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 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A4HQI9
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006370 | 7-methylguanosine mRNA capping | 8 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006397 | mRNA processing | 7 | 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:0009451 | RNA modification | 5 | 12 |
GO:0009452 | 7-methylguanosine RNA capping | 8 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0016071 | mRNA metabolic process | 6 | 12 |
GO:0016556 | mRNA modification | 6 | 12 |
GO:0032259 | methylation | 2 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0036260 | RNA capping | 7 | 12 |
GO:0036451 | cap mRNA methylation | 6 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0043414 | macromolecule methylation | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0080009 | mRNA methylation | 5 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:0097309 | cap1 mRNA methylation | 7 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004483 | mRNA (nucleoside-2'-O-)-methyltransferase activity | 6 | 12 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0008171 | O-methyltransferase activity | 5 | 12 |
GO:0008173 | RNA methyltransferase activity | 4 | 12 |
GO:0008174 | mRNA methyltransferase activity | 5 | 12 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0003676 | nucleic acid binding | 3 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 394 | 398 | PF00656 | 0.735 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.347 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.350 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.512 |
CLV_PCSK_PC1ET2_1 | 117 | 119 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.363 |
DEG_APCC_DBOX_1 | 48 | 56 | PF00400 | 0.518 |
DEG_APCC_DBOX_1 | 70 | 78 | PF00400 | 0.447 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.583 |
DOC_MAPK_DCC_7 | 71 | 79 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 71 | 79 | PF00069 | 0.526 |
DOC_MAPK_MEF2A_6 | 201 | 209 | PF00069 | 0.503 |
DOC_MAPK_MEF2A_6 | 290 | 297 | PF00069 | 0.487 |
DOC_PP1_RVXF_1 | 5 | 12 | PF00149 | 0.434 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.637 |
DOC_USP7_UBL2_3 | 140 | 144 | PF12436 | 0.400 |
DOC_USP7_UBL2_3 | 241 | 245 | PF12436 | 0.547 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.735 |
LIG_14-3-3_CanoR_1 | 284 | 293 | PF00244 | 0.476 |
LIG_BRCT_BRCA1_1 | 171 | 175 | PF00533 | 0.518 |
LIG_BRCT_BRCA1_1 | 214 | 218 | PF00533 | 0.400 |
LIG_BRCT_BRCA1_1 | 7 | 11 | PF00533 | 0.533 |
LIG_Clathr_ClatBox_1 | 292 | 296 | PF01394 | 0.562 |
LIG_deltaCOP1_diTrp_1 | 303 | 312 | PF00928 | 0.452 |
LIG_deltaCOP1_diTrp_1 | 330 | 338 | PF00928 | 0.508 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.482 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.550 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.462 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.476 |
LIG_LIR_Gen_1 | 101 | 111 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 121 | 131 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 164 | 173 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 121 | 127 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 164 | 169 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 255 | 260 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 296 | 300 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 310 | 315 | PF02991 | 0.385 |
LIG_MYND_1 | 324 | 328 | PF01753 | 0.516 |
LIG_NRBOX | 106 | 112 | PF00104 | 0.581 |
LIG_Pex14_1 | 37 | 41 | PF04695 | 0.392 |
LIG_Pex14_2 | 214 | 218 | PF04695 | 0.487 |
LIG_Rb_pABgroove_1 | 248 | 256 | PF01858 | 0.476 |
LIG_SH2_CRK | 166 | 170 | PF00017 | 0.430 |
LIG_SH2_CRK | 272 | 276 | PF00017 | 0.476 |
LIG_SH2_STAT3 | 31 | 34 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.454 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.460 |
LIG_SUMO_SIM_par_1 | 194 | 200 | PF11976 | 0.522 |
LIG_SUMO_SIM_par_1 | 75 | 80 | PF11976 | 0.466 |
LIG_TRAF2_1 | 366 | 369 | PF00917 | 0.475 |
LIG_WRC_WIRS_1 | 254 | 259 | PF05994 | 0.487 |
MOD_CDK_SPxxK_3 | 255 | 262 | PF00069 | 0.476 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.517 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.737 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.650 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.562 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.312 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.456 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.657 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.370 |
MOD_Cter_Amidation | 141 | 144 | PF01082 | 0.381 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.340 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.355 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.465 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.509 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.483 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.503 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.427 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.550 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.508 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.497 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.533 |
MOD_N-GLC_1 | 345 | 350 | PF02516 | 0.317 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.501 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.537 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.471 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.482 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.429 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.283 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.501 |
MOD_PIKK_1 | 132 | 138 | PF00454 | 0.476 |
MOD_PIKK_1 | 54 | 60 | PF00454 | 0.565 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.487 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.462 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.515 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.572 |
MOD_Plk_1 | 345 | 351 | PF00069 | 0.344 |
MOD_Plk_1 | 5 | 11 | PF00069 | 0.416 |
MOD_Plk_2-3 | 44 | 50 | PF00069 | 0.373 |
MOD_Plk_2-3 | 5 | 11 | PF00069 | 0.533 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.481 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.562 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.476 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.736 |
MOD_SUMO_rev_2 | 365 | 373 | PF00179 | 0.565 |
TRG_DiLeu_BaEn_1 | 106 | 111 | PF01217 | 0.581 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.466 |
TRG_ER_diArg_1 | 116 | 119 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 13 | 15 | PF00400 | 0.498 |
TRG_NLS_MonoExtC_3 | 115 | 120 | PF00514 | 0.511 |
TRG_NLS_MonoExtN_4 | 114 | 120 | PF00514 | 0.551 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P800 | Leptomonas seymouri | 73% | 99% |
A0A0S4IIT9 | Bodo saltans | 45% | 97% |
A0A1X0NL91 | Trypanosomatidae | 56% | 100% |
A0A3S5IS12 | Trypanosoma rangeli | 54% | 100% |
A0A3S7XCC2 | Leishmania donovani | 85% | 100% |
A4HQI9 | Leishmania braziliensis | 100% | 100% |
D0A3N7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9AHZ8 | Leishmania infantum | 85% | 100% |
E9AUA2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q38AH0 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 49% | 100% |
Q4E123 | Trypanosoma cruzi (strain CL Brener) | 55% | 100% |
Q4Q089 | Leishmania major | 83% | 100% |
V5BD10 | Trypanosoma cruzi | 54% | 100% |