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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043228 | non-membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0030684 | preribosome | 3 | 1 |
GO:0030686 | 90S preribosome | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4I3R4
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 12 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 11 |
GO:0042254 | ribosome biogenesis | 5 | 11 |
GO:0044085 | cellular component biogenesis | 3 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
GO:0000462 | maturation of SSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 1 |
GO:0000469 | cleavage involved in rRNA processing | 7 | 1 |
GO:0000478 | endonucleolytic cleavage involved in rRNA processing | 8 | 1 |
GO:0000479 | endonucleolytic cleavage of tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 9 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 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:0016070 | RNA metabolic process | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0030490 | maturation of SSU-rRNA | 9 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 1 |
GO:0090501 | RNA phosphodiester bond hydrolysis | 6 | 1 |
GO:0090502 | RNA phosphodiester bond hydrolysis, endonucleolytic | 7 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005525 | GTP binding | 5 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0019001 | guanyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0003924 | GTPase activity | 7 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
GO:0030515 | snoRNA binding | 5 | 1 |
GO:0034511 | U3 snoRNA binding | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1204 | 1208 | PF00656 | 0.427 |
CLV_C14_Caspase3-7 | 452 | 456 | PF00656 | 0.679 |
CLV_C14_Caspase3-7 | 521 | 525 | PF00656 | 0.553 |
CLV_C14_Caspase3-7 | 600 | 604 | PF00656 | 0.662 |
CLV_C14_Caspase3-7 | 676 | 680 | PF00656 | 0.697 |
CLV_C14_Caspase3-7 | 753 | 757 | PF00656 | 0.695 |
CLV_NRD_NRD_1 | 1133 | 1135 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 1194 | 1196 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 1258 | 1260 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 638 | 640 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 764 | 766 | PF00675 | 0.727 |
CLV_NRD_NRD_1 | 931 | 933 | PF00675 | 0.237 |
CLV_PCSK_FUR_1 | 128 | 132 | PF00082 | 0.337 |
CLV_PCSK_FUR_1 | 26 | 30 | PF00082 | 0.610 |
CLV_PCSK_FUR_1 | 407 | 411 | PF00082 | 0.468 |
CLV_PCSK_FUR_1 | 760 | 764 | PF00082 | 0.729 |
CLV_PCSK_FUR_1 | 907 | 911 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 1132 | 1134 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 1194 | 1196 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 1218 | 1220 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 638 | 640 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 762 | 764 | PF00082 | 0.697 |
CLV_PCSK_KEX2_1 | 805 | 807 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 909 | 911 | PF00082 | 0.237 |
CLV_PCSK_KEX2_1 | 931 | 933 | PF00082 | 0.237 |
CLV_PCSK_PC1ET2_1 | 1132 | 1134 | PF00082 | 0.455 |
CLV_PCSK_PC1ET2_1 | 1218 | 1220 | PF00082 | 0.430 |
CLV_PCSK_PC1ET2_1 | 201 | 203 | PF00082 | 0.362 |
CLV_PCSK_PC1ET2_1 | 27 | 29 | PF00082 | 0.615 |
CLV_PCSK_PC1ET2_1 | 805 | 807 | PF00082 | 0.321 |
CLV_PCSK_PC1ET2_1 | 909 | 911 | PF00082 | 0.237 |
CLV_PCSK_PC7_1 | 403 | 409 | PF00082 | 0.526 |
CLV_PCSK_PC7_1 | 581 | 587 | PF00082 | 0.561 |
CLV_PCSK_PC7_1 | 760 | 766 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 1007 | 1011 | PF00082 | 0.237 |
CLV_PCSK_SKI1_1 | 1026 | 1030 | PF00082 | 0.237 |
CLV_PCSK_SKI1_1 | 1148 | 1152 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 1153 | 1157 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 1181 | 1185 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 1195 | 1199 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 1223 | 1227 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 1240 | 1244 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.237 |
CLV_PCSK_SKI1_1 | 529 | 533 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 577 | 581 | PF00082 | 0.676 |
CLV_PCSK_SKI1_1 | 726 | 730 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 801 | 805 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 916 | 920 | PF00082 | 0.237 |
CLV_PCSK_SKI1_1 | 949 | 953 | PF00082 | 0.237 |
CLV_Separin_Metazoa | 1087 | 1091 | PF03568 | 0.474 |
DEG_Kelch_Keap1_1 | 456 | 461 | PF01344 | 0.700 |
DEG_MDM2_SWIB_1 | 1079 | 1086 | PF02201 | 0.252 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.593 |
DEG_ODPH_VHL_1 | 502 | 515 | PF01847 | 0.615 |
DOC_CDC14_PxL_1 | 300 | 308 | PF14671 | 0.272 |
DOC_CKS1_1 | 1001 | 1006 | PF01111 | 0.408 |
DOC_CYCLIN_RxL_1 | 1004 | 1014 | PF00134 | 0.239 |
DOC_CYCLIN_RxL_1 | 1145 | 1152 | PF00134 | 0.514 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 1150 | 1159 | PF00134 | 0.530 |
DOC_MAPK_gen_1 | 1110 | 1120 | PF00069 | 0.410 |
DOC_MAPK_gen_1 | 26 | 34 | PF00069 | 0.478 |
DOC_MAPK_gen_1 | 293 | 303 | PF00069 | 0.237 |
DOC_MAPK_gen_1 | 407 | 414 | PF00069 | 0.635 |
DOC_MAPK_gen_1 | 64 | 71 | PF00069 | 0.405 |
DOC_MAPK_gen_1 | 916 | 926 | PF00069 | 0.237 |
DOC_MAPK_MEF2A_6 | 149 | 158 | PF00069 | 0.257 |
DOC_MAPK_MEF2A_6 | 415 | 424 | PF00069 | 0.540 |
DOC_MAPK_MEF2A_6 | 881 | 889 | PF00069 | 0.272 |
DOC_MAPK_MEF2A_6 | 919 | 928 | PF00069 | 0.237 |
DOC_PP1_RVXF_1 | 128 | 135 | PF00149 | 0.305 |
DOC_PP1_RVXF_1 | 280 | 287 | PF00149 | 0.237 |
DOC_PP2B_LxvP_1 | 348 | 351 | PF13499 | 0.450 |
DOC_PP2B_LxvP_1 | 69 | 72 | PF13499 | 0.384 |
DOC_PP2B_LxvP_1 | 976 | 979 | PF13499 | 0.380 |
DOC_PP4_FxxP_1 | 45 | 48 | PF00568 | 0.486 |
DOC_PP4_FxxP_1 | 964 | 967 | PF00568 | 0.237 |
DOC_PP4_FxxP_1 | 988 | 991 | PF00568 | 0.331 |
DOC_USP7_MATH_1 | 1082 | 1086 | PF00917 | 0.380 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.312 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.341 |
DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 642 | 646 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 689 | 693 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 983 | 987 | PF00917 | 0.313 |
DOC_USP7_UBL2_3 | 1054 | 1058 | PF12436 | 0.237 |
DOC_USP7_UBL2_3 | 1213 | 1217 | PF12436 | 0.434 |
DOC_USP7_UBL2_3 | 1226 | 1230 | PF12436 | 0.390 |
DOC_USP7_UBL2_3 | 1240 | 1244 | PF12436 | 0.327 |
DOC_USP7_UBL2_3 | 18 | 22 | PF12436 | 0.482 |
DOC_USP7_UBL2_3 | 197 | 201 | PF12436 | 0.365 |
DOC_USP7_UBL2_3 | 800 | 804 | PF12436 | 0.240 |
DOC_WW_Pin1_4 | 1000 | 1005 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 1011 | 1016 | PF00397 | 0.209 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.400 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.395 |
DOC_WW_Pin1_4 | 652 | 657 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 951 | 956 | PF00397 | 0.237 |
LIG_14-3-3_CanoR_1 | 1065 | 1069 | PF00244 | 0.237 |
LIG_14-3-3_CanoR_1 | 1090 | 1095 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 113 | 119 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 130 | 135 | PF00244 | 0.257 |
LIG_14-3-3_CanoR_1 | 254 | 262 | PF00244 | 0.237 |
LIG_14-3-3_CanoR_1 | 339 | 344 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 6 | 15 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 726 | 733 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 931 | 937 | PF00244 | 0.237 |
LIG_14-3-3_CanoR_1 | 984 | 989 | PF00244 | 0.290 |
LIG_Actin_WH2_2 | 179 | 196 | PF00022 | 0.343 |
LIG_Actin_WH2_2 | 853 | 871 | PF00022 | 0.253 |
LIG_Actin_WH2_2 | 994 | 1012 | PF00022 | 0.331 |
LIG_BRCT_BRCA1_1 | 160 | 164 | PF00533 | 0.326 |
LIG_Clathr_ClatBox_1 | 155 | 159 | PF01394 | 0.257 |
LIG_Clathr_ClatBox_1 | 243 | 247 | PF01394 | 0.252 |
LIG_FHA_1 | 1001 | 1007 | PF00498 | 0.252 |
LIG_FHA_1 | 1020 | 1026 | PF00498 | 0.151 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.252 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.638 |
LIG_FHA_1 | 728 | 734 | PF00498 | 0.589 |
LIG_FHA_1 | 812 | 818 | PF00498 | 0.406 |
LIG_FHA_1 | 933 | 939 | PF00498 | 0.237 |
LIG_FHA_1 | 971 | 977 | PF00498 | 0.237 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.399 |
LIG_FHA_2 | 1065 | 1071 | PF00498 | 0.237 |
LIG_FHA_2 | 1199 | 1205 | PF00498 | 0.491 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.283 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.335 |
LIG_FHA_2 | 450 | 456 | PF00498 | 0.493 |
LIG_FHA_2 | 578 | 584 | PF00498 | 0.512 |
LIG_FHA_2 | 744 | 750 | PF00498 | 0.656 |
LIG_FXI_DFP_1 | 306 | 310 | PF00024 | 0.237 |
LIG_Integrin_isoDGR_2 | 724 | 726 | PF01839 | 0.597 |
LIG_Integrin_isoDGR_2 | 945 | 947 | PF01839 | 0.237 |
LIG_LIR_Apic_2 | 1115 | 1119 | PF02991 | 0.464 |
LIG_LIR_Apic_2 | 986 | 991 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 167 | 177 | PF02991 | 0.270 |
LIG_LIR_Gen_1 | 669 | 677 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 826 | 835 | PF02991 | 0.252 |
LIG_LIR_Gen_1 | 864 | 875 | PF02991 | 0.237 |
LIG_LIR_Gen_1 | 973 | 983 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 1081 | 1086 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 1125 | 1131 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 1165 | 1170 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 167 | 172 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 665 | 671 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 823 | 828 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 864 | 870 | PF02991 | 0.252 |
LIG_LIR_Nem_3 | 898 | 904 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 927 | 933 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 973 | 978 | PF02991 | 0.245 |
LIG_MAD2 | 403 | 411 | PF02301 | 0.591 |
LIG_NRBOX | 238 | 244 | PF00104 | 0.237 |
LIG_PCNA_PIPBox_1 | 183 | 192 | PF02747 | 0.285 |
LIG_PCNA_PIPBox_1 | 958 | 967 | PF02747 | 0.272 |
LIG_Pex14_2 | 1079 | 1083 | PF04695 | 0.237 |
LIG_Pex14_2 | 180 | 184 | PF04695 | 0.301 |
LIG_Pex14_2 | 879 | 883 | PF04695 | 0.237 |
LIG_SH2_CRK | 1116 | 1120 | PF00017 | 0.537 |
LIG_SH2_CRK | 828 | 832 | PF00017 | 0.297 |
LIG_SH2_CRK | 953 | 957 | PF00017 | 0.281 |
LIG_SH2_CRK | 965 | 969 | PF00017 | 0.187 |
LIG_SH2_GRB2like | 110 | 113 | PF00017 | 0.359 |
LIG_SH2_NCK_1 | 965 | 969 | PF00017 | 0.252 |
LIG_SH2_SRC | 965 | 968 | PF00017 | 0.237 |
LIG_SH2_STAP1 | 360 | 364 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 1091 | 1094 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 1128 | 1131 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 1235 | 1238 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 862 | 865 | PF00017 | 0.241 |
LIG_SH2_STAT5 | 867 | 870 | PF00017 | 0.233 |
LIG_SH2_STAT5 | 950 | 953 | PF00017 | 0.237 |
LIG_SH2_STAT5 | 995 | 998 | PF00017 | 0.237 |
LIG_SH3_1 | 291 | 297 | PF00018 | 0.252 |
LIG_SH3_3 | 1083 | 1089 | PF00018 | 0.238 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.338 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.280 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.265 |
LIG_SH3_3 | 424 | 430 | PF00018 | 0.575 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.385 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.280 |
LIG_SH3_3 | 882 | 888 | PF00018 | 0.237 |
LIG_SH3_3 | 964 | 970 | PF00018 | 0.237 |
LIG_SH3_3 | 977 | 983 | PF00018 | 0.237 |
LIG_SH3_3 | 998 | 1004 | PF00018 | 0.265 |
LIG_SUMO_SIM_anti_2 | 152 | 159 | PF11976 | 0.258 |
LIG_SUMO_SIM_par_1 | 154 | 159 | PF11976 | 0.279 |
LIG_SUMO_SIM_par_1 | 922 | 927 | PF11976 | 0.237 |
LIG_TRAF2_1 | 1175 | 1178 | PF00917 | 0.525 |
LIG_TRAF2_1 | 554 | 557 | PF00917 | 0.648 |
LIG_TRAF2_1 | 697 | 700 | PF00917 | 0.599 |
LIG_TRAF2_1 | 768 | 771 | PF00917 | 0.690 |
LIG_TYR_ITIM | 951 | 956 | PF00017 | 0.331 |
LIG_UBA3_1 | 102 | 108 | PF00899 | 0.301 |
LIG_UBA3_1 | 527 | 532 | PF00899 | 0.448 |
LIG_ULM_U2AF65_1 | 909 | 914 | PF00076 | 0.237 |
LIG_WRC_WIRS_1 | 1199 | 1204 | PF05994 | 0.489 |
LIG_WRC_WIRS_1 | 166 | 171 | PF05994 | 0.274 |
LIG_WRC_WIRS_1 | 705 | 710 | PF05994 | 0.513 |
LIG_WRC_WIRS_1 | 985 | 990 | PF05994 | 0.380 |
LIG_WW_1 | 1088 | 1091 | PF00397 | 0.341 |
LIG_WW_3 | 1087 | 1091 | PF00397 | 0.474 |
MOD_CDK_SPK_2 | 652 | 657 | PF00069 | 0.632 |
MOD_CDK_SPxK_1 | 1011 | 1017 | PF00069 | 0.252 |
MOD_CDK_SPxxK_3 | 1000 | 1007 | PF00069 | 0.423 |
MOD_CDK_SPxxK_3 | 221 | 228 | PF00069 | 0.464 |
MOD_CK1_1 | 1126 | 1132 | PF00069 | 0.484 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.667 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.528 |
MOD_CK1_1 | 595 | 601 | PF00069 | 0.656 |
MOD_CK1_1 | 630 | 636 | PF00069 | 0.549 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.607 |
MOD_CK2_1 | 1028 | 1034 | PF00069 | 0.237 |
MOD_CK2_1 | 1105 | 1111 | PF00069 | 0.420 |
MOD_CK2_1 | 1221 | 1227 | PF00069 | 0.443 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.287 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.540 |
MOD_CK2_1 | 561 | 567 | PF00069 | 0.533 |
MOD_CK2_1 | 595 | 601 | PF00069 | 0.664 |
MOD_CK2_1 | 786 | 792 | PF00069 | 0.485 |
MOD_GlcNHglycan | 1046 | 1049 | PF01048 | 0.252 |
MOD_GlcNHglycan | 1080 | 1083 | PF01048 | 0.265 |
MOD_GlcNHglycan | 1222 | 1226 | PF01048 | 0.466 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.691 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.639 |
MOD_GlcNHglycan | 377 | 381 | PF01048 | 0.453 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.424 |
MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.695 |
MOD_GlcNHglycan | 684 | 688 | PF01048 | 0.653 |
MOD_GlcNHglycan | 715 | 718 | PF01048 | 0.684 |
MOD_GlcNHglycan | 863 | 866 | PF01048 | 0.237 |
MOD_GSK3_1 | 1078 | 1085 | PF00069 | 0.265 |
MOD_GSK3_1 | 1251 | 1258 | PF00069 | 0.461 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.324 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.325 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.391 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.640 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.613 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.691 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.304 |
MOD_N-GLC_1 | 449 | 454 | PF02516 | 0.750 |
MOD_N-GLC_1 | 6 | 11 | PF02516 | 0.528 |
MOD_N-GLC_1 | 627 | 632 | PF02516 | 0.567 |
MOD_N-GLC_1 | 821 | 826 | PF02516 | 0.272 |
MOD_NEK2_1 | 1009 | 1014 | PF00069 | 0.245 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.293 |
MOD_NEK2_1 | 1198 | 1203 | PF00069 | 0.411 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.529 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.483 |
MOD_NEK2_1 | 704 | 709 | PF00069 | 0.494 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.453 |
MOD_NEK2_1 | 924 | 929 | PF00069 | 0.237 |
MOD_NEK2_2 | 1105 | 1110 | PF00069 | 0.399 |
MOD_NEK2_2 | 642 | 647 | PF00069 | 0.413 |
MOD_PIKK_1 | 1207 | 1213 | PF00454 | 0.533 |
MOD_PIKK_1 | 1251 | 1257 | PF00454 | 0.457 |
MOD_PIKK_1 | 932 | 938 | PF00454 | 0.237 |
MOD_PKA_1 | 1243 | 1249 | PF00069 | 0.410 |
MOD_PKA_1 | 130 | 136 | PF00069 | 0.287 |
MOD_PKA_1 | 27 | 33 | PF00069 | 0.508 |
MOD_PKA_1 | 64 | 70 | PF00069 | 0.386 |
MOD_PKA_2 | 1064 | 1070 | PF00069 | 0.237 |
MOD_PKA_2 | 1171 | 1177 | PF00069 | 0.491 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.301 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.321 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.237 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.600 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.498 |
MOD_PKA_2 | 584 | 590 | PF00069 | 0.735 |
MOD_PKA_2 | 630 | 636 | PF00069 | 0.587 |
MOD_PKA_2 | 983 | 989 | PF00069 | 0.290 |
MOD_PKB_1 | 1219 | 1227 | PF00069 | 0.492 |
MOD_PKB_1 | 128 | 136 | PF00069 | 0.320 |
MOD_PKB_1 | 337 | 345 | PF00069 | 0.559 |
MOD_PKB_1 | 625 | 633 | PF00069 | 0.567 |
MOD_Plk_1 | 416 | 422 | PF00069 | 0.570 |
MOD_Plk_1 | 449 | 455 | PF00069 | 0.492 |
MOD_Plk_1 | 523 | 529 | PF00069 | 0.499 |
MOD_Plk_1 | 74 | 80 | PF00069 | 0.369 |
MOD_Plk_1 | 743 | 749 | PF00069 | 0.719 |
MOD_Plk_1 | 821 | 827 | PF00069 | 0.271 |
MOD_Plk_2-3 | 165 | 171 | PF00069 | 0.276 |
MOD_Plk_2-3 | 266 | 272 | PF00069 | 0.380 |
MOD_Plk_2-3 | 416 | 422 | PF00069 | 0.614 |
MOD_Plk_4 | 1052 | 1058 | PF00069 | 0.297 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.370 |
MOD_Plk_4 | 449 | 455 | PF00069 | 0.492 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.548 |
MOD_Plk_4 | 689 | 695 | PF00069 | 0.631 |
MOD_Plk_4 | 704 | 710 | PF00069 | 0.467 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.306 |
MOD_ProDKin_1 | 1000 | 1006 | PF00069 | 0.335 |
MOD_ProDKin_1 | 1011 | 1017 | PF00069 | 0.209 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.405 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.395 |
MOD_ProDKin_1 | 652 | 658 | PF00069 | 0.737 |
MOD_ProDKin_1 | 951 | 957 | PF00069 | 0.237 |
MOD_SUMO_for_1 | 1016 | 1019 | PF00179 | 0.380 |
MOD_SUMO_rev_2 | 61 | 67 | PF00179 | 0.477 |
MOD_SUMO_rev_2 | 848 | 857 | PF00179 | 0.301 |
TRG_DiLeu_BaEn_1 | 381 | 386 | PF01217 | 0.512 |
TRG_DiLeu_BaEn_1 | 700 | 705 | PF01217 | 0.498 |
TRG_DiLeu_BaEn_1 | 793 | 798 | PF01217 | 0.272 |
TRG_DiLeu_BaEn_1 | 84 | 89 | PF01217 | 0.314 |
TRG_DiLeu_BaEn_2 | 1033 | 1039 | PF01217 | 0.272 |
TRG_DiLeu_BaEn_2 | 166 | 172 | PF01217 | 0.271 |
TRG_DiLeu_BaEn_4 | 1139 | 1145 | PF01217 | 0.556 |
TRG_DiLeu_BaLyEn_6 | 238 | 243 | PF01217 | 0.237 |
TRG_DiLeu_BaLyEn_6 | 502 | 507 | PF01217 | 0.687 |
TRG_DiLeu_BaLyEn_6 | 83 | 88 | PF01217 | 0.330 |
TRG_DiLeu_BaLyEn_6 | 885 | 890 | PF01217 | 0.272 |
TRG_DiLeu_BaLyEn_6 | 920 | 925 | PF01217 | 0.252 |
TRG_DiLeu_LyEn_5 | 793 | 798 | PF01217 | 0.297 |
TRG_ENDOCYTIC_2 | 1091 | 1094 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 1128 | 1131 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 671 | 674 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 828 | 831 | PF00928 | 0.237 |
TRG_ENDOCYTIC_2 | 867 | 870 | PF00928 | 0.237 |
TRG_ENDOCYTIC_2 | 953 | 956 | PF00928 | 0.256 |
TRG_ENDOCYTIC_2 | 965 | 968 | PF00928 | 0.206 |
TRG_ER_diArg_1 | 1133 | 1136 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 128 | 131 | PF00400 | 0.335 |
TRG_ER_diArg_1 | 206 | 209 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 25 | 28 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 406 | 409 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 637 | 639 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 759 | 762 | PF00400 | 0.723 |
TRG_ER_diArg_1 | 763 | 765 | PF00400 | 0.725 |
TRG_ER_diArg_1 | 910 | 913 | PF00400 | 0.237 |
TRG_ER_diArg_1 | 930 | 932 | PF00400 | 0.108 |
TRG_ER_diArg_1 | 947 | 950 | PF00400 | 0.237 |
TRG_NES_CRM1_1 | 165 | 176 | PF08389 | 0.274 |
TRG_NES_CRM1_1 | 418 | 432 | PF08389 | 0.694 |
TRG_NLS_MonoCore_2 | 199 | 204 | PF00514 | 0.369 |
TRG_NLS_MonoCore_2 | 25 | 30 | PF00514 | 0.463 |
TRG_NLS_MonoExtC_3 | 1131 | 1136 | PF00514 | 0.472 |
TRG_NLS_MonoExtC_3 | 1216 | 1221 | PF00514 | 0.442 |
TRG_NLS_MonoExtC_3 | 1239 | 1244 | PF00514 | 0.392 |
TRG_NLS_MonoExtC_3 | 199 | 204 | PF00514 | 0.354 |
TRG_NLS_MonoExtC_3 | 803 | 809 | PF00514 | 0.255 |
TRG_NLS_MonoExtN_4 | 1004 | 1011 | PF00514 | 0.265 |
TRG_NLS_MonoExtN_4 | 197 | 204 | PF00514 | 0.357 |
TRG_NLS_MonoExtN_4 | 26 | 31 | PF00514 | 0.471 |
TRG_NLS_MonoExtN_4 | 801 | 808 | PF00514 | 0.252 |
TRG_NLS_MonoExtN_4 | 907 | 913 | PF00514 | 0.237 |
TRG_Pf-PMV_PEXEL_1 | 1096 | 1100 | PF00026 | 0.364 |
TRG_Pf-PMV_PEXEL_1 | 1110 | 1115 | PF00026 | 0.334 |
TRG_Pf-PMV_PEXEL_1 | 1153 | 1158 | PF00026 | 0.531 |
TRG_Pf-PMV_PEXEL_1 | 505 | 509 | PF00026 | 0.671 |
TRG_Pf-PMV_PEXEL_1 | 529 | 533 | PF00026 | 0.579 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PET3 | Leptomonas seymouri | 75% | 99% |
A0A0S4KP78 | Bodo saltans | 52% | 100% |
A0A1X0NSK0 | Trypanosomatidae | 57% | 100% |
A0A3Q8IE00 | Leishmania donovani | 100% | 100% |
A0A3R7LAY5 | Trypanosoma rangeli | 59% | 100% |
A4HGP1 | Leishmania braziliensis | 85% | 99% |
D0A894 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
E9B007 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q878 | Leishmania major | 96% | 100% |
V5DBA6 | Trypanosoma cruzi | 59% | 100% |