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: 3 |
NetGPI | no | yes: 0, no: 3 |
Related structures:
AlphaFold database: A0A3S7X6K8
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 4 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 4 |
GO:0006807 | nitrogen compound metabolic process | 2 | 4 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0009056 | catabolic process | 2 | 4 |
GO:0009057 | macromolecule catabolic process | 4 | 4 |
GO:0009987 | cellular process | 1 | 4 |
GO:0019538 | protein metabolic process | 3 | 4 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 4 |
GO:0043170 | macromolecule metabolic process | 3 | 4 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 4 |
GO:0044237 | cellular metabolic process | 2 | 4 |
GO:0044238 | primary metabolic process | 2 | 4 |
GO:0044248 | cellular catabolic process | 3 | 4 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 4 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 4 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 4 |
GO:0071704 | organic substance metabolic process | 2 | 4 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 4 |
GO:1901575 | organic substance catabolic process | 3 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 119 | 123 | PF00656 | 0.664 |
CLV_C14_Caspase3-7 | 270 | 274 | PF00656 | 0.354 |
CLV_C14_Caspase3-7 | 47 | 51 | PF00656 | 0.416 |
CLV_C14_Caspase3-7 | 96 | 100 | PF00656 | 0.587 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.415 |
CLV_PCSK_PC1ET2_1 | 34 | 36 | PF00082 | 0.415 |
CLV_PCSK_PC7_1 | 30 | 36 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.393 |
DEG_APCC_DBOX_1 | 63 | 71 | PF00400 | 0.637 |
DEG_MDM2_SWIB_1 | 279 | 287 | PF02201 | 0.341 |
DOC_MAPK_JIP1_4 | 262 | 268 | PF00069 | 0.392 |
DOC_MAPK_RevD_3 | 20 | 35 | PF00069 | 0.412 |
DOC_PP2B_LxvP_1 | 3 | 6 | PF13499 | 0.561 |
DOC_PP4_FxxP_1 | 110 | 113 | PF00568 | 0.515 |
DOC_PP4_FxxP_1 | 95 | 98 | PF00568 | 0.565 |
DOC_PP4_MxPP_1 | 209 | 212 | PF00568 | 0.535 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.576 |
DOC_USP7_UBL2_3 | 129 | 133 | PF12436 | 0.564 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.632 |
LIG_14-3-3_CanoR_1 | 174 | 181 | PF00244 | 0.729 |
LIG_14-3-3_CanoR_1 | 232 | 237 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 239 | 244 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 262 | 267 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 35 | 45 | PF00244 | 0.371 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.592 |
LIG_BRCT_BRCA1_1 | 171 | 175 | PF00533 | 0.648 |
LIG_BRCT_BRCA1_1 | 234 | 238 | PF00533 | 0.335 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.621 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.335 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.418 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.570 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.610 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.568 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.486 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.580 |
LIG_IRF3_LxIS_1 | 151 | 156 | PF10401 | 0.571 |
LIG_LIR_Apic_2 | 92 | 98 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 282 | 291 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 141 | 145 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 216 | 222 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 247 | 253 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 282 | 286 | PF02991 | 0.356 |
LIG_MYND_1 | 208 | 212 | PF01753 | 0.603 |
LIG_MYND_1 | 6 | 10 | PF01753 | 0.589 |
LIG_NRBOX | 44 | 50 | PF00104 | 0.383 |
LIG_Pex14_2 | 279 | 283 | PF04695 | 0.370 |
LIG_SH2_SRC | 271 | 274 | PF00017 | 0.345 |
LIG_SH2_STAP1 | 181 | 185 | PF00017 | 0.569 |
LIG_SH2_STAP1 | 253 | 257 | PF00017 | 0.400 |
LIG_SH2_STAP1 | 300 | 304 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.379 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.657 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.553 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.595 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.563 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.416 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.509 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.645 |
LIG_SUMO_SIM_par_1 | 150 | 156 | PF11976 | 0.622 |
LIG_SUMO_SIM_par_1 | 20 | 27 | PF11976 | 0.350 |
LIG_TYR_ITIM | 298 | 303 | PF00017 | 0.328 |
LIG_UBA3_1 | 303 | 310 | PF00899 | 0.364 |
LIG_WRC_WIRS_1 | 240 | 245 | PF05994 | 0.424 |
LIG_WW_3 | 111 | 115 | PF00397 | 0.652 |
MOD_CDC14_SPxK_1 | 200 | 203 | PF00782 | 0.646 |
MOD_CDK_SPK_2 | 169 | 174 | PF00069 | 0.563 |
MOD_CDK_SPK_2 | 78 | 83 | PF00069 | 0.599 |
MOD_CDK_SPxK_1 | 197 | 203 | PF00069 | 0.652 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.578 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.630 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.454 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.518 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.608 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.724 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.517 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.576 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.667 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.467 |
MOD_GlcNHglycan | 154 | 158 | PF01048 | 0.642 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.681 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.307 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.720 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.659 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.636 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.410 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.535 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.616 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.563 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.675 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.619 |
MOD_N-GLC_1 | 6 | 11 | PF02516 | 0.523 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.661 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.449 |
MOD_PIKK_1 | 113 | 119 | PF00454 | 0.582 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.608 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.559 |
MOD_PKA_2 | 238 | 244 | PF00069 | 0.399 |
MOD_PKB_1 | 237 | 245 | PF00069 | 0.401 |
MOD_Plk_1 | 39 | 45 | PF00069 | 0.354 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.649 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.331 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.344 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.354 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.630 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.622 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.509 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.524 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.586 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.637 |
MOD_SUMO_for_1 | 341 | 344 | PF00179 | 0.393 |
TRG_DiLeu_BaEn_4 | 301 | 307 | PF01217 | 0.323 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.326 |
TRG_NES_CRM1_1 | 319 | 332 | PF08389 | 0.375 |
TRG_Pf-PMV_PEXEL_1 | 46 | 50 | PF00026 | 0.393 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF05 | Leptomonas seymouri | 54% | 100% |
A4I8W2 | Leishmania infantum | 100% | 100% |