SitesBLAST
Comparing WP_028312975.1 NCBI__GCF_000482785.1:WP_028312975.1 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)
2opxA Crystal structure of lactaldehyde dehydrogenase from escherichia coli
59% identity, 99% coverage: 4:478/479 of query aligns to 4:477/477 of 2opxA
- active site: N151 (= N151), K174 (= K174), E249 (= E249), C283 (= C283), E381 (= E382), A458 (= A459)
- binding (3alpha,5beta,12alpha)-3,12-dihydroxycholan-24-oic acid: F105 (= F105), F152 (= F152), N284 (= N284), F312 (≠ Y312), G313 (= G313), R318 (≠ E318), D320 (≠ G320), I321 (≠ L321), A322 (≠ D322), Y362 (≠ H363), F440 (= F441), F440 (= F441), E441 (= E442)
2impA Crystal structure of lactaldehyde dehydrogenase from e. Coli: the ternary complex with lactate (occupancy 0.5) and nadh. Crystals soaked with (l)-lactate. (see paper)
58% identity, 99% coverage: 3:478/479 of query aligns to 3:477/477 of 2impA
- active site: N151 (= N151), K174 (= K174), E249 (= E249), C283 (= C283), E381 (= E382), A458 (= A459)
- binding 1,4-dihydronicotinamide adenine dinucleotide: I147 (= I147), L148 (= L148), P149 (= P149), W150 (= W150), K174 (= K174), E177 (= E177), F178 (≠ E178), G207 (= G207), G211 (= G211), Q212 (≠ A212), S228 (= S228), A231 (≠ T231), K234 (≠ A234), R334 (≠ K334)
2iluA Crystal structure of lactaldehyde dehydrogenase from e. Coli: the binary complex with NADPH (see paper)
58% identity, 99% coverage: 3:478/479 of query aligns to 3:477/477 of 2iluA
- active site: N151 (= N151), K174 (= K174), E249 (= E249), C283 (= C283), E381 (= E382), A458 (= A459)
- binding nadph dihydro-nicotinamide-adenine-dinucleotide phosphate: I147 (= I147), L148 (= L148), P149 (= P149), W150 (= W150), K174 (= K174), S176 (= S176), E177 (= E177), R206 (= R206), G207 (= G207), G211 (= G211), Q212 (≠ A212), S228 (= S228), A231 (≠ T231), K234 (≠ A234), I235 (= I235), N328 (= N328), R334 (≠ K334), F383 (= F384)
P25553 Lactaldehyde dehydrogenase; Aldehyde dehydrogenase A; Glycolaldehyde dehydrogenase; EC 1.2.1.22; EC 1.2.1.21 from Escherichia coli (strain K12) (see 5 papers)
58% identity, 99% coverage: 3:478/479 of query aligns to 5:479/479 of P25553
- L150 (= L148) binding NAD(+)
- R161 (= R159) binding (S)-lactate
- KPSE 176:179 (= KPSE 174:177) binding NAD(+)
- F180 (≠ E178) mutation to T: Can bind and use NADP(+) as coenzyme. 16-fold increase in catalytic efficiency with NAD(+) as coenzyme.
- Q214 (≠ A212) binding NAD(+)
- S230 (= S228) binding NAD(+)
- E251 (= E249) binding (S)-lactate
- N286 (= N284) binding (S)-lactate; mutation to E: 4-fold increase in catalytic efficiency with L-lactaldehyde as substrate. Shows expanded substrate specificity.; mutation to H: 15-fold increase in catalytic efficiency with L-lactaldehyde as substrate. Shows expanded substrate specificity.; mutation to T: 6-fold increase in catalytic efficiency with L-lactaldehyde as substrate. Shows expanded substrate specificity.
- R336 (≠ K334) binding NAD(+)
- E443 (= E442) binding (S)-lactate
- H449 (= H448) binding (S)-lactate
Sites not aligning to the query:
- 1 modified: Initiator methionine, Removed
6j76A Structure of 3,6-anhydro-l-galactose dehydrogenase in complex with nap (see paper)
43% identity, 99% coverage: 4:477/479 of query aligns to 1:476/477 of 6j76A
- active site: N148 (= N151), E246 (= E249), C280 (= C283), E458 (≠ A459)
- binding nadp nicotinamide-adenine-dinucleotide phosphate: I144 (= I147), T145 (≠ L148), A146 (≠ P149), W147 (= W150), N148 (= N151), K171 (= K174), T173 (≠ S176), S174 (≠ E177), G204 (= G207), G208 (= G211), T223 (= T226), G224 (= G227), S225 (= S228), A228 (≠ T231), S231 (≠ A234), I232 (= I235), E246 (= E249), L247 (= L250), C280 (= C283), E381 (= E382), F383 (= F384), H447 (= H448)
5izdA Wild-type glyceraldehyde dehydrogenase from thermoplasma acidophilum in complex with NADP
37% identity, 98% coverage: 8:476/479 of query aligns to 6:475/494 of 5izdA
- active site: N149 (= N151), K172 (= K174), E247 (= E249), C281 (= C283), E381 (= E382), E458 (≠ A459)
- binding nadp nicotinamide-adenine-dinucleotide phosphate: L145 (≠ I147), T146 (≠ L148), W148 (= W150), K172 (= K174), P173 (= P175), S174 (= S176), S175 (≠ E177), R204 (= R206), G205 (= G207), G209 (= G211), D210 (≠ A212), G225 (= G227), S226 (= S228), T229 (= T231)
8of1A Structure of aldh5f1 from moss physcomitrium patens in complex with NAD+ in the contracted conformation
38% identity, 99% coverage: 4:476/479 of query aligns to 27:497/505 of 8of1A
- binding nicotinamide-adenine-dinucleotide: I170 (= I147), A171 (≠ L148), P172 (= P149), W173 (= W150), K197 (= K174), A230 (≠ G207), F248 (= F225), G250 (= G227), S251 (= S228), V254 (≠ T231), M257 (≠ A234), L273 (= L250), C306 (= C283), K356 (= K334), E403 (= E382), F405 (= F384)
P17202 Aminoaldehyde dehydrogenase BADH; 4-trimethylammoniobutyraldehyde dehydrogenase BADH; Aminobutyraldehyde dehydrogenase BADH; Betaine aldehyde dehydrogenase; SoBADH; EC 1.2.1.-; EC 1.2.1.47; EC 1.2.1.19; EC 1.2.1.8 from Spinacia oleracea (Spinach) (see 3 papers)
37% identity, 96% coverage: 8:468/479 of query aligns to 11:476/497 of P17202
- I28 (≠ R25) binding K(+)
- D96 (≠ E91) binding K(+)
- SPW 156:158 (≠ LPW 148:150) binding NAD(+)
- Y160 (≠ F152) mutation to A: Decreases binding affinity for betaine aldehyde; increases binding affinity for 4-(trimethylamino)butanal.
- W167 (≠ R159) mutation to A: Decreases binding affinity for betaine aldehyde; increases binding affinity for 4-aminobutanal.
- KPSE 182:185 (= KPSE 174:177) binding NAD(+)
- L186 (≠ E178) binding K(+)
- SSAT 236:239 (≠ SVAT 228:231) binding NAD(+)
- V251 (≠ L243) binding in other chain
- L258 (= L250) binding NAD(+)
- W285 (≠ I277) mutation to A: Decreases binding affinity for betaine aldehyde.
- E390 (= E382) binding NAD(+)
- A441 (≠ E433) mutation to I: Decreases binding affinity for betaine aldehyde; increases binding affinity for 4-aminobutanal.
- C450 (≠ E442) mutation to S: Loss of partial inactivation by betaine aldehyde in the absence of NAD(+).
- W456 (≠ H448) binding NAD(+); mutation to A: Decreases binding affinity for betaine aldehyde.
- K460 (≠ R452) binding K(+)
3jz4A Crystal structure of e. Coli NADP dependent enzyme (see paper)
36% identity, 96% coverage: 9:470/479 of query aligns to 14:473/481 of 3jz4A
- active site: N156 (= N151), K179 (= K174), E254 (= E249), C288 (= C283), E385 (= E382), E462 (≠ A459)
- binding nadp nicotinamide-adenine-dinucleotide phosphate: P154 (= P149), W155 (= W150), K179 (= K174), A181 (≠ S176), S182 (≠ E177), A212 (≠ G207), G216 (= G211), G232 (= G227), S233 (= S228), I236 (≠ T231), C288 (= C283), K338 (= K334), E385 (= E382), F387 (= F384)
P25526 Succinate-semialdehyde dehydrogenase [NADP(+)] GabD; SSDH; Glutarate-semialdehyde dehydrogenase; EC 1.2.1.79; EC 1.2.1.- from Escherichia coli (strain K12) (see paper)
36% identity, 96% coverage: 9:470/479 of query aligns to 15:474/482 of P25526
4v37A Crystal structure of betaine aldehyde dehydrogenase from spinach showing a thiohemiacetal with 3-aminopropionaldehyde
37% identity, 96% coverage: 8:468/479 of query aligns to 9:474/495 of 4v37A
- active site: N157 (= N151), K180 (= K174), E255 (= E249), A289 (≠ C283), E388 (= E382), E465 (≠ A459)
- binding 3-aminopropan-1-ol: C448 (≠ E442), W454 (≠ H448)
- binding nicotinamide-adenine-dinucleotide: I153 (= I147), S154 (≠ L148), P155 (= P149), W156 (= W150), N157 (= N151), M162 (≠ L156), K180 (= K174), S182 (= S176), E183 (= E177), G213 (= G207), G217 (= G211), A218 (= A212), T232 (= T226), G233 (= G227), S234 (= S228), T237 (= T231), E255 (= E249), L256 (= L250), A289 (≠ C283), E388 (= E382), F390 (= F384)
8rwkA Cryoem structure of the central ald4 filament determined by filamentid (see paper)
36% identity, 97% coverage: 8:474/479 of query aligns to 24:489/495 of 8rwkA
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)
37% identity, 98% coverage: 8:477/479 of query aligns to 10:482/490 of Q9HTJ1
- GAWN 150:153 (≠ LPWN 148:151) binding NADPH
- K162 (= K160) active site, Charge relay system
- KPSE 176:179 (= KPSE 174:177) binding NADPH
- G209 (= G207) binding NADPH
- GTST 230:233 (≠ SVAT 228:231) binding NADPH
- E252 (= E249) active site, Proton acceptor
- C286 (= C283) binding covalent; modified: Cysteine sulfenic acid (-SOH)
- E387 (= E382) binding NADPH
- E464 (≠ A459) active site, Charge relay system
4cazA Crystal structure of betaine aldehyde dehydrogenase from pseudomonas aeruginosa in complex with nadh
37% identity, 98% coverage: 8:477/479 of query aligns to 9:481/489 of 4cazA
- active site: N152 (= N151), K175 (= K174), E251 (= E249), C285 (= C283), E386 (= E382), E463 (≠ A459)
- 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 (= I147), G149 (≠ L148), W151 (= W150), N152 (= N151), K175 (= K174), E178 (= E177), G208 (= G207), G212 (= G211), F226 (= F225), T227 (= T226), G228 (= G227), G229 (≠ S228), T232 (= T231), V236 (≠ I235), E251 (= E249), L252 (= L250), C285 (= C283), E386 (= E382), F388 (= F384)
2woxA Betaine aldehyde dehydrogenase from pseudomonas aeruginosa with NAD(p) h-catalytic thiol adduct. (see paper)
37% identity, 98% coverage: 8:477/479 of query aligns to 9:481/489 of 2woxA
- active site: N152 (= N151), K175 (= K174), E251 (= E249), C285 (= C283), E386 (= E382), E463 (≠ A459)
- binding nadph dihydro-nicotinamide-adenine-dinucleotide phosphate: I148 (= I147), G149 (≠ L148), W151 (= W150), N152 (= N151), K175 (= K174), S177 (= S176), E178 (= E177), G208 (= G207), G212 (= G211), F226 (= F225), T227 (= T226), G228 (= G227), G229 (≠ S228), T232 (= T231), V236 (≠ I235), E251 (= E249), L252 (= L250), C285 (= C283), E386 (= E382), F388 (= F384)
2wmeA Crystallographic structure of betaine aldehyde dehydrogenase from pseudomonas aeruginosa (see paper)
37% identity, 98% coverage: 8:477/479 of query aligns to 9:481/489 of 2wmeA
- active site: N152 (= N151), K175 (= K174), E251 (= E249), C285 (= C283), E386 (= E382), E463 (≠ A459)
- binding nadp nicotinamide-adenine-dinucleotide phosphate: G149 (≠ L148), W151 (= W150), K175 (= K174), S177 (= S176), E178 (= E177), G208 (= G207), G212 (= G211), F226 (= F225), G228 (= G227), G229 (≠ S228), T232 (= T231), V236 (≠ I235)
7a6qB Crystal structure of human aldehyde dehydrogenase 1a3 in complex with selective nr6 inhibitor compound (see paper)
37% identity, 98% coverage: 8:477/479 of query aligns to 17:488/489 of 7a6qB
- active site: N163 (= N151), E262 (= E249), C296 (= C283), E470 (≠ A459)
- binding nicotinamide-adenine-dinucleotide: I159 (= I147), W162 (= W150), K186 (= K174), E189 (= E177), G219 (= G207), G223 (= G211), S240 (= S228), V243 (≠ T231), K342 (≠ V330)
- binding (3-oxidanylidene-3-sodiooxy-propanoyl)oxysodium: A32 (≠ E23), T33 (≠ V24), C34 (≠ R25), P36 (= P27), D103 (≠ E91), E189 (= E177), Q190 (≠ E178), F218 (≠ R206), I339 (≠ V327), D340 (≠ N328)
- binding 3-(2-phenylimidazo[1,2-a]pyridin-6-yl)benzenecarbonitrile: G118 (≠ F105), D141 (= D128), N143 (= N131), N451 (≠ H440), L453 (≠ E442), A455 (≠ M444)
7a6qA Crystal structure of human aldehyde dehydrogenase 1a3 in complex with selective nr6 inhibitor compound (see paper)
37% identity, 98% coverage: 8:477/479 of query aligns to 17:488/489 of 7a6qA
- active site: N163 (= N151), E262 (= E249), C296 (= C283), E470 (≠ A459)
- binding nicotinamide-adenine-dinucleotide: I159 (= I147), T160 (≠ L148), W162 (= W150), K186 (= K174), A188 (≠ S176), E189 (= E177), G219 (= G207), G223 (= G211), S240 (= S228), V243 (≠ T231), K342 (≠ V330), K346 (= K334)
- binding 3-(2-phenylimidazo[1,2-a]pyridin-6-yl)benzenecarbonitrile: G118 (≠ F105), D141 (= D128), N143 (= N131), N451 (≠ H440), L453 (≠ E442), Y454 (≠ A443)
5fhzA Human aldehyde dehydrogenase 1a3 complexed with NAD(+) and retinoic acid (see paper)
37% identity, 98% coverage: 8:477/479 of query aligns to 17:488/489 of 5fhzA
- active site: N163 (= N151), K186 (= K174), E262 (= E249), C296 (= C283), E393 (= E382), E470 (≠ A459)
- binding nicotinamide-adenine-dinucleotide: I159 (= I147), T160 (≠ L148), W162 (= W150), K186 (= K174), E189 (= E177), G219 (= G207), G223 (= G211), F237 (= F225), G239 (= G227), S240 (= S228), T241 (≠ V229), V243 (≠ T231), G264 (= G251), Q343 (≠ G331), E393 (= E382)
- binding retinoic acid: G118 (≠ F105), R121 (≠ D108), F164 (= F152), M168 (≠ L156), W171 (≠ R159), C295 (≠ V282), C296 (= C283), L453 (≠ E442)
7qk9A Crystal structure of the aldh1a3-atp complex (see paper)
37% identity, 98% coverage: 8:477/479 of query aligns to 16:487/489 of 7qk9A
- binding adenosine-5'-triphosphate: I158 (= I147), T159 (≠ L148), P160 (= P149), W161 (= W150), K185 (= K174), E188 (= E177), G218 (= G207), G222 (= G211), F236 (= F225), S239 (= S228), V242 (≠ T231)
Query Sequence
>WP_028312975.1 NCBI__GCF_000482785.1:WP_028312975.1
MVTKYSNYVNGEFVSPASEATIEVRNPADHALIALIPDSAPSVVDDAVAAARQAQRGWEK
LPAIQRAGYLRKISAKLREQRDRLAEVITREQGKVLPLARIEVDFTADYIDYMAEWARRI
EGEVIPSDRPNETIFLLRKPIGVTAGILPWNFPFFLIARKMAPALVTGNTIVVKPSEETP
VNAFEFAKLVAETDLPPGVFNLVSGRGATTGAALTGHPDVGLVSFTGSVATGQAIMKAAA
ANLTRVNLELGGKAPAIVLASADLDLAAKSIVASRTINTGQVCNCAERVYVQESVAEAFA
DKVVKLMAATRYGDPLREDGLDMGPLVNQVGLDKVAAMVERARGEGAQVLLGGKVADLGA
GFHYEPTVIAGCRADMEIMRKEIFGPVLPLQTVADLDEAITLANDCEYGLTSSIFTQDID
AAFKACRELSFGETYVNREHFEAMQGFHAGRRKSGIGGADGRHGLLEYTETHVVYLQSR
Or try a new SitesBLAST search
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