Amino acid metabolism, Homoserine dehydrogenase
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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HT44
Term | Name | Level | Count |
---|---|---|---|
GO:0000096 | sulfur amino acid metabolic process | 4 | 5 |
GO:0000097 | sulfur amino acid biosynthetic process | 5 | 5 |
GO:0006082 | organic acid metabolic process | 3 | 6 |
GO:0006520 | amino acid metabolic process | 3 | 6 |
GO:0006549 | isoleucine metabolic process | 5 | 5 |
GO:0006555 | methionine metabolic process | 5 | 5 |
GO:0006566 | threonine metabolic process | 6 | 5 |
GO:0006790 | sulfur compound metabolic process | 3 | 5 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0008652 | amino acid biosynthetic process | 4 | 5 |
GO:0009058 | biosynthetic process | 2 | 5 |
GO:0009066 | aspartate family amino acid metabolic process | 5 | 5 |
GO:0009067 | aspartate family amino acid biosynthetic process | 6 | 5 |
GO:0009081 | branched-chain amino acid metabolic process | 4 | 5 |
GO:0009082 | branched-chain amino acid biosynthetic process | 5 | 5 |
GO:0009086 | methionine biosynthetic process | 6 | 5 |
GO:0009088 | threonine biosynthetic process | 7 | 5 |
GO:0009097 | isoleucine biosynthetic process | 6 | 5 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016053 | organic acid biosynthetic process | 4 | 5 |
GO:0019752 | carboxylic acid metabolic process | 5 | 6 |
GO:0043436 | oxoacid metabolic process | 4 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0044249 | cellular biosynthetic process | 3 | 5 |
GO:0044272 | sulfur compound biosynthetic process | 4 | 5 |
GO:0044281 | small molecule metabolic process | 2 | 6 |
GO:0044283 | small molecule biosynthetic process | 3 | 5 |
GO:0046394 | carboxylic acid biosynthetic process | 5 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 6 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 5 |
GO:1901576 | organic substance biosynthetic process | 3 | 5 |
GO:1901605 | alpha-amino acid metabolic process | 4 | 5 |
GO:1901607 | alpha-amino acid biosynthetic process | 5 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 5 |
GO:0003824 | catalytic activity | 1 | 6 |
GO:0004412 | homoserine dehydrogenase activity | 5 | 6 |
GO:0005488 | binding | 1 | 5 |
GO:0016491 | oxidoreductase activity | 2 | 6 |
GO:0016614 | oxidoreductase activity, acting on CH-OH group of donors | 3 | 6 |
GO:0016616 | oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor | 4 | 6 |
GO:0036094 | small molecule binding | 2 | 5 |
GO:0050661 | NADP binding | 4 | 5 |
GO:0097159 | organic cyclic compound binding | 2 | 5 |
GO:1901265 | nucleoside phosphate binding | 3 | 5 |
GO:1901363 | heterocyclic compound binding | 2 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.422 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.424 |
CLV_PCSK_PC1ET2_1 | 50 | 52 | PF00082 | 0.387 |
CLV_PCSK_PC7_1 | 46 | 52 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.426 |
DEG_SPOP_SBC_1 | 273 | 277 | PF00917 | 0.406 |
DOC_MAPK_gen_1 | 30 | 38 | PF00069 | 0.290 |
DOC_MAPK_MEF2A_6 | 221 | 230 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 32 | 40 | PF00069 | 0.290 |
DOC_MAPK_MEF2A_6 | 75 | 82 | PF00069 | 0.426 |
DOC_PP1_RVXF_1 | 109 | 115 | PF00149 | 0.426 |
DOC_PP4_FxxP_1 | 363 | 366 | PF00568 | 0.551 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.347 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.407 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.352 |
LIG_14-3-3_CanoR_1 | 300 | 306 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 58 | 66 | PF00244 | 0.290 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.426 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.357 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.415 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.325 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.476 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.415 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.433 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.290 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.426 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.426 |
LIG_GBD_Chelix_1 | 40 | 48 | PF00786 | 0.426 |
LIG_LIR_Apic_2 | 361 | 366 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 189 | 199 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 217 | 227 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 89 | 100 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 137 | 143 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 189 | 195 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 89 | 95 | PF02991 | 0.426 |
LIG_Pex14_1 | 359 | 363 | PF04695 | 0.468 |
LIG_SH2_NCK_1 | 19 | 23 | PF00017 | 0.329 |
LIG_SH2_NCK_1 | 204 | 208 | PF00017 | 0.504 |
LIG_SH2_SRC | 204 | 207 | PF00017 | 0.504 |
LIG_SH2_STAP1 | 356 | 360 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 346 | 349 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.426 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.367 |
LIG_SUMO_SIM_anti_2 | 37 | 42 | PF11976 | 0.324 |
LIG_SUMO_SIM_par_1 | 334 | 339 | PF11976 | 0.504 |
LIG_TRAF2_1 | 120 | 123 | PF00917 | 0.426 |
LIG_TRAF2_1 | 191 | 194 | PF00917 | 0.465 |
LIG_TRAF2_1 | 284 | 287 | PF00917 | 0.290 |
LIG_TYR_ITIM | 260 | 265 | PF00017 | 0.504 |
LIG_TYR_ITSM | 328 | 335 | PF00017 | 0.504 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.343 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.426 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.426 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.387 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.426 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.372 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.426 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.364 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.500 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.173 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.287 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.589 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.339 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.364 |
MOD_N-GLC_1 | 173 | 178 | PF02516 | 0.504 |
MOD_N-GLC_2 | 159 | 161 | PF02516 | 0.426 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.582 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.522 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.343 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.329 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.469 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.480 |
MOD_PKA_1 | 49 | 55 | PF00069 | 0.406 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.504 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.387 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.401 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.387 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.426 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.357 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.426 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.604 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.352 |
MOD_SUMO_rev_2 | 57 | 66 | PF00179 | 0.426 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 262 | 265 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.505 |
TRG_ER_diArg_1 | 293 | 296 | PF00400 | 0.290 |
TRG_ER_diArg_1 | 363 | 365 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 48 | 51 | PF00400 | 0.426 |
TRG_NES_CRM1_1 | 68 | 83 | PF08389 | 0.329 |
TRG_NLS_MonoExtC_3 | 48 | 53 | PF00514 | 0.387 |
TRG_NLS_MonoExtN_4 | 46 | 53 | PF00514 | 0.387 |
TRG_Pf-PMV_PEXEL_1 | 295 | 299 | PF00026 | 0.290 |
TRG_Pf-PMV_PEXEL_1 | 53 | 57 | PF00026 | 0.426 |
TRG_Pf-PMV_PEXEL_1 | 97 | 101 | PF00026 | 0.426 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WPS1 | Leishmania donovani | 100% | 100% |
A4H4X1 | Leishmania braziliensis | 73% | 100% |
E9AL36 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
O94671 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 97% |
P08499 | Corynebacterium glutamicum (strain ATCC 13032 / DSM 20300 / BCRC 11384 / JCM 1318 / LMG 3730 / NCIMB 10025) | 31% | 82% |
P19582 | Bacillus subtilis (strain 168) | 33% | 85% |
P29365 | Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) | 33% | 84% |
P37143 | Methylobacillus glycogenes | 28% | 84% |
P37144 | Methylobacillus glycogenes | 31% | 89% |
P46806 | Mycobacterium leprae (strain TN) | 33% | 83% |
P52985 | Lactococcus lactis subsp. cremoris | 34% | 86% |
P52986 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 35% | 85% |
P56429 | Helicobacter pylori (strain ATCC 700392 / 26695) | 30% | 87% |
P63630 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 34% | 83% |
P9WPX0 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 34% | 83% |
P9WPX1 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 34% | 83% |
Q4QIR8 | Leishmania major | 94% | 100% |
Q9CGD8 | Lactococcus lactis subsp. lactis (strain IL1403) | 32% | 86% |
Q9ZL20 | Helicobacter pylori (strain J99 / ATCC 700824) | 30% | 87% |