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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 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 | 2 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
Related structures:
AlphaFold database: A4HII5
Term | Name | Level | Count |
---|---|---|---|
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 1 |
GO:0042254 | ribosome biogenesis | 5 | 1 |
GO:0043085 | positive regulation of catalytic activity | 4 | 1 |
GO:0044085 | cellular component biogenesis | 3 | 1 |
GO:0044093 | positive regulation of molecular function | 3 | 1 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050790 | regulation of catalytic activity | 3 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051052 | regulation of DNA metabolic process | 5 | 1 |
GO:0051054 | positive regulation of DNA metabolic process | 6 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051338 | regulation of transferase activity | 4 | 1 |
GO:0051347 | positive regulation of transferase activity | 5 | 1 |
GO:0051972 | regulation of telomerase activity | 5 | 1 |
GO:0051973 | positive regulation of telomerase activity | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065009 | regulation of molecular function | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:2000278 | regulation of DNA biosynthetic process | 6 | 1 |
GO:2000573 | positive regulation of DNA biosynthetic process | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 16 |
GO:0003824 | catalytic activity | 1 | 16 |
GO:0005488 | binding | 1 | 16 |
GO:0005524 | ATP binding | 5 | 16 |
GO:0016462 | pyrophosphatase activity | 5 | 16 |
GO:0016787 | hydrolase activity | 2 | 16 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 16 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 16 |
GO:0016887 | ATP hydrolysis activity | 7 | 16 |
GO:0017076 | purine nucleotide binding | 4 | 16 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 16 |
GO:0030554 | adenyl nucleotide binding | 5 | 16 |
GO:0032553 | ribonucleotide binding | 3 | 16 |
GO:0032555 | purine ribonucleotide binding | 4 | 16 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 16 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 16 |
GO:0036094 | small molecule binding | 2 | 16 |
GO:0043167 | ion binding | 2 | 16 |
GO:0043168 | anion binding | 3 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:0097367 | carbohydrate derivative binding | 2 | 16 |
GO:1901265 | nucleoside phosphate binding | 3 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 1 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
GO:1990275 | preribosome binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 775 | 779 | PF00656 | 0.352 |
CLV_C14_Caspase3-7 | 799 | 803 | PF00656 | 0.352 |
CLV_C14_Caspase3-7 | 825 | 829 | PF00656 | 0.424 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 461 | 463 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 540 | 542 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.730 |
CLV_NRD_NRD_1 | 839 | 841 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 936 | 938 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.475 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 461 | 463 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 540 | 542 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 812 | 814 | PF00082 | 0.207 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.719 |
CLV_PCSK_KEX2_1 | 839 | 841 | PF00082 | 0.336 |
CLV_PCSK_PC1ET2_1 | 812 | 814 | PF00082 | 0.207 |
CLV_PCSK_PC7_1 | 79 | 85 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 710 | 714 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 722 | 726 | PF00082 | 0.222 |
CLV_PCSK_SKI1_1 | 758 | 762 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 812 | 816 | PF00082 | 0.420 |
DEG_APCC_DBOX_1 | 336 | 344 | PF00400 | 0.432 |
DEG_APCC_DBOX_1 | 586 | 594 | PF00400 | 0.490 |
DEG_COP1_1 | 296 | 304 | PF00400 | 0.483 |
DEG_SPOP_SBC_1 | 42 | 46 | PF00917 | 0.720 |
DOC_ANK_TNKS_1 | 11 | 18 | PF00023 | 0.563 |
DOC_CDC14_PxL_1 | 547 | 555 | PF14671 | 0.279 |
DOC_CDC14_PxL_1 | 842 | 850 | PF14671 | 0.495 |
DOC_CYCLIN_RxL_1 | 427 | 438 | PF00134 | 0.347 |
DOC_CYCLIN_RxL_1 | 810 | 821 | PF00134 | 0.207 |
DOC_CYCLIN_yCln2_LP_2 | 125 | 131 | PF00134 | 0.532 |
DOC_CYCLIN_yCln2_LP_2 | 7 | 10 | PF00134 | 0.709 |
DOC_MAPK_gen_1 | 461 | 469 | PF00069 | 0.410 |
DOC_MAPK_gen_1 | 540 | 546 | PF00069 | 0.405 |
DOC_MAPK_gen_1 | 811 | 818 | PF00069 | 0.420 |
DOC_MAPK_gen_1 | 833 | 843 | PF00069 | 0.352 |
DOC_MAPK_MEF2A_6 | 587 | 595 | PF00069 | 0.436 |
DOC_MAPK_MEF2A_6 | 765 | 773 | PF00069 | 0.352 |
DOC_MAPK_MEF2A_6 | 836 | 845 | PF00069 | 0.352 |
DOC_PP1_RVXF_1 | 811 | 818 | PF00149 | 0.207 |
DOC_PP1_RVXF_1 | 923 | 930 | PF00149 | 0.403 |
DOC_PP2B_LxvP_1 | 125 | 128 | PF13499 | 0.499 |
DOC_PP2B_LxvP_1 | 434 | 437 | PF13499 | 0.510 |
DOC_PP2B_LxvP_1 | 573 | 576 | PF13499 | 0.532 |
DOC_PP2B_LxvP_1 | 7 | 10 | PF13499 | 0.709 |
DOC_PP2B_LxvP_1 | 706 | 709 | PF13499 | 0.384 |
DOC_PP2B_LxvP_1 | 90 | 93 | PF13499 | 0.533 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 718 | 722 | PF00917 | 0.318 |
DOC_USP7_MATH_1 | 730 | 734 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 901 | 905 | PF00917 | 0.443 |
DOC_USP7_UBL2_3 | 107 | 111 | PF12436 | 0.528 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.359 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 704 | 709 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 765 | 770 | PF00397 | 0.420 |
LIG_14-3-3_CanoR_1 | 171 | 178 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 222 | 228 | PF00244 | 0.347 |
LIG_14-3-3_CanoR_1 | 279 | 284 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 315 | 319 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 328 | 334 | PF00244 | 0.323 |
LIG_14-3-3_CanoR_1 | 430 | 435 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 461 | 469 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 492 | 498 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 520 | 526 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 650 | 658 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 786 | 794 | PF00244 | 0.313 |
LIG_14-3-3_CanoR_1 | 82 | 92 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 851 | 859 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 919 | 929 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 937 | 944 | PF00244 | 0.570 |
LIG_BRCT_BRCA1_1 | 697 | 701 | PF00533 | 0.448 |
LIG_Clathr_ClatBox_1 | 908 | 912 | PF01394 | 0.280 |
LIG_deltaCOP1_diTrp_1 | 309 | 314 | PF00928 | 0.540 |
LIG_deltaCOP1_diTrp_1 | 691 | 699 | PF00928 | 0.518 |
LIG_deltaCOP1_diTrp_1 | 926 | 933 | PF00928 | 0.399 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.786 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.526 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.560 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.505 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.546 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.476 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.441 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.322 |
LIG_FHA_1 | 628 | 634 | PF00498 | 0.410 |
LIG_FHA_2 | 402 | 408 | PF00498 | 0.596 |
LIG_FHA_2 | 618 | 624 | PF00498 | 0.362 |
LIG_FHA_2 | 643 | 649 | PF00498 | 0.551 |
LIG_FHA_2 | 670 | 676 | PF00498 | 0.402 |
LIG_FHA_2 | 683 | 689 | PF00498 | 0.330 |
LIG_FHA_2 | 797 | 803 | PF00498 | 0.352 |
LIG_FHA_2 | 845 | 851 | PF00498 | 0.583 |
LIG_FHA_2 | 879 | 885 | PF00498 | 0.359 |
LIG_FHA_2 | 905 | 911 | PF00498 | 0.376 |
LIG_FHA_2 | 99 | 105 | PF00498 | 0.588 |
LIG_GBD_Chelix_1 | 526 | 534 | PF00786 | 0.366 |
LIG_LIR_Gen_1 | 307 | 318 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 429 | 439 | PF02991 | 0.616 |
LIG_LIR_Gen_1 | 464 | 473 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 670 | 680 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 698 | 709 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 891 | 901 | PF02991 | 0.287 |
LIG_LIR_LC3C_4 | 418 | 421 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 224 | 230 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 307 | 313 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 362 | 368 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 429 | 434 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 464 | 469 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 670 | 676 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 698 | 704 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 856 | 862 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 891 | 897 | PF02991 | 0.287 |
LIG_MYND_1 | 267 | 271 | PF01753 | 0.477 |
LIG_MYND_1 | 9 | 13 | PF01753 | 0.580 |
LIG_PCNA_yPIPBox_3 | 615 | 628 | PF02747 | 0.397 |
LIG_Pex14_1 | 310 | 314 | PF04695 | 0.533 |
LIG_Pex14_2 | 20 | 24 | PF04695 | 0.520 |
LIG_RPA_C_Fungi | 536 | 548 | PF08784 | 0.400 |
LIG_SH2_CRK | 231 | 235 | PF00017 | 0.447 |
LIG_SH2_CRK | 715 | 719 | PF00017 | 0.352 |
LIG_SH2_PTP2 | 842 | 845 | PF00017 | 0.352 |
LIG_SH2_STAP1 | 463 | 467 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 463 | 466 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 842 | 845 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 872 | 875 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 880 | 883 | PF00017 | 0.287 |
LIG_SH3_2 | 846 | 851 | PF14604 | 0.394 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.529 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.416 |
LIG_SH3_3 | 573 | 579 | PF00018 | 0.428 |
LIG_SH3_3 | 663 | 669 | PF00018 | 0.441 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.585 |
LIG_SH3_3 | 737 | 743 | PF00018 | 0.287 |
LIG_SH3_3 | 828 | 834 | PF00018 | 0.318 |
LIG_SH3_3 | 840 | 846 | PF00018 | 0.400 |
LIG_SUMO_SIM_anti_2 | 884 | 891 | PF11976 | 0.287 |
LIG_SUMO_SIM_anti_2 | 904 | 910 | PF11976 | 0.288 |
LIG_SUMO_SIM_par_1 | 256 | 261 | PF11976 | 0.565 |
LIG_SUMO_SIM_par_1 | 341 | 346 | PF11976 | 0.526 |
LIG_SUMO_SIM_par_1 | 499 | 505 | PF11976 | 0.269 |
LIG_SUMO_SIM_par_1 | 533 | 539 | PF11976 | 0.544 |
LIG_SUMO_SIM_par_1 | 569 | 574 | PF11976 | 0.457 |
LIG_SUMO_SIM_par_1 | 608 | 614 | PF11976 | 0.481 |
LIG_SUMO_SIM_par_1 | 907 | 912 | PF11976 | 0.281 |
LIG_TRAF2_1 | 404 | 407 | PF00917 | 0.638 |
LIG_TRFH_1 | 704 | 708 | PF08558 | 0.386 |
LIG_TYR_ITIM | 322 | 327 | PF00017 | 0.515 |
LIG_TYR_ITSM | 223 | 230 | PF00017 | 0.559 |
MOD_CDC14_SPxK_1 | 150 | 153 | PF00782 | 0.524 |
MOD_CDK_SPxK_1 | 147 | 153 | PF00069 | 0.522 |
MOD_CDK_SPxK_1 | 704 | 710 | PF00069 | 0.442 |
MOD_CDK_SPxxK_3 | 147 | 154 | PF00069 | 0.564 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.675 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.593 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.634 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.598 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.737 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.709 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.505 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.513 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.705 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.518 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.343 |
MOD_CK1_1 | 569 | 575 | PF00069 | 0.360 |
MOD_CK1_1 | 667 | 673 | PF00069 | 0.444 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.698 |
MOD_CK1_1 | 904 | 910 | PF00069 | 0.515 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.638 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.499 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.636 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.657 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.518 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.673 |
MOD_CK2_1 | 844 | 850 | PF00069 | 0.499 |
MOD_CK2_1 | 878 | 884 | PF00069 | 0.294 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.515 |
MOD_DYRK1A_RPxSP_1 | 765 | 769 | PF00069 | 0.420 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.493 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.510 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.763 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.672 |
MOD_GlcNHglycan | 16 | 20 | PF01048 | 0.533 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.602 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.466 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.686 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.597 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.756 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.777 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.556 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.543 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.551 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.345 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.530 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.337 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.413 |
MOD_GlcNHglycan | 597 | 600 | PF01048 | 0.534 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.672 |
MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.477 |
MOD_GlcNHglycan | 678 | 681 | PF01048 | 0.477 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.741 |
MOD_GlcNHglycan | 901 | 904 | PF01048 | 0.456 |
MOD_GlcNHglycan | 922 | 925 | PF01048 | 0.497 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.759 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.573 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.611 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.595 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.623 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.473 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.447 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.504 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.749 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.630 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.716 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.596 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.602 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.734 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.632 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.489 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.704 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.407 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.333 |
MOD_GSK3_1 | 638 | 645 | PF00069 | 0.524 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.697 |
MOD_GSK3_1 | 695 | 702 | PF00069 | 0.519 |
MOD_GSK3_1 | 792 | 799 | PF00069 | 0.297 |
MOD_GSK3_1 | 874 | 881 | PF00069 | 0.287 |
MOD_GSK3_1 | 895 | 902 | PF00069 | 0.307 |
MOD_N-GLC_1 | 31 | 36 | PF02516 | 0.632 |
MOD_N-GLC_1 | 595 | 600 | PF02516 | 0.577 |
MOD_N-GLC_1 | 704 | 709 | PF02516 | 0.534 |
MOD_N-GLC_1 | 730 | 735 | PF02516 | 0.352 |
MOD_N-GLC_1 | 899 | 904 | PF02516 | 0.321 |
MOD_N-GLC_2 | 295 | 297 | PF02516 | 0.437 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.584 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.343 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.449 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.591 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.354 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.685 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.561 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.525 |
MOD_NEK2_1 | 595 | 600 | PF00069 | 0.539 |
MOD_NEK2_1 | 627 | 632 | PF00069 | 0.377 |
MOD_NEK2_1 | 664 | 669 | PF00069 | 0.427 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.632 |
MOD_PIKK_1 | 119 | 125 | PF00454 | 0.524 |
MOD_PIKK_1 | 327 | 333 | PF00454 | 0.466 |
MOD_PIKK_1 | 346 | 352 | PF00454 | 0.487 |
MOD_PIKK_1 | 617 | 623 | PF00454 | 0.376 |
MOD_PIKK_1 | 792 | 798 | PF00454 | 0.287 |
MOD_PK_1 | 823 | 829 | PF00069 | 0.311 |
MOD_PKA_1 | 461 | 467 | PF00069 | 0.332 |
MOD_PKA_1 | 82 | 88 | PF00069 | 0.520 |
MOD_PKA_1 | 937 | 943 | PF00069 | 0.701 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.661 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.592 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.626 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.441 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.664 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.294 |
MOD_PKA_2 | 461 | 467 | PF00069 | 0.350 |
MOD_PKA_2 | 493 | 499 | PF00069 | 0.527 |
MOD_PKA_2 | 638 | 644 | PF00069 | 0.503 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.687 |
MOD_PKA_2 | 920 | 926 | PF00069 | 0.463 |
MOD_PKA_2 | 936 | 942 | PF00069 | 0.605 |
MOD_Plk_1 | 664 | 670 | PF00069 | 0.514 |
MOD_Plk_1 | 730 | 736 | PF00069 | 0.420 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.505 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.538 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.428 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.443 |
MOD_Plk_4 | 521 | 527 | PF00069 | 0.449 |
MOD_Plk_4 | 561 | 567 | PF00069 | 0.461 |
MOD_Plk_4 | 638 | 644 | PF00069 | 0.341 |
MOD_Plk_4 | 695 | 701 | PF00069 | 0.494 |
MOD_Plk_4 | 720 | 726 | PF00069 | 0.352 |
MOD_Plk_4 | 904 | 910 | PF00069 | 0.288 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.576 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.573 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.428 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.354 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.519 |
MOD_ProDKin_1 | 704 | 710 | PF00069 | 0.418 |
MOD_ProDKin_1 | 765 | 771 | PF00069 | 0.420 |
MOD_SUMO_rev_2 | 675 | 685 | PF00179 | 0.420 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.569 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 842 | 845 | PF00928 | 0.352 |
TRG_ER_diArg_1 | 24 | 27 | PF00400 | 0.772 |
TRG_ER_diArg_1 | 314 | 316 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 461 | 463 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 540 | 542 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 82 | 84 | PF00400 | 0.705 |
TRG_ER_diArg_1 | 839 | 841 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 918 | 921 | PF00400 | 0.415 |
TRG_Pf-PMV_PEXEL_1 | 758 | 762 | PF00026 | 0.420 |
TRG_Pf-PMV_PEXEL_1 | 792 | 796 | PF00026 | 0.287 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2H1 | Leptomonas seymouri | 61% | 100% |
A0A1X0P1J4 | Trypanosomatidae | 50% | 100% |
A0A3Q8IS46 | Leishmania donovani | 76% | 97% |
A0A3R7M308 | Trypanosoma rangeli | 50% | 100% |
A0A3S7X0L3 | Leishmania donovani | 32% | 100% |
A4HFM9 | Leishmania braziliensis | 32% | 100% |
A4I2Q7 | Leishmania infantum | 32% | 100% |
A4I5S8 | Leishmania infantum | 76% | 90% |
C9ZR48 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9AD83 | Leishmania major | 32% | 100% |
E9AZ07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B124 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4Q741 | Leishmania major | 80% | 100% |
V5AUZ1 | Trypanosoma cruzi | 50% | 100% |