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 | 1 |
GO:0005845 | mRNA cap binding complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0034518 | RNA cap binding complex | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: E9AVJ4
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006370 | 7-methylguanosine mRNA capping | 8 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009452 | 7-methylguanosine RNA capping | 8 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0036260 | RNA capping | 7 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004482 | mRNA (guanine-N7-)-methyltransferase activity | 6 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0008170 | N-methyltransferase activity | 5 | 12 |
GO:0008173 | RNA methyltransferase activity | 4 | 12 |
GO:0008174 | mRNA methyltransferase activity | 5 | 12 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0000166 | nucleotide binding | 3 | 2 |
GO:0004484 | mRNA guanylyltransferase activity | 5 | 2 |
GO:0005524 | ATP binding | 5 | 2 |
GO:0005525 | GTP binding | 5 | 2 |
GO:0008192 | RNA guanylyltransferase activity | 4 | 2 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 3 |
GO:0016779 | nucleotidyltransferase activity | 4 | 3 |
GO:0017076 | purine nucleotide binding | 4 | 2 |
GO:0019001 | guanyl nucleotide binding | 5 | 2 |
GO:0030554 | adenyl nucleotide binding | 5 | 2 |
GO:0032553 | ribonucleotide binding | 3 | 2 |
GO:0032555 | purine ribonucleotide binding | 4 | 2 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 2 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 2 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 2 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043168 | anion binding | 3 | 2 |
GO:0070568 | guanylyltransferase activity | 5 | 2 |
GO:0097367 | carbohydrate derivative binding | 2 | 2 |
GO:1901265 | nucleoside phosphate binding | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.385 |
CLV_C14_Caspase3-7 | 367 | 371 | PF00656 | 0.401 |
CLV_C14_Caspase3-7 | 40 | 44 | PF00656 | 0.565 |
CLV_C14_Caspase3-7 | 541 | 545 | PF00656 | 0.652 |
CLV_NRD_NRD_1 | 1040 | 1042 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 591 | 593 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 688 | 690 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 729 | 731 | PF00675 | 0.387 |
CLV_NRD_NRD_1 | 748 | 750 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 991 | 993 | PF00675 | 0.427 |
CLV_PCSK_FUR_1 | 157 | 161 | PF00082 | 0.476 |
CLV_PCSK_FUR_1 | 222 | 226 | PF00082 | 0.488 |
CLV_PCSK_FUR_1 | 991 | 995 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 1039 | 1041 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 690 | 692 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 729 | 731 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 748 | 750 | PF00082 | 0.226 |
CLV_PCSK_KEX2_1 | 838 | 840 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 991 | 993 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 300 | 302 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 690 | 692 | PF00082 | 0.537 |
CLV_PCSK_PC1ET2_1 | 838 | 840 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 993 | 995 | PF00082 | 0.385 |
CLV_PCSK_PC7_1 | 159 | 165 | PF00082 | 0.508 |
CLV_PCSK_PC7_1 | 725 | 731 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 550 | 554 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 555 | 559 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 736 | 740 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 748 | 752 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 777 | 781 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 963 | 967 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 984 | 988 | PF00082 | 0.398 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.589 |
DEG_SPOP_SBC_1 | 383 | 387 | PF00917 | 0.530 |
DOC_CKS1_1 | 373 | 378 | PF01111 | 0.399 |
DOC_CKS1_1 | 90 | 95 | PF01111 | 0.550 |
DOC_CYCLIN_yCln2_LP_2 | 437 | 443 | PF00134 | 0.383 |
DOC_CYCLIN_yCln2_LP_2 | 751 | 757 | PF00134 | 0.428 |
DOC_MAPK_gen_1 | 391 | 400 | PF00069 | 0.375 |
DOC_MAPK_gen_1 | 436 | 443 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 562 | 572 | PF00069 | 0.533 |
DOC_MAPK_gen_1 | 592 | 600 | PF00069 | 0.544 |
DOC_MAPK_gen_1 | 689 | 697 | PF00069 | 0.546 |
DOC_MAPK_gen_1 | 748 | 759 | PF00069 | 0.398 |
DOC_MAPK_JIP1_4 | 777 | 783 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 112 | 120 | PF00069 | 0.437 |
DOC_PP2B_LxvP_1 | 751 | 754 | PF13499 | 0.359 |
DOC_PP4_FxxP_1 | 449 | 452 | PF00568 | 0.427 |
DOC_PP4_FxxP_1 | 86 | 89 | PF00568 | 0.401 |
DOC_PP4_FxxP_1 | 928 | 931 | PF00568 | 0.449 |
DOC_USP7_MATH_1 | 1026 | 1030 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.547 |
DOC_USP7_UBL2_3 | 1023 | 1027 | PF12436 | 0.603 |
DOC_USP7_UBL2_3 | 752 | 756 | PF12436 | 0.449 |
DOC_WW_Pin1_4 | 1003 | 1008 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.386 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 607 | 612 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.411 |
LIG_14-3-3_CanoR_1 | 175 | 181 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 183 | 188 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 265 | 275 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 350 | 359 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 676 | 681 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 797 | 806 | PF00244 | 0.368 |
LIG_14-3-3_CterR_2 | 1039 | 1043 | PF00244 | 0.603 |
LIG_Actin_WH2_2 | 335 | 352 | PF00022 | 0.453 |
LIG_Actin_WH2_2 | 60 | 75 | PF00022 | 0.512 |
LIG_Actin_WH2_2 | 949 | 965 | PF00022 | 0.398 |
LIG_BIR_III_2 | 136 | 140 | PF00653 | 0.370 |
LIG_BIR_III_2 | 59 | 63 | PF00653 | 0.572 |
LIG_BRCT_BRCA1_1 | 197 | 201 | PF00533 | 0.573 |
LIG_BRCT_BRCA1_1 | 416 | 420 | PF00533 | 0.413 |
LIG_BRCT_BRCA1_1 | 845 | 849 | PF00533 | 0.328 |
LIG_BRCT_BRCA1_1 | 917 | 921 | PF00533 | 0.477 |
LIG_BRCT_BRCA1_2 | 416 | 422 | PF00533 | 0.413 |
LIG_Clathr_ClatBox_1 | 1018 | 1022 | PF01394 | 0.449 |
LIG_Clathr_ClatBox_1 | 397 | 401 | PF01394 | 0.413 |
LIG_Clathr_ClatBox_1 | 507 | 511 | PF01394 | 0.557 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.530 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.531 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.368 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.462 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.396 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.430 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.479 |
LIG_FHA_1 | 942 | 948 | PF00498 | 0.428 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.480 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.508 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.622 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.635 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.398 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.411 |
LIG_FHA_2 | 677 | 683 | PF00498 | 0.582 |
LIG_FHA_2 | 880 | 886 | PF00498 | 0.329 |
LIG_LIR_Apic_2 | 582 | 588 | PF02991 | 0.527 |
LIG_LIR_Apic_2 | 85 | 89 | PF02991 | 0.410 |
LIG_LIR_Apic_2 | 927 | 931 | PF02991 | 0.470 |
LIG_LIR_Apic_2 | 944 | 949 | PF02991 | 0.197 |
LIG_LIR_Gen_1 | 238 | 246 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 249 | 259 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 27 | 38 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 305 | 314 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 490 | 499 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 617 | 626 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 645 | 655 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 661 | 671 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 911 | 921 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 951 | 958 | PF02991 | 0.451 |
LIG_LIR_LC3C_4 | 692 | 697 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 249 | 255 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 27 | 33 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 305 | 310 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 490 | 495 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 617 | 623 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 644 | 650 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 661 | 667 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 710 | 716 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 911 | 916 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 951 | 956 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 967 | 973 | PF02991 | 0.195 |
LIG_MLH1_MIPbox_1 | 416 | 420 | PF16413 | 0.413 |
LIG_MYND_3 | 612 | 616 | PF01753 | 0.565 |
LIG_NRBOX | 503 | 509 | PF00104 | 0.490 |
LIG_NRBOX | 670 | 676 | PF00104 | 0.389 |
LIG_Pex14_1 | 124 | 128 | PF04695 | 0.521 |
LIG_Pex14_2 | 816 | 820 | PF04695 | 0.449 |
LIG_PTB_Apo_2 | 77 | 84 | PF02174 | 0.337 |
LIG_PTB_Apo_2 | 898 | 905 | PF02174 | 0.328 |
LIG_PTB_Phospho_1 | 77 | 83 | PF10480 | 0.334 |
LIG_PTB_Phospho_1 | 898 | 904 | PF10480 | 0.328 |
LIG_REV1ctd_RIR_1 | 417 | 427 | PF16727 | 0.344 |
LIG_SH2_CRK | 30 | 34 | PF00017 | 0.481 |
LIG_SH2_CRK | 307 | 311 | PF00017 | 0.467 |
LIG_SH2_CRK | 360 | 364 | PF00017 | 0.420 |
LIG_SH2_CRK | 713 | 717 | PF00017 | 0.430 |
LIG_SH2_GRB2like | 575 | 578 | PF00017 | 0.529 |
LIG_SH2_NCK_1 | 463 | 467 | PF00017 | 0.398 |
LIG_SH2_PTP2 | 620 | 623 | PF00017 | 0.387 |
LIG_SH2_PTP2 | 946 | 949 | PF00017 | 0.413 |
LIG_SH2_SRC | 571 | 574 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 351 | 355 | PF00017 | 0.265 |
LIG_SH2_STAP1 | 414 | 418 | PF00017 | 0.396 |
LIG_SH2_STAP1 | 492 | 496 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 932 | 936 | PF00017 | 0.340 |
LIG_SH2_STAT3 | 165 | 168 | PF00017 | 0.587 |
LIG_SH2_STAT3 | 973 | 976 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 571 | 574 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 620 | 623 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 635 | 638 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 863 | 866 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 946 | 949 | PF00017 | 0.305 |
LIG_SH3_1 | 360 | 366 | PF00018 | 0.553 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.451 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.644 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.553 |
LIG_SH3_3 | 580 | 586 | PF00018 | 0.535 |
LIG_SH3_3 | 694 | 700 | PF00018 | 0.609 |
LIG_SH3_3 | 998 | 1004 | PF00018 | 0.475 |
LIG_SH3_4 | 752 | 759 | PF00018 | 0.475 |
LIG_SUMO_SIM_anti_2 | 884 | 890 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 117 | 122 | PF11976 | 0.401 |
LIG_SUMO_SIM_par_1 | 150 | 156 | PF11976 | 0.438 |
LIG_SUMO_SIM_par_1 | 377 | 387 | PF11976 | 0.533 |
LIG_SUMO_SIM_par_1 | 396 | 401 | PF11976 | 0.223 |
LIG_SUMO_SIM_par_1 | 692 | 698 | PF11976 | 0.599 |
LIG_TRAF2_1 | 614 | 617 | PF00917 | 0.539 |
LIG_TRAF2_1 | 721 | 724 | PF00917 | 0.398 |
LIG_TRAF2_1 | 939 | 942 | PF00917 | 0.259 |
LIG_WRC_WIRS_1 | 252 | 257 | PF05994 | 0.428 |
LIG_WW_3 | 699 | 703 | PF00397 | 0.362 |
MOD_CDK_SPxxK_3 | 89 | 96 | PF00069 | 0.457 |
MOD_CK1_1 | 1030 | 1036 | PF00069 | 0.692 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.495 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.665 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.328 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.558 |
MOD_CK1_1 | 703 | 709 | PF00069 | 0.579 |
MOD_CK1_1 | 857 | 863 | PF00069 | 0.379 |
MOD_CK2_1 | 1003 | 1009 | PF00069 | 0.335 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.518 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.566 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.501 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.308 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.466 |
MOD_CK2_1 | 487 | 493 | PF00069 | 0.328 |
MOD_CK2_1 | 611 | 617 | PF00069 | 0.575 |
MOD_CK2_1 | 676 | 682 | PF00069 | 0.587 |
MOD_CK2_1 | 796 | 802 | PF00069 | 0.412 |
MOD_CK2_1 | 881 | 887 | PF00069 | 0.363 |
MOD_CK2_1 | 936 | 942 | PF00069 | 0.190 |
MOD_DYRK1A_RPxSP_1 | 607 | 611 | PF00069 | 0.430 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.591 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.585 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.539 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.567 |
MOD_GlcNHglycan | 644 | 647 | PF01048 | 0.497 |
MOD_GlcNHglycan | 829 | 832 | PF01048 | 0.448 |
MOD_GlcNHglycan | 917 | 920 | PF01048 | 0.465 |
MOD_GSK3_1 | 1026 | 1033 | PF00069 | 0.678 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.551 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.524 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.448 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.539 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.353 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.455 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.603 |
MOD_GSK3_1 | 703 | 710 | PF00069 | 0.509 |
MOD_GSK3_1 | 734 | 741 | PF00069 | 0.371 |
MOD_GSK3_1 | 798 | 805 | PF00069 | 0.344 |
MOD_GSK3_1 | 843 | 850 | PF00069 | 0.335 |
MOD_GSK3_1 | 932 | 939 | PF00069 | 0.318 |
MOD_N-GLC_1 | 144 | 149 | PF02516 | 0.557 |
MOD_N-GLC_1 | 292 | 297 | PF02516 | 0.299 |
MOD_N-GLC_1 | 576 | 581 | PF02516 | 0.564 |
MOD_N-GLC_1 | 75 | 80 | PF02516 | 0.567 |
MOD_NEK2_1 | 1021 | 1026 | PF00069 | 0.454 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.276 |
MOD_NEK2_1 | 695 | 700 | PF00069 | 0.644 |
MOD_NEK2_1 | 739 | 744 | PF00069 | 0.370 |
MOD_NEK2_1 | 842 | 847 | PF00069 | 0.388 |
MOD_NEK2_1 | 878 | 883 | PF00069 | 0.339 |
MOD_NEK2_2 | 216 | 221 | PF00069 | 0.414 |
MOD_NEK2_2 | 414 | 419 | PF00069 | 0.449 |
MOD_NEK2_2 | 847 | 852 | PF00069 | 0.328 |
MOD_PIKK_1 | 464 | 470 | PF00454 | 0.475 |
MOD_PIKK_1 | 703 | 709 | PF00454 | 0.591 |
MOD_PKA_1 | 265 | 271 | PF00069 | 0.357 |
MOD_PKA_1 | 96 | 102 | PF00069 | 0.469 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.573 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.588 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.470 |
MOD_PKA_2 | 561 | 567 | PF00069 | 0.491 |
MOD_PKA_2 | 796 | 802 | PF00069 | 0.344 |
MOD_PKB_1 | 527 | 535 | PF00069 | 0.612 |
MOD_Plk_1 | 144 | 150 | PF00069 | 0.529 |
MOD_Plk_1 | 233 | 239 | PF00069 | 0.406 |
MOD_Plk_1 | 245 | 251 | PF00069 | 0.399 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.290 |
MOD_Plk_1 | 579 | 585 | PF00069 | 0.626 |
MOD_Plk_1 | 784 | 790 | PF00069 | 0.449 |
MOD_Plk_1 | 936 | 942 | PF00069 | 0.337 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.425 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.538 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.411 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.496 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.387 |
MOD_Plk_4 | 481 | 487 | PF00069 | 0.328 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.328 |
MOD_Plk_4 | 579 | 585 | PF00069 | 0.602 |
MOD_Plk_4 | 734 | 740 | PF00069 | 0.372 |
MOD_Plk_4 | 868 | 874 | PF00069 | 0.398 |
MOD_ProDKin_1 | 1003 | 1009 | PF00069 | 0.411 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.656 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.651 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.397 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.617 |
MOD_ProDKin_1 | 607 | 613 | PF00069 | 0.617 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.536 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.407 |
TRG_DiLeu_BaEn_1 | 368 | 373 | PF01217 | 0.455 |
TRG_DiLeu_BaEn_1 | 682 | 687 | PF01217 | 0.578 |
TRG_DiLeu_BaEn_2 | 353 | 359 | PF01217 | 0.526 |
TRG_DiLeu_BaEn_4 | 723 | 729 | PF01217 | 0.398 |
TRG_ENDOCYTIC_2 | 1016 | 1019 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 307 | 310 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 492 | 495 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 620 | 623 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 647 | 650 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 713 | 716 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.394 |
TRG_ER_diArg_1 | 1039 | 1041 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 157 | 160 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 162 | 164 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 19 | 21 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 222 | 225 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 264 | 266 | PF00400 | 0.283 |
TRG_ER_diArg_1 | 435 | 438 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 527 | 530 | PF00400 | 0.664 |
TRG_ER_diArg_1 | 675 | 678 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 728 | 730 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 747 | 749 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 991 | 994 | PF00400 | 0.460 |
TRG_NLS_MonoExtC_3 | 991 | 997 | PF00514 | 0.398 |
TRG_NLS_MonoExtN_4 | 991 | 996 | PF00514 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 559 | 563 | PF00026 | 0.545 |
TRG_Pf-PMV_PEXEL_1 | 592 | 596 | PF00026 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 7 | 11 | PF00026 | 0.527 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P391 | Leptomonas seymouri | 62% | 99% |
A0A0S4JKH1 | Bodo saltans | 30% | 84% |
A0A1X0NT41 | Trypanosomatidae | 36% | 100% |
A0A3S7WX21 | Leishmania donovani | 93% | 100% |
A0A422N4N7 | Trypanosoma rangeli | 36% | 100% |
A4HC60 | Leishmania braziliensis | 81% | 100% |
C9ZSC4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 99% |
E9AGY9 | Leishmania infantum | 93% | 100% |
Q4QBY5 | Leishmania major | 92% | 100% |
V5BB69 | Trypanosoma cruzi | 37% | 99% |