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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0005794 | Golgi apparatus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A0A3S7WSS8
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 1 |
GO:0006605 | protein targeting | 5 | 1 |
GO:0006612 | protein targeting to membrane | 5 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018198 | peptidyl-cysteine modification | 6 | 1 |
GO:0018230 | peptidyl-L-cysteine S-palmitoylation | 7 | 1 |
GO:0018231 | peptidyl-S-diacylglycerol-L-cysteine biosynthetic process from peptidyl-cysteine | 7 | 1 |
GO:0018345 | protein palmitoylation | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043543 | protein acylation | 5 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0051668 | localization within membrane | 3 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0072657 | protein localization to membrane | 4 | 1 |
GO:0090150 | establishment of protein localization to membrane | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0016409 | palmitoyltransferase activity | 5 | 7 |
GO:0016417 | S-acyltransferase activity | 5 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016746 | acyltransferase activity | 3 | 7 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 7 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 7 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.230 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.354 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.245 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.245 |
DEG_APCC_DBOX_1 | 176 | 184 | PF00400 | 0.445 |
DEG_MDM2_SWIB_1 | 62 | 69 | PF02201 | 0.275 |
DOC_MAPK_DCC_7 | 80 | 90 | PF00069 | 0.245 |
DOC_MAPK_gen_1 | 151 | 159 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 176 | 183 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 207 | 216 | PF00069 | 0.260 |
DOC_MAPK_NFAT4_5 | 207 | 215 | PF00069 | 0.260 |
DOC_PP1_RVXF_1 | 36 | 42 | PF00149 | 0.532 |
DOC_PP2B_PxIxI_1 | 85 | 91 | PF00149 | 0.344 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.344 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.338 |
LIG_14-3-3_CanoR_1 | 259 | 265 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 70 | 74 | PF00244 | 0.324 |
LIG_Actin_WH2_2 | 223 | 241 | PF00022 | 0.300 |
LIG_Actin_WH2_2 | 57 | 72 | PF00022 | 0.341 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.662 |
LIG_CSL_BTD_1 | 40 | 43 | PF09270 | 0.513 |
LIG_CtBP_PxDLS_1 | 118 | 122 | PF00389 | 0.561 |
LIG_EH1_1 | 46 | 54 | PF00400 | 0.279 |
LIG_eIF4E_1 | 178 | 184 | PF01652 | 0.279 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.532 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.353 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.303 |
LIG_GBD_Chelix_1 | 230 | 238 | PF00786 | 0.300 |
LIG_LIR_Apic_2 | 68 | 74 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 2 | 11 | PF02991 | 0.632 |
LIG_LIR_Gen_1 | 263 | 273 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 46 | 56 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 59 | 69 | PF02991 | 0.213 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 263 | 268 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 46 | 51 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.213 |
LIG_NRBOX | 60 | 66 | PF00104 | 0.333 |
LIG_Pex14_2 | 62 | 66 | PF04695 | 0.279 |
LIG_SH2_CRK | 71 | 75 | PF00017 | 0.341 |
LIG_SH2_GRB2like | 250 | 253 | PF00017 | 0.460 |
LIG_SH2_NCK_1 | 71 | 75 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.335 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.289 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.539 |
LIG_SUMO_SIM_par_1 | 222 | 227 | PF11976 | 0.344 |
LIG_SUMO_SIM_par_1 | 48 | 54 | PF11976 | 0.265 |
LIG_SUMO_SIM_par_1 | 91 | 97 | PF11976 | 0.308 |
LIG_SUMO_SIM_par_1 | 98 | 105 | PF11976 | 0.256 |
LIG_TYR_ITIM | 197 | 202 | PF00017 | 0.322 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.545 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.331 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.640 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.358 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.260 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.472 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.406 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.408 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.300 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.559 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.678 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.414 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.344 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.510 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.279 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.327 |
MOD_N-GLC_2 | 154 | 156 | PF02516 | 0.271 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.279 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.498 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.330 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.344 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.309 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.313 |
MOD_NEK2_2 | 135 | 140 | PF00069 | 0.491 |
MOD_NEK2_2 | 260 | 265 | PF00069 | 0.525 |
MOD_PIKK_1 | 142 | 148 | PF00454 | 0.497 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.457 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.516 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.315 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.588 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.393 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.500 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.341 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.309 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.509 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.336 |
TRG_DiLeu_BaLyEn_6 | 162 | 167 | PF01217 | 0.491 |
TRG_DiLeu_BaLyEn_6 | 236 | 241 | PF01217 | 0.445 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.279 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.193 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.568 |
TRG_ER_diArg_1 | 176 | 178 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 256 | 259 | PF00400 | 0.504 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5B1 | Leptomonas seymouri | 60% | 100% |
A0A0S4IR23 | Bodo saltans | 31% | 80% |
A0A0S4JCH4 | Bodo saltans | 31% | 76% |
A0A3S7WZD9 | Leishmania donovani | 27% | 85% |
A4H7G8 | Leishmania braziliensis | 81% | 100% |
A4HVU9 | Leishmania infantum | 100% | 100% |
A4I1S8 | Leishmania infantum | 27% | 85% |
E9APK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
E9AXW2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
F1QAM1 | Danio rerio | 33% | 81% |
F1QHM7 | Danio rerio | 27% | 69% |
O80685 | Arabidopsis thaliana | 28% | 68% |
Q2TGK3 | Rattus norvegicus | 26% | 93% |
Q4Q9K8 | Leishmania major | 26% | 85% |
Q4QFX8 | Leishmania major | 96% | 100% |
Q5FVR1 | Rattus norvegicus | 30% | 81% |
Q5PNZ1 | Arabidopsis thaliana | 29% | 68% |
Q5R5J8 | Pongo abelii | 30% | 77% |
Q6CQB5 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 29% | 79% |
Q8R173 | Mus musculus | 26% | 93% |
Q91WU6 | Mus musculus | 26% | 91% |
Q923G5 | Rattus norvegicus | 26% | 91% |
Q9FLM3 | Arabidopsis thaliana | 25% | 68% |
Q9NYG2 | Homo sapiens | 28% | 93% |