Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | yes | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: Q4QG44
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 11 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006399 | tRNA metabolic process | 7 | 11 |
GO:0006418 | tRNA aminoacylation for protein translation | 6 | 11 |
GO:0006429 | leucyl-tRNA aminoacylation | 7 | 11 |
GO:0006520 | amino acid metabolic process | 3 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0019752 | carboxylic acid metabolic process | 5 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0034660 | ncRNA metabolic process | 6 | 11 |
GO:0043038 | amino acid activation | 4 | 11 |
GO:0043039 | tRNA aminoacylation | 5 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043436 | oxoacid metabolic process | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044281 | small molecule metabolic process | 2 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0002161 | aminoacyl-tRNA editing activity | 5 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004812 | aminoacyl-tRNA ligase activity | 4 | 11 |
GO:0004823 | leucine-tRNA ligase activity | 5 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 11 |
GO:0016874 | ligase activity | 2 | 11 |
GO:0016875 | ligase activity, forming carbon-oxygen bonds | 3 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0052689 | carboxylic ester hydrolase activity | 4 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 11 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 599 | 603 | PF00656 | 0.349 |
CLV_C14_Caspase3-7 | 760 | 764 | PF00656 | 0.477 |
CLV_NRD_NRD_1 | 1056 | 1058 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.294 |
CLV_NRD_NRD_1 | 863 | 865 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 947 | 949 | PF00675 | 0.500 |
CLV_PCSK_KEX2_1 | 1056 | 1058 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.299 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 863 | 865 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 935 | 937 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 947 | 949 | PF00082 | 0.451 |
CLV_PCSK_PC1ET2_1 | 139 | 141 | PF00082 | 0.630 |
CLV_PCSK_PC1ET2_1 | 227 | 229 | PF00082 | 0.280 |
CLV_PCSK_PC1ET2_1 | 935 | 937 | PF00082 | 0.293 |
CLV_PCSK_PC7_1 | 73 | 79 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 717 | 721 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 731 | 735 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 831 | 835 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 916 | 920 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 931 | 935 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 955 | 959 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.328 |
CLV_Separin_Metazoa | 513 | 517 | PF03568 | 0.575 |
DEG_APCC_DBOX_1 | 5 | 13 | PF00400 | 0.399 |
DEG_APCC_DBOX_1 | 954 | 962 | PF00400 | 0.511 |
DEG_ODPH_VHL_1 | 370 | 381 | PF01847 | 0.528 |
DEG_SPOP_SBC_1 | 917 | 921 | PF00917 | 0.437 |
DOC_ANK_TNKS_1 | 244 | 251 | PF00023 | 0.480 |
DOC_CDC14_PxL_1 | 435 | 443 | PF14671 | 0.575 |
DOC_CKS1_1 | 121 | 126 | PF01111 | 0.725 |
DOC_CYCLIN_yCln2_LP_2 | 366 | 372 | PF00134 | 0.511 |
DOC_MAPK_DCC_7 | 1032 | 1041 | PF00069 | 0.404 |
DOC_MAPK_FxFP_2 | 45 | 48 | PF00069 | 0.480 |
DOC_MAPK_gen_1 | 316 | 326 | PF00069 | 0.575 |
DOC_MAPK_gen_1 | 5 | 12 | PF00069 | 0.423 |
DOC_MAPK_gen_1 | 734 | 742 | PF00069 | 0.480 |
DOC_MAPK_gen_1 | 863 | 871 | PF00069 | 0.528 |
DOC_MAPK_HePTP_8 | 410 | 422 | PF00069 | 0.498 |
DOC_MAPK_HePTP_8 | 861 | 873 | PF00069 | 0.575 |
DOC_MAPK_JIP1_4 | 147 | 153 | PF00069 | 0.531 |
DOC_MAPK_MEF2A_6 | 1032 | 1041 | PF00069 | 0.404 |
DOC_MAPK_MEF2A_6 | 413 | 422 | PF00069 | 0.594 |
DOC_MAPK_MEF2A_6 | 864 | 873 | PF00069 | 0.575 |
DOC_PP1_RVXF_1 | 206 | 213 | PF00149 | 0.493 |
DOC_PP2B_LxvP_1 | 366 | 369 | PF13499 | 0.493 |
DOC_PP4_FxxP_1 | 166 | 169 | PF00568 | 0.396 |
DOC_PP4_FxxP_1 | 28 | 31 | PF00568 | 0.621 |
DOC_PP4_FxxP_1 | 45 | 48 | PF00568 | 0.399 |
DOC_PP4_FxxP_1 | 900 | 903 | PF00568 | 0.493 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 666 | 670 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 710 | 714 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 761 | 765 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 994 | 998 | PF00917 | 0.614 |
DOC_USP7_UBL2_3 | 307 | 311 | PF12436 | 0.569 |
DOC_USP7_UBL2_3 | 419 | 423 | PF12436 | 0.480 |
DOC_USP7_UBL2_3 | 540 | 544 | PF12436 | 0.493 |
DOC_USP7_UBL2_3 | 931 | 935 | PF12436 | 0.493 |
DOC_USP7_UBL2_3 | 986 | 990 | PF12436 | 0.537 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.480 |
LIG_14-3-3_CanoR_1 | 1040 | 1049 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 195 | 205 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 77 | 81 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 916 | 925 | PF00244 | 0.476 |
LIG_Actin_WH2_2 | 910 | 925 | PF00022 | 0.483 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.468 |
LIG_BRCT_BRCA1_1 | 304 | 308 | PF00533 | 0.456 |
LIG_BRCT_BRCA1_1 | 577 | 581 | PF00533 | 0.511 |
LIG_Clathr_ClatBox_1 | 353 | 357 | PF01394 | 0.466 |
LIG_Clathr_ClatBox_1 | 9 | 13 | PF01394 | 0.400 |
LIG_CtBP_PxDLS_1 | 682 | 686 | PF00389 | 0.333 |
LIG_CtBP_PxDLS_1 | 973 | 977 | PF00389 | 0.521 |
LIG_deltaCOP1_diTrp_1 | 192 | 197 | PF00928 | 0.536 |
LIG_deltaCOP1_diTrp_1 | 424 | 430 | PF00928 | 0.511 |
LIG_deltaCOP1_diTrp_1 | 574 | 581 | PF00928 | 0.515 |
LIG_deltaCOP1_diTrp_1 | 711 | 720 | PF00928 | 0.528 |
LIG_EH1_1 | 865 | 873 | PF00400 | 0.536 |
LIG_eIF4E_1 | 256 | 262 | PF01652 | 0.575 |
LIG_eIF4E_1 | 866 | 872 | PF01652 | 0.536 |
LIG_FHA_1 | 1011 | 1017 | PF00498 | 0.451 |
LIG_FHA_1 | 1025 | 1031 | PF00498 | 0.364 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.623 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.669 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.533 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.480 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.480 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.567 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.480 |
LIG_FHA_1 | 592 | 598 | PF00498 | 0.390 |
LIG_FHA_1 | 640 | 646 | PF00498 | 0.455 |
LIG_FHA_1 | 696 | 702 | PF00498 | 0.480 |
LIG_FHA_1 | 781 | 787 | PF00498 | 0.380 |
LIG_FHA_1 | 902 | 908 | PF00498 | 0.550 |
LIG_FHA_1 | 917 | 923 | PF00498 | 0.493 |
LIG_FHA_2 | 1046 | 1052 | PF00498 | 0.583 |
LIG_FHA_2 | 346 | 352 | PF00498 | 0.498 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.493 |
LIG_FHA_2 | 496 | 502 | PF00498 | 0.553 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.493 |
LIG_FHA_2 | 782 | 788 | PF00498 | 0.373 |
LIG_FHA_2 | 817 | 823 | PF00498 | 0.564 |
LIG_FHA_2 | 919 | 925 | PF00498 | 0.437 |
LIG_FHA_2 | 944 | 950 | PF00498 | 0.520 |
LIG_FHA_2 | 969 | 975 | PF00498 | 0.608 |
LIG_IBAR_NPY_1 | 203 | 205 | PF08397 | 0.476 |
LIG_IBAR_NPY_1 | 632 | 634 | PF08397 | 0.529 |
LIG_LIR_Apic_2 | 174 | 178 | PF02991 | 0.385 |
LIG_LIR_Apic_2 | 27 | 31 | PF02991 | 0.566 |
LIG_LIR_Apic_2 | 374 | 380 | PF02991 | 0.483 |
LIG_LIR_Apic_2 | 424 | 429 | PF02991 | 0.566 |
LIG_LIR_Apic_2 | 43 | 48 | PF02991 | 0.408 |
LIG_LIR_Apic_2 | 676 | 682 | PF02991 | 0.336 |
LIG_LIR_Apic_2 | 897 | 903 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 255 | 263 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 402 | 411 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 644 | 653 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 69 | 75 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 800 | 810 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 822 | 833 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 836 | 845 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 882 | 889 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 906 | 917 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 255 | 259 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 402 | 407 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 483 | 489 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 532 | 538 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 541 | 546 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 555 | 561 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 603 | 609 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 613 | 618 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 644 | 649 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 678 | 683 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 800 | 806 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 836 | 841 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 842 | 848 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 882 | 888 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 906 | 912 | PF02991 | 0.488 |
LIG_PCNA_yPIPBox_3 | 808 | 818 | PF02747 | 0.529 |
LIG_Pex14_1 | 172 | 176 | PF04695 | 0.356 |
LIG_Pex14_1 | 193 | 197 | PF04695 | 0.536 |
LIG_Pex14_1 | 426 | 430 | PF04695 | 0.575 |
LIG_Pex14_1 | 534 | 538 | PF04695 | 0.480 |
LIG_Pex14_1 | 81 | 85 | PF04695 | 0.536 |
LIG_Pex14_2 | 67 | 71 | PF04695 | 0.480 |
LIG_Pex14_2 | 806 | 810 | PF04695 | 0.315 |
LIG_PTB_Apo_2 | 200 | 207 | PF02174 | 0.459 |
LIG_PTB_Apo_2 | 640 | 647 | PF02174 | 0.415 |
LIG_PTB_Apo_2 | 832 | 839 | PF02174 | 0.500 |
LIG_SH2_CRK | 106 | 110 | PF00017 | 0.457 |
LIG_SH2_CRK | 256 | 260 | PF00017 | 0.480 |
LIG_SH2_CRK | 373 | 377 | PF00017 | 0.482 |
LIG_SH2_CRK | 486 | 490 | PF00017 | 0.516 |
LIG_SH2_CRK | 650 | 654 | PF00017 | 0.574 |
LIG_SH2_CRK | 909 | 913 | PF00017 | 0.493 |
LIG_SH2_GRB2like | 337 | 340 | PF00017 | 0.543 |
LIG_SH2_GRB2like | 341 | 344 | PF00017 | 0.529 |
LIG_SH2_GRB2like | 404 | 407 | PF00017 | 0.480 |
LIG_SH2_GRB2like | 49 | 52 | PF00017 | 0.480 |
LIG_SH2_NCK_1 | 373 | 377 | PF00017 | 0.536 |
LIG_SH2_NCK_1 | 702 | 706 | PF00017 | 0.480 |
LIG_SH2_NCK_1 | 866 | 870 | PF00017 | 0.528 |
LIG_SH2_SRC | 341 | 344 | PF00017 | 0.575 |
LIG_SH2_SRC | 512 | 515 | PF00017 | 0.511 |
LIG_SH2_SRC | 648 | 651 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 373 | 377 | PF00017 | 0.536 |
LIG_SH2_STAP1 | 866 | 870 | PF00017 | 0.575 |
LIG_SH2_STAP1 | 909 | 913 | PF00017 | 0.493 |
LIG_SH2_STAT3 | 1006 | 1009 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 535 | 538 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 586 | 589 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 610 | 613 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 648 | 651 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 851 | 854 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 945 | 948 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 950 | 953 | PF00017 | 0.408 |
LIG_SH3_1 | 1058 | 1064 | PF00018 | 0.477 |
LIG_SH3_1 | 142 | 148 | PF00018 | 0.585 |
LIG_SH3_3 | 1058 | 1064 | PF00018 | 0.442 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.450 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.586 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.550 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.480 |
LIG_SH3_3 | 260 | 266 | PF00018 | 0.503 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.501 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.499 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.486 |
LIG_SH3_3 | 627 | 633 | PF00018 | 0.347 |
LIG_SH3_3 | 660 | 666 | PF00018 | 0.549 |
LIG_SH3_3 | 872 | 878 | PF00018 | 0.480 |
LIG_SH3_3 | 893 | 899 | PF00018 | 0.522 |
LIG_SUMO_SIM_anti_2 | 867 | 873 | PF11976 | 0.543 |
LIG_SUMO_SIM_par_1 | 434 | 440 | PF11976 | 0.575 |
LIG_SUMO_SIM_par_1 | 524 | 532 | PF11976 | 0.480 |
LIG_SUMO_SIM_par_1 | 7 | 13 | PF11976 | 0.438 |
LIG_TRAF2_1 | 938 | 941 | PF00917 | 0.505 |
LIG_TRFH_1 | 634 | 638 | PF08558 | 0.512 |
LIG_TYR_ITIM | 907 | 912 | PF00017 | 0.493 |
LIG_UBA3_1 | 992 | 1000 | PF00899 | 0.473 |
LIG_WRC_WIRS_1 | 995 | 1000 | PF05994 | 0.473 |
MOD_CDK_SPK_2 | 230 | 235 | PF00069 | 0.575 |
MOD_CDK_SPxxK_3 | 120 | 127 | PF00069 | 0.567 |
MOD_CK1_1 | 1024 | 1030 | PF00069 | 0.506 |
MOD_CK1_1 | 1031 | 1037 | PF00069 | 0.444 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.490 |
MOD_CK1_1 | 601 | 607 | PF00069 | 0.334 |
MOD_CK1_1 | 894 | 900 | PF00069 | 0.544 |
MOD_CK2_1 | 1045 | 1051 | PF00069 | 0.539 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.565 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.493 |
MOD_CK2_1 | 519 | 525 | PF00069 | 0.480 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.480 |
MOD_CK2_1 | 738 | 744 | PF00069 | 0.480 |
MOD_CK2_1 | 781 | 787 | PF00069 | 0.423 |
MOD_CK2_1 | 816 | 822 | PF00069 | 0.564 |
MOD_CK2_1 | 918 | 924 | PF00069 | 0.437 |
MOD_CK2_1 | 943 | 949 | PF00069 | 0.472 |
MOD_CK2_1 | 968 | 974 | PF00069 | 0.500 |
MOD_Cter_Amidation | 225 | 228 | PF01082 | 0.280 |
MOD_Cter_Amidation | 75 | 78 | PF01082 | 0.293 |
MOD_Cter_Amidation | 861 | 864 | PF01082 | 0.328 |
MOD_GlcNHglycan | 1033 | 1036 | PF01048 | 0.392 |
MOD_GlcNHglycan | 1042 | 1045 | PF01048 | 0.431 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.795 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.293 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.311 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.302 |
MOD_GlcNHglycan | 687 | 690 | PF01048 | 0.280 |
MOD_GlcNHglycan | 799 | 802 | PF01048 | 0.548 |
MOD_GSK3_1 | 1024 | 1031 | PF00069 | 0.434 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.559 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.437 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.351 |
MOD_GSK3_1 | 789 | 796 | PF00069 | 0.485 |
MOD_GSK3_1 | 839 | 846 | PF00069 | 0.483 |
MOD_GSK3_1 | 912 | 919 | PF00069 | 0.580 |
MOD_N-GLC_1 | 1024 | 1029 | PF02516 | 0.484 |
MOD_N-GLC_1 | 405 | 410 | PF02516 | 0.280 |
MOD_N-GLC_1 | 458 | 463 | PF02516 | 0.375 |
MOD_N-GLC_1 | 810 | 815 | PF02516 | 0.362 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.493 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.538 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.343 |
MOD_NEK2_1 | 685 | 690 | PF00069 | 0.315 |
MOD_NEK2_1 | 732 | 737 | PF00069 | 0.480 |
MOD_NEK2_1 | 780 | 785 | PF00069 | 0.375 |
MOD_NEK2_1 | 810 | 815 | PF00069 | 0.493 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.480 |
MOD_NEK2_1 | 884 | 889 | PF00069 | 0.477 |
MOD_NEK2_1 | 907 | 912 | PF00069 | 0.541 |
MOD_NEK2_1 | 918 | 923 | PF00069 | 0.521 |
MOD_NEK2_2 | 287 | 292 | PF00069 | 0.480 |
MOD_NEK2_2 | 372 | 377 | PF00069 | 0.536 |
MOD_NEK2_2 | 666 | 671 | PF00069 | 0.447 |
MOD_PIKK_1 | 1010 | 1016 | PF00454 | 0.480 |
MOD_PIKK_1 | 265 | 271 | PF00454 | 0.553 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.480 |
MOD_PIKK_1 | 843 | 849 | PF00454 | 0.493 |
MOD_PIKK_1 | 894 | 900 | PF00454 | 0.575 |
MOD_PIKK_1 | 924 | 930 | PF00454 | 0.497 |
MOD_PKA_2 | 1031 | 1037 | PF00069 | 0.506 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.508 |
MOD_PKA_2 | 685 | 691 | PF00069 | 0.315 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.511 |
MOD_PKA_2 | 771 | 777 | PF00069 | 0.462 |
MOD_Plk_1 | 1028 | 1034 | PF00069 | 0.518 |
MOD_Plk_1 | 1045 | 1051 | PF00069 | 0.380 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.459 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.538 |
MOD_Plk_1 | 405 | 411 | PF00069 | 0.480 |
MOD_Plk_1 | 565 | 571 | PF00069 | 0.480 |
MOD_Plk_1 | 601 | 607 | PF00069 | 0.325 |
MOD_Plk_1 | 751 | 757 | PF00069 | 0.480 |
MOD_Plk_1 | 810 | 816 | PF00069 | 0.521 |
MOD_Plk_1 | 843 | 849 | PF00069 | 0.486 |
MOD_Plk_1 | 907 | 913 | PF00069 | 0.543 |
MOD_Plk_2-3 | 1045 | 1051 | PF00069 | 0.593 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.459 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.510 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.473 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.528 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.518 |
MOD_Plk_4 | 591 | 597 | PF00069 | 0.377 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.220 |
MOD_Plk_4 | 695 | 701 | PF00069 | 0.493 |
MOD_Plk_4 | 781 | 787 | PF00069 | 0.452 |
MOD_Plk_4 | 813 | 819 | PF00069 | 0.511 |
MOD_Plk_4 | 884 | 890 | PF00069 | 0.548 |
MOD_Plk_4 | 891 | 897 | PF00069 | 0.482 |
MOD_Plk_4 | 907 | 913 | PF00069 | 0.480 |
MOD_Plk_4 | 994 | 1000 | PF00069 | 0.601 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.629 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.480 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.480 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.480 |
MOD_SUMO_for_1 | 1072 | 1075 | PF00179 | 0.604 |
MOD_SUMO_for_1 | 318 | 321 | PF00179 | 0.528 |
MOD_SUMO_for_1 | 422 | 425 | PF00179 | 0.480 |
MOD_SUMO_rev_2 | 115 | 121 | PF00179 | 0.600 |
MOD_SUMO_rev_2 | 182 | 187 | PF00179 | 0.536 |
MOD_SUMO_rev_2 | 268 | 278 | PF00179 | 0.483 |
MOD_SUMO_rev_2 | 462 | 470 | PF00179 | 0.495 |
MOD_SUMO_rev_2 | 492 | 496 | PF00179 | 0.575 |
MOD_SUMO_rev_2 | 537 | 546 | PF00179 | 0.474 |
MOD_SUMO_rev_2 | 711 | 716 | PF00179 | 0.572 |
TRG_DiLeu_BaEn_1 | 444 | 449 | PF01217 | 0.437 |
TRG_DiLeu_BaEn_1 | 668 | 673 | PF01217 | 0.432 |
TRG_DiLeu_BaEn_1 | 867 | 872 | PF01217 | 0.480 |
TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 486 | 489 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 512 | 515 | PF00928 | 0.575 |
TRG_ENDOCYTIC_2 | 609 | 612 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 650 | 653 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 803 | 806 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 825 | 828 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 865 | 868 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 909 | 912 | PF00928 | 0.493 |
TRG_ER_diArg_1 | 193 | 195 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 217 | 219 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 863 | 865 | PF00400 | 0.538 |
TRG_NLS_MonoExtC_3 | 933 | 938 | PF00514 | 0.493 |
TRG_NLS_MonoExtN_4 | 137 | 143 | PF00514 | 0.630 |
TRG_NLS_MonoExtN_4 | 931 | 938 | PF00514 | 0.493 |
TRG_Pf-PMV_PEXEL_1 | 1040 | 1045 | PF00026 | 0.487 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0Z6 | Leptomonas seymouri | 78% | 100% |
A0A0S4J826 | Bodo saltans | 62% | 99% |
A0A1X0NNK0 | Trypanosomatidae | 65% | 100% |
A0A3Q8II14 | Leishmania donovani | 96% | 100% |
A0A422NLI7 | Trypanosoma rangeli | 65% | 100% |
A0B7B7 | Methanothrix thermoacetophila (strain DSM 6194 / JCM 14653 / NBRC 101360 / PT) | 31% | 100% |
A1RTX9 | Pyrobaculum islandicum (strain DSM 4184 / JCM 9189 / GEO3) | 29% | 100% |
A3DKS1 | Staphylothermus marinus (strain ATCC 43588 / DSM 3639 / JCM 9404 / F1) | 29% | 100% |
A3MU00 | Pyrobaculum calidifontis (strain DSM 21063 / JCM 11548 / VA1) | 29% | 100% |
A4FYA3 | Methanococcus maripaludis (strain C5 / ATCC BAA-1333) | 30% | 100% |
A4H796 | Leishmania braziliensis | 92% | 100% |
A4HVN8 | Leishmania infantum | 96% | 100% |
A4WHK6 | Pyrobaculum arsenaticum (strain DSM 13514 / JCM 11321 / PZ6) | 28% | 100% |
A4YE96 | Metallosphaera sedula (strain ATCC 51363 / DSM 5348 / JCM 9185 / NBRC 15509 / TH2) | 27% | 100% |
A4YI28 | Metallosphaera sedula (strain ATCC 51363 / DSM 5348 / JCM 9185 / NBRC 15509 / TH2) | 28% | 100% |
A6USJ5 | Methanococcus vannielii (strain ATCC 35089 / DSM 1224 / JCM 13029 / OCM 148 / SB) | 29% | 100% |
A6UTK3 | Methanococcus aeolicus (strain ATCC BAA-1280 / DSM 17508 / OCM 812 / Nankai-3) | 29% | 100% |
A6VK04 | Methanococcus maripaludis (strain C7 / ATCC BAA-1331) | 30% | 100% |
A8A8T2 | Ignicoccus hospitalis (strain KIN4/I / DSM 18386 / JCM 14125) | 29% | 100% |
B1YAS9 | Pyrobaculum neutrophilum (strain DSM 2338 / JCM 9278 / NBRC 100436 / V24Sta) | 30% | 100% |
B6YST9 | Thermococcus onnurineus (strain NA1) | 30% | 100% |
E9APD4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
F4I116 | Arabidopsis thaliana | 42% | 99% |
O27552 | Methanothermobacter thermautotrophicus (strain ATCC 29096 / DSM 1053 / JCM 10044 / NBRC 100330 / Delta H) | 28% | 100% |
O30250 | Archaeoglobus fulgidus (strain ATCC 49558 / DSM 4304 / JCM 9628 / NBRC 100126 / VC-16) | 31% | 100% |
O33768 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 28% | 100% |
O58698 | Pyrococcus horikoshii (strain ATCC 700860 / DSM 12428 / JCM 9974 / NBRC 100139 / OT-3) | 29% | 100% |
P10857 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 37% | 96% |
P26637 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 39% | 99% |
P58176 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 24% | 100% |
Q09996 | Caenorhabditis elegans | 44% | 91% |
Q10490 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 39% | 97% |
Q12WA2 | Methanococcoides burtonii (strain DSM 6242 / NBRC 107633 / OCM 468 / ACE-M) | 30% | 100% |
Q46AW0 | Methanosarcina barkeri (strain Fusaro / DSM 804) | 30% | 100% |
Q4J8J7 | Sulfolobus acidocaldarius (strain ATCC 33909 / DSM 639 / JCM 8929 / NBRC 15157 / NCIMB 11770) | 28% | 100% |
Q4JBP0 | Sulfolobus acidocaldarius (strain ATCC 33909 / DSM 639 / JCM 8929 / NBRC 15157 / NCIMB 11770) | 25% | 100% |
Q54N83 | Dictyostelium discoideum | 42% | 100% |
Q58050 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 29% | 100% |
Q5R614 | Pongo abelii | 42% | 91% |
Q6LZD2 | Methanococcus maripaludis (strain S2 / LL) | 30% | 100% |
Q8BMJ2 | Mus musculus | 41% | 91% |
Q8NKR7 | Thermococcus kodakarensis (strain ATCC BAA-918 / JCM 12380 / KOD1) | 30% | 100% |
Q8Q054 | Methanosarcina mazei (strain ATCC BAA-159 / DSM 3647 / Goe1 / Go1 / JCM 11833 / OCM 88) | 30% | 100% |
Q8TQD3 | Methanosarcina acetivorans (strain ATCC 35395 / DSM 2834 / JCM 12185 / C2A) | 30% | 100% |
Q8TVM4 | Methanopyrus kandleri (strain AV19 / DSM 6324 / JCM 9639 / NBRC 100938) | 30% | 100% |
Q8U2E6 | Pyrococcus furiosus (strain ATCC 43587 / DSM 3638 / JCM 8422 / Vc1) | 30% | 100% |
Q8ZXT6 | Pyrobaculum aerophilum (strain ATCC 51768 / DSM 7523 / JCM 9630 / CIP 104966 / NBRC 100827 / IM2) | 29% | 100% |
Q970Z6 | Sulfurisphaera tokodaii (strain DSM 16993 / JCM 10545 / NBRC 100140 / 7) | 29% | 100% |
Q974N4 | Sulfurisphaera tokodaii (strain DSM 16993 / JCM 10545 / NBRC 100140 / 7) | 27% | 100% |
Q97AN8 | Thermoplasma volcanium (strain ATCC 51530 / DSM 4299 / JCM 9571 / NBRC 15438 / GSS1) | 27% | 100% |
Q9HK31 | Thermoplasma acidophilum (strain ATCC 25905 / DSM 1728 / JCM 9062 / NBRC 15155 / AMRC-C165) | 29% | 100% |
Q9P2J5 | Homo sapiens | 42% | 91% |
Q9V0B9 | Pyrococcus abyssi (strain GE5 / Orsay) | 28% | 100% |
Q9YD97 | Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1) | 35% | 100% |
V5B774 | Trypanosoma cruzi | 66% | 100% |