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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030870 | Mre11 complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
Related structures:
AlphaFold database: A0A3S5H703
Term | Name | Level | Count |
---|---|---|---|
GO:0000075 | cell cycle checkpoint signaling | 4 | 2 |
GO:0000077 | DNA damage checkpoint signaling | 5 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006259 | DNA metabolic process | 4 | 2 |
GO:0006281 | DNA repair | 5 | 2 |
GO:0006302 | double-strand break repair | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006950 | response to stress | 2 | 2 |
GO:0006974 | DNA damage response | 4 | 2 |
GO:0007093 | mitotic cell cycle checkpoint signaling | 4 | 2 |
GO:0007095 | mitotic G2 DNA damage checkpoint signaling | 6 | 2 |
GO:0007165 | signal transduction | 2 | 2 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010389 | regulation of G2/M transition of mitotic cell cycle | 7 | 2 |
GO:0010564 | regulation of cell cycle process | 5 | 2 |
GO:0010948 | negative regulation of cell cycle process | 6 | 2 |
GO:0010972 | negative regulation of G2/M transition of mitotic cell cycle | 8 | 2 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0031570 | DNA integrity checkpoint signaling | 5 | 2 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0035556 | intracellular signal transduction | 3 | 2 |
GO:0042770 | signal transduction in response to DNA damage | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044773 | mitotic DNA damage checkpoint signaling | 6 | 2 |
GO:0044774 | mitotic DNA integrity checkpoint signaling | 5 | 2 |
GO:0044818 | mitotic G2/M transition checkpoint | 5 | 2 |
GO:0045786 | negative regulation of cell cycle | 5 | 2 |
GO:0045930 | negative regulation of mitotic cell cycle | 6 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0048519 | negative regulation of biological process | 3 | 2 |
GO:0048523 | negative regulation of cellular process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0051726 | regulation of cell cycle | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 2 |
GO:1901988 | negative regulation of cell cycle phase transition | 7 | 2 |
GO:1901990 | regulation of mitotic cell cycle phase transition | 6 | 2 |
GO:1901991 | negative regulation of mitotic cell cycle phase transition | 7 | 2 |
GO:1902749 | regulation of cell cycle G2/M phase transition | 7 | 2 |
GO:1902750 | negative regulation of cell cycle G2/M phase transition | 8 | 2 |
GO:1903047 | mitotic cell cycle process | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 114 | 118 | PF00656 | 0.601 |
CLV_C14_Caspase3-7 | 207 | 211 | PF00656 | 0.505 |
CLV_C14_Caspase3-7 | 683 | 687 | PF00656 | 0.807 |
CLV_C14_Caspase3-7 | 721 | 725 | PF00656 | 0.751 |
CLV_C14_Caspase3-7 | 775 | 779 | PF00656 | 0.640 |
CLV_C14_Caspase3-7 | 965 | 969 | PF00656 | 0.713 |
CLV_NRD_NRD_1 | 1054 | 1056 | PF00675 | 0.795 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.723 |
CLV_NRD_NRD_1 | 555 | 557 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 675 | 677 | PF00675 | 0.652 |
CLV_NRD_NRD_1 | 680 | 682 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 688 | 690 | PF00675 | 0.698 |
CLV_NRD_NRD_1 | 803 | 805 | PF00675 | 0.780 |
CLV_NRD_NRD_1 | 863 | 865 | PF00675 | 0.835 |
CLV_NRD_NRD_1 | 906 | 908 | PF00675 | 0.810 |
CLV_PCSK_FUR_1 | 553 | 557 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 493 | 495 | PF00082 | 0.780 |
CLV_PCSK_KEX2_1 | 553 | 555 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 675 | 677 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 680 | 682 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 688 | 690 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 803 | 805 | PF00082 | 0.783 |
CLV_PCSK_KEX2_1 | 859 | 861 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 906 | 908 | PF00082 | 0.810 |
CLV_PCSK_PC1ET2_1 | 859 | 861 | PF00082 | 0.629 |
CLV_PCSK_PC7_1 | 489 | 495 | PF00082 | 0.689 |
CLV_PCSK_PC7_1 | 676 | 682 | PF00082 | 0.756 |
CLV_PCSK_PC7_1 | 799 | 805 | PF00082 | 0.761 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 593 | 597 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 675 | 679 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 688 | 692 | PF00082 | 0.751 |
CLV_PCSK_SKI1_1 | 694 | 698 | PF00082 | 0.737 |
DEG_APCC_DBOX_1 | 881 | 889 | PF00400 | 0.808 |
DEG_COP1_1 | 964 | 975 | PF00400 | 0.711 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.409 |
DEG_SPOP_SBC_1 | 264 | 268 | PF00917 | 0.635 |
DEG_SPOP_SBC_1 | 462 | 466 | PF00917 | 0.744 |
DEG_SPOP_SBC_1 | 947 | 951 | PF00917 | 0.715 |
DOC_CYCLIN_yCln2_LP_2 | 881 | 887 | PF00134 | 0.593 |
DOC_MAPK_gen_1 | 101 | 109 | PF00069 | 0.349 |
DOC_MAPK_gen_1 | 152 | 160 | PF00069 | 0.363 |
DOC_MAPK_gen_1 | 553 | 560 | PF00069 | 0.671 |
DOC_MAPK_MEF2A_6 | 101 | 109 | PF00069 | 0.382 |
DOC_MAPK_MEF2A_6 | 152 | 160 | PF00069 | 0.396 |
DOC_PP1_RVXF_1 | 299 | 305 | PF00149 | 0.486 |
DOC_PP2B_LxvP_1 | 248 | 251 | PF13499 | 0.514 |
DOC_PP2B_LxvP_1 | 881 | 884 | PF13499 | 0.790 |
DOC_PP4_FxxP_1 | 254 | 257 | PF00568 | 0.464 |
DOC_PP4_FxxP_1 | 282 | 285 | PF00568 | 0.632 |
DOC_PP4_FxxP_1 | 446 | 449 | PF00568 | 0.687 |
DOC_SPAK_OSR1_1 | 253 | 257 | PF12202 | 0.534 |
DOC_USP7_MATH_1 | 1010 | 1014 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 648 | 652 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 690 | 694 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 717 | 721 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 741 | 745 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 757 | 761 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 810 | 814 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 832 | 836 | PF00917 | 0.782 |
DOC_USP7_MATH_1 | 990 | 994 | PF00917 | 0.838 |
DOC_USP7_MATH_2 | 762 | 768 | PF00917 | 0.708 |
DOC_WW_Pin1_4 | 1006 | 1011 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 523 | 528 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 704 | 709 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 781 | 786 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 806 | 811 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 867 | 872 | PF00397 | 0.778 |
DOC_WW_Pin1_4 | 893 | 898 | PF00397 | 0.746 |
LIG_14-3-3_CanoR_1 | 483 | 490 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 493 | 499 | PF00244 | 0.681 |
LIG_14-3-3_CanoR_1 | 500 | 508 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 518 | 523 | PF00244 | 0.646 |
LIG_14-3-3_CanoR_1 | 666 | 674 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 688 | 696 | PF00244 | 0.717 |
LIG_14-3-3_CanoR_1 | 803 | 810 | PF00244 | 0.769 |
LIG_14-3-3_CanoR_1 | 864 | 873 | PF00244 | 0.765 |
LIG_APCC_ABBA_1 | 451 | 456 | PF00400 | 0.774 |
LIG_BIR_III_4 | 943 | 947 | PF00653 | 0.622 |
LIG_BRCT_BRCA1_1 | 412 | 416 | PF00533 | 0.506 |
LIG_DLG_GKlike_1 | 518 | 526 | PF00625 | 0.618 |
LIG_FHA_1 | 1006 | 1012 | PF00498 | 0.621 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.476 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.589 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.490 |
LIG_FHA_1 | 638 | 644 | PF00498 | 0.531 |
LIG_FHA_1 | 943 | 949 | PF00498 | 0.752 |
LIG_FHA_1 | 995 | 1001 | PF00498 | 0.621 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.587 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.472 |
LIG_FHA_2 | 653 | 659 | PF00498 | 0.443 |
LIG_FHA_2 | 773 | 779 | PF00498 | 0.650 |
LIG_FHA_2 | 924 | 930 | PF00498 | 0.784 |
LIG_FHA_2 | 934 | 940 | PF00498 | 0.775 |
LIG_LIR_Apic_2 | 252 | 257 | PF02991 | 0.554 |
LIG_LIR_Apic_2 | 266 | 272 | PF02991 | 0.493 |
LIG_LIR_Apic_2 | 280 | 285 | PF02991 | 0.564 |
LIG_LIR_Apic_2 | 444 | 449 | PF02991 | 0.677 |
LIG_LIR_Gen_1 | 219 | 230 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 232 | 242 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 276 | 285 | PF02991 | 0.596 |
LIG_LIR_Gen_1 | 357 | 364 | PF02991 | 0.547 |
LIG_LIR_Gen_1 | 406 | 416 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 571 | 581 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 14 | 20 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 312 | 318 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 357 | 363 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 37 | 43 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 406 | 411 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 571 | 576 | PF02991 | 0.470 |
LIG_LYPXL_yS_3 | 878 | 881 | PF13949 | 0.724 |
LIG_PCNA_yPIPBox_3 | 556 | 570 | PF02747 | 0.492 |
LIG_Pex14_2 | 569 | 573 | PF04695 | 0.522 |
LIG_PTAP_UEV_1 | 972 | 977 | PF05743 | 0.746 |
LIG_PTB_Apo_2 | 297 | 304 | PF02174 | 0.446 |
LIG_PTB_Apo_2 | 411 | 418 | PF02174 | 0.518 |
LIG_PTB_Phospho_1 | 411 | 417 | PF10480 | 0.510 |
LIG_RPA_C_Fungi | 478 | 490 | PF08784 | 0.682 |
LIG_RPA_C_Fungi | 505 | 517 | PF08784 | 0.551 |
LIG_SH2_CRK | 153 | 157 | PF00017 | 0.483 |
LIG_SH2_CRK | 18 | 22 | PF00017 | 0.430 |
LIG_SH2_CRK | 222 | 226 | PF00017 | 0.382 |
LIG_SH2_CRK | 581 | 585 | PF00017 | 0.512 |
LIG_SH2_GRB2like | 169 | 172 | PF00017 | 0.530 |
LIG_SH2_NCK_1 | 222 | 226 | PF00017 | 0.382 |
LIG_SH2_NCK_1 | 31 | 35 | PF00017 | 0.325 |
LIG_SH2_PTP2 | 360 | 363 | PF00017 | 0.390 |
LIG_SH2_SRC | 360 | 363 | PF00017 | 0.471 |
LIG_SH2_SRC | 417 | 420 | PF00017 | 0.525 |
LIG_SH2_STAP1 | 18 | 22 | PF00017 | 0.358 |
LIG_SH2_STAP1 | 2 | 6 | PF00017 | 0.538 |
LIG_SH2_STAP1 | 581 | 585 | PF00017 | 0.512 |
LIG_SH2_STAP1 | 611 | 615 | PF00017 | 0.574 |
LIG_SH2_STAP1 | 639 | 643 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 572 | 575 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 602 | 605 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 639 | 642 | PF00017 | 0.510 |
LIG_SH3_2 | 877 | 882 | PF14604 | 0.723 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.487 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.503 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.507 |
LIG_SH3_3 | 786 | 792 | PF00018 | 0.711 |
LIG_SH3_3 | 873 | 879 | PF00018 | 0.705 |
LIG_SH3_3 | 953 | 959 | PF00018 | 0.724 |
LIG_SH3_3 | 970 | 976 | PF00018 | 0.697 |
LIG_SUMO_SIM_anti_2 | 49 | 55 | PF11976 | 0.404 |
LIG_TRAF2_1 | 83 | 86 | PF00917 | 0.788 |
LIG_TRAF2_1 | 918 | 921 | PF00917 | 0.827 |
LIG_TRFH_1 | 279 | 283 | PF08558 | 0.548 |
LIG_TYR_ITIM | 38 | 43 | PF00017 | 0.536 |
LIG_TYR_ITIM | 570 | 575 | PF00017 | 0.505 |
LIG_TYR_ITIM | 876 | 881 | PF00017 | 0.686 |
LIG_UBA3_1 | 407 | 415 | PF00899 | 0.502 |
MOD_CDC14_SPxK_1 | 10 | 13 | PF00782 | 0.627 |
MOD_CDK_SPxK_1 | 1006 | 1012 | PF00069 | 0.798 |
MOD_CDK_SPxK_1 | 7 | 13 | PF00069 | 0.617 |
MOD_CK1_1 | 1006 | 1012 | PF00069 | 0.811 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.592 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.448 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.682 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.736 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.698 |
MOD_CK1_1 | 684 | 690 | PF00069 | 0.726 |
MOD_CK1_1 | 692 | 698 | PF00069 | 0.691 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.655 |
MOD_CK1_1 | 707 | 713 | PF00069 | 0.475 |
MOD_CK1_1 | 784 | 790 | PF00069 | 0.796 |
MOD_CK1_1 | 793 | 799 | PF00069 | 0.757 |
MOD_CK1_1 | 805 | 811 | PF00069 | 0.776 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.604 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.587 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.576 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.491 |
MOD_CK2_1 | 652 | 658 | PF00069 | 0.407 |
MOD_CK2_1 | 915 | 921 | PF00069 | 0.776 |
MOD_CK2_1 | 923 | 929 | PF00069 | 0.792 |
MOD_CK2_1 | 933 | 939 | PF00069 | 0.776 |
MOD_GlcNHglycan | 1005 | 1008 | PF01048 | 0.689 |
MOD_GlcNHglycan | 1033 | 1037 | PF01048 | 0.831 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.515 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.539 |
MOD_GlcNHglycan | 308 | 312 | PF01048 | 0.425 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.553 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.280 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.707 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.713 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.749 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.683 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.740 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.652 |
MOD_GlcNHglycan | 668 | 671 | PF01048 | 0.600 |
MOD_GlcNHglycan | 709 | 712 | PF01048 | 0.719 |
MOD_GlcNHglycan | 805 | 808 | PF01048 | 0.744 |
MOD_GlcNHglycan | 814 | 817 | PF01048 | 0.731 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.785 |
MOD_GlcNHglycan | 903 | 906 | PF01048 | 0.770 |
MOD_GlcNHglycan | 909 | 912 | PF01048 | 0.743 |
MOD_GlcNHglycan | 973 | 976 | PF01048 | 0.712 |
MOD_GSK3_1 | 1006 | 1013 | PF00069 | 0.779 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.514 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.554 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.555 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.439 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.492 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.590 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.313 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.678 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.745 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.674 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.561 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.631 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.630 |
MOD_GSK3_1 | 648 | 655 | PF00069 | 0.426 |
MOD_GSK3_1 | 676 | 683 | PF00069 | 0.777 |
MOD_GSK3_1 | 684 | 691 | PF00069 | 0.642 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.610 |
MOD_GSK3_1 | 790 | 797 | PF00069 | 0.767 |
MOD_GSK3_1 | 798 | 805 | PF00069 | 0.693 |
MOD_GSK3_1 | 806 | 813 | PF00069 | 0.606 |
MOD_GSK3_1 | 867 | 874 | PF00069 | 0.790 |
MOD_GSK3_1 | 938 | 945 | PF00069 | 0.681 |
MOD_GSK3_1 | 967 | 974 | PF00069 | 0.702 |
MOD_GSK3_1 | 985 | 992 | PF00069 | 0.585 |
MOD_LATS_1 | 1030 | 1036 | PF00433 | 0.748 |
MOD_N-GLC_1 | 1003 | 1008 | PF02516 | 0.821 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.477 |
MOD_N-GLC_1 | 290 | 295 | PF02516 | 0.572 |
MOD_N-GLC_1 | 364 | 369 | PF02516 | 0.500 |
MOD_N-GLC_1 | 741 | 746 | PF02516 | 0.724 |
MOD_N-GLC_1 | 840 | 845 | PF02516 | 0.784 |
MOD_N-GLC_1 | 961 | 966 | PF02516 | 0.740 |
MOD_N-GLC_2 | 633 | 635 | PF02516 | 0.568 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.527 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.377 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.501 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.608 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.541 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.505 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.630 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.609 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.545 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.715 |
MOD_NEK2_1 | 629 | 634 | PF00069 | 0.520 |
MOD_NEK2_1 | 948 | 953 | PF00069 | 0.772 |
MOD_NEK2_2 | 403 | 408 | PF00069 | 0.417 |
MOD_NEK2_2 | 449 | 454 | PF00069 | 0.515 |
MOD_NEK2_2 | 639 | 644 | PF00069 | 0.521 |
MOD_PIKK_1 | 1043 | 1049 | PF00454 | 0.760 |
MOD_PIKK_1 | 341 | 347 | PF00454 | 0.612 |
MOD_PIKK_1 | 757 | 763 | PF00454 | 0.803 |
MOD_PIKK_1 | 840 | 846 | PF00454 | 0.716 |
MOD_PIKK_1 | 915 | 921 | PF00454 | 0.764 |
MOD_PIKK_1 | 949 | 955 | PF00454 | 0.838 |
MOD_PIKK_1 | 967 | 973 | PF00454 | 0.592 |
MOD_PK_1 | 821 | 827 | PF00069 | 0.735 |
MOD_PKA_1 | 493 | 499 | PF00069 | 0.725 |
MOD_PKA_1 | 680 | 686 | PF00069 | 0.776 |
MOD_PKA_1 | 688 | 694 | PF00069 | 0.690 |
MOD_PKA_1 | 803 | 809 | PF00069 | 0.756 |
MOD_PKA_2 | 1043 | 1049 | PF00069 | 0.616 |
MOD_PKA_2 | 1051 | 1057 | PF00069 | 0.647 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.509 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.593 |
MOD_PKA_2 | 488 | 494 | PF00069 | 0.708 |
MOD_PKA_2 | 499 | 505 | PF00069 | 0.706 |
MOD_PKA_2 | 605 | 611 | PF00069 | 0.531 |
MOD_PKA_2 | 680 | 686 | PF00069 | 0.759 |
MOD_PKA_2 | 688 | 694 | PF00069 | 0.738 |
MOD_PKA_2 | 798 | 804 | PF00069 | 0.775 |
MOD_PKA_2 | 988 | 994 | PF00069 | 0.828 |
MOD_PKB_1 | 483 | 491 | PF00069 | 0.761 |
MOD_PKB_1 | 510 | 518 | PF00069 | 0.699 |
MOD_Plk_1 | 1032 | 1038 | PF00069 | 0.753 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.513 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.441 |
MOD_Plk_1 | 403 | 409 | PF00069 | 0.419 |
MOD_Plk_1 | 664 | 670 | PF00069 | 0.666 |
MOD_Plk_1 | 967 | 973 | PF00069 | 0.756 |
MOD_Plk_2-3 | 41 | 47 | PF00069 | 0.458 |
MOD_Plk_2-3 | 605 | 611 | PF00069 | 0.531 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.478 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.482 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.391 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.670 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.436 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.422 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.493 |
MOD_Plk_4 | 895 | 901 | PF00069 | 0.696 |
MOD_ProDKin_1 | 1006 | 1012 | PF00069 | 0.764 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.563 |
MOD_ProDKin_1 | 523 | 529 | PF00069 | 0.759 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.617 |
MOD_ProDKin_1 | 704 | 710 | PF00069 | 0.748 |
MOD_ProDKin_1 | 781 | 787 | PF00069 | 0.759 |
MOD_ProDKin_1 | 806 | 812 | PF00069 | 0.654 |
MOD_ProDKin_1 | 867 | 873 | PF00069 | 0.777 |
MOD_ProDKin_1 | 893 | 899 | PF00069 | 0.748 |
MOD_SUMO_rev_2 | 587 | 591 | PF00179 | 0.511 |
MOD_SUMO_rev_2 | 610 | 617 | PF00179 | 0.506 |
TRG_DiLeu_BaEn_2 | 381 | 387 | PF01217 | 0.531 |
TRG_DiLeu_BaEn_2 | 564 | 570 | PF01217 | 0.552 |
TRG_DiLeu_BaEn_4 | 418 | 424 | PF01217 | 0.601 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 572 | 575 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 581 | 584 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 878 | 881 | PF00928 | 0.724 |
TRG_ER_diArg_1 | 1050 | 1053 | PF00400 | 0.666 |
TRG_ER_diArg_1 | 173 | 175 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 511 | 514 | PF00400 | 0.645 |
TRG_ER_diArg_1 | 553 | 556 | PF00400 | 0.719 |
TRG_ER_diArg_1 | 576 | 579 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 674 | 676 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 680 | 682 | PF00400 | 0.679 |
TRG_ER_diArg_1 | 900 | 903 | PF00400 | 0.767 |
TRG_NES_CRM1_1 | 574 | 588 | PF08389 | 0.465 |
TRG_NLS_MonoExtN_4 | 984 | 990 | PF00514 | 0.802 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2V4 | Leptomonas seymouri | 47% | 96% |
A0A3S5IS81 | Trypanosoma rangeli | 30% | 100% |
A4H8Y4 | Leishmania braziliensis | 56% | 99% |
A4HXB4 | Leishmania infantum | 99% | 100% |
E9AR10 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 99% |
Q4QEF3 | Leishmania major | 87% | 99% |
V5D6I4 | Trypanosoma cruzi | 30% | 100% |