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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032991 | protein-containing complex | 1 | 10 |
GO:0043564 | Ku70:Ku80 complex | 3 | 10 |
GO:0140513 | nuclear protein-containing complex | 2 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000723 | telomere maintenance | 5 | 10 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006259 | DNA metabolic process | 4 | 10 |
GO:0006281 | DNA repair | 5 | 10 |
GO:0006302 | double-strand break repair | 6 | 10 |
GO:0006303 | double-strand break repair via nonhomologous end joining | 7 | 10 |
GO:0006310 | DNA recombination | 5 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0006950 | response to stress | 2 | 10 |
GO:0006974 | DNA damage response | 4 | 10 |
GO:0006996 | organelle organization | 4 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016043 | cellular component organization | 3 | 10 |
GO:0032200 | telomere organization | 6 | 10 |
GO:0033554 | cellular response to stress | 3 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0050896 | response to stimulus | 1 | 10 |
GO:0051276 | chromosome organization | 5 | 10 |
GO:0051716 | cellular response to stimulus | 2 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0071840 | cellular component organization or biogenesis | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
GO:0009314 | response to radiation | 3 | 1 |
GO:0009628 | response to abiotic stimulus | 2 | 1 |
GO:0010165 | response to X-ray | 5 | 1 |
GO:0010212 | response to ionizing radiation | 4 | 1 |
GO:0010332 | response to gamma radiation | 5 | 1 |
GO:0071214 | cellular response to abiotic stimulus | 3 | 1 |
GO:0071478 | cellular response to radiation | 4 | 1 |
GO:0071479 | cellular response to ionizing radiation | 5 | 1 |
GO:0071480 | cellular response to gamma radiation | 6 | 1 |
GO:0071481 | cellular response to X-ray | 6 | 1 |
GO:0104004 | cellular response to environmental stimulus | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003677 | DNA binding | 4 | 10 |
GO:0003684 | damaged DNA binding | 5 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004386 | helicase activity | 2 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0042162 | telomeric DNA binding | 6 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0043565 | sequence-specific DNA binding | 5 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 10 |
GO:0140657 | ATP-dependent activity | 1 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0003678 | DNA helicase activity | 3 | 1 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 270 | 274 | PF00656 | 0.463 |
CLV_C14_Caspase3-7 | 525 | 529 | PF00656 | 0.510 |
CLV_C14_Caspase3-7 | 636 | 640 | PF00656 | 0.488 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.401 |
CLV_NRD_NRD_1 | 459 | 461 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 613 | 615 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 648 | 650 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 673 | 675 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 791 | 793 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 883 | 885 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 919 | 921 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 950 | 952 | PF00675 | 0.405 |
CLV_PCSK_FUR_1 | 256 | 260 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 459 | 461 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.263 |
CLV_PCSK_KEX2_1 | 615 | 617 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 642 | 644 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 648 | 650 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 673 | 675 | PF00082 | 0.315 |
CLV_PCSK_KEX2_1 | 711 | 713 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 883 | 885 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 919 | 921 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 950 | 952 | PF00082 | 0.393 |
CLV_PCSK_PC1ET2_1 | 615 | 617 | PF00082 | 0.288 |
CLV_PCSK_PC1ET2_1 | 642 | 644 | PF00082 | 0.288 |
CLV_PCSK_PC1ET2_1 | 711 | 713 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 747 | 751 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 799 | 803 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 859 | 863 | PF00082 | 0.418 |
DEG_APCC_DBOX_1 | 467 | 475 | PF00400 | 0.518 |
DEG_COP1_1 | 731 | 739 | PF00400 | 0.485 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.592 |
DEG_SCF_TRCP1_1 | 563 | 568 | PF00400 | 0.464 |
DOC_ANK_TNKS_1 | 413 | 420 | PF00023 | 0.374 |
DOC_CDC14_PxL_1 | 733 | 741 | PF14671 | 0.484 |
DOC_CYCLIN_RxL_1 | 241 | 251 | PF00134 | 0.355 |
DOC_CYCLIN_RxL_1 | 255 | 264 | PF00134 | 0.348 |
DOC_CYCLIN_yCln2_LP_2 | 332 | 338 | PF00134 | 0.393 |
DOC_MAPK_gen_1 | 37 | 46 | PF00069 | 0.358 |
DOC_MAPK_gen_1 | 465 | 474 | PF00069 | 0.513 |
DOC_MAPK_gen_1 | 533 | 541 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 614 | 620 | PF00069 | 0.584 |
DOC_MAPK_gen_1 | 673 | 683 | PF00069 | 0.488 |
DOC_MAPK_gen_1 | 711 | 717 | PF00069 | 0.472 |
DOC_MAPK_gen_1 | 950 | 958 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 135 | 142 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 289 | 296 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 325 | 332 | PF00069 | 0.388 |
DOC_MAPK_MEF2A_6 | 507 | 516 | PF00069 | 0.243 |
DOC_MAPK_RevD_3 | 245 | 259 | PF00069 | 0.389 |
DOC_PP1_RVXF_1 | 604 | 610 | PF00149 | 0.487 |
DOC_PP2B_LxvP_1 | 332 | 335 | PF13499 | 0.399 |
DOC_PP2B_LxvP_1 | 512 | 515 | PF13499 | 0.457 |
DOC_PP2B_LxvP_1 | 930 | 933 | PF13499 | 0.409 |
DOC_PP4_FxxP_1 | 398 | 401 | PF00568 | 0.417 |
DOC_PP4_FxxP_1 | 963 | 966 | PF00568 | 0.428 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 754 | 758 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 885 | 889 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 942 | 946 | PF00917 | 0.395 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 563 | 568 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 699 | 704 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 747 | 752 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 830 | 835 | PF00397 | 0.529 |
LIG_14-3-3_CanoR_1 | 146 | 150 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 244 | 250 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 360 | 365 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 507 | 513 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 648 | 653 | PF00244 | 0.524 |
LIG_Actin_WH2_2 | 718 | 736 | PF00022 | 0.484 |
LIG_APCC_ABBA_1 | 631 | 636 | PF00400 | 0.510 |
LIG_BRCT_BRCA1_1 | 110 | 114 | PF00533 | 0.477 |
LIG_BRCT_BRCA1_1 | 150 | 154 | PF00533 | 0.488 |
LIG_BRCT_BRCA1_1 | 350 | 354 | PF00533 | 0.470 |
LIG_CaM_IQ_9 | 851 | 866 | PF13499 | 0.357 |
LIG_CtBP_PxDLS_1 | 329 | 333 | PF00389 | 0.402 |
LIG_Dynein_DLC8_1 | 62 | 68 | PF01221 | 0.444 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.453 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.442 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.439 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.518 |
LIG_FHA_1 | 566 | 572 | PF00498 | 0.461 |
LIG_FHA_1 | 628 | 634 | PF00498 | 0.510 |
LIG_FHA_1 | 748 | 754 | PF00498 | 0.588 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.449 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.502 |
LIG_FHA_1 | 939 | 945 | PF00498 | 0.461 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.500 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.444 |
LIG_FHA_2 | 490 | 496 | PF00498 | 0.494 |
LIG_FHA_2 | 608 | 614 | PF00498 | 0.486 |
LIG_FHA_2 | 621 | 627 | PF00498 | 0.544 |
LIG_FHA_2 | 759 | 765 | PF00498 | 0.352 |
LIG_FHA_2 | 831 | 837 | PF00498 | 0.650 |
LIG_FHA_2 | 838 | 844 | PF00498 | 0.496 |
LIG_LIR_Apic_2 | 396 | 401 | PF02991 | 0.487 |
LIG_LIR_Apic_2 | 595 | 601 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 185 | 195 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 626 | 637 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 865 | 873 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 396 | 402 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 511 | 516 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 626 | 632 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 865 | 869 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 924 | 930 | PF02991 | 0.490 |
LIG_NBox_RRM_1 | 235 | 245 | PF00076 | 0.370 |
LIG_NRBOX | 449 | 455 | PF00104 | 0.486 |
LIG_PCNA_yPIPBox_3 | 451 | 465 | PF02747 | 0.431 |
LIG_PCNA_yPIPBox_3 | 50 | 64 | PF02747 | 0.417 |
LIG_PCNA_yPIPBox_3 | 530 | 539 | PF02747 | 0.486 |
LIG_PCNA_yPIPBox_3 | 911 | 920 | PF02747 | 0.348 |
LIG_Pex14_2 | 393 | 397 | PF04695 | 0.509 |
LIG_Pex14_2 | 850 | 854 | PF04695 | 0.515 |
LIG_RPA_C_Fungi | 669 | 681 | PF08784 | 0.393 |
LIG_SH2_CRK | 599 | 603 | PF00017 | 0.313 |
LIG_SH2_CRK | 791 | 795 | PF00017 | 0.409 |
LIG_SH2_GRB2like | 442 | 445 | PF00017 | 0.317 |
LIG_SH2_NCK_1 | 599 | 603 | PF00017 | 0.383 |
LIG_SH2_PTP2 | 513 | 516 | PF00017 | 0.243 |
LIG_SH2_PTP2 | 723 | 726 | PF00017 | 0.300 |
LIG_SH2_SRC | 599 | 602 | PF00017 | 0.297 |
LIG_SH2_STAP1 | 729 | 733 | PF00017 | 0.300 |
LIG_SH2_STAT3 | 158 | 161 | PF00017 | 0.349 |
LIG_SH2_STAT3 | 871 | 874 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 513 | 516 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 608 | 611 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 686 | 689 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 723 | 726 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 871 | 874 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 938 | 941 | PF00017 | 0.375 |
LIG_SH3_1 | 460 | 466 | PF00018 | 0.380 |
LIG_SH3_2 | 463 | 468 | PF14604 | 0.467 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.380 |
LIG_SH3_3 | 697 | 703 | PF00018 | 0.301 |
LIG_SH3_3 | 722 | 728 | PF00018 | 0.321 |
LIG_SH3_3 | 779 | 785 | PF00018 | 0.426 |
LIG_SH3_3 | 805 | 811 | PF00018 | 0.487 |
LIG_SUMO_SIM_anti_2 | 136 | 142 | PF11976 | 0.318 |
LIG_SUMO_SIM_anti_2 | 83 | 89 | PF11976 | 0.329 |
LIG_SUMO_SIM_anti_2 | 954 | 960 | PF11976 | 0.455 |
LIG_SUMO_SIM_par_1 | 245 | 251 | PF11976 | 0.350 |
LIG_SUMO_SIM_par_1 | 327 | 333 | PF11976 | 0.397 |
LIG_SUMO_SIM_par_1 | 420 | 427 | PF11976 | 0.355 |
LIG_TRAF2_1 | 187 | 190 | PF00917 | 0.492 |
LIG_TRAF2_1 | 610 | 613 | PF00917 | 0.263 |
LIG_TRAF2_1 | 820 | 823 | PF00917 | 0.571 |
LIG_TRAF2_1 | 833 | 836 | PF00917 | 0.496 |
LIG_TRAF2_1 | 904 | 907 | PF00917 | 0.525 |
LIG_TRAF2_1 | 913 | 916 | PF00917 | 0.395 |
LIG_UBA3_1 | 122 | 129 | PF00899 | 0.341 |
LIG_UBA3_1 | 633 | 642 | PF00899 | 0.425 |
LIG_UBA3_1 | 931 | 936 | PF00899 | 0.411 |
LIG_UBA3_1 | 955 | 960 | PF00899 | 0.515 |
LIG_WRC_WIRS_1 | 854 | 859 | PF05994 | 0.363 |
MOD_CDC14_SPxK_1 | 566 | 569 | PF00782 | 0.297 |
MOD_CDK_SPxK_1 | 563 | 569 | PF00069 | 0.297 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.407 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.458 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.609 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.475 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.356 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.568 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.484 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.644 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.572 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.630 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.536 |
MOD_CK1_1 | 688 | 694 | PF00069 | 0.337 |
MOD_CK1_1 | 771 | 777 | PF00069 | 0.359 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.514 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.366 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.405 |
MOD_CK2_1 | 607 | 613 | PF00069 | 0.279 |
MOD_CK2_1 | 620 | 626 | PF00069 | 0.368 |
MOD_CK2_1 | 758 | 764 | PF00069 | 0.594 |
MOD_CK2_1 | 830 | 836 | PF00069 | 0.722 |
MOD_CK2_1 | 901 | 907 | PF00069 | 0.642 |
MOD_CK2_1 | 910 | 916 | PF00069 | 0.463 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.368 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.501 |
MOD_GlcNHglycan | 267 | 272 | PF01048 | 0.573 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.568 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.529 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.626 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.726 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.471 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.312 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.366 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.562 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.646 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.326 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.486 |
MOD_GlcNHglycan | 770 | 773 | PF01048 | 0.443 |
MOD_GlcNHglycan | 879 | 882 | PF01048 | 0.548 |
MOD_GlcNHglycan | 887 | 890 | PF01048 | 0.568 |
MOD_GlcNHglycan | 903 | 906 | PF01048 | 0.594 |
MOD_GlcNHglycan | 945 | 948 | PF01048 | 0.464 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.561 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.334 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.286 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.414 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.547 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.436 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.545 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.705 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.538 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.483 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.590 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.446 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.643 |
MOD_GSK3_1 | 648 | 655 | PF00069 | 0.308 |
MOD_GSK3_1 | 685 | 692 | PF00069 | 0.341 |
MOD_GSK3_1 | 699 | 706 | PF00069 | 0.211 |
MOD_GSK3_1 | 743 | 750 | PF00069 | 0.502 |
MOD_GSK3_1 | 754 | 761 | PF00069 | 0.539 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.450 |
MOD_GSK3_1 | 938 | 945 | PF00069 | 0.383 |
MOD_LATS_1 | 78 | 84 | PF00433 | 0.414 |
MOD_N-GLC_1 | 321 | 326 | PF02516 | 0.364 |
MOD_N-GLC_1 | 578 | 583 | PF02516 | 0.297 |
MOD_N-GLC_1 | 910 | 915 | PF02516 | 0.365 |
MOD_N-GLC_1 | 942 | 947 | PF02516 | 0.438 |
MOD_N-GLC_2 | 278 | 280 | PF02516 | 0.450 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.388 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.335 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.578 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.299 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.550 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.536 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.509 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.491 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.299 |
MOD_NEK2_1 | 652 | 657 | PF00069 | 0.397 |
MOD_NEK2_1 | 753 | 758 | PF00069 | 0.596 |
MOD_NEK2_1 | 773 | 778 | PF00069 | 0.217 |
MOD_NEK2_1 | 837 | 842 | PF00069 | 0.533 |
MOD_NEK2_1 | 853 | 858 | PF00069 | 0.300 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.534 |
MOD_PKA_1 | 648 | 654 | PF00069 | 0.357 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.297 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.527 |
MOD_PKA_2 | 543 | 549 | PF00069 | 0.436 |
MOD_PKA_2 | 647 | 653 | PF00069 | 0.392 |
MOD_PKA_2 | 743 | 749 | PF00069 | 0.470 |
MOD_PKA_2 | 885 | 891 | PF00069 | 0.550 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.372 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.578 |
MOD_Plk_1 | 371 | 377 | PF00069 | 0.584 |
MOD_Plk_1 | 754 | 760 | PF00069 | 0.505 |
MOD_Plk_1 | 837 | 843 | PF00069 | 0.522 |
MOD_Plk_1 | 910 | 916 | PF00069 | 0.363 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.417 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.538 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.334 |
MOD_Plk_4 | 581 | 587 | PF00069 | 0.337 |
MOD_Plk_4 | 648 | 654 | PF00069 | 0.289 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.384 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.629 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.436 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.578 |
MOD_ProDKin_1 | 563 | 569 | PF00069 | 0.372 |
MOD_ProDKin_1 | 699 | 705 | PF00069 | 0.368 |
MOD_ProDKin_1 | 747 | 753 | PF00069 | 0.537 |
MOD_ProDKin_1 | 830 | 836 | PF00069 | 0.525 |
MOD_SUMO_for_1 | 641 | 644 | PF00179 | 0.341 |
MOD_SUMO_rev_2 | 212 | 222 | PF00179 | 0.370 |
MOD_SUMO_rev_2 | 611 | 617 | PF00179 | 0.376 |
TRG_DiLeu_BaEn_3 | 612 | 618 | PF01217 | 0.297 |
TRG_DiLeu_BaLyEn_6 | 398 | 403 | PF01217 | 0.468 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 513 | 516 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 599 | 602 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 791 | 794 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 844 | 847 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 866 | 869 | PF00928 | 0.547 |
TRG_ER_diArg_1 | 255 | 258 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 458 | 460 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 517 | 520 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 535 | 537 | PF00400 | 0.221 |
TRG_ER_diArg_1 | 614 | 617 | PF00400 | 0.376 |
TRG_ER_diArg_1 | 647 | 649 | PF00400 | 0.372 |
TRG_ER_diArg_1 | 672 | 674 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 883 | 886 | PF00400 | 0.638 |
TRG_ER_diArg_1 | 918 | 920 | PF00400 | 0.347 |
TRG_NES_CRM1_1 | 764 | 778 | PF08389 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 792 | 796 | PF00026 | 0.585 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8R7 | Leptomonas seymouri | 42% | 100% |
A0A0S4JJL6 | Bodo saltans | 27% | 100% |
A0A3R7KD14 | Trypanosoma rangeli | 31% | 100% |
A4HHB7 | Leishmania braziliensis | 73% | 99% |
A4I4G4 | Leishmania infantum | 100% | 100% |
E9ADW3 | Leishmania major | 87% | 96% |
E9ALW7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 98% |
V5BH85 | Trypanosoma cruzi | 30% | 100% |