SitesBLAST
Comparing GFF2617 FitnessBrowser__WCS417:GFF2617 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)
Q3L181 Perakine reductase; EC 1.1.1.317 from Rauvolfia serpentina (Serpentine wood) (Ophioxylon serpentinum) (see paper)
41% identity, 95% coverage: 5:316/328 of query aligns to 4:317/337 of Q3L181
- D52 (= D52) mutation to A: 99% loss of activity.
- Y57 (= Y57) mutation to A: 99% loss of activity.
- K84 (= K82) mutation to A: Total loss of activity.
- H126 (= H124) mutation to A: 98% loss of activity.
3v0sA Crystal structure of perakine reductase, founder member of a novel akr subfamily with unique conformational changes during NADPH binding (see paper)
39% identity, 91% coverage: 5:304/328 of query aligns to 4:273/287 of 3v0sA
- active site: D45 (= D52), Y50 (= Y57), G87 (≠ I92), H119 (= H124)
- binding 2'-monophosphoadenosine-5'-diphosphate: S198 (≠ C203), P199 (= P204), I200 (≠ L205), G201 (= G206), L204 (≠ F209), P246 (= P277), G247 (= G278), T248 (= T279), T249 (≠ K280), N253 (≠ Y284), N256 (≠ E287), N257 (= N288)
O14295 Pyridoxal reductase; PL reductase; PL-red; EC 1.1.1.65 from Schizosaccharomyces pombe (strain 972 / ATCC 24843) (Fission yeast) (see paper)
31% identity, 95% coverage: 10:322/328 of query aligns to 5:327/333 of O14295
- S292 (≠ E287) modified: Phosphoserine
P80874 Aldo-keto reductase YhdN; AKR11B; General stress protein 69; GSP69; EC 1.1.1.- from Bacillus subtilis (strain 168) (see paper)
31% identity, 92% coverage: 6:308/328 of query aligns to 5:310/331 of P80874
- TW 20:21 (vs. gap) binding NADP(+)
- D52 (= D52) binding NADP(+)
- Q175 (= Q174) binding NADP(+)
- YGSLCR 203:208 (≠ FCPLGR 202:207) binding NADP(+)
- K214 (= K213) binding NADP(+)
- R227 (= R226) binding NADP(+)
- GAR 280:282 (≠ GTK 278:280) binding NADP(+)
- Q286 (≠ Y284) binding NADP(+)
8hnqA The structure of a alcohol dehydrogenase akr13b2 with NADP
35% identity, 88% coverage: 12:298/328 of query aligns to 23:279/286 of 8hnqA
- binding nadp nicotinamide-adenine-dinucleotide phosphate: G31 (= G20), M33 (= M22), R34 (vs. gap), Y71 (= Y57), R138 (= R125), Q187 (= Q174), W214 (≠ F202), A215 (≠ C203), P216 (= P204), L217 (= L205), S219 (≠ R207), G220 (= G208), I257 (= I276), P258 (= P277), G259 (= G278), T260 (= T279), K262 (≠ R281), H265 (≠ Y284), E268 (= E287), N269 (= N288)
- binding 1,4,7,10,13,16-hexaoxacyclooctadecane: L98 (≠ F85), W106 (≠ V93), R138 (= R125)
1pz1A Structure of NADPH-dependent family 11 aldo-keto reductase akr11b(holo) (see paper)
31% identity, 92% coverage: 6:308/328 of query aligns to 5:310/333 of 1pz1A
- active site: D52 (= D52), Y57 (= Y57), K90 (≠ V88), Q93 (= Q91), H125 (= H124)
- binding nadp nicotinamide-adenine-dinucleotide phosphate: G19 (= G20), W21 (vs. gap), Q175 (= Q174), Y203 (≠ F202), G204 (≠ C203), L206 (= L205), R208 (= R207), K214 (= K213), G280 (= G278), R282 (≠ K280), Q286 (≠ Y284)
P46336 Aldo-keto reductase IolS; AKR11A; Vegetative protein 147; VEG147; EC 1.1.1.- from Bacillus subtilis (strain 168) (see paper)
31% identity, 92% coverage: 7:309/328 of query aligns to 6:310/310 of P46336
1pz0A Structure of NADPH-dependent family 11 aldo-keto reductase akr11a(holo) (see paper)
31% identity, 92% coverage: 7:309/328 of query aligns to 5:309/311 of 1pz0A
- active site: D52 (= D52), Y57 (= Y57), N91 (≠ G90), H124 (= H124)
- binding nadp nicotinamide-adenine-dinucleotide phosphate: H124 (= H124), Q174 (= Q174), Y202 (≠ F202), F203 (≠ C203), P204 (= P204), L205 (= L205), S207 (≠ R207), G208 (= G208), A211 (≠ T211), K213 (= K213)
4aubB The complex structure of the bacterial aldo-keto reductase akr14a1 with NADP and citrate (see paper)
33% identity, 87% coverage: 8:291/328 of query aligns to 17:303/335 of 4aubB
- binding nadp nicotinamide-adenine-dinucleotide phosphate: G29 (= G20), W31 (= W27), D59 (= D52), Y64 (= Y57), H136 (= H124), Q191 (= Q174), F220 (= F202), T221 (≠ C203), P222 (= P204), L223 (= L205), Q225 (≠ R207), G226 (= G208), K231 (= K213), R241 (= R226), R244 (≠ D229), L288 (≠ I276), G290 (= G278), S292 (≠ K280), Q296 (≠ Y284), E299 (= E287), N300 (= N288)
Sites not aligning to the query:
8jwmB Crystal structure of akrtyl-NADP-tylosin complex (see paper)
35% identity, 89% coverage: 7:299/328 of query aligns to 6:310/331 of 8jwmB
- binding nadp nicotinamide-adenine-dinucleotide phosphate: G19 (= G20), M21 (= M22), D48 (= D52), Y53 (= Y57), N161 (≠ E155), Q186 (= Q174), W214 (≠ F202), S215 (≠ C203), P216 (= P204), L217 (= L205), G219 (≠ R207), G220 (= G208), R235 (vs. gap), R236 (≠ K213), A237 (= A214), I287 (= I276), G289 (= G278), R291 (≠ K280), Q295 (≠ Y284), S298 (≠ E287)
- binding tylosin: Y53 (= Y57), W55 (≠ P59), H130 (= H124), C192 (≠ W180), E193 (= E181), R195 (≠ N183), G240 (≠ A217), R241 (≠ T218), Q250 (≠ R231), E253 (= E234), Q254 (≠ E235), R257 (≠ S246)
Sites not aligning to the query:
8jwkD The second purified state crystal structure of akrtyl (see paper)
35% identity, 89% coverage: 7:299/328 of query aligns to 6:293/314 of 8jwkD
- binding nadph dihydro-nicotinamide-adenine-dinucleotide phosphate: G19 (= G20), M21 (= M22), D48 (= D52), Y53 (= Y57), H130 (= H124), Q186 (= Q174), W214 (≠ F202), S215 (≠ C203), P216 (= P204), L217 (= L205), I270 (= I276), G272 (= G278), R274 (≠ K280), Q278 (≠ Y284), S281 (≠ E287)
8jwoL Crystal structure of akrtyl-tylosin complex (see paper)
35% identity, 89% coverage: 7:299/328 of query aligns to 6:290/311 of 8jwoL
Sites not aligning to the query:
8jwkH The second purified state crystal structure of akrtyl (see paper)
34% identity, 92% coverage: 7:308/328 of query aligns to 6:295/307 of 8jwkH
- binding nadph dihydro-nicotinamide-adenine-dinucleotide phosphate: G19 (= G20), M21 (= M22), D48 (= D52), Y53 (= Y57), H129 (= H124), N160 (≠ E155), Q185 (= Q174), W213 (≠ F202), S214 (≠ C203), P215 (= P204), L216 (= L205), G218 (≠ R207), I263 (= I276), G265 (= G278), R267 (≠ K280), Q271 (≠ Y284), S274 (≠ E287)
3n6qD Crystal structure of yghz from e. Coli (see paper)
32% identity, 87% coverage: 8:291/328 of query aligns to 18:290/315 of 3n6qD
6ow0A Crystal structure of mithramycin 3-side chain keto-reductase mtmw in complex with NAD+ and peg (see paper)
35% identity, 80% coverage: 6:267/328 of query aligns to 5:275/323 of 6ow0A
- binding nadp nicotinamide-adenine-dinucleotide phosphate: G19 (= G20), L21 (≠ M22), D49 (= D52), Y54 (= Y57), S151 (≠ C154), Y204 (≠ F202), F205 (≠ C203), L207 (= L205), Q209 (≠ R207), G210 (= G208), T213 (= T211), K215 (= K213), R227 (= R226)
Sites not aligning to the query:
8tf1A Crystal structure of pyridoxal reductase (pdxi)in complex with NADPH and pyridoxal
33% identity, 91% coverage: 3:299/328 of query aligns to 5:276/286 of 8tf1A
- binding magnesium ion: M22 (= M22), Q23 (vs. gap), G255 (= G278)
- binding nadp nicotinamide-adenine-dinucleotide phosphate: G20 (= G20), M22 (= M22), Q23 (vs. gap), D55 (= D52), Y60 (= Y57), K85 (= K82), R127 (≠ H124), Q183 (= Q174), F210 (= F202), F211 (≠ C203), P212 (= P204), M236 (≠ A259), I253 (= I276), G255 (= G278), T256 (= T279), S257 (≠ K280), H261 (≠ Y284), E264 (= E287), N265 (= N288)
- binding 4,5-bis(hydroxymethyl)-2-methyl-pyridin-3-ol: W96 (≠ V93), R127 (≠ H124)
P77256 NADH-specific methylglyoxal reductase; AKR11B2; EC 1.1.1.- from Escherichia coli (strain K12) (see paper)
31% identity, 96% coverage: 2:317/328 of query aligns to 1:326/326 of P77256
- D232 (≠ H219) mutation D->A,E: Converts the protein into an enzyme with dual specificity, i.e. that is able to use both NADPH and NADH as cosubstrates.
4aubE The complex structure of the bacterial aldo-keto reductase akr14a1 with NADP and citrate (see paper)
31% identity, 87% coverage: 8:291/328 of query aligns to 18:278/297 of 4aubE
- binding nadp nicotinamide-adenine-dinucleotide phosphate: G30 (= G20), W32 (= W27), D60 (= D52), Y65 (= Y57), Q192 (= Q174), F221 (= F202), T222 (≠ C203), P223 (= P204), L224 (= L205), Q226 (≠ R207), T230 (= T211), K232 (= K213), L263 (≠ I276), G265 (= G278), S267 (≠ K280), Q271 (≠ Y284), E274 (= E287), N275 (= N288)
Sites not aligning to the query:
1ynqB Aldo-keto reductase akr11c1 from bacillus halodurans (holo form) (see paper)
29% identity, 92% coverage: 7:307/328 of query aligns to 7:287/298 of 1ynqB
- active site: D47 (= D52), Y52 (= Y57), K86 (≠ Q91), H120 (= H124)
- binding beta-D-fructofuranose: N44 (= N49), D71 (≠ E76)
- binding nadph dihydro-nicotinamide-adenine-dinucleotide phosphate: G20 (= G20), C21 (= C21), M22 (= M22), S23 (≠ G23), D47 (= D52), Y52 (= Y57), K77 (= K82), S150 (≠ C154), M170 (≠ Q174), R197 (≠ F202), G198 (≠ C203), P199 (= P204), V200 (≠ L205), R202 (= R207), S206 (≠ T211), R208 (≠ K213), A255 (≠ I276), A256 (≠ P277), G257 (= G278), S259 (≠ K280), Q263 (≠ Y284), N267 (= N288)
Sites not aligning to the query:
1ynpB Aldo-keto reductase akr11c1 from bacillus halodurans (apo form) (see paper)
29% identity, 92% coverage: 7:307/328 of query aligns to 7:287/298 of 1ynpB
Sites not aligning to the query:
Query Sequence
>GFF2617 FitnessBrowser__WCS417:GFF2617
MVSTITLGTQGLQVGRIGLGCMGMSQWYGATDDNESLRTLHRALELGVNFFDSAEAYGPF
TNERLLQRAFAGRRGEVVIATKFGFRIVDGQIVGVDSSESNLQRVVEASLKRLGTDYIDV
LYQHRLDPTVPIEEVVGAMGRLVEQGKVKYLGLCEVGTRTIERAHATHPISVIQGEYSLW
ERNVEQEILPLLHNLGIGYVAFCPLGRGFLTGKAASATHYDANDFRQQDPRFREENFAAN
TFLTESILALADSWSMTPAQLALAWLLTRSPHLAVIPGTKRVAYLEENVAADACVLNDEQ
SHAIQALLGQWAVAGERYEQRMMQFIDR
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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