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 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0031974 | membrane-enclosed lumen | 2 | 2 |
GO:0031981 | nuclear lumen | 5 | 2 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043233 | organelle lumen | 3 | 2 |
GO:0070013 | intracellular organelle lumen | 4 | 2 |
GO:0097014 | ciliary plasm | 5 | 2 |
GO:0099568 | cytoplasmic region | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0005694 | chromosome | 5 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: Q4Q199
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006265 | DNA topological change | 5 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006996 | organelle organization | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0051276 | chromosome organization | 5 | 12 |
GO:0071103 | DNA conformation change | 6 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003916 | DNA topoisomerase activity | 3 | 12 |
GO:0003917 | DNA topoisomerase type I (single strand cut, ATP-independent) activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008270 | zinc ion binding | 6 | 11 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0046914 | transition metal ion binding | 5 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 328 | 332 | PF00656 | 0.323 |
CLV_C14_Caspase3-7 | 492 | 496 | PF00656 | 0.393 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 881 | 883 | PF00675 | 0.690 |
CLV_NRD_NRD_1 | 922 | 924 | PF00675 | 0.345 |
CLV_PCSK_FUR_1 | 928 | 932 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 519 | 521 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 599 | 601 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 881 | 883 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 930 | 932 | PF00082 | 0.334 |
CLV_PCSK_PC1ET2_1 | 131 | 133 | PF00082 | 0.310 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.265 |
CLV_PCSK_PC1ET2_1 | 162 | 164 | PF00082 | 0.428 |
CLV_PCSK_PC1ET2_1 | 519 | 521 | PF00082 | 0.290 |
CLV_PCSK_PC1ET2_1 | 599 | 601 | PF00082 | 0.541 |
CLV_PCSK_PC1ET2_1 | 930 | 932 | PF00082 | 0.380 |
CLV_PCSK_PC7_1 | 280 | 286 | PF00082 | 0.344 |
CLV_PCSK_PC7_1 | 515 | 521 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 930 | 934 | PF00082 | 0.317 |
CLV_Separin_Metazoa | 342 | 346 | PF03568 | 0.392 |
DEG_APCC_DBOX_1 | 147 | 155 | PF00400 | 0.439 |
DEG_APCC_DBOX_1 | 396 | 404 | PF00400 | 0.316 |
DEG_APCC_DBOX_1 | 405 | 413 | PF00400 | 0.291 |
DEG_APCC_DBOX_1 | 86 | 94 | PF00400 | 0.516 |
DOC_ANK_TNKS_1 | 816 | 823 | PF00023 | 0.588 |
DOC_MAPK_DCC_7 | 817 | 825 | PF00069 | 0.582 |
DOC_MAPK_gen_1 | 131 | 137 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 284 | 290 | PF00069 | 0.374 |
DOC_MAPK_gen_1 | 397 | 405 | PF00069 | 0.379 |
DOC_MAPK_gen_1 | 836 | 843 | PF00069 | 0.500 |
DOC_MAPK_MEF2A_6 | 103 | 111 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 171 | 178 | PF00069 | 0.323 |
DOC_MAPK_MEF2A_6 | 552 | 559 | PF00069 | 0.307 |
DOC_MAPK_MEF2A_6 | 817 | 825 | PF00069 | 0.582 |
DOC_MAPK_NFAT4_5 | 171 | 179 | PF00069 | 0.323 |
DOC_MAPK_NFAT4_5 | 552 | 560 | PF00069 | 0.307 |
DOC_PP2B_LxvP_1 | 157 | 160 | PF13499 | 0.408 |
DOC_PP2B_LxvP_1 | 303 | 306 | PF13499 | 0.411 |
DOC_PP4_FxxP_1 | 702 | 705 | PF00568 | 0.409 |
DOC_PP4_FxxP_1 | 78 | 81 | PF00568 | 0.541 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.307 |
DOC_USP7_MATH_1 | 790 | 794 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 796 | 800 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 803 | 807 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 851 | 855 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 859 | 863 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 880 | 884 | PF00917 | 0.724 |
DOC_USP7_UBL2_3 | 158 | 162 | PF12436 | 0.523 |
DOC_USP7_UBL2_3 | 42 | 46 | PF12436 | 0.515 |
DOC_WW_Pin1_4 | 410 | 415 | PF00397 | 0.321 |
DOC_WW_Pin1_4 | 668 | 673 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 701 | 706 | PF00397 | 0.434 |
DOC_WW_Pin1_4 | 794 | 799 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 899 | 904 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 912 | 917 | PF00397 | 0.308 |
LIG_14-3-3_CanoR_1 | 184 | 189 | PF00244 | 0.347 |
LIG_14-3-3_CanoR_1 | 452 | 461 | PF00244 | 0.289 |
LIG_14-3-3_CanoR_1 | 663 | 668 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 785 | 789 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 881 | 885 | PF00244 | 0.747 |
LIG_14-3-3_CanoR_1 | 938 | 943 | PF00244 | 0.372 |
LIG_Actin_WH2_2 | 161 | 179 | PF00022 | 0.323 |
LIG_Actin_WH2_2 | 357 | 375 | PF00022 | 0.433 |
LIG_APCC_ABBA_1 | 577 | 582 | PF00400 | 0.387 |
LIG_BRCT_BRCA1_1 | 331 | 335 | PF00533 | 0.323 |
LIG_BRCT_BRCA1_1 | 423 | 427 | PF00533 | 0.428 |
LIG_Clathr_ClatBox_1 | 809 | 813 | PF01394 | 0.480 |
LIG_eIF4E_1 | 72 | 78 | PF01652 | 0.496 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.468 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.325 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.406 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.323 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.323 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.559 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.350 |
LIG_FHA_1 | 527 | 533 | PF00498 | 0.454 |
LIG_FHA_1 | 673 | 679 | PF00498 | 0.544 |
LIG_FHA_1 | 751 | 757 | PF00498 | 0.447 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.484 |
LIG_FHA_1 | 826 | 832 | PF00498 | 0.459 |
LIG_FHA_1 | 868 | 874 | PF00498 | 0.579 |
LIG_FHA_2 | 144 | 150 | PF00498 | 0.383 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.335 |
LIG_FHA_2 | 391 | 397 | PF00498 | 0.393 |
LIG_FHA_2 | 509 | 515 | PF00498 | 0.322 |
LIG_GBD_Chelix_1 | 505 | 513 | PF00786 | 0.342 |
LIG_Integrin_isoDGR_2 | 661 | 663 | PF01839 | 0.489 |
LIG_LIR_Apic_2 | 868 | 874 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 183 | 193 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 247 | 257 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 3 | 11 | PF02991 | 0.366 |
LIG_LIR_Gen_1 | 536 | 546 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 581 | 589 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 839 | 847 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 941 | 947 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 183 | 188 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 227 | 232 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 247 | 252 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 3 | 7 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 33 | 38 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 536 | 541 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 581 | 587 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 712 | 717 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 731 | 735 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 839 | 843 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 941 | 946 | PF02991 | 0.379 |
LIG_NRBOX | 542 | 548 | PF00104 | 0.323 |
LIG_PCNA_yPIPBox_3 | 397 | 409 | PF02747 | 0.323 |
LIG_Pex14_1 | 444 | 448 | PF04695 | 0.307 |
LIG_Pex14_2 | 190 | 194 | PF04695 | 0.323 |
LIG_Pex14_2 | 74 | 78 | PF04695 | 0.541 |
LIG_PTB_Apo_2 | 33 | 40 | PF02174 | 0.466 |
LIG_PTB_Phospho_1 | 33 | 39 | PF10480 | 0.515 |
LIG_SH2_CRK | 185 | 189 | PF00017 | 0.428 |
LIG_SH2_CRK | 249 | 253 | PF00017 | 0.393 |
LIG_SH2_CRK | 401 | 405 | PF00017 | 0.323 |
LIG_SH2_CRK | 714 | 718 | PF00017 | 0.452 |
LIG_SH2_CRK | 871 | 875 | PF00017 | 0.433 |
LIG_SH2_NCK_1 | 249 | 253 | PF00017 | 0.346 |
LIG_SH2_NCK_1 | 580 | 584 | PF00017 | 0.411 |
LIG_SH2_NCK_1 | 871 | 875 | PF00017 | 0.449 |
LIG_SH2_PTP2 | 840 | 843 | PF00017 | 0.455 |
LIG_SH2_SRC | 318 | 321 | PF00017 | 0.307 |
LIG_SH2_SRC | 461 | 464 | PF00017 | 0.428 |
LIG_SH2_SRC | 580 | 583 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 249 | 253 | PF00017 | 0.346 |
LIG_SH2_STAP1 | 258 | 262 | PF00017 | 0.350 |
LIG_SH2_STAP1 | 356 | 360 | PF00017 | 0.406 |
LIG_SH2_STAP1 | 39 | 43 | PF00017 | 0.515 |
LIG_SH2_STAP1 | 580 | 584 | PF00017 | 0.411 |
LIG_SH2_STAT3 | 218 | 221 | PF00017 | 0.428 |
LIG_SH2_STAT3 | 333 | 336 | PF00017 | 0.428 |
LIG_SH2_STAT3 | 72 | 75 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 517 | 520 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 601 | 604 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 840 | 843 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 871 | 874 | PF00017 | 0.455 |
LIG_SH3_2 | 383 | 388 | PF14604 | 0.307 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.319 |
LIG_SH3_3 | 365 | 371 | PF00018 | 0.385 |
LIG_SH3_3 | 380 | 386 | PF00018 | 0.207 |
LIG_SH3_3 | 666 | 672 | PF00018 | 0.541 |
LIG_SH3_3 | 783 | 789 | PF00018 | 0.410 |
LIG_SUMO_SIM_anti_2 | 337 | 345 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 486 | 496 | PF11976 | 0.328 |
LIG_SxIP_EBH_1 | 452 | 464 | PF03271 | 0.419 |
LIG_TRAF2_1 | 170 | 173 | PF00917 | 0.342 |
LIG_TRAF2_1 | 334 | 337 | PF00917 | 0.432 |
LIG_TYR_ITSM | 181 | 188 | PF00017 | 0.428 |
LIG_TYR_ITSM | 710 | 717 | PF00017 | 0.436 |
LIG_WRC_WIRS_1 | 200 | 205 | PF05994 | 0.323 |
LIG_WRC_WIRS_1 | 809 | 814 | PF05994 | 0.505 |
MOD_CDC14_SPxK_1 | 704 | 707 | PF00782 | 0.584 |
MOD_CDK_SPxK_1 | 701 | 707 | PF00069 | 0.560 |
MOD_CDK_SPxK_1 | 912 | 918 | PF00069 | 0.227 |
MOD_CDK_SPxxK_3 | 794 | 801 | PF00069 | 0.508 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.521 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.407 |
MOD_CK1_1 | 710 | 716 | PF00069 | 0.429 |
MOD_CK1_1 | 862 | 868 | PF00069 | 0.664 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.324 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.454 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.323 |
MOD_CK2_1 | 919 | 925 | PF00069 | 0.341 |
MOD_Cter_Amidation | 928 | 931 | PF01082 | 0.323 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.266 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.316 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.370 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.418 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.313 |
MOD_GlcNHglycan | 766 | 769 | PF01048 | 0.528 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.321 |
MOD_GlcNHglycan | 805 | 808 | PF01048 | 0.490 |
MOD_GlcNHglycan | 813 | 817 | PF01048 | 0.545 |
MOD_GlcNHglycan | 848 | 851 | PF01048 | 0.651 |
MOD_GlcNHglycan | 853 | 856 | PF01048 | 0.658 |
MOD_GlcNHglycan | 857 | 860 | PF01048 | 0.646 |
MOD_GlcNHglycan | 867 | 870 | PF01048 | 0.602 |
MOD_GlcNHglycan | 878 | 881 | PF01048 | 0.649 |
MOD_GlcNHglycan | 903 | 906 | PF01048 | 0.644 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.323 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.342 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.312 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.295 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.329 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.267 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.514 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.456 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.365 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.365 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.515 |
MOD_GSK3_1 | 668 | 675 | PF00069 | 0.510 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.426 |
MOD_GSK3_1 | 790 | 797 | PF00069 | 0.509 |
MOD_GSK3_1 | 808 | 815 | PF00069 | 0.412 |
MOD_GSK3_1 | 846 | 853 | PF00069 | 0.623 |
MOD_GSK3_1 | 855 | 862 | PF00069 | 0.644 |
MOD_GSK3_1 | 863 | 870 | PF00069 | 0.477 |
MOD_GSK3_1 | 872 | 879 | PF00069 | 0.574 |
MOD_LATS_1 | 302 | 308 | PF00433 | 0.365 |
MOD_N-GLC_1 | 390 | 395 | PF02516 | 0.378 |
MOD_N-GLC_1 | 453 | 458 | PF02516 | 0.380 |
MOD_N-GLC_1 | 67 | 72 | PF02516 | 0.341 |
MOD_N-GLC_1 | 851 | 856 | PF02516 | 0.678 |
MOD_N-GLC_2 | 119 | 121 | PF02516 | 0.266 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.520 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.404 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.338 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.338 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.394 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.294 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.466 |
MOD_NEK2_1 | 485 | 490 | PF00069 | 0.365 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.365 |
MOD_NEK2_1 | 588 | 593 | PF00069 | 0.524 |
MOD_NEK2_1 | 772 | 777 | PF00069 | 0.433 |
MOD_NEK2_1 | 784 | 789 | PF00069 | 0.429 |
MOD_NEK2_1 | 812 | 817 | PF00069 | 0.553 |
MOD_NEK2_1 | 825 | 830 | PF00069 | 0.322 |
MOD_NEK2_2 | 790 | 795 | PF00069 | 0.534 |
MOD_NEK2_2 | 880 | 885 | PF00069 | 0.709 |
MOD_OFUCOSY | 776 | 782 | PF10250 | 0.499 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.544 |
MOD_PIKK_1 | 390 | 396 | PF00454 | 0.419 |
MOD_PIKK_1 | 418 | 424 | PF00454 | 0.392 |
MOD_PIKK_1 | 796 | 802 | PF00454 | 0.542 |
MOD_PK_1 | 707 | 713 | PF00069 | 0.574 |
MOD_PKA_1 | 162 | 168 | PF00069 | 0.428 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.407 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.393 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.360 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.324 |
MOD_PKA_2 | 784 | 790 | PF00069 | 0.503 |
MOD_PKA_2 | 880 | 886 | PF00069 | 0.772 |
MOD_Plk_1 | 453 | 459 | PF00069 | 0.385 |
MOD_Plk_1 | 501 | 507 | PF00069 | 0.307 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.559 |
MOD_Plk_1 | 851 | 857 | PF00069 | 0.638 |
MOD_Plk_2-3 | 331 | 337 | PF00069 | 0.316 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.484 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.391 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.349 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.393 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.307 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.357 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.533 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.307 |
MOD_Plk_4 | 521 | 527 | PF00069 | 0.307 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.323 |
MOD_Plk_4 | 613 | 619 | PF00069 | 0.557 |
MOD_Plk_4 | 938 | 944 | PF00069 | 0.379 |
MOD_ProDKin_1 | 410 | 416 | PF00069 | 0.321 |
MOD_ProDKin_1 | 668 | 674 | PF00069 | 0.527 |
MOD_ProDKin_1 | 701 | 707 | PF00069 | 0.448 |
MOD_ProDKin_1 | 794 | 800 | PF00069 | 0.507 |
MOD_ProDKin_1 | 899 | 905 | PF00069 | 0.679 |
MOD_ProDKin_1 | 912 | 918 | PF00069 | 0.308 |
MOD_SUMO_for_1 | 41 | 44 | PF00179 | 0.515 |
MOD_SUMO_for_1 | 518 | 521 | PF00179 | 0.290 |
MOD_SUMO_rev_2 | 40 | 48 | PF00179 | 0.496 |
TRG_DiLeu_BaEn_1 | 339 | 344 | PF01217 | 0.428 |
TRG_DiLeu_BaEn_1 | 521 | 526 | PF01217 | 0.323 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 538 | 541 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 580 | 583 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 595 | 598 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 714 | 717 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 840 | 843 | PF00928 | 0.436 |
TRG_ER_diArg_1 | 215 | 217 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.351 |
TRG_ER_diArg_1 | 367 | 370 | PF00400 | 0.299 |
TRG_ER_diArg_1 | 397 | 400 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 763 | 766 | PF00400 | 0.401 |
TRG_NES_CRM1_1 | 149 | 161 | PF08389 | 0.530 |
TRG_NES_CRM1_1 | 339 | 352 | PF08389 | 0.412 |
TRG_Pf-PMV_PEXEL_1 | 600 | 605 | PF00026 | 0.576 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0P1 | Leptomonas seymouri | 33% | 100% |
A0A0N1PAL1 | Leptomonas seymouri | 77% | 98% |
A0A0S4J933 | Bodo saltans | 31% | 100% |
A0A0S4JI21 | Bodo saltans | 48% | 97% |
A0A1X0NSK9 | Trypanosomatidae | 32% | 100% |
A0A1X0P3I0 | Trypanosomatidae | 58% | 100% |
A0A3R7KDV1 | Trypanosoma rangeli | 59% | 100% |
A0A3S7WW83 | Leishmania donovani | 22% | 100% |
A0A3S7X1K1 | Leishmania donovani | 33% | 100% |
A0A3S7XB89 | Leishmania donovani | 97% | 100% |
A0A422NYW0 | Trypanosoma rangeli | 32% | 100% |
A0R979 | Bacillus thuringiensis (strain Al Hakam) | 22% | 100% |
A4HGN1 | Leishmania braziliensis | 33% | 100% |
A4HPI6 | Leishmania braziliensis | 87% | 100% |
A4I3Q5 | Leishmania infantum | 33% | 100% |
A4IDA8 | Leishmania infantum | 97% | 100% |
D0A8A5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A8E9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E9AT98 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
E9AZZ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
F4ISQ7 | Arabidopsis thaliana | 32% | 100% |
O27661 | Methanothermobacter thermautotrophicus (strain ATCC 29096 / DSM 1053 / JCM 10044 / NBRC 100330 / Delta H) | 25% | 100% |
O28469 | Archaeoglobus fulgidus (strain ATCC 49558 / DSM 4304 / JCM 9628 / NBRC 100126 / VC-16) | 27% | 100% |
O58356 | Pyrococcus horikoshii (strain ATCC 700860 / DSM 12428 / JCM 9974 / NBRC 100139 / OT-3) | 30% | 100% |
O67226 | Aquifex aeolicus (strain VF5) | 23% | 82% |
O95985 | Homo sapiens | 31% | 100% |
O96651 | Drosophila melanogaster | 33% | 100% |
P13099 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 36% | 100% |
P34184 | Alkalihalophilus pseudofirmus (strain ATCC BAA-2126 / JCM 17055 / OF4) | 23% | 100% |
P39814 | Bacillus subtilis (strain 168) | 22% | 100% |
P40114 | Bacillus anthracis | 22% | 100% |
P43012 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 23% | 100% |
P43704 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 26% | 100% |
P96583 | Bacillus subtilis (strain 168) | 24% | 100% |
Q0J0S6 | Oryza sativa subsp. japonica | 33% | 100% |
Q2FEN5 | Staphylococcus aureus (strain USA300) | 23% | 100% |
Q2FW03 | Staphylococcus aureus (strain NCTC 8325 / PS 47) | 23% | 100% |
Q49ZH2 | Staphylococcus saprophyticus subsp. saprophyticus (strain ATCC 15305 / DSM 20229 / NCIMB 8711 / NCTC 7292 / S-41) | 21% | 100% |
Q4L8B8 | Staphylococcus haemolyticus (strain JCSC1435) | 21% | 100% |
Q4Q888 | Leishmania major | 33% | 100% |
Q59046 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 24% | 100% |
Q5HDV4 | Staphylococcus aureus (strain COL) | 23% | 100% |
Q5HLZ4 | Staphylococcus epidermidis (strain ATCC 35984 / RP62A) | 21% | 100% |
Q5WAX6 | Alkalihalobacillus clausii (strain KSM-K16) | 26% | 100% |
Q63GK5 | Bacillus cereus (strain ZK / E33L) | 22% | 100% |
Q65N90 | Bacillus licheniformis (strain ATCC 14580 / DSM 13 / JCM 2505 / CCUG 7422 / NBRC 12200 / NCIMB 9375 / NCTC 10341 / NRRL NRS-1264 / Gibson 46) | 24% | 100% |
Q6G767 | Staphylococcus aureus (strain MSSA476) | 23% | 100% |
Q6GEH9 | Staphylococcus aureus (strain MRSA252) | 23% | 100% |
Q6HP19 | Bacillus thuringiensis subsp. konkukian (strain 97-27) | 22% | 100% |
Q73E74 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 22% | 100% |
Q7A075 | Staphylococcus aureus (strain MW2) | 23% | 100% |
Q7A455 | Staphylococcus aureus (strain N315) | 23% | 100% |
Q81IH1 | Bacillus cereus (strain ATCC 14579 / DSM 31 / CCUG 7414 / JCM 2152 / NBRC 15305 / NCIMB 9373 / NCTC 2599 / NRRL B-3711) | 23% | 100% |
Q81Z97 | Bacillus anthracis | 22% | 100% |
Q8CRF7 | Staphylococcus epidermidis (strain ATCC 12228 / FDA PCI 1200) | 21% | 100% |
Q8T2T7 | Dictyostelium discoideum | 37% | 100% |
Q8ZXT5 | Pyrobaculum aerophilum (strain ATCC 51768 / DSM 7523 / JCM 9630 / CIP 104966 / NBRC 100827 / IM2) | 23% | 77% |
Q99S17 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 23% | 100% |
Q9CN30 | Pasteurella multocida (strain Pm70) | 23% | 100% |
Q9CP53 | Pasteurella multocida (strain Pm70) | 24% | 100% |
Q9HM08 | Thermoplasma acidophilum (strain ATCC 25905 / DSM 1728 / JCM 9062 / NBRC 15155 / AMRC-C165) | 26% | 100% |
Q9KRB2 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 24% | 100% |
Q9LVP1 | Arabidopsis thaliana | 42% | 100% |
Q9UYS8 | Pyrococcus abyssi (strain GE5 / Orsay) | 29% | 100% |
Q9YB01 | Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1) | 27% | 100% |
Q9Z321 | Mus musculus | 31% | 100% |
Q9ZMV7 | Helicobacter pylori (strain J99 / ATCC 700824) | 22% | 100% |
V5AV88 | Trypanosoma cruzi | 31% | 100% |
V5BE78 | Trypanosoma cruzi | 54% | 100% |