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Comparing WP_012049704.1 NCBI__GCF_000016765.1:WP_012049704.1 to proteins with known functional sites using BLASTp with E ≤ 0.001.
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Found 20 (the maximum) hits to proteins with known functional sites (download)
4u3wA X-ray crystal structure of 2-aminomuconate 6-semialdehyde dehydrogenase from burkholderia cenocepacia
66% identity, 97% coverage: 17:496/496 of query aligns to 4:484/485 of 4u3wA
5kj5B Crystal structure of 2-aminomuconate 6-semialdehyde dehydrogenase n169d in complex with NAD+ (see paper)
60% identity, 97% coverage: 14:496/496 of query aligns to 1:484/484 of 5kj5B
- active site: D153 (≠ N165), K176 (= K188), E252 (= E264), C286 (= C298), E388 (= E400), E465 (= E477)
- binding nicotinamide-adenine-dinucleotide: I149 (≠ V161), S150 (= S162), P151 (= P163), W152 (= W164), D153 (≠ N165), L158 (= L170), K176 (= K188), G209 (= G221), K210 (≠ P222), G214 (= G226), F228 (= F240), T229 (= T241), G230 (= G242), E231 (= E243), T234 (= T246), E252 (= E264), L253 (= L265), C286 (= C298), E388 (= E400), F390 (= F402), F454 (= F466)
4npiA 1.94 angstroms x-ray crystal structure of NAD- and intermediate- bound alpha-aminomuconate-epsilon-semialdehyde dehydrogenase from pseudomonas fluorescens (see paper)
60% identity, 96% coverage: 20:496/496 of query aligns to 6:483/483 of 4npiA
- active site: N152 (= N165), K175 (= K188), E251 (= E264), C285 (= C298), E387 (= E400), E464 (= E477)
- binding (2Z,4E)-2-hydroxy-6-oxohexa-2,4-dienoic acid: R103 (= R116), L157 (= L170), W160 (= W173), E251 (= E264), C285 (= C298), Y445 (≠ F458), R447 (= R460), F453 (= F466)
- binding nicotinamide-adenine-dinucleotide: I148 (≠ V161), S149 (= S162), P150 (= P163), W151 (= W164), K175 (= K188), E178 (= E191), G208 (= G221), G213 (= G226), E214 (= E227), F227 (= F240), G229 (= G242), E230 (= E243), T233 (= T246), G253 (= G266), C285 (= C298), K335 (= K348), E387 (= E400), F389 (= F402)
4i2rA 2.15 angstroms x-ray crystal structure of NAD- and alternative substrate-bound 2-aminomuconate 6-semialdehyde dehydrogenase from pseudomonas fluorescens (see paper)
60% identity, 96% coverage: 20:496/496 of query aligns to 6:483/483 of 4i2rA
- active site: N152 (= N165), K175 (= K188), E251 (= E264), C285 (= C298), E387 (= E400), E464 (= E477)
- binding (2E,4E)-2-hydroxy-6-oxohexa-2,4-dienoic acid: R103 (= R116), L157 (= L170), C285 (= C298), Y445 (≠ F458), R447 (= R460), F453 (= F466)
- binding nicotinamide-adenine-dinucleotide: I148 (≠ V161), S149 (= S162), W151 (= W164), N152 (= N165), K175 (= K188), E178 (= E191), G208 (= G221), F227 (= F240), T228 (= T241), G229 (= G242), E230 (= E243), T233 (= T246), E251 (= E264), L252 (= L265), G253 (= G266), C285 (= C298), E387 (= E400), F389 (= F402)
4i25A 2.00 angstroms x-ray crystal structure of NAD- and substrate-bound 2- aminomuconate 6-semialdehyde dehydrogenase from pseudomonas fluorescens (see paper)
60% identity, 96% coverage: 20:496/496 of query aligns to 6:483/483 of 4i25A
- active site: N152 (= N165), K175 (= K188), E251 (= E264), C285 (= C298), E387 (= E400), E464 (= E477)
- binding (2E,4E)-2-amino-6-oxohexa-2,4-dienoic acid: R103 (= R116), L157 (= L170), C285 (= C298), Y445 (≠ F458), R447 (= R460), F453 (= F466)
- binding nicotinamide-adenine-dinucleotide: I148 (≠ V161), S149 (= S162), P150 (= P163), W151 (= W164), N152 (= N165), K175 (= K188), E178 (= E191), G208 (= G221), G213 (= G226), F227 (= F240), T228 (= T241), G229 (= G242), E230 (= E243), T233 (= T246), E251 (= E264), L252 (= L265), C285 (= C298), E387 (= E400), F389 (= F402)
5kllA Crystal structure of 2-hydroxymuconate-6-semialdehyde derived tautomeric intermediate in 2-aminomuconate 6-semialdehyde dehydrogenase n169d (see paper)
60% identity, 96% coverage: 20:496/496 of query aligns to 6:483/483 of 5kllA
- active site: D152 (≠ N165), K175 (= K188), E251 (= E264), C285 (= C298), E387 (= E400), E464 (= E477)
- binding (3~{E},5~{E})-6-oxidanyl-2-oxidanylidene-hexa-3,5-dienoic acid: R103 (= R116), D152 (≠ N165), L157 (= L170), W160 (= W173), C285 (= C298), Y445 (≠ F458), R447 (= R460), F453 (= F466)
4ou2A A 2.15 angstroms x-ray crystal structure of e268a 2-aminomuconate 6- semialdehyde dehydrogenase catalytic intermediate from pseudomonas fluorescens (see paper)
60% identity, 96% coverage: 20:496/496 of query aligns to 6:483/483 of 4ou2A
- active site: N152 (= N165), K175 (= K188), A251 (≠ E264), C285 (= C298), E387 (= E400), E464 (= E477)
- binding (2Z,4E)-2,6-dihydroxyhexa-2,4-dienoic acid: R103 (= R116), L157 (= L170), C285 (= C298), Y445 (≠ F458), R447 (= R460), F453 (= F466)
- binding nicotinamide-adenine-dinucleotide: I148 (≠ V161), S149 (= S162), P150 (= P163), W151 (= W164), N152 (= N165), K175 (= K188), G208 (= G221), G213 (= G226), E214 (= E227), F227 (= F240), T228 (= T241), G229 (= G242), E230 (= E243), T233 (= T246), A251 (≠ E264), L252 (= L265), G253 (= G266), C285 (= C298), E387 (= E400), F389 (= F402)
Q9H2A2 2-aminomuconic semialdehyde dehydrogenase; Aldehyde dehydrogenase 12; Aldehyde dehydrogenase family 8 member A1; EC 1.2.1.32 from Homo sapiens (Human) (see paper)
41% identity, 98% coverage: 10:495/496 of query aligns to 3:486/487 of Q9H2A2
- R109 (= R116) mutation to A: About 65-fold loss of catalytic efficiency.
- N155 (= N165) mutation to A: Complete loss of activity.
- R451 (= R460) mutation to A: Complete loss of activity.
4o6rA Crystal structure of a putative aldehyde dehydrogenase from burkholderia cenocepacia
41% identity, 97% coverage: 18:496/496 of query aligns to 5:479/489 of 4o6rA
- active site: N150 (= N165), K173 (= K188), E248 (= E264), C282 (= C298), E383 (= E400), E460 (= E477)
- binding adenosine monophosphate: I146 (≠ V161), V147 (≠ S162), K173 (= K188), G206 (= G221), G210 (= G226), Q211 (≠ E227), F224 (= F240), G226 (= G242), S227 (≠ E243), T230 (= T246), R233 (≠ A249)
2d4eC Crystal structure of the hpcc from thermus thermophilus hb8
42% identity, 96% coverage: 20:496/496 of query aligns to 30:505/515 of 2d4eC
- active site: N173 (= N165), K196 (= K188), E271 (= E264), C305 (= C298), E409 (= E400), E486 (= E477)
- binding nicotinamide-adenine-dinucleotide: I169 (≠ V161), T170 (≠ S162), P171 (= P163), W172 (= W164), K196 (= K188), A198 (≠ S190), G229 (= G221), G233 (= G226), A234 (≠ E227), T248 (= T241), G249 (= G242), E250 (= E243), T253 (= T246), E271 (= E264), L272 (= L265), C305 (= C298), E409 (= E400), F411 (= F402), F475 (= F466)
4go4A Crystal structure of pnpe in complex with nicotinamide adenine dinucleotide
41% identity, 96% coverage: 20:496/496 of query aligns to 6:477/487 of 4go4A
- active site: N149 (= N165), K172 (= K188), E247 (= E264), C281 (= C298), E381 (= E400), E458 (= E477)
- binding nicotinamide-adenine-dinucleotide: I145 (≠ V161), V146 (≠ S162), W148 (= W164), N149 (= N165), F154 (≠ L170), K172 (= K188), G205 (= G221), G209 (= G226), Q210 (≠ E227), F223 (= F240), T224 (= T241), G225 (= G242), S226 (≠ E243), T229 (= T246), E247 (= E264), G249 (= G266), C281 (= C298), E381 (= E400), F383 (= F402)
6vr6D Structure of aldh9a1 complexed with NAD+ in space group p1 (see paper)
37% identity, 93% coverage: 35:496/496 of query aligns to 31:486/493 of 6vr6D
- active site: N156 (= N165), E253 (= E264), C287 (= C298), E467 (= E477)
- binding nicotinamide-adenine-dinucleotide: I152 (≠ V161), G153 (≠ S162), W155 (= W164), K179 (= K188), A212 (≠ G221), G215 (= G226), Q216 (≠ E227), F229 (= F240), G231 (= G242), S232 (≠ E243), T235 (= T246), I239 (= I250)
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)
37% identity, 93% coverage: 35:496/496 of query aligns to 32:487/494 of P49189
- C116 (≠ N120) 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
5gtlA NADPH complex structure of aldehyde dehydrogenase from bacillus cereus
36% identity, 97% coverage: 17:496/496 of query aligns to 17:490/491 of 5gtlA
- active site: N165 (= N165), K188 (= K188), E263 (= E264), C297 (= C298), E394 (= E400), E471 (= E477)
- binding nadph dihydro-nicotinamide-adenine-dinucleotide phosphate: I161 (≠ V161), P163 (= P163), K188 (= K188), A190 (≠ S190), E191 (= E191), Q192 (≠ E192), G221 (= G221), G225 (= G226), G241 (= G242), S242 (≠ E243), T245 (= T246), L264 (= L265), C297 (= C298), E394 (= E400), F396 (= F402)
5gtkA NAD+ complex structure of aldehyde dehydrogenase from bacillus cereus
36% identity, 97% coverage: 17:496/496 of query aligns to 17:490/491 of 5gtkA
- active site: N165 (= N165), K188 (= K188), E263 (= E264), C297 (= C298), E394 (= E400), E471 (= E477)
- binding nicotinamide-adenine-dinucleotide: I161 (≠ V161), I162 (≠ S162), P163 (= P163), W164 (= W164), K188 (= K188), E191 (= E191), G221 (= G221), G225 (= G226), A226 (≠ E227), F239 (= F240), G241 (= G242), S242 (≠ E243), T245 (= T246), Y248 (≠ A249), L264 (= L265), C297 (= C298), Q344 (≠ H345), R347 (≠ K348), E394 (= E400), F396 (= F402)
4neaA 1.90 angstrom resolution crystal structure of betaine aldehyde dehydrogenase (betb) from staphylococcus aureus in complex with NAD+ and bme-free cys289 (see paper)
39% identity, 94% coverage: 20:486/496 of query aligns to 21:485/505 of 4neaA
- active site: N166 (= N165), K189 (= K188), E264 (= E264), C298 (= C298), E399 (= E400), E476 (= E477)
- binding nicotinamide-adenine-dinucleotide: P164 (= P163), K189 (= K188), E192 (= E191), G222 (= G221), G226 (= G226), G242 (= G242), G243 (≠ E243), T246 (= T246), H249 (≠ A249), I250 (= I250), C298 (= C298), E399 (= E400), F401 (= F402)
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)
38% identity, 96% coverage: 20:496/496 of query aligns to 10:483/490 of Q9HTJ1
- GAWN 150:153 (≠ SPWN 162:165) binding NADPH
- K162 (= K174) active site, Charge relay system
- KPSE 176:179 (= KPSE 188:191) binding NADPH
- G209 (= G221) binding NADPH
- GTST 230:233 (≠ ETRT 243:246) binding NADPH
- E252 (= E264) active site, Proton acceptor
- C286 (= C298) binding covalent; modified: Cysteine sulfenic acid (-SOH)
- E387 (= E400) binding NADPH
- E464 (= E477) active site, Charge relay system
4cazA Crystal structure of betaine aldehyde dehydrogenase from pseudomonas aeruginosa in complex with nadh
38% identity, 96% coverage: 20:496/496 of query aligns to 9:482/489 of 4cazA
- active site: N152 (= N165), K175 (= K188), E251 (= E264), C285 (= C298), E386 (= E400), E463 (= E477)
- 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 (≠ V161), G149 (≠ S162), W151 (= W164), N152 (= N165), K175 (= K188), E178 (= E191), G208 (= G221), G212 (= G226), F226 (= F240), T227 (= T241), G228 (= G242), G229 (≠ E243), T232 (= T246), V236 (≠ I250), E251 (= E264), L252 (= L265), C285 (= C298), E386 (= E400), F388 (= F402)
2woxA Betaine aldehyde dehydrogenase from pseudomonas aeruginosa with NAD(p) h-catalytic thiol adduct. (see paper)
38% identity, 96% coverage: 20:496/496 of query aligns to 9:482/489 of 2woxA
- active site: N152 (= N165), K175 (= K188), E251 (= E264), C285 (= C298), E386 (= E400), E463 (= E477)
- binding nadph dihydro-nicotinamide-adenine-dinucleotide phosphate: I148 (≠ V161), G149 (≠ S162), W151 (= W164), N152 (= N165), K175 (= K188), S177 (= S190), E178 (= E191), G208 (= G221), G212 (= G226), F226 (= F240), T227 (= T241), G228 (= G242), G229 (≠ E243), T232 (= T246), V236 (≠ I250), E251 (= E264), L252 (= L265), C285 (= C298), E386 (= E400), F388 (= F402)
2wmeA Crystallographic structure of betaine aldehyde dehydrogenase from pseudomonas aeruginosa (see paper)
38% identity, 96% coverage: 20:496/496 of query aligns to 9:482/489 of 2wmeA
- active site: N152 (= N165), K175 (= K188), E251 (= E264), C285 (= C298), E386 (= E400), E463 (= E477)
- binding nadp nicotinamide-adenine-dinucleotide phosphate: G149 (≠ S162), W151 (= W164), K175 (= K188), S177 (= S190), E178 (= E191), G208 (= G221), G212 (= G226), F226 (= F240), G228 (= G242), G229 (≠ E243), T232 (= T246), V236 (≠ I250)
Query Sequence
>WP_012049704.1 NCBI__GCF_000016765.1:WP_012049704.1
METRLKAILGTRPPRSLSCYVNGAWRPGVSRFTKYSPIDGSPVAEVEEAGAALVDEAVAA
ARAASRRWRETPLSERHRLLHRIADEIERRFDAFVEAEVLDTGRPESQARTLDIPRGAAN
FRTFADLVGAESGEVFETETPDGAGAINYTIRKPHGVVAIVSPWNLPFLLLTWKVAPALA
LGNCVVAKPSEETPATATLLAEVMHAVGLPEGVFNLVHGHGPEATGEFLTRHPGVDAITF
TGETRTGAAIMRAAAEGVRPISFELGGKNAAIIFADCDLEKTLDGVARSTFLNCGQVCLC
TERIYVERPIFDRFVQGLKERAERLAPGMPDDPATTLGPLISREHRDKVLSYYALARDEG
AVVVTGGGVPSLGDGLDGGCWVEPTILTGLPQTARLLQEEVFGPIAHIAPFDTEEEAIML
ANDTRYGLAAAIWTENLSRGHRVARAMETGIAWVNSWFLRDLRTPFGGVRLSGLGREGGA
HSLAFYGEPMNICVKL
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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