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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 10 |
GO:0005730 | nucleolus | 5 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043228 | non-membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: E9AF71
Term | Name | Level | Count |
---|---|---|---|
GO:0000027 | ribosomal large subunit assembly | 7 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006364 | rRNA processing | 8 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016072 | rRNA metabolic process | 7 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 2 |
GO:0034470 | ncRNA processing | 7 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034660 | ncRNA metabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0065003 | protein-containing complex assembly | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 8 |
GO:0042254 | ribosome biogenesis | 5 | 8 |
GO:0044085 | cellular component biogenesis | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0008097 | 5S rRNA binding | 6 | 2 |
GO:0019843 | rRNA binding | 5 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.299 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.329 |
CLV_PCSK_FUR_1 | 242 | 246 | PF00082 | 0.308 |
CLV_PCSK_FUR_1 | 325 | 329 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.299 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.298 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.329 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.317 |
CLV_PCSK_PC1ET2_1 | 203 | 205 | PF00082 | 0.421 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.298 |
CLV_PCSK_PC1ET2_1 | 237 | 239 | PF00082 | 0.291 |
CLV_PCSK_PC1ET2_1 | 244 | 246 | PF00082 | 0.316 |
CLV_PCSK_PC1ET2_1 | 314 | 316 | PF00082 | 0.532 |
CLV_PCSK_PC1ET2_1 | 327 | 329 | PF00082 | 0.541 |
CLV_PCSK_PC7_1 | 209 | 215 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.384 |
DOC_CKS1_1 | 262 | 267 | PF01111 | 0.400 |
DOC_MAPK_gen_1 | 244 | 255 | PF00069 | 0.326 |
DOC_MAPK_gen_1 | 314 | 326 | PF00069 | 0.519 |
DOC_MAPK_HePTP_8 | 216 | 228 | PF00069 | 0.288 |
DOC_MAPK_MEF2A_6 | 219 | 228 | PF00069 | 0.288 |
DOC_MAPK_MEF2A_6 | 58 | 65 | PF00069 | 0.360 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.369 |
DOC_USP7_UBL2_3 | 133 | 137 | PF12436 | 0.358 |
DOC_USP7_UBL2_3 | 185 | 189 | PF12436 | 0.296 |
DOC_USP7_UBL2_3 | 191 | 195 | PF12436 | 0.289 |
DOC_USP7_UBL2_3 | 90 | 94 | PF12436 | 0.298 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.284 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.284 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.388 |
LIG_14-3-3_CanoR_1 | 139 | 144 | PF00244 | 0.251 |
LIG_14-3-3_CanoR_1 | 204 | 212 | PF00244 | 0.293 |
LIG_14-3-3_CanoR_1 | 294 | 299 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 307 | 313 | PF00244 | 0.564 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.245 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.403 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.400 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.333 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.366 |
LIG_FHA_2 | 117 | 123 | PF00498 | 0.284 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.397 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.400 |
LIG_LIR_Apic_2 | 284 | 290 | PF02991 | 0.567 |
LIG_LIR_Gen_1 | 95 | 104 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 69 | 73 | PF02991 | 0.344 |
LIG_MYND_1 | 35 | 39 | PF01753 | 0.360 |
LIG_NRBOX | 223 | 229 | PF00104 | 0.400 |
LIG_PDZ_Class_1 | 334 | 339 | PF00595 | 0.524 |
LIG_SH2_CRK | 262 | 266 | PF00017 | 0.400 |
LIG_SH2_CRK | 50 | 54 | PF00017 | 0.344 |
LIG_SH2_PTP2 | 287 | 290 | PF00017 | 0.467 |
LIG_SH2_SRC | 287 | 290 | PF00017 | 0.467 |
LIG_SH2_SRC | 50 | 53 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.467 |
LIG_SH3_1 | 49 | 55 | PF00018 | 0.344 |
LIG_SH3_2 | 42 | 47 | PF14604 | 0.308 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.308 |
LIG_SH3_3 | 314 | 320 | PF00018 | 0.578 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.331 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.266 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.267 |
LIG_SUMO_SIM_anti_2 | 220 | 228 | PF11976 | 0.288 |
LIG_SUMO_SIM_par_1 | 264 | 269 | PF11976 | 0.284 |
LIG_TRAF2_1 | 119 | 122 | PF00917 | 0.284 |
LIG_TRAF2_1 | 198 | 201 | PF00917 | 0.366 |
LIG_TRAF2_1 | 297 | 300 | PF00917 | 0.392 |
LIG_UBA3_1 | 101 | 109 | PF00899 | 0.400 |
MOD_CDK_SPK_2 | 131 | 136 | PF00069 | 0.288 |
MOD_CDK_SPxK_1 | 131 | 137 | PF00069 | 0.288 |
MOD_CDK_SPxxK_3 | 131 | 138 | PF00069 | 0.254 |
MOD_CDK_SPxxK_3 | 268 | 275 | PF00069 | 0.400 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.422 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.410 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.284 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.397 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.403 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.298 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.470 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.489 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.546 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.305 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.364 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.271 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.372 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.386 |
MOD_N-GLC_1 | 112 | 117 | PF02516 | 0.278 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.308 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.536 |
MOD_PKA_1 | 108 | 114 | PF00069 | 0.288 |
MOD_PKA_1 | 137 | 143 | PF00069 | 0.288 |
MOD_PKA_1 | 191 | 197 | PF00069 | 0.316 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.559 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.284 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.454 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.477 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.284 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.284 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.388 |
MOD_SUMO_for_1 | 168 | 171 | PF00179 | 0.288 |
MOD_SUMO_for_1 | 320 | 323 | PF00179 | 0.510 |
MOD_SUMO_for_1 | 326 | 329 | PF00179 | 0.513 |
MOD_SUMO_for_1 | 93 | 96 | PF00179 | 0.400 |
MOD_SUMO_rev_2 | 200 | 205 | PF00179 | 0.336 |
MOD_SUMO_rev_2 | 89 | 99 | PF00179 | 0.272 |
TRG_DiLeu_BaEn_1 | 223 | 228 | PF01217 | 0.400 |
TRG_DiLeu_BaEn_1 | 299 | 304 | PF01217 | 0.428 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.155 |
TRG_ER_diArg_1 | 45 | 48 | PF00400 | 0.324 |
TRG_NLS_MonoCore_2 | 135 | 140 | PF00514 | 0.215 |
TRG_NLS_MonoExtC_3 | 136 | 141 | PF00514 | 0.235 |
TRG_NLS_MonoExtC_3 | 187 | 192 | PF00514 | 0.286 |
TRG_NLS_MonoExtC_3 | 89 | 94 | PF00514 | 0.360 |
TRG_NLS_MonoExtN_4 | 133 | 140 | PF00514 | 0.263 |
TRG_NLS_MonoExtN_4 | 185 | 192 | PF00514 | 0.285 |
TRG_NLS_MonoExtN_4 | 242 | 248 | PF00514 | 0.400 |
TRG_Pf-PMV_PEXEL_1 | 296 | 300 | PF00026 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 7 | 12 | PF00026 | 0.400 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8R6 | Leptomonas seymouri | 66% | 100% |
A0A0S4KHQ3 | Bodo saltans | 48% | 100% |
A0A1X0P5V5 | Trypanosomatidae | 54% | 97% |
A0A3Q8IF61 | Leishmania donovani | 91% | 100% |
A0A422NEC3 | Trypanosoma rangeli | 54% | 100% |
A4HMS1 | Leishmania braziliensis | 79% | 100% |
A4IBF7 | Leishmania infantum | 92% | 100% |
E9B6C7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |