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: E9AGY9
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 | 0.396 |
CLV_C14_Caspase3-7 | 135 | 139 | PF00656 | 0.620 |
CLV_C14_Caspase3-7 | 367 | 371 | PF00656 | 0.402 |
CLV_C14_Caspase3-7 | 40 | 44 | PF00656 | 0.562 |
CLV_C14_Caspase3-7 | 542 | 546 | PF00656 | 0.636 |
CLV_NRD_NRD_1 | 1036 | 1038 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 592 | 594 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 689 | 691 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 730 | 732 | PF00675 | 0.387 |
CLV_NRD_NRD_1 | 749 | 751 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 992 | 994 | PF00675 | 0.369 |
CLV_PCSK_FUR_1 | 157 | 161 | PF00082 | 0.462 |
CLV_PCSK_FUR_1 | 222 | 226 | PF00082 | 0.477 |
CLV_PCSK_FUR_1 | 992 | 996 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 691 | 693 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 730 | 732 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 749 | 751 | PF00082 | 0.226 |
CLV_PCSK_KEX2_1 | 839 | 841 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 992 | 994 | PF00082 | 0.335 |
CLV_PCSK_PC1ET2_1 | 300 | 302 | PF00082 | 0.482 |
CLV_PCSK_PC1ET2_1 | 691 | 693 | PF00082 | 0.533 |
CLV_PCSK_PC1ET2_1 | 839 | 841 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 994 | 996 | PF00082 | 0.385 |
CLV_PCSK_PC7_1 | 159 | 165 | PF00082 | 0.493 |
CLV_PCSK_PC7_1 | 726 | 732 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 737 | 741 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 750 | 754 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 778 | 782 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 939 | 943 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 964 | 968 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 985 | 989 | PF00082 | 0.398 |
DEG_APCC_DBOX_1 | 748 | 756 | PF00400 | 0.262 |
DEG_COP1_1 | 609 | 616 | PF00400 | 0.516 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.583 |
DEG_SPOP_SBC_1 | 383 | 387 | PF00917 | 0.537 |
DOC_CKS1_1 | 373 | 378 | PF01111 | 0.400 |
DOC_CKS1_1 | 90 | 95 | PF01111 | 0.565 |
DOC_CYCLIN_yCln2_LP_2 | 437 | 443 | PF00134 | 0.383 |
DOC_MAPK_gen_1 | 391 | 400 | PF00069 | 0.369 |
DOC_MAPK_gen_1 | 436 | 443 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 563 | 573 | PF00069 | 0.522 |
DOC_MAPK_gen_1 | 593 | 601 | PF00069 | 0.525 |
DOC_MAPK_gen_1 | 690 | 698 | PF00069 | 0.532 |
DOC_MAPK_gen_1 | 749 | 760 | PF00069 | 0.398 |
DOC_MAPK_JIP1_4 | 778 | 784 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 112 | 120 | PF00069 | 0.443 |
DOC_PP4_FxxP_1 | 449 | 452 | PF00568 | 0.427 |
DOC_PP4_FxxP_1 | 86 | 89 | PF00568 | 0.418 |
DOC_PP4_FxxP_1 | 929 | 932 | PF00568 | 0.449 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 612 | 616 | PF00917 | 0.528 |
DOC_USP7_UBL2_3 | 1024 | 1028 | PF12436 | 0.596 |
DOC_USP7_UBL2_3 | 753 | 757 | PF12436 | 0.449 |
DOC_WW_Pin1_4 | 1004 | 1009 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 608 | 613 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.426 |
LIG_14-3-3_CanoR_1 | 183 | 188 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 266 | 272 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 350 | 358 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 677 | 682 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 749 | 753 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 798 | 807 | PF00244 | 0.368 |
LIG_14-3-3_CterR_2 | 1041 | 1044 | PF00244 | 0.584 |
LIG_Actin_WH2_2 | 335 | 352 | PF00022 | 0.447 |
LIG_Actin_WH2_2 | 60 | 75 | PF00022 | 0.508 |
LIG_Actin_WH2_2 | 950 | 966 | PF00022 | 0.398 |
LIG_BIR_III_2 | 211 | 215 | PF00653 | 0.558 |
LIG_BIR_III_2 | 59 | 63 | PF00653 | 0.578 |
LIG_BRCT_BRCA1_1 | 197 | 201 | PF00533 | 0.571 |
LIG_BRCT_BRCA1_1 | 354 | 358 | PF00533 | 0.512 |
LIG_BRCT_BRCA1_1 | 416 | 420 | PF00533 | 0.413 |
LIG_BRCT_BRCA1_1 | 846 | 850 | PF00533 | 0.328 |
LIG_BRCT_BRCA1_1 | 918 | 922 | PF00533 | 0.477 |
LIG_BRCT_BRCA1_2 | 416 | 422 | PF00533 | 0.413 |
LIG_Clathr_ClatBox_1 | 1019 | 1023 | PF01394 | 0.449 |
LIG_Clathr_ClatBox_1 | 397 | 401 | PF01394 | 0.413 |
LIG_Clathr_ClatBox_1 | 507 | 511 | PF01394 | 0.539 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.513 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.433 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.362 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.455 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.517 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.396 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.435 |
LIG_FHA_1 | 932 | 938 | PF00498 | 0.465 |
LIG_FHA_1 | 943 | 949 | PF00498 | 0.428 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.492 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.518 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.612 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.649 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.400 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.412 |
LIG_FHA_2 | 678 | 684 | PF00498 | 0.584 |
LIG_FHA_2 | 881 | 887 | PF00498 | 0.329 |
LIG_LIR_Apic_2 | 583 | 589 | PF02991 | 0.497 |
LIG_LIR_Apic_2 | 83 | 89 | PF02991 | 0.456 |
LIG_LIR_Apic_2 | 928 | 932 | PF02991 | 0.470 |
LIG_LIR_Apic_2 | 945 | 950 | PF02991 | 0.197 |
LIG_LIR_Gen_1 | 188 | 195 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 238 | 246 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 249 | 259 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 27 | 35 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 305 | 314 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 490 | 499 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 618 | 627 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 646 | 656 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 662 | 672 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 912 | 922 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 952 | 959 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 188 | 193 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 249 | 255 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 27 | 33 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 305 | 310 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 377 | 382 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 490 | 495 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 532 | 537 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 618 | 624 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 645 | 651 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 662 | 668 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 711 | 717 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 912 | 917 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 952 | 957 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 968 | 974 | PF02991 | 0.195 |
LIG_MLH1_MIPbox_1 | 416 | 420 | PF16413 | 0.413 |
LIG_MYND_3 | 613 | 617 | PF01753 | 0.551 |
LIG_NRBOX | 503 | 509 | PF00104 | 0.481 |
LIG_NRBOX | 671 | 677 | PF00104 | 0.388 |
LIG_Pex14_1 | 124 | 128 | PF04695 | 0.511 |
LIG_Pex14_2 | 817 | 821 | PF04695 | 0.449 |
LIG_PTB_Apo_2 | 899 | 906 | PF02174 | 0.328 |
LIG_PTB_Phospho_1 | 899 | 905 | PF10480 | 0.328 |
LIG_REV1ctd_RIR_1 | 417 | 427 | PF16727 | 0.344 |
LIG_SH2_CRK | 30 | 34 | PF00017 | 0.478 |
LIG_SH2_CRK | 307 | 311 | PF00017 | 0.465 |
LIG_SH2_CRK | 360 | 364 | PF00017 | 0.422 |
LIG_SH2_CRK | 714 | 718 | PF00017 | 0.430 |
LIG_SH2_GRB2like | 576 | 579 | PF00017 | 0.499 |
LIG_SH2_NCK_1 | 463 | 467 | PF00017 | 0.398 |
LIG_SH2_PTP2 | 621 | 624 | PF00017 | 0.380 |
LIG_SH2_PTP2 | 947 | 950 | PF00017 | 0.413 |
LIG_SH2_SRC | 463 | 466 | PF00017 | 0.359 |
LIG_SH2_SRC | 572 | 575 | PF00017 | 0.420 |
LIG_SH2_STAP1 | 414 | 418 | PF00017 | 0.396 |
LIG_SH2_STAP1 | 492 | 496 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 933 | 937 | PF00017 | 0.340 |
LIG_SH2_STAT3 | 165 | 168 | PF00017 | 0.567 |
LIG_SH2_STAT3 | 974 | 977 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 572 | 575 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 576 | 579 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 621 | 624 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 636 | 639 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 864 | 867 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 933 | 936 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 947 | 950 | PF00017 | 0.305 |
LIG_SH3_1 | 360 | 366 | PF00018 | 0.555 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.441 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.633 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.555 |
LIG_SH3_3 | 581 | 587 | PF00018 | 0.496 |
LIG_SH3_3 | 999 | 1005 | PF00018 | 0.475 |
LIG_SH3_4 | 753 | 760 | PF00018 | 0.475 |
LIG_SUMO_SIM_anti_2 | 885 | 891 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 117 | 122 | PF11976 | 0.402 |
LIG_SUMO_SIM_par_1 | 151 | 156 | PF11976 | 0.424 |
LIG_SUMO_SIM_par_1 | 184 | 191 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 377 | 387 | PF11976 | 0.542 |
LIG_SUMO_SIM_par_1 | 396 | 401 | PF11976 | 0.213 |
LIG_SUMO_SIM_par_1 | 693 | 699 | PF11976 | 0.582 |
LIG_TRAF2_1 | 615 | 618 | PF00917 | 0.530 |
LIG_TRAF2_1 | 722 | 725 | PF00917 | 0.398 |
LIG_TYR_ITIM | 619 | 624 | PF00017 | 0.298 |
LIG_WRC_WIRS_1 | 252 | 257 | PF05994 | 0.421 |
MOD_CDK_SPxxK_3 | 89 | 96 | PF00069 | 0.471 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.483 |
MOD_CK1_1 | 1031 | 1037 | PF00069 | 0.665 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.646 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.452 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.328 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.558 |
MOD_CK1_1 | 704 | 710 | PF00069 | 0.575 |
MOD_CK1_1 | 858 | 864 | PF00069 | 0.379 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.447 |
MOD_CK2_1 | 1004 | 1010 | PF00069 | 0.336 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.531 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.560 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.506 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.318 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.466 |
MOD_CK2_1 | 487 | 493 | PF00069 | 0.328 |
MOD_CK2_1 | 612 | 618 | PF00069 | 0.560 |
MOD_CK2_1 | 677 | 683 | PF00069 | 0.587 |
MOD_CK2_1 | 797 | 803 | PF00069 | 0.412 |
MOD_CK2_1 | 882 | 888 | PF00069 | 0.363 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.607 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.573 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.640 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.574 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.585 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.420 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.524 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.550 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.488 |
MOD_GlcNHglycan | 830 | 833 | PF01048 | 0.448 |
MOD_GlcNHglycan | 918 | 921 | PF01048 | 0.465 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.534 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.523 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.431 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.533 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.353 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.578 |
MOD_GSK3_1 | 696 | 703 | PF00069 | 0.570 |
MOD_GSK3_1 | 704 | 711 | PF00069 | 0.507 |
MOD_GSK3_1 | 735 | 742 | PF00069 | 0.371 |
MOD_GSK3_1 | 799 | 806 | PF00069 | 0.344 |
MOD_GSK3_1 | 844 | 851 | PF00069 | 0.335 |
MOD_GSK3_1 | 933 | 940 | PF00069 | 0.318 |
MOD_N-GLC_1 | 144 | 149 | PF02516 | 0.542 |
MOD_N-GLC_1 | 497 | 502 | PF02516 | 0.370 |
MOD_N-GLC_1 | 577 | 582 | PF02516 | 0.517 |
MOD_N-GLC_1 | 75 | 80 | PF02516 | 0.606 |
MOD_NEK2_1 | 1022 | 1027 | PF00069 | 0.448 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.426 |
MOD_NEK2_1 | 696 | 701 | PF00069 | 0.629 |
MOD_NEK2_1 | 740 | 745 | PF00069 | 0.370 |
MOD_NEK2_1 | 843 | 848 | PF00069 | 0.388 |
MOD_NEK2_1 | 879 | 884 | PF00069 | 0.339 |
MOD_NEK2_2 | 216 | 221 | PF00069 | 0.406 |
MOD_NEK2_2 | 414 | 419 | PF00069 | 0.449 |
MOD_NEK2_2 | 848 | 853 | PF00069 | 0.328 |
MOD_PIKK_1 | 352 | 358 | PF00454 | 0.509 |
MOD_PIKK_1 | 464 | 470 | PF00454 | 0.475 |
MOD_PIKK_1 | 704 | 710 | PF00454 | 0.587 |
MOD_PKA_1 | 96 | 102 | PF00069 | 0.480 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.549 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.462 |
MOD_PKA_2 | 562 | 568 | PF00069 | 0.476 |
MOD_PKA_2 | 748 | 754 | PF00069 | 0.347 |
MOD_PKA_2 | 797 | 803 | PF00069 | 0.344 |
MOD_PKB_1 | 527 | 535 | PF00069 | 0.564 |
MOD_Plk_1 | 144 | 150 | PF00069 | 0.514 |
MOD_Plk_1 | 233 | 239 | PF00069 | 0.414 |
MOD_Plk_1 | 245 | 251 | PF00069 | 0.386 |
MOD_Plk_1 | 497 | 503 | PF00069 | 0.320 |
MOD_Plk_1 | 580 | 586 | PF00069 | 0.580 |
MOD_Plk_1 | 75 | 81 | PF00069 | 0.431 |
MOD_Plk_1 | 785 | 791 | PF00069 | 0.449 |
MOD_Plk_1 | 937 | 943 | PF00069 | 0.337 |
MOD_Plk_2-3 | 683 | 689 | PF00069 | 0.467 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.424 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.525 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.404 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.491 |
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 | 529 | 535 | PF00069 | 0.351 |
MOD_Plk_4 | 580 | 586 | PF00069 | 0.556 |
MOD_Plk_4 | 683 | 689 | PF00069 | 0.545 |
MOD_Plk_4 | 735 | 741 | PF00069 | 0.372 |
MOD_Plk_4 | 869 | 875 | PF00069 | 0.398 |
MOD_ProDKin_1 | 1004 | 1010 | PF00069 | 0.411 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.637 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.638 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.397 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.617 |
MOD_ProDKin_1 | 608 | 614 | PF00069 | 0.591 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.422 |
TRG_DiLeu_BaEn_1 | 368 | 373 | PF01217 | 0.455 |
TRG_DiLeu_BaEn_1 | 683 | 688 | PF01217 | 0.578 |
TRG_DiLeu_BaEn_2 | 353 | 359 | PF01217 | 0.523 |
TRG_DiLeu_BaEn_4 | 724 | 730 | PF01217 | 0.398 |
TRG_ENDOCYTIC_2 | 1017 | 1020 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 307 | 310 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 492 | 495 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 621 | 624 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 648 | 651 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 714 | 717 | PF00928 | 0.449 |
TRG_ER_diArg_1 | 157 | 160 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 162 | 164 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 220 | 222 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 224 | 227 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 435 | 438 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 474 | 477 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 527 | 530 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 676 | 679 | PF00400 | 0.565 |
TRG_ER_diArg_1 | 729 | 731 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 748 | 750 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 992 | 995 | PF00400 | 0.417 |
TRG_NLS_MonoExtC_3 | 992 | 998 | PF00514 | 0.398 |
TRG_NLS_MonoExtN_4 | 992 | 997 | PF00514 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 560 | 564 | PF00026 | 0.534 |
TRG_Pf-PMV_PEXEL_1 | 593 | 597 | PF00026 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 7 | 11 | PF00026 | 0.580 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P391 | Leptomonas seymouri | 63% | 99% |
A0A0S4JKH1 | Bodo saltans | 30% | 84% |
A0A1X0NT41 | Trypanosomatidae | 36% | 100% |
A0A3S7WX21 | Leishmania donovani | 100% | 100% |
A0A422N4N7 | Trypanosoma rangeli | 36% | 100% |
A4HC60 | Leishmania braziliensis | 81% | 100% |
C9ZSC4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 99% |
E9AVJ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4QBY5 | Leishmania major | 95% | 100% |
V5BB69 | Trypanosoma cruzi | 37% | 99% |