SitesBLAST
Comparing WP_090273754.1 NCBI__GCF_900105005.1:WP_090273754.1 to proteins with known functional sites using BLASTp with E ≤ 0.001.
Or try Sites on a Tree, PaperBLAST, Conserved Domains, or compare to all protein structures
Found 20 (the maximum) hits to proteins with known functional sites (download)
P42412 Malonate-semialdehyde dehydrogenase; MSA dehydrogenase; Methylmalonate-semialdehyde dehydrogenase; MMSA dehydrogenase; MMSDH; MSDH; EC 1.2.1.27 from Bacillus subtilis (strain 168) (see 3 papers)
48% identity, 95% coverage: 9:485/502 of query aligns to 7:481/487 of P42412
- C36 (≠ A38) mutation to A: No effect at either the structural or enzymatic levels; when associated with A-160; A-287; A-351 and A-413.
- R107 (= R109) mutation to L: At least 50-fold decrease of the second-order rate constant for the acylation step.
- A150 (≠ T152) binding NAD(+)
- F152 (= F154) binding NAD(+)
- C160 (≠ L162) mutation to A: No effect at either the structural or enzymatic levels; when associated with A-36; A-287; A-351 and A-413.
- K176 (= K178) binding NAD(+)
- E179 (= E181) binding NAD(+)
- R180 (≠ Q182) binding NAD(+)
- S229 (= S231) binding NAD(+)
- T251 (≠ M253) binding NAD(+)
- R283 (= R285) mutation to L: At least 50-fold decrease of the second-order rate constant for the acylation step.
- C287 (≠ L289) mutation to A: No effect at either the structural or enzymatic levels; when associated with A-36; A-160; A-351 and A-413.
- C351 (≠ L352) mutation to A: No effect at either the structural or enzymatic levels; when associated with A-36; A-160; A-287 and A-413.
- E382 (= E386) binding NAD(+)
- C413 (≠ A417) mutation to A: No effect at either the structural or enzymatic levels; when associated with A-36; A-160; A-287 and A-351.
1t90A Crystal structure of methylmalonate semialdehyde dehydrogenase from bacillus subtilis
48% identity, 95% coverage: 9:485/502 of query aligns to 5:479/484 of 1t90A
- active site: N151 (= N155), K174 (= K178), L248 (≠ M252), C282 (= C286), E380 (= E386), A460 (≠ P466)
- binding nicotinamide-adenine-dinucleotide: I147 (= I151), A148 (≠ T152), P149 (= P153), F150 (= F154), N151 (= N155), W159 (= W163), K174 (= K178), E177 (= E181), R178 (≠ Q182), H207 (≠ V211), V225 (= V229), G226 (= G230), S227 (= S231), V230 (= V234), L248 (≠ M252), T249 (≠ M253), C282 (= C286), E380 (= E386), F382 (= F388)
4zz7A Crystal structure of methylmalonate-semialdehyde dehydrogenase (dddc) from oceanimonas doudoroffii (see paper)
46% identity, 96% coverage: 6:485/502 of query aligns to 1:481/489 of 4zz7A
- active site: N149 (= N155), K172 (= K178), L246 (≠ M252), C280 (= C286), E382 (= E386), A462 (≠ P466)
- binding nicotinamide-adenine-dinucleotide: T146 (= T152), P147 (= P153), F148 (= F154), N149 (= N155), K172 (= K178), E175 (= E181), K205 (≠ V211), V208 (= V214), F222 (= F228), V223 (= V229), G224 (= G230), S225 (= S231), I228 (≠ V234), L246 (≠ M252), G247 (≠ M253), C280 (= C286), E382 (= E386), F384 (= F388)
4iymC Crystal structure of putative methylmalonate-semialdehyde dehydrogenase from sinorhizobium meliloti 1021 complexed with NAD, target 011934
48% identity, 94% coverage: 12:485/502 of query aligns to 10:485/491 of 4iymC
- active site: N153 (= N155), K176 (= K178), F250 (≠ M252), C284 (= C286), E386 (= E386), Q466 (≠ P466)
- binding nicotinamide-adenine-dinucleotide: I149 (= I151), T150 (= T152), P151 (= P153), F152 (= F154), N153 (= N155), F154 (= F156), K176 (= K178), K209 (≠ V211), V212 (= V214), F226 (= F228), V227 (= V229), G228 (= G230), S229 (= S231), I232 (≠ V234), G251 (≠ M253), C284 (= C286), E386 (= E386), F388 (= F388)
5tjrD X-ray crystal structure of a methylmalonate semialdehyde dehydrogenase from pseudomonas sp. Aac (see paper)
45% identity, 97% coverage: 9:494/502 of query aligns to 3:464/468 of 5tjrD
- active site: N144 (= N155), K167 (= K178), L241 (≠ M252), C270 (= C286), E356 (= E386), A436 (≠ P466)
- binding adenosine-5'-diphosphate: I140 (= I151), T141 (= T152), F143 (= F154), K167 (= K178), E170 (= E181), K200 (≠ V211), F217 (= F228), S220 (= S231), I223 (≠ V234)
4cazA Crystal structure of betaine aldehyde dehydrogenase from pseudomonas aeruginosa in complex with nadh
32% identity, 92% coverage: 10:469/502 of query aligns to 7:474/489 of 4cazA
- active site: N152 (= N155), K175 (= K178), E251 (≠ M252), C285 (= C286), E386 (= E386), E463 (≠ G458)
- binding [[(2R,3S,4R,5R)-5-[(3R)-3-aminocarbonyl-3,4-dihydro-2H-pyridin-1-yl]-3,4-bis(oxidanyl)oxolan-2-yl]methoxy-oxidanidyl-phosphoryl] [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-bis(oxidanyl)oxolan-2-yl]methyl phosphate: I148 (= I151), G149 (≠ T152), W151 (≠ F154), N152 (= N155), K175 (= K178), E178 (= E181), G208 (= G210), G212 (≠ V214), F226 (= F228), T227 (≠ V229), G228 (= G230), G229 (≠ S231), T232 (≠ V234), V236 (= V238), E251 (≠ M252), L252 (≠ M253), C285 (= C286), E386 (= E386), F388 (= F388)
2woxA Betaine aldehyde dehydrogenase from pseudomonas aeruginosa with NAD(p) h-catalytic thiol adduct. (see paper)
32% identity, 92% coverage: 10:469/502 of query aligns to 7:474/489 of 2woxA
- active site: N152 (= N155), K175 (= K178), E251 (≠ M252), C285 (= C286), E386 (= E386), E463 (≠ G458)
- binding nadph dihydro-nicotinamide-adenine-dinucleotide phosphate: I148 (= I151), G149 (≠ T152), W151 (≠ F154), N152 (= N155), K175 (= K178), S177 (= S180), E178 (= E181), G208 (= G210), G212 (≠ V214), F226 (= F228), T227 (≠ V229), G228 (= G230), G229 (≠ S231), T232 (≠ V234), V236 (= V238), E251 (≠ M252), L252 (≠ M253), C285 (= C286), E386 (= E386), F388 (= F388)
2wmeA Crystallographic structure of betaine aldehyde dehydrogenase from pseudomonas aeruginosa (see paper)
32% identity, 92% coverage: 10:469/502 of query aligns to 7:474/489 of 2wmeA
- active site: N152 (= N155), K175 (= K178), E251 (≠ M252), C285 (= C286), E386 (= E386), E463 (≠ G458)
- binding nadp nicotinamide-adenine-dinucleotide phosphate: G149 (≠ T152), W151 (≠ F154), K175 (= K178), S177 (= S180), E178 (= E181), G208 (= G210), G212 (≠ V214), F226 (= F228), G228 (= G230), G229 (≠ S231), T232 (≠ V234), V236 (= V238)
Q9HTJ1 NAD/NADP-dependent betaine aldehyde dehydrogenase; BADH; EC 1.2.1.8 from Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) (see 2 papers)
32% identity, 92% coverage: 10:469/502 of query aligns to 8:475/490 of Q9HTJ1
- GAWN 150:153 (≠ TPFN 152:155) binding NADPH
- K162 (≠ M164) active site, Charge relay system
- KPSE 176:179 (= KPSE 178:181) binding NADPH
- G209 (= G210) binding NADPH
- GTST 230:233 (≠ STHV 231:234) binding NADPH
- E252 (≠ M252) active site, Proton acceptor
- C286 (= C286) binding covalent; modified: Cysteine sulfenic acid (-SOH)
- E387 (= E386) binding NADPH
- E464 (≠ G458) active site, Charge relay system
5gtlA NADPH complex structure of aldehyde dehydrogenase from bacillus cereus
32% identity, 94% coverage: 9:481/502 of query aligns to 17:486/491 of 5gtlA
- active site: N165 (= N155), K188 (= K178), E263 (≠ M252), C297 (= C286), E394 (= E386), E471 (≠ D463)
- binding nadph dihydro-nicotinamide-adenine-dinucleotide phosphate: I161 (= I151), P163 (= P153), K188 (= K178), A190 (≠ S180), E191 (= E181), Q192 (= Q182), G221 (= G210), G225 (≠ V214), G241 (= G230), S242 (= S231), T245 (≠ V234), L264 (≠ M253), C297 (= C286), E394 (= E386), F396 (= F388)
5gtkA NAD+ complex structure of aldehyde dehydrogenase from bacillus cereus
32% identity, 94% coverage: 9:481/502 of query aligns to 17:486/491 of 5gtkA
- active site: N165 (= N155), K188 (= K178), E263 (≠ M252), C297 (= C286), E394 (= E386), E471 (≠ D463)
- binding nicotinamide-adenine-dinucleotide: I161 (= I151), I162 (≠ T152), P163 (= P153), W164 (≠ F154), K188 (= K178), E191 (= E181), G221 (= G210), G225 (≠ V214), A226 (≠ N215), F239 (= F228), G241 (= G230), S242 (= S231), T245 (≠ V234), Y248 (≠ H237), L264 (≠ M253), C297 (= C286), Q344 (≠ A332), R347 (= R335), E394 (= E386), F396 (= F388)
P49189 4-trimethylaminobutyraldehyde dehydrogenase; TMABA-DH; TMABALDH; Aldehyde dehydrogenase E3 isozyme; Aldehyde dehydrogenase family 9 member A1; Formaldehyde dehydrogenase; Gamma-aminobutyraldehyde dehydrogenase; R-aminobutyraldehyde dehydrogenase; EC 1.2.1.47; EC 1.2.1.3; EC 1.2.1.46; EC 1.2.1.19 from Homo sapiens (Human) (see 2 papers)
31% identity, 91% coverage: 29:487/502 of query aligns to 32:489/494 of P49189
- C116 (≠ V113) to S: in allele ALDH9A1*2
Sites not aligning to the query:
- 1 modified: Initiator methionine, Removed; alternate
- 2 modified: N-acetylserine; in 4-trimethylaminobutyraldehyde dehydrogenase, N-terminally processed
6vr6D Structure of aldh9a1 complexed with NAD+ in space group p1 (see paper)
31% identity, 91% coverage: 29:487/502 of query aligns to 31:488/493 of 6vr6D
- active site: N156 (= N155), E253 (≠ M252), C287 (= C286), E467 (≠ L464)
- binding nicotinamide-adenine-dinucleotide: I152 (= I151), G153 (≠ T152), W155 (≠ F154), K179 (= K178), A212 (≠ V211), G215 (≠ V214), Q216 (≠ N215), F229 (= F228), G231 (= G230), S232 (= S231), T235 (≠ V234), I239 (≠ V238)
7radA Crystal structure analysis of aldh1b1
31% identity, 96% coverage: 3:484/502 of query aligns to 7:487/493 of 7radA
- binding nicotinamide-adenine-dinucleotide: I158 (= I151), I159 (≠ T152), P160 (= P153), W161 (≠ F154), N162 (= N155), M167 (≠ I160), K185 (= K178), E188 (= E181), G218 (= G210), G222 (≠ V214), A223 (≠ N215), T237 (≠ V229), G238 (= G230), S239 (= S231), V242 (= V234), E261 (≠ M252), L262 (≠ M253), C295 (= C286), E392 (= E386), F394 (= F388)
- binding 3-(2-methoxyphenyl)-1-(4-phenylphenyl)-6,7,8,9-tetrahydro-5~{H}-imidazo[1,2-a][1,3]diazepine: L113 (vs. gap), E117 (≠ R109), F163 (= F156), E285 (≠ G276), F289 (≠ G280), N450 (vs. gap), V452 (= V442)
7mjdA Crystal structure analysis of aldh1b1
31% identity, 96% coverage: 3:484/502 of query aligns to 7:487/493 of 7mjdA
- binding nicotinamide-adenine-dinucleotide: I158 (= I151), I159 (≠ T152), P160 (= P153), W161 (≠ F154), N162 (= N155), M167 (≠ I160), K185 (= K178), E188 (= E181), G218 (= G210), G222 (≠ V214), F236 (= F228), T237 (≠ V229), G238 (= G230), S239 (= S231), V242 (= V234), E261 (≠ M252), L262 (≠ M253), C295 (= C286), E392 (= E386), F394 (= F388)
- binding 8-(2-methoxyphenyl)-10-(4-phenylphenyl)-1$l^{4},8-diazabicyclo[5.3.0]deca-1(7),9-diene: E117 (≠ R109), E285 (≠ G276), F289 (≠ G280), N450 (vs. gap), V452 (= V442)
7mjcA Crystal structure analysis of aldh1b1
31% identity, 96% coverage: 3:484/502 of query aligns to 7:487/493 of 7mjcA
- binding nicotinamide-adenine-dinucleotide: I158 (= I151), I159 (≠ T152), P160 (= P153), W161 (≠ F154), N162 (= N155), K185 (= K178), E188 (= E181), G218 (= G210), G222 (≠ V214), T237 (≠ V229), G238 (= G230), S239 (= S231), V242 (= V234), E261 (≠ M252), L262 (≠ M253), C295 (= C286), E392 (= E386), F394 (= F388)
1bpwA Betaine aldehyde dehydrogenase from cod liver (see paper)
31% identity, 92% coverage: 28:489/502 of query aligns to 40:500/503 of 1bpwA
- active site: N166 (= N155), K189 (= K178), E263 (≠ M252), C297 (= C286), E400 (= E386), E477 (≠ L464)
- binding nicotinamide-adenine-dinucleotide: I162 (= I151), L163 (≠ T152), W165 (≠ F154), N166 (= N155), K189 (= K178), G221 (= G210), G225 (≠ V214), T240 (≠ V229), G241 (= G230), S242 (= S231), T245 (≠ V234), E263 (≠ M252), L264 (≠ M253), C297 (= C286), E400 (= E386), F402 (= F388), F466 (= F453)
P56533 4-trimethylaminobutyraldehyde dehydrogenase; TMABA-DH; TMABADH; Aldehyde dehydrogenase family 9 member A1; Betaine aldehyde dehydrogenase; BADH; EC 1.2.1.47; EC 1.2.1.3 from Gadus morhua subsp. callarias (Baltic cod) (Gadus callarias) (see paper)
31% identity, 92% coverage: 28:489/502 of query aligns to 40:500/503 of P56533
8rwkA Cryoem structure of the central ald4 filament determined by filamentid (see paper)
31% identity, 86% coverage: 11:441/502 of query aligns to 23:452/495 of 8rwkA
2d4eC Crystal structure of the hpcc from thermus thermophilus hb8
31% identity, 94% coverage: 12:481/502 of query aligns to 30:501/515 of 2d4eC
- active site: N173 (= N155), K196 (= K178), E271 (≠ M252), C305 (= C286), E409 (= E386), E486 (≠ P466)
- binding nicotinamide-adenine-dinucleotide: I169 (= I151), T170 (= T152), P171 (= P153), W172 (≠ F154), K196 (= K178), A198 (≠ S180), G229 (= G210), G233 (≠ V214), A234 (≠ N215), T248 (≠ V229), G249 (= G230), E250 (≠ S231), T253 (≠ V234), E271 (≠ M252), L272 (≠ M253), C305 (= C286), E409 (= E386), F411 (= F388), F475 (= F453)
Query Sequence
>WP_090273754.1 NCBI__GCF_900105005.1:WP_090273754.1
MSNNNLPTVKLLINGEFVESKTDQWRDVINPATQEVLARVPFATQDEINAAVASAKEAFK
TWRKTPIGARARIFLKYQQLIRENIKELAAILTAEQGKTMADAEGDVFRGLEVVEHASAV
GNLQLGELANNVAGGVDTYTLLQPLGVCAGITPFNFPAMIPLWMFPMAIATGNTFVLKPS
EQDPMVTMRLVELALEAGIPPGVLNVIHGGVDAVNGVCDHPDIKAVSFVGSTHVGTHVYN
RASQAGKRVQCMMGAKNHAVIMPDANKEQTLNNLIGAAFGAAGQRCMALPVIILVGESRN
WLPELARKAETLKVSAGIEAGTDVGPVISTSALERVNGLIQKGIDEGAELVLDGRNPNVA
GYADGNFVGPTIFAGVKPGMTVYDEEIFGPVLCVMQADSLDEAIDIINANPNGNGTAIFT
RSGGIARRFQEDIDVGQVGINVPIPVPVPLFSFSGSRGSKLGDLGPYGKQVILFYTQTKT
ITARWFDDDEQAAAVNTTITLK
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SitesBLAST's Database
SitesBLAST's database includes
(1) SwissProt
entries with experimentally-supported functional features;
and (2) protein structures with bound ligands, from the
BioLip database.
by Morgan Price,
Arkin group
Lawrence Berkeley National Laboratory