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: A4HC60
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:0000166 | nucleotide binding | 3 | 3 |
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:0004484 | mRNA guanylyltransferase activity | 5 | 3 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 3 |
GO:0005525 | GTP binding | 5 | 3 |
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:0008192 | RNA guanylyltransferase activity | 4 | 3 |
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:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 4 |
GO:0016779 | nucleotidyltransferase activity | 4 | 4 |
GO:0017076 | purine nucleotide binding | 4 | 3 |
GO:0019001 | guanyl nucleotide binding | 5 | 3 |
GO:0030554 | adenyl nucleotide binding | 5 | 3 |
GO:0032553 | ribonucleotide binding | 3 | 3 |
GO:0032555 | purine ribonucleotide binding | 4 | 3 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 3 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 3 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 3 |
GO:0036094 | small molecule binding | 2 | 3 |
GO:0043167 | ion binding | 2 | 3 |
GO:0043168 | anion binding | 3 | 3 |
GO:0070568 | guanylyltransferase activity | 5 | 3 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 3 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 3 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.321 |
CLV_C14_Caspase3-7 | 135 | 139 | PF00656 | 0.534 |
CLV_C14_Caspase3-7 | 366 | 370 | PF00656 | 0.324 |
CLV_C14_Caspase3-7 | 540 | 544 | PF00656 | 0.646 |
CLV_C14_Caspase3-7 | 880 | 884 | PF00656 | 0.238 |
CLV_C14_Caspase3-7 | 997 | 1001 | PF00656 | 0.187 |
CLV_NRD_NRD_1 | 1038 | 1040 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 590 | 592 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 689 | 691 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 728 | 730 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.262 |
CLV_NRD_NRD_1 | 989 | 991 | PF00675 | 0.409 |
CLV_PCSK_KEX2_1 | 1038 | 1040 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 515 | 517 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 688 | 690 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 728 | 730 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 836 | 838 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 991 | 993 | PF00082 | 0.183 |
CLV_PCSK_PC1ET2_1 | 515 | 517 | PF00082 | 0.300 |
CLV_PCSK_PC1ET2_1 | 836 | 838 | PF00082 | 0.325 |
CLV_PCSK_PC1ET2_1 | 991 | 993 | PF00082 | 0.322 |
CLV_PCSK_PC7_1 | 724 | 730 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 549 | 553 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 735 | 739 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 747 | 751 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 776 | 780 | PF00082 | 0.307 |
DEG_APCC_DBOX_1 | 158 | 166 | PF00400 | 0.295 |
DEG_COP1_1 | 607 | 614 | PF00400 | 0.421 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.526 |
DOC_AGCK_PIF_1 | 281 | 286 | PF00069 | 0.209 |
DOC_CKS1_1 | 372 | 377 | PF01111 | 0.327 |
DOC_CKS1_1 | 90 | 95 | PF01111 | 0.393 |
DOC_CKS1_1 | 926 | 931 | PF01111 | 0.187 |
DOC_CYCLIN_RxL_1 | 390 | 400 | PF00134 | 0.332 |
DOC_CYCLIN_yCln2_LP_2 | 436 | 442 | PF00134 | 0.412 |
DOC_CYCLIN_yCln2_LP_2 | 750 | 756 | PF00134 | 0.378 |
DOC_MAPK_gen_1 | 390 | 399 | PF00069 | 0.305 |
DOC_MAPK_gen_1 | 435 | 442 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 561 | 571 | PF00069 | 0.478 |
DOC_MAPK_gen_1 | 591 | 599 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 688 | 696 | PF00069 | 0.500 |
DOC_MAPK_gen_1 | 96 | 102 | PF00069 | 0.255 |
DOC_MAPK_gen_1 | 976 | 986 | PF00069 | 0.187 |
DOC_MAPK_JIP1_4 | 776 | 782 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 112 | 120 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 234 | 243 | PF00069 | 0.242 |
DOC_PP1_RVXF_1 | 913 | 920 | PF00149 | 0.371 |
DOC_PP2B_LxvP_1 | 750 | 753 | PF13499 | 0.262 |
DOC_PP4_FxxP_1 | 448 | 451 | PF00568 | 0.375 |
DOC_PP4_FxxP_1 | 86 | 89 | PF00568 | 0.330 |
DOC_PP4_FxxP_1 | 926 | 929 | PF00568 | 0.409 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.397 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.187 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 722 | 726 | PF00917 | 0.312 |
DOC_USP7_UBL2_3 | 1021 | 1025 | PF12436 | 0.456 |
DOC_USP7_UBL2_3 | 751 | 755 | PF12436 | 0.409 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.318 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.338 |
DOC_WW_Pin1_4 | 925 | 930 | PF00397 | 0.323 |
DOC_WW_Pin1_4 | 998 | 1003 | PF00397 | 0.361 |
LIG_14-3-3_CanoR_1 | 175 | 181 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 183 | 188 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 226 | 231 | PF00244 | 0.309 |
LIG_14-3-3_CanoR_1 | 265 | 271 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 349 | 358 | PF00244 | 0.394 |
LIG_14-3-3_CanoR_1 | 675 | 680 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 710 | 716 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 796 | 805 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 905 | 911 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 990 | 999 | PF00244 | 0.187 |
LIG_APCC_ABBA_1 | 239 | 244 | PF00400 | 0.214 |
LIG_BIR_III_4 | 533 | 537 | PF00653 | 0.425 |
LIG_BRCT_BRCA1_1 | 197 | 201 | PF00533 | 0.571 |
LIG_BRCT_BRCA1_1 | 353 | 357 | PF00533 | 0.435 |
LIG_BRCT_BRCA1_1 | 415 | 419 | PF00533 | 0.396 |
LIG_BRCT_BRCA1_1 | 843 | 847 | PF00533 | 0.264 |
LIG_BRCT_BRCA1_1 | 915 | 919 | PF00533 | 0.459 |
LIG_BRCT_BRCA1_2 | 415 | 421 | PF00533 | 0.421 |
LIG_Clathr_ClatBox_1 | 1016 | 1020 | PF01394 | 0.409 |
LIG_Clathr_ClatBox_1 | 396 | 400 | PF01394 | 0.391 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.507 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.308 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.439 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.404 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.502 |
LIG_FHA_1 | 550 | 556 | PF00498 | 0.389 |
LIG_FHA_1 | 926 | 932 | PF00498 | 0.450 |
LIG_FHA_1 | 940 | 946 | PF00498 | 0.377 |
LIG_FHA_1 | 959 | 965 | PF00498 | 0.145 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.467 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.562 |
LIG_FHA_2 | 245 | 251 | PF00498 | 0.535 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.301 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.606 |
LIG_FHA_2 | 364 | 370 | PF00498 | 0.322 |
LIG_FHA_2 | 372 | 378 | PF00498 | 0.323 |
LIG_FHA_2 | 676 | 682 | PF00498 | 0.437 |
LIG_FHA_2 | 878 | 884 | PF00498 | 0.264 |
LIG_FHA_2 | 908 | 914 | PF00498 | 0.270 |
LIG_LIR_Apic_2 | 85 | 89 | PF02991 | 0.342 |
LIG_LIR_Apic_2 | 923 | 929 | PF02991 | 0.311 |
LIG_LIR_Apic_2 | 942 | 947 | PF02991 | 0.172 |
LIG_LIR_Gen_1 | 211 | 219 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 237 | 245 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 248 | 258 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 304 | 313 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 489 | 498 | PF02991 | 0.386 |
LIG_LIR_Gen_1 | 616 | 625 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 644 | 654 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 660 | 670 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 81 | 90 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 909 | 919 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 949 | 956 | PF02991 | 0.412 |
LIG_LIR_LC3C_4 | 691 | 696 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 304 | 309 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 489 | 494 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 616 | 622 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 643 | 649 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 660 | 666 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 81 | 86 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 909 | 914 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 949 | 954 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 965 | 971 | PF02991 | 0.181 |
LIG_MLH1_MIPbox_1 | 415 | 419 | PF16413 | 0.396 |
LIG_MYND_3 | 611 | 615 | PF01753 | 0.502 |
LIG_NRBOX | 502 | 508 | PF00104 | 0.426 |
LIG_NRBOX | 669 | 675 | PF00104 | 0.326 |
LIG_Pex14_1 | 124 | 128 | PF04695 | 0.483 |
LIG_Pex14_2 | 814 | 818 | PF04695 | 0.409 |
LIG_PTB_Apo_2 | 896 | 903 | PF02174 | 0.264 |
LIG_PTB_Phospho_1 | 896 | 902 | PF10480 | 0.264 |
LIG_REV1ctd_RIR_1 | 416 | 426 | PF16727 | 0.403 |
LIG_SH2_CRK | 306 | 310 | PF00017 | 0.403 |
LIG_SH2_CRK | 712 | 716 | PF00017 | 0.522 |
LIG_SH2_GRB2like | 570 | 573 | PF00017 | 0.471 |
LIG_SH2_GRB2like | 574 | 577 | PF00017 | 0.498 |
LIG_SH2_NCK_1 | 712 | 716 | PF00017 | 0.353 |
LIG_SH2_PTP2 | 619 | 622 | PF00017 | 0.308 |
LIG_SH2_PTP2 | 944 | 947 | PF00017 | 0.357 |
LIG_SH2_SRC | 570 | 573 | PF00017 | 0.330 |
LIG_SH2_STAP1 | 491 | 495 | PF00017 | 0.409 |
LIG_SH2_STAP1 | 712 | 716 | PF00017 | 0.416 |
LIG_SH2_STAP1 | 902 | 906 | PF00017 | 0.213 |
LIG_SH2_STAT3 | 971 | 974 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 570 | 573 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 574 | 577 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 619 | 622 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 634 | 637 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 861 | 864 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 930 | 933 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 944 | 947 | PF00017 | 0.244 |
LIG_SH3_1 | 359 | 365 | PF00018 | 0.390 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.391 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.610 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.390 |
LIG_SH3_3 | 579 | 585 | PF00018 | 0.493 |
LIG_SH3_3 | 693 | 699 | PF00018 | 0.561 |
LIG_SH3_3 | 996 | 1002 | PF00018 | 0.325 |
LIG_SH3_4 | 751 | 758 | PF00018 | 0.325 |
LIG_SUMO_SIM_par_1 | 117 | 122 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 150 | 156 | PF11976 | 0.375 |
LIG_SUMO_SIM_par_1 | 201 | 211 | PF11976 | 0.322 |
LIG_SUMO_SIM_par_1 | 377 | 385 | PF11976 | 0.489 |
LIG_SUMO_SIM_par_1 | 395 | 400 | PF11976 | 0.316 |
LIG_SUMO_SIM_par_1 | 691 | 697 | PF11976 | 0.523 |
LIG_SUMO_SIM_par_1 | 960 | 966 | PF11976 | 0.361 |
LIG_TRAF2_1 | 613 | 616 | PF00917 | 0.477 |
LIG_UBA3_1 | 417 | 422 | PF00899 | 0.385 |
LIG_UBA3_1 | 503 | 510 | PF00899 | 0.389 |
LIG_WRC_WIRS_1 | 251 | 256 | PF05994 | 0.358 |
MOD_CDK_SPxxK_3 | 1001 | 1008 | PF00069 | 0.187 |
MOD_CDK_SPxxK_3 | 89 | 96 | PF00069 | 0.388 |
MOD_CK1_1 | 1001 | 1007 | PF00069 | 0.297 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.458 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.444 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.481 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.630 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.264 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.499 |
MOD_CK1_1 | 907 | 913 | PF00069 | 0.270 |
MOD_CK1_1 | 922 | 928 | PF00069 | 0.273 |
MOD_CK2_1 | 1001 | 1007 | PF00069 | 0.270 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.477 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.519 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.515 |
MOD_CK2_1 | 298 | 304 | PF00069 | 0.425 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.300 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.250 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.264 |
MOD_CK2_1 | 610 | 616 | PF00069 | 0.510 |
MOD_CK2_1 | 675 | 681 | PF00069 | 0.438 |
MOD_CK2_1 | 795 | 801 | PF00069 | 0.383 |
MOD_CK2_1 | 879 | 885 | PF00069 | 0.297 |
MOD_CK2_1 | 907 | 913 | PF00069 | 0.392 |
MOD_Cter_Amidation | 1036 | 1039 | PF01082 | 0.486 |
MOD_Cter_Amidation | 809 | 812 | PF01082 | 0.187 |
MOD_GlcNHglycan | 138 | 142 | PF01048 | 0.621 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.488 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.544 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.424 |
MOD_GlcNHglycan | 533 | 537 | PF01048 | 0.572 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.505 |
MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.459 |
MOD_GlcNHglycan | 825 | 830 | PF01048 | 0.441 |
MOD_GlcNHglycan | 906 | 909 | PF01048 | 0.478 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.552 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.469 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.486 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.474 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.500 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.427 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.287 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.518 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.279 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.315 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.397 |
MOD_GSK3_1 | 694 | 701 | PF00069 | 0.511 |
MOD_GSK3_1 | 733 | 740 | PF00069 | 0.348 |
MOD_GSK3_1 | 797 | 804 | PF00069 | 0.279 |
MOD_GSK3_1 | 841 | 848 | PF00069 | 0.278 |
MOD_N-GLC_1 | 144 | 149 | PF02516 | 0.406 |
MOD_N-GLC_1 | 496 | 501 | PF02516 | 0.305 |
MOD_N-GLC_1 | 575 | 580 | PF02516 | 0.536 |
MOD_N-GLC_1 | 75 | 80 | PF02516 | 0.526 |
MOD_NEK2_1 | 1019 | 1024 | PF00069 | 0.387 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.390 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.465 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.580 |
MOD_NEK2_1 | 694 | 699 | PF00069 | 0.591 |
MOD_NEK2_1 | 702 | 707 | PF00069 | 0.529 |
MOD_NEK2_1 | 738 | 743 | PF00069 | 0.333 |
MOD_NEK2_1 | 824 | 829 | PF00069 | 0.472 |
MOD_NEK2_1 | 840 | 845 | PF00069 | 0.352 |
MOD_NEK2_1 | 876 | 881 | PF00069 | 0.274 |
MOD_NEK2_2 | 413 | 418 | PF00069 | 0.448 |
MOD_NEK2_2 | 553 | 558 | PF00069 | 0.236 |
MOD_NEK2_2 | 845 | 850 | PF00069 | 0.264 |
MOD_PIKK_1 | 351 | 357 | PF00454 | 0.381 |
MOD_PIKK_1 | 463 | 469 | PF00454 | 0.367 |
MOD_PIKK_1 | 702 | 708 | PF00454 | 0.532 |
MOD_PKA_1 | 990 | 996 | PF00069 | 0.202 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.613 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.515 |
MOD_PKA_2 | 560 | 566 | PF00069 | 0.422 |
MOD_PKA_2 | 795 | 801 | PF00069 | 0.328 |
MOD_PKA_2 | 904 | 910 | PF00069 | 0.187 |
MOD_PKA_2 | 991 | 997 | PF00069 | 0.199 |
MOD_PKB_1 | 224 | 232 | PF00069 | 0.238 |
MOD_Plk_1 | 144 | 150 | PF00069 | 0.488 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.502 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.346 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.326 |
MOD_Plk_1 | 496 | 502 | PF00069 | 0.257 |
MOD_Plk_1 | 578 | 584 | PF00069 | 0.496 |
MOD_Plk_1 | 636 | 642 | PF00069 | 0.240 |
MOD_Plk_1 | 783 | 789 | PF00069 | 0.409 |
MOD_Plk_1 | 934 | 940 | PF00069 | 0.282 |
MOD_Plk_2-3 | 245 | 251 | PF00069 | 0.250 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.365 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.414 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.522 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.340 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.405 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.446 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.365 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.264 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.264 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.435 |
MOD_Plk_4 | 578 | 584 | PF00069 | 0.613 |
MOD_Plk_4 | 681 | 687 | PF00069 | 0.418 |
MOD_Plk_4 | 733 | 739 | PF00069 | 0.308 |
MOD_Plk_4 | 958 | 964 | PF00069 | 0.264 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.615 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.327 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.335 |
MOD_ProDKin_1 | 925 | 931 | PF00069 | 0.323 |
MOD_ProDKin_1 | 998 | 1004 | PF00069 | 0.361 |
MOD_SUMO_rev_2 | 907 | 917 | PF00179 | 0.187 |
MOD_SUMO_rev_2 | 973 | 980 | PF00179 | 0.187 |
TRG_DiLeu_BaEn_1 | 367 | 372 | PF01217 | 0.382 |
TRG_DiLeu_BaEn_1 | 681 | 686 | PF01217 | 0.435 |
TRG_DiLeu_BaEn_2 | 249 | 255 | PF01217 | 0.245 |
TRG_DiLeu_BaEn_2 | 352 | 358 | PF01217 | 0.484 |
TRG_DiLeu_BaEn_2 | 545 | 551 | PF01217 | 0.274 |
TRG_ENDOCYTIC_2 | 1014 | 1017 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 306 | 309 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 491 | 494 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 619 | 622 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 646 | 649 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 712 | 715 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.344 |
TRG_ER_diArg_1 | 100 | 103 | PF00400 | 0.382 |
TRG_ER_diArg_1 | 19 | 21 | PF00400 | 0.332 |
TRG_ER_diArg_1 | 434 | 437 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 473 | 476 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 526 | 529 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 674 | 677 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 688 | 690 | PF00400 | 0.273 |
TRG_ER_diArg_1 | 727 | 729 | PF00400 | 0.361 |
TRG_NES_CRM1_1 | 608 | 621 | PF08389 | 0.282 |
TRG_Pf-PMV_PEXEL_1 | 558 | 562 | PF00026 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 591 | 595 | PF00026 | 0.400 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P391 | Leptomonas seymouri | 60% | 99% |
A0A0S4JKH1 | Bodo saltans | 32% | 84% |
A0A1X0NT41 | Trypanosomatidae | 34% | 100% |
A0A3S7WX21 | Leishmania donovani | 81% | 100% |
A0A422N4N7 | Trypanosoma rangeli | 36% | 100% |
C9ZSC4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 99% |
E9AGY9 | Leishmania infantum | 81% | 100% |
E9AVJ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4QBY5 | Leishmania major | 80% | 100% |
V5BB69 | Trypanosoma cruzi | 37% | 99% |