SitesBLAST
Comparing WP_013133826.1 NCBI__GCF_000092245.1:WP_013133826.1 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
65% identity, 98% coverage: 7:477/483 of query aligns to 5:476/477 of 2opxA
- active site: N151 (= N152), K174 (= K175), E249 (= E250), C283 (= C284), E381 (= E382), A458 (= A459)
- binding (3alpha,5beta,12alpha)-3,12-dihydroxycholan-24-oic acid: F105 (= F106), F152 (= F153), N284 (= N285), F312 (≠ C313), G313 (= G314), R318 (≠ E319), D320 (vs. gap), I321 (= I321), A322 (≠ D322), Y362 (≠ F363), F440 (= F441), F440 (= F441), E441 (= E442)
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)
65% identity, 99% coverage: 1:477/483 of query aligns to 1:478/479 of P25553
- M1 (= M1) modified: Initiator methionine, Removed
- L150 (= L149) binding NAD(+)
- R161 (= R160) binding (S)-lactate
- KPSE 176:179 (≠ KPSG 175:178) binding NAD(+)
- F180 (≠ E179) mutation to T: Can bind and use NADP(+) as coenzyme. 16-fold increase in catalytic efficiency with NAD(+) as coenzyme.
- Q214 (≠ N213) binding NAD(+)
- S230 (= S229) binding NAD(+)
- E251 (= E250) binding (S)-lactate
- N286 (= N285) 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 (≠ H334) binding NAD(+)
- E443 (= E442) binding (S)-lactate
- H449 (= H448) binding (S)-lactate
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)
65% identity, 98% coverage: 7:477/483 of query aligns to 5:476/477 of 2impA
- active site: N151 (= N152), K174 (= K175), E249 (= E250), C283 (= C284), E381 (= E382), A458 (= A459)
- binding 1,4-dihydronicotinamide adenine dinucleotide: I147 (≠ V148), L148 (= L149), P149 (= P150), W150 (= W151), K174 (= K175), E177 (≠ G178), F178 (≠ E179), G207 (= G208), G211 (= G212), Q212 (≠ N213), S228 (= S229), A231 (≠ T232), K234 (= K235), R334 (≠ H334)
2iluA Crystal structure of lactaldehyde dehydrogenase from e. Coli: the binary complex with NADPH (see paper)
65% identity, 98% coverage: 7:477/483 of query aligns to 5:476/477 of 2iluA
- active site: N151 (= N152), K174 (= K175), E249 (= E250), C283 (= C284), E381 (= E382), A458 (= A459)
- binding nadph dihydro-nicotinamide-adenine-dinucleotide phosphate: I147 (≠ V148), L148 (= L149), P149 (= P150), W150 (= W151), K174 (= K175), S176 (= S177), E177 (≠ G178), R206 (≠ S207), G207 (= G208), G211 (= G212), Q212 (≠ N213), S228 (= S229), A231 (≠ T232), K234 (= K235), I235 (= I236), N328 (= N328), R334 (≠ H334), F383 (= F384)
6j76A Structure of 3,6-anhydro-l-galactose dehydrogenase in complex with nap (see paper)
45% identity, 98% coverage: 7:478/483 of query aligns to 2:477/477 of 6j76A
- active site: N148 (= N152), E246 (= E250), C280 (= C284), E458 (≠ A459)
- binding nadp nicotinamide-adenine-dinucleotide phosphate: I144 (≠ V148), T145 (≠ L149), A146 (≠ P150), W147 (= W151), N148 (= N152), K171 (= K175), T173 (≠ S177), S174 (≠ G178), G204 (= G208), G208 (= G212), T223 (= T227), G224 (= G228), S225 (= S229), A228 (≠ T232), S231 (≠ K235), I232 (= I236), E246 (= E250), L247 (= L251), C280 (= C284), E381 (= E382), F383 (= F384), H447 (= H448)
5izdA Wild-type glyceraldehyde dehydrogenase from thermoplasma acidophilum in complex with NADP
38% identity, 98% coverage: 8:478/483 of query aligns to 4:477/494 of 5izdA
- active site: N149 (= N152), K172 (= K175), E247 (= E250), C281 (= C284), E381 (= E382), E458 (≠ A459)
- binding nadp nicotinamide-adenine-dinucleotide phosphate: L145 (≠ V148), T146 (≠ L149), W148 (= W151), K172 (= K175), P173 (= P176), S174 (= S177), S175 (≠ G178), R204 (≠ S207), G205 (= G208), G209 (= G212), D210 (≠ N213), G225 (= G228), S226 (= S229), T229 (= T232)
3jz4A Crystal structure of e. Coli NADP dependent enzyme (see paper)
39% identity, 97% coverage: 8:476/483 of query aligns to 11:479/481 of 3jz4A
- active site: N156 (= N152), K179 (= K175), E254 (= E250), C288 (= C284), E385 (= E382), E462 (≠ A459)
- binding nadp nicotinamide-adenine-dinucleotide phosphate: P154 (= P150), W155 (= W151), K179 (= K175), A181 (≠ S177), S182 (≠ G178), A212 (≠ G208), G216 (= G212), G232 (= G228), S233 (= S229), I236 (≠ T232), C288 (= C284), K338 (≠ H334), 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)
39% identity, 97% coverage: 8:476/483 of query aligns to 12:480/482 of P25526
8of1A Structure of aldh5f1 from moss physcomitrium patens in complex with NAD+ in the contracted conformation
41% identity, 95% coverage: 20:476/483 of query aligns to 42:497/505 of 8of1A
- binding nicotinamide-adenine-dinucleotide: I170 (≠ V148), A171 (≠ L149), P172 (= P150), W173 (= W151), K197 (= K175), A230 (≠ G208), F248 (= F226), G250 (= G228), S251 (= S229), V254 (≠ T232), M257 (≠ K235), L273 (= L251), C306 (= C284), K356 (≠ H334), E403 (= E382), F405 (= F384)
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)
38% identity, 96% coverage: 10:474/483 of query aligns to 21:491/505 of 4neaA
- active site: N166 (= N152), K189 (= K175), E264 (= E250), C298 (= C284), E399 (= E382), E476 (≠ A459)
- binding nicotinamide-adenine-dinucleotide: P164 (= P150), K189 (= K175), E192 (≠ G178), G222 (= G208), G226 (= G212), G242 (= G228), G243 (≠ S229), T246 (= T232), H249 (≠ K235), I250 (= I236), C298 (= C284), E399 (= E382), F401 (= F384)
8rwkA Cryoem structure of the central ald4 filament determined by filamentid (see paper)
37% identity, 98% coverage: 9:479/483 of query aligns to 23:494/495 of 8rwkA
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, 97% coverage: 8:474/483 of query aligns to 9:482/497 of P17202
- I28 (= I26) binding K(+)
- D96 (≠ E92) binding K(+)
- SPW 156:158 (≠ LPW 149:151) binding NAD(+)
- Y160 (≠ F153) mutation to A: Decreases binding affinity for betaine aldehyde; increases binding affinity for 4-(trimethylamino)butanal.
- W167 (≠ R160) mutation to A: Decreases binding affinity for betaine aldehyde; increases binding affinity for 4-aminobutanal.
- KPSE 182:185 (≠ KPSG 175:178) binding NAD(+)
- L186 (≠ E179) binding K(+)
- SSAT 236:239 (≠ SVPT 229:232) binding NAD(+)
- V251 (= V244) binding in other chain
- L258 (= L251) binding NAD(+)
- W285 (≠ T278) 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 (= K452) binding K(+)
8c54A Cryo-em structure of nadh bound sla dehydrogenase rlgabd from rhizobium leguminosarum bv. Trifolii srd1565 (see paper)
38% identity, 97% coverage: 10:476/483 of query aligns to 13:479/482 of 8c54A
- binding 1,4-dihydronicotinamide adenine dinucleotide: I152 (≠ V148), T153 (≠ L149), P154 (= P150), K179 (= K175), A212 (≠ G208), K213 (≠ S209), F230 (= F226), T231 (= T227), G232 (= G228), S233 (= S229), V236 (≠ T232), W239 (≠ K235), G256 (= G252)
5ekcE Thermostable aldehyde dehydrogenase from pyrobaculum sp.1860 complexed with NADP+
37% identity, 95% coverage: 10:467/483 of query aligns to 11:467/490 of 5ekcE
- active site: N154 (= N152), K177 (= K175), E252 (= E250), C286 (= C284), E381 (= E382), E459 (≠ A459)
- binding nadp nicotinamide-adenine-dinucleotide phosphate: I150 (≠ V148), T151 (≠ L149), P152 (= P150), W153 (= W151), K177 (= K175), S180 (≠ G178), G210 (= G208), G214 (= G212), F228 (= F226), G230 (= G228), E231 (≠ S229), T234 (= T232), N331 (= N328), R333 (≠ D330), Q334 (≠ A331)
5ek6A Thermostable aldehyde dehydrogenase from pyrobaculum sp. 1860 complexed with NADP and isobutyraldehyde (see paper)
37% identity, 95% coverage: 10:467/483 of query aligns to 4:460/482 of 5ek6A
- active site: N147 (= N152), K170 (= K175), E245 (= E250), C279 (= C284), E374 (= E382), E452 (≠ A459)
- binding 2-methylpropanal: I152 (≠ L157), K155 (≠ R160), T222 (= T227), E245 (= E250), F441 (≠ H448)
- binding nadp nicotinamide-adenine-dinucleotide phosphate: I143 (≠ V148), T144 (≠ L149), W146 (= W151), N147 (= N152), I152 (≠ L157), K170 (= K175), A172 (≠ S177), S173 (≠ G178), P202 (≠ S207), G203 (= G208), G207 (= G212), F221 (= F226), T222 (= T227), G223 (= G228), E224 (≠ S229), T227 (= T232), I231 (= I236), E245 (= E250), L246 (= L251), C279 (= C284), E374 (= E382)
4h73A Thermostable aldehyde dehydrogenase from pyrobaculum sp. Complexed with NADP+
37% identity, 95% coverage: 10:467/483 of query aligns to 4:460/482 of 4h73A
- active site: N147 (= N152), K170 (= K175), E245 (= E250), C279 (= C284), E374 (= E382), E452 (≠ A459)
- binding nadph dihydro-nicotinamide-adenine-dinucleotide phosphate: I143 (≠ V148), T144 (≠ L149), P145 (= P150), W146 (= W151), K170 (= K175), A172 (≠ S177), S173 (≠ G178), G203 (= G208), G207 (= G212), F221 (= F226), G223 (= G228), E224 (≠ S229), T227 (= T232)
O14293 Putative aldehyde dehydrogenase-like protein C9E9.09c; EC 1.2.1.- from Schizosaccharomyces pombe (strain 972 / ATCC 24843) (Fission yeast) (see paper)
36% identity, 98% coverage: 9:481/483 of query aligns to 25:500/503 of O14293
- S248 (= S229) modified: Phosphoserine
Sites not aligning to the query:
- 501 modified: Phosphoserine
4v37A Crystal structure of betaine aldehyde dehydrogenase from spinach showing a thiohemiacetal with 3-aminopropionaldehyde
36% identity, 97% coverage: 8:474/483 of query aligns to 7:480/495 of 4v37A
- active site: N157 (= N152), K180 (= K175), E255 (= E250), A289 (≠ C284), E388 (= E382), E465 (≠ A459)
- binding 3-aminopropan-1-ol: C448 (≠ E442), W454 (≠ H448)
- binding nicotinamide-adenine-dinucleotide: I153 (≠ V148), S154 (≠ L149), P155 (= P150), W156 (= W151), N157 (= N152), M162 (≠ L157), K180 (= K175), S182 (= S177), E183 (≠ G178), G213 (= G208), G217 (= G212), A218 (≠ N213), T232 (= T227), G233 (= G228), S234 (= S229), T237 (= T232), E255 (= E250), L256 (= L251), A289 (≠ C284), E388 (= E382), F390 (= F384)
7a6qB Crystal structure of human aldehyde dehydrogenase 1a3 in complex with selective nr6 inhibitor compound (see paper)
36% identity, 98% coverage: 3:477/483 of query aligns to 10:488/489 of 7a6qB
- active site: N163 (= N152), E262 (= E250), C296 (= C284), E470 (≠ A459)
- binding nicotinamide-adenine-dinucleotide: I159 (≠ V148), W162 (= W151), K186 (= K175), E189 (≠ G178), G219 (= G208), G223 (= G212), S240 (= S229), V243 (≠ T232), K342 (≠ D330)
- binding (3-oxidanylidene-3-sodiooxy-propanoyl)oxysodium: A32 (≠ P24), T33 (≠ V25), C34 (≠ I26), P36 (= P28), D103 (≠ E92), E189 (≠ G178), Q190 (≠ E179), F218 (≠ S207), I339 (= I327), D340 (≠ N328)
- binding 3-(2-phenylimidazo[1,2-a]pyridin-6-yl)benzenecarbonitrile: G118 (≠ F106), D141 (= D129), N143 (= N134), N451 (= N440), L453 (≠ E442), A455 (≠ M444)
7a6qA Crystal structure of human aldehyde dehydrogenase 1a3 in complex with selective nr6 inhibitor compound (see paper)
36% identity, 98% coverage: 3:477/483 of query aligns to 10:488/489 of 7a6qA
- active site: N163 (= N152), E262 (= E250), C296 (= C284), E470 (≠ A459)
- binding nicotinamide-adenine-dinucleotide: I159 (≠ V148), T160 (≠ L149), W162 (= W151), K186 (= K175), A188 (≠ S177), E189 (≠ G178), G219 (= G208), G223 (= G212), S240 (= S229), V243 (≠ T232), K342 (≠ D330), K346 (≠ H334)
- binding 3-(2-phenylimidazo[1,2-a]pyridin-6-yl)benzenecarbonitrile: G118 (≠ F106), D141 (= D129), N143 (= N134), N451 (= N440), L453 (≠ E442), Y454 (≠ A443)
Query Sequence
>WP_013133826.1 NCBI__GCF_000092245.1:WP_013133826.1
MSEKRVYEMYINGEFVSNKGETTPVINPSTKEIISYIPKGNAEDAKVAIDAAHNAQDAWA
KLPAVERGNYLRKIAQKIRENSDMLAKTITQEQGKVLGLAEVEVNFTADYLDYMAEWARR
YEGEIIQSDRPNENIFLFKLPIGVATGVLPWNFPFFLIARKLAPALLTGNTIVIKPSGET
PNNAFEFAKLVDQIDLPKGVFNLVSGSGSTVGNELAANEKVGIVSFTGSVPTGVKIMEAA
SKNVTKVSLELGGKAPAIVMADANLDIAVEAIKNSRVTNNGQVCNCAERVYVHKSIAKEF
TDRITKSMAALTCGNPLTEKIDMGPLINEDAITHVQKLVDSAVAAGASITTGGKRCDRDD
GYFYEPTVVIDVKQDMDIIKEEIFGPVLPIVTFDTLDEAIALANDSEFGLTSSIYTQNLD
IAMRACKEIKCGETYINRENFEAMQGFHAGWKKSGIGGADGKHGLEEFLQTKVVYLQYDL
NKQ
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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