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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0030684 | preribosome | 3 | 1 |
GO:0030687 | preribosome, large subunit precursor | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A0A451EJH4
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 11 |
GO:0002128 | tRNA nucleoside ribose methylation | 6 | 10 |
GO:0002181 | cytoplasmic translation | 5 | 10 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006396 | RNA processing | 6 | 11 |
GO:0006399 | tRNA metabolic process | 7 | 10 |
GO:0006400 | tRNA modification | 6 | 10 |
GO:0006412 | translation | 4 | 10 |
GO:0006518 | peptide metabolic process | 4 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008033 | tRNA processing | 8 | 10 |
GO:0008152 | metabolic process | 1 | 14 |
GO:0009058 | biosynthetic process | 2 | 10 |
GO:0009059 | macromolecule biosynthetic process | 4 | 10 |
GO:0009451 | RNA modification | 5 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0019538 | protein metabolic process | 3 | 10 |
GO:0030488 | tRNA methylation | 5 | 10 |
GO:0032259 | methylation | 2 | 14 |
GO:0034470 | ncRNA processing | 7 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 10 |
GO:0034660 | ncRNA metabolic process | 6 | 11 |
GO:0043043 | peptide biosynthetic process | 5 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0043414 | macromolecule methylation | 3 | 11 |
GO:0043603 | amide metabolic process | 3 | 10 |
GO:0043604 | amide biosynthetic process | 4 | 10 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044249 | cellular biosynthetic process | 3 | 10 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 11 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 10 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 10 |
GO:1901576 | organic substance biosynthetic process | 3 | 10 |
GO:0000154 | rRNA modification | 6 | 1 |
GO:0000460 | maturation of 5.8S rRNA | 9 | 1 |
GO:0000463 | maturation of LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 1 |
GO:0000466 | maturation of 5.8S rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 1 |
GO:0000470 | maturation of LSU-rRNA | 9 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0031167 | rRNA methylation | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 14 |
GO:0008168 | methyltransferase activity | 4 | 14 |
GO:0008173 | RNA methyltransferase activity | 4 | 11 |
GO:0008175 | tRNA methyltransferase activity | 5 | 10 |
GO:0016740 | transferase activity | 2 | 14 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 14 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 11 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 10 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:0008171 | O-methyltransferase activity | 5 | 1 |
GO:0008649 | rRNA methyltransferase activity | 5 | 1 |
GO:0008650 | rRNA (uridine-2'-O-)-methyltransferase activity | 6 | 1 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 1 |
GO:0016435 | rRNA (guanine) methyltransferase activity | 6 | 1 |
GO:0016436 | rRNA (uridine) methyltransferase activity | 6 | 1 |
GO:0062105 | RNA 2'-O-methyltransferase activity | 5 | 1 |
GO:0140102 | catalytic activity, acting on a rRNA | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 309 | 313 | PF00656 | 0.527 |
CLV_C14_Caspase3-7 | 419 | 423 | PF00656 | 0.581 |
CLV_C14_Caspase3-7 | 426 | 430 | PF00656 | 0.592 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.290 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.436 |
CLV_PCSK_PC1ET2_1 | 8 | 10 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.323 |
DEG_APCC_DBOX_1 | 251 | 259 | PF00400 | 0.377 |
DEG_SPOP_SBC_1 | 281 | 285 | PF00917 | 0.745 |
DOC_CYCLIN_yCln2_LP_2 | 402 | 408 | PF00134 | 0.603 |
DOC_MAPK_gen_1 | 160 | 166 | PF00069 | 0.465 |
DOC_PP2B_LxvP_1 | 123 | 126 | PF13499 | 0.532 |
DOC_PP2B_LxvP_1 | 402 | 405 | PF13499 | 0.559 |
DOC_PP4_FxxP_1 | 146 | 149 | PF00568 | 0.410 |
DOC_PP4_FxxP_1 | 210 | 213 | PF00568 | 0.449 |
DOC_PP4_FxxP_1 | 251 | 254 | PF00568 | 0.361 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.509 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 410 | 415 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.500 |
LIG_14-3-3_CanoR_1 | 211 | 219 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 22 | 30 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 238 | 243 | PF00244 | 0.449 |
LIG_Actin_WH2_2 | 185 | 202 | PF00022 | 0.465 |
LIG_APCC_ABBA_1 | 30 | 35 | PF00400 | 0.441 |
LIG_BRCT_BRCA1_1 | 221 | 225 | PF00533 | 0.469 |
LIG_eIF4E_1 | 182 | 188 | PF01652 | 0.449 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.487 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.472 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.470 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.633 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.451 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.487 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.449 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.485 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.543 |
LIG_FHA_2 | 346 | 352 | PF00498 | 0.604 |
LIG_FHA_2 | 424 | 430 | PF00498 | 0.606 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.628 |
LIG_LIR_Apic_2 | 144 | 149 | PF02991 | 0.410 |
LIG_LIR_Apic_2 | 207 | 213 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 34 | 44 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 57 | 66 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 25 | 30 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 34 | 39 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 57 | 61 | PF02991 | 0.465 |
LIG_PCNA_PIPBox_1 | 176 | 185 | PF02747 | 0.465 |
LIG_PCNA_yPIPBox_3 | 233 | 246 | PF02747 | 0.449 |
LIG_SH2_CRK | 27 | 31 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 329 | 333 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.652 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.531 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.532 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.554 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.495 |
LIG_SH3_3 | 391 | 397 | PF00018 | 0.522 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.692 |
LIG_SUMO_SIM_anti_2 | 101 | 107 | PF11976 | 0.487 |
LIG_SUMO_SIM_par_1 | 88 | 93 | PF11976 | 0.480 |
LIG_TRAF2_1 | 16 | 19 | PF00917 | 0.363 |
LIG_WRC_WIRS_1 | 194 | 199 | PF05994 | 0.449 |
LIG_WRC_WIRS_1 | 242 | 247 | PF05994 | 0.532 |
MOD_CDC14_SPxK_1 | 158 | 161 | PF00782 | 0.506 |
MOD_CDK_SPK_2 | 155 | 160 | PF00069 | 0.506 |
MOD_CDK_SPK_2 | 83 | 88 | PF00069 | 0.487 |
MOD_CDK_SPxK_1 | 155 | 161 | PF00069 | 0.506 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.469 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.522 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.532 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.670 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.593 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.735 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.449 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.547 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.625 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.630 |
MOD_DYRK1A_RPxSP_1 | 437 | 441 | PF00069 | 0.608 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.231 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.280 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.685 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.691 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.689 |
MOD_GlcNHglycan | 376 | 380 | PF01048 | 0.490 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.452 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.495 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.480 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.586 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.794 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.638 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.561 |
MOD_N-GLC_1 | 142 | 147 | PF02516 | 0.315 |
MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.249 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.291 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.459 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.620 |
MOD_NEK2_2 | 345 | 350 | PF00069 | 0.679 |
MOD_PIKK_1 | 412 | 418 | PF00454 | 0.699 |
MOD_PIKK_1 | 428 | 434 | PF00454 | 0.543 |
MOD_PIKK_1 | 56 | 62 | PF00454 | 0.451 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.483 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.637 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.676 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.608 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.630 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.478 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.449 |
MOD_Plk_2-3 | 306 | 312 | PF00069 | 0.539 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.459 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.473 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.521 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.485 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.549 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.485 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.656 |
MOD_ProDKin_1 | 410 | 416 | PF00069 | 0.511 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.609 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.500 |
MOD_SUMO_for_1 | 16 | 19 | PF00179 | 0.363 |
MOD_SUMO_for_1 | 300 | 303 | PF00179 | 0.609 |
TRG_DiLeu_BaEn_1 | 118 | 123 | PF01217 | 0.485 |
TRG_DiLeu_BaEn_4 | 34 | 40 | PF01217 | 0.465 |
TRG_DiLeu_LyEn_5 | 118 | 123 | PF01217 | 0.465 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.467 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.446 |
TRG_NES_CRM1_1 | 95 | 109 | PF08389 | 0.449 |
TRG_NLS_MonoExtC_3 | 432 | 437 | PF00514 | 0.651 |
TRG_NLS_MonoExtN_4 | 433 | 438 | PF00514 | 0.699 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTF7 | Leptomonas seymouri | 61% | 100% |
A0A0S4JD71 | Bodo saltans | 45% | 100% |
A0A3S7X469 | Leishmania donovani | 24% | 100% |
A4H3D4 | Leishmania braziliensis | 76% | 99% |
A4HRN5 | Leishmania infantum | 100% | 100% |
A4I6F9 | Leishmania infantum | 24% | 100% |
C9ZJ17 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9ACB3 | Leishmania major | 95% | 100% |
E9AJK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 99% |
E9B1L6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
Q9BHC8 | Leishmania major | 24% | 100% |
V5BCX7 | Trypanosoma cruzi | 50% | 100% |