SitesBLAST
Comparing 17649 FitnessBrowser__Keio:17649 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)
P37685 Aldehyde dehydrogenase B; Acetaldehyde dehydrogenase; EC 1.2.1.4 from Escherichia coli (strain K12) (see paper)
100% identity, 100% coverage: 1:512/512 of query aligns to 1:512/512 of P37685
- R197 (= R197) mutation to E: Less than 10% of wild-type acetaldehyde dehydrogenase activity.
9kokA Crystal structure of exac, an NAD+-dependent aldehyde dehydrogenase, from pseudomonas aeruginosa (see paper)
67% identity, 98% coverage: 12:512/512 of query aligns to 7:507/507 of 9kokA
- binding nicotinamide-adenine-dinucleotide: I162 (= I167), I163 (= I168), P164 (= P169), W165 (= W170), K189 (= K194), E192 (≠ R197), G221 (= G226), G225 (= G230), E226 (= E231), F239 (= F244), T240 (= T245), G241 (= G246), S242 (= S247), V245 (= V250), E263 (= E268), G265 (= G270), C302 (= C307), Q349 (= Q354), K352 (≠ T357), E403 (= E408), F405 (= F410)
O14293 Putative aldehyde dehydrogenase-like protein C9E9.09c; EC 1.2.1.- from Schizosaccharomyces pombe (strain 972 / ATCC 24843) (Fission yeast) (see paper)
44% identity, 94% coverage: 28:509/512 of query aligns to 26:503/503 of O14293
- S248 (= S247) modified: Phosphoserine
- S501 (≠ K507) modified: Phosphoserine
P05091 Aldehyde dehydrogenase, mitochondrial; ALDH class 2; ALDH-E2; ALDHI; EC 1.2.1.3 from Homo sapiens (Human) (see 5 papers)
43% identity, 94% coverage: 28:507/512 of query aligns to 40:515/517 of P05091
- E337 (= E325) to V: in dbSNP:rs1062136
- E496 (≠ K488) to K: in allele ALDH2*3; dbSNP:rs769724893
- E504 (≠ Q496) to K: in AMEDS; allele ALDH2*2; drastic reduction of enzyme activity; dbSNP:rs671
Sites not aligning to the query:
5l13A Structure of aldh2 in complex with 2p3 (see paper)
43% identity, 94% coverage: 28:507/512 of query aligns to 17:492/494 of 5l13A
- active site: N163 (= N171), K186 (= K194), E262 (= E268), C296 (= C307), E393 (= E408), E470 (= E485)
- binding 2,3,5-trimethyl-6-propyl-7H-furo[3,2-g][1]benzopyran-7-one: F164 (= F172), M168 (= M176), W171 (= W179), F290 (= F301), C295 (≠ V306), C296 (= C307), C297 (≠ T308), D451 (≠ H466), F453 (≠ Y468)
4kwgA Crystal structure analysis of aldh2+aldib13 (see paper)
43% identity, 94% coverage: 28:507/512 of query aligns to 17:492/494 of 4kwgA
- active site: N163 (= N171), K186 (= K194), E262 (= E268), C296 (= C307), E393 (= E408), E470 (= E485)
- binding 7-bromo-5-methyl-1H-indole-2,3-dione: F164 (= F172), M168 (= M176), C295 (≠ V306), C296 (= C307), C297 (≠ T308), D451 (≠ H466), F453 (≠ Y468)
4kwfA Crystal structure analysis of aldh2+aldib33 (see paper)
43% identity, 94% coverage: 28:507/512 of query aligns to 17:492/494 of 4kwfA
- active site: N163 (= N171), K186 (= K194), E262 (= E268), C296 (= C307), E393 (= E408), E470 (= E485)
- binding 1-benzyl-1H-indole-2,3-dione: F164 (= F172), M168 (= M176), W171 (= W179), E262 (= E268), C295 (≠ V306), C296 (= C307), C297 (≠ T308), D451 (≠ H466), F453 (≠ Y468), F459 (= F474)
3sz9A Crystal structure of human aldh2 modified with the beta-elimination product of aldi-3; 1-(4-ethylbenzene)prop-2-en-1-one (see paper)
43% identity, 94% coverage: 28:507/512 of query aligns to 17:492/494 of 3sz9A
- active site: N163 (= N171), K186 (= K194), E262 (= E268), C296 (= C307), E393 (= E408), E470 (= E485)
- binding 1-(4-ethylphenyl)propan-1-one: F164 (= F172), C295 (≠ V306), C296 (= C307), D451 (≠ H466), F453 (≠ Y468), F459 (= F474)
3injA Human mitochondrial aldehyde dehydrogenase complexed with agonist alda-1 (see paper)
43% identity, 94% coverage: 28:507/512 of query aligns to 17:492/494 of 3injA
- active site: N163 (= N171), K186 (= K194), E262 (= E268), C296 (= C307), E393 (= E408), E470 (= E485)
- binding N-(1,3-benzodioxol-5-ylmethyl)-2,6-dichlorobenzamide: M118 (≠ L126), F164 (= F172), L167 (= L175), F286 (= F296), F290 (= F301), D451 (≠ H466), F453 (≠ Y468)
2vleA The structure of daidzin, a naturally occurring anti alcohol- addiction agent, in complex with human mitochondrial aldehyde dehydrogenase (see paper)
43% identity, 94% coverage: 28:507/512 of query aligns to 17:492/494 of 2vleA
- active site: N163 (= N171), K186 (= K194), E262 (= E268), C296 (= C307), E393 (= E408), E470 (= E485)
- binding daidzin: M118 (≠ L126), F164 (= F172), M168 (= M176), W171 (= W179), F286 (= F296), F290 (= F301), C295 (≠ V306), C296 (= C307), D451 (≠ H466), V452 (≠ A467), F453 (≠ Y468)
1o01B Human mitochondrial aldehyde dehydrogenase complexed with crotonaldehyde, NAD(h) and mg2+ (see paper)
43% identity, 94% coverage: 28:507/512 of query aligns to 17:492/494 of 1o01B
- active site: N163 (= N171), K186 (= K194), E262 (= E268), C296 (= C307), E393 (= E408), E470 (= E485)
- binding (2e)-but-2-enal: C296 (= C307), C297 (≠ T308), F453 (≠ Y468)
- binding nicotinamide-adenine-dinucleotide: I159 (= I167), I160 (= I168), P161 (= P169), W162 (= W170), K186 (= K194), E189 (≠ R197), G219 (= G226), G223 (= G230), A224 (≠ E231), F237 (= F244), G239 (= G246), S240 (= S247), I243 (≠ V250), L263 (= L269), G264 (= G270), C296 (= C307), Q343 (= Q354), E393 (= E408), F395 (= F410)
1cw3A Human mitochondrial aldehyde dehydrogenase complexed with NAD+ and mn2+ (see paper)
43% identity, 94% coverage: 28:507/512 of query aligns to 17:492/494 of 1cw3A
- active site: N163 (= N171), K186 (= K194), E262 (= E268), C296 (= C307), E393 (= E408), E470 (= E485)
- binding magnesium ion: V34 (≠ L45), D103 (= D111), Q190 (≠ L198)
- binding nicotinamide-adenine-dinucleotide: I159 (= I167), I160 (= I168), P161 (= P169), W162 (= W170), K186 (= K194), G219 (= G226), G223 (= G230), A224 (≠ E231), F237 (= F244), G239 (= G246), S240 (= S247), I243 (≠ V250), L263 (= L269), G264 (= G270), C296 (= C307), Q343 (= Q354), K346 (≠ T357), E393 (= E408), F395 (= F410)
4fr8C Crystal structure of human aldehyde dehydrogenase-2 in complex with nitroglycerin (see paper)
42% identity, 94% coverage: 28:507/512 of query aligns to 19:494/496 of 4fr8C
- active site: N165 (= N171), K188 (= K194), Q264 (≠ E268), C298 (= C307), E395 (= E408), E472 (= E485)
- binding nicotinamide-adenine-dinucleotide: I161 (= I167), I162 (= I168), W164 (= W170), K188 (= K194), G221 (= G226), G225 (= G230), A226 (≠ E231), F239 (= F244), G241 (= G246), S242 (= S247), I245 (≠ V250), Q345 (= Q354), E395 (= E408), F397 (= F410)
4fr8A Crystal structure of human aldehyde dehydrogenase-2 in complex with nitroglycerin (see paper)
42% identity, 94% coverage: 28:507/512 of query aligns to 16:491/493 of 4fr8A
- active site: N162 (= N171), K185 (= K194), Q261 (≠ E268), C295 (= C307), E392 (= E408), E469 (= E485)
- binding nicotinamide-adenine-dinucleotide: I158 (= I167), I159 (= I168), W161 (= W170), K185 (= K194), G218 (= G226), G222 (= G230), A223 (≠ E231), F236 (= F244), G238 (= G246), S239 (= S247), I242 (≠ V250), Q342 (= Q354), K345 (≠ T357), E392 (= E408), F394 (= F410)
- binding propane-1,2,3-triyl trinitrate: F163 (= F172), L166 (= L175), W170 (= W179), F289 (= F301), S294 (≠ V306), C295 (= C307), D450 (≠ H466), F452 (≠ Y468)
P20000 Aldehyde dehydrogenase, mitochondrial; ALDH class 2; ALDH-E2; ALDHI; EC 1.2.1.3 from Bos taurus (Bovine) (see 2 papers)
43% identity, 94% coverage: 28:507/512 of query aligns to 43:518/520 of P20000
Sites not aligning to the query:
- 1:21 modified: transit peptide, Mitochondrion
1nzwA Cys302ser mutant of human mitochondrial aldehyde dehydrogenase complexed with nadh and mg2+ (see paper)
43% identity, 94% coverage: 28:507/512 of query aligns to 17:492/494 of 1nzwA
- active site: N163 (= N171), K186 (= K194), E262 (= E268), S296 (≠ T308), E393 (= E408), E470 (= E485)
- binding 1,4-dihydronicotinamide adenine dinucleotide: I159 (= I167), I160 (= I168), P161 (= P169), K186 (= K194), E189 (≠ R197), G219 (= G226), P220 (≠ G227), G223 (= G230), A224 (≠ E231), F237 (= F244), G239 (= G246), S240 (= S247), I243 (≠ V250), E262 (= E268), G264 (= G270), S296 (≠ T308), Q343 (= Q354), E393 (= E408), F395 (= F410)
2onmA Human mitochondrial aldehyde dehydrogenase asian variant, aldh2 2, Complexed with NAD+ (see paper)
43% identity, 91% coverage: 28:494/512 of query aligns to 17:479/494 of 2onmA
- active site: N163 (= N171), K186 (= K194), E262 (= E268), C296 (= C307), E393 (= E408), E470 (= E485)
- binding adenosine-5'-diphosphate: E189 (≠ R197), G219 (= G226), G223 (= G230), A224 (≠ E231), F237 (= F244), G239 (= G246), S240 (= S247), I243 (≠ V250)
7radA Crystal structure analysis of aldh1b1
42% identity, 94% coverage: 28:507/512 of query aligns to 16:491/493 of 7radA
- binding nicotinamide-adenine-dinucleotide: I158 (= I167), I159 (= I168), P160 (= P169), W161 (= W170), N162 (= N171), M167 (= M176), K185 (= K194), E188 (≠ R197), G218 (= G226), G222 (= G230), A223 (≠ E231), T237 (= T245), G238 (= G246), S239 (= S247), V242 (= V250), E261 (= E268), L262 (= L269), C295 (= C307), E392 (= E408), F394 (= F410)
- binding 3-(2-methoxyphenyl)-1-(4-phenylphenyl)-6,7,8,9-tetrahydro-5~{H}-imidazo[1,2-a][1,3]diazepine: L113 (≠ A122), E117 (≠ L126), F163 (= F172), E285 (= E294), F289 (= F301), N450 (≠ H466), V452 (≠ Y468)
7mjdA Crystal structure analysis of aldh1b1
42% identity, 94% coverage: 28:507/512 of query aligns to 16:491/493 of 7mjdA
- binding nicotinamide-adenine-dinucleotide: I158 (= I167), I159 (= I168), P160 (= P169), W161 (= W170), N162 (= N171), M167 (= M176), K185 (= K194), E188 (≠ R197), G218 (= G226), G222 (= G230), F236 (= F244), T237 (= T245), G238 (= G246), S239 (= S247), V242 (= V250), E261 (= E268), L262 (= L269), C295 (= C307), E392 (= E408), F394 (= F410)
- binding 8-(2-methoxyphenyl)-10-(4-phenylphenyl)-1$l^{4},8-diazabicyclo[5.3.0]deca-1(7),9-diene: E117 (≠ L126), E285 (= E294), F289 (= F301), N450 (≠ H466), V452 (≠ Y468)
7mjcA Crystal structure analysis of aldh1b1
42% identity, 94% coverage: 28:507/512 of query aligns to 16:491/493 of 7mjcA
- binding nicotinamide-adenine-dinucleotide: I158 (= I167), I159 (= I168), P160 (= P169), W161 (= W170), N162 (= N171), K185 (= K194), E188 (≠ R197), G218 (= G226), G222 (= G230), T237 (= T245), G238 (= G246), S239 (= S247), V242 (= V250), E261 (= E268), L262 (= L269), C295 (= C307), E392 (= E408), F394 (= F410)
Query Sequence
>17649 FitnessBrowser__Keio:17649
MTNNPPSAQIKPGEYGFPLKLKARYDNFIGGEWVAPADGEYYQNLTPVTGQLLCEVASSG
KRDIDLALDAAHKVKDKWAHTSVQDRAAILFKIADRMEQNLELLATAETWDNGKPIRETS
AADVPLAIDHFRYFASCIRAQEGGISEVDSETVAYHFHEPLGVVGQIIPWNFPLLMASWK
MAPALAAGNCVVLKPARLTPLSVLLLMEIVGDLLPPGVVNVVNGAGGVIGEYLATSKRIA
KVAFTGSTEVGQQIMQYATQNIIPVTLELGGKSPNIFFADVMDEEDAFFDKALEGFALFA
FNQGEVCTCPSRALVQESIYERFMERAIRRVESIRSGNPLDSVTQMGAQVSHGQLETILN
YIDIGKKEGADVLTGGRRKLLEGELKDGYYLEPTILFGQNNMRVFQEEIFGPVLAVTTFK
TMEEALELANDTQYGLGAGVWSRNGNLAYKMGRGIQAGRVWTNCYHAYPAHAAFGGYKQS
GIGRETHKMMLEHYQQTKCLLVSYSDKPLGLF
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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