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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7WSQ8
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 6 |
GO:0006644 | phospholipid metabolic process | 4 | 6 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 6 |
GO:0006661 | phosphatidylinositol biosynthetic process | 6 | 6 |
GO:0006793 | phosphorus metabolic process | 3 | 8 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 8 |
GO:0007165 | signal transduction | 2 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0008610 | lipid biosynthetic process | 4 | 6 |
GO:0008654 | phospholipid biosynthetic process | 5 | 6 |
GO:0009058 | biosynthetic process | 2 | 6 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016310 | phosphorylation | 5 | 8 |
GO:0019637 | organophosphate metabolic process | 3 | 6 |
GO:0035556 | intracellular signal transduction | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0044249 | cellular biosynthetic process | 3 | 6 |
GO:0044255 | cellular lipid metabolic process | 3 | 6 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 6 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 6 |
GO:0046486 | glycerolipid metabolic process | 4 | 6 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 6 |
GO:0046854 | phosphatidylinositol phosphate biosynthetic process | 7 | 6 |
GO:0048015 | phosphatidylinositol-mediated signaling | 5 | 8 |
GO:0048017 | inositol lipid-mediated signaling | 4 | 8 |
GO:0050789 | regulation of biological process | 2 | 8 |
GO:0050794 | regulation of cellular process | 3 | 8 |
GO:0065007 | biological regulation | 1 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:0090407 | organophosphate biosynthetic process | 4 | 6 |
GO:1901576 | organic substance biosynthetic process | 3 | 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0016301 | kinase activity | 4 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
GO:0016303 | 1-phosphatidylinositol-3-kinase activity | 6 | 2 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 2 |
GO:0035004 | phosphatidylinositol 3-kinase activity | 5 | 2 |
GO:0052742 | phosphatidylinositol kinase activity | 5 | 2 |
GO:0046934 | phosphatidylinositol-4,5-bisphosphate 3-kinase activity | 6 | 1 |
GO:0052812 | phosphatidylinositol-3,4-bisphosphate 5-kinase activity | 6 | 1 |
GO:0052813 | phosphatidylinositol bisphosphate kinase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 154 | 158 | PF00656 | 0.347 |
CLV_C14_Caspase3-7 | 277 | 281 | PF00656 | 0.374 |
CLV_C14_Caspase3-7 | 601 | 605 | PF00656 | 0.226 |
CLV_C14_Caspase3-7 | 807 | 811 | PF00656 | 0.186 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 500 | 502 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 507 | 509 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 589 | 591 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 655 | 657 | PF00675 | 0.401 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 851 | 853 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 976 | 978 | PF00675 | 0.172 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.388 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 500 | 502 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 507 | 509 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 533 | 535 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 589 | 591 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 655 | 657 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 694 | 696 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 851 | 853 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 937 | 939 | PF00082 | 0.186 |
CLV_PCSK_KEX2_1 | 976 | 978 | PF00082 | 0.172 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.400 |
CLV_PCSK_PC1ET2_1 | 243 | 245 | PF00082 | 0.390 |
CLV_PCSK_PC1ET2_1 | 500 | 502 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 533 | 535 | PF00082 | 0.386 |
CLV_PCSK_PC1ET2_1 | 694 | 696 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 937 | 939 | PF00082 | 0.186 |
CLV_PCSK_PC7_1 | 173 | 179 | PF00082 | 0.463 |
CLV_PCSK_PC7_1 | 651 | 657 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 1007 | 1011 | PF00082 | 0.225 |
CLV_PCSK_SKI1_1 | 1035 | 1039 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 530 | 534 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 549 | 553 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 651 | 655 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 677 | 681 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 714 | 718 | PF00082 | 0.447 |
DEG_APCC_DBOX_1 | 42 | 50 | PF00400 | 0.306 |
DEG_APCC_DBOX_1 | 731 | 739 | PF00400 | 0.228 |
DEG_APCC_DBOX_1 | 796 | 804 | PF00400 | 0.186 |
DEG_SPOP_SBC_1 | 394 | 398 | PF00917 | 0.240 |
DOC_ANK_TNKS_1 | 461 | 468 | PF00023 | 0.268 |
DOC_CKS1_1 | 944 | 949 | PF01111 | 0.386 |
DOC_CYCLIN_RxL_1 | 382 | 392 | PF00134 | 0.201 |
DOC_CYCLIN_RxL_1 | 54 | 65 | PF00134 | 0.319 |
DOC_CYCLIN_RxL_1 | 645 | 657 | PF00134 | 0.186 |
DOC_MAPK_gen_1 | 243 | 251 | PF00069 | 0.190 |
DOC_MAPK_gen_1 | 460 | 468 | PF00069 | 0.325 |
DOC_MAPK_gen_1 | 768 | 776 | PF00069 | 0.214 |
DOC_MAPK_MEF2A_6 | 139 | 146 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 206 | 215 | PF00069 | 0.221 |
DOC_MAPK_MEF2A_6 | 243 | 251 | PF00069 | 0.268 |
DOC_MAPK_MEF2A_6 | 768 | 776 | PF00069 | 0.230 |
DOC_MAPK_MEF2A_6 | 797 | 805 | PF00069 | 0.199 |
DOC_MAPK_MEF2A_6 | 814 | 822 | PF00069 | 0.203 |
DOC_MAPK_NFAT4_5 | 139 | 147 | PF00069 | 0.363 |
DOC_MAPK_NFAT4_5 | 244 | 252 | PF00069 | 0.190 |
DOC_PP1_RVXF_1 | 363 | 369 | PF00149 | 0.240 |
DOC_PP1_RVXF_1 | 386 | 392 | PF00149 | 0.275 |
DOC_PP1_RVXF_1 | 487 | 494 | PF00149 | 0.328 |
DOC_PP1_RVXF_1 | 547 | 554 | PF00149 | 0.201 |
DOC_PP1_RVXF_1 | 55 | 62 | PF00149 | 0.305 |
DOC_PP1_RVXF_1 | 735 | 741 | PF00149 | 0.229 |
DOC_PP2B_LxvP_1 | 7 | 10 | PF13499 | 0.369 |
DOC_PP2B_PxIxI_1 | 210 | 216 | PF00149 | 0.190 |
DOC_PP4_FxxP_1 | 132 | 135 | PF00568 | 0.267 |
DOC_PP4_FxxP_1 | 259 | 262 | PF00568 | 0.331 |
DOC_PP4_FxxP_1 | 487 | 490 | PF00568 | 0.269 |
DOC_SPAK_OSR1_1 | 15 | 19 | PF12202 | 0.358 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.293 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.246 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.215 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.387 |
DOC_USP7_UBL2_3 | 564 | 568 | PF12436 | 0.226 |
DOC_USP7_UBL2_3 | 725 | 729 | PF12436 | 0.252 |
DOC_USP7_UBL2_3 | 933 | 937 | PF12436 | 0.386 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.190 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 589 | 594 | PF00397 | 0.268 |
DOC_WW_Pin1_4 | 693 | 698 | PF00397 | 0.268 |
DOC_WW_Pin1_4 | 943 | 948 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 955 | 960 | PF00397 | 0.405 |
LIG_14-3-3_CanoR_1 | 173 | 181 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 191 | 200 | PF00244 | 0.214 |
LIG_14-3-3_CanoR_1 | 31 | 38 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 405 | 413 | PF00244 | 0.229 |
LIG_14-3-3_CanoR_1 | 44 | 50 | PF00244 | 0.246 |
LIG_14-3-3_CanoR_1 | 655 | 659 | PF00244 | 0.228 |
LIG_14-3-3_CanoR_1 | 732 | 736 | PF00244 | 0.288 |
LIG_14-3-3_CanoR_1 | 743 | 747 | PF00244 | 0.174 |
LIG_14-3-3_CanoR_1 | 85 | 94 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 976 | 986 | PF00244 | 0.468 |
LIG_Actin_WH2_2 | 519 | 535 | PF00022 | 0.238 |
LIG_Actin_WH2_2 | 993 | 1009 | PF00022 | 0.434 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.386 |
LIG_BIR_III_4 | 1029 | 1033 | PF00653 | 0.497 |
LIG_BRCT_BRCA1_1 | 325 | 329 | PF00533 | 0.306 |
LIG_BRCT_BRCA1_1 | 428 | 432 | PF00533 | 0.229 |
LIG_BRCT_BRCA1_1 | 766 | 770 | PF00533 | 0.286 |
LIG_BRCT_BRCA1_1 | 957 | 961 | PF00533 | 0.415 |
LIG_Clathr_ClatBox_1 | 576 | 580 | PF01394 | 0.215 |
LIG_Clathr_ClatBox_1 | 918 | 922 | PF01394 | 0.386 |
LIG_deltaCOP1_diTrp_1 | 108 | 112 | PF00928 | 0.242 |
LIG_eIF4E_1 | 226 | 232 | PF01652 | 0.186 |
LIG_eIF4E_1 | 582 | 588 | PF01652 | 0.201 |
LIG_eIF4E_1 | 707 | 713 | PF01652 | 0.201 |
LIG_FHA_1 | 1006 | 1012 | PF00498 | 0.446 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.258 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.215 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.377 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.334 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.213 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.276 |
LIG_FHA_1 | 477 | 483 | PF00498 | 0.317 |
LIG_FHA_1 | 743 | 749 | PF00498 | 0.207 |
LIG_FHA_1 | 800 | 806 | PF00498 | 0.186 |
LIG_FHA_1 | 895 | 901 | PF00498 | 0.227 |
LIG_FHA_2 | 1013 | 1019 | PF00498 | 0.486 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.309 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.342 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.240 |
LIG_FHA_2 | 66 | 72 | PF00498 | 0.272 |
LIG_FHA_2 | 678 | 684 | PF00498 | 0.215 |
LIG_FHA_2 | 848 | 854 | PF00498 | 0.226 |
LIG_FHA_2 | 997 | 1003 | PF00498 | 0.520 |
LIG_IRF3_LxIS_1 | 306 | 312 | PF10401 | 0.345 |
LIG_LIR_Apic_2 | 257 | 262 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 1040 | 1046 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 199 | 205 | PF02991 | 0.221 |
LIG_LIR_Gen_1 | 326 | 337 | PF02991 | 0.250 |
LIG_LIR_Gen_1 | 604 | 612 | PF02991 | 0.201 |
LIG_LIR_Gen_1 | 784 | 794 | PF02991 | 0.232 |
LIG_LIR_LC3C_4 | 246 | 251 | PF02991 | 0.190 |
LIG_LIR_Nem_3 | 1020 | 1026 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 1040 | 1044 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 108 | 112 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 325 | 331 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 481 | 487 | PF02991 | 0.231 |
LIG_LIR_Nem_3 | 604 | 610 | PF02991 | 0.226 |
LIG_LIR_Nem_3 | 783 | 789 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 922 | 926 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 958 | 964 | PF02991 | 0.386 |
LIG_MLH1_MIPbox_1 | 325 | 329 | PF16413 | 0.233 |
LIG_MLH1_MIPbox_1 | 428 | 432 | PF16413 | 0.215 |
LIG_PCNA_APIM_2 | 649 | 655 | PF02747 | 0.186 |
LIG_PCNA_yPIPBox_3 | 655 | 668 | PF02747 | 0.268 |
LIG_Pex14_1 | 575 | 579 | PF04695 | 0.186 |
LIG_Pex14_1 | 868 | 872 | PF04695 | 0.186 |
LIG_Pex14_2 | 480 | 484 | PF04695 | 0.261 |
LIG_Pex14_2 | 740 | 744 | PF04695 | 0.301 |
LIG_Pex14_2 | 786 | 790 | PF04695 | 0.196 |
LIG_Pex14_2 | 919 | 923 | PF04695 | 0.386 |
LIG_Pex14_2 | 926 | 930 | PF04695 | 0.386 |
LIG_PTB_Apo_2 | 230 | 237 | PF02174 | 0.172 |
LIG_PTB_Phospho_1 | 230 | 236 | PF10480 | 0.172 |
LIG_SH2_CRK | 1023 | 1027 | PF00017 | 0.512 |
LIG_SH2_CRK | 234 | 238 | PF00017 | 0.190 |
LIG_SH2_CRK | 538 | 542 | PF00017 | 0.268 |
LIG_SH2_CRK | 646 | 650 | PF00017 | 0.226 |
LIG_SH2_CRK | 825 | 829 | PF00017 | 0.186 |
LIG_SH2_CRK | 972 | 976 | PF00017 | 0.426 |
LIG_SH2_GRB2like | 105 | 108 | PF00017 | 0.242 |
LIG_SH2_NCK_1 | 893 | 897 | PF00017 | 0.224 |
LIG_SH2_PTP2 | 1041 | 1044 | PF00017 | 0.430 |
LIG_SH2_SRC | 1041 | 1044 | PF00017 | 0.430 |
LIG_SH2_SRC | 166 | 169 | PF00017 | 0.266 |
LIG_SH2_SRC | 224 | 227 | PF00017 | 0.186 |
LIG_SH2_SRC | 949 | 952 | PF00017 | 0.468 |
LIG_SH2_STAP1 | 443 | 447 | PF00017 | 0.268 |
LIG_SH2_STAP1 | 607 | 611 | PF00017 | 0.240 |
LIG_SH2_STAP1 | 646 | 650 | PF00017 | 0.268 |
LIG_SH2_STAT3 | 226 | 229 | PF00017 | 0.268 |
LIG_SH2_STAT3 | 702 | 705 | PF00017 | 0.199 |
LIG_SH2_STAT5 | 1041 | 1044 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.242 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.201 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.186 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.227 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 520 | 523 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 619 | 622 | PF00017 | 0.232 |
LIG_SH2_STAT5 | 667 | 670 | PF00017 | 0.186 |
LIG_SH2_STAT5 | 671 | 674 | PF00017 | 0.186 |
LIG_SH2_STAT5 | 702 | 705 | PF00017 | 0.199 |
LIG_SH2_STAT5 | 707 | 710 | PF00017 | 0.201 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.206 |
LIG_SH2_STAT5 | 893 | 896 | PF00017 | 0.214 |
LIG_SH2_STAT5 | 898 | 901 | PF00017 | 0.214 |
LIG_SH2_STAT5 | 949 | 952 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 963 | 966 | PF00017 | 0.390 |
LIG_SH3_2 | 117 | 122 | PF14604 | 0.304 |
LIG_SH3_2 | 266 | 271 | PF14604 | 0.275 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.296 |
LIG_SH3_3 | 247 | 253 | PF00018 | 0.309 |
LIG_SH3_3 | 263 | 269 | PF00018 | 0.268 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.254 |
LIG_SH3_3 | 488 | 494 | PF00018 | 0.269 |
LIG_SH3_3 | 735 | 741 | PF00018 | 0.322 |
LIG_SH3_3 | 953 | 959 | PF00018 | 0.331 |
LIG_SUMO_SIM_anti_2 | 1008 | 1013 | PF11976 | 0.436 |
LIG_SUMO_SIM_anti_2 | 246 | 252 | PF11976 | 0.301 |
LIG_SUMO_SIM_anti_2 | 598 | 604 | PF11976 | 0.186 |
LIG_SUMO_SIM_par_1 | 986 | 992 | PF11976 | 0.386 |
LIG_TRAF2_1 | 1015 | 1018 | PF00917 | 0.444 |
LIG_TRAF2_1 | 408 | 411 | PF00917 | 0.201 |
LIG_TRAF2_1 | 415 | 418 | PF00917 | 0.201 |
LIG_TYR_ITIM | 232 | 237 | PF00017 | 0.220 |
LIG_TYR_ITIM | 536 | 541 | PF00017 | 0.330 |
LIG_TYR_ITIM | 823 | 828 | PF00017 | 0.236 |
LIG_UBA3_1 | 632 | 640 | PF00899 | 0.318 |
LIG_UBA3_1 | 688 | 694 | PF00899 | 0.279 |
LIG_UBA3_1 | 805 | 814 | PF00899 | 0.214 |
MOD_CDC14_SPxK_1 | 696 | 699 | PF00782 | 0.381 |
MOD_CDK_SPxK_1 | 693 | 699 | PF00069 | 0.330 |
MOD_CDK_SPxxK_3 | 955 | 962 | PF00069 | 0.330 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.542 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.401 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.565 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.483 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.473 |
MOD_CK1_1 | 657 | 663 | PF00069 | 0.224 |
MOD_CK2_1 | 1012 | 1018 | PF00069 | 0.307 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.445 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.348 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.615 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.438 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.262 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.282 |
MOD_CK2_1 | 621 | 627 | PF00069 | 0.214 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.244 |
MOD_CK2_1 | 677 | 683 | PF00069 | 0.220 |
MOD_CK2_1 | 826 | 832 | PF00069 | 0.270 |
MOD_CK2_1 | 847 | 853 | PF00069 | 0.330 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.306 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.535 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.220 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.505 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.424 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.361 |
MOD_GlcNHglycan | 646 | 649 | PF01048 | 0.255 |
MOD_GlcNHglycan | 791 | 794 | PF01048 | 0.330 |
MOD_GlcNHglycan | 815 | 818 | PF01048 | 0.404 |
MOD_GlcNHglycan | 979 | 982 | PF01048 | 0.272 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.395 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.539 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.421 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.617 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.535 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.245 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.347 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.172 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.457 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.303 |
MOD_N-GLC_1 | 1012 | 1017 | PF02516 | 0.457 |
MOD_N-GLC_1 | 677 | 682 | PF02516 | 0.214 |
MOD_N-GLC_1 | 847 | 852 | PF02516 | 0.214 |
MOD_N-GLC_1 | 87 | 92 | PF02516 | 0.289 |
MOD_N-GLC_2 | 476 | 478 | PF02516 | 0.352 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.357 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.549 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.535 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.225 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.270 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.219 |
MOD_NEK2_1 | 731 | 736 | PF00069 | 0.304 |
MOD_NEK2_1 | 808 | 813 | PF00069 | 0.214 |
MOD_NEK2_1 | 886 | 891 | PF00069 | 0.273 |
MOD_NEK2_1 | 988 | 993 | PF00069 | 0.280 |
MOD_NEK2_2 | 111 | 116 | PF00069 | 0.316 |
MOD_NEK2_2 | 158 | 163 | PF00069 | 0.324 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.290 |
MOD_PIKK_1 | 435 | 441 | PF00454 | 0.316 |
MOD_PKA_1 | 937 | 943 | PF00069 | 0.214 |
MOD_PKA_1 | 976 | 982 | PF00069 | 0.246 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.354 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.219 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.424 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.440 |
MOD_PKA_2 | 654 | 660 | PF00069 | 0.236 |
MOD_PKA_2 | 731 | 737 | PF00069 | 0.337 |
MOD_PKA_2 | 742 | 748 | PF00069 | 0.203 |
MOD_PKA_2 | 937 | 943 | PF00069 | 0.214 |
MOD_PKA_2 | 976 | 982 | PF00069 | 0.322 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.357 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.476 |
MOD_Plk_1 | 547 | 553 | PF00069 | 0.282 |
MOD_Plk_1 | 677 | 683 | PF00069 | 0.215 |
MOD_Plk_2-3 | 199 | 205 | PF00069 | 0.220 |
MOD_Plk_2-3 | 621 | 627 | PF00069 | 0.330 |
MOD_Plk_2-3 | 996 | 1002 | PF00069 | 0.407 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.323 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.418 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.425 |
MOD_Plk_4 | 516 | 522 | PF00069 | 0.386 |
MOD_Plk_4 | 547 | 553 | PF00069 | 0.255 |
MOD_Plk_4 | 808 | 814 | PF00069 | 0.239 |
MOD_Plk_4 | 894 | 900 | PF00069 | 0.214 |
MOD_Plk_4 | 914 | 920 | PF00069 | 0.115 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.220 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.640 |
MOD_ProDKin_1 | 589 | 595 | PF00069 | 0.330 |
MOD_ProDKin_1 | 693 | 699 | PF00069 | 0.330 |
MOD_ProDKin_1 | 943 | 949 | PF00069 | 0.221 |
MOD_ProDKin_1 | 955 | 961 | PF00069 | 0.241 |
MOD_SUMO_for_1 | 316 | 319 | PF00179 | 0.332 |
MOD_SUMO_for_1 | 639 | 642 | PF00179 | 0.214 |
MOD_SUMO_for_1 | 936 | 939 | PF00179 | 0.227 |
MOD_SUMO_rev_2 | 102 | 112 | PF00179 | 0.353 |
MOD_SUMO_rev_2 | 246 | 256 | PF00179 | 0.255 |
MOD_SUMO_rev_2 | 381 | 389 | PF00179 | 0.210 |
MOD_SUMO_rev_2 | 545 | 551 | PF00179 | 0.253 |
MOD_SUMO_rev_2 | 758 | 765 | PF00179 | 0.400 |
TRG_DiLeu_BaEn_1 | 583 | 588 | PF01217 | 0.236 |
TRG_DiLeu_BaEn_1 | 683 | 688 | PF01217 | 0.214 |
TRG_DiLeu_BaEn_2 | 938 | 944 | PF01217 | 0.214 |
TRG_DiLeu_BaLyEn_6 | 208 | 213 | PF01217 | 0.405 |
TRG_DiLeu_BaLyEn_6 | 227 | 232 | PF01217 | 0.155 |
TRG_DiLeu_BaLyEn_6 | 54 | 59 | PF01217 | 0.315 |
TRG_ENDOCYTIC_2 | 1023 | 1026 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 1041 | 1044 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.220 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 538 | 541 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 555 | 558 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 607 | 610 | PF00928 | 0.270 |
TRG_ENDOCYTIC_2 | 646 | 649 | PF00928 | 0.270 |
TRG_ENDOCYTIC_2 | 825 | 828 | PF00928 | 0.227 |
TRG_ENDOCYTIC_2 | 972 | 975 | PF00928 | 0.279 |
TRG_ER_diArg_1 | 177 | 179 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 3 | 6 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 588 | 590 | PF00400 | 0.255 |
TRG_ER_diArg_1 | 654 | 656 | PF00400 | 0.236 |
TRG_ER_diArg_1 | 85 | 87 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 97 | 99 | PF00400 | 0.242 |
TRG_ER_diArg_1 | 975 | 977 | PF00400 | 0.195 |
TRG_NES_CRM1_1 | 1001 | 1016 | PF08389 | 0.318 |
TRG_NES_CRM1_1 | 527 | 539 | PF08389 | 0.255 |
TRG_NES_CRM1_1 | 627 | 642 | PF08389 | 0.236 |
TRG_NES_CRM1_1 | 794 | 807 | PF08389 | 0.214 |
TRG_Pf-PMV_PEXEL_1 | 1035 | 1040 | PF00026 | 0.278 |
TRG_Pf-PMV_PEXEL_1 | 126 | 130 | PF00026 | 0.362 |
TRG_Pf-PMV_PEXEL_1 | 31 | 35 | PF00026 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 36 | 40 | PF00026 | 0.369 |
TRG_Pf-PMV_PEXEL_1 | 534 | 539 | PF00026 | 0.214 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0G2K344 | Rattus norvegicus | 33% | 98% |
A0A0N1I4K0 | Leptomonas seymouri | 74% | 100% |
A0A1X0NPD0 | Trypanosomatidae | 55% | 99% |
A0A3R7MRK8 | Trypanosoma rangeli | 51% | 99% |
A4HVU4 | Leishmania infantum | 100% | 100% |
E9APJ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
O00329 | Homo sapiens | 33% | 100% |
O02697 | Sus scrofa | 33% | 95% |
O35904 | Mus musculus | 34% | 100% |
P0C5E7 | Caenorhabditis briggsae | 28% | 90% |
P32871 | Bos taurus | 33% | 98% |
P42336 | Homo sapiens | 33% | 98% |
P42337 | Mus musculus | 33% | 98% |
P42338 | Homo sapiens | 33% | 98% |
P48736 | Homo sapiens | 34% | 95% |
Q8BTI9 | Mus musculus | 33% | 98% |
Q94125 | Caenorhabditis elegans | 29% | 89% |
Q9JHG7 | Mus musculus | 34% | 95% |
Q9Z1L0 | Rattus norvegicus | 33% | 98% |
V5AXQ0 | Trypanosoma cruzi | 52% | 99% |