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: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005778 | peroxisomal membrane | 6 | 12 |
GO:0005829 | cytosol | 2 | 2 |
GO:0016020 | membrane | 2 | 12 |
GO:0031090 | organelle membrane | 3 | 12 |
GO:0031903 | microbody membrane | 5 | 12 |
GO:0042579 | microbody | 5 | 12 |
GO:0043226 | organelle | 2 | 13 |
GO:0043227 | membrane-bounded organelle | 3 | 13 |
GO:0043229 | intracellular organelle | 3 | 13 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 13 |
GO:0098588 | bounding membrane of organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:0005634 | nucleus | 5 | 1 |
Related structures:
AlphaFold database: Q4Q2J2
Term | Name | Level | Count |
---|---|---|---|
GO:0006605 | protein targeting | 5 | 12 |
GO:0006625 | protein targeting to peroxisome | 5 | 12 |
GO:0006810 | transport | 3 | 12 |
GO:0006886 | intracellular protein transport | 4 | 12 |
GO:0006996 | organelle organization | 4 | 12 |
GO:0007031 | peroxisome organization | 5 | 12 |
GO:0008104 | protein localization | 4 | 12 |
GO:0009987 | cellular process | 1 | 13 |
GO:0015031 | protein transport | 4 | 12 |
GO:0015919 | peroxisomal membrane transport | 5 | 2 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0016558 | protein import into peroxisome matrix | 5 | 2 |
GO:0033036 | macromolecule localization | 2 | 12 |
GO:0033365 | protein localization to organelle | 5 | 12 |
GO:0043574 | peroxisomal transport | 4 | 12 |
GO:0044743 | protein transmembrane import into intracellular organelle | 4 | 2 |
GO:0045184 | establishment of protein localization | 3 | 12 |
GO:0046907 | intracellular transport | 3 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051641 | cellular localization | 2 | 12 |
GO:0051649 | establishment of localization in cell | 3 | 12 |
GO:0055085 | transmembrane transport | 2 | 2 |
GO:0065002 | intracellular protein transmembrane transport | 4 | 2 |
GO:0070727 | cellular macromolecule localization | 3 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0071705 | nitrogen compound transport | 4 | 12 |
GO:0071806 | protein transmembrane transport | 3 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 13 |
GO:0072594 | establishment of protein localization to organelle | 4 | 12 |
GO:0072662 | protein localization to peroxisome | 6 | 12 |
GO:0072663 | establishment of protein localization to peroxisome | 5 | 12 |
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: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: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 | 17 |
GO:0003824 | catalytic activity | 1 | 17 |
GO:0005488 | binding | 1 | 17 |
GO:0005524 | ATP binding | 5 | 17 |
GO:0016462 | pyrophosphatase activity | 5 | 17 |
GO:0016787 | hydrolase activity | 2 | 17 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 17 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 17 |
GO:0016887 | ATP hydrolysis activity | 7 | 17 |
GO:0017076 | purine nucleotide binding | 4 | 17 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 17 |
GO:0030554 | adenyl nucleotide binding | 5 | 17 |
GO:0032553 | ribonucleotide binding | 3 | 17 |
GO:0032555 | purine ribonucleotide binding | 4 | 17 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 17 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 17 |
GO:0036094 | small molecule binding | 2 | 17 |
GO:0043167 | ion binding | 2 | 17 |
GO:0043168 | anion binding | 3 | 17 |
GO:0097159 | organic cyclic compound binding | 2 | 17 |
GO:0097367 | carbohydrate derivative binding | 2 | 17 |
GO:1901265 | nucleoside phosphate binding | 3 | 17 |
GO:1901363 | heterocyclic compound binding | 2 | 17 |
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 | 158 | 162 | PF00656 | 0.452 |
CLV_C14_Caspase3-7 | 327 | 331 | PF00656 | 0.586 |
CLV_C14_Caspase3-7 | 500 | 504 | PF00656 | 0.430 |
CLV_C14_Caspase3-7 | 756 | 760 | PF00656 | 0.334 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 516 | 518 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 742 | 744 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 807 | 809 | PF00675 | 0.572 |
CLV_PCSK_FUR_1 | 184 | 188 | PF00082 | 0.659 |
CLV_PCSK_FUR_1 | 228 | 232 | PF00082 | 0.417 |
CLV_PCSK_FUR_1 | 568 | 572 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 516 | 518 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 570 | 572 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 807 | 809 | PF00082 | 0.520 |
CLV_PCSK_PC1ET2_1 | 570 | 572 | PF00082 | 0.558 |
CLV_PCSK_PC7_1 | 566 | 572 | PF00082 | 0.332 |
CLV_PCSK_PC7_1 | 803 | 809 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 516 | 520 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 529 | 533 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 561 | 565 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 692 | 696 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 744 | 748 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 787 | 791 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 950 | 954 | PF00082 | 0.626 |
DEG_APCC_DBOX_1 | 266 | 274 | PF00400 | 0.581 |
DEG_APCC_DBOX_1 | 404 | 412 | PF00400 | 0.430 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.571 |
DEG_SCF_FBW7_1 | 94 | 101 | PF00400 | 0.394 |
DEG_SCF_TRCP1_1 | 216 | 222 | PF00400 | 0.490 |
DOC_CKS1_1 | 307 | 312 | PF01111 | 0.601 |
DOC_CKS1_1 | 589 | 594 | PF01111 | 0.398 |
DOC_CKS1_1 | 95 | 100 | PF01111 | 0.396 |
DOC_CYCLIN_RxL_1 | 514 | 522 | PF00134 | 0.481 |
DOC_CYCLIN_RxL_1 | 782 | 794 | PF00134 | 0.529 |
DOC_CYCLIN_yCln2_LP_2 | 104 | 110 | PF00134 | 0.541 |
DOC_CYCLIN_yCln2_LP_2 | 40 | 46 | PF00134 | 0.379 |
DOC_CYCLIN_yCln2_LP_2 | 440 | 446 | PF00134 | 0.430 |
DOC_CYCLIN_yCln2_LP_2 | 625 | 631 | PF00134 | 0.413 |
DOC_CYCLIN_yCln2_LP_2 | 71 | 77 | PF00134 | 0.386 |
DOC_MAPK_DCC_7 | 102 | 110 | PF00069 | 0.554 |
DOC_MAPK_DCC_7 | 68 | 77 | PF00069 | 0.499 |
DOC_MAPK_DCC_7 | 873 | 883 | PF00069 | 0.486 |
DOC_MAPK_gen_1 | 641 | 648 | PF00069 | 0.379 |
DOC_MAPK_gen_1 | 66 | 73 | PF00069 | 0.516 |
DOC_MAPK_JIP1_4 | 442 | 448 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 240 | 247 | PF00069 | 0.541 |
DOC_MAPK_MEF2A_6 | 37 | 46 | PF00069 | 0.519 |
DOC_MAPK_MEF2A_6 | 570 | 579 | PF00069 | 0.457 |
DOC_MAPK_NFAT4_5 | 240 | 248 | PF00069 | 0.405 |
DOC_PP1_RVXF_1 | 603 | 609 | PF00149 | 0.597 |
DOC_PP1_RVXF_1 | 806 | 813 | PF00149 | 0.429 |
DOC_PP2B_LxvP_1 | 104 | 107 | PF13499 | 0.541 |
DOC_PP2B_LxvP_1 | 40 | 43 | PF13499 | 0.391 |
DOC_PP2B_LxvP_1 | 625 | 628 | PF13499 | 0.359 |
DOC_PP4_FxxP_1 | 589 | 592 | PF00568 | 0.392 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.783 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 720 | 724 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 750 | 754 | PF00917 | 0.286 |
DOC_USP7_MATH_1 | 819 | 823 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 841 | 845 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 891 | 895 | PF00917 | 0.638 |
DOC_USP7_UBL2_3 | 236 | 240 | PF12436 | 0.548 |
DOC_USP7_UBL2_3 | 396 | 400 | PF12436 | 0.320 |
DOC_USP7_UBL2_3 | 923 | 927 | PF12436 | 0.533 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 553 | 558 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 588 | 593 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 810 | 815 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.573 |
LIG_14-3-3_CanoR_1 | 12 | 19 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 230 | 239 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 471 | 475 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 516 | 522 | PF00244 | 0.348 |
LIG_14-3-3_CanoR_1 | 526 | 532 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 807 | 811 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 917 | 925 | PF00244 | 0.458 |
LIG_14-3-3_CterR_2 | 950 | 954 | PF00244 | 0.730 |
LIG_AP2alpha_1 | 707 | 711 | PF02296 | 0.286 |
LIG_BRCT_BRCA1_1 | 793 | 797 | PF00533 | 0.570 |
LIG_Clathr_ClatBox_1 | 903 | 907 | PF01394 | 0.524 |
LIG_EH1_1 | 657 | 665 | PF00400 | 0.317 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.461 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.642 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.547 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.459 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.382 |
LIG_FHA_1 | 531 | 537 | PF00498 | 0.593 |
LIG_FHA_1 | 622 | 628 | PF00498 | 0.410 |
LIG_FHA_1 | 655 | 661 | PF00498 | 0.286 |
LIG_FHA_1 | 724 | 730 | PF00498 | 0.286 |
LIG_FHA_1 | 894 | 900 | PF00498 | 0.694 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.359 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.496 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.541 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.541 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.629 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.327 |
LIG_FHA_2 | 554 | 560 | PF00498 | 0.389 |
LIG_FHA_2 | 811 | 817 | PF00498 | 0.416 |
LIG_GBD_Chelix_1 | 362 | 370 | PF00786 | 0.488 |
LIG_GBD_Chelix_1 | 729 | 737 | PF00786 | 0.345 |
LIG_LIR_Apic_2 | 588 | 592 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 449 | 457 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 607 | 614 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 620 | 629 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 67 | 77 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 709 | 716 | PF02991 | 0.286 |
LIG_LIR_Gen_1 | 907 | 918 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 143 | 148 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 449 | 454 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 553 | 558 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 588 | 593 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 607 | 611 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 620 | 625 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 678 | 683 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 709 | 714 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 907 | 913 | PF02991 | 0.459 |
LIG_MYND_1 | 342 | 346 | PF01753 | 0.541 |
LIG_NRBOX | 785 | 791 | PF00104 | 0.450 |
LIG_PCNA_yPIPBox_3 | 236 | 248 | PF02747 | 0.388 |
LIG_Pex14_2 | 481 | 485 | PF04695 | 0.380 |
LIG_Pex14_2 | 69 | 73 | PF04695 | 0.483 |
LIG_Pex14_2 | 707 | 711 | PF04695 | 0.286 |
LIG_PTAP_UEV_1 | 314 | 319 | PF05743 | 0.504 |
LIG_PTB_Apo_2 | 826 | 833 | PF02174 | 0.514 |
LIG_PTB_Apo_2 | 892 | 899 | PF02174 | 0.453 |
LIG_SH2_CRK | 622 | 626 | PF00017 | 0.366 |
LIG_SH2_SRC | 736 | 739 | PF00017 | 0.317 |
LIG_SH2_STAP1 | 622 | 626 | PF00017 | 0.296 |
LIG_SH2_STAT3 | 683 | 686 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 513 | 516 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 683 | 686 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 736 | 739 | PF00017 | 0.317 |
LIG_SH3_1 | 336 | 342 | PF00018 | 0.499 |
LIG_SH3_2 | 146 | 151 | PF14604 | 0.480 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.493 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.493 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.513 |
LIG_SH3_3 | 312 | 318 | PF00018 | 0.655 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.559 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.445 |
LIG_SH3_3 | 535 | 541 | PF00018 | 0.543 |
LIG_SH3_3 | 769 | 775 | PF00018 | 0.341 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.523 |
LIG_SH3_3 | 940 | 946 | PF00018 | 0.759 |
LIG_SUMO_SIM_anti_2 | 274 | 279 | PF11976 | 0.464 |
LIG_SUMO_SIM_anti_2 | 779 | 788 | PF11976 | 0.408 |
LIG_SUMO_SIM_par_1 | 106 | 114 | PF11976 | 0.538 |
LIG_SUMO_SIM_par_1 | 137 | 143 | PF11976 | 0.588 |
LIG_SUMO_SIM_par_1 | 348 | 353 | PF11976 | 0.560 |
LIG_SUMO_SIM_par_1 | 415 | 420 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 444 | 449 | PF11976 | 0.286 |
LIG_SUMO_SIM_par_1 | 492 | 498 | PF11976 | 0.325 |
LIG_SUMO_SIM_par_1 | 517 | 522 | PF11976 | 0.430 |
LIG_TRAF2_1 | 289 | 292 | PF00917 | 0.680 |
LIG_TRAF2_1 | 798 | 801 | PF00917 | 0.564 |
LIG_UBA3_1 | 634 | 641 | PF00899 | 0.462 |
LIG_UBA3_1 | 785 | 792 | PF00899 | 0.444 |
MOD_CDK_SPK_2 | 94 | 99 | PF00069 | 0.402 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.542 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.799 |
MOD_CK1_1 | 607 | 613 | PF00069 | 0.401 |
MOD_CK1_1 | 723 | 729 | PF00069 | 0.301 |
MOD_CK1_1 | 788 | 794 | PF00069 | 0.443 |
MOD_CK1_1 | 822 | 828 | PF00069 | 0.404 |
MOD_CK1_1 | 912 | 918 | PF00069 | 0.529 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.515 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.413 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.413 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.728 |
MOD_CK2_1 | 458 | 464 | PF00069 | 0.308 |
MOD_CK2_1 | 575 | 581 | PF00069 | 0.572 |
MOD_CK2_1 | 795 | 801 | PF00069 | 0.479 |
MOD_CK2_1 | 916 | 922 | PF00069 | 0.510 |
MOD_Cter_Amidation | 741 | 744 | PF01082 | 0.393 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.344 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.777 |
MOD_GlcNHglycan | 314 | 318 | PF01048 | 0.764 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.686 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.547 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.366 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.628 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.277 |
MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.363 |
MOD_GlcNHglycan | 651 | 654 | PF01048 | 0.315 |
MOD_GlcNHglycan | 721 | 725 | PF01048 | 0.301 |
MOD_GlcNHglycan | 793 | 796 | PF01048 | 0.457 |
MOD_GlcNHglycan | 816 | 820 | PF01048 | 0.445 |
MOD_GlcNHglycan | 822 | 825 | PF01048 | 0.408 |
MOD_GlcNHglycan | 843 | 846 | PF01048 | 0.701 |
MOD_GlcNHglycan | 939 | 942 | PF01048 | 0.759 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.505 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.260 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.430 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.413 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.745 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.270 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.298 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.500 |
MOD_GSK3_1 | 791 | 798 | PF00069 | 0.498 |
MOD_GSK3_1 | 806 | 813 | PF00069 | 0.335 |
MOD_GSK3_1 | 815 | 822 | PF00069 | 0.381 |
MOD_GSK3_1 | 889 | 896 | PF00069 | 0.462 |
MOD_GSK3_1 | 909 | 916 | PF00069 | 0.501 |
MOD_GSK3_1 | 933 | 940 | PF00069 | 0.582 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.582 |
MOD_GSK3_1 | 946 | 953 | PF00069 | 0.739 |
MOD_LATS_1 | 269 | 275 | PF00433 | 0.457 |
MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.715 |
MOD_N-GLC_1 | 553 | 558 | PF02516 | 0.462 |
MOD_N-GLC_1 | 810 | 815 | PF02516 | 0.486 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.556 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.311 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.540 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.419 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.523 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.300 |
MOD_NEK2_1 | 593 | 598 | PF00069 | 0.422 |
MOD_NEK2_1 | 621 | 626 | PF00069 | 0.406 |
MOD_NEK2_1 | 820 | 825 | PF00069 | 0.377 |
MOD_NEK2_1 | 909 | 914 | PF00069 | 0.514 |
MOD_NEK2_2 | 169 | 174 | PF00069 | 0.413 |
MOD_NEK2_2 | 483 | 488 | PF00069 | 0.430 |
MOD_NEK2_2 | 57 | 62 | PF00069 | 0.289 |
MOD_NEK2_2 | 575 | 580 | PF00069 | 0.453 |
MOD_NEK2_2 | 585 | 590 | PF00069 | 0.383 |
MOD_NEK2_2 | 617 | 622 | PF00069 | 0.396 |
MOD_PIKK_1 | 19 | 25 | PF00454 | 0.524 |
MOD_PIKK_1 | 298 | 304 | PF00454 | 0.370 |
MOD_PKA_1 | 230 | 236 | PF00069 | 0.641 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.540 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.414 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.449 |
MOD_PKA_2 | 470 | 476 | PF00069 | 0.454 |
MOD_PKA_2 | 525 | 531 | PF00069 | 0.492 |
MOD_PKA_2 | 806 | 812 | PF00069 | 0.524 |
MOD_PKA_2 | 834 | 840 | PF00069 | 0.553 |
MOD_PKA_2 | 916 | 922 | PF00069 | 0.468 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.370 |
MOD_PKB_1 | 228 | 236 | PF00069 | 0.468 |
MOD_Plk_1 | 474 | 480 | PF00069 | 0.359 |
MOD_Plk_1 | 815 | 821 | PF00069 | 0.511 |
MOD_Plk_1 | 889 | 895 | PF00069 | 0.733 |
MOD_Plk_2-3 | 604 | 610 | PF00069 | 0.477 |
MOD_Plk_2-3 | 902 | 908 | PF00069 | 0.520 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.378 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.492 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.477 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.507 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.402 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.388 |
MOD_Plk_4 | 617 | 623 | PF00069 | 0.427 |
MOD_Plk_4 | 654 | 660 | PF00069 | 0.361 |
MOD_Plk_4 | 823 | 829 | PF00069 | 0.450 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.560 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.591 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.625 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.550 |
MOD_ProDKin_1 | 553 | 559 | PF00069 | 0.433 |
MOD_ProDKin_1 | 588 | 594 | PF00069 | 0.413 |
MOD_ProDKin_1 | 810 | 816 | PF00069 | 0.384 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.566 |
MOD_SUMO_for_1 | 664 | 667 | PF00179 | 0.210 |
MOD_SUMO_rev_2 | 158 | 166 | PF00179 | 0.420 |
MOD_SUMO_rev_2 | 553 | 563 | PF00179 | 0.396 |
MOD_SUMO_rev_2 | 610 | 620 | PF00179 | 0.430 |
MOD_SUMO_rev_2 | 687 | 691 | PF00179 | 0.286 |
TRG_DiLeu_BaEn_2 | 174 | 180 | PF01217 | 0.320 |
TRG_ENDOCYTIC_2 | 555 | 558 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 622 | 625 | PF00928 | 0.372 |
TRG_ER_diArg_1 | 184 | 187 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 206 | 209 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 227 | 230 | PF00400 | 0.621 |
TRG_ER_diArg_1 | 515 | 517 | PF00400 | 0.404 |
TRG_NES_CRM1_1 | 409 | 420 | PF08389 | 0.327 |
TRG_Pf-PMV_PEXEL_1 | 433 | 437 | PF00026 | 0.401 |
TRG_Pf-PMV_PEXEL_1 | 517 | 522 | PF00026 | 0.288 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I568 | Leptomonas seymouri | 76% | 99% |
A0A0S4IKL1 | Bodo saltans | 42% | 100% |
A0A1X0PA10 | Trypanosomatidae | 45% | 100% |
A0A3Q8IIU8 | Leishmania donovani | 93% | 100% |
A0A3R7MK02 | Trypanosoma rangeli | 48% | 100% |
A0A3S7X0L3 | Leishmania donovani | 33% | 100% |
A4HB70 | Leishmania braziliensis | 84% | 100% |
A4HFM9 | Leishmania braziliensis | 32% | 100% |
A4I2Q7 | Leishmania infantum | 33% | 100% |
A4IAB8 | Leishmania infantum | 93% | 100% |
C9ZLX8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9AD83 | Leishmania major | 33% | 100% |
E9AZ07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9B5E1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5BKY8 | Trypanosoma cruzi | 47% | 100% |