Glycosylation, alpha-1,2-mannosyltransferase
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005789 | endoplasmic reticulum membrane | 4 | 5 |
GO:0031090 | organelle membrane | 3 | 5 |
Related structures:
AlphaFold database: A4IC43
Term | Name | Level | Count |
---|---|---|---|
GO:0006486 | protein glycosylation | 4 | 5 |
GO:0006487 | protein N-linked glycosylation | 5 | 1 |
GO:0006490 | oligosaccharide-lipid intermediate biosynthetic process | 4 | 1 |
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019538 | protein metabolic process | 3 | 5 |
GO:0036211 | protein modification process | 4 | 5 |
GO:0043170 | macromolecule metabolic process | 3 | 5 |
GO:0043412 | macromolecule modification | 4 | 5 |
GO:0043413 | macromolecule glycosylation | 3 | 5 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0070085 | glycosylation | 2 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 1 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 5 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000026 | alpha-1,2-mannosyltransferase activity | 6 | 12 |
GO:0000030 | mannosyltransferase activity | 5 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004376 | glycolipid mannosyltransferase activity | 6 | 12 |
GO:0004377 | GDP-Man:Man3GlcNAc2-PP-Dol alpha-1,2-mannosyltransferase activity | 7 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016757 | glycosyltransferase activity | 3 | 12 |
GO:0016758 | hexosyltransferase activity | 4 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.339 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.384 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.299 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.286 |
CLV_PCSK_PC1ET2_1 | 20 | 22 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 324 | 326 | PF00082 | 0.279 |
CLV_PCSK_PC1ET2_1 | 437 | 439 | PF00082 | 0.306 |
CLV_PCSK_PC1ET2_1 | 62 | 64 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.307 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.442 |
DOC_CYCLIN_yCln2_LP_2 | 99 | 105 | PF00134 | 0.270 |
DOC_MAPK_FxFP_2 | 159 | 162 | PF00069 | 0.329 |
DOC_MAPK_gen_1 | 286 | 295 | PF00069 | 0.263 |
DOC_MAPK_gen_1 | 59 | 68 | PF00069 | 0.273 |
DOC_MAPK_gen_1 | 98 | 108 | PF00069 | 0.302 |
DOC_MAPK_MEF2A_6 | 390 | 398 | PF00069 | 0.339 |
DOC_PP1_RVXF_1 | 41 | 47 | PF00149 | 0.245 |
DOC_PP1_RVXF_1 | 429 | 436 | PF00149 | 0.321 |
DOC_PP1_RVXF_1 | 99 | 106 | PF00149 | 0.388 |
DOC_PP2B_LxvP_1 | 256 | 259 | PF13499 | 0.360 |
DOC_PP4_FxxP_1 | 159 | 162 | PF00568 | 0.368 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.273 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.420 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.299 |
DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.305 |
LIG_14-3-3_CanoR_1 | 123 | 127 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 25 | 29 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 278 | 283 | PF00244 | 0.398 |
LIG_Actin_WH2_2 | 93 | 111 | PF00022 | 0.378 |
LIG_BIR_III_2 | 119 | 123 | PF00653 | 0.321 |
LIG_eIF4E_1 | 121 | 127 | PF01652 | 0.245 |
LIG_eIF4E_1 | 161 | 167 | PF01652 | 0.260 |
LIG_eIF4E_1 | 216 | 222 | PF01652 | 0.339 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.426 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.259 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.214 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.267 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.317 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.446 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.431 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.339 |
LIG_FHA_2 | 364 | 370 | PF00498 | 0.196 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.281 |
LIG_LIR_Gen_1 | 217 | 226 | PF02991 | 0.236 |
LIG_LIR_Gen_1 | 3 | 12 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 403 | 414 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 453 | 463 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 119 | 124 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 174 | 178 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 3 | 7 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 369 | 375 | PF02991 | 0.241 |
LIG_LIR_Nem_3 | 403 | 409 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 430 | 435 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 453 | 458 | PF02991 | 0.446 |
LIG_LYPXL_S_1 | 160 | 164 | PF13949 | 0.218 |
LIG_LYPXL_yS_3 | 121 | 124 | PF13949 | 0.279 |
LIG_LYPXL_yS_3 | 161 | 164 | PF13949 | 0.245 |
LIG_LYPXL_yS_3 | 178 | 181 | PF13949 | 0.245 |
LIG_NRBOX | 123 | 129 | PF00104 | 0.329 |
LIG_PDZ_Class_2 | 461 | 466 | PF00595 | 0.417 |
LIG_Pex14_2 | 451 | 455 | PF04695 | 0.307 |
LIG_SH2_SRC | 462 | 465 | PF00017 | 0.374 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.279 |
LIG_SH2_STAP1 | 414 | 418 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 432 | 435 | PF00017 | 0.278 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.269 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.245 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.260 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.164 |
LIG_SUMO_SIM_anti_2 | 395 | 401 | PF11976 | 0.321 |
LIG_SUMO_SIM_anti_2 | 5 | 11 | PF11976 | 0.438 |
LIG_SUMO_SIM_par_1 | 124 | 130 | PF11976 | 0.294 |
LIG_SUMO_SIM_par_1 | 148 | 154 | PF11976 | 0.305 |
LIG_SUMO_SIM_par_1 | 373 | 378 | PF11976 | 0.260 |
LIG_SUMO_SIM_par_1 | 417 | 423 | PF11976 | 0.333 |
LIG_SUMO_SIM_par_1 | 5 | 11 | PF11976 | 0.388 |
LIG_SUMO_SIM_par_1 | 86 | 92 | PF11976 | 0.321 |
LIG_TRAF2_1 | 410 | 413 | PF00917 | 0.282 |
LIG_TYR_ITIM | 213 | 218 | PF00017 | 0.238 |
LIG_TYR_ITSM | 174 | 181 | PF00017 | 0.260 |
LIG_UBA3_1 | 87 | 93 | PF00899 | 0.371 |
LIG_Vh1_VBS_1 | 207 | 225 | PF01044 | 0.321 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.390 |
LIG_WRC_WIRS_1 | 128 | 133 | PF05994 | 0.381 |
LIG_WRC_WIRS_1 | 443 | 448 | PF05994 | 0.410 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.341 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.245 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.299 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.319 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.371 |
MOD_CK2_1 | 407 | 413 | PF00069 | 0.261 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.346 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.331 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.388 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.251 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.407 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.353 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.323 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.365 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.480 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.360 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.305 |
MOD_N-GLC_1 | 346 | 351 | PF02516 | 0.371 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.300 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.401 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.249 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.254 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.439 |
MOD_NEK2_2 | 363 | 368 | PF00069 | 0.321 |
MOD_PIKK_1 | 183 | 189 | PF00454 | 0.368 |
MOD_PIKK_1 | 237 | 243 | PF00454 | 0.317 |
MOD_PIKK_1 | 266 | 272 | PF00454 | 0.365 |
MOD_PK_1 | 278 | 284 | PF00069 | 0.321 |
MOD_PK_1 | 93 | 99 | PF00069 | 0.273 |
MOD_PKA_1 | 437 | 443 | PF00069 | 0.411 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.356 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.339 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.317 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.321 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.305 |
MOD_Plk_1 | 346 | 352 | PF00069 | 0.371 |
MOD_Plk_1 | 446 | 452 | PF00069 | 0.296 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.260 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.250 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.415 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.395 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.299 |
MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.305 |
MOD_SUMO_rev_2 | 321 | 326 | PF00179 | 0.283 |
TRG_DiLeu_BaEn_1 | 217 | 222 | PF01217 | 0.236 |
TRG_DiLeu_BaLyEn_6 | 159 | 164 | PF01217 | 0.245 |
TRG_DiLeu_BaLyEn_6 | 95 | 100 | PF01217 | 0.455 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.245 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.251 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.249 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.253 |
TRG_ENDOCYTIC_2 | 223 | 226 | PF00928 | 0.258 |
TRG_ENDOCYTIC_2 | 432 | 435 | PF00928 | 0.260 |
TRG_ENDOCYTIC_2 | 65 | 68 | PF00928 | 0.393 |
TRG_ER_diArg_1 | 188 | 191 | PF00400 | 0.314 |
TRG_ER_diArg_1 | 323 | 326 | PF00400 | 0.261 |
TRG_ER_diArg_1 | 424 | 427 | PF00400 | 0.416 |
TRG_ER_diArg_1 | 451 | 454 | PF00400 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 114 | 119 | PF00026 | 0.305 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6F7 | Leptomonas seymouri | 66% | 100% |
A0A0S4INF7 | Bodo saltans | 24% | 92% |
A0A0S4JLQ0 | Bodo saltans | 42% | 99% |
A0A1X0P5V7 | Trypanosomatidae | 50% | 98% |
A0A3R7K7Z3 | Trypanosoma rangeli | 49% | 98% |
A0A3S7XA76 | Leishmania donovani | 100% | 100% |
A4HNI6 | Leishmania braziliensis | 87% | 100% |
C9ZYD9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 99% |
E9AFZ8 | Leishmania major | 94% | 100% |
E9B751 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
O74878 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 99% |
P53954 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 85% |
P53993 | Caenorhabditis elegans | 33% | 99% |
Q08B22 | Xenopus laevis | 38% | 96% |
Q2TAA5 | Homo sapiens | 38% | 95% |
Q3TZM9 | Mus musculus | 38% | 95% |
Q54DM9 | Dictyostelium discoideum | 36% | 92% |
Q59S72 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 31% | 77% |
Q5R7Z6 | Pongo abelii | 38% | 95% |
Q6BVB2 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 32% | 76% |
Q6C9T3 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 36% | 73% |
Q6CLD6 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 29% | 82% |
Q6FWD1 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 34% | 92% |
Q6P312 | Xenopus tropicalis | 38% | 96% |
Q75B12 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 33% | 80% |
Q7ZW24 | Danio rerio | 37% | 93% |
Q8X092 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 32% | 84% |
Q9XEE9 | Arabidopsis thaliana | 38% | 100% |
V5BPD4 | Trypanosoma cruzi | 50% | 98% |