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. | yes | yes: 25 |
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: Q4QEX2
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 3 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 3 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 3 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009058 | biosynthetic process | 2 | 3 |
GO:0009117 | nucleotide metabolic process | 5 | 3 |
GO:0009165 | nucleotide biosynthetic process | 6 | 3 |
GO:0009225 | nucleotide-sugar metabolic process | 4 | 3 |
GO:0009226 | nucleotide-sugar biosynthetic process | 5 | 3 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016310 | phosphorylation | 5 | 11 |
GO:0018130 | heterocycle biosynthetic process | 4 | 3 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 3 |
GO:0019637 | organophosphate metabolic process | 3 | 3 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 3 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 3 |
GO:0042350 | GDP-L-fucose biosynthetic process | 5 | 3 |
GO:0042352 | GDP-L-fucose salvage | 5 | 3 |
GO:0043094 | cellular metabolic compound salvage | 3 | 3 |
GO:0043173 | nucleotide salvage | 4 | 3 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0044249 | cellular biosynthetic process | 3 | 3 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 3 |
GO:0044281 | small molecule metabolic process | 2 | 3 |
GO:0046368 | GDP-L-fucose metabolic process | 4 | 3 |
GO:0046483 | heterocycle metabolic process | 3 | 3 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:0090407 | organophosphate biosynthetic process | 4 | 3 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 3 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 3 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 3 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 3 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 3 |
GO:1901576 | organic substance biosynthetic process | 3 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0016301 | kinase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 11 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0050201 | fucokinase activity | 5 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 265 | 269 | PF00656 | 0.412 |
CLV_C14_Caspase3-7 | 313 | 317 | PF00656 | 0.568 |
CLV_C14_Caspase3-7 | 751 | 755 | PF00656 | 0.651 |
CLV_MEL_PAP_1 | 930 | 936 | PF00089 | 0.604 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 1155 | 1157 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 609 | 611 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 767 | 769 | PF00675 | 0.660 |
CLV_NRD_NRD_1 | 982 | 984 | PF00675 | 0.396 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 1108 | 1110 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 1155 | 1157 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 609 | 611 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 767 | 769 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 982 | 984 | PF00082 | 0.368 |
CLV_PCSK_PC1ET2_1 | 1108 | 1110 | PF00082 | 0.630 |
CLV_PCSK_PC1ET2_1 | 82 | 84 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 1049 | 1053 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 1060 | 1064 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 1158 | 1162 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 609 | 613 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 768 | 772 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 906 | 910 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 982 | 986 | PF00082 | 0.369 |
CLV_Separin_Metazoa | 1057 | 1061 | PF03568 | 0.539 |
DEG_APCC_DBOX_1 | 169 | 177 | PF00400 | 0.495 |
DEG_APCC_DBOX_1 | 608 | 616 | PF00400 | 0.626 |
DEG_APCC_DBOX_1 | 82 | 90 | PF00400 | 0.577 |
DEG_Kelch_Keap1_1 | 877 | 882 | PF01344 | 0.648 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.702 |
DEG_ODPH_VHL_1 | 355 | 368 | PF01847 | 0.754 |
DEG_SCF_FBW7_1 | 341 | 346 | PF00400 | 0.702 |
DEG_SCF_TRCP1_1 | 879 | 885 | PF00400 | 0.607 |
DOC_ANK_TNKS_1 | 225 | 232 | PF00023 | 0.468 |
DOC_CKS1_1 | 347 | 352 | PF01111 | 0.650 |
DOC_CKS1_1 | 377 | 382 | PF01111 | 0.660 |
DOC_CYCLIN_RxL_1 | 1155 | 1162 | PF00134 | 0.563 |
DOC_CYCLIN_RxL_1 | 129 | 140 | PF00134 | 0.470 |
DOC_CYCLIN_RxL_1 | 205 | 213 | PF00134 | 0.536 |
DOC_CYCLIN_RxL_1 | 764 | 775 | PF00134 | 0.453 |
DOC_CYCLIN_RxL_1 | 978 | 988 | PF00134 | 0.594 |
DOC_CYCLIN_yCln2_LP_2 | 633 | 639 | PF00134 | 0.667 |
DOC_MAPK_gen_1 | 609 | 616 | PF00069 | 0.628 |
DOC_MAPK_HePTP_8 | 863 | 875 | PF00069 | 0.532 |
DOC_MAPK_MEF2A_6 | 232 | 241 | PF00069 | 0.473 |
DOC_MAPK_MEF2A_6 | 609 | 618 | PF00069 | 0.567 |
DOC_MAPK_MEF2A_6 | 656 | 664 | PF00069 | 0.587 |
DOC_MAPK_MEF2A_6 | 807 | 816 | PF00069 | 0.576 |
DOC_MAPK_MEF2A_6 | 823 | 830 | PF00069 | 0.495 |
DOC_MAPK_MEF2A_6 | 866 | 875 | PF00069 | 0.461 |
DOC_MAPK_NFAT4_5 | 609 | 617 | PF00069 | 0.566 |
DOC_PP2B_LxvP_1 | 1133 | 1136 | PF13499 | 0.534 |
DOC_PP2B_LxvP_1 | 120 | 123 | PF13499 | 0.409 |
DOC_PP2B_LxvP_1 | 446 | 449 | PF13499 | 0.498 |
DOC_PP2B_LxvP_1 | 660 | 663 | PF13499 | 0.593 |
DOC_PP4_FxxP_1 | 7 | 10 | PF00568 | 0.626 |
DOC_PP4_FxxP_1 | 902 | 905 | PF00568 | 0.455 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.313 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 665 | 669 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 700 | 704 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 740 | 744 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 810 | 814 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 948 | 952 | PF00917 | 0.558 |
DOC_USP7_UBL2_3 | 17 | 21 | PF12436 | 0.623 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 627 | 632 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 713 | 718 | PF00397 | 0.827 |
DOC_WW_Pin1_4 | 834 | 839 | PF00397 | 0.491 |
LIG_14-3-3_CanoR_1 | 135 | 145 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 155 | 160 | PF00244 | 0.213 |
LIG_14-3-3_CanoR_1 | 232 | 236 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 275 | 283 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 326 | 335 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 490 | 496 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 508 | 513 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 585 | 592 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 593 | 601 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 609 | 615 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 83 | 89 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 893 | 899 | PF00244 | 0.660 |
LIG_Actin_WH2_2 | 300 | 317 | PF00022 | 0.627 |
LIG_Actin_WH2_2 | 587 | 604 | PF00022 | 0.548 |
LIG_APCC_ABBA_1 | 142 | 147 | PF00400 | 0.423 |
LIG_APCC_ABBA_1 | 812 | 817 | PF00400 | 0.526 |
LIG_BIR_III_2 | 372 | 376 | PF00653 | 0.656 |
LIG_BIR_III_4 | 168 | 172 | PF00653 | 0.495 |
LIG_BIR_III_4 | 678 | 682 | PF00653 | 0.739 |
LIG_BRCT_BRCA1_1 | 3 | 7 | PF00533 | 0.701 |
LIG_BRCT_BRCA1_1 | 506 | 510 | PF00533 | 0.587 |
LIG_deltaCOP1_diTrp_1 | 420 | 428 | PF00928 | 0.565 |
LIG_deltaCOP1_diTrp_1 | 503 | 510 | PF00928 | 0.586 |
LIG_EH_1 | 899 | 903 | PF12763 | 0.563 |
LIG_EVH1_1 | 120 | 124 | PF00568 | 0.460 |
LIG_FHA_1 | 1067 | 1073 | PF00498 | 0.543 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.588 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.480 |
LIG_FHA_1 | 611 | 617 | PF00498 | 0.551 |
LIG_FHA_1 | 953 | 959 | PF00498 | 0.581 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.388 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.495 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.648 |
LIG_FHA_2 | 923 | 929 | PF00498 | 0.538 |
LIG_HP1_1 | 636 | 640 | PF01393 | 0.528 |
LIG_LIR_Apic_2 | 1028 | 1034 | PF02991 | 0.540 |
LIG_LIR_Apic_2 | 346 | 350 | PF02991 | 0.749 |
LIG_LIR_Apic_2 | 4 | 10 | PF02991 | 0.658 |
LIG_LIR_Gen_1 | 284 | 293 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 549 | 558 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 706 | 711 | PF02991 | 0.746 |
LIG_LIR_Gen_1 | 837 | 848 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 87 | 92 | PF02991 | 0.587 |
LIG_LIR_Gen_1 | 887 | 896 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 921 | 931 | PF02991 | 0.545 |
LIG_LIR_Gen_1 | 942 | 948 | PF02991 | 0.597 |
LIG_LIR_Gen_1 | 969 | 974 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 1090 | 1096 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 281 | 286 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 316 | 322 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 493 | 499 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 549 | 553 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 671 | 677 | PF02991 | 0.767 |
LIG_LIR_Nem_3 | 706 | 710 | PF02991 | 0.624 |
LIG_LIR_Nem_3 | 837 | 843 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 87 | 91 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 887 | 892 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 921 | 926 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 942 | 947 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 969 | 973 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 999 | 1004 | PF02991 | 0.614 |
LIG_Pex14_1 | 707 | 711 | PF04695 | 0.756 |
LIG_Pex14_1 | 997 | 1001 | PF04695 | 0.596 |
LIG_Pex14_2 | 914 | 918 | PF04695 | 0.462 |
LIG_PTB_Apo_2 | 600 | 607 | PF02174 | 0.585 |
LIG_PTB_Phospho_1 | 600 | 606 | PF10480 | 0.588 |
LIG_RPA_C_Fungi | 567 | 579 | PF08784 | 0.562 |
LIG_RPA_C_Fungi | 762 | 774 | PF08784 | 0.604 |
LIG_SH2_CRK | 1001 | 1005 | PF00017 | 0.488 |
LIG_SH2_CRK | 1044 | 1048 | PF00017 | 0.522 |
LIG_SH2_CRK | 1085 | 1089 | PF00017 | 0.561 |
LIG_SH2_CRK | 1096 | 1100 | PF00017 | 0.539 |
LIG_SH2_CRK | 496 | 500 | PF00017 | 0.565 |
LIG_SH2_CRK | 840 | 844 | PF00017 | 0.478 |
LIG_SH2_CRK | 923 | 927 | PF00017 | 0.532 |
LIG_SH2_NCK_1 | 1085 | 1089 | PF00017 | 0.559 |
LIG_SH2_PTP2 | 864 | 867 | PF00017 | 0.522 |
LIG_SH2_STAP1 | 1096 | 1100 | PF00017 | 0.531 |
LIG_SH2_STAP1 | 286 | 290 | PF00017 | 0.414 |
LIG_SH2_STAP1 | 533 | 537 | PF00017 | 0.491 |
LIG_SH2_STAP1 | 607 | 611 | PF00017 | 0.565 |
LIG_SH2_STAT3 | 214 | 217 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 1031 | 1034 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 1044 | 1047 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 1129 | 1132 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 552 | 555 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 864 | 867 | PF00017 | 0.442 |
LIG_SH3_1 | 338 | 344 | PF00018 | 0.620 |
LIG_SH3_2 | 121 | 126 | PF14604 | 0.470 |
LIG_SH3_2 | 410 | 415 | PF14604 | 0.673 |
LIG_SH3_3 | 1012 | 1018 | PF00018 | 0.551 |
LIG_SH3_3 | 1111 | 1117 | PF00018 | 0.578 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.469 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.663 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.686 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.665 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.622 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.768 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.615 |
LIG_SH3_3 | 620 | 626 | PF00018 | 0.572 |
LIG_SH3_3 | 628 | 634 | PF00018 | 0.550 |
LIG_SH3_3 | 659 | 665 | PF00018 | 0.605 |
LIG_SH3_3 | 689 | 695 | PF00018 | 0.763 |
LIG_SH3_3 | 942 | 948 | PF00018 | 0.477 |
LIG_SUMO_SIM_anti_2 | 1121 | 1127 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 1121 | 1127 | PF11976 | 0.596 |
LIG_SUMO_SIM_par_1 | 207 | 213 | PF11976 | 0.536 |
LIG_SUMO_SIM_par_1 | 310 | 316 | PF11976 | 0.492 |
LIG_SUMO_SIM_par_1 | 782 | 788 | PF11976 | 0.569 |
LIG_SUMO_SIM_par_1 | 983 | 988 | PF11976 | 0.414 |
LIG_TRAF2_1 | 776 | 779 | PF00917 | 0.631 |
LIG_TYR_ITIM | 1042 | 1047 | PF00017 | 0.498 |
LIG_TYR_ITSM | 492 | 499 | PF00017 | 0.571 |
LIG_UBA3_1 | 1004 | 1009 | PF00899 | 0.485 |
LIG_WRC_WIRS_1 | 886 | 891 | PF05994 | 0.501 |
LIG_WW_3 | 122 | 126 | PF00397 | 0.320 |
MOD_CDC14_SPxK_1 | 412 | 415 | PF00782 | 0.688 |
MOD_CDK_SPxK_1 | 409 | 415 | PF00069 | 0.715 |
MOD_CK1_1 | 1029 | 1035 | PF00069 | 0.567 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.536 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.621 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.535 |
MOD_CK1_1 | 668 | 674 | PF00069 | 0.705 |
MOD_CK1_1 | 703 | 709 | PF00069 | 0.743 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.535 |
MOD_CK1_1 | 844 | 850 | PF00069 | 0.584 |
MOD_CK1_1 | 877 | 883 | PF00069 | 0.550 |
MOD_CK1_1 | 885 | 891 | PF00069 | 0.518 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.498 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.366 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.470 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.591 |
MOD_CK2_1 | 758 | 764 | PF00069 | 0.702 |
MOD_CK2_1 | 772 | 778 | PF00069 | 0.361 |
MOD_CK2_1 | 885 | 891 | PF00069 | 0.560 |
MOD_CK2_1 | 922 | 928 | PF00069 | 0.551 |
MOD_CK2_1 | 963 | 969 | PF00069 | 0.470 |
MOD_DYRK1A_RPxSP_1 | 627 | 631 | PF00069 | 0.585 |
MOD_GlcNHglycan | 1177 | 1180 | PF01048 | 0.618 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.510 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.559 |
MOD_GlcNHglycan | 395 | 399 | PF01048 | 0.703 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.598 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.493 |
MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.469 |
MOD_GlcNHglycan | 667 | 670 | PF01048 | 0.683 |
MOD_GlcNHglycan | 702 | 705 | PF01048 | 0.732 |
MOD_GlcNHglycan | 717 | 720 | PF01048 | 0.828 |
MOD_GlcNHglycan | 760 | 763 | PF01048 | 0.656 |
MOD_GlcNHglycan | 775 | 778 | PF01048 | 0.371 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.658 |
MOD_GlcNHglycan | 843 | 846 | PF01048 | 0.565 |
MOD_GlcNHglycan | 879 | 882 | PF01048 | 0.581 |
MOD_GlcNHglycan | 950 | 953 | PF01048 | 0.416 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.667 |
MOD_GSK3_1 | 1173 | 1180 | PF00069 | 0.563 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.434 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.516 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.552 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.557 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.574 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.530 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.511 |
MOD_GSK3_1 | 709 | 716 | PF00069 | 0.801 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.604 |
MOD_GSK3_1 | 918 | 925 | PF00069 | 0.544 |
MOD_GSK3_1 | 948 | 955 | PF00069 | 0.416 |
MOD_GSK3_1 | 959 | 966 | PF00069 | 0.416 |
MOD_N-GLC_1 | 1 | 6 | PF02516 | 0.702 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.639 |
MOD_NEK2_1 | 1042 | 1047 | PF00069 | 0.498 |
MOD_NEK2_1 | 1175 | 1180 | PF00069 | 0.559 |
MOD_NEK2_1 | 1182 | 1187 | PF00069 | 0.566 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.414 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.514 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.701 |
MOD_NEK2_1 | 772 | 777 | PF00069 | 0.498 |
MOD_NEK2_1 | 884 | 889 | PF00069 | 0.606 |
MOD_NEK2_1 | 939 | 944 | PF00069 | 0.468 |
MOD_NEK2_1 | 953 | 958 | PF00069 | 0.349 |
MOD_NEK2_2 | 191 | 196 | PF00069 | 0.266 |
MOD_NEK2_2 | 59 | 64 | PF00069 | 0.533 |
MOD_NEK2_2 | 810 | 815 | PF00069 | 0.478 |
MOD_PIKK_1 | 128 | 134 | PF00454 | 0.470 |
MOD_PIKK_1 | 137 | 143 | PF00454 | 0.470 |
MOD_PIKK_1 | 579 | 585 | PF00454 | 0.621 |
MOD_PK_1 | 508 | 514 | PF00069 | 0.608 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.422 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.488 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.495 |
MOD_PKA_2 | 584 | 590 | PF00069 | 0.489 |
MOD_PKA_2 | 592 | 598 | PF00069 | 0.514 |
MOD_PKA_2 | 601 | 607 | PF00069 | 0.532 |
MOD_PKA_2 | 665 | 671 | PF00069 | 0.724 |
MOD_PKA_2 | 772 | 778 | PF00069 | 0.450 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.714 |
MOD_Plk_1 | 1173 | 1179 | PF00069 | 0.563 |
MOD_Plk_1 | 191 | 197 | PF00069 | 0.320 |
MOD_Plk_1 | 419 | 425 | PF00069 | 0.550 |
MOD_Plk_1 | 810 | 816 | PF00069 | 0.421 |
MOD_Plk_1 | 939 | 945 | PF00069 | 0.449 |
MOD_Plk_2-3 | 922 | 928 | PF00069 | 0.541 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.691 |
MOD_Plk_4 | 1026 | 1032 | PF00069 | 0.580 |
MOD_Plk_4 | 1118 | 1124 | PF00069 | 0.601 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.448 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.536 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.519 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.650 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.525 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.504 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.545 |
MOD_Plk_4 | 610 | 616 | PF00069 | 0.624 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.579 |
MOD_Plk_4 | 844 | 850 | PF00069 | 0.536 |
MOD_Plk_4 | 954 | 960 | PF00069 | 0.416 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.652 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.744 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.663 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.701 |
MOD_ProDKin_1 | 627 | 633 | PF00069 | 0.602 |
MOD_ProDKin_1 | 713 | 719 | PF00069 | 0.829 |
MOD_ProDKin_1 | 834 | 840 | PF00069 | 0.492 |
MOD_SUMO_for_1 | 1148 | 1151 | PF00179 | 0.537 |
TRG_DiLeu_BaEn_1 | 1006 | 1011 | PF01217 | 0.494 |
TRG_DiLeu_BaEn_1 | 779 | 784 | PF01217 | 0.610 |
TRG_DiLeu_BaEn_2 | 939 | 945 | PF01217 | 0.569 |
TRG_DiLeu_BaLyEn_6 | 372 | 377 | PF01217 | 0.653 |
TRG_ENDOCYTIC_2 | 1001 | 1004 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 1044 | 1047 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 1085 | 1088 | PF00928 | 0.563 |
TRG_ENDOCYTIC_2 | 1096 | 1099 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 1143 | 1146 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 496 | 499 | PF00928 | 0.597 |
TRG_ENDOCYTIC_2 | 738 | 741 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 840 | 843 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 864 | 867 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 895 | 898 | PF00928 | 0.548 |
TRG_ENDOCYTIC_2 | 923 | 926 | PF00928 | 0.523 |
TRG_ER_diArg_1 | 107 | 109 | PF00400 | 0.416 |
TRG_ER_diArg_1 | 1155 | 1158 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 124 | 126 | PF00400 | 0.416 |
TRG_ER_diArg_1 | 224 | 227 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 609 | 611 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 626 | 629 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 767 | 769 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 865 | 868 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 982 | 984 | PF00400 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 1155 | 1159 | PF00026 | 0.575 |
TRG_Pf-PMV_PEXEL_1 | 208 | 213 | PF00026 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 415 | 420 | PF00026 | 0.606 |
TRG_Pf-PMV_PEXEL_1 | 965 | 969 | PF00026 | 0.549 |
TRG_Pf-PMV_PEXEL_1 | 983 | 988 | PF00026 | 0.342 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7Y3 | Leptomonas seymouri | 64% | 97% |
A0A381MFR4 | Leishmania infantum | 95% | 100% |
A0A3Q8I9C4 | Leishmania donovani | 95% | 100% |
A0A3S7WTT9 | Leishmania donovani | 95% | 100% |
A4H8H4 | Leishmania braziliensis | 76% | 97% |
A4HWU2 | Leishmania infantum | 95% | 100% |
E9AQK6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 99% |
Q4QEX6 | Leishmania major | 100% | 100% |
V5B4L9 | Trypanosoma cruzi | 34% | 100% |