Phosphoglycan beta 1,3 galactosyltransferase (required for proper protective coat formation). Probably part of a much larger group. Expanded in Leishmaniids. Localization: Golgi (by homology)
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: 1, no: 18 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000139 | Golgi membrane | 5 | 17 |
GO:0016020 | membrane | 2 | 18 |
GO:0031090 | organelle membrane | 3 | 17 |
GO:0098588 | bounding membrane of organelle | 4 | 17 |
GO:0110165 | cellular anatomical entity | 1 | 18 |
Related structures:
AlphaFold database: E9AI30
Term | Name | Level | Count |
---|---|---|---|
GO:0006486 | protein glycosylation | 4 | 18 |
GO:0006807 | nitrogen compound metabolic process | 2 | 18 |
GO:0008152 | metabolic process | 1 | 18 |
GO:0019538 | protein metabolic process | 3 | 18 |
GO:0036211 | protein modification process | 4 | 18 |
GO:0043170 | macromolecule metabolic process | 3 | 18 |
GO:0043412 | macromolecule modification | 4 | 18 |
GO:0043413 | macromolecule glycosylation | 3 | 18 |
GO:0044238 | primary metabolic process | 2 | 18 |
GO:0070085 | glycosylation | 2 | 18 |
GO:0071704 | organic substance metabolic process | 2 | 18 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 19 |
GO:0016740 | transferase activity | 2 | 19 |
GO:0016757 | glycosyltransferase activity | 3 | 19 |
GO:0016758 | hexosyltransferase activity | 4 | 18 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.471 |
CLV_PCSK_FUR_1 | 333 | 337 | PF00082 | 0.256 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.261 |
CLV_PCSK_PC1ET2_1 | 267 | 269 | PF00082 | 0.373 |
CLV_PCSK_PC1ET2_1 | 335 | 337 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.273 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.345 |
DOC_CDC14_PxL_1 | 64 | 72 | PF14671 | 0.226 |
DOC_MAPK_MEF2A_6 | 16 | 23 | PF00069 | 0.331 |
DOC_MAPK_MEF2A_6 | 72 | 81 | PF00069 | 0.224 |
DOC_MAPK_NFAT4_5 | 16 | 24 | PF00069 | 0.286 |
DOC_PP1_RVXF_1 | 231 | 237 | PF00149 | 0.444 |
DOC_PP1_RVXF_1 | 50 | 57 | PF00149 | 0.349 |
DOC_PP2B_LxvP_1 | 79 | 82 | PF13499 | 0.216 |
DOC_PP4_FxxP_1 | 243 | 246 | PF00568 | 0.247 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.332 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.453 |
DOC_USP7_UBL2_3 | 257 | 261 | PF12436 | 0.370 |
LIG_14-3-3_CanoR_1 | 16 | 20 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 233 | 237 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 316 | 320 | PF00244 | 0.321 |
LIG_14-3-3_CanoR_1 | 89 | 96 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 98 | 103 | PF00244 | 0.319 |
LIG_Actin_WH2_2 | 245 | 263 | PF00022 | 0.406 |
LIG_Actin_WH2_2 | 74 | 91 | PF00022 | 0.405 |
LIG_EH_1 | 155 | 159 | PF12763 | 0.224 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.288 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.243 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.327 |
LIG_LIR_Apic_2 | 241 | 246 | PF02991 | 0.231 |
LIG_LIR_Apic_2 | 38 | 44 | PF02991 | 0.516 |
LIG_LIR_Apic_2 | 95 | 99 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 18 | 24 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 180 | 188 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 235 | 243 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 75 | 85 | PF02991 | 0.247 |
LIG_LIR_Nem_3 | 18 | 23 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 180 | 184 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 235 | 239 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 62 | 67 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.323 |
LIG_NRBOX | 164 | 170 | PF00104 | 0.229 |
LIG_Pex14_1 | 129 | 133 | PF04695 | 0.456 |
LIG_RPA_C_Fungi | 215 | 227 | PF08784 | 0.239 |
LIG_SH2_SRC | 188 | 191 | PF00017 | 0.309 |
LIG_SH2_STAP1 | 188 | 192 | PF00017 | 0.315 |
LIG_SH2_STAP1 | 330 | 334 | PF00017 | 0.295 |
LIG_SH2_STAP1 | 59 | 63 | PF00017 | 0.457 |
LIG_SH2_STAT3 | 90 | 93 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.201 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.267 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.261 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.208 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.243 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.362 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.506 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.243 |
LIG_SUMO_SIM_anti_2 | 180 | 186 | PF11976 | 0.369 |
LIG_SUMO_SIM_par_1 | 304 | 309 | PF11976 | 0.271 |
LIG_TYR_ITIM | 131 | 136 | PF00017 | 0.254 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.371 |
MOD_Cter_Amidation | 209 | 212 | PF01082 | 0.495 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.547 |
MOD_N-GLC_1 | 173 | 178 | PF02516 | 0.318 |
MOD_N-GLC_1 | 281 | 286 | PF02516 | 0.375 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.419 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.381 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.258 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.609 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.300 |
MOD_NEK2_2 | 173 | 178 | PF00069 | 0.431 |
MOD_PIKK_1 | 290 | 296 | PF00454 | 0.243 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.242 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.264 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.475 |
MOD_PKA_2 | 218 | 224 | PF00069 | 0.369 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.255 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.285 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.536 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.416 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.221 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.413 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.443 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.296 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.249 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.192 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.266 |
MOD_SUMO_rev_2 | 259 | 269 | PF00179 | 0.370 |
TRG_DiLeu_BaEn_1 | 180 | 185 | PF01217 | 0.212 |
TRG_DiLeu_BaEn_1 | 265 | 270 | PF01217 | 0.452 |
TRG_DiLeu_LyEn_5 | 265 | 270 | PF01217 | 0.242 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.490 |
TRG_ER_diArg_1 | 148 | 150 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 211 | 213 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 219 | 222 | PF00400 | 0.436 |
TRG_NLS_MonoExtN_4 | 333 | 339 | PF00514 | 0.265 |
TRG_Pf-PMV_PEXEL_1 | 148 | 152 | PF00026 | 0.343 |
TRG_Pf-PMV_PEXEL_1 | 167 | 171 | PF00026 | 0.200 |
TRG_Pf-PMV_PEXEL_1 | 267 | 271 | PF00026 | 0.259 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NJF0 | Trypanosomatidae | 27% | 100% |
A0A1X0NJG9 | Trypanosomatidae | 26% | 100% |
A0A1X0NJQ2 | Trypanosomatidae | 29% | 90% |
A0A1X0NJS8 | Trypanosomatidae | 29% | 91% |
A0A1X0NPR7 | Trypanosomatidae | 29% | 98% |
A0A1X0NPV0 | Trypanosomatidae | 30% | 91% |
A0A1X0NPW4 | Trypanosomatidae | 32% | 93% |
A0A1X0NQ61 | Trypanosomatidae | 31% | 91% |
A0A1X0NQ97 | Trypanosomatidae | 28% | 93% |
A0A1X0NQX6 | Trypanosomatidae | 28% | 100% |
A0A1X0NRK5 | Trypanosomatidae | 29% | 100% |
A0A1X0NVK8 | Trypanosomatidae | 25% | 78% |
A0A1X0P6H4 | Trypanosomatidae | 30% | 93% |
A0A3R7KQD7 | Trypanosoma rangeli | 28% | 87% |
A4H3B5 | Leishmania braziliensis | 37% | 66% |
A4H3H1 | Leishmania braziliensis | 26% | 100% |
C9ZPC0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 91% |
E8NHL6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |