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 |
Related structures:
AlphaFold database: E9ALW7
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 | 0.505 |
CLV_C14_Caspase3-7 | 514 | 518 | PF00656 | 0.515 |
CLV_C14_Caspase3-7 | 625 | 629 | PF00656 | 0.502 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 459 | 461 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 525 | 527 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 602 | 604 | PF00675 | 0.287 |
CLV_NRD_NRD_1 | 637 | 639 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 662 | 664 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 780 | 782 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 872 | 874 | PF00675 | 0.713 |
CLV_NRD_NRD_1 | 900 | 902 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 931 | 933 | PF00675 | 0.499 |
CLV_PCSK_FUR_1 | 256 | 260 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 459 | 461 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 525 | 527 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 604 | 606 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 631 | 633 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 637 | 639 | PF00082 | 0.341 |
CLV_PCSK_KEX2_1 | 662 | 664 | PF00082 | 0.341 |
CLV_PCSK_KEX2_1 | 872 | 874 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 900 | 902 | PF00082 | 0.381 |
CLV_PCSK_KEX2_1 | 931 | 933 | PF00082 | 0.492 |
CLV_PCSK_PC1ET2_1 | 604 | 606 | PF00082 | 0.302 |
CLV_PCSK_PC1ET2_1 | 631 | 633 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 638 | 642 | PF00082 | 0.172 |
CLV_PCSK_SKI1_1 | 736 | 740 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 788 | 792 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 848 | 852 | PF00082 | 0.536 |
DEG_COP1_1 | 720 | 728 | PF00400 | 0.506 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.713 |
DEG_SCF_TRCP1_1 | 552 | 557 | PF00400 | 0.467 |
DOC_ANK_TNKS_1 | 413 | 420 | PF00023 | 0.484 |
DOC_CDC14_PxL_1 | 722 | 730 | PF14671 | 0.600 |
DOC_CYCLIN_RxL_1 | 241 | 251 | PF00134 | 0.409 |
DOC_CYCLIN_RxL_1 | 255 | 264 | PF00134 | 0.330 |
DOC_CYCLIN_RxL_1 | 782 | 795 | PF00134 | 0.425 |
DOC_MAPK_gen_1 | 36 | 46 | PF00069 | 0.384 |
DOC_MAPK_gen_1 | 522 | 530 | PF00069 | 0.500 |
DOC_MAPK_gen_1 | 603 | 609 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 662 | 672 | PF00069 | 0.575 |
DOC_MAPK_gen_1 | 931 | 939 | PF00069 | 0.473 |
DOC_MAPK_MEF2A_6 | 135 | 142 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 289 | 296 | PF00069 | 0.468 |
DOC_MAPK_MEF2A_6 | 496 | 505 | PF00069 | 0.251 |
DOC_MAPK_RevD_3 | 245 | 259 | PF00069 | 0.450 |
DOC_PP1_RVXF_1 | 349 | 355 | PF00149 | 0.473 |
DOC_PP1_RVXF_1 | 593 | 599 | PF00149 | 0.493 |
DOC_PP2B_LxvP_1 | 501 | 504 | PF13499 | 0.467 |
DOC_PP2B_LxvP_1 | 85 | 88 | PF13499 | 0.467 |
DOC_PP2B_LxvP_1 | 911 | 914 | PF13499 | 0.442 |
DOC_PP4_FxxP_1 | 398 | 401 | PF00568 | 0.440 |
DOC_PP4_FxxP_1 | 944 | 947 | PF00568 | 0.535 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 743 | 747 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 882 | 886 | PF00917 | 0.790 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.656 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.792 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 552 | 557 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 688 | 693 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 736 | 741 | PF00397 | 0.581 |
LIG_14-3-3_CanoR_1 | 146 | 150 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 244 | 250 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 309 | 316 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 360 | 365 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 496 | 502 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 637 | 641 | PF00244 | 0.530 |
LIG_Actin_WH2_2 | 707 | 725 | PF00022 | 0.490 |
LIG_APCC_ABBA_1 | 620 | 625 | PF00400 | 0.515 |
LIG_BRCT_BRCA1_1 | 110 | 114 | PF00533 | 0.519 |
LIG_BRCT_BRCA1_1 | 150 | 154 | PF00533 | 0.502 |
LIG_BRCT_BRCA1_1 | 229 | 233 | PF00533 | 0.560 |
LIG_BRCT_BRCA1_1 | 429 | 433 | PF00533 | 0.430 |
LIG_CaM_IQ_9 | 840 | 855 | PF13499 | 0.424 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.541 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.554 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.591 |
LIG_FHA_1 | 555 | 561 | PF00498 | 0.472 |
LIG_FHA_1 | 617 | 623 | PF00498 | 0.532 |
LIG_FHA_1 | 728 | 734 | PF00498 | 0.474 |
LIG_FHA_1 | 737 | 743 | PF00498 | 0.562 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.660 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.641 |
LIG_FHA_1 | 920 | 926 | PF00498 | 0.494 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.612 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.406 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.497 |
LIG_FHA_2 | 597 | 603 | PF00498 | 0.490 |
LIG_FHA_2 | 610 | 616 | PF00498 | 0.490 |
LIG_FHA_2 | 730 | 736 | PF00498 | 0.388 |
LIG_FHA_2 | 748 | 754 | PF00498 | 0.384 |
LIG_FHA_2 | 827 | 833 | PF00498 | 0.469 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.712 |
LIG_GBD_Chelix_1 | 754 | 762 | PF00786 | 0.461 |
LIG_LIR_Apic_2 | 396 | 401 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 185 | 195 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 615 | 626 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 838 | 846 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 854 | 862 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 905 | 916 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 396 | 402 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 500 | 505 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 615 | 621 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 838 | 842 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 854 | 858 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 905 | 911 | PF02991 | 0.522 |
LIG_NBox_RRM_1 | 235 | 245 | PF00076 | 0.413 |
LIG_NRBOX | 449 | 455 | PF00104 | 0.525 |
LIG_PCNA_yPIPBox_3 | 50 | 64 | PF02747 | 0.498 |
LIG_PCNA_yPIPBox_3 | 519 | 528 | PF02747 | 0.500 |
LIG_Pex14_2 | 393 | 397 | PF04695 | 0.562 |
LIG_Pex14_2 | 839 | 843 | PF04695 | 0.460 |
LIG_RPA_C_Fungi | 658 | 670 | PF08784 | 0.400 |
LIG_SH2_CRK | 588 | 592 | PF00017 | 0.322 |
LIG_SH2_CRK | 780 | 784 | PF00017 | 0.417 |
LIG_SH2_NCK_1 | 588 | 592 | PF00017 | 0.391 |
LIG_SH2_PTP2 | 502 | 505 | PF00017 | 0.251 |
LIG_SH2_PTP2 | 712 | 715 | PF00017 | 0.308 |
LIG_SH2_STAP1 | 718 | 722 | PF00017 | 0.308 |
LIG_SH2_STAT3 | 158 | 161 | PF00017 | 0.358 |
LIG_SH2_STAT3 | 860 | 863 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 597 | 600 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 675 | 678 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 712 | 715 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 860 | 863 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 919 | 922 | PF00017 | 0.389 |
LIG_SH3_1 | 460 | 466 | PF00018 | 0.407 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.444 |
LIG_SH3_3 | 686 | 692 | PF00018 | 0.320 |
LIG_SH3_3 | 711 | 717 | PF00018 | 0.333 |
LIG_SH3_3 | 768 | 774 | PF00018 | 0.458 |
LIG_SH3_3 | 794 | 800 | PF00018 | 0.576 |
LIG_SUMO_SIM_anti_2 | 136 | 142 | PF11976 | 0.327 |
LIG_SUMO_SIM_anti_2 | 935 | 941 | PF11976 | 0.479 |
LIG_SUMO_SIM_par_1 | 245 | 251 | PF11976 | 0.413 |
LIG_TRAF2_1 | 187 | 190 | PF00917 | 0.400 |
LIG_TRAF2_1 | 599 | 602 | PF00917 | 0.270 |
LIG_TRAF2_1 | 809 | 812 | PF00917 | 0.649 |
LIG_TRAF2_1 | 822 | 825 | PF00917 | 0.467 |
LIG_TRAF2_1 | 885 | 888 | PF00917 | 0.669 |
LIG_TRAF2_1 | 90 | 93 | PF00917 | 0.536 |
LIG_TRAF2_2 | 822 | 827 | PF00917 | 0.435 |
LIG_UBA3_1 | 122 | 129 | PF00899 | 0.360 |
LIG_UBA3_1 | 622 | 631 | PF00899 | 0.312 |
LIG_UBA3_1 | 912 | 917 | PF00899 | 0.456 |
LIG_UBA3_1 | 936 | 941 | PF00899 | 0.498 |
LIG_WRC_WIRS_1 | 836 | 841 | PF05994 | 0.448 |
LIG_WRC_WIRS_1 | 843 | 848 | PF05994 | 0.412 |
MOD_CDC14_SPxK_1 | 555 | 558 | PF00782 | 0.312 |
MOD_CDK_SPxK_1 | 552 | 558 | PF00069 | 0.312 |
MOD_CDK_SPxxK_3 | 227 | 234 | PF00069 | 0.523 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.451 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.462 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.522 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.285 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.678 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.453 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.702 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.754 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.639 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.733 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.202 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.664 |
MOD_CK1_1 | 678 | 684 | PF00069 | 0.390 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.587 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.635 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.541 |
MOD_CK2_1 | 596 | 602 | PF00069 | 0.284 |
MOD_CK2_1 | 609 | 615 | PF00069 | 0.284 |
MOD_CK2_1 | 747 | 753 | PF00069 | 0.602 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.710 |
MOD_CK2_1 | 882 | 888 | PF00069 | 0.773 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.312 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.345 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.693 |
MOD_GlcNHglycan | 267 | 272 | PF01048 | 0.568 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.659 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.750 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.780 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.617 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.455 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.522 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.705 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.343 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.317 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.617 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.657 |
MOD_GlcNHglycan | 868 | 871 | PF01048 | 0.651 |
MOD_GlcNHglycan | 884 | 887 | PF01048 | 0.746 |
MOD_GlcNHglycan | 926 | 929 | PF01048 | 0.554 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.739 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.376 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.423 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.312 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.681 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.726 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.719 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.662 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.719 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.259 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.415 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.709 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.360 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.360 |
MOD_GSK3_1 | 743 | 750 | PF00069 | 0.667 |
MOD_GSK3_1 | 878 | 885 | PF00069 | 0.660 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.685 |
MOD_N-GLC_1 | 371 | 376 | PF02516 | 0.575 |
MOD_N-GLC_1 | 567 | 572 | PF02516 | 0.312 |
MOD_N-GLC_2 | 278 | 280 | PF02516 | 0.425 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.408 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.309 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.517 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.251 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.574 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.703 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.520 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.308 |
MOD_NEK2_1 | 609 | 614 | PF00069 | 0.354 |
MOD_NEK2_1 | 641 | 646 | PF00069 | 0.404 |
MOD_NEK2_1 | 742 | 747 | PF00069 | 0.574 |
MOD_NEK2_1 | 762 | 767 | PF00069 | 0.521 |
MOD_NEK2_1 | 826 | 831 | PF00069 | 0.510 |
MOD_NEK2_1 | 842 | 847 | PF00069 | 0.454 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.620 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.312 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.764 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.628 |
MOD_PKA_2 | 532 | 538 | PF00069 | 0.472 |
MOD_PKA_2 | 636 | 642 | PF00069 | 0.399 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.379 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.717 |
MOD_Plk_1 | 371 | 377 | PF00069 | 0.630 |
MOD_Plk_1 | 743 | 749 | PF00069 | 0.555 |
MOD_Plk_1 | 826 | 832 | PF00069 | 0.389 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.450 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.542 |
MOD_Plk_4 | 497 | 503 | PF00069 | 0.311 |
MOD_Plk_4 | 570 | 576 | PF00069 | 0.312 |
MOD_Plk_4 | 729 | 735 | PF00069 | 0.380 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.482 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.769 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.508 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.606 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.702 |
MOD_ProDKin_1 | 552 | 558 | PF00069 | 0.405 |
MOD_ProDKin_1 | 688 | 694 | PF00069 | 0.385 |
MOD_ProDKin_1 | 736 | 742 | PF00069 | 0.582 |
MOD_SUMO_for_1 | 630 | 633 | PF00179 | 0.360 |
MOD_SUMO_for_1 | 807 | 810 | PF00179 | 0.516 |
MOD_SUMO_rev_2 | 214 | 222 | PF00179 | 0.560 |
MOD_SUMO_rev_2 | 600 | 606 | PF00179 | 0.384 |
TRG_DiLeu_BaEn_3 | 601 | 607 | PF01217 | 0.312 |
TRG_DiLeu_BaLyEn_6 | 348 | 353 | PF01217 | 0.527 |
TRG_DiLeu_BaLyEn_6 | 398 | 403 | PF01217 | 0.502 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 502 | 505 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 588 | 591 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 780 | 783 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 833 | 836 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 855 | 858 | PF00928 | 0.505 |
TRG_ER_diArg_1 | 255 | 258 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 35 | 37 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 458 | 460 | PF00400 | 0.492 |
TRG_ER_diArg_1 | 524 | 526 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 603 | 606 | PF00400 | 0.340 |
TRG_ER_diArg_1 | 636 | 638 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 661 | 663 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 872 | 875 | PF00400 | 0.720 |
TRG_ER_diArg_1 | 899 | 901 | PF00400 | 0.377 |
TRG_NES_CRM1_1 | 753 | 767 | PF08389 | 0.506 |
TRG_Pf-PMV_PEXEL_1 | 781 | 785 | PF00026 | 0.578 |
TRG_Pf-PMV_PEXEL_1 | 821 | 825 | PF00026 | 0.456 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8R7 | Leptomonas seymouri | 43% | 100% |
A0A0S4JJL6 | Bodo saltans | 27% | 100% |
A0A3R7KD14 | Trypanosoma rangeli | 32% | 100% |
A4HHB7 | Leishmania braziliensis | 72% | 100% |
A4I4G4 | Leishmania infantum | 86% | 98% |
E5KZN0 | Leishmania donovani | 86% | 98% |
E9ADW3 | Leishmania major | 82% | 96% |
V5BH85 | Trypanosoma cruzi | 30% | 100% |