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: 23 |
NetGPI | no | yes: 0, no: 23 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005739 | mitochondrion | 5 | 2 |
GO:0020023 | kinetoplast | 2 | 2 |
GO:0031019 | mitochondrial mRNA editing complex | 3 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 2 |
GO:0031981 | nuclear lumen | 5 | 2 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043233 | organelle lumen | 3 | 2 |
GO:0045293 | mRNA editing complex | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 2 |
GO:0097014 | ciliary plasm | 5 | 2 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
GO:0099568 | cytoplasmic region | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:1902494 | catalytic complex | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0009895 | negative regulation of catabolic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0010628 | positive regulation of gene expression | 6 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0016553 | base conversion or substitution editing | 6 | 1 |
GO:0016554 | cytidine to uridine editing | 7 | 1 |
GO:0016556 | mRNA modification | 6 | 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:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0031330 | negative regulation of cellular catabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043487 | regulation of RNA stability | 3 | 1 |
GO:0043488 | regulation of mRNA stability | 4 | 1 |
GO:0043489 | RNA stabilization | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0048255 | mRNA stabilization | 5 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 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:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051172 | negative 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:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0061013 | regulation of mRNA catabolic process | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1902369 | negative regulation of RNA catabolic process | 7 | 1 |
GO:1902373 | negative regulation of mRNA catabolic process | 7 | 1 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 1 |
GO:1903312 | negative regulation of mRNA metabolic process | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 24 |
GO:0003676 | nucleic acid binding | 3 | 23 |
GO:0003824 | catalytic activity | 1 | 24 |
GO:0004386 | helicase activity | 2 | 24 |
GO:0005488 | binding | 1 | 24 |
GO:0005524 | ATP binding | 5 | 24 |
GO:0016787 | hydrolase activity | 2 | 15 |
GO:0017076 | purine nucleotide binding | 4 | 24 |
GO:0030554 | adenyl nucleotide binding | 5 | 24 |
GO:0032553 | ribonucleotide binding | 3 | 24 |
GO:0032555 | purine ribonucleotide binding | 4 | 24 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 24 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 24 |
GO:0036094 | small molecule binding | 2 | 24 |
GO:0043167 | ion binding | 2 | 24 |
GO:0043168 | anion binding | 3 | 24 |
GO:0097159 | organic cyclic compound binding | 2 | 24 |
GO:0097367 | carbohydrate derivative binding | 2 | 24 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 24 |
GO:0140657 | ATP-dependent activity | 1 | 24 |
GO:1901265 | nucleoside phosphate binding | 3 | 24 |
GO:1901363 | heterocyclic compound binding | 2 | 24 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003724 | RNA helicase activity | 3 | 1 |
GO:0003729 | mRNA binding | 5 | 1 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 1 |
GO:0034458 | 3'-5' RNA helicase activity | 4 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0008270 | zinc ion binding | 6 | 3 |
GO:0043169 | cation binding | 3 | 3 |
GO:0046872 | metal ion binding | 4 | 3 |
GO:0046914 | transition metal ion binding | 5 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1141 | 1145 | PF00656 | 0.633 |
CLV_C14_Caspase3-7 | 1179 | 1183 | PF00656 | 0.459 |
CLV_C14_Caspase3-7 | 123 | 127 | PF00656 | 0.503 |
CLV_C14_Caspase3-7 | 1468 | 1472 | PF00656 | 0.351 |
CLV_C14_Caspase3-7 | 183 | 187 | PF00656 | 0.409 |
CLV_C14_Caspase3-7 | 424 | 428 | PF00656 | 0.432 |
CLV_C14_Caspase3-7 | 800 | 804 | PF00656 | 0.437 |
CLV_C14_Caspase3-7 | 896 | 900 | PF00656 | 0.382 |
CLV_C14_Caspase3-7 | 990 | 994 | PF00656 | 0.414 |
CLV_NRD_NRD_1 | 1065 | 1067 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 1250 | 1252 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 1272 | 1274 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 1331 | 1333 | PF00675 | 0.263 |
CLV_NRD_NRD_1 | 1418 | 1420 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 544 | 546 | PF00675 | 0.278 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 728 | 730 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 923 | 925 | PF00675 | 0.260 |
CLV_PCSK_FUR_1 | 1066 | 1070 | PF00082 | 0.364 |
CLV_PCSK_FUR_1 | 255 | 259 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 1068 | 1070 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 1272 | 1274 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 1331 | 1333 | PF00082 | 0.263 |
CLV_PCSK_KEX2_1 | 1418 | 1420 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.299 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 544 | 546 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 728 | 730 | PF00082 | 0.602 |
CLV_PCSK_PC1ET2_1 | 1068 | 1070 | PF00082 | 0.428 |
CLV_PCSK_PC1ET2_1 | 169 | 171 | PF00082 | 0.385 |
CLV_PCSK_PC1ET2_1 | 226 | 228 | PF00082 | 0.544 |
CLV_PCSK_PC1ET2_1 | 366 | 368 | PF00082 | 0.299 |
CLV_PCSK_PC7_1 | 165 | 171 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 1029 | 1033 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 1069 | 1073 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 1121 | 1125 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 1264 | 1268 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 1297 | 1301 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 1332 | 1336 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 1418 | 1422 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 579 | 583 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 625 | 629 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 635 | 639 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 729 | 733 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 758 | 762 | PF00082 | 0.239 |
CLV_PCSK_SKI1_1 | 768 | 772 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 820 | 824 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 938 | 942 | PF00082 | 0.447 |
CLV_Separin_Metazoa | 148 | 152 | PF03568 | 0.685 |
CLV_Separin_Metazoa | 162 | 166 | PF03568 | 0.485 |
CLV_Separin_Metazoa | 997 | 1001 | PF03568 | 0.416 |
DEG_APCC_DBOX_1 | 1331 | 1339 | PF00400 | 0.428 |
DEG_APCC_DBOX_1 | 957 | 965 | PF00400 | 0.354 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.490 |
DEG_SCF_FBW7_1 | 306 | 311 | PF00400 | 0.599 |
DEG_SCF_FBW7_2 | 1011 | 1016 | PF00400 | 0.540 |
DEG_SCF_FBW7_2 | 1420 | 1427 | PF00400 | 0.249 |
DEG_SCF_SKP2-CKS1_1 | 704 | 711 | PF00560 | 0.451 |
DEG_SPOP_SBC_1 | 1304 | 1308 | PF00917 | 0.429 |
DEG_SPOP_SBC_1 | 869 | 873 | PF00917 | 0.403 |
DOC_ANK_TNKS_1 | 246 | 253 | PF00023 | 0.487 |
DOC_CKS1_1 | 110 | 115 | PF01111 | 0.681 |
DOC_CKS1_1 | 1421 | 1426 | PF01111 | 0.262 |
DOC_CYCLIN_RxL_1 | 1066 | 1076 | PF00134 | 0.425 |
DOC_CYCLIN_RxL_1 | 1415 | 1423 | PF00134 | 0.234 |
DOC_CYCLIN_RxL_1 | 60 | 74 | PF00134 | 0.514 |
DOC_CYCLIN_RxL_1 | 622 | 632 | PF00134 | 0.448 |
DOC_MAPK_gen_1 | 1246 | 1255 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 470 | 476 | PF00069 | 0.507 |
DOC_MAPK_gen_1 | 60 | 70 | PF00069 | 0.466 |
DOC_MAPK_gen_1 | 630 | 638 | PF00069 | 0.492 |
DOC_MAPK_HePTP_8 | 1416 | 1428 | PF00069 | 0.333 |
DOC_MAPK_MEF2A_6 | 1419 | 1428 | PF00069 | 0.336 |
DOC_MAPK_MEF2A_6 | 32 | 39 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 630 | 638 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 958 | 966 | PF00069 | 0.288 |
DOC_MAPK_NFAT4_5 | 32 | 40 | PF00069 | 0.545 |
DOC_PP1_RVXF_1 | 64 | 71 | PF00149 | 0.538 |
DOC_PP2B_LxvP_1 | 1234 | 1237 | PF13499 | 0.532 |
DOC_PP2B_LxvP_1 | 35 | 38 | PF13499 | 0.485 |
DOC_PP2B_LxvP_1 | 715 | 718 | PF13499 | 0.584 |
DOC_PP2B_LxvP_1 | 984 | 987 | PF13499 | 0.602 |
DOC_PP4_FxxP_1 | 15 | 18 | PF00568 | 0.758 |
DOC_PP4_FxxP_1 | 685 | 688 | PF00568 | 0.447 |
DOC_PP4_FxxP_1 | 983 | 986 | PF00568 | 0.468 |
DOC_USP7_MATH_1 | 1168 | 1172 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 1176 | 1180 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 1190 | 1194 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 1240 | 1244 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 1266 | 1270 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 1304 | 1308 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 1351 | 1355 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 692 | 696 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 709 | 713 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 788 | 792 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 813 | 817 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 869 | 873 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.489 |
DOC_USP7_UBL2_3 | 707 | 711 | PF12436 | 0.443 |
DOC_WW_Pin1_4 | 1009 | 1014 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 1128 | 1133 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 1306 | 1311 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 1420 | 1425 | PF00397 | 0.282 |
DOC_WW_Pin1_4 | 1430 | 1435 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 1444 | 1449 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 304 | 309 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 653 | 658 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 684 | 689 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 705 | 710 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 872 | 877 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.548 |
LIG_14-3-3_CanoR_1 | 1211 | 1215 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 1377 | 1381 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 1387 | 1391 | PF00244 | 0.346 |
LIG_14-3-3_CanoR_1 | 1405 | 1413 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 329 | 335 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 437 | 445 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 446 | 452 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 482 | 487 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 544 | 551 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 559 | 564 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 579 | 584 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 854 | 860 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 927 | 937 | PF00244 | 0.562 |
LIG_Actin_WH2_2 | 1095 | 1113 | PF00022 | 0.460 |
LIG_Actin_WH2_2 | 1450 | 1467 | PF00022 | 0.373 |
LIG_Actin_WH2_2 | 18 | 34 | PF00022 | 0.456 |
LIG_Actin_WH2_2 | 388 | 406 | PF00022 | 0.564 |
LIG_Actin_WH2_2 | 620 | 637 | PF00022 | 0.503 |
LIG_AP2alpha_1 | 1321 | 1325 | PF02296 | 0.445 |
LIG_APCC_ABBA_1 | 1318 | 1323 | PF00400 | 0.423 |
LIG_APCC_ABBA_1 | 1371 | 1376 | PF00400 | 0.318 |
LIG_BIR_III_2 | 1147 | 1151 | PF00653 | 0.392 |
LIG_BIR_III_4 | 243 | 247 | PF00653 | 0.535 |
LIG_BRCT_BRCA1_1 | 686 | 690 | PF00533 | 0.342 |
LIG_BRCT_BRCA1_1 | 874 | 878 | PF00533 | 0.404 |
LIG_CaM_IQ_9 | 919 | 934 | PF13499 | 0.437 |
LIG_CaM_NSCaTE_8 | 1344 | 1351 | PF13499 | 0.352 |
LIG_Clathr_ClatBox_1 | 1483 | 1487 | PF01394 | 0.476 |
LIG_deltaCOP1_diTrp_1 | 943 | 951 | PF00928 | 0.333 |
LIG_FHA_1 | 1105 | 1111 | PF00498 | 0.238 |
LIG_FHA_1 | 1144 | 1150 | PF00498 | 0.695 |
LIG_FHA_1 | 1199 | 1205 | PF00498 | 0.567 |
LIG_FHA_1 | 1377 | 1383 | PF00498 | 0.352 |
LIG_FHA_1 | 1421 | 1427 | PF00498 | 0.252 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.615 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.390 |
LIG_FHA_1 | 514 | 520 | PF00498 | 0.466 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.477 |
LIG_FHA_1 | 654 | 660 | PF00498 | 0.409 |
LIG_FHA_1 | 708 | 714 | PF00498 | 0.647 |
LIG_FHA_1 | 816 | 822 | PF00498 | 0.545 |
LIG_FHA_1 | 841 | 847 | PF00498 | 0.427 |
LIG_FHA_1 | 939 | 945 | PF00498 | 0.397 |
LIG_FHA_2 | 1055 | 1061 | PF00498 | 0.426 |
LIG_FHA_2 | 1161 | 1167 | PF00498 | 0.443 |
LIG_FHA_2 | 1306 | 1312 | PF00498 | 0.368 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.529 |
LIG_FHA_2 | 593 | 599 | PF00498 | 0.478 |
LIG_FHA_2 | 831 | 837 | PF00498 | 0.462 |
LIG_FHA_2 | 847 | 853 | PF00498 | 0.462 |
LIG_FHA_2 | 980 | 986 | PF00498 | 0.599 |
LIG_FHA_2 | 988 | 994 | PF00498 | 0.538 |
LIG_GBD_Chelix_1 | 1382 | 1390 | PF00786 | 0.447 |
LIG_GBD_Chelix_1 | 395 | 403 | PF00786 | 0.567 |
LIG_GBD_Chelix_1 | 837 | 845 | PF00786 | 0.176 |
LIG_Integrin_isoDGR_2 | 40 | 42 | PF01839 | 0.371 |
LIG_Integrin_RGD_1 | 1278 | 1280 | PF01839 | 0.572 |
LIG_LIR_Apic_2 | 12 | 18 | PF02991 | 0.700 |
LIG_LIR_Apic_2 | 682 | 688 | PF02991 | 0.485 |
LIG_LIR_Apic_2 | 779 | 783 | PF02991 | 0.524 |
LIG_LIR_Apic_2 | 982 | 986 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 1016 | 1025 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 1097 | 1105 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 1257 | 1266 | PF02991 | 0.558 |
LIG_LIR_Gen_1 | 1342 | 1351 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 1368 | 1378 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 1379 | 1386 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 1389 | 1398 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 1447 | 1457 | PF02991 | 0.634 |
LIG_LIR_Gen_1 | 687 | 697 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 734 | 743 | PF02991 | 0.257 |
LIG_LIR_Gen_1 | 875 | 886 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 943 | 952 | PF02991 | 0.377 |
LIG_LIR_LC3C_4 | 394 | 397 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 1016 | 1020 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 1097 | 1102 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 120 | 124 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 1257 | 1263 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 1342 | 1347 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 1368 | 1373 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 1379 | 1383 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 1389 | 1394 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 1447 | 1452 | PF02991 | 0.648 |
LIG_LIR_Nem_3 | 646 | 651 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 687 | 693 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 734 | 739 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 875 | 881 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 943 | 948 | PF02991 | 0.420 |
LIG_NRBOX | 1342 | 1348 | PF00104 | 0.306 |
LIG_NRBOX | 964 | 970 | PF00104 | 0.348 |
LIG_Pex14_2 | 1321 | 1325 | PF04695 | 0.445 |
LIG_Pex14_2 | 648 | 652 | PF04695 | 0.385 |
LIG_Pex14_2 | 763 | 767 | PF04695 | 0.438 |
LIG_PTAP_UEV_1 | 274 | 279 | PF05743 | 0.472 |
LIG_SH2_CRK | 1380 | 1384 | PF00017 | 0.430 |
LIG_SH2_CRK | 1398 | 1402 | PF00017 | 0.587 |
LIG_SH2_CRK | 171 | 175 | PF00017 | 0.530 |
LIG_SH2_CRK | 290 | 294 | PF00017 | 0.343 |
LIG_SH2_CRK | 736 | 740 | PF00017 | 0.328 |
LIG_SH2_CRK | 780 | 784 | PF00017 | 0.468 |
LIG_SH2_NCK_1 | 1380 | 1384 | PF00017 | 0.338 |
LIG_SH2_NCK_1 | 1398 | 1402 | PF00017 | 0.392 |
LIG_SH2_NCK_1 | 686 | 690 | PF00017 | 0.570 |
LIG_SH2_NCK_1 | 736 | 740 | PF00017 | 0.369 |
LIG_SH2_SRC | 124 | 127 | PF00017 | 0.464 |
LIG_SH2_STAP1 | 364 | 368 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 458 | 462 | PF00017 | 0.413 |
LIG_SH2_STAP1 | 569 | 573 | PF00017 | 0.461 |
LIG_SH2_STAP1 | 784 | 788 | PF00017 | 0.376 |
LIG_SH2_STAP1 | 915 | 919 | PF00017 | 0.451 |
LIG_SH2_STAT3 | 1116 | 1119 | PF00017 | 0.286 |
LIG_SH2_STAT3 | 1319 | 1322 | PF00017 | 0.324 |
LIG_SH2_STAT3 | 458 | 461 | PF00017 | 0.349 |
LIG_SH2_STAT3 | 475 | 478 | PF00017 | 0.428 |
LIG_SH2_STAT3 | 915 | 918 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 1017 | 1020 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 1070 | 1073 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 1319 | 1322 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 522 | 525 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 651 | 654 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 672 | 675 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 741 | 744 | PF00017 | 0.357 |
LIG_SH3_1 | 104 | 110 | PF00018 | 0.535 |
LIG_SH3_1 | 1398 | 1404 | PF00018 | 0.592 |
LIG_SH3_3 | 1019 | 1025 | PF00018 | 0.459 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.704 |
LIG_SH3_3 | 1146 | 1152 | PF00018 | 0.432 |
LIG_SH3_3 | 1307 | 1313 | PF00018 | 0.450 |
LIG_SH3_3 | 1398 | 1404 | PF00018 | 0.613 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.625 |
LIG_SH3_3 | 537 | 543 | PF00018 | 0.474 |
LIG_SH3_3 | 759 | 765 | PF00018 | 0.456 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.628 |
LIG_SH3_3 | 946 | 952 | PF00018 | 0.467 |
LIG_SUMO_SIM_anti_2 | 1016 | 1022 | PF11976 | 0.416 |
LIG_SUMO_SIM_anti_2 | 1215 | 1220 | PF11976 | 0.322 |
LIG_SUMO_SIM_anti_2 | 835 | 843 | PF11976 | 0.443 |
LIG_SUMO_SIM_par_1 | 1029 | 1035 | PF11976 | 0.558 |
LIG_SUMO_SIM_par_1 | 1480 | 1491 | PF11976 | 0.429 |
LIG_SUMO_SIM_par_1 | 203 | 208 | PF11976 | 0.426 |
LIG_SUMO_SIM_par_1 | 394 | 401 | PF11976 | 0.360 |
LIG_SUMO_SIM_par_1 | 794 | 801 | PF11976 | 0.449 |
LIG_TRAF2_1 | 100 | 103 | PF00917 | 0.600 |
LIG_TRAF2_1 | 145 | 148 | PF00917 | 0.613 |
LIG_TRAF2_2 | 1448 | 1453 | PF00917 | 0.399 |
LIG_TYR_ITIM | 1118 | 1123 | PF00017 | 0.234 |
LIG_TYR_ITIM | 294 | 299 | PF00017 | 0.328 |
LIG_TYR_ITSM | 732 | 739 | PF00017 | 0.286 |
LIG_UBA3_1 | 1390 | 1397 | PF00899 | 0.572 |
LIG_UBA3_1 | 620 | 625 | PF00899 | 0.357 |
LIG_UBA3_1 | 760 | 768 | PF00899 | 0.321 |
LIG_UBA3_1 | 961 | 967 | PF00899 | 0.447 |
LIG_WRC_WIRS_1 | 980 | 985 | PF05994 | 0.528 |
LIG_WW_3 | 106 | 110 | PF00397 | 0.529 |
MOD_CDC14_SPxK_1 | 1309 | 1312 | PF00782 | 0.346 |
MOD_CDK_SPK_2 | 109 | 114 | PF00069 | 0.487 |
MOD_CDK_SPxK_1 | 1306 | 1312 | PF00069 | 0.376 |
MOD_CDK_SPxK_1 | 705 | 711 | PF00069 | 0.450 |
MOD_CK1_1 | 1042 | 1048 | PF00069 | 0.250 |
MOD_CK1_1 | 1073 | 1079 | PF00069 | 0.374 |
MOD_CK1_1 | 1210 | 1216 | PF00069 | 0.404 |
MOD_CK1_1 | 1290 | 1296 | PF00069 | 0.337 |
MOD_CK1_1 | 1303 | 1309 | PF00069 | 0.472 |
MOD_CK1_1 | 1339 | 1345 | PF00069 | 0.313 |
MOD_CK1_1 | 1352 | 1358 | PF00069 | 0.397 |
MOD_CK1_1 | 1433 | 1439 | PF00069 | 0.460 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.364 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.648 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.563 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.383 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.263 |
MOD_CK1_1 | 830 | 836 | PF00069 | 0.271 |
MOD_CK1_1 | 853 | 859 | PF00069 | 0.296 |
MOD_CK1_1 | 870 | 876 | PF00069 | 0.294 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.578 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.514 |
MOD_CK2_1 | 1351 | 1357 | PF00069 | 0.298 |
MOD_CK2_1 | 1386 | 1392 | PF00069 | 0.278 |
MOD_CK2_1 | 1405 | 1411 | PF00069 | 0.616 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.541 |
MOD_CK2_1 | 547 | 553 | PF00069 | 0.291 |
MOD_CK2_1 | 691 | 697 | PF00069 | 0.539 |
MOD_CK2_1 | 784 | 790 | PF00069 | 0.382 |
MOD_CK2_1 | 846 | 852 | PF00069 | 0.467 |
MOD_CK2_1 | 979 | 985 | PF00069 | 0.601 |
MOD_Cter_Amidation | 1005 | 1008 | PF01082 | 0.214 |
MOD_DYRK1A_RPxSP_1 | 109 | 113 | PF00069 | 0.492 |
MOD_GlcNHglycan | 1178 | 1181 | PF01048 | 0.434 |
MOD_GlcNHglycan | 1182 | 1186 | PF01048 | 0.436 |
MOD_GlcNHglycan | 1190 | 1193 | PF01048 | 0.544 |
MOD_GlcNHglycan | 126 | 130 | PF01048 | 0.322 |
MOD_GlcNHglycan | 1302 | 1305 | PF01048 | 0.597 |
MOD_GlcNHglycan | 1338 | 1341 | PF01048 | 0.283 |
MOD_GlcNHglycan | 1407 | 1410 | PF01048 | 0.499 |
MOD_GlcNHglycan | 1438 | 1441 | PF01048 | 0.477 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.514 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.653 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.648 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.552 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.664 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.462 |
MOD_GlcNHglycan | 546 | 549 | PF01048 | 0.294 |
MOD_GlcNHglycan | 639 | 642 | PF01048 | 0.333 |
MOD_GlcNHglycan | 771 | 774 | PF01048 | 0.425 |
MOD_GlcNHglycan | 786 | 789 | PF01048 | 0.200 |
MOD_GlcNHglycan | 803 | 806 | PF01048 | 0.417 |
MOD_GlcNHglycan | 815 | 818 | PF01048 | 0.275 |
MOD_GlcNHglycan | 829 | 832 | PF01048 | 0.240 |
MOD_GlcNHglycan | 872 | 875 | PF01048 | 0.406 |
MOD_GlcNHglycan | 895 | 898 | PF01048 | 0.399 |
MOD_GSK3_1 | 1075 | 1082 | PF00069 | 0.399 |
MOD_GSK3_1 | 1160 | 1167 | PF00069 | 0.575 |
MOD_GSK3_1 | 1176 | 1183 | PF00069 | 0.644 |
MOD_GSK3_1 | 1190 | 1197 | PF00069 | 0.483 |
MOD_GSK3_1 | 1203 | 1210 | PF00069 | 0.384 |
MOD_GSK3_1 | 1235 | 1242 | PF00069 | 0.520 |
MOD_GSK3_1 | 1293 | 1300 | PF00069 | 0.523 |
MOD_GSK3_1 | 1302 | 1309 | PF00069 | 0.547 |
MOD_GSK3_1 | 1349 | 1356 | PF00069 | 0.394 |
MOD_GSK3_1 | 1405 | 1412 | PF00069 | 0.608 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.554 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.742 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.500 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.631 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.455 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.644 |
MOD_GSK3_1 | 579 | 586 | PF00069 | 0.357 |
MOD_GSK3_1 | 675 | 682 | PF00069 | 0.260 |
MOD_GSK3_1 | 705 | 712 | PF00069 | 0.507 |
MOD_GSK3_1 | 716 | 723 | PF00069 | 0.509 |
MOD_GSK3_1 | 752 | 759 | PF00069 | 0.300 |
MOD_GSK3_1 | 784 | 791 | PF00069 | 0.387 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.466 |
MOD_GSK3_1 | 797 | 804 | PF00069 | 0.369 |
MOD_GSK3_1 | 846 | 853 | PF00069 | 0.344 |
MOD_GSK3_1 | 864 | 871 | PF00069 | 0.349 |
MOD_GSK3_1 | 905 | 912 | PF00069 | 0.249 |
MOD_LATS_1 | 480 | 486 | PF00433 | 0.378 |
MOD_LATS_1 | 530 | 536 | PF00433 | 0.225 |
MOD_N-GLC_1 | 1405 | 1410 | PF02516 | 0.620 |
MOD_N-GLC_1 | 180 | 185 | PF02516 | 0.552 |
MOD_N-GLC_1 | 752 | 757 | PF02516 | 0.416 |
MOD_N-GLC_1 | 919 | 924 | PF02516 | 0.315 |
MOD_NEK2_1 | 1032 | 1037 | PF00069 | 0.458 |
MOD_NEK2_1 | 1104 | 1109 | PF00069 | 0.388 |
MOD_NEK2_1 | 1334 | 1339 | PF00069 | 0.396 |
MOD_NEK2_1 | 1386 | 1391 | PF00069 | 0.362 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.520 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.359 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.483 |
MOD_NEK2_1 | 639 | 644 | PF00069 | 0.312 |
MOD_NEK2_1 | 797 | 802 | PF00069 | 0.274 |
MOD_NEK2_1 | 845 | 850 | PF00069 | 0.467 |
MOD_NEK2_1 | 944 | 949 | PF00069 | 0.454 |
MOD_NEK2_2 | 487 | 492 | PF00069 | 0.413 |
MOD_NEK2_2 | 815 | 820 | PF00069 | 0.225 |
MOD_PIKK_1 | 1073 | 1079 | PF00454 | 0.301 |
MOD_PIKK_1 | 1287 | 1293 | PF00454 | 0.575 |
MOD_PIKK_1 | 1381 | 1387 | PF00454 | 0.325 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.374 |
MOD_PIKK_1 | 398 | 404 | PF00454 | 0.445 |
MOD_PIKK_1 | 474 | 480 | PF00454 | 0.427 |
MOD_PIKK_1 | 514 | 520 | PF00454 | 0.356 |
MOD_PIKK_1 | 538 | 544 | PF00454 | 0.328 |
MOD_PIKK_1 | 720 | 726 | PF00454 | 0.450 |
MOD_PIKK_1 | 906 | 912 | PF00454 | 0.266 |
MOD_PIKK_1 | 914 | 920 | PF00454 | 0.290 |
MOD_PIKK_1 | 928 | 934 | PF00454 | 0.283 |
MOD_PKA_1 | 482 | 488 | PF00069 | 0.392 |
MOD_PKA_1 | 544 | 550 | PF00069 | 0.290 |
MOD_PKA_2 | 1137 | 1143 | PF00069 | 0.459 |
MOD_PKA_2 | 1210 | 1216 | PF00069 | 0.506 |
MOD_PKA_2 | 1376 | 1382 | PF00069 | 0.351 |
MOD_PKA_2 | 1386 | 1392 | PF00069 | 0.344 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.597 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.415 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.436 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.465 |
MOD_PKA_2 | 544 | 550 | PF00069 | 0.273 |
MOD_PKA_2 | 558 | 564 | PF00069 | 0.335 |
MOD_PKA_2 | 629 | 635 | PF00069 | 0.185 |
MOD_PKA_2 | 853 | 859 | PF00069 | 0.387 |
MOD_PKB_1 | 435 | 443 | PF00069 | 0.377 |
MOD_Plk_1 | 1164 | 1170 | PF00069 | 0.568 |
MOD_Plk_1 | 1360 | 1366 | PF00069 | 0.424 |
MOD_Plk_1 | 1405 | 1411 | PF00069 | 0.611 |
MOD_Plk_1 | 185 | 191 | PF00069 | 0.529 |
MOD_Plk_1 | 196 | 202 | PF00069 | 0.322 |
MOD_Plk_1 | 440 | 446 | PF00069 | 0.460 |
MOD_Plk_1 | 992 | 998 | PF00069 | 0.280 |
MOD_Plk_2-3 | 1160 | 1166 | PF00069 | 0.594 |
MOD_Plk_2-3 | 117 | 123 | PF00069 | 0.580 |
MOD_Plk_2-3 | 1453 | 1459 | PF00069 | 0.542 |
MOD_Plk_2-3 | 1485 | 1491 | PF00069 | 0.613 |
MOD_Plk_4 | 1032 | 1038 | PF00069 | 0.459 |
MOD_Plk_4 | 1039 | 1045 | PF00069 | 0.384 |
MOD_Plk_4 | 1339 | 1345 | PF00069 | 0.301 |
MOD_Plk_4 | 1386 | 1392 | PF00069 | 0.446 |
MOD_Plk_4 | 1453 | 1459 | PF00069 | 0.542 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.537 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.524 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.313 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.590 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.628 |
MOD_Plk_4 | 756 | 762 | PF00069 | 0.276 |
MOD_Plk_4 | 979 | 985 | PF00069 | 0.567 |
MOD_ProDKin_1 | 1009 | 1015 | PF00069 | 0.288 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.598 |
MOD_ProDKin_1 | 1128 | 1134 | PF00069 | 0.571 |
MOD_ProDKin_1 | 1306 | 1312 | PF00069 | 0.544 |
MOD_ProDKin_1 | 1420 | 1426 | PF00069 | 0.287 |
MOD_ProDKin_1 | 1430 | 1436 | PF00069 | 0.475 |
MOD_ProDKin_1 | 1444 | 1450 | PF00069 | 0.545 |
MOD_ProDKin_1 | 304 | 310 | PF00069 | 0.525 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.569 |
MOD_ProDKin_1 | 653 | 659 | PF00069 | 0.459 |
MOD_ProDKin_1 | 684 | 690 | PF00069 | 0.432 |
MOD_ProDKin_1 | 705 | 711 | PF00069 | 0.655 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.656 |
MOD_ProDKin_1 | 872 | 878 | PF00069 | 0.467 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.548 |
MOD_SUMO_rev_2 | 1505 | 1515 | PF00179 | 0.488 |
MOD_SUMO_rev_2 | 750 | 760 | PF00179 | 0.394 |
TRG_DiLeu_BaEn_1 | 1016 | 1021 | PF01217 | 0.242 |
TRG_DiLeu_BaEn_2 | 196 | 202 | PF01217 | 0.319 |
TRG_DiLeu_BaLyEn_6 | 1416 | 1421 | PF01217 | 0.314 |
TRG_DiLeu_BaLyEn_6 | 235 | 240 | PF01217 | 0.316 |
TRG_ENDOCYTIC_2 | 1017 | 1020 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 1087 | 1090 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 1120 | 1123 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 1380 | 1383 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 736 | 739 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 937 | 940 | PF00928 | 0.371 |
TRG_ER_diArg_1 | 1272 | 1274 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 1330 | 1332 | PF00400 | 0.260 |
TRG_ER_diArg_1 | 1418 | 1420 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 164 | 166 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 255 | 258 | PF00400 | 0.747 |
TRG_ER_diArg_1 | 469 | 471 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 481 | 483 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 501 | 504 | PF00400 | 0.242 |
TRG_ER_diArg_1 | 543 | 545 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 633 | 636 | PF00400 | 0.354 |
TRG_ER_FFAT_2 | 679 | 691 | PF00635 | 0.486 |
TRG_NES_CRM1_1 | 1009 | 1024 | PF08389 | 0.242 |
TRG_NES_CRM1_1 | 598 | 609 | PF08389 | 0.432 |
TRG_NLS_MonoCore_2 | 1065 | 1070 | PF00514 | 0.454 |
TRG_NLS_MonoExtN_4 | 1066 | 1071 | PF00514 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 238 | 242 | PF00026 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 291 | 295 | PF00026 | 0.327 |
TRG_Pf-PMV_PEXEL_1 | 671 | 675 | PF00026 | 0.353 |
TRG_Pf-PMV_PEXEL_1 | 942 | 946 | PF00026 | 0.377 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5H2 | Leptomonas seymouri | 59% | 83% |
A0A0S4ILP1 | Bodo saltans | 29% | 71% |
A0A0S4IND4 | Bodo saltans | 34% | 89% |
A0A1X0P9B9 | Trypanosomatidae | 43% | 100% |
A0A1X0P9W8 | Trypanosomatidae | 31% | 69% |
A0A3R7M0Y1 | Trypanosoma rangeli | 30% | 70% |
A0A3R7MLF0 | Trypanosoma rangeli | 44% | 100% |
A0A3S7WQG7 | Leishmania donovani | 30% | 100% |
A4HAN8 | Leishmania braziliensis | 78% | 100% |
A4HB41 | Leishmania braziliensis | 32% | 68% |
A4HDG6 | Leishmania braziliensis | 26% | 100% |
A4HTS5 | Leishmania infantum | 30% | 100% |
A4I9T1 | Leishmania infantum | 100% | 100% |
C9ZM05 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 70% |
C9ZMU8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AMK8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9B4U2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
E9B5B2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 68% |
Q4Q2M1 | Leishmania major | 31% | 68% |
Q4Q384 | Leishmania major | 92% | 100% |
Q581T1 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 29% | 70% |
V5BKW2 | Trypanosoma cruzi | 32% | 95% |
V5BND8 | Trypanosoma cruzi | 44% | 100% |