Uncharacterized Protein, Uncharacterized
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 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4ID25
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 | 1 |
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 | 1 |
GO:0031123 | RNA 3'-end processing | 7 | 1 |
GO:0031124 | mRNA 3'-end processing | 8 | 1 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.414 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.487 |
CLV_PCSK_PC1ET2_1 | 102 | 104 | PF00082 | 0.521 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.489 |
CLV_Separin_Metazoa | 263 | 267 | PF03568 | 0.271 |
CLV_Separin_Metazoa | 317 | 321 | PF03568 | 0.412 |
DEG_ODPH_VHL_1 | 353 | 365 | PF01847 | 0.395 |
DEG_ODPH_VHL_1 | 390 | 402 | PF01847 | 0.345 |
DOC_CYCLIN_RxL_1 | 335 | 348 | PF00134 | 0.474 |
DOC_MAPK_gen_1 | 102 | 109 | PF00069 | 0.346 |
DOC_MAPK_gen_1 | 134 | 142 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 4 | 13 | PF00069 | 0.567 |
DOC_PP1_RVXF_1 | 339 | 346 | PF00149 | 0.430 |
DOC_PP2B_LxvP_1 | 149 | 152 | PF13499 | 0.360 |
DOC_PP4_FxxP_1 | 302 | 305 | PF00568 | 0.480 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.381 |
DOC_USP7_MATH_2 | 309 | 315 | PF00917 | 0.420 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.398 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.328 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.353 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.388 |
LIG_14-3-3_CanoR_1 | 113 | 119 | PF00244 | 0.278 |
LIG_14-3-3_CanoR_1 | 282 | 287 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 312 | 319 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 437 | 446 | PF00244 | 0.352 |
LIG_14-3-3_CanoR_1 | 47 | 52 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 57 | 63 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 9 | 14 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 96 | 106 | PF00244 | 0.400 |
LIG_APCC_ABBA_1 | 51 | 56 | PF00400 | 0.478 |
LIG_BRCT_BRCA1_1 | 341 | 345 | PF00533 | 0.489 |
LIG_Clathr_ClatBox_1 | 62 | 66 | PF01394 | 0.462 |
LIG_deltaCOP1_diTrp_1 | 280 | 286 | PF00928 | 0.301 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.391 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.397 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.421 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.343 |
LIG_FHA_2 | 443 | 449 | PF00498 | 0.536 |
LIG_LIR_Apic_2 | 299 | 305 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 17 | 27 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 280 | 291 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 369 | 379 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 447 | 452 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 163 | 169 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 17 | 22 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 280 | 286 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 326 | 331 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 369 | 375 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 447 | 452 | PF02991 | 0.430 |
LIG_MYND_1 | 173 | 177 | PF01753 | 0.281 |
LIG_NRBOX | 122 | 128 | PF00104 | 0.411 |
LIG_PCNA_yPIPBox_3 | 282 | 295 | PF02747 | 0.331 |
LIG_PDZ_Class_2 | 447 | 452 | PF00595 | 0.409 |
LIG_SH2_CRK | 19 | 23 | PF00017 | 0.376 |
LIG_SH2_CRK | 200 | 204 | PF00017 | 0.331 |
LIG_SH2_CRK | 258 | 262 | PF00017 | 0.469 |
LIG_SH2_NCK_1 | 19 | 23 | PF00017 | 0.376 |
LIG_SH2_PTP2 | 449 | 452 | PF00017 | 0.444 |
LIG_SH2_SRC | 230 | 233 | PF00017 | 0.287 |
LIG_SH2_STAP1 | 49 | 53 | PF00017 | 0.433 |
LIG_SH2_STAT3 | 199 | 202 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 322 | 325 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.391 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.331 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.459 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.354 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.387 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.491 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.435 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.495 |
LIG_SH3_3 | 386 | 392 | PF00018 | 0.352 |
LIG_SUMO_SIM_anti_2 | 104 | 110 | PF11976 | 0.309 |
LIG_SUMO_SIM_anti_2 | 268 | 275 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 176 | 182 | PF11976 | 0.276 |
LIG_SUMO_SIM_par_1 | 268 | 275 | PF11976 | 0.282 |
LIG_TRAF2_1 | 15 | 18 | PF00917 | 0.360 |
LIG_TRAF2_1 | 415 | 418 | PF00917 | 0.570 |
LIG_TRAF2_1 | 445 | 448 | PF00917 | 0.417 |
LIG_TYR_ITIM | 256 | 261 | PF00017 | 0.411 |
MOD_CDK_SPK_2 | 169 | 174 | PF00069 | 0.331 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.340 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.364 |
MOD_CK2_1 | 230 | 236 | PF00069 | 0.465 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.391 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.412 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.517 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.330 |
MOD_CK2_1 | 442 | 448 | PF00069 | 0.443 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.328 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.281 |
MOD_GlcNHglycan | 213 | 217 | PF01048 | 0.331 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.432 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.578 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.322 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.481 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.411 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.483 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.538 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.385 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.595 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.442 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.383 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.349 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.511 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.440 |
MOD_NEK2_2 | 432 | 437 | PF00069 | 0.495 |
MOD_PKA_1 | 4 | 10 | PF00069 | 0.484 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.411 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.292 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.298 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.521 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.506 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.491 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.436 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.328 |
MOD_Plk_1 | 368 | 374 | PF00069 | 0.520 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.360 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.378 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.355 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.227 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.326 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.307 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.482 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.367 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.404 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.398 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.328 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.353 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.382 |
TRG_DiLeu_BaEn_1 | 17 | 22 | PF01217 | 0.378 |
TRG_DiLeu_BaEn_1 | 408 | 413 | PF01217 | 0.344 |
TRG_DiLeu_BaLyEn_6 | 416 | 421 | PF01217 | 0.472 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 449 | 452 | PF00928 | 0.515 |
TRG_ER_diArg_1 | 421 | 423 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.533 |
TRG_NLS_MonoExtN_4 | 2 | 8 | PF00514 | 0.634 |
TRG_Pf-PMV_PEXEL_1 | 259 | 263 | PF00026 | 0.285 |
TRG_Pf-PMV_PEXEL_1 | 293 | 297 | PF00026 | 0.375 |
TRG_Pf-PMV_PEXEL_1 | 316 | 321 | PF00026 | 0.423 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJZ5 | Leptomonas seymouri | 77% | 100% |
A0A0S4JES6 | Bodo saltans | 30% | 100% |
A0A1X0P3J8 | Trypanosomatidae | 45% | 100% |
A0A3Q8IL58 | Leishmania donovani | 100% | 100% |
A0A422N1N1 | Trypanosoma rangeli | 45% | 100% |
A4HPN9 | Leishmania braziliensis | 94% | 100% |
D0A8H5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9ATF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
Q4Q144 | Leishmania major | 97% | 100% |
V5AU86 | Trypanosoma cruzi | 45% | 100% |