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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043227 | membrane-bounded organelle | 3 | 7 |
GO:0043229 | intracellular organelle | 3 | 7 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0031010 | ISWI-type complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0070603 | SWI/SNF superfamily-type complex | 3 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1904949 | ATPase complex | 3 | 1 |
Related structures:
AlphaFold database: E9ASM6
Term | Name | Level | Count |
---|---|---|---|
GO:0006325 | chromatin organization | 4 | 1 |
GO:0006338 | chromatin remodeling | 5 | 1 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009890 | negative regulation of biosynthetic process | 5 | 1 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010558 | negative regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031327 | negative regulation of cellular biosynthetic process | 6 | 1 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 1 |
GO:0031554 | regulation of termination of DNA-templated transcription | 6 | 1 |
GO:0031555 | transcriptional attenuation | 7 | 1 |
GO:0043244 | regulation of protein-containing complex disassembly | 5 | 1 |
GO:0045892 | negative regulation of DNA-templated transcription | 7 | 1 |
GO:0045893 | positive regulation of DNA-templated transcription | 7 | 1 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051128 | regulation of cellular component organization | 4 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0051253 | negative regulation of RNA metabolic process | 6 | 1 |
GO:0051254 | positive regulation of RNA metabolic process | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1902679 | negative regulation of RNA biosynthetic process | 7 | 1 |
GO:1902680 | positive regulation of RNA biosynthetic process | 7 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:1903507 | negative regulation of nucleic acid-templated transcription | 8 | 1 |
GO:1903508 | positive regulation of nucleic acid-templated transcription | 8 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 189 | 193 | PF00656 | 0.562 |
CLV_C14_Caspase3-7 | 593 | 597 | PF00656 | 0.676 |
CLV_C14_Caspase3-7 | 787 | 791 | PF00656 | 0.485 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 579 | 581 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 752 | 754 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 819 | 821 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 851 | 853 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 888 | 890 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 910 | 912 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 953 | 955 | PF00675 | 0.284 |
CLV_PCSK_FUR_1 | 202 | 206 | PF00082 | 0.647 |
CLV_PCSK_FUR_1 | 849 | 853 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 578 | 580 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 821 | 823 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 851 | 853 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 888 | 890 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 909 | 911 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 953 | 955 | PF00082 | 0.284 |
CLV_PCSK_PC1ET2_1 | 332 | 334 | PF00082 | 0.558 |
CLV_PCSK_PC1ET2_1 | 415 | 417 | PF00082 | 0.464 |
CLV_PCSK_PC1ET2_1 | 420 | 422 | PF00082 | 0.467 |
CLV_PCSK_PC1ET2_1 | 578 | 580 | PF00082 | 0.582 |
CLV_PCSK_PC1ET2_1 | 821 | 823 | PF00082 | 0.479 |
CLV_PCSK_PC7_1 | 202 | 208 | PF00082 | 0.701 |
CLV_PCSK_PC7_1 | 416 | 422 | PF00082 | 0.553 |
CLV_PCSK_PC7_1 | 441 | 447 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 554 | 558 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 735 | 739 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 893 | 897 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 914 | 918 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 962 | 966 | PF00082 | 0.400 |
DEG_APCC_DBOX_1 | 961 | 969 | PF00400 | 0.284 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.520 |
DEG_SCF_FBW7_1 | 244 | 250 | PF00400 | 0.486 |
DEG_SPOP_SBC_1 | 601 | 605 | PF00917 | 0.646 |
DEG_SPOP_SBC_1 | 609 | 613 | PF00917 | 0.575 |
DOC_ANK_TNKS_1 | 445 | 452 | PF00023 | 0.606 |
DOC_CKS1_1 | 244 | 249 | PF01111 | 0.488 |
DOC_CKS1_1 | 465 | 470 | PF01111 | 0.721 |
DOC_CKS1_1 | 482 | 487 | PF01111 | 0.478 |
DOC_CKS1_1 | 550 | 555 | PF01111 | 0.593 |
DOC_CYCLIN_RxL_1 | 500 | 508 | PF00134 | 0.522 |
DOC_CYCLIN_RxL_1 | 532 | 541 | PF00134 | 0.516 |
DOC_CYCLIN_yCln2_LP_2 | 371 | 377 | PF00134 | 0.349 |
DOC_MAPK_DCC_7 | 162 | 171 | PF00069 | 0.604 |
DOC_MAPK_gen_1 | 162 | 169 | PF00069 | 0.537 |
DOC_MAPK_gen_1 | 558 | 567 | PF00069 | 0.318 |
DOC_MAPK_gen_1 | 89 | 95 | PF00069 | 0.518 |
DOC_MAPK_MEF2A_6 | 162 | 171 | PF00069 | 0.594 |
DOC_MAPK_MEF2A_6 | 535 | 542 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 560 | 569 | PF00069 | 0.294 |
DOC_PP1_RVXF_1 | 849 | 856 | PF00149 | 0.346 |
DOC_PP1_RVXF_1 | 996 | 1002 | PF00149 | 0.608 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 601 | 605 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 609 | 613 | PF00917 | 0.828 |
DOC_USP7_MATH_1 | 619 | 623 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 698 | 702 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 773 | 777 | PF00917 | 0.504 |
DOC_USP7_UBL2_3 | 426 | 430 | PF12436 | 0.563 |
DOC_USP7_UBL2_3 | 757 | 761 | PF12436 | 0.540 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 481 | 486 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 546 | 551 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 605 | 610 | PF00397 | 0.748 |
LIG_14-3-3_CanoR_1 | 204 | 214 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 674 | 680 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 69 | 79 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 84 | 93 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 888 | 897 | PF00244 | 0.253 |
LIG_14-3-3_CanoR_1 | 914 | 923 | PF00244 | 0.227 |
LIG_Actin_WH2_2 | 300 | 315 | PF00022 | 0.392 |
LIG_AP2alpha_2 | 657 | 659 | PF02296 | 0.604 |
LIG_BIR_III_4 | 410 | 414 | PF00653 | 0.331 |
LIG_BIR_III_4 | 525 | 529 | PF00653 | 0.572 |
LIG_BRCT_BRCA1_1 | 353 | 357 | PF00533 | 0.426 |
LIG_Clathr_ClatBox_1 | 996 | 1000 | PF01394 | 0.538 |
LIG_CtBP_PxDLS_1 | 399 | 403 | PF00389 | 0.412 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.797 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.627 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.514 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.505 |
LIG_FHA_1 | 550 | 556 | PF00498 | 0.636 |
LIG_FHA_1 | 873 | 879 | PF00498 | 0.441 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.431 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.289 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.399 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.588 |
LIG_FHA_2 | 587 | 593 | PF00498 | 0.719 |
LIG_FHA_2 | 619 | 625 | PF00498 | 0.706 |
LIG_FHA_2 | 638 | 644 | PF00498 | 0.711 |
LIG_FHA_2 | 647 | 653 | PF00498 | 0.699 |
LIG_FHA_2 | 791 | 797 | PF00498 | 0.699 |
LIG_LIR_Gen_1 | 296 | 305 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 336 | 346 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 823 | 832 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 296 | 301 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 391 | 397 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 470 | 476 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 568 | 572 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 6 | 11 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 678 | 682 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 77 | 81 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 823 | 829 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 848 | 853 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 875 | 879 | PF02991 | 0.268 |
LIG_MAD2 | 861 | 869 | PF02301 | 0.379 |
LIG_NRBOX | 736 | 742 | PF00104 | 0.555 |
LIG_PALB2_WD40_1 | 558 | 566 | PF16756 | 0.540 |
LIG_PCNA_yPIPBox_3 | 231 | 245 | PF02747 | 0.605 |
LIG_Pex14_2 | 294 | 298 | PF04695 | 0.591 |
LIG_RPA_C_Fungi | 884 | 896 | PF08784 | 0.251 |
LIG_SH2_CRK | 826 | 830 | PF00017 | 0.547 |
LIG_SH2_CRK | 850 | 854 | PF00017 | 0.344 |
LIG_SH2_GRB2like | 993 | 996 | PF00017 | 0.496 |
LIG_SH2_PTP2 | 78 | 81 | PF00017 | 0.467 |
LIG_SH2_PTP2 | 993 | 996 | PF00017 | 0.451 |
LIG_SH2_STAP1 | 476 | 480 | PF00017 | 0.562 |
LIG_SH2_STAP1 | 60 | 64 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 826 | 830 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 473 | 476 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 864 | 867 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 943 | 946 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 971 | 974 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 993 | 996 | PF00017 | 0.518 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.710 |
LIG_SH3_3 | 547 | 553 | PF00018 | 0.646 |
LIG_SH3_3 | 871 | 877 | PF00018 | 0.298 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 167 | 174 | PF11976 | 0.651 |
LIG_SUMO_SIM_par_1 | 536 | 541 | PF11976 | 0.513 |
LIG_SxIP_EBH_1 | 72 | 84 | PF03271 | 0.387 |
LIG_TRAF2_1 | 27 | 30 | PF00917 | 0.533 |
LIG_TRAF2_1 | 38 | 41 | PF00917 | 0.455 |
LIG_TRAF2_1 | 398 | 401 | PF00917 | 0.498 |
LIG_TRAF2_1 | 622 | 625 | PF00917 | 0.733 |
LIG_TRAF2_1 | 649 | 652 | PF00917 | 0.729 |
LIG_TYR_ITIM | 76 | 81 | PF00017 | 0.450 |
LIG_WRC_WIRS_1 | 512 | 517 | PF05994 | 0.520 |
MOD_CDC14_SPxK_1 | 174 | 177 | PF00782 | 0.630 |
MOD_CDK_SPK_2 | 243 | 248 | PF00069 | 0.487 |
MOD_CDK_SPK_2 | 549 | 554 | PF00069 | 0.606 |
MOD_CDK_SPxK_1 | 171 | 177 | PF00069 | 0.630 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.709 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.725 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.725 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.519 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.506 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.372 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.468 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.616 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.551 |
MOD_CK1_1 | 603 | 609 | PF00069 | 0.773 |
MOD_CK1_1 | 610 | 616 | PF00069 | 0.779 |
MOD_CK1_1 | 675 | 681 | PF00069 | 0.641 |
MOD_CK1_1 | 746 | 752 | PF00069 | 0.571 |
MOD_CK1_1 | 891 | 897 | PF00069 | 0.490 |
MOD_CK2_1 | 104 | 110 | PF00069 | 0.432 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.501 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.778 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.405 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.435 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.594 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.394 |
MOD_CK2_1 | 584 | 590 | PF00069 | 0.726 |
MOD_CK2_1 | 610 | 616 | PF00069 | 0.734 |
MOD_CK2_1 | 618 | 624 | PF00069 | 0.649 |
MOD_CK2_1 | 637 | 643 | PF00069 | 0.685 |
MOD_CK2_1 | 646 | 652 | PF00069 | 0.640 |
MOD_CK2_1 | 773 | 779 | PF00069 | 0.639 |
MOD_CK2_1 | 790 | 796 | PF00069 | 0.520 |
MOD_Cter_Amidation | 907 | 910 | PF01082 | 0.358 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.514 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.605 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.492 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.453 |
MOD_GlcNHglycan | 621 | 624 | PF01048 | 0.822 |
MOD_GlcNHglycan | 944 | 947 | PF01048 | 0.462 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.718 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.747 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.550 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.438 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.615 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.425 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.713 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.699 |
MOD_GSK3_1 | 610 | 617 | PF00069 | 0.779 |
MOD_GSK3_1 | 642 | 649 | PF00069 | 0.748 |
MOD_GSK3_1 | 653 | 660 | PF00069 | 0.635 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.316 |
MOD_GSK3_1 | 743 | 750 | PF00069 | 0.533 |
MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.664 |
MOD_N-GLC_1 | 195 | 200 | PF02516 | 0.692 |
MOD_N-GLC_1 | 505 | 510 | PF02516 | 0.560 |
MOD_N-GLC_1 | 869 | 874 | PF02516 | 0.379 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.551 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.525 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.532 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.639 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.481 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.516 |
MOD_NEK2_1 | 740 | 745 | PF00069 | 0.510 |
MOD_PIKK_1 | 505 | 511 | PF00454 | 0.485 |
MOD_PIKK_1 | 82 | 88 | PF00454 | 0.545 |
MOD_PKA_1 | 205 | 211 | PF00069 | 0.719 |
MOD_PKA_1 | 888 | 894 | PF00069 | 0.251 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.707 |
MOD_PKA_2 | 888 | 894 | PF00069 | 0.290 |
MOD_PKA_2 | 981 | 987 | PF00069 | 0.612 |
MOD_PKB_1 | 205 | 213 | PF00069 | 0.735 |
MOD_PKB_1 | 268 | 276 | PF00069 | 0.430 |
MOD_Plk_1 | 339 | 345 | PF00069 | 0.471 |
MOD_Plk_1 | 39 | 45 | PF00069 | 0.345 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.597 |
MOD_Plk_1 | 505 | 511 | PF00069 | 0.560 |
MOD_Plk_1 | 538 | 544 | PF00069 | 0.594 |
MOD_Plk_1 | 716 | 722 | PF00069 | 0.673 |
MOD_Plk_1 | 869 | 875 | PF00069 | 0.312 |
MOD_Plk_1 | 900 | 906 | PF00069 | 0.356 |
MOD_Plk_2-3 | 126 | 132 | PF00069 | 0.508 |
MOD_Plk_2-3 | 592 | 598 | PF00069 | 0.716 |
MOD_Plk_2-3 | 657 | 663 | PF00069 | 0.548 |
MOD_Plk_2-3 | 792 | 798 | PF00069 | 0.537 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.516 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.345 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.606 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.503 |
MOD_Plk_4 | 901 | 907 | PF00069 | 0.239 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.627 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.713 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.492 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.554 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.732 |
MOD_ProDKin_1 | 481 | 487 | PF00069 | 0.515 |
MOD_ProDKin_1 | 546 | 552 | PF00069 | 0.637 |
MOD_ProDKin_1 | 605 | 611 | PF00069 | 0.748 |
MOD_SUMO_for_1 | 230 | 233 | PF00179 | 0.599 |
MOD_SUMO_for_1 | 414 | 417 | PF00179 | 0.425 |
MOD_SUMO_for_1 | 429 | 432 | PF00179 | 0.480 |
MOD_SUMO_for_1 | 767 | 770 | PF00179 | 0.559 |
MOD_SUMO_rev_2 | 425 | 431 | PF00179 | 0.563 |
MOD_SUMO_rev_2 | 612 | 622 | PF00179 | 0.600 |
MOD_SUMO_rev_2 | 657 | 666 | PF00179 | 0.602 |
MOD_SUMO_rev_2 | 717 | 726 | PF00179 | 0.501 |
MOD_SUMO_rev_2 | 731 | 740 | PF00179 | 0.372 |
MOD_SUMO_rev_2 | 776 | 785 | PF00179 | 0.586 |
MOD_SUMO_rev_2 | 921 | 931 | PF00179 | 0.300 |
TRG_DiLeu_BaEn_1 | 439 | 444 | PF01217 | 0.493 |
TRG_DiLeu_BaEn_1 | 461 | 466 | PF01217 | 0.630 |
TRG_DiLeu_BaEn_1 | 736 | 741 | PF01217 | 0.455 |
TRG_DiLeu_BaEn_1 | 901 | 906 | PF01217 | 0.179 |
TRG_DiLeu_BaEn_4 | 880 | 886 | PF01217 | 0.179 |
TRG_DiLeu_BaEn_4 | 901 | 907 | PF01217 | 0.355 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 826 | 829 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 850 | 853 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 854 | 857 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 993 | 996 | PF00928 | 0.524 |
TRG_ER_diArg_1 | 201 | 204 | PF00400 | 0.660 |
TRG_ER_diArg_1 | 205 | 207 | PF00400 | 0.673 |
TRG_ER_diArg_1 | 421 | 423 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 444 | 447 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 545 | 548 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 850 | 852 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 909 | 911 | PF00400 | 0.358 |
TRG_NLS_Bipartite_1 | 404 | 424 | PF00514 | 0.559 |
TRG_NLS_MonoCore_2 | 576 | 581 | PF00514 | 0.602 |
TRG_NLS_MonoCore_2 | 752 | 757 | PF00514 | 0.608 |
TRG_NLS_MonoExtC_3 | 419 | 425 | PF00514 | 0.560 |
TRG_NLS_MonoExtC_3 | 752 | 757 | PF00514 | 0.533 |
TRG_NLS_MonoExtN_4 | 577 | 582 | PF00514 | 0.617 |
TRG_NLS_MonoExtN_4 | 753 | 759 | PF00514 | 0.614 |
TRG_Pf-PMV_PEXEL_1 | 421 | 425 | PF00026 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 446 | 450 | PF00026 | 0.645 |
TRG_Pf-PMV_PEXEL_1 | 457 | 461 | PF00026 | 0.685 |
TRG_Pf-PMV_PEXEL_1 | 724 | 728 | PF00026 | 0.516 |
TRG_Pf-PMV_PEXEL_1 | 893 | 898 | PF00026 | 0.430 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD66 | Leptomonas seymouri | 57% | 93% |
A0A1X0P937 | Trypanosomatidae | 39% | 100% |
A0A3S7XAG3 | Leishmania donovani | 89% | 100% |
A0A422NTX5 | Trypanosoma rangeli | 38% | 100% |
A4HNW6 | Leishmania braziliensis | 75% | 100% |
A4ICM8 | Leishmania infantum | 90% | 100% |
D0A2T4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
Q4Q1X0 | Leishmania major | 88% | 100% |