 | PF00026 | 0.394 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I302 | Leptomonas seymouri | 48% | 78% |
A0A3S7WYI2 | Leishmania donovani | 99% | 74% |
A4HDK0 | Leishmania braziliensis | 75% | 100% |
E9AWY5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QAI9 | Leishmania major | 92% | 100% |