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:0005634 | nucleus | 5 | 2 |
GO:0005654 | nucleoplasm | 2 | 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:0110165 | cellular anatomical entity | 1 | 3 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: E9B114
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0000394 | RNA splicing, via endonucleolytic cleavage and ligation | 8 | 1 |
GO:0006378 | mRNA polyadenylation | 7 | 1 |
GO:0006388 | tRNA splicing, via endonucleolytic cleavage and ligation | 9 | 1 |
GO:0006397 | mRNA processing | 7 | 2 |
GO:0006399 | tRNA metabolic process | 7 | 1 |
GO:0008033 | tRNA processing | 8 | 1 |
GO:0008380 | RNA splicing | 7 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 2 |
GO:0031123 | RNA 3'-end processing | 7 | 2 |
GO:0031124 | mRNA 3'-end processing | 8 | 2 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043631 | RNA polyadenylation | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0016301 | kinase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 12 |
GO:0019205 | nucleobase-containing compound kinase activity | 5 | 12 |
GO:0051731 | polynucleotide 5'-hydroxyl-kinase activity | 5 | 12 |
GO:0046404 | polydeoxyribonucleotide 5'-hydroxyl-kinase activity | 7 | 1 |
GO:0051733 | polydeoxyribonucleotide kinase activity | 6 | 1 |
GO:0051734 | polynucleotide kinase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 116 | 120 | PF00656 | 0.646 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.391 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.387 |
CLV_PCSK_PC1ET2_1 | 210 | 212 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.508 |
DEG_APCC_DBOX_1 | 323 | 331 | PF00400 | 0.548 |
DEG_COP1_1 | 348 | 358 | PF00400 | 0.452 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.746 |
DEG_ODPH_VHL_1 | 394 | 407 | PF01847 | 0.518 |
DEG_SCF_FBW7_1 | 76 | 83 | PF00400 | 0.249 |
DEG_SPOP_SBC_1 | 110 | 114 | PF00917 | 0.486 |
DOC_CDC14_PxL_1 | 290 | 298 | PF14671 | 0.453 |
DOC_CKS1_1 | 320 | 325 | PF01111 | 0.417 |
DOC_CKS1_1 | 77 | 82 | PF01111 | 0.501 |
DOC_CYCLIN_yCln2_LP_2 | 401 | 407 | PF00134 | 0.392 |
DOC_CYCLIN_yCln2_LP_2 | 418 | 424 | PF00134 | 0.564 |
DOC_MAPK_DCC_7 | 416 | 424 | PF00069 | 0.614 |
DOC_MAPK_gen_1 | 210 | 217 | PF00069 | 0.322 |
DOC_MAPK_gen_1 | 4 | 12 | PF00069 | 0.597 |
DOC_MAPK_MEF2A_6 | 141 | 148 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 210 | 217 | PF00069 | 0.365 |
DOC_MAPK_MEF2A_6 | 353 | 360 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 416 | 424 | PF00069 | 0.614 |
DOC_MAPK_NFAT4_5 | 141 | 149 | PF00069 | 0.427 |
DOC_MAPK_NFAT4_5 | 210 | 218 | PF00069 | 0.375 |
DOC_PP1_RVXF_1 | 284 | 291 | PF00149 | 0.371 |
DOC_PP2B_LxvP_1 | 412 | 415 | PF13499 | 0.429 |
DOC_PP2B_LxvP_1 | 418 | 421 | PF13499 | 0.478 |
DOC_PP4_FxxP_1 | 320 | 323 | PF00568 | 0.514 |
DOC_PP4_FxxP_1 | 393 | 396 | PF00568 | 0.368 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.349 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.384 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.483 |
LIG_14-3-3_CanoR_1 | 335 | 342 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 4 | 12 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 41 | 45 | PF00244 | 0.479 |
LIG_APCC_ABBA_1 | 340 | 345 | PF00400 | 0.498 |
LIG_BRCT_BRCA1_1 | 174 | 178 | PF00533 | 0.427 |
LIG_BRCT_BRCA1_1 | 224 | 228 | PF00533 | 0.427 |
LIG_deltaCOP1_diTrp_1 | 272 | 278 | PF00928 | 0.278 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.491 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.366 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.356 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.531 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.521 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.441 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.448 |
LIG_LIR_Apic_2 | 119 | 124 | PF02991 | 0.557 |
LIG_LIR_Apic_2 | 392 | 396 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 248 | 258 | PF02991 | 0.177 |
LIG_LIR_Gen_1 | 287 | 297 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.177 |
LIG_LIR_Nem_3 | 287 | 293 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 345 | 350 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 351 | 355 | PF02991 | 0.376 |
LIG_PCNA_TLS_4 | 312 | 319 | PF02747 | 0.375 |
LIG_PTB_Apo_2 | 227 | 234 | PF02174 | 0.427 |
LIG_RPA_C_Fungi | 91 | 103 | PF08784 | 0.462 |
LIG_SH2_CRK | 251 | 255 | PF00017 | 0.276 |
LIG_SH2_CRK | 280 | 284 | PF00017 | 0.337 |
LIG_SH2_CRK | 50 | 54 | PF00017 | 0.431 |
LIG_SH2_PTP2 | 158 | 161 | PF00017 | 0.453 |
LIG_SH2_SRC | 158 | 161 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.306 |
LIG_SH3_2 | 326 | 331 | PF14604 | 0.412 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.417 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.310 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.374 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.370 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.299 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.420 |
LIG_SH3_3 | 404 | 410 | PF00018 | 0.508 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.541 |
LIG_SUMO_SIM_anti_2 | 29 | 34 | PF11976 | 0.422 |
LIG_SUMO_SIM_anti_2 | 337 | 343 | PF11976 | 0.410 |
LIG_SUMO_SIM_par_1 | 125 | 131 | PF11976 | 0.395 |
LIG_SUMO_SIM_par_1 | 29 | 34 | PF11976 | 0.371 |
LIG_SUMO_SIM_par_1 | 98 | 105 | PF11976 | 0.547 |
LIG_TRAF2_1 | 113 | 116 | PF00917 | 0.661 |
LIG_TYR_ITIM | 156 | 161 | PF00017 | 0.375 |
LIG_TYR_ITIM | 249 | 254 | PF00017 | 0.276 |
LIG_UBA3_1 | 100 | 108 | PF00899 | 0.569 |
LIG_WRC_WIRS_1 | 390 | 395 | PF05994 | 0.368 |
MOD_CDK_SPK_2 | 319 | 324 | PF00069 | 0.511 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.394 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.394 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.528 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.589 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.441 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.462 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.453 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.205 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.510 |
MOD_Cter_Amidation | 106 | 109 | PF01082 | 0.316 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.427 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.375 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.440 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.466 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.473 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.269 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.443 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.308 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.529 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.415 |
MOD_N-GLC_1 | 21 | 26 | PF02516 | 0.269 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.596 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.454 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.391 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.304 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.382 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.371 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.462 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.419 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.433 |
MOD_PIKK_1 | 21 | 27 | PF00454 | 0.343 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.636 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.487 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.495 |
MOD_Plk_2-3 | 348 | 354 | PF00069 | 0.416 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.319 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.325 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.391 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.424 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.422 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.427 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.415 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.391 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.393 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.401 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.484 |
MOD_SUMO_rev_2 | 112 | 120 | PF00179 | 0.637 |
TRG_DiLeu_BaEn_1 | 87 | 92 | PF01217 | 0.489 |
TRG_DiLeu_BaEn_2 | 233 | 239 | PF01217 | 0.453 |
TRG_DiLeu_BaEn_2 | 273 | 279 | PF01217 | 0.457 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 212 | 215 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 280 | 283 | PF00928 | 0.337 |
TRG_ER_diArg_1 | 310 | 312 | PF00400 | 0.448 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HT73 | Leptomonas seymouri | 70% | 99% |
A0A0S4IVZ6 | Bodo saltans | 33% | 98% |
A0A1X0P2B1 | Trypanosomatidae | 39% | 100% |
A0A3R7KU37 | Trypanosoma rangeli | 36% | 100% |
A0A3S5H7N4 | Leishmania donovani | 92% | 100% |
A1DE49 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 23% | 76% |
A2RAW3 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 24% | 89% |
A2VE01 | Bos taurus | 25% | 100% |
A4HEC1 | Leishmania braziliensis | 25% | 100% |
A4HIH2 | Leishmania braziliensis | 86% | 100% |
A4I5R9 | Leishmania infantum | 92% | 100% |
A6S936 | Botryotinia fuckeliana (strain B05.10) | 25% | 92% |
A7RG82 | Nematostella vectensis | 27% | 99% |
A8PB32 | Brugia malayi | 28% | 98% |
A8X9U4 | Caenorhabditis briggsae | 27% | 99% |
B0VZR4 | Culex quinquefasciatus | 25% | 100% |
B3MGZ0 | Drosophila ananassae | 26% | 100% |
B3NRK6 | Drosophila erecta | 26% | 100% |
B4GGT6 | Drosophila persimilis | 25% | 100% |
B4HQJ2 | Drosophila sechellia | 25% | 100% |
B4JVN0 | Drosophila grimshawi | 24% | 100% |
B4KML2 | Drosophila mojavensis | 26% | 100% |
B4MCL6 | Drosophila virilis | 25% | 100% |
B4MRZ9 | Drosophila willistoni | 25% | 100% |
B4P4H2 | Drosophila yakuba | 26% | 100% |
B4QEE3 | Drosophila simulans | 25% | 100% |
C9ZKC3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 96% |
C9ZR38 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E7F3I6 | Danio rerio | 30% | 96% |
P52874 | Caenorhabditis elegans | 26% | 99% |
Q0CEZ9 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 24% | 76% |
Q0U2G5 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 23% | 91% |
Q16WA6 | Aedes aegypti | 24% | 100% |
Q1DKL9 | Coccidioides immitis (strain RS) | 22% | 76% |
Q28ZT4 | Drosophila pseudoobscura pseudoobscura | 25% | 100% |
Q2H1L0 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 24% | 86% |
Q4Q752 | Leishmania major | 93% | 100% |
Q4R7R3 | Macaca fascicularis | 26% | 100% |
Q54N48 | Dictyostelium discoideum | 23% | 93% |
Q5BH19 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 24% | 78% |
Q5PQL4 | Rattus norvegicus | 26% | 100% |
Q5ZJL4 | Gallus gallus | 26% | 100% |
Q66JK4 | Xenopus tropicalis | 30% | 97% |
Q6NS21 | Xenopus laevis | 27% | 97% |
Q7K284 | Drosophila melanogaster | 25% | 100% |
Q7QJW7 | Anopheles gambiae | 26% | 100% |
Q92989 | Homo sapiens | 26% | 100% |
Q99LI9 | Mus musculus | 26% | 100% |
Q9FLE2 | Arabidopsis thaliana | 24% | 100% |
Q9SR06 | Arabidopsis thaliana | 27% | 96% |
V5DD01 | Trypanosoma cruzi | 39% | 92% |