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 | 11 |
GO:0016020 | membrane | 2 | 7 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: E9AZY0
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 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:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006289 | nucleotide-excision repair | 6 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022414 | reproductive process | 1 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1903046 | meiotic cell cycle process | 2 | 1 |
GO:1990918 | double-strand break repair involved in meiotic recombination | 3 | 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:0003678 | DNA helicase activity | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 12 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 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: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:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016887 | ATP hydrolysis activity | 7 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1029 | 1033 | PF00656 | 0.732 |
CLV_C14_Caspase3-7 | 157 | 161 | PF00656 | 0.524 |
CLV_NRD_NRD_1 | 1037 | 1039 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 104 | 106 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.719 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.731 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 521 | 523 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 807 | 809 | PF00675 | 0.293 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 953 | 955 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 978 | 980 | PF00675 | 0.378 |
CLV_PCSK_FUR_1 | 102 | 106 | PF00082 | 0.597 |
CLV_PCSK_FUR_1 | 465 | 469 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 1037 | 1039 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.664 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.758 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 467 | 469 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 471 | 473 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 521 | 523 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 565 | 567 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 953 | 955 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 978 | 980 | PF00082 | 0.378 |
CLV_PCSK_PC1ET2_1 | 117 | 119 | PF00082 | 0.757 |
CLV_PCSK_PC1ET2_1 | 123 | 125 | PF00082 | 0.779 |
CLV_PCSK_PC1ET2_1 | 471 | 473 | PF00082 | 0.728 |
CLV_PCSK_PC1ET2_1 | 565 | 567 | PF00082 | 0.247 |
CLV_PCSK_PC1ET2_1 | 90 | 92 | PF00082 | 0.603 |
CLV_PCSK_PC7_1 | 467 | 473 | PF00082 | 0.656 |
CLV_PCSK_PC7_1 | 517 | 523 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 1089 | 1093 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 1101 | 1105 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 566 | 570 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 572 | 576 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 586 | 590 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 660 | 664 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 780 | 784 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 854 | 858 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 900 | 904 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 953 | 957 | PF00082 | 0.416 |
DEG_APCC_DBOX_1 | 180 | 188 | PF00400 | 0.296 |
DEG_APCC_DBOX_1 | 381 | 389 | PF00400 | 0.293 |
DEG_SCF_TRCP1_1 | 625 | 631 | PF00400 | 0.645 |
DEG_SPOP_SBC_1 | 409 | 413 | PF00917 | 0.478 |
DEG_SPOP_SBC_1 | 708 | 712 | PF00917 | 0.575 |
DOC_CDC14_PxL_1 | 333 | 341 | PF14671 | 0.335 |
DOC_CKS1_1 | 35 | 40 | PF01111 | 0.404 |
DOC_CKS1_1 | 966 | 971 | PF01111 | 0.663 |
DOC_CYCLIN_RxL_1 | 425 | 436 | PF00134 | 0.385 |
DOC_CYCLIN_RxL_1 | 600 | 610 | PF00134 | 0.604 |
DOC_CYCLIN_yCln2_LP_2 | 32 | 38 | PF00134 | 0.417 |
DOC_CYCLIN_yCln2_LP_2 | 734 | 740 | PF00134 | 0.524 |
DOC_CYCLIN_yCln2_LP_2 | 859 | 865 | PF00134 | 0.535 |
DOC_MAPK_gen_1 | 178 | 186 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 565 | 573 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 777 | 785 | PF00069 | 0.478 |
DOC_MAPK_gen_1 | 839 | 848 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 900 | 910 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 382 | 389 | PF00069 | 0.366 |
DOC_MAPK_MEF2A_6 | 565 | 573 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 854 | 863 | PF00069 | 0.431 |
DOC_MAPK_NFAT4_5 | 382 | 390 | PF00069 | 0.369 |
DOC_MAPK_NFAT4_5 | 566 | 574 | PF00069 | 0.548 |
DOC_MAPK_NFAT4_5 | 854 | 862 | PF00069 | 0.478 |
DOC_PP1_RVXF_1 | 321 | 328 | PF00149 | 0.242 |
DOC_PP2B_LxvP_1 | 1009 | 1012 | PF13499 | 0.661 |
DOC_PP2B_LxvP_1 | 197 | 200 | PF13499 | 0.372 |
DOC_PP2B_LxvP_1 | 32 | 35 | PF13499 | 0.397 |
DOC_PP2B_LxvP_1 | 764 | 767 | PF13499 | 0.446 |
DOC_PP2B_LxvP_1 | 859 | 862 | PF13499 | 0.535 |
DOC_PP4_FxxP_1 | 196 | 199 | PF00568 | 0.409 |
DOC_PP4_FxxP_1 | 524 | 527 | PF00568 | 0.393 |
DOC_PP4_FxxP_1 | 804 | 807 | PF00568 | 0.456 |
DOC_PP4_FxxP_1 | 956 | 959 | PF00568 | 0.504 |
DOC_USP7_MATH_1 | 1028 | 1032 | PF00917 | 0.828 |
DOC_USP7_MATH_1 | 1054 | 1058 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 1095 | 1099 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 596 | 600 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 708 | 712 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 865 | 869 | PF00917 | 0.442 |
DOC_USP7_UBL2_3 | 119 | 123 | PF12436 | 0.504 |
DOC_WW_Pin1_4 | 1030 | 1035 | PF00397 | 0.791 |
DOC_WW_Pin1_4 | 1064 | 1069 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.311 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 525 | 530 | PF00397 | 0.326 |
DOC_WW_Pin1_4 | 666 | 671 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.360 |
DOC_WW_Pin1_4 | 959 | 964 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 965 | 970 | PF00397 | 0.637 |
LIG_14-3-3_CanoR_1 | 1017 | 1023 | PF00244 | 0.751 |
LIG_14-3-3_CanoR_1 | 1042 | 1048 | PF00244 | 0.736 |
LIG_14-3-3_CanoR_1 | 1055 | 1065 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 173 | 180 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 515 | 524 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 539 | 544 | PF00244 | 0.310 |
LIG_14-3-3_CanoR_1 | 577 | 582 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 586 | 592 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 728 | 732 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 839 | 848 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 929 | 933 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 946 | 956 | PF00244 | 0.609 |
LIG_Actin_WH2_2 | 199 | 216 | PF00022 | 0.278 |
LIG_Actin_WH2_2 | 642 | 658 | PF00022 | 0.507 |
LIG_Actin_WH2_2 | 740 | 757 | PF00022 | 0.574 |
LIG_Actin_WH2_2 | 884 | 902 | PF00022 | 0.526 |
LIG_APCC_ABBA_1 | 359 | 364 | PF00400 | 0.245 |
LIG_APCC_ABBA_1 | 451 | 456 | PF00400 | 0.304 |
LIG_BRCT_BRCA1_1 | 451 | 455 | PF00533 | 0.270 |
LIG_BRCT_BRCA1_1 | 647 | 651 | PF00533 | 0.456 |
LIG_deltaCOP1_diTrp_1 | 160 | 169 | PF00928 | 0.339 |
LIG_DLG_GKlike_1 | 577 | 585 | PF00625 | 0.391 |
LIG_EH_1 | 551 | 555 | PF12763 | 0.266 |
LIG_eIF4E_1 | 338 | 344 | PF01652 | 0.275 |
LIG_eIF4E_1 | 905 | 911 | PF01652 | 0.439 |
LIG_EVH1_2 | 165 | 169 | PF00568 | 0.374 |
LIG_FHA_1 | 1082 | 1088 | PF00498 | 0.696 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.337 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.251 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.424 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.532 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.224 |
LIG_FHA_1 | 637 | 643 | PF00498 | 0.508 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.286 |
LIG_FHA_1 | 749 | 755 | PF00498 | 0.487 |
LIG_FHA_1 | 812 | 818 | PF00498 | 0.501 |
LIG_FHA_1 | 829 | 835 | PF00498 | 0.404 |
LIG_FHA_1 | 883 | 889 | PF00498 | 0.498 |
LIG_FHA_1 | 998 | 1004 | PF00498 | 0.710 |
LIG_FHA_2 | 1027 | 1033 | PF00498 | 0.762 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.566 |
LIG_FHA_2 | 346 | 352 | PF00498 | 0.335 |
LIG_FHA_2 | 434 | 440 | PF00498 | 0.276 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.391 |
LIG_FHA_2 | 587 | 593 | PF00498 | 0.529 |
LIG_FHA_2 | 751 | 757 | PF00498 | 0.545 |
LIG_LIR_Apic_2 | 160 | 165 | PF02991 | 0.366 |
LIG_LIR_Apic_2 | 589 | 594 | PF02991 | 0.593 |
LIG_LIR_Apic_2 | 801 | 807 | PF02991 | 0.525 |
LIG_LIR_Apic_2 | 912 | 918 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 280 | 290 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 439 | 448 | PF02991 | 0.185 |
LIG_LIR_Gen_1 | 648 | 658 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 730 | 739 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 167 | 172 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 280 | 285 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 330 | 336 | PF02991 | 0.245 |
LIG_LIR_Nem_3 | 439 | 444 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 452 | 457 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 550 | 554 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 604 | 609 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 648 | 654 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 669 | 674 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 730 | 734 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 868 | 872 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 904 | 908 | PF02991 | 0.439 |
LIG_LYPXL_yS_3 | 336 | 339 | PF13949 | 0.335 |
LIG_MLH1_MIPbox_1 | 451 | 455 | PF16413 | 0.270 |
LIG_MYND_1 | 722 | 726 | PF01753 | 0.552 |
LIG_MYND_1 | 965 | 969 | PF01753 | 0.576 |
LIG_NRBOX | 570 | 576 | PF00104 | 0.531 |
LIG_Pex14_1 | 952 | 956 | PF04695 | 0.566 |
LIG_Pex14_2 | 168 | 172 | PF04695 | 0.336 |
LIG_PTB_Apo_2 | 733 | 740 | PF02174 | 0.580 |
LIG_REV1ctd_RIR_1 | 166 | 174 | PF16727 | 0.367 |
LIG_SH2_CRK | 541 | 545 | PF00017 | 0.231 |
LIG_SH2_CRK | 731 | 735 | PF00017 | 0.530 |
LIG_SH2_CRK | 769 | 773 | PF00017 | 0.522 |
LIG_SH2_CRK | 905 | 909 | PF00017 | 0.457 |
LIG_SH2_NCK_1 | 1078 | 1082 | PF00017 | 0.639 |
LIG_SH2_NCK_1 | 328 | 332 | PF00017 | 0.282 |
LIG_SH2_NCK_1 | 915 | 919 | PF00017 | 0.498 |
LIG_SH2_SRC | 328 | 331 | PF00017 | 0.322 |
LIG_SH2_STAP1 | 1078 | 1082 | PF00017 | 0.704 |
LIG_SH2_STAP1 | 541 | 545 | PF00017 | 0.160 |
LIG_SH2_STAP1 | 699 | 703 | PF00017 | 0.509 |
LIG_SH2_STAP1 | 883 | 887 | PF00017 | 0.498 |
LIG_SH2_STAT3 | 100 | 103 | PF00017 | 0.343 |
LIG_SH2_STAT3 | 39 | 42 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.256 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.242 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.231 |
LIG_SH2_STAT5 | 883 | 886 | PF00017 | 0.453 |
LIG_SH3_2 | 723 | 728 | PF14604 | 0.477 |
LIG_SH3_2 | 862 | 867 | PF14604 | 0.439 |
LIG_SH3_3 | 1012 | 1018 | PF00018 | 0.670 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.317 |
LIG_SH3_3 | 690 | 696 | PF00018 | 0.537 |
LIG_SH3_3 | 720 | 726 | PF00018 | 0.492 |
LIG_SH3_3 | 859 | 865 | PF00018 | 0.439 |
LIG_SUMO_SIM_anti_2 | 183 | 189 | PF11976 | 0.295 |
LIG_SUMO_SIM_anti_2 | 383 | 391 | PF11976 | 0.347 |
LIG_SUMO_SIM_par_1 | 436 | 442 | PF11976 | 0.299 |
LIG_SUMO_SIM_par_1 | 61 | 67 | PF11976 | 0.316 |
LIG_SUMO_SIM_par_1 | 907 | 913 | PF11976 | 0.431 |
LIG_TRAF2_1 | 1109 | 1112 | PF00917 | 0.748 |
LIG_TRFH_1 | 338 | 342 | PF08558 | 0.231 |
LIG_WRC_WIRS_1 | 440 | 445 | PF05994 | 0.314 |
MOD_CDK_SPK_2 | 90 | 95 | PF00069 | 0.439 |
MOD_CDK_SPxxK_3 | 1030 | 1037 | PF00069 | 0.586 |
MOD_CK1_1 | 1026 | 1032 | PF00069 | 0.810 |
MOD_CK1_1 | 1106 | 1112 | PF00069 | 0.683 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.527 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.528 |
MOD_CK1_1 | 587 | 593 | PF00069 | 0.652 |
MOD_CK1_1 | 710 | 716 | PF00069 | 0.679 |
MOD_CK2_1 | 1106 | 1112 | PF00069 | 0.719 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.556 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.335 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.297 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.286 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.387 |
MOD_CK2_1 | 596 | 602 | PF00069 | 0.756 |
MOD_CK2_1 | 750 | 756 | PF00069 | 0.587 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.336 |
MOD_GlcNHglycan | 1012 | 1015 | PF01048 | 0.497 |
MOD_GlcNHglycan | 1060 | 1063 | PF01048 | 0.504 |
MOD_GlcNHglycan | 1105 | 1109 | PF01048 | 0.470 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.702 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.706 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.439 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.547 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.506 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.708 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.766 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.591 |
MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.386 |
MOD_GlcNHglycan | 598 | 601 | PF01048 | 0.411 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.492 |
MOD_GlcNHglycan | 625 | 628 | PF01048 | 0.452 |
MOD_GlcNHglycan | 664 | 667 | PF01048 | 0.260 |
MOD_GlcNHglycan | 756 | 760 | PF01048 | 0.320 |
MOD_GlcNHglycan | 877 | 880 | PF01048 | 0.231 |
MOD_GlcNHglycan | 956 | 959 | PF01048 | 0.365 |
MOD_GlcNHglycan | 969 | 972 | PF01048 | 0.506 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.522 |
MOD_GSK3_1 | 1026 | 1033 | PF00069 | 0.764 |
MOD_GSK3_1 | 1054 | 1061 | PF00069 | 0.682 |
MOD_GSK3_1 | 1077 | 1084 | PF00069 | 0.653 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.473 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.516 |
MOD_GSK3_1 | 645 | 652 | PF00069 | 0.534 |
MOD_GSK3_1 | 662 | 669 | PF00069 | 0.417 |
MOD_GSK3_1 | 707 | 714 | PF00069 | 0.607 |
MOD_GSK3_1 | 750 | 757 | PF00069 | 0.515 |
MOD_GSK3_1 | 877 | 884 | PF00069 | 0.407 |
MOD_GSK3_1 | 961 | 968 | PF00069 | 0.703 |
MOD_GSK3_1 | 989 | 996 | PF00069 | 0.651 |
MOD_LATS_1 | 109 | 115 | PF00433 | 0.588 |
MOD_LATS_1 | 171 | 177 | PF00433 | 0.422 |
MOD_N-GLC_1 | 252 | 257 | PF02516 | 0.481 |
MOD_N-GLC_1 | 715 | 720 | PF02516 | 0.474 |
MOD_N-GLC_1 | 821 | 826 | PF02516 | 0.342 |
MOD_N-GLC_2 | 156 | 158 | PF02516 | 0.559 |
MOD_N-GLC_2 | 332 | 334 | PF02516 | 0.528 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.589 |
MOD_NEK2_1 | 1043 | 1048 | PF00069 | 0.720 |
MOD_NEK2_1 | 1069 | 1074 | PF00069 | 0.625 |
MOD_NEK2_1 | 1077 | 1082 | PF00069 | 0.639 |
MOD_NEK2_1 | 1103 | 1108 | PF00069 | 0.719 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.353 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.301 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.335 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.326 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.379 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.278 |
MOD_NEK2_1 | 554 | 559 | PF00069 | 0.266 |
MOD_NEK2_1 | 645 | 650 | PF00069 | 0.461 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.476 |
MOD_NEK2_1 | 727 | 732 | PF00069 | 0.560 |
MOD_NEK2_1 | 739 | 744 | PF00069 | 0.514 |
MOD_NEK2_1 | 750 | 755 | PF00069 | 0.504 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.299 |
MOD_NEK2_1 | 833 | 838 | PF00069 | 0.518 |
MOD_NEK2_1 | 945 | 950 | PF00069 | 0.534 |
MOD_NEK2_1 | 993 | 998 | PF00069 | 0.714 |
MOD_PIKK_1 | 173 | 179 | PF00454 | 0.521 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.431 |
MOD_PIKK_1 | 494 | 500 | PF00454 | 0.452 |
MOD_PIKK_1 | 694 | 700 | PF00454 | 0.610 |
MOD_PIKK_1 | 717 | 723 | PF00454 | 0.726 |
MOD_PIKK_1 | 748 | 754 | PF00454 | 0.552 |
MOD_PIKK_1 | 798 | 804 | PF00454 | 0.490 |
MOD_PIKK_1 | 821 | 827 | PF00454 | 0.545 |
MOD_PIKK_1 | 947 | 953 | PF00454 | 0.484 |
MOD_PK_1 | 539 | 545 | PF00069 | 0.160 |
MOD_PKA_1 | 111 | 117 | PF00069 | 0.541 |
MOD_PKA_2 | 1054 | 1060 | PF00069 | 0.717 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.564 |
MOD_PKA_2 | 473 | 479 | PF00069 | 0.383 |
MOD_PKA_2 | 636 | 642 | PF00069 | 0.442 |
MOD_PKA_2 | 727 | 733 | PF00069 | 0.594 |
MOD_PKA_2 | 754 | 760 | PF00069 | 0.513 |
MOD_PKA_2 | 922 | 928 | PF00069 | 0.474 |
MOD_PKA_2 | 945 | 951 | PF00069 | 0.627 |
MOD_PKB_1 | 995 | 1003 | PF00069 | 0.723 |
MOD_Plk_1 | 252 | 258 | PF00069 | 0.313 |
MOD_Plk_1 | 601 | 607 | PF00069 | 0.719 |
MOD_Plk_1 | 934 | 940 | PF00069 | 0.576 |
MOD_Plk_1 | 988 | 994 | PF00069 | 0.574 |
MOD_Plk_2-3 | 374 | 380 | PF00069 | 0.242 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.381 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.271 |
MOD_Plk_4 | 449 | 455 | PF00069 | 0.364 |
MOD_Plk_4 | 539 | 545 | PF00069 | 0.225 |
MOD_Plk_4 | 559 | 565 | PF00069 | 0.224 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.300 |
MOD_ProDKin_1 | 1030 | 1036 | PF00069 | 0.791 |
MOD_ProDKin_1 | 1064 | 1070 | PF00069 | 0.679 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.444 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.313 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.535 |
MOD_ProDKin_1 | 525 | 531 | PF00069 | 0.323 |
MOD_ProDKin_1 | 666 | 672 | PF00069 | 0.545 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.360 |
MOD_ProDKin_1 | 959 | 965 | PF00069 | 0.639 |
TRG_DiLeu_BaEn_2 | 438 | 444 | PF01217 | 0.314 |
TRG_DiLeu_BaLyEn_6 | 21 | 26 | PF01217 | 0.351 |
TRG_DiLeu_BaLyEn_6 | 339 | 344 | PF01217 | 0.242 |
TRG_DiLeu_BaLyEn_6 | 720 | 725 | PF01217 | 0.655 |
TRG_DiLeu_BaLyEn_6 | 962 | 967 | PF01217 | 0.567 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.244 |
TRG_ENDOCYTIC_2 | 336 | 339 | PF00928 | 0.219 |
TRG_ENDOCYTIC_2 | 541 | 544 | PF00928 | 0.231 |
TRG_ENDOCYTIC_2 | 731 | 734 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 769 | 772 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 905 | 908 | PF00928 | 0.439 |
TRG_ER_diArg_1 | 101 | 104 | PF00400 | 0.359 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 192 | 195 | PF00400 | 0.382 |
TRG_ER_diArg_1 | 220 | 222 | PF00400 | 0.298 |
TRG_ER_diArg_1 | 503 | 505 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 514 | 517 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 952 | 954 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 977 | 979 | PF00400 | 0.669 |
TRG_ER_diArg_1 | 995 | 998 | PF00400 | 0.747 |
TRG_NES_CRM1_1 | 300 | 310 | PF08389 | 0.303 |
TRG_NES_CRM1_1 | 391 | 405 | PF08389 | 0.397 |
TRG_NES_CRM1_1 | 449 | 463 | PF08389 | 0.293 |
TRG_NES_CRM1_1 | 850 | 864 | PF08389 | 0.439 |
TRG_NLS_Bipartite_1 | 111 | 127 | PF00514 | 0.554 |
TRG_NLS_MonoExtC_3 | 177 | 183 | PF00514 | 0.391 |
TRG_NLS_MonoExtC_3 | 89 | 94 | PF00514 | 0.458 |
TRG_NLS_MonoExtN_4 | 121 | 127 | PF00514 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 105 | 110 | PF00026 | 0.588 |
TRG_Pf-PMV_PEXEL_1 | 1075 | 1079 | PF00026 | 0.394 |
TRG_Pf-PMV_PEXEL_1 | 47 | 51 | PF00026 | 0.514 |
TRG_Pf-PMV_PEXEL_1 | 572 | 576 | PF00026 | 0.301 |
TRG_Pf-PMV_PEXEL_1 | 676 | 681 | PF00026 | 0.329 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8F0 | Leptomonas seymouri | 57% | 88% |
A0A0S4IQT3 | Bodo saltans | 38% | 100% |
A0A1X0NRE3 | Trypanosomatidae | 42% | 100% |
A0A3R7P0G4 | Trypanosoma rangeli | 43% | 100% |
A0A3S5H7J4 | Leishmania donovani | 90% | 100% |
A4HGL3 | Leishmania braziliensis | 79% | 100% |
A4I3N9 | Leishmania infantum | 89% | 88% |
D0A8C5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
Q4Q8A5 | Leishmania major | 90% | 100% |
V5BAP9 | Trypanosoma cruzi | 39% | 100% |