Amino acid metabolism, Uncharacterized
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | yes | yes: 2 |
Forrest at al. (procyclic) | yes | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 9 |
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 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4IE04
Term | Name | Level | Count |
---|---|---|---|
GO:0000096 | sulfur amino acid metabolic process | 4 | 4 |
GO:0000097 | sulfur amino acid biosynthetic process | 5 | 4 |
GO:0006082 | organic acid metabolic process | 3 | 4 |
GO:0006520 | amino acid metabolic process | 3 | 4 |
GO:0006555 | methionine metabolic process | 5 | 4 |
GO:0006790 | sulfur compound metabolic process | 3 | 4 |
GO:0006807 | nitrogen compound metabolic process | 2 | 4 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0008652 | amino acid biosynthetic process | 4 | 4 |
GO:0009058 | biosynthetic process | 2 | 4 |
GO:0009066 | aspartate family amino acid metabolic process | 5 | 4 |
GO:0009067 | aspartate family amino acid biosynthetic process | 6 | 4 |
GO:0009086 | methionine biosynthetic process | 6 | 4 |
GO:0009987 | cellular process | 1 | 4 |
GO:0016053 | organic acid biosynthetic process | 4 | 4 |
GO:0019509 | L-methionine salvage from methylthioadenosine | 6 | 4 |
GO:0019752 | carboxylic acid metabolic process | 5 | 4 |
GO:0043094 | cellular metabolic compound salvage | 3 | 4 |
GO:0043102 | amino acid salvage | 4 | 4 |
GO:0043436 | oxoacid metabolic process | 4 | 4 |
GO:0044237 | cellular metabolic process | 2 | 4 |
GO:0044238 | primary metabolic process | 2 | 4 |
GO:0044249 | cellular biosynthetic process | 3 | 4 |
GO:0044272 | sulfur compound biosynthetic process | 4 | 4 |
GO:0044281 | small molecule metabolic process | 2 | 4 |
GO:0044283 | small molecule biosynthetic process | 3 | 4 |
GO:0046394 | carboxylic acid biosynthetic process | 5 | 4 |
GO:0071265 | L-methionine biosynthetic process | 7 | 4 |
GO:0071267 | L-methionine salvage | 5 | 4 |
GO:0071704 | organic substance metabolic process | 2 | 4 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 4 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 4 |
GO:1901576 | organic substance biosynthetic process | 3 | 4 |
GO:1901605 | alpha-amino acid metabolic process | 4 | 4 |
GO:1901607 | alpha-amino acid biosynthetic process | 5 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000287 | magnesium ion binding | 5 | 4 |
GO:0003824 | catalytic activity | 1 | 4 |
GO:0005488 | binding | 1 | 4 |
GO:0016787 | hydrolase activity | 2 | 4 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 4 |
GO:0016791 | phosphatase activity | 5 | 4 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 4 |
GO:0043167 | ion binding | 2 | 4 |
GO:0043169 | cation binding | 3 | 4 |
GO:0043874 | acireductone synthase activity | 6 | 4 |
GO:0046872 | metal ion binding | 4 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.479 |
CLV_PCSK_PC1ET2_1 | 180 | 182 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.425 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.554 |
DOC_CYCLIN_RxL_1 | 274 | 285 | PF00134 | 0.523 |
DOC_PP2B_LxvP_1 | 287 | 290 | PF13499 | 0.465 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.301 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.333 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.579 |
DOC_USP7_UBL2_3 | 270 | 274 | PF12436 | 0.429 |
DOC_USP7_UBL2_3 | 365 | 369 | PF12436 | 0.507 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.395 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.387 |
LIG_14-3-3_CanoR_1 | 3 | 13 | PF00244 | 0.422 |
LIG_BRCT_BRCA1_1 | 142 | 146 | PF00533 | 0.476 |
LIG_BRCT_BRCA1_1 | 206 | 210 | PF00533 | 0.506 |
LIG_BRCT_BRCA1_1 | 213 | 217 | PF00533 | 0.390 |
LIG_Clathr_ClatBox_1 | 81 | 85 | PF01394 | 0.493 |
LIG_deltaCOP1_diTrp_1 | 327 | 331 | PF00928 | 0.427 |
LIG_EH_1 | 254 | 258 | PF12763 | 0.409 |
LIG_EH1_1 | 67 | 75 | PF00400 | 0.365 |
LIG_eIF4E_1 | 261 | 267 | PF01652 | 0.514 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.468 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.441 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.537 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.437 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.334 |
LIG_LIR_Apic_2 | 259 | 264 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 117 | 128 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 169 | 179 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 25 | 35 | PF02991 | 0.545 |
LIG_LIR_Gen_1 | 275 | 284 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 327 | 335 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 344 | 349 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 117 | 123 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 207 | 213 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 214 | 219 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 249 | 254 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 25 | 31 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 259 | 265 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 275 | 279 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 327 | 331 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 344 | 348 | PF02991 | 0.396 |
LIG_MLH1_MIPbox_1 | 213 | 217 | PF16413 | 0.292 |
LIG_Pex14_1 | 196 | 200 | PF04695 | 0.418 |
LIG_Pex14_2 | 171 | 175 | PF04695 | 0.516 |
LIG_REV1ctd_RIR_1 | 214 | 222 | PF16727 | 0.414 |
LIG_SH2_CRK | 276 | 280 | PF00017 | 0.413 |
LIG_SH2_NCK_1 | 142 | 146 | PF00017 | 0.476 |
LIG_SH2_NCK_1 | 68 | 72 | PF00017 | 0.568 |
LIG_SH2_STAP1 | 142 | 146 | PF00017 | 0.476 |
LIG_SH2_STAP1 | 28 | 32 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.493 |
LIG_SH3_3 | 124 | 130 | PF00018 | 0.598 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.568 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.433 |
LIG_SUMO_SIM_par_1 | 263 | 269 | PF11976 | 0.521 |
LIG_WRC_WIRS_1 | 213 | 218 | PF05994 | 0.436 |
LIG_WRC_WIRS_1 | 342 | 347 | PF05994 | 0.394 |
MOD_CDK_SPxxK_3 | 130 | 137 | PF00069 | 0.653 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.374 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.443 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.453 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.545 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.484 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.494 |
MOD_GlcNHglycan | 305 | 309 | PF01048 | 0.431 |
MOD_GlcNHglycan | 310 | 314 | PF01048 | 0.457 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.401 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.544 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.494 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.429 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.541 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.376 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.457 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.432 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.509 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.415 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.498 |
MOD_NEK2_2 | 290 | 295 | PF00069 | 0.329 |
MOD_PIKK_1 | 204 | 210 | PF00454 | 0.392 |
MOD_PIKK_1 | 343 | 349 | PF00454 | 0.391 |
MOD_PKA_1 | 180 | 186 | PF00069 | 0.441 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.536 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.402 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.338 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.403 |
MOD_Plk_2-3 | 327 | 333 | PF00069 | 0.535 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.434 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.471 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.357 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.457 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.652 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.397 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.390 |
MOD_SUMO_rev_2 | 198 | 205 | PF00179 | 0.550 |
TRG_DiLeu_BaEn_3 | 29 | 35 | PF01217 | 0.341 |
TRG_DiLeu_BaLyEn_6 | 261 | 266 | PF01217 | 0.439 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.457 |
TRG_ER_diArg_1 | 228 | 231 | PF00400 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 280 | 285 | PF00026 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 323 | 327 | PF00026 | 0.408 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEN0 | Leptomonas seymouri | 47% | 96% |
A0A0S4JWP4 | Bodo saltans | 31% | 100% |
A0A1X0NM36 | Trypanosomatidae | 29% | 100% |
A0A3Q8IJW9 | Leishmania donovani | 99% | 100% |
A0A3R7M5E0 | Trypanosoma rangeli | 28% | 100% |
A4HQB3 | Leishmania braziliensis | 75% | 100% |
A6SRT0 | Botryotinia fuckeliana (strain B05.10) | 28% | 100% |
A7E3Z4 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 27% | 100% |
A9RBS1 | Physcomitrium patens | 31% | 74% |
A9V2Y9 | Monosiga brevicollis | 30% | 100% |
B3M173 | Drosophila ananassae | 33% | 100% |
B4G0F3 | Zea mays | 30% | 72% |
B4GFE6 | Drosophila persimilis | 32% | 100% |
B4I3X6 | Drosophila sechellia | 35% | 100% |
B4PV71 | Drosophila yakuba | 33% | 100% |
B4QW91 | Drosophila simulans | 33% | 100% |
B5X2D1 | Salmo salar | 32% | 100% |
B8BKI7 | Oryza sativa subsp. indica | 29% | 72% |
B9N1F9 | Populus trichocarpa | 30% | 72% |
B9SQI7 | Ricinus communis | 30% | 71% |
B9WAM8 | Candida dubliniensis (strain CD36 / ATCC MYA-646 / CBS 7987 / NCPF 3949 / NRRL Y-17841) | 24% | 100% |
C3XR70 | Branchiostoma floridae | 26% | 100% |
C4YJE1 | Candida albicans (strain WO-1) | 24% | 100% |
C9SUS0 | Verticillium alfalfae (strain VaMs.102 / ATCC MYA-4576 / FGSC 10136) | 30% | 100% |
D2UYP1 | Naegleria gruberi | 27% | 100% |
E0CTF3 | Vitis vinifera | 29% | 70% |
E9AU26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q0VD27 | Bos taurus | 33% | 100% |
Q28C69 | Xenopus tropicalis | 29% | 100% |
Q296B0 | Drosophila pseudoobscura pseudoobscura | 31% | 100% |
Q2R483 | Oryza sativa subsp. japonica | 29% | 72% |
Q4Q0G9 | Leishmania major | 91% | 100% |
Q55FM6 | Dictyostelium discoideum | 27% | 100% |
Q5PPH0 | Rattus norvegicus | 32% | 100% |
Q6FLR5 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 25% | 100% |
Q6GMI7 | Danio rerio | 31% | 100% |
Q7Q9C0 | Anopheles gambiae | 28% | 100% |
Q8BGB7 | Mus musculus | 33% | 100% |
Q9FN41 | Arabidopsis thaliana | 32% | 74% |
Q9UHY7 | Homo sapiens | 32% | 100% |
Q9VN95 | Drosophila melanogaster | 34% | 100% |
V5BJ24 | Trypanosoma cruzi | 27% | 100% |