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 | 2 |
GO:0005654 | nucleoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000724 | double-strand break repair via homologous recombination | 7 | 11 |
GO:0000725 | recombinational repair | 6 | 11 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006259 | DNA metabolic process | 4 | 11 |
GO:0006281 | DNA repair | 5 | 11 |
GO:0006302 | double-strand break repair | 6 | 11 |
GO:0006310 | DNA recombination | 5 | 11 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0006950 | response to stress | 2 | 11 |
GO:0006974 | DNA damage response | 4 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009605 | response to external stimulus | 2 | 2 |
GO:0009607 | response to biotic stimulus | 2 | 2 |
GO:0009889 | regulation of biosynthetic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 11 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 2 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0020033 | antigenic variation | 7 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 2 |
GO:0033554 | cellular response to stress | 3 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0042783 | evasion of host immune response | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043207 | response to external biotic stimulus | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 11 |
GO:0044403 | biological process involved in symbiotic interaction | 2 | 2 |
GO:0044419 | biological process involved in interspecies interaction between organisms | 1 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0050896 | response to stimulus | 1 | 11 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051252 | regulation of RNA metabolic process | 5 | 2 |
GO:0051701 | biological process involved in interaction with host | 3 | 2 |
GO:0051707 | response to other organism | 2 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 11 |
GO:0052173 | response to defenses of other organism | 3 | 2 |
GO:0052200 | response to host defenses | 4 | 2 |
GO:0052572 | response to host immune response | 5 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0075136 | response to host | 3 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 2 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003677 | DNA binding | 4 | 2 |
GO:0003684 | damaged DNA binding | 5 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 460 | 464 | PF00656 | 0.536 |
CLV_C14_Caspase3-7 | 613 | 617 | PF00656 | 0.438 |
CLV_C14_Caspase3-7 | 873 | 877 | PF00656 | 0.592 |
CLV_NRD_NRD_1 | 1020 | 1022 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 1083 | 1085 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 608 | 610 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 696 | 698 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 712 | 714 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 846 | 848 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 995 | 997 | PF00675 | 0.530 |
CLV_PCSK_FUR_1 | 606 | 610 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 1020 | 1022 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 1083 | 1085 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 608 | 610 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 712 | 714 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 995 | 997 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 163 | 165 | PF00082 | 0.489 |
CLV_PCSK_PC1ET2_1 | 29 | 31 | PF00082 | 0.502 |
CLV_PCSK_PC7_1 | 25 | 31 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 1093 | 1097 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 589 | 593 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 651 | 655 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 691 | 695 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 824 | 828 | PF00082 | 0.460 |
CLV_Separin_Metazoa | 1145 | 1149 | PF03568 | 0.489 |
DEG_APCC_DBOX_1 | 124 | 132 | PF00400 | 0.496 |
DEG_APCC_DBOX_1 | 422 | 430 | PF00400 | 0.279 |
DEG_APCC_DBOX_1 | 780 | 788 | PF00400 | 0.470 |
DEG_COP1_1 | 142 | 150 | PF00400 | 0.552 |
DEG_COP1_1 | 873 | 883 | PF00400 | 0.608 |
DEG_SCF_FBW7_1 | 314 | 319 | PF00400 | 0.409 |
DEG_SCF_FBW7_2 | 235 | 242 | PF00400 | 0.543 |
DEG_SPOP_SBC_1 | 83 | 87 | PF00917 | 0.534 |
DOC_ANK_TNKS_1 | 426 | 433 | PF00023 | 0.475 |
DOC_CDC14_PxL_1 | 102 | 110 | PF14671 | 0.587 |
DOC_CKS1_1 | 39 | 44 | PF01111 | 0.544 |
DOC_CKS1_1 | 527 | 532 | PF01111 | 0.557 |
DOC_CKS1_1 | 938 | 943 | PF01111 | 0.714 |
DOC_CYCLIN_RxL_1 | 767 | 778 | PF00134 | 0.479 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 923 | 932 | PF00134 | 0.502 |
DOC_CYCLIN_yCln2_LP_2 | 1001 | 1007 | PF00134 | 0.594 |
DOC_CYCLIN_yCln2_LP_2 | 1101 | 1107 | PF00134 | 0.475 |
DOC_CYCLIN_yCln2_LP_2 | 539 | 545 | PF00134 | 0.456 |
DOC_CYCLIN_yCln2_LP_2 | 938 | 944 | PF00134 | 0.585 |
DOC_MAPK_DCC_7 | 875 | 885 | PF00069 | 0.605 |
DOC_MAPK_gen_1 | 1083 | 1090 | PF00069 | 0.500 |
DOC_MAPK_gen_1 | 17 | 26 | PF00069 | 0.518 |
DOC_MAPK_gen_1 | 448 | 458 | PF00069 | 0.468 |
DOC_MAPK_MEF2A_6 | 17 | 26 | PF00069 | 0.572 |
DOC_MAPK_RevD_3 | 1069 | 1084 | PF00069 | 0.445 |
DOC_PP1_RVXF_1 | 1076 | 1083 | PF00149 | 0.442 |
DOC_PP1_RVXF_1 | 383 | 389 | PF00149 | 0.291 |
DOC_PP1_RVXF_1 | 689 | 695 | PF00149 | 0.468 |
DOC_PP2B_LxvP_1 | 138 | 141 | PF13499 | 0.569 |
DOC_PP2B_LxvP_1 | 539 | 542 | PF13499 | 0.457 |
DOC_PP2B_LxvP_1 | 761 | 764 | PF13499 | 0.478 |
DOC_PP2B_LxvP_1 | 772 | 775 | PF13499 | 0.386 |
DOC_PP2B_LxvP_1 | 80 | 83 | PF13499 | 0.563 |
DOC_PP4_FxxP_1 | 11 | 14 | PF00568 | 0.528 |
DOC_PP4_FxxP_1 | 272 | 275 | PF00568 | 0.623 |
DOC_PP4_MxPP_1 | 205 | 208 | PF00568 | 0.519 |
DOC_USP7_MATH_1 | 1007 | 1011 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.783 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.337 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 619 | 623 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 677 | 681 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 764 | 768 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 894 | 898 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 967 | 971 | PF00917 | 0.695 |
DOC_WW_Pin1_4 | 1100 | 1105 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.786 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 892 | 897 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 899 | 904 | PF00397 | 0.778 |
DOC_WW_Pin1_4 | 937 | 942 | PF00397 | 0.672 |
LIG_14-3-3_CanoR_1 | 1093 | 1101 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 1151 | 1159 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 155 | 160 | PF00244 | 0.682 |
LIG_14-3-3_CanoR_1 | 213 | 218 | PF00244 | 0.755 |
LIG_14-3-3_CanoR_1 | 457 | 462 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 589 | 595 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 627 | 632 | PF00244 | 0.327 |
LIG_14-3-3_CanoR_1 | 770 | 775 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 781 | 785 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 817 | 823 | PF00244 | 0.474 |
LIG_Actin_WH2_2 | 1135 | 1150 | PF00022 | 0.438 |
LIG_Actin_WH2_2 | 454 | 471 | PF00022 | 0.536 |
LIG_Actin_WH2_2 | 472 | 488 | PF00022 | 0.442 |
LIG_BIR_III_2 | 36 | 40 | PF00653 | 0.629 |
LIG_BIR_III_2 | 838 | 842 | PF00653 | 0.479 |
LIG_BRCT_BRCA1_1 | 324 | 328 | PF00533 | 0.504 |
LIG_CSL_BTD_1 | 1116 | 1119 | PF09270 | 0.478 |
LIG_CSL_BTD_1 | 997 | 1000 | PF09270 | 0.543 |
LIG_CtBP_PxDLS_1 | 542 | 546 | PF00389 | 0.502 |
LIG_deltaCOP1_diTrp_1 | 1113 | 1122 | PF00928 | 0.384 |
LIG_FHA_1 | 1000 | 1006 | PF00498 | 0.553 |
LIG_FHA_1 | 1035 | 1041 | PF00498 | 0.498 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.526 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.795 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.650 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.331 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.475 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.485 |
LIG_FHA_1 | 602 | 608 | PF00498 | 0.534 |
LIG_FHA_1 | 627 | 633 | PF00498 | 0.351 |
LIG_FHA_1 | 722 | 728 | PF00498 | 0.553 |
LIG_FHA_1 | 745 | 751 | PF00498 | 0.383 |
LIG_FHA_1 | 755 | 761 | PF00498 | 0.407 |
LIG_FHA_1 | 777 | 783 | PF00498 | 0.404 |
LIG_FHA_1 | 810 | 816 | PF00498 | 0.359 |
LIG_FHA_1 | 899 | 905 | PF00498 | 0.584 |
LIG_FHA_1 | 927 | 933 | PF00498 | 0.579 |
LIG_FHA_2 | 1046 | 1052 | PF00498 | 0.539 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.615 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.672 |
LIG_FHA_2 | 458 | 464 | PF00498 | 0.536 |
LIG_FHA_2 | 505 | 511 | PF00498 | 0.536 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.647 |
LIG_FHA_2 | 645 | 651 | PF00498 | 0.555 |
LIG_FHA_2 | 791 | 797 | PF00498 | 0.503 |
LIG_FHA_2 | 871 | 877 | PF00498 | 0.732 |
LIG_Integrin_isoDGR_2 | 920 | 922 | PF01839 | 0.523 |
LIG_LIR_Apic_2 | 10 | 14 | PF02991 | 0.604 |
LIG_LIR_Apic_2 | 1113 | 1119 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 516 | 526 | PF02991 | 0.553 |
LIG_LIR_Gen_1 | 666 | 677 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 747 | 753 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 756 | 766 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 810 | 815 | PF02991 | 0.358 |
LIG_LIR_LC3C_4 | 436 | 441 | PF02991 | 0.476 |
LIG_LIR_LC3C_4 | 783 | 786 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 1089 | 1095 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 399 | 404 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 516 | 522 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 666 | 672 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 747 | 751 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 756 | 761 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 810 | 814 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 850 | 855 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 976 | 982 | PF02991 | 0.388 |
LIG_MYND_1 | 106 | 110 | PF01753 | 0.563 |
LIG_NRBOX | 338 | 344 | PF00104 | 0.381 |
LIG_Pex14_1 | 1091 | 1095 | PF04695 | 0.460 |
LIG_Pex14_1 | 669 | 673 | PF04695 | 0.470 |
LIG_PTB_Apo_2 | 752 | 759 | PF02174 | 0.401 |
LIG_PTB_Apo_2 | 785 | 792 | PF02174 | 0.328 |
LIG_PTB_Phospho_1 | 752 | 758 | PF10480 | 0.405 |
LIG_Rb_pABgroove_1 | 983 | 991 | PF01858 | 0.508 |
LIG_REV1ctd_RIR_1 | 691 | 702 | PF16727 | 0.491 |
LIG_SH2_CRK | 519 | 523 | PF00017 | 0.536 |
LIG_SH2_CRK | 758 | 762 | PF00017 | 0.434 |
LIG_SH2_CRK | 811 | 815 | PF00017 | 0.371 |
LIG_SH2_CRK | 979 | 983 | PF00017 | 0.480 |
LIG_SH2_SRC | 701 | 704 | PF00017 | 0.573 |
LIG_SH2_STAP1 | 811 | 815 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 1139 | 1142 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 701 | 704 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 737 | 740 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 811 | 814 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 915 | 918 | PF00017 | 0.683 |
LIG_SH3_1 | 875 | 881 | PF00018 | 0.507 |
LIG_SH3_2 | 39 | 44 | PF14604 | 0.544 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.509 |
LIG_SH3_3 | 195 | 201 | PF00018 | 0.686 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.659 |
LIG_SH3_3 | 481 | 487 | PF00018 | 0.497 |
LIG_SH3_3 | 875 | 881 | PF00018 | 0.610 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.723 |
LIG_SH3_3 | 928 | 934 | PF00018 | 0.706 |
LIG_SH3_3 | 938 | 944 | PF00018 | 0.687 |
LIG_SH3_3 | 957 | 963 | PF00018 | 0.746 |
LIG_Sin3_3 | 437 | 444 | PF02671 | 0.461 |
LIG_SUMO_SIM_anti_2 | 296 | 303 | PF11976 | 0.456 |
LIG_SUMO_SIM_anti_2 | 319 | 325 | PF11976 | 0.392 |
LIG_SUMO_SIM_anti_2 | 402 | 408 | PF11976 | 0.390 |
LIG_SUMO_SIM_anti_2 | 438 | 443 | PF11976 | 0.442 |
LIG_SUMO_SIM_anti_2 | 629 | 636 | PF11976 | 0.485 |
LIG_SUMO_SIM_anti_2 | 778 | 786 | PF11976 | 0.486 |
LIG_SUMO_SIM_par_1 | 341 | 346 | PF11976 | 0.303 |
LIG_SUMO_SIM_par_1 | 457 | 463 | PF11976 | 0.536 |
LIG_SUMO_SIM_par_1 | 629 | 636 | PF11976 | 0.486 |
LIG_TRAF2_1 | 1055 | 1058 | PF00917 | 0.442 |
LIG_TYR_ITIM | 517 | 522 | PF00017 | 0.410 |
LIG_UBA3_1 | 322 | 331 | PF00899 | 0.290 |
LIG_UBA3_1 | 359 | 368 | PF00899 | 0.381 |
LIG_WRC_WIRS_1 | 327 | 332 | PF05994 | 0.376 |
LIG_WRC_WIRS_1 | 564 | 569 | PF05994 | 0.480 |
MOD_CDK_SPK_2 | 363 | 368 | PF00069 | 0.413 |
MOD_CDK_SPxK_1 | 38 | 44 | PF00069 | 0.656 |
MOD_CDK_SPxxK_3 | 450 | 457 | PF00069 | 0.342 |
MOD_CK1_1 | 1029 | 1035 | PF00069 | 0.594 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.371 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.649 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.603 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.446 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.699 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.434 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.355 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.610 |
MOD_CK1_1 | 626 | 632 | PF00069 | 0.341 |
MOD_CK1_1 | 668 | 674 | PF00069 | 0.430 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.638 |
MOD_CK1_1 | 952 | 958 | PF00069 | 0.671 |
MOD_CK2_1 | 1045 | 1051 | PF00069 | 0.443 |
MOD_CK2_1 | 1155 | 1161 | PF00069 | 0.574 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.615 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.665 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.578 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.286 |
MOD_CK2_1 | 504 | 510 | PF00069 | 0.331 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.644 |
MOD_CK2_1 | 644 | 650 | PF00069 | 0.478 |
MOD_Cter_Amidation | 44 | 47 | PF01082 | 0.656 |
MOD_DYRK1A_RPxSP_1 | 312 | 316 | PF00069 | 0.439 |
MOD_GlcNHglycan | 1009 | 1012 | PF01048 | 0.591 |
MOD_GlcNHglycan | 1028 | 1031 | PF01048 | 0.598 |
MOD_GlcNHglycan | 1129 | 1132 | PF01048 | 0.457 |
MOD_GlcNHglycan | 1142 | 1145 | PF01048 | 0.479 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.321 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.645 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.649 |
MOD_GlcNHglycan | 344 | 348 | PF01048 | 0.486 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.432 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.624 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.521 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.411 |
MOD_GlcNHglycan | 575 | 579 | PF01048 | 0.660 |
MOD_GlcNHglycan | 766 | 769 | PF01048 | 0.551 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.704 |
MOD_GlcNHglycan | 896 | 899 | PF01048 | 0.783 |
MOD_GlcNHglycan | 934 | 937 | PF01048 | 0.627 |
MOD_GlcNHglycan | 951 | 954 | PF01048 | 0.789 |
MOD_GSK3_1 | 1041 | 1048 | PF00069 | 0.531 |
MOD_GSK3_1 | 1069 | 1076 | PF00069 | 0.469 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.291 |
MOD_GSK3_1 | 1093 | 1100 | PF00069 | 0.381 |
MOD_GSK3_1 | 1151 | 1158 | PF00069 | 0.538 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.562 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.755 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.537 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.354 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.381 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.386 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.399 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.430 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.759 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.440 |
MOD_GSK3_1 | 619 | 626 | PF00069 | 0.451 |
MOD_GSK3_1 | 716 | 723 | PF00069 | 0.555 |
MOD_GSK3_1 | 776 | 783 | PF00069 | 0.408 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.679 |
MOD_GSK3_1 | 866 | 873 | PF00069 | 0.693 |
MOD_GSK3_1 | 894 | 901 | PF00069 | 0.613 |
MOD_LATS_1 | 1149 | 1155 | PF00433 | 0.511 |
MOD_LATS_1 | 211 | 217 | PF00433 | 0.563 |
MOD_LATS_1 | 455 | 461 | PF00433 | 0.406 |
MOD_N-GLC_1 | 720 | 725 | PF02516 | 0.625 |
MOD_N-GLC_1 | 754 | 759 | PF02516 | 0.410 |
MOD_N-GLC_1 | 787 | 792 | PF02516 | 0.331 |
MOD_N-GLC_1 | 926 | 931 | PF02516 | 0.504 |
MOD_NEK2_1 | 1005 | 1010 | PF00069 | 0.599 |
MOD_NEK2_1 | 1095 | 1100 | PF00069 | 0.358 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.279 |
MOD_NEK2_1 | 1138 | 1143 | PF00069 | 0.386 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.580 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.778 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.608 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.475 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.445 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.308 |
MOD_NEK2_1 | 692 | 697 | PF00069 | 0.443 |
MOD_NEK2_1 | 787 | 792 | PF00069 | 0.463 |
MOD_NEK2_1 | 815 | 820 | PF00069 | 0.532 |
MOD_NEK2_1 | 866 | 871 | PF00069 | 0.776 |
MOD_NEK2_2 | 443 | 448 | PF00069 | 0.311 |
MOD_PIKK_1 | 64 | 70 | PF00454 | 0.646 |
MOD_PIKK_1 | 816 | 822 | PF00454 | 0.509 |
MOD_PKA_1 | 124 | 130 | PF00069 | 0.410 |
MOD_PKA_2 | 1026 | 1032 | PF00069 | 0.567 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.410 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.783 |
MOD_PKA_2 | 626 | 632 | PF00069 | 0.348 |
MOD_PKA_2 | 780 | 786 | PF00069 | 0.402 |
MOD_PKA_2 | 816 | 822 | PF00069 | 0.509 |
MOD_PKB_1 | 213 | 221 | PF00069 | 0.594 |
MOD_PKB_1 | 28 | 36 | PF00069 | 0.586 |
MOD_Plk_1 | 1040 | 1046 | PF00069 | 0.509 |
MOD_Plk_1 | 1069 | 1075 | PF00069 | 0.480 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.598 |
MOD_Plk_1 | 30 | 36 | PF00069 | 0.567 |
MOD_Plk_1 | 754 | 760 | PF00069 | 0.404 |
MOD_Plk_1 | 787 | 793 | PF00069 | 0.375 |
MOD_Plk_1 | 809 | 815 | PF00069 | 0.398 |
MOD_Plk_2-3 | 1155 | 1161 | PF00069 | 0.482 |
MOD_Plk_4 | 1041 | 1047 | PF00069 | 0.470 |
MOD_Plk_4 | 1058 | 1064 | PF00069 | 0.520 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.279 |
MOD_Plk_4 | 1086 | 1092 | PF00069 | 0.399 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.514 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.591 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.494 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.351 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.363 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.279 |
MOD_Plk_4 | 495 | 501 | PF00069 | 0.361 |
MOD_Plk_4 | 541 | 547 | PF00069 | 0.473 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.427 |
MOD_Plk_4 | 627 | 633 | PF00069 | 0.363 |
MOD_Plk_4 | 665 | 671 | PF00069 | 0.373 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.560 |
MOD_Plk_4 | 780 | 786 | PF00069 | 0.385 |
MOD_Plk_4 | 787 | 793 | PF00069 | 0.334 |
MOD_Plk_4 | 942 | 948 | PF00069 | 0.585 |
MOD_ProDKin_1 | 1100 | 1106 | PF00069 | 0.609 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.786 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.630 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.525 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.676 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.430 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.439 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.410 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.650 |
MOD_ProDKin_1 | 526 | 532 | PF00069 | 0.340 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.681 |
MOD_ProDKin_1 | 892 | 898 | PF00069 | 0.742 |
MOD_ProDKin_1 | 899 | 905 | PF00069 | 0.778 |
MOD_ProDKin_1 | 937 | 943 | PF00069 | 0.675 |
TRG_DiLeu_BaEn_1 | 780 | 785 | PF01217 | 0.375 |
TRG_DiLeu_BaEn_4 | 1041 | 1047 | PF01217 | 0.394 |
TRG_DiLeu_BaLyEn_6 | 1148 | 1153 | PF01217 | 0.503 |
TRG_DiLeu_BaLyEn_6 | 22 | 27 | PF01217 | 0.559 |
TRG_ENDOCYTIC_2 | 1139 | 1142 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 519 | 522 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 758 | 761 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 811 | 814 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 979 | 982 | PF00928 | 0.480 |
TRG_ER_diArg_1 | 1019 | 1021 | PF00400 | 0.336 |
TRG_ER_diArg_1 | 1082 | 1084 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 123 | 125 | PF00400 | 0.353 |
TRG_ER_diArg_1 | 212 | 215 | PF00400 | 0.745 |
TRG_ER_diArg_1 | 27 | 30 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 587 | 590 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 606 | 609 | PF00400 | 0.315 |
TRG_ER_diArg_1 | 711 | 713 | PF00400 | 0.515 |
TRG_Pf-PMV_PEXEL_1 | 1151 | 1155 | PF00026 | 0.493 |
TRG_Pf-PMV_PEXEL_1 | 215 | 219 | PF00026 | 0.578 |
TRG_Pf-PMV_PEXEL_1 | 651 | 656 | PF00026 | 0.570 |
TRG_Pf-PMV_PEXEL_1 | 834 | 838 | PF00026 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 853 | 857 | PF00026 | 0.444 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAP2 | Leptomonas seymouri | 51% | 95% |
A0A1X0NWJ4 | Trypanosomatidae | 27% | 100% |
A0A3S7WVQ6 | Leishmania donovani | 91% | 100% |
A0A422N7U4 | Trypanosoma rangeli | 30% | 100% |
A4HBH5 | Leishmania braziliensis | 74% | 99% |
A4HYJ9 | Leishmania infantum | 91% | 100% |
C9ZHU4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AUE6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
V5BQX8 | Trypanosoma cruzi | 29% | 100% |