Nuclear proteins, NPL4 family, putative
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: 1 |
NetGPI | no | yes: 0, no: 1 |
Related structures:
AlphaFold database: A4I1H3
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 2 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 2 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.326 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.326 |
CLV_PCSK_PC1ET2_1 | 188 | 190 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.299 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.374 |
DOC_MAPK_gen_1 | 185 | 194 | PF00069 | 0.310 |
DOC_MAPK_MEF2A_6 | 2 | 11 | PF00069 | 0.317 |
DOC_PP2B_PxIxI_1 | 67 | 73 | PF00149 | 0.375 |
DOC_PP4_FxxP_1 | 155 | 158 | PF00568 | 0.311 |
DOC_PP4_MxPP_1 | 172 | 175 | PF00568 | 0.314 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.275 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.491 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.310 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.265 |
LIG_14-3-3_CanoR_1 | 144 | 150 | PF00244 | 0.288 |
LIG_14-3-3_CanoR_1 | 189 | 195 | PF00244 | 0.287 |
LIG_14-3-3_CanoR_1 | 219 | 225 | PF00244 | 0.278 |
LIG_BRCT_BRCA1_1 | 190 | 194 | PF00533 | 0.300 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.317 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.292 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.375 |
LIG_FHA_2 | 120 | 126 | PF00498 | 0.356 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.287 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.241 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.273 |
LIG_LIR_Gen_1 | 147 | 155 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 200 | 208 | PF02991 | 0.236 |
LIG_LIR_Nem_3 | 143 | 149 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 200 | 204 | PF02991 | 0.235 |
LIG_MYND_1 | 64 | 68 | PF01753 | 0.438 |
LIG_NRBOX | 203 | 209 | PF00104 | 0.238 |
LIG_Pex14_1 | 145 | 149 | PF04695 | 0.285 |
LIG_SH2_CRK | 237 | 241 | PF00017 | 0.262 |
LIG_SH2_PTP2 | 149 | 152 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.244 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.345 |
LIG_SUMO_SIM_par_1 | 67 | 73 | PF11976 | 0.375 |
LIG_TYR_ITSM | 145 | 152 | PF00017 | 0.294 |
MOD_CDK_SPxxK_3 | 154 | 161 | PF00069 | 0.316 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.509 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.452 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.288 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.273 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.324 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.516 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.522 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.507 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.477 |
MOD_GlcNHglycan | 94 | 98 | PF01048 | 0.320 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.374 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.272 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.281 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.254 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.286 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.511 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.502 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.443 |
MOD_LATS_1 | 129 | 135 | PF00433 | 0.396 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.341 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.238 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.308 |
MOD_PIKK_1 | 206 | 212 | PF00454 | 0.247 |
MOD_PKA_1 | 188 | 194 | PF00069 | 0.303 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.344 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.303 |
MOD_Plk_1 | 19 | 25 | PF00069 | 0.270 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.292 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.392 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.313 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.259 |
TRG_ENDOCYTIC_2 | 149 | 152 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.272 |
TRG_NES_CRM1_1 | 196 | 210 | PF08389 | 0.244 |
TRG_NES_CRM1_1 | 5 | 20 | PF08389 | 0.274 |
TRG_NLS_MonoExtN_4 | 185 | 192 | PF00514 | 0.322 |