SitesBLAST
Comparing WP_020173974.1 NCBI__GCF_000385335.1:WP_020173974.1 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)
P15770 Shikimate dehydrogenase (NADP(+)); SD; SDH; EC 1.1.1.25 from Escherichia coli (strain K12) (see paper)
39% identity, 94% coverage: 10:274/282 of query aligns to 6:268/272 of P15770
1nytA Shikimate dehydrogenase aroe complexed with NADP+ (see paper)
39% identity, 94% coverage: 10:274/282 of query aligns to 6:268/271 of 1nytA
- binding nadp nicotinamide-adenine-dinucleotide phosphate: K65 (= K69), D102 (= D105), G128 (= G133), G129 (= G134), A130 (= A135), N149 (= N155), R150 (= R156), T151 (= T157), R154 (= R160), T188 (= T194), S189 (= S195), S190 (≠ L196), M213 (≠ I220), G237 (= G243), M240 (= M246), L241 (= L247)
Q5HNV1 Shikimate dehydrogenase (NADP(+)); SDH; EC 1.1.1.25 from Staphylococcus epidermidis (strain ATCC 35984 / RP62A) (see paper)
35% identity, 92% coverage: 7:265/282 of query aligns to 2:254/269 of Q5HNV1
- SLS 13:15 (≠ SRS 18:20) binding shikimate
- T60 (= T65) binding shikimate
- N85 (= N90) binding shikimate
- D100 (= D105) binding shikimate
- Y211 (= Y222) Plays a major role in the catalytic process and a minor role in the substrate binding; mutation to F: Leads to a 345-fold decrease in the catalytic efficiency and a 3-fold decrease in the affinity binding for shikimate.
- Q239 (= Q250) binding shikimate
Q9KVT3 Shikimate dehydrogenase (NADP(+)); SDH; EC 1.1.1.25 from Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961)
38% identity, 93% coverage: 1:263/282 of query aligns to 1:261/278 of Q9KVT3
- SKS 18:20 (≠ SRS 18:20) binding shikimate
- N90 (= N90) binding shikimate
- D106 (= D105) binding shikimate
- NRTFAK 154:159 (≠ NRTLER 155:160) binding NADP(+)
- Q248 (= Q250) binding shikimate
3pgjA 2.49 angstrom resolution crystal structure of shikimate 5- dehydrogenase (aroe) from vibrio cholerae o1 biovar eltor str. N16961 in complex with shikimate
39% identity, 90% coverage: 10:263/282 of query aligns to 6:257/272 of 3pgjA
- binding (3r,4s,5r)-3,4,5-trihydroxycyclohex-1-ene-1-carboxylic acid: S14 (= S18), S16 (= S20), N59 (= N63), T61 (= T65), K65 (= K69), N86 (= N90), D102 (= D105), Q244 (= Q250)
3dooA Crystal structure of shikimate dehydrogenase from staphylococcus epidermidis complexed with shikimate (see paper)
34% identity, 92% coverage: 7:265/282 of query aligns to 2:245/258 of 3dooA
- binding (3r,4s,5r)-3,4,5-trihydroxycyclohex-1-ene-1-carboxylic acid: S13 (= S18), S15 (= S20), N58 (= N63), T60 (= T65), K64 (= K69), N85 (= N90), D100 (= D105), F227 (≠ L247), Q230 (= Q250)
2hk9B Crystal structure of shikimate dehydrogenase from aquifex aeolicus in complex with shikimate and NADP+ at 2.2 angstrom resolution (see paper)
36% identity, 89% coverage: 10:260/282 of query aligns to 11:252/267 of 2hk9B
- binding nadp nicotinamide-adenine-dinucleotide phosphate: V67 (≠ L66), G130 (= G131), G133 (= G134), A134 (= A135), N153 (= N155), R154 (= R156), T155 (= T157), K158 (≠ R160), T188 (= T194), S189 (= S195), V190 (≠ L196), I214 (= I220), M238 (= M246), L239 (= L247)
- binding (3r,4s,5r)-3,4,5-trihydroxycyclohex-1-ene-1-carboxylic acid: S19 (= S18), S21 (= S20), N64 (= N63), T66 (= T65), K70 (= K69), N91 (= N90), D106 (= D105), Y216 (= Y222), L239 (= L247), Q242 (= Q250)
2hk9A Crystal structure of shikimate dehydrogenase from aquifex aeolicus in complex with shikimate and NADP+ at 2.2 angstrom resolution (see paper)
36% identity, 89% coverage: 10:260/282 of query aligns to 11:252/269 of 2hk9A
- binding 2'-monophosphoadenosine-5'-diphosphate: V67 (≠ L66), G132 (= G133), G133 (= G134), A134 (= A135), N153 (= N155), R154 (= R156), T155 (= T157), T188 (= T194), S189 (= S195), V190 (≠ L196)
- binding (3r,4s,5r)-3,4,5-trihydroxycyclohex-1-ene-1-carboxylic acid: S19 (= S18), S21 (= S20), N64 (= N63), K70 (= K69), N91 (= N90), D106 (= D105), Y216 (= Y222), L239 (= L247), Q242 (= Q250)
O67049 Shikimate dehydrogenase (NADP(+)); SD; SDH; EC 1.1.1.25 from Aquifex aeolicus (strain VF5) (see paper)
36% identity, 89% coverage: 10:260/282 of query aligns to 11:252/269 of O67049
- SLS 19:21 (≠ SRS 18:20) binding shikimate
- D82 (≠ E81) binding NADP(+)
- N91 (= N90) binding shikimate
- D106 (= D105) binding shikimate
- GAGGA 130:134 (= GAGGA 131:135) binding NADP(+)
- I214 (= I220) binding NADP(+)
- Y216 (= Y222) binding shikimate
- G235 (= G243) binding NADP(+)
- Q242 (= Q250) binding shikimate
3sefC 2.4 angstrom resolution crystal structure of shikimate 5-dehydrogenase (aroe) from vibrio cholerae o1 biovar eltor str. N16961 in complex with shikimate and NADPH
37% identity, 90% coverage: 10:263/282 of query aligns to 6:230/244 of 3sefC
3sefA 2.4 angstrom resolution crystal structure of shikimate 5-dehydrogenase (aroe) from vibrio cholerae o1 biovar eltor str. N16961 in complex with shikimate and NADPH
38% identity, 90% coverage: 10:263/282 of query aligns to 6:253/268 of 3sefA
1nvtB Crystal structure of shikimate dehydrogenase (aroe or mj1084) in complex with NADP+ (see paper)
33% identity, 94% coverage: 10:274/282 of query aligns to 16:283/287 of 1nvtB
- active site: K75 (= K69), D111 (= D105)
- binding nadp nicotinamide-adenine-dinucleotide phosphate: I72 (≠ L66), G135 (≠ A132), G137 (= G134), G138 (≠ A135), A139 (= A136), N157 (= N155), R158 (= R156), T159 (= T157), K162 (≠ R160), A200 (≠ T193), T201 (= T194), P202 (≠ S195), I203 (≠ L196), M205 (= M198), L229 (≠ I220), Y231 (= Y222), M255 (= M246), L256 (= L247)
- binding zinc ion: E22 (≠ K16), H23 (= H17)
1nvtA Crystal structure of shikimate dehydrogenase (aroe or mj1084) in complex with NADP+ (see paper)
33% identity, 94% coverage: 10:274/282 of query aligns to 16:283/287 of 1nvtA
- active site: K75 (= K69), D111 (= D105)
- binding nadp nicotinamide-adenine-dinucleotide phosphate: G135 (≠ A132), A139 (= A136), N157 (= N155), R158 (= R156), T159 (= T157), K162 (≠ R160), A200 (≠ T193), T201 (= T194), P202 (≠ S195), I203 (≠ L196), M205 (= M198), L229 (≠ I220), Y231 (= Y222), G252 (= G243), M255 (= M246), L256 (= L247)
Q58484 Shikimate dehydrogenase (NADP(+)); SDH; EC 1.1.1.25 from Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) (Methanococcus jannaschii) (see paper)
33% identity, 94% coverage: 10:274/282 of query aligns to 11:278/282 of Q58484
P43876 Shikimate dehydrogenase (NADP(+)); SDH; EC 1.1.1.25 from Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) (see paper)
32% identity, 94% coverage: 10:274/282 of query aligns to 6:265/272 of P43876
3tnlA 1.45 angstrom crystal structure of shikimate 5-dehydrogenase from listeria monocytogenes in complex with shikimate and NAD.
31% identity, 88% coverage: 10:258/282 of query aligns to 15:273/288 of 3tnlA
- binding nicotinamide-adenine-dinucleotide: M71 (≠ L66), G134 (= G131), A135 (= A132), G136 (= G133), G137 (= G134), A138 (= A135), N158 (= N155), R159 (= R156), D161 (≠ L158), F163 (vs. gap), T207 (= T194), V209 (≠ L196), M211 (= M198), F214 (≠ L204), V235 (≠ I220), Y237 (= Y222), M261 (= M246), M262 (≠ L247)
- binding (3r,4s,5r)-3,4,5-trihydroxycyclohex-1-ene-1-carboxylic acid: S23 (= S18), S25 (= S20), N68 (= N63), S70 (≠ T65), K74 (= K69), N95 (= N90), D110 (= D105), Q265 (= Q250)
3tozA 2.2 angstrom crystal structure of shikimate 5-dehydrogenase from listeria monocytogenes in complex with NAD.
31% identity, 88% coverage: 10:258/282 of query aligns to 18:276/291 of 3tozA
- binding nicotinamide-adenine-dinucleotide: G137 (= G131), A138 (= A132), G139 (= G133), G140 (= G134), A141 (= A135), N161 (= N155), R162 (= R156), D164 (≠ L158), F166 (vs. gap), T210 (= T194), G211 (≠ S195), V212 (≠ L196), M214 (= M198), F217 (≠ L204), V238 (≠ I220), Y240 (= Y222), G261 (= G243), M264 (= M246), M265 (≠ L247)
Q8Y9N5 Shikimate dehydrogenase (NADP(+)); SDH; EC 1.1.1.25 from Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e)
31% identity, 88% coverage: 10:258/282 of query aligns to 18:276/291 of Q8Y9N5
1npdB X-ray structure of shikimate dehydrogenase complexed with NAD+ from e.Coli (ydib) northeast structural genomics research consortium (nesg) target er24 (see paper)
31% identity, 89% coverage: 10:261/282 of query aligns to 12:273/288 of 1npdB
- binding nicotinamide-adenine-dinucleotide: A132 (= A132), G133 (= G133), G134 (= G134), A135 (= A135), N155 (= N155), R156 (= R156), D158 (≠ L158), F160 (vs. gap), T204 (= T194), K205 (≠ S195), V206 (≠ L196), M208 (= M198), C232 (≠ I220), M258 (= M246), L259 (= L247)
P0A6D5 Quinate/shikimate dehydrogenase; NAD-dependent shikimate 5-dehydrogenase; EC 1.1.1.282 from Escherichia coli (strain K12) (see 4 papers)
31% identity, 89% coverage: 10:261/282 of query aligns to 12:273/288 of P0A6D5
- S22 (= S20) mutation to A: Kinetically unchanged as compared with the wild-type.
- Y39 (= Y37) mutation to F: Kinetically unchanged as compared with the wild-type.
- S67 (≠ T65) mutation to A: Reduces activity towards quinate about 6-fold, but has a little effect on shikimate conversion.
- K71 (= K69) mutation to A: 3200-fold decrease in the affinity for quinate. 170-fold decrease in the affinity for shikimate.; mutation to G: 10-fold greater reduction in catalytic efficiency is observed with quinate than with shikimate.
- N92 (= N90) mutation to A: Alters protein structure. Loss of activity for both substrates.
- T106 (= T104) mutation to A: 2000-fold decrease in the affinity for quinate. 70-fold decrease in the affinity for shikimate. 10-fold greater reduction in catalytic efficiency is observed with quinate than with shikimate.
- D107 (= D105) mutation to A: Loss of activity towards quinate. 20000-fold decrease in the affinity for shikimate.
- AGGA 132:135 (= AGGA 132:135) binding NAD(+)
- NRRD 155:158 (≠ NRTL 155:158) binding NAD(+)
- K205 (≠ S195) binding NAD(+)
- CVYN 232:235 (≠ IVYV 220:223) binding NAD(+)
- G255 (= G243) binding NAD(+)
- Q262 (= Q250) mutation to A: 3-fold reduction in catalytic efficiency for both substrates.
Sites not aligning to the query:
- 1 modified: Initiator methionine, Removed
Query Sequence
>WP_020173974.1 NCBI__GCF_000385335.1:WP_020173974.1
MSTNPPRACVIGWPVKHSRSPLIHTYWLQQLGIEGSYGRAEVAPADFQNFVSHLAEKGYR
GGNVTLPHKEMAYRLATRRTERADSLQAVNTLWIEGGELWGDNTDIIGFLGGLDAEVQGW
EKTGDKAVVLGAGGAARAIVQALLLRNIKNILIFNRTLERAEELARLFGSGVTARPWQQL
GESLAGVDLLVNTTSLGMAGQPPLDIDLSALPSYAVVDDIVYVPLETPLLAQAHRRGLRT
VGGLSMLLHQAVPGFEHWFGQRPEVTPELLALIEADVTSTPK
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