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: 19 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0005739 | mitochondrion | 5 | 3 |
GO:0020023 | kinetoplast | 2 | 3 |
GO:0031974 | membrane-enclosed lumen | 2 | 3 |
GO:0031981 | nuclear lumen | 5 | 3 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0043233 | organelle lumen | 3 | 3 |
GO:0070013 | intracellular organelle lumen | 4 | 3 |
GO:0097014 | ciliary plasm | 5 | 3 |
GO:0099568 | cytoplasmic region | 3 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0031019 | mitochondrial mRNA editing complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0045293 | mRNA editing complex | 3 | 1 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
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 | 20 |
GO:0003676 | nucleic acid binding | 3 | 20 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 20 |
GO:0004386 | helicase activity | 2 | 20 |
GO:0005488 | binding | 1 | 20 |
GO:0005524 | ATP binding | 5 | 20 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 20 |
GO:0030554 | adenyl nucleotide binding | 5 | 20 |
GO:0032553 | ribonucleotide binding | 3 | 20 |
GO:0032555 | purine ribonucleotide binding | 4 | 20 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 20 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 20 |
GO:0036094 | small molecule binding | 2 | 20 |
GO:0043167 | ion binding | 2 | 20 |
GO:0043168 | anion binding | 3 | 20 |
GO:0097159 | organic cyclic compound binding | 2 | 20 |
GO:0097367 | carbohydrate derivative binding | 2 | 20 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 20 |
GO:0140657 | ATP-dependent activity | 1 | 20 |
GO:1901265 | nucleoside phosphate binding | 3 | 20 |
GO:1901363 | heterocyclic compound binding | 2 | 20 |
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 | 1147 | 1151 | PF00656 | 0.620 |
CLV_C14_Caspase3-7 | 1185 | 1189 | PF00656 | 0.453 |
CLV_C14_Caspase3-7 | 123 | 127 | PF00656 | 0.496 |
CLV_C14_Caspase3-7 | 1283 | 1287 | PF00656 | 0.351 |
CLV_C14_Caspase3-7 | 183 | 187 | PF00656 | 0.438 |
CLV_C14_Caspase3-7 | 430 | 434 | PF00656 | 0.649 |
CLV_C14_Caspase3-7 | 806 | 810 | PF00656 | 0.450 |
CLV_C14_Caspase3-7 | 996 | 1000 | PF00656 | 0.392 |
CLV_NRD_NRD_1 | 1071 | 1073 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 1256 | 1258 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 1278 | 1280 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 1299 | 1301 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 1424 | 1426 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 1471 | 1473 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 488 | 490 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 550 | 552 | PF00675 | 0.274 |
CLV_NRD_NRD_1 | 734 | 736 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 929 | 931 | PF00675 | 0.250 |
CLV_NRD_NRD_1 | 963 | 965 | PF00675 | 0.491 |
CLV_PCSK_FUR_1 | 1072 | 1076 | PF00082 | 0.365 |
CLV_PCSK_FUR_1 | 255 | 259 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 1074 | 1076 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 1278 | 1280 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 1299 | 1301 | PF00082 | 0.378 |
CLV_PCSK_KEX2_1 | 1424 | 1426 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 1471 | 1473 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 488 | 490 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 550 | 552 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 734 | 736 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 963 | 965 | PF00082 | 0.246 |
CLV_PCSK_PC1ET2_1 | 1074 | 1076 | PF00082 | 0.448 |
CLV_PCSK_PC1ET2_1 | 226 | 228 | PF00082 | 0.582 |
CLV_PCSK_PC1ET2_1 | 366 | 368 | PF00082 | 0.322 |
CLV_PCSK_PC7_1 | 730 | 736 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 1035 | 1039 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 1075 | 1079 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 1127 | 1131 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 1270 | 1274 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 1303 | 1307 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 1424 | 1428 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 585 | 589 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 631 | 635 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 641 | 645 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 735 | 739 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 764 | 768 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 774 | 778 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 826 | 830 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 944 | 948 | PF00082 | 0.452 |
CLV_Separin_Metazoa | 1003 | 1007 | PF03568 | 0.436 |
CLV_Separin_Metazoa | 148 | 152 | PF03568 | 0.697 |
CLV_Separin_Metazoa | 162 | 166 | PF03568 | 0.501 |
DEG_APCC_DBOX_1 | 330 | 338 | PF00400 | 0.412 |
DEG_APCC_DBOX_1 | 963 | 971 | PF00400 | 0.368 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.507 |
DEG_ODPH_VHL_1 | 954 | 967 | PF01847 | 0.260 |
DEG_SCF_FBW7_1 | 306 | 311 | PF00400 | 0.416 |
DEG_SCF_FBW7_1 | 907 | 914 | PF00400 | 0.495 |
DEG_SCF_FBW7_2 | 1017 | 1022 | PF00400 | 0.536 |
DEG_SCF_SKP2-CKS1_1 | 710 | 717 | PF00560 | 0.504 |
DEG_SPOP_SBC_1 | 1310 | 1314 | PF00917 | 0.463 |
DEG_SPOP_SBC_1 | 875 | 879 | PF00917 | 0.420 |
DOC_ANK_TNKS_1 | 246 | 253 | PF00023 | 0.468 |
DOC_CDC14_PxL_1 | 1426 | 1434 | PF14671 | 0.346 |
DOC_CKS1_1 | 110 | 115 | PF01111 | 0.677 |
DOC_CKS1_1 | 908 | 913 | PF01111 | 0.392 |
DOC_CYCLIN_RxL_1 | 1072 | 1082 | PF00134 | 0.412 |
DOC_CYCLIN_RxL_1 | 60 | 74 | PF00134 | 0.512 |
DOC_CYCLIN_RxL_1 | 628 | 635 | PF00134 | 0.458 |
DOC_MAPK_gen_1 | 1252 | 1261 | PF00069 | 0.546 |
DOC_MAPK_gen_1 | 30 | 39 | PF00069 | 0.378 |
DOC_MAPK_gen_1 | 476 | 482 | PF00069 | 0.504 |
DOC_MAPK_gen_1 | 60 | 70 | PF00069 | 0.515 |
DOC_MAPK_gen_1 | 636 | 644 | PF00069 | 0.496 |
DOC_MAPK_gen_1 | 734 | 740 | PF00069 | 0.388 |
DOC_MAPK_gen_1 | 963 | 970 | PF00069 | 0.238 |
DOC_MAPK_HePTP_8 | 1422 | 1434 | PF00069 | 0.346 |
DOC_MAPK_MEF2A_6 | 1425 | 1434 | PF00069 | 0.350 |
DOC_MAPK_MEF2A_6 | 30 | 39 | PF00069 | 0.555 |
DOC_MAPK_MEF2A_6 | 636 | 644 | PF00069 | 0.477 |
DOC_MAPK_MEF2A_6 | 963 | 972 | PF00069 | 0.311 |
DOC_MAPK_NFAT4_5 | 32 | 40 | PF00069 | 0.550 |
DOC_PP1_RVXF_1 | 64 | 71 | PF00149 | 0.538 |
DOC_PP2B_LxvP_1 | 1240 | 1243 | PF13499 | 0.524 |
DOC_PP2B_LxvP_1 | 1427 | 1430 | PF13499 | 0.491 |
DOC_PP2B_LxvP_1 | 35 | 38 | PF13499 | 0.515 |
DOC_PP2B_LxvP_1 | 990 | 993 | PF13499 | 0.585 |
DOC_PP4_FxxP_1 | 15 | 18 | PF00568 | 0.533 |
DOC_PP4_FxxP_1 | 691 | 694 | PF00568 | 0.478 |
DOC_PP4_FxxP_1 | 989 | 992 | PF00568 | 0.463 |
DOC_SPAK_OSR1_1 | 798 | 802 | PF12202 | 0.396 |
DOC_USP7_MATH_1 | 1182 | 1186 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 1246 | 1250 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 1272 | 1276 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 1310 | 1314 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 1357 | 1361 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 606 | 610 | PF00917 | 0.382 |
DOC_USP7_MATH_1 | 698 | 702 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 715 | 719 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 794 | 798 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 819 | 823 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 875 | 879 | PF00917 | 0.567 |
DOC_USP7_UBL2_3 | 713 | 717 | PF12436 | 0.500 |
DOC_WW_Pin1_4 | 1015 | 1020 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 1134 | 1139 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 1312 | 1317 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 1436 | 1441 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 1450 | 1455 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 304 | 309 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 659 | 664 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 690 | 695 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 711 | 716 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 721 | 726 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 878 | 883 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 907 | 912 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.563 |
LIG_14-3-3_CanoR_1 | 1217 | 1221 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 1383 | 1387 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 1393 | 1397 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 1411 | 1419 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 329 | 335 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 452 | 460 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 488 | 493 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 550 | 557 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 565 | 570 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 585 | 590 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 860 | 866 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 933 | 943 | PF00244 | 0.544 |
LIG_Actin_WH2_2 | 1101 | 1119 | PF00022 | 0.456 |
LIG_Actin_WH2_2 | 1456 | 1473 | PF00022 | 0.395 |
LIG_Actin_WH2_2 | 18 | 34 | PF00022 | 0.467 |
LIG_Actin_WH2_2 | 388 | 406 | PF00022 | 0.557 |
LIG_Actin_WH2_2 | 626 | 643 | PF00022 | 0.496 |
LIG_AP2alpha_1 | 1327 | 1331 | PF02296 | 0.439 |
LIG_APCC_ABBA_1 | 1324 | 1329 | PF00400 | 0.445 |
LIG_APCC_ABBA_1 | 1377 | 1382 | PF00400 | 0.306 |
LIG_APCC_ABBA_1 | 954 | 959 | PF00400 | 0.319 |
LIG_BIR_III_2 | 1286 | 1290 | PF00653 | 0.351 |
LIG_BIR_III_2 | 1503 | 1507 | PF00653 | 0.513 |
LIG_BRCT_BRCA1_1 | 692 | 696 | PF00533 | 0.344 |
LIG_BRCT_BRCA1_1 | 880 | 884 | PF00533 | 0.421 |
LIG_CaM_IQ_9 | 925 | 940 | PF13499 | 0.441 |
LIG_CaM_NSCaTE_8 | 1350 | 1357 | PF13499 | 0.400 |
LIG_Clathr_ClatBox_1 | 1489 | 1493 | PF01394 | 0.479 |
LIG_deltaCOP1_diTrp_1 | 949 | 957 | PF00928 | 0.331 |
LIG_FHA_1 | 1179 | 1185 | PF00498 | 0.376 |
LIG_FHA_1 | 1205 | 1211 | PF00498 | 0.556 |
LIG_FHA_1 | 1383 | 1389 | PF00498 | 0.407 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.608 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.410 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.473 |
LIG_FHA_1 | 589 | 595 | PF00498 | 0.476 |
LIG_FHA_1 | 660 | 666 | PF00498 | 0.422 |
LIG_FHA_1 | 714 | 720 | PF00498 | 0.666 |
LIG_FHA_1 | 822 | 828 | PF00498 | 0.437 |
LIG_FHA_1 | 847 | 853 | PF00498 | 0.432 |
LIG_FHA_1 | 907 | 913 | PF00498 | 0.419 |
LIG_FHA_1 | 945 | 951 | PF00498 | 0.382 |
LIG_FHA_2 | 1061 | 1067 | PF00498 | 0.429 |
LIG_FHA_2 | 1167 | 1173 | PF00498 | 0.483 |
LIG_FHA_2 | 1312 | 1318 | PF00498 | 0.387 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.553 |
LIG_FHA_2 | 417 | 423 | PF00498 | 0.690 |
LIG_FHA_2 | 599 | 605 | PF00498 | 0.453 |
LIG_FHA_2 | 837 | 843 | PF00498 | 0.474 |
LIG_FHA_2 | 853 | 859 | PF00498 | 0.474 |
LIG_FHA_2 | 986 | 992 | PF00498 | 0.586 |
LIG_FHA_2 | 994 | 1000 | PF00498 | 0.523 |
LIG_GBD_Chelix_1 | 1388 | 1396 | PF00786 | 0.439 |
LIG_GBD_Chelix_1 | 395 | 403 | PF00786 | 0.566 |
LIG_Integrin_isoDGR_2 | 40 | 42 | PF01839 | 0.382 |
LIG_Integrin_RGD_1 | 1284 | 1286 | PF01839 | 0.391 |
LIG_LIR_Apic_2 | 12 | 18 | PF02991 | 0.782 |
LIG_LIR_Apic_2 | 688 | 694 | PF02991 | 0.467 |
LIG_LIR_Apic_2 | 785 | 789 | PF02991 | 0.557 |
LIG_LIR_Apic_2 | 988 | 992 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 1022 | 1031 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 1103 | 1111 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 1263 | 1272 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 1348 | 1357 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 1374 | 1384 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 1385 | 1392 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 1395 | 1404 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 1453 | 1463 | PF02991 | 0.632 |
LIG_LIR_Gen_1 | 741 | 749 | PF02991 | 0.258 |
LIG_LIR_Gen_1 | 796 | 804 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 881 | 892 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 949 | 958 | PF02991 | 0.391 |
LIG_LIR_LC3C_4 | 394 | 397 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 1022 | 1026 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 1103 | 1108 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 120 | 124 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 1263 | 1269 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 1348 | 1353 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 1374 | 1379 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 1385 | 1389 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 1395 | 1400 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 1453 | 1458 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 652 | 657 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 693 | 699 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 741 | 745 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 796 | 802 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 881 | 887 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 949 | 954 | PF02991 | 0.407 |
LIG_NRBOX | 1348 | 1354 | PF00104 | 0.296 |
LIG_NRBOX | 970 | 976 | PF00104 | 0.333 |
LIG_NRP_CendR_1 | 1529 | 1531 | PF00754 | 0.520 |
LIG_Pex14_2 | 1327 | 1331 | PF04695 | 0.439 |
LIG_Pex14_2 | 654 | 658 | PF04695 | 0.374 |
LIG_Pex14_2 | 769 | 773 | PF04695 | 0.450 |
LIG_PTAP_UEV_1 | 274 | 279 | PF05743 | 0.492 |
LIG_SH2_CRK | 1386 | 1390 | PF00017 | 0.408 |
LIG_SH2_CRK | 171 | 175 | PF00017 | 0.499 |
LIG_SH2_CRK | 290 | 294 | PF00017 | 0.352 |
LIG_SH2_CRK | 742 | 746 | PF00017 | 0.323 |
LIG_SH2_CRK | 786 | 790 | PF00017 | 0.494 |
LIG_SH2_NCK_1 | 1386 | 1390 | PF00017 | 0.378 |
LIG_SH2_NCK_1 | 1404 | 1408 | PF00017 | 0.336 |
LIG_SH2_NCK_1 | 692 | 696 | PF00017 | 0.328 |
LIG_SH2_NCK_1 | 742 | 746 | PF00017 | 0.384 |
LIG_SH2_NCK_1 | 790 | 794 | PF00017 | 0.421 |
LIG_SH2_SRC | 124 | 127 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 364 | 368 | PF00017 | 0.393 |
LIG_SH2_STAP1 | 464 | 468 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 575 | 579 | PF00017 | 0.452 |
LIG_SH2_STAP1 | 921 | 925 | PF00017 | 0.459 |
LIG_SH2_STAT3 | 1122 | 1125 | PF00017 | 0.283 |
LIG_SH2_STAT3 | 1325 | 1328 | PF00017 | 0.315 |
LIG_SH2_STAT3 | 464 | 467 | PF00017 | 0.388 |
LIG_SH2_STAT3 | 481 | 484 | PF00017 | 0.448 |
LIG_SH2_STAT3 | 921 | 924 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 1023 | 1026 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 1076 | 1079 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 1325 | 1328 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 481 | 484 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 657 | 660 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 678 | 681 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 747 | 750 | PF00017 | 0.348 |
LIG_SH3_1 | 104 | 110 | PF00018 | 0.552 |
LIG_SH3_1 | 1404 | 1410 | PF00018 | 0.584 |
LIG_SH3_3 | 1025 | 1031 | PF00018 | 0.450 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.655 |
LIG_SH3_3 | 1152 | 1158 | PF00018 | 0.437 |
LIG_SH3_3 | 1189 | 1195 | PF00018 | 0.550 |
LIG_SH3_3 | 1313 | 1319 | PF00018 | 0.439 |
LIG_SH3_3 | 1404 | 1410 | PF00018 | 0.584 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.569 |
LIG_SH3_3 | 543 | 549 | PF00018 | 0.478 |
LIG_SH3_3 | 765 | 771 | PF00018 | 0.469 |
LIG_SH3_3 | 905 | 911 | PF00018 | 0.392 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.639 |
LIG_SUMO_SIM_anti_2 | 1022 | 1028 | PF11976 | 0.436 |
LIG_SUMO_SIM_anti_2 | 1221 | 1226 | PF11976 | 0.311 |
LIG_SUMO_SIM_par_1 | 1035 | 1041 | PF11976 | 0.425 |
LIG_SUMO_SIM_par_1 | 203 | 208 | PF11976 | 0.412 |
LIG_SUMO_SIM_par_1 | 394 | 401 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 800 | 807 | PF11976 | 0.441 |
LIG_TRAF2_1 | 100 | 103 | PF00917 | 0.572 |
LIG_TRAF2_1 | 145 | 148 | PF00917 | 0.658 |
LIG_TRAF2_2 | 1454 | 1459 | PF00917 | 0.421 |
LIG_TYR_ITIM | 294 | 299 | PF00017 | 0.345 |
LIG_TYR_ITIM | 740 | 745 | PF00017 | 0.384 |
LIG_UBA3_1 | 1396 | 1403 | PF00899 | 0.607 |
LIG_UBA3_1 | 626 | 631 | PF00899 | 0.308 |
LIG_UBA3_1 | 766 | 774 | PF00899 | 0.352 |
LIG_UBA3_1 | 967 | 973 | PF00899 | 0.435 |
LIG_WRC_WIRS_1 | 986 | 991 | PF05994 | 0.506 |
LIG_WW_3 | 106 | 110 | PF00397 | 0.549 |
MOD_CDC14_SPxK_1 | 1315 | 1318 | PF00782 | 0.368 |
MOD_CDK_SPK_2 | 109 | 114 | PF00069 | 0.510 |
MOD_CDK_SPxK_1 | 1312 | 1318 | PF00069 | 0.401 |
MOD_CDK_SPxK_1 | 711 | 717 | PF00069 | 0.503 |
MOD_CK1_1 | 1048 | 1054 | PF00069 | 0.253 |
MOD_CK1_1 | 1079 | 1085 | PF00069 | 0.366 |
MOD_CK1_1 | 1216 | 1222 | PF00069 | 0.442 |
MOD_CK1_1 | 1309 | 1315 | PF00069 | 0.518 |
MOD_CK1_1 | 1345 | 1351 | PF00069 | 0.307 |
MOD_CK1_1 | 1358 | 1364 | PF00069 | 0.337 |
MOD_CK1_1 | 1439 | 1445 | PF00069 | 0.481 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.399 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.591 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.670 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.518 |
MOD_CK1_1 | 724 | 730 | PF00069 | 0.557 |
MOD_CK1_1 | 836 | 842 | PF00069 | 0.287 |
MOD_CK1_1 | 859 | 865 | PF00069 | 0.323 |
MOD_CK1_1 | 876 | 882 | PF00069 | 0.392 |
MOD_CK2_1 | 1153 | 1159 | PF00069 | 0.628 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.541 |
MOD_CK2_1 | 1172 | 1178 | PF00069 | 0.476 |
MOD_CK2_1 | 1357 | 1363 | PF00069 | 0.304 |
MOD_CK2_1 | 1392 | 1398 | PF00069 | 0.312 |
MOD_CK2_1 | 1411 | 1417 | PF00069 | 0.512 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.588 |
MOD_CK2_1 | 416 | 422 | PF00069 | 0.592 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.384 |
MOD_CK2_1 | 852 | 858 | PF00069 | 0.465 |
MOD_CK2_1 | 985 | 991 | PF00069 | 0.585 |
MOD_Cter_Amidation | 1011 | 1014 | PF01082 | 0.270 |
MOD_DYRK1A_RPxSP_1 | 109 | 113 | PF00069 | 0.515 |
MOD_GlcNHglycan | 1112 | 1115 | PF01048 | 0.440 |
MOD_GlcNHglycan | 1184 | 1187 | PF01048 | 0.428 |
MOD_GlcNHglycan | 1188 | 1192 | PF01048 | 0.428 |
MOD_GlcNHglycan | 1198 | 1201 | PF01048 | 0.453 |
MOD_GlcNHglycan | 126 | 130 | PF01048 | 0.354 |
MOD_GlcNHglycan | 1308 | 1311 | PF01048 | 0.597 |
MOD_GlcNHglycan | 1344 | 1347 | PF01048 | 0.332 |
MOD_GlcNHglycan | 1413 | 1416 | PF01048 | 0.473 |
MOD_GlcNHglycan | 1444 | 1447 | PF01048 | 0.490 |
MOD_GlcNHglycan | 1493 | 1496 | PF01048 | 0.652 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.548 |
MOD_GlcNHglycan | 1518 | 1524 | PF01048 | 0.664 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.607 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.709 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.560 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.660 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.579 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.308 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.328 |
MOD_GlcNHglycan | 700 | 703 | PF01048 | 0.578 |
MOD_GlcNHglycan | 777 | 780 | PF01048 | 0.408 |
MOD_GlcNHglycan | 809 | 812 | PF01048 | 0.437 |
MOD_GlcNHglycan | 821 | 824 | PF01048 | 0.275 |
MOD_GlcNHglycan | 835 | 838 | PF01048 | 0.267 |
MOD_GlcNHglycan | 878 | 881 | PF01048 | 0.423 |
MOD_GlcNHglycan | 897 | 900 | PF01048 | 0.348 |
MOD_GlcNHglycan | 901 | 904 | PF01048 | 0.452 |
MOD_GSK3_1 | 1081 | 1088 | PF00069 | 0.382 |
MOD_GSK3_1 | 1166 | 1173 | PF00069 | 0.579 |
MOD_GSK3_1 | 1178 | 1185 | PF00069 | 0.561 |
MOD_GSK3_1 | 1196 | 1203 | PF00069 | 0.483 |
MOD_GSK3_1 | 1209 | 1216 | PF00069 | 0.399 |
MOD_GSK3_1 | 1241 | 1248 | PF00069 | 0.551 |
MOD_GSK3_1 | 1299 | 1306 | PF00069 | 0.543 |
MOD_GSK3_1 | 1308 | 1315 | PF00069 | 0.550 |
MOD_GSK3_1 | 1355 | 1362 | PF00069 | 0.405 |
MOD_GSK3_1 | 1411 | 1418 | PF00069 | 0.645 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.569 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.615 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.464 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.607 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.452 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.617 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.359 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.280 |
MOD_GSK3_1 | 711 | 718 | PF00069 | 0.545 |
MOD_GSK3_1 | 726 | 733 | PF00069 | 0.400 |
MOD_GSK3_1 | 758 | 765 | PF00069 | 0.314 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.508 |
MOD_GSK3_1 | 803 | 810 | PF00069 | 0.389 |
MOD_GSK3_1 | 852 | 859 | PF00069 | 0.351 |
MOD_GSK3_1 | 870 | 877 | PF00069 | 0.388 |
MOD_GSK3_1 | 895 | 902 | PF00069 | 0.350 |
MOD_GSK3_1 | 907 | 914 | PF00069 | 0.299 |
MOD_LATS_1 | 486 | 492 | PF00433 | 0.386 |
MOD_LATS_1 | 536 | 542 | PF00433 | 0.246 |
MOD_N-GLC_1 | 1342 | 1347 | PF02516 | 0.309 |
MOD_N-GLC_1 | 1411 | 1416 | PF02516 | 0.447 |
MOD_N-GLC_1 | 180 | 185 | PF02516 | 0.558 |
MOD_N-GLC_1 | 758 | 763 | PF02516 | 0.361 |
MOD_N-GLC_1 | 925 | 930 | PF02516 | 0.327 |
MOD_NEK2_1 | 1038 | 1043 | PF00069 | 0.253 |
MOD_NEK2_1 | 1110 | 1115 | PF00069 | 0.406 |
MOD_NEK2_1 | 1392 | 1397 | PF00069 | 0.356 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.526 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.266 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.435 |
MOD_NEK2_1 | 645 | 650 | PF00069 | 0.305 |
MOD_NEK2_1 | 803 | 808 | PF00069 | 0.274 |
MOD_NEK2_1 | 851 | 856 | PF00069 | 0.474 |
MOD_NEK2_1 | 950 | 955 | PF00069 | 0.473 |
MOD_NEK2_2 | 493 | 498 | PF00069 | 0.454 |
MOD_NEK2_2 | 821 | 826 | PF00069 | 0.255 |
MOD_PIKK_1 | 1079 | 1085 | PF00454 | 0.286 |
MOD_PIKK_1 | 1293 | 1299 | PF00454 | 0.610 |
MOD_PIKK_1 | 1387 | 1393 | PF00454 | 0.368 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.420 |
MOD_PIKK_1 | 398 | 404 | PF00454 | 0.596 |
MOD_PIKK_1 | 480 | 486 | PF00454 | 0.448 |
MOD_PIKK_1 | 520 | 526 | PF00454 | 0.351 |
MOD_PIKK_1 | 544 | 550 | PF00454 | 0.321 |
MOD_PIKK_1 | 912 | 918 | PF00454 | 0.246 |
MOD_PIKK_1 | 920 | 926 | PF00454 | 0.239 |
MOD_PIKK_1 | 934 | 940 | PF00454 | 0.245 |
MOD_PKA_1 | 1299 | 1305 | PF00069 | 0.383 |
MOD_PKA_1 | 488 | 494 | PF00069 | 0.383 |
MOD_PKA_1 | 550 | 556 | PF00069 | 0.287 |
MOD_PKA_2 | 1216 | 1222 | PF00069 | 0.504 |
MOD_PKA_2 | 1299 | 1305 | PF00069 | 0.383 |
MOD_PKA_2 | 1382 | 1388 | PF00069 | 0.362 |
MOD_PKA_2 | 1392 | 1398 | PF00069 | 0.314 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.573 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.466 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.540 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.468 |
MOD_PKA_2 | 487 | 493 | PF00069 | 0.441 |
MOD_PKA_2 | 550 | 556 | PF00069 | 0.266 |
MOD_PKA_2 | 564 | 570 | PF00069 | 0.287 |
MOD_PKA_2 | 859 | 865 | PF00069 | 0.349 |
MOD_Plk_1 | 1342 | 1348 | PF00069 | 0.456 |
MOD_Plk_1 | 1366 | 1372 | PF00069 | 0.449 |
MOD_Plk_1 | 1411 | 1417 | PF00069 | 0.441 |
MOD_Plk_1 | 185 | 191 | PF00069 | 0.585 |
MOD_Plk_1 | 196 | 202 | PF00069 | 0.472 |
MOD_Plk_1 | 446 | 452 | PF00069 | 0.638 |
MOD_Plk_1 | 998 | 1004 | PF00069 | 0.285 |
MOD_Plk_2-3 | 117 | 123 | PF00069 | 0.547 |
MOD_Plk_2-3 | 1459 | 1465 | PF00069 | 0.530 |
MOD_Plk_4 | 1038 | 1044 | PF00069 | 0.462 |
MOD_Plk_4 | 1045 | 1051 | PF00069 | 0.422 |
MOD_Plk_4 | 1345 | 1351 | PF00069 | 0.339 |
MOD_Plk_4 | 1392 | 1398 | PF00069 | 0.456 |
MOD_Plk_4 | 1459 | 1465 | PF00069 | 0.530 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.575 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.398 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.667 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.632 |
MOD_Plk_4 | 762 | 768 | PF00069 | 0.289 |
MOD_Plk_4 | 985 | 991 | PF00069 | 0.535 |
MOD_ProDKin_1 | 1015 | 1021 | PF00069 | 0.295 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.597 |
MOD_ProDKin_1 | 1134 | 1140 | PF00069 | 0.579 |
MOD_ProDKin_1 | 1312 | 1318 | PF00069 | 0.561 |
MOD_ProDKin_1 | 1436 | 1442 | PF00069 | 0.477 |
MOD_ProDKin_1 | 1450 | 1456 | PF00069 | 0.574 |
MOD_ProDKin_1 | 304 | 310 | PF00069 | 0.464 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.598 |
MOD_ProDKin_1 | 659 | 665 | PF00069 | 0.446 |
MOD_ProDKin_1 | 690 | 696 | PF00069 | 0.455 |
MOD_ProDKin_1 | 711 | 717 | PF00069 | 0.681 |
MOD_ProDKin_1 | 721 | 727 | PF00069 | 0.535 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.646 |
MOD_ProDKin_1 | 878 | 884 | PF00069 | 0.465 |
MOD_ProDKin_1 | 907 | 913 | PF00069 | 0.477 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.562 |
MOD_SUMO_rev_2 | 756 | 766 | PF00179 | 0.421 |
TRG_DiLeu_BaEn_1 | 1022 | 1027 | PF01217 | 0.267 |
TRG_DiLeu_BaEn_2 | 196 | 202 | PF01217 | 0.336 |
TRG_DiLeu_BaLyEn_6 | 1422 | 1427 | PF01217 | 0.326 |
TRG_DiLeu_BaLyEn_6 | 235 | 240 | PF01217 | 0.321 |
TRG_ENDOCYTIC_2 | 1023 | 1026 | PF00928 | 0.267 |
TRG_ENDOCYTIC_2 | 1093 | 1096 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 1126 | 1129 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 1386 | 1389 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 742 | 745 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 943 | 946 | PF00928 | 0.359 |
TRG_ER_diArg_1 | 1278 | 1280 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 1298 | 1300 | PF00400 | 0.311 |
TRG_ER_diArg_1 | 1424 | 1426 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 1470 | 1472 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 164 | 166 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 255 | 258 | PF00400 | 0.734 |
TRG_ER_diArg_1 | 328 | 331 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 475 | 477 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 487 | 489 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 507 | 510 | PF00400 | 0.403 |
TRG_ER_diArg_1 | 549 | 551 | PF00400 | 0.321 |
TRG_ER_diArg_1 | 638 | 641 | PF00400 | 0.350 |
TRG_ER_diArg_1 | 962 | 964 | PF00400 | 0.252 |
TRG_ER_FFAT_2 | 685 | 697 | PF00635 | 0.470 |
TRG_NES_CRM1_1 | 1015 | 1030 | PF08389 | 0.267 |
TRG_NES_CRM1_1 | 604 | 615 | PF08389 | 0.286 |
TRG_NLS_MonoCore_2 | 1071 | 1076 | PF00514 | 0.495 |
TRG_NLS_MonoExtN_4 | 1072 | 1077 | PF00514 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 238 | 242 | PF00026 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 291 | 295 | PF00026 | 0.345 |
TRG_Pf-PMV_PEXEL_1 | 677 | 681 | PF00026 | 0.336 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5H2 | Leptomonas seymouri | 58% | 84% |
A0A1X0P9B9 | Trypanosomatidae | 43% | 100% |
A0A1X0P9W8 | Trypanosomatidae | 28% | 69% |
A0A3R7MLF0 | Trypanosoma rangeli | 44% | 100% |
A0A3S7WQG7 | Leishmania donovani | 29% | 100% |
A0A3S7X7P0 | Leishmania donovani | 92% | 100% |
A4HAN8 | Leishmania braziliensis | 78% | 79% |
A4HB41 | Leishmania braziliensis | 31% | 68% |
A4HTS5 | Leishmania infantum | 29% | 100% |
A4I9T1 | Leishmania infantum | 93% | 84% |
C9ZM05 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 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) | 90% | 100% |
E9B5B2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 69% |
Q4Q2M1 | Leishmania major | 31% | 69% |
Q581T1 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 31% | 71% |
V5BKW2 | Trypanosoma cruzi | 31% | 95% |
V5BND8 | Trypanosoma cruzi | 44% | 100% |