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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000228 | nuclear chromosome | 6 | 2 |
GO:0000793 | condensed chromosome | 6 | 2 |
GO:0000794 | condensed nuclear chromosome | 7 | 2 |
GO:0005634 | nucleus | 5 | 2 |
GO:0005694 | chromosome | 5 | 2 |
GO:0030870 | Mre11 complex | 3 | 10 |
GO:0032991 | protein-containing complex | 1 | 10 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000722 | telomere maintenance via recombination | 6 | 2 |
GO:0000723 | telomere maintenance | 5 | 10 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006259 | DNA metabolic process | 4 | 10 |
GO:0006278 | RNA-templated DNA biosynthetic process | 6 | 2 |
GO:0006281 | DNA repair | 5 | 10 |
GO:0006302 | double-strand break repair | 6 | 2 |
GO:0006310 | DNA recombination | 5 | 2 |
GO:0006312 | mitotic recombination | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0006950 | response to stress | 2 | 10 |
GO:0006974 | DNA damage response | 4 | 10 |
GO:0006996 | organelle organization | 4 | 10 |
GO:0007004 | telomere maintenance via telomerase | 7 | 2 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009059 | macromolecule biosynthetic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 10 |
GO:0010833 | telomere maintenance via telomere lengthening | 6 | 2 |
GO:0016043 | cellular component organization | 3 | 10 |
GO:0018130 | heterocycle biosynthetic process | 4 | 2 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 2 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0022414 | reproductive process | 1 | 2 |
GO:0032200 | telomere organization | 6 | 10 |
GO:0032392 | DNA geometric change | 7 | 2 |
GO:0032508 | DNA duplex unwinding | 8 | 2 |
GO:0033554 | cellular response to stress | 3 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 10 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0050896 | response to stimulus | 1 | 10 |
GO:0051276 | chromosome organization | 5 | 10 |
GO:0051716 | cellular response to stimulus | 2 | 10 |
GO:0070192 | chromosome organization involved in meiotic cell cycle | 3 | 2 |
GO:0071103 | DNA conformation change | 6 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0071840 | cellular component organization or biogenesis | 2 | 10 |
GO:0071897 | DNA biosynthetic process | 5 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
GO:1903046 | meiotic cell cycle process | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003677 | DNA binding | 4 | 2 |
GO:0003690 | double-stranded DNA binding | 5 | 2 |
GO:0003691 | double-stranded telomeric DNA binding | 6 | 2 |
GO:0003697 | single-stranded DNA binding | 5 | 2 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 10 |
GO:0016462 | pyrophosphatase activity | 5 | 10 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 10 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 10 |
GO:0016887 | ATP hydrolysis activity | 7 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0042162 | telomeric DNA binding | 6 | 2 |
GO:0043047 | single-stranded telomeric DNA binding | 7 | 2 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0043565 | sequence-specific DNA binding | 5 | 2 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0051880 | G-quadruplex DNA binding | 5 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0098847 | sequence-specific single stranded DNA binding | 6 | 2 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 10 |
GO:0140299 | small molecule sensor activity | 1 | 10 |
GO:0140612 | DNA damage sensor activity | 2 | 10 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 10 |
GO:0140657 | ATP-dependent activity | 1 | 10 |
GO:0140664 | ATP-dependent DNA damage sensor activity | 3 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 114 | 118 | PF00656 | 0.487 |
CLV_C14_Caspase3-7 | 1286 | 1290 | PF00656 | 0.559 |
CLV_C14_Caspase3-7 | 1295 | 1299 | PF00656 | 0.506 |
CLV_NRD_NRD_1 | 1040 | 1042 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 1049 | 1051 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 1204 | 1206 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 1230 | 1232 | PF00675 | 0.232 |
CLV_NRD_NRD_1 | 1307 | 1309 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.232 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 635 | 637 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 714 | 716 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 824 | 826 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 843 | 845 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 905 | 907 | PF00675 | 0.591 |
CLV_PCSK_KEX2_1 | 1049 | 1051 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 1154 | 1156 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 1204 | 1206 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 1230 | 1232 | PF00082 | 0.221 |
CLV_PCSK_KEX2_1 | 1240 | 1242 | PF00082 | 0.221 |
CLV_PCSK_KEX2_1 | 1307 | 1309 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.222 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 452 | 454 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 635 | 637 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 672 | 674 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 945 | 947 | PF00082 | 0.642 |
CLV_PCSK_PC1ET2_1 | 1154 | 1156 | PF00082 | 0.395 |
CLV_PCSK_PC1ET2_1 | 1240 | 1242 | PF00082 | 0.226 |
CLV_PCSK_PC1ET2_1 | 177 | 179 | PF00082 | 0.320 |
CLV_PCSK_PC1ET2_1 | 328 | 330 | PF00082 | 0.523 |
CLV_PCSK_PC1ET2_1 | 672 | 674 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 945 | 947 | PF00082 | 0.638 |
CLV_PCSK_PC7_1 | 1236 | 1242 | PF00082 | 0.221 |
CLV_PCSK_PC7_1 | 282 | 288 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 1265 | 1269 | PF00082 | 0.225 |
CLV_PCSK_SKI1_1 | 1308 | 1312 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.222 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.216 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.184 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.226 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 596 | 600 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 673 | 677 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 882 | 886 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 977 | 981 | PF00082 | 0.560 |
DEG_APCC_DBOX_1 | 258 | 266 | PF00400 | 0.546 |
DEG_APCC_DBOX_1 | 557 | 565 | PF00400 | 0.448 |
DEG_APCC_DBOX_1 | 672 | 680 | PF00400 | 0.501 |
DEG_COP1_1 | 137 | 147 | PF00400 | 0.451 |
DEG_Kelch_Keap1_1 | 124 | 129 | PF01344 | 0.369 |
DEG_SPOP_SBC_1 | 130 | 134 | PF00917 | 0.464 |
DOC_CYCLIN_RxL_1 | 604 | 614 | PF00134 | 0.457 |
DOC_CYCLIN_RxL_1 | 958 | 968 | PF00134 | 0.641 |
DOC_CYCLIN_RxL_1 | 985 | 993 | PF00134 | 0.568 |
DOC_MAPK_gen_1 | 1154 | 1163 | PF00069 | 0.388 |
DOC_MAPK_gen_1 | 1307 | 1318 | PF00069 | 0.298 |
DOC_MAPK_gen_1 | 346 | 353 | PF00069 | 0.525 |
DOC_MAPK_gen_1 | 755 | 763 | PF00069 | 0.495 |
DOC_MAPK_gen_1 | 985 | 994 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 1257 | 1266 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 746 | 754 | PF00069 | 0.515 |
DOC_MAPK_MEF2A_6 | 81 | 88 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 985 | 994 | PF00069 | 0.503 |
DOC_MAPK_NFAT4_5 | 81 | 89 | PF00069 | 0.432 |
DOC_PP1_RVXF_1 | 108 | 114 | PF00149 | 0.520 |
DOC_PP1_RVXF_1 | 83 | 89 | PF00149 | 0.421 |
DOC_PP2B_LxvP_1 | 170 | 173 | PF13499 | 0.428 |
DOC_PP2B_LxvP_1 | 992 | 995 | PF13499 | 0.555 |
DOC_PP4_FxxP_1 | 27 | 30 | PF00568 | 0.421 |
DOC_PP4_FxxP_1 | 580 | 583 | PF00568 | 0.339 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 1183 | 1187 | PF00917 | 0.360 |
DOC_USP7_MATH_1 | 1229 | 1233 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 678 | 682 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 702 | 706 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 740 | 744 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 951 | 955 | PF00917 | 0.587 |
DOC_USP7_UBL2_3 | 1038 | 1042 | PF12436 | 0.529 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 720 | 725 | PF00397 | 0.456 |
LIG_14-3-3_CanoR_1 | 1041 | 1045 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 1079 | 1085 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 110 | 120 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 1101 | 1106 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 1155 | 1161 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 1204 | 1208 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 1230 | 1234 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 1249 | 1259 | PF00244 | 0.354 |
LIG_14-3-3_CanoR_1 | 136 | 144 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 309 | 319 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 408 | 416 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 589 | 598 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 719 | 724 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 882 | 890 | PF00244 | 0.628 |
LIG_Actin_WH2_2 | 248 | 265 | PF00022 | 0.538 |
LIG_Actin_WH2_2 | 805 | 822 | PF00022 | 0.524 |
LIG_AP2alpha_1 | 180 | 184 | PF02296 | 0.464 |
LIG_BRCT_BRCA1_1 | 1268 | 1272 | PF00533 | 0.421 |
LIG_BRCT_BRCA1_1 | 199 | 203 | PF00533 | 0.446 |
LIG_Clathr_ClatBox_1 | 508 | 512 | PF01394 | 0.501 |
LIG_DLG_GKlike_1 | 1101 | 1108 | PF00625 | 0.430 |
LIG_EH1_1 | 1089 | 1097 | PF00400 | 0.509 |
LIG_FHA_1 | 1111 | 1117 | PF00498 | 0.506 |
LIG_FHA_1 | 1163 | 1169 | PF00498 | 0.354 |
LIG_FHA_1 | 1212 | 1218 | PF00498 | 0.446 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.432 |
LIG_FHA_1 | 1283 | 1289 | PF00498 | 0.426 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.421 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.421 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.421 |
LIG_FHA_1 | 606 | 612 | PF00498 | 0.492 |
LIG_FHA_1 | 626 | 632 | PF00498 | 0.451 |
LIG_FHA_1 | 814 | 820 | PF00498 | 0.529 |
LIG_FHA_1 | 872 | 878 | PF00498 | 0.543 |
LIG_FHA_2 | 1041 | 1047 | PF00498 | 0.661 |
LIG_FHA_2 | 1105 | 1111 | PF00498 | 0.483 |
LIG_FHA_2 | 1115 | 1121 | PF00498 | 0.494 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.487 |
LIG_FHA_2 | 1284 | 1290 | PF00498 | 0.421 |
LIG_FHA_2 | 1317 | 1323 | PF00498 | 0.295 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.523 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.537 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.429 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.421 |
LIG_FHA_2 | 720 | 726 | PF00498 | 0.501 |
LIG_FHA_2 | 734 | 740 | PF00498 | 0.464 |
LIG_FHA_2 | 809 | 815 | PF00498 | 0.467 |
LIG_FHA_2 | 937 | 943 | PF00498 | 0.667 |
LIG_Integrin_isoDGR_2 | 280 | 282 | PF01839 | 0.460 |
LIG_Integrin_RGD_1 | 1145 | 1147 | PF01839 | 0.508 |
LIG_LIR_Apic_2 | 578 | 583 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 112 | 121 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 1147 | 1156 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 1158 | 1168 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 1174 | 1184 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 1344 | 1355 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 653 | 662 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 681 | 690 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 739 | 747 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 800 | 809 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 862 | 871 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 112 | 116 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 1147 | 1152 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 1158 | 1163 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 1174 | 1180 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 119 | 125 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 1232 | 1238 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 1334 | 1339 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 1344 | 1350 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 1352 | 1358 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 653 | 658 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 681 | 686 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 739 | 744 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 800 | 806 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 862 | 866 | PF02991 | 0.425 |
LIG_LYPXL_SIV_4 | 869 | 877 | PF13949 | 0.520 |
LIG_NRBOX | 301 | 307 | PF00104 | 0.578 |
LIG_NRBOX | 390 | 396 | PF00104 | 0.540 |
LIG_PCNA_yPIPBox_3 | 1191 | 1203 | PF02747 | 0.327 |
LIG_PDZ_Class_2 | 1355 | 1360 | PF00595 | 0.291 |
LIG_Pex14_1 | 1203 | 1207 | PF04695 | 0.325 |
LIG_Pex14_2 | 1355 | 1359 | PF04695 | 0.272 |
LIG_Pex14_2 | 180 | 184 | PF04695 | 0.421 |
LIG_RPA_C_Fungi | 544 | 556 | PF08784 | 0.382 |
LIG_RPA_C_Plants | 966 | 977 | PF08784 | 0.533 |
LIG_SH2_CRK | 1235 | 1239 | PF00017 | 0.262 |
LIG_SH2_GRB2like | 1149 | 1152 | PF00017 | 0.499 |
LIG_SH2_NCK_1 | 330 | 334 | PF00017 | 0.471 |
LIG_SH2_NCK_1 | 870 | 874 | PF00017 | 0.396 |
LIG_SH2_SRC | 1149 | 1152 | PF00017 | 0.499 |
LIG_SH2_SRC | 655 | 658 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 330 | 334 | PF00017 | 0.597 |
LIG_SH2_STAP1 | 655 | 659 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 1000 | 1003 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 1338 | 1341 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.262 |
LIG_SH3_2 | 169 | 174 | PF14604 | 0.278 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.278 |
LIG_SH3_3 | 566 | 572 | PF00018 | 0.507 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.262 |
LIG_SUMO_SIM_anti_2 | 537 | 542 | PF11976 | 0.501 |
LIG_SUMO_SIM_par_1 | 1213 | 1222 | PF11976 | 0.448 |
LIG_SUMO_SIM_par_1 | 1277 | 1283 | PF11976 | 0.262 |
LIG_SUMO_SIM_par_1 | 1314 | 1319 | PF11976 | 0.298 |
LIG_SUMO_SIM_par_1 | 189 | 194 | PF11976 | 0.278 |
LIG_SUMO_SIM_par_1 | 814 | 822 | PF11976 | 0.506 |
LIG_TRAF2_1 | 1026 | 1029 | PF00917 | 0.543 |
LIG_TRAF2_1 | 264 | 267 | PF00917 | 0.451 |
LIG_TRAF2_1 | 339 | 342 | PF00917 | 0.557 |
LIG_TRAF2_1 | 490 | 493 | PF00917 | 0.518 |
LIG_TRAF2_1 | 618 | 621 | PF00917 | 0.510 |
LIG_TRAF2_1 | 654 | 657 | PF00917 | 0.358 |
LIG_TRAF2_1 | 862 | 865 | PF00917 | 0.455 |
LIG_WRC_WIRS_1 | 12 | 17 | PF05994 | 0.262 |
LIG_WRC_WIRS_1 | 709 | 714 | PF05994 | 0.521 |
LIG_WRC_WIRS_1 | 99 | 104 | PF05994 | 0.278 |
MOD_CK1_1 | 1083 | 1089 | PF00069 | 0.548 |
MOD_CK1_1 | 1104 | 1110 | PF00069 | 0.478 |
MOD_CK1_1 | 587 | 593 | PF00069 | 0.399 |
MOD_CK1_1 | 625 | 631 | PF00069 | 0.467 |
MOD_CK1_1 | 705 | 711 | PF00069 | 0.525 |
MOD_CK1_1 | 723 | 729 | PF00069 | 0.593 |
MOD_CK2_1 | 1023 | 1029 | PF00069 | 0.506 |
MOD_CK2_1 | 1104 | 1110 | PF00069 | 0.454 |
MOD_CK2_1 | 1114 | 1120 | PF00069 | 0.391 |
MOD_CK2_1 | 1175 | 1181 | PF00069 | 0.494 |
MOD_CK2_1 | 1216 | 1222 | PF00069 | 0.551 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.190 |
MOD_CK2_1 | 1316 | 1322 | PF00069 | 0.295 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.434 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.526 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.262 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.262 |
MOD_CK2_1 | 624 | 630 | PF00069 | 0.478 |
MOD_CK2_1 | 719 | 725 | PF00069 | 0.459 |
MOD_CK2_1 | 733 | 739 | PF00069 | 0.430 |
MOD_CK2_1 | 808 | 814 | PF00069 | 0.514 |
MOD_CK2_1 | 859 | 865 | PF00069 | 0.464 |
MOD_CK2_1 | 936 | 942 | PF00069 | 0.685 |
MOD_GlcNHglycan | 1020 | 1023 | PF01048 | 0.600 |
MOD_GlcNHglycan | 1025 | 1028 | PF01048 | 0.631 |
MOD_GlcNHglycan | 1050 | 1053 | PF01048 | 0.625 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.401 |
MOD_GlcNHglycan | 1177 | 1180 | PF01048 | 0.438 |
MOD_GlcNHglycan | 1252 | 1255 | PF01048 | 0.262 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.260 |
MOD_GlcNHglycan | 847 | 850 | PF01048 | 0.676 |
MOD_GlcNHglycan | 924 | 927 | PF01048 | 0.519 |
MOD_GSK3_1 | 1110 | 1117 | PF00069 | 0.509 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.197 |
MOD_GSK3_1 | 1162 | 1169 | PF00069 | 0.481 |
MOD_GSK3_1 | 1203 | 1210 | PF00069 | 0.340 |
MOD_GSK3_1 | 1218 | 1225 | PF00069 | 0.313 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.322 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.584 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.504 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.254 |
MOD_GSK3_1 | 719 | 726 | PF00069 | 0.497 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.577 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.269 |
MOD_N-GLC_1 | 514 | 519 | PF02516 | 0.548 |
MOD_N-GLC_1 | 734 | 739 | PF02516 | 0.328 |
MOD_N-GLC_2 | 1003 | 1005 | PF02516 | 0.501 |
MOD_N-GLC_2 | 51 | 53 | PF02516 | 0.278 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.262 |
MOD_NEK2_1 | 1077 | 1082 | PF00069 | 0.541 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.174 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.262 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.556 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.360 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.493 |
MOD_NEK2_1 | 808 | 813 | PF00069 | 0.453 |
MOD_NEK2_1 | 819 | 824 | PF00069 | 0.517 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.262 |
MOD_NEK2_1 | 990 | 995 | PF00069 | 0.532 |
MOD_NEK2_2 | 584 | 589 | PF00069 | 0.322 |
MOD_NEK2_2 | 678 | 683 | PF00069 | 0.366 |
MOD_PIKK_1 | 296 | 302 | PF00454 | 0.576 |
MOD_PIKK_1 | 469 | 475 | PF00454 | 0.423 |
MOD_PIKK_1 | 501 | 507 | PF00454 | 0.574 |
MOD_PIKK_1 | 587 | 593 | PF00454 | 0.468 |
MOD_PIKK_1 | 839 | 845 | PF00454 | 0.587 |
MOD_PK_1 | 746 | 752 | PF00069 | 0.572 |
MOD_PKA_2 | 1016 | 1022 | PF00069 | 0.609 |
MOD_PKA_2 | 1040 | 1046 | PF00069 | 0.653 |
MOD_PKA_2 | 1048 | 1054 | PF00069 | 0.610 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.412 |
MOD_PKA_2 | 1156 | 1162 | PF00069 | 0.373 |
MOD_PKA_2 | 1203 | 1209 | PF00069 | 0.336 |
MOD_PKA_2 | 1229 | 1235 | PF00069 | 0.278 |
MOD_PKA_2 | 1250 | 1256 | PF00069 | 0.298 |
MOD_PKA_2 | 135 | 141 | PF00069 | 0.355 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.613 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.312 |
MOD_PKA_2 | 819 | 825 | PF00069 | 0.589 |
MOD_PKB_1 | 195 | 203 | PF00069 | 0.298 |
MOD_PKB_1 | 406 | 414 | PF00069 | 0.507 |
MOD_Plk_1 | 1063 | 1069 | PF00069 | 0.564 |
MOD_Plk_1 | 1077 | 1083 | PF00069 | 0.512 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.293 |
MOD_Plk_1 | 1166 | 1172 | PF00069 | 0.468 |
MOD_Plk_1 | 1351 | 1357 | PF00069 | 0.281 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.322 |
MOD_Plk_1 | 387 | 393 | PF00069 | 0.540 |
MOD_Plk_1 | 514 | 520 | PF00069 | 0.524 |
MOD_Plk_1 | 705 | 711 | PF00069 | 0.441 |
MOD_Plk_1 | 813 | 819 | PF00069 | 0.562 |
MOD_Plk_2-3 | 1211 | 1217 | PF00069 | 0.419 |
MOD_Plk_2-3 | 1351 | 1357 | PF00069 | 0.281 |
MOD_Plk_4 | 1156 | 1162 | PF00069 | 0.373 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.355 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.495 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.283 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.298 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.262 |
MOD_Plk_4 | 708 | 714 | PF00069 | 0.555 |
MOD_Plk_4 | 746 | 752 | PF00069 | 0.436 |
MOD_Plk_4 | 798 | 804 | PF00069 | 0.438 |
MOD_Plk_4 | 996 | 1002 | PF00069 | 0.470 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.298 |
MOD_ProDKin_1 | 720 | 726 | PF00069 | 0.460 |
MOD_SUMO_for_1 | 598 | 601 | PF00179 | 0.494 |
MOD_SUMO_for_1 | 690 | 693 | PF00179 | 0.325 |
MOD_SUMO_rev_2 | 67 | 75 | PF00179 | 0.265 |
MOD_SUMO_rev_2 | 767 | 775 | PF00179 | 0.535 |
MOD_SUMO_rev_2 | 77 | 82 | PF00179 | 0.268 |
MOD_SUMO_rev_2 | 900 | 909 | PF00179 | 0.511 |
TRG_DiLeu_BaEn_2 | 63 | 69 | PF01217 | 0.278 |
TRG_DiLeu_BaEn_4 | 601 | 607 | PF01217 | 0.418 |
TRG_DiLeu_BaLyEn_6 | 390 | 395 | PF01217 | 0.539 |
TRG_DiLeu_BaLyEn_6 | 82 | 87 | PF01217 | 0.278 |
TRG_ENDOCYTIC_2 | 1149 | 1152 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 1177 | 1180 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 1235 | 1238 | PF00928 | 0.270 |
TRG_ENDOCYTIC_2 | 655 | 658 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 683 | 686 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 741 | 744 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 803 | 806 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 863 | 866 | PF00928 | 0.416 |
TRG_ER_diArg_1 | 1203 | 1205 | PF00400 | 0.261 |
TRG_ER_diArg_1 | 1248 | 1251 | PF00400 | 0.278 |
TRG_ER_diArg_1 | 203 | 205 | PF00400 | 0.278 |
TRG_ER_diArg_1 | 290 | 292 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 336 | 338 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 451 | 454 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 758 | 761 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 938 | 941 | PF00400 | 0.618 |
TRG_NES_CRM1_1 | 559 | 573 | PF08389 | 0.489 |
TRG_Pf-PMV_PEXEL_1 | 1007 | 1011 | PF00026 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 1294 | 1298 | PF00026 | 0.264 |
TRG_Pf-PMV_PEXEL_1 | 1301 | 1305 | PF00026 | 0.318 |
TRG_Pf-PMV_PEXEL_1 | 1326 | 1331 | PF00026 | 0.309 |
TRG_Pf-PMV_PEXEL_1 | 205 | 209 | PF00026 | 0.355 |
TRG_Pf-PMV_PEXEL_1 | 253 | 257 | PF00026 | 0.567 |
TRG_Pf-PMV_PEXEL_1 | 369 | 373 | PF00026 | 0.552 |
TRG_Pf-PMV_PEXEL_1 | 453 | 457 | PF00026 | 0.562 |
TRG_Pf-PMV_PEXEL_1 | 506 | 510 | PF00026 | 0.571 |
TRG_Pf-PMV_PEXEL_1 | 596 | 601 | PF00026 | 0.459 |
TRG_Pf-PMV_PEXEL_1 | 609 | 614 | PF00026 | 0.332 |
TRG_Pf-PMV_PEXEL_1 | 901 | 905 | PF00026 | 0.635 |
TRG_Pf-PMV_PEXEL_1 | 928 | 932 | PF00026 | 0.605 |
TRG_Pf-PMV_PEXEL_1 | 985 | 989 | PF00026 | 0.565 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3D5 | Leptomonas seymouri | 69% | 100% |
A0A0S4JAY7 | Bodo saltans | 38% | 100% |
A0A1X0NYH4 | Trypanosomatidae | 46% | 100% |
A0A3R7N260 | Trypanosoma rangeli | 47% | 100% |
A0A3S7X1A7 | Leishmania donovani | 94% | 100% |
A4HG93 | Leishmania braziliensis | 83% | 100% |
A4I3C7 | Leishmania infantum | 93% | 100% |
D0A818 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AZL4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q92878 | Homo sapiens | 28% | 100% |
V5BQC9 | Trypanosoma cruzi | 45% | 100% |