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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030870 | Mre11 complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: E9AR10
Term | Name | Level | Count |
---|---|---|---|
GO:0000075 | cell cycle checkpoint signaling | 4 | 1 |
GO:0000077 | DNA damage checkpoint signaling | 5 | 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: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:0007093 | mitotic cell cycle checkpoint signaling | 4 | 1 |
GO:0007095 | mitotic G2 DNA damage checkpoint signaling | 6 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010389 | regulation of G2/M transition of mitotic cell cycle | 7 | 1 |
GO:0010564 | regulation of cell cycle process | 5 | 1 |
GO:0010948 | negative regulation of cell cycle process | 6 | 1 |
GO:0010972 | negative regulation of G2/M transition of mitotic cell cycle | 8 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0031570 | DNA integrity checkpoint signaling | 5 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0042770 | signal transduction in response to DNA damage | 4 | 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:0044773 | mitotic DNA damage checkpoint signaling | 6 | 1 |
GO:0044774 | mitotic DNA integrity checkpoint signaling | 5 | 1 |
GO:0044818 | mitotic G2/M transition checkpoint | 5 | 1 |
GO:0045786 | negative regulation of cell cycle | 5 | 1 |
GO:0045930 | negative regulation of mitotic cell cycle | 6 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0051726 | regulation of cell cycle | 4 | 1 |
GO:0065007 | biological regulation | 1 | 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 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 1 |
GO:1901988 | negative regulation of cell cycle phase transition | 7 | 1 |
GO:1901990 | regulation of mitotic cell cycle phase transition | 6 | 1 |
GO:1901991 | negative regulation of mitotic cell cycle phase transition | 7 | 1 |
GO:1902749 | regulation of cell cycle G2/M phase transition | 7 | 1 |
GO:1902750 | negative regulation of cell cycle G2/M phase transition | 8 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 114 | 118 | PF00656 | 0.585 |
CLV_C14_Caspase3-7 | 207 | 211 | PF00656 | 0.482 |
CLV_C14_Caspase3-7 | 441 | 445 | PF00656 | 0.656 |
CLV_C14_Caspase3-7 | 683 | 687 | PF00656 | 0.787 |
CLV_C14_Caspase3-7 | 721 | 725 | PF00656 | 0.729 |
CLV_C14_Caspase3-7 | 96 | 100 | PF00656 | 0.590 |
CLV_NRD_NRD_1 | 1065 | 1067 | PF00675 | 0.742 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 644 | 646 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 680 | 682 | PF00675 | 0.661 |
CLV_NRD_NRD_1 | 688 | 690 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 805 | 807 | PF00675 | 0.770 |
CLV_NRD_NRD_1 | 866 | 868 | PF00675 | 0.772 |
CLV_NRD_NRD_1 | 908 | 910 | PF00675 | 0.785 |
CLV_NRD_NRD_1 | 996 | 998 | PF00675 | 0.737 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 493 | 495 | PF00082 | 0.739 |
CLV_PCSK_KEX2_1 | 554 | 556 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 644 | 646 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 680 | 682 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 688 | 690 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 805 | 807 | PF00082 | 0.774 |
CLV_PCSK_KEX2_1 | 866 | 868 | PF00082 | 0.780 |
CLV_PCSK_KEX2_1 | 908 | 910 | PF00082 | 0.785 |
CLV_PCSK_KEX2_1 | 988 | 990 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 996 | 998 | PF00082 | 0.827 |
CLV_PCSK_PC1ET2_1 | 988 | 990 | PF00082 | 0.561 |
CLV_PCSK_PC7_1 | 801 | 807 | PF00082 | 0.750 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 512 | 516 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 593 | 597 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 688 | 692 | PF00082 | 0.638 |
DEG_APCC_DBOX_1 | 883 | 891 | PF00400 | 0.821 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.432 |
DEG_SCF_FBW7_1 | 791 | 797 | PF00400 | 0.804 |
DEG_SPOP_SBC_1 | 264 | 268 | PF00917 | 0.649 |
DEG_SPOP_SBC_1 | 462 | 466 | PF00917 | 0.725 |
DOC_CKS1_1 | 791 | 796 | PF01111 | 0.537 |
DOC_MAPK_gen_1 | 152 | 160 | PF00069 | 0.380 |
DOC_MAPK_gen_1 | 174 | 185 | PF00069 | 0.382 |
DOC_MAPK_gen_1 | 554 | 560 | PF00069 | 0.620 |
DOC_MAPK_MEF2A_6 | 152 | 160 | PF00069 | 0.414 |
DOC_MAPK_RevD_3 | 479 | 494 | PF00069 | 0.485 |
DOC_PP1_RVXF_1 | 299 | 305 | PF00149 | 0.463 |
DOC_PP2B_LxvP_1 | 248 | 251 | PF13499 | 0.547 |
DOC_PP2B_LxvP_1 | 883 | 886 | PF13499 | 0.746 |
DOC_PP4_FxxP_1 | 254 | 257 | PF00568 | 0.477 |
DOC_PP4_FxxP_1 | 282 | 285 | PF00568 | 0.609 |
DOC_PP4_FxxP_1 | 446 | 449 | PF00568 | 0.710 |
DOC_SPAK_OSR1_1 | 253 | 257 | PF12202 | 0.576 |
DOC_USP7_MATH_1 | 1009 | 1013 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 1021 | 1025 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 447 | 451 | PF00917 | 0.791 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 527 | 531 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 690 | 694 | PF00917 | 0.786 |
DOC_USP7_MATH_1 | 717 | 721 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 741 | 745 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 784 | 788 | PF00917 | 0.832 |
DOC_USP7_MATH_1 | 808 | 812 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 833 | 837 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 992 | 996 | PF00917 | 0.831 |
DOC_WW_Pin1_4 | 1017 | 1022 | PF00397 | 0.759 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 523 | 528 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 704 | 709 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 790 | 795 | PF00397 | 0.795 |
DOC_WW_Pin1_4 | 804 | 809 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 869 | 874 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 895 | 900 | PF00397 | 0.729 |
LIG_14-3-3_CanoR_1 | 493 | 499 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 500 | 508 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 518 | 523 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 579 | 584 | PF00244 | 0.354 |
LIG_14-3-3_CanoR_1 | 644 | 653 | PF00244 | 0.284 |
LIG_14-3-3_CanoR_1 | 666 | 674 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 688 | 696 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 801 | 808 | PF00244 | 0.713 |
LIG_14-3-3_CanoR_1 | 866 | 875 | PF00244 | 0.746 |
LIG_14-3-3_CanoR_1 | 903 | 910 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 989 | 998 | PF00244 | 0.649 |
LIG_APCC_ABBA_1 | 451 | 456 | PF00400 | 0.777 |
LIG_BIR_III_4 | 82 | 86 | PF00653 | 0.498 |
LIG_BRCT_BRCA1_1 | 412 | 416 | PF00533 | 0.513 |
LIG_DLG_GKlike_1 | 518 | 526 | PF00625 | 0.623 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.495 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.626 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.366 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.506 |
LIG_FHA_1 | 580 | 586 | PF00498 | 0.362 |
LIG_FHA_1 | 638 | 644 | PF00498 | 0.490 |
LIG_FHA_1 | 791 | 797 | PF00498 | 0.713 |
LIG_FHA_1 | 945 | 951 | PF00498 | 0.755 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.580 |
LIG_FHA_2 | 653 | 659 | PF00498 | 0.474 |
LIG_FHA_2 | 66 | 72 | PF00498 | 0.514 |
LIG_FHA_2 | 767 | 773 | PF00498 | 0.734 |
LIG_FHA_2 | 936 | 942 | PF00498 | 0.624 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.506 |
LIG_LIR_Apic_2 | 252 | 257 | PF02991 | 0.545 |
LIG_LIR_Apic_2 | 266 | 272 | PF02991 | 0.544 |
LIG_LIR_Apic_2 | 280 | 285 | PF02991 | 0.543 |
LIG_LIR_Apic_2 | 415 | 420 | PF02991 | 0.349 |
LIG_LIR_Apic_2 | 444 | 449 | PF02991 | 0.700 |
LIG_LIR_Gen_1 | 219 | 230 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 232 | 242 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 276 | 285 | PF02991 | 0.599 |
LIG_LIR_Gen_1 | 357 | 364 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 406 | 416 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 505 | 514 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 571 | 581 | PF02991 | 0.482 |
LIG_LIR_LC3C_4 | 897 | 902 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 14 | 20 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 312 | 318 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 357 | 363 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 37 | 43 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 406 | 411 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 571 | 576 | PF02991 | 0.477 |
LIG_LYPXL_yS_3 | 880 | 883 | PF13949 | 0.741 |
LIG_MYND_1 | 449 | 453 | PF01753 | 0.508 |
LIG_PCNA_yPIPBox_3 | 563 | 577 | PF02747 | 0.368 |
LIG_Pex14_2 | 569 | 573 | PF04695 | 0.476 |
LIG_PTAP_UEV_1 | 974 | 979 | PF05743 | 0.753 |
LIG_PTB_Apo_2 | 297 | 304 | PF02174 | 0.361 |
LIG_PTB_Apo_2 | 411 | 418 | PF02174 | 0.519 |
LIG_PTB_Phospho_1 | 411 | 417 | PF10480 | 0.513 |
LIG_SH2_CRK | 153 | 157 | PF00017 | 0.472 |
LIG_SH2_CRK | 18 | 22 | PF00017 | 0.416 |
LIG_SH2_CRK | 222 | 226 | PF00017 | 0.408 |
LIG_SH2_CRK | 581 | 585 | PF00017 | 0.489 |
LIG_SH2_GRB2like | 169 | 172 | PF00017 | 0.531 |
LIG_SH2_NCK_1 | 222 | 226 | PF00017 | 0.408 |
LIG_SH2_PTP2 | 360 | 363 | PF00017 | 0.410 |
LIG_SH2_SRC | 360 | 363 | PF00017 | 0.464 |
LIG_SH2_SRC | 417 | 420 | PF00017 | 0.566 |
LIG_SH2_STAP1 | 18 | 22 | PF00017 | 0.345 |
LIG_SH2_STAP1 | 2 | 6 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 581 | 585 | PF00017 | 0.489 |
LIG_SH2_STAP1 | 611 | 615 | PF00017 | 0.561 |
LIG_SH2_STAP1 | 639 | 643 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 572 | 575 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 581 | 584 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 602 | 605 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 639 | 642 | PF00017 | 0.485 |
LIG_SH3_2 | 879 | 884 | PF14604 | 0.742 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.482 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.503 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.455 |
LIG_SH3_3 | 876 | 882 | PF00018 | 0.710 |
LIG_SH3_3 | 972 | 978 | PF00018 | 0.729 |
LIG_SUMO_SIM_anti_2 | 49 | 55 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 941 | 952 | PF11976 | 0.538 |
LIG_TRAF2_1 | 919 | 922 | PF00917 | 0.780 |
LIG_TRAF2_1 | 928 | 931 | PF00917 | 0.737 |
LIG_TRFH_1 | 279 | 283 | PF08558 | 0.557 |
LIG_TYR_ITIM | 38 | 43 | PF00017 | 0.522 |
LIG_TYR_ITIM | 570 | 575 | PF00017 | 0.482 |
LIG_ULM_U2AF65_1 | 858 | 863 | PF00076 | 0.546 |
LIG_WRC_WIRS_1 | 580 | 585 | PF05994 | 0.509 |
MOD_CDC14_SPxK_1 | 10 | 13 | PF00782 | 0.614 |
MOD_CDK_SPxK_1 | 1017 | 1023 | PF00069 | 0.760 |
MOD_CDK_SPxK_1 | 7 | 13 | PF00069 | 0.601 |
MOD_CK1_1 | 1017 | 1023 | PF00069 | 0.818 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.569 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.448 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.671 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.642 |
MOD_CK1_1 | 684 | 690 | PF00069 | 0.724 |
MOD_CK1_1 | 692 | 698 | PF00069 | 0.733 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.601 |
MOD_CK1_1 | 707 | 713 | PF00069 | 0.664 |
MOD_CK1_1 | 786 | 792 | PF00069 | 0.789 |
MOD_CK1_1 | 795 | 801 | PF00069 | 0.742 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.574 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.617 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.510 |
MOD_CK2_1 | 504 | 510 | PF00069 | 0.522 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.404 |
MOD_CK2_1 | 652 | 658 | PF00069 | 0.436 |
MOD_CK2_1 | 935 | 941 | PF00069 | 0.618 |
MOD_Cter_Amidation | 491 | 494 | PF01082 | 0.493 |
MOD_Cter_Amidation | 552 | 555 | PF01082 | 0.633 |
MOD_GlcNHglycan | 1007 | 1010 | PF01048 | 0.739 |
MOD_GlcNHglycan | 1016 | 1019 | PF01048 | 0.758 |
MOD_GlcNHglycan | 1044 | 1048 | PF01048 | 0.750 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.521 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.578 |
MOD_GlcNHglycan | 161 | 165 | PF01048 | 0.486 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.535 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.259 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.721 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.670 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.655 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.715 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.685 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.551 |
MOD_GlcNHglycan | 668 | 671 | PF01048 | 0.606 |
MOD_GlcNHglycan | 709 | 712 | PF01048 | 0.689 |
MOD_GlcNHglycan | 724 | 728 | PF01048 | 0.556 |
MOD_GlcNHglycan | 779 | 782 | PF01048 | 0.771 |
MOD_GlcNHglycan | 785 | 789 | PF01048 | 0.728 |
MOD_GlcNHglycan | 905 | 908 | PF01048 | 0.749 |
MOD_GlcNHglycan | 911 | 914 | PF01048 | 0.758 |
MOD_GlcNHglycan | 956 | 959 | PF01048 | 0.616 |
MOD_GlcNHglycan | 975 | 978 | PF01048 | 0.713 |
MOD_GlcNHglycan | 998 | 1001 | PF01048 | 0.733 |
MOD_GSK3_1 | 1005 | 1012 | PF00069 | 0.691 |
MOD_GSK3_1 | 1017 | 1024 | PF00069 | 0.800 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.496 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.491 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.606 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.523 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.522 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.320 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.791 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.629 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.675 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.585 |
MOD_GSK3_1 | 648 | 655 | PF00069 | 0.415 |
MOD_GSK3_1 | 676 | 683 | PF00069 | 0.692 |
MOD_GSK3_1 | 684 | 691 | PF00069 | 0.650 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.618 |
MOD_GSK3_1 | 719 | 726 | PF00069 | 0.747 |
MOD_GSK3_1 | 786 | 793 | PF00069 | 0.733 |
MOD_GSK3_1 | 795 | 802 | PF00069 | 0.672 |
MOD_GSK3_1 | 804 | 811 | PF00069 | 0.622 |
MOD_GSK3_1 | 869 | 876 | PF00069 | 0.776 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.786 |
MOD_GSK3_1 | 940 | 947 | PF00069 | 0.791 |
MOD_GSK3_1 | 969 | 976 | PF00069 | 0.731 |
MOD_GSK3_1 | 987 | 994 | PF00069 | 0.758 |
MOD_LATS_1 | 1041 | 1047 | PF00433 | 0.748 |
MOD_N-GLC_1 | 1005 | 1010 | PF02516 | 0.808 |
MOD_N-GLC_1 | 1014 | 1019 | PF02516 | 0.723 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.456 |
MOD_N-GLC_1 | 290 | 295 | PF02516 | 0.558 |
MOD_N-GLC_1 | 364 | 369 | PF02516 | 0.482 |
MOD_N-GLC_1 | 741 | 746 | PF02516 | 0.738 |
MOD_N-GLC_1 | 969 | 974 | PF02516 | 0.677 |
MOD_N-GLC_2 | 633 | 635 | PF02516 | 0.515 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.482 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.608 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.537 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.527 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.714 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.672 |
MOD_NEK2_1 | 629 | 634 | PF00069 | 0.486 |
MOD_NEK2_1 | 777 | 782 | PF00069 | 0.635 |
MOD_NEK2_1 | 812 | 817 | PF00069 | 0.716 |
MOD_NEK2_1 | 948 | 953 | PF00069 | 0.779 |
MOD_NEK2_2 | 403 | 408 | PF00069 | 0.437 |
MOD_NEK2_2 | 639 | 644 | PF00069 | 0.484 |
MOD_PIKK_1 | 1054 | 1060 | PF00454 | 0.760 |
MOD_PIKK_1 | 341 | 347 | PF00454 | 0.579 |
MOD_PIKK_1 | 867 | 873 | PF00454 | 0.620 |
MOD_PIKK_1 | 969 | 975 | PF00454 | 0.593 |
MOD_PK_1 | 681 | 687 | PF00069 | 0.630 |
MOD_PK_1 | 822 | 828 | PF00069 | 0.720 |
MOD_PKA_1 | 493 | 499 | PF00069 | 0.709 |
MOD_PKA_1 | 680 | 686 | PF00069 | 0.783 |
MOD_PKA_1 | 688 | 694 | PF00069 | 0.671 |
MOD_PKA_1 | 908 | 914 | PF00069 | 0.532 |
MOD_PKA_1 | 996 | 1002 | PF00069 | 0.820 |
MOD_PKA_2 | 1062 | 1068 | PF00069 | 0.649 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.491 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.263 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.578 |
MOD_PKA_2 | 493 | 499 | PF00069 | 0.717 |
MOD_PKA_2 | 605 | 611 | PF00069 | 0.507 |
MOD_PKA_2 | 680 | 686 | PF00069 | 0.693 |
MOD_PKA_2 | 688 | 694 | PF00069 | 0.743 |
MOD_PKA_2 | 800 | 806 | PF00069 | 0.722 |
MOD_PKA_2 | 908 | 914 | PF00069 | 0.540 |
MOD_PKA_2 | 990 | 996 | PF00069 | 0.801 |
MOD_PKB_1 | 516 | 524 | PF00069 | 0.677 |
MOD_PKB_1 | 577 | 585 | PF00069 | 0.366 |
MOD_PKB_1 | 989 | 997 | PF00069 | 0.545 |
MOD_Plk_1 | 1043 | 1049 | PF00069 | 0.754 |
MOD_Plk_1 | 160 | 166 | PF00069 | 0.403 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.455 |
MOD_Plk_1 | 403 | 409 | PF00069 | 0.446 |
MOD_Plk_1 | 664 | 670 | PF00069 | 0.637 |
MOD_Plk_1 | 944 | 950 | PF00069 | 0.580 |
MOD_Plk_1 | 969 | 975 | PF00069 | 0.728 |
MOD_Plk_2-3 | 41 | 47 | PF00069 | 0.463 |
MOD_Plk_2-3 | 605 | 611 | PF00069 | 0.507 |
MOD_Plk_2-3 | 93 | 99 | PF00069 | 0.550 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.345 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.433 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.394 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.724 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.455 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.425 |
MOD_Plk_4 | 579 | 585 | PF00069 | 0.362 |
MOD_Plk_4 | 944 | 950 | PF00069 | 0.541 |
MOD_ProDKin_1 | 1017 | 1023 | PF00069 | 0.760 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.539 |
MOD_ProDKin_1 | 523 | 529 | PF00069 | 0.751 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.601 |
MOD_ProDKin_1 | 704 | 710 | PF00069 | 0.716 |
MOD_ProDKin_1 | 790 | 796 | PF00069 | 0.799 |
MOD_ProDKin_1 | 804 | 810 | PF00069 | 0.664 |
MOD_ProDKin_1 | 869 | 875 | PF00069 | 0.709 |
MOD_ProDKin_1 | 895 | 901 | PF00069 | 0.731 |
MOD_SUMO_rev_2 | 587 | 591 | PF00179 | 0.488 |
MOD_SUMO_rev_2 | 610 | 617 | PF00179 | 0.494 |
TRG_DiLeu_BaEn_1 | 101 | 106 | PF01217 | 0.456 |
TRG_DiLeu_BaEn_2 | 381 | 387 | PF01217 | 0.507 |
TRG_DiLeu_BaEn_2 | 564 | 570 | PF01217 | 0.503 |
TRG_DiLeu_BaEn_4 | 418 | 424 | PF01217 | 0.591 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 572 | 575 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 581 | 584 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 880 | 883 | PF00928 | 0.741 |
TRG_ER_diArg_1 | 1061 | 1064 | PF00400 | 0.664 |
TRG_ER_diArg_1 | 173 | 175 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 576 | 579 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 643 | 645 | PF00400 | 0.342 |
TRG_ER_diArg_1 | 866 | 868 | PF00400 | 0.728 |
TRG_ER_diArg_1 | 902 | 905 | PF00400 | 0.737 |
TRG_ER_diArg_1 | 908 | 910 | PF00400 | 0.744 |
TRG_ER_diArg_1 | 996 | 998 | PF00400 | 0.630 |
TRG_NES_CRM1_1 | 574 | 588 | PF08389 | 0.487 |
TRG_NLS_MonoExtN_4 | 849 | 855 | PF00514 | 0.612 |
TRG_NLS_MonoExtN_4 | 986 | 992 | PF00514 | 0.785 |
TRG_Pf-PMV_PEXEL_1 | 512 | 517 | PF00026 | 0.515 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2V4 | Leptomonas seymouri | 47% | 97% |
A0A3S5H703 | Leishmania donovani | 82% | 100% |
A0A3S5IS81 | Trypanosoma rangeli | 31% | 100% |
A4H8Y4 | Leishmania braziliensis | 55% | 98% |
A4HXB4 | Leishmania infantum | 79% | 100% |
Q4QEF3 | Leishmania major | 81% | 98% |