SitesBLAST
Comparing WP_012707665.1 NCBI__GCF_000018545.1:WP_012707665.1 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)
2f2aA Structure of tRNA-dependent amidotransferase gatcab complexed with gln (see paper)
48% identity, 94% coverage: 19:481/493 of query aligns to 18:473/485 of 2f2aA
- active site: K79 (= K79), S154 (= S159), S155 (= S160), S173 (≠ T178), T175 (= T180), G176 (= G181), G177 (= G182), S178 (= S183), Q181 (= Q186)
- binding glutamine: G130 (= G130), S154 (= S159), D174 (= D179), T175 (= T180), G176 (= G181), S178 (= S183), F206 (= F211), Y309 (= Y314), Y310 (= Y315), R358 (= R362), D425 (= D432)
2dqnA Structure of tRNA-dependent amidotransferase gatcab complexed with asn (see paper)
48% identity, 94% coverage: 19:481/493 of query aligns to 18:473/485 of 2dqnA
- active site: K79 (= K79), S154 (= S159), S155 (= S160), S173 (≠ T178), T175 (= T180), G176 (= G181), G177 (= G182), S178 (= S183), Q181 (= Q186)
- binding asparagine: M129 (= M129), G130 (= G130), T175 (= T180), G176 (= G181), S178 (= S183), Y309 (= Y314), Y310 (= Y315), R358 (= R362), D425 (= D432)
3h0mA Structure of tRNA-dependent amidotransferase gatcab from aquifex aeolicus (see paper)
47% identity, 98% coverage: 4:487/493 of query aligns to 2:472/478 of 3h0mA
- active site: K72 (= K79), S147 (= S159), S148 (= S160), S166 (≠ T178), T168 (= T180), G169 (= G181), G170 (= G182), S171 (= S183), Q174 (= Q186)
- binding glutamine: M122 (= M129), G123 (= G130), D167 (= D179), T168 (= T180), G169 (= G181), G170 (= G182), S171 (= S183), F199 (= F211), Y302 (= Y314), R351 (= R362), D418 (= D432)
3h0lA Structure of tRNA-dependent amidotransferase gatcab from aquifex aeolicus (see paper)
47% identity, 98% coverage: 4:487/493 of query aligns to 2:472/478 of 3h0lA
- active site: K72 (= K79), S147 (= S159), S148 (= S160), S166 (≠ T178), T168 (= T180), G169 (= G181), G170 (= G182), S171 (= S183), Q174 (= Q186)
- binding asparagine: G123 (= G130), S147 (= S159), G169 (= G181), G170 (= G182), S171 (= S183), Y302 (= Y314), R351 (= R362), D418 (= D432)
3kfuE Crystal structure of the transamidosome (see paper)
43% identity, 97% coverage: 11:486/493 of query aligns to 4:459/468 of 3kfuE
4n0iA Crystal structure of s. Cerevisiae mitochondrial gatfab in complex with glutamine (see paper)
36% identity, 82% coverage: 70:474/493 of query aligns to 29:443/450 of 4n0iA
- active site: K38 (= K79), S116 (= S159), S117 (= S160), T135 (= T178), T137 (= T180), G138 (= G181), G139 (= G182), S140 (= S183), L143 (≠ Q186)
- binding glutamine: G89 (= G130), T137 (= T180), G138 (= G181), S140 (= S183), Y168 (≠ F211), Y271 (= Y314), Y272 (= Y315), R320 (= R362), D404 (= D432)
1m21A Crystal structure analysis of the peptide amidase pam in complex with the competitive inhibitor chymostatin (see paper)
33% identity, 96% coverage: 9:482/493 of query aligns to 8:477/487 of 1m21A
- active site: K81 (= K79), S160 (= S159), S161 (= S160), T179 (= T178), T181 (= T180), D182 (≠ G181), G183 (= G182), S184 (= S183), C187 (≠ Q186)
- binding : A129 (= A128), N130 (≠ M129), F131 (≠ G130), C158 (≠ G157), G159 (= G158), S160 (= S159), S184 (= S183), C187 (≠ Q186), I212 (≠ F211), R318 (≠ Y315), L321 (≠ A318), L365 (≠ M364), F426 (≠ I433)
6c6gA An unexpected vestigial protein complex reveals the evolutionary origins of an s-triazine catabolic enzyme. Inhibitor bound complex. (see paper)
30% identity, 95% coverage: 16:481/493 of query aligns to 10:448/457 of 6c6gA
Q84DC4 Mandelamide hydrolase; EC 3.5.1.86 from Pseudomonas putida (Arthrobacter siderocapsulatus) (see 2 papers)
30% identity, 98% coverage: 4:486/493 of query aligns to 25:492/507 of Q84DC4
- T31 (≠ A10) mutation to I: More active on the (S)-enantiomers of mandelamide and lactamide than the (R)-enantiomers; when associated with N-437.
- K100 (= K79) mutation to A: Abolishes activity on mandelamide.
- S180 (= S159) mutation to A: Significantly decreases activity on mandelamide.
- S181 (= S160) mutation to A: Significantly decreases activity on mandelamide.
- G202 (= G181) mutation to A: Increase in KM values for aromatic substrates, but not aliphatic substrates. Active against lactamide but not against mandelamide; when associated with H-207 and E-382.; mutation to V: Increase in KM values for aromatic substrates, but not aliphatic substrates.
- S204 (= S183) mutation to A: Abolishes activity on mandelamide.
- Q207 (= Q186) mutation to H: Increases activity on lactamide, does not affect activity on mandelamide; when associated with E-382. Active against lactamide but not against mandelamide; when associated with A-202 and E-382. More active on the (S)-enantiomers of mandelamide and lactamide than the (R)-enantiomers; when associated with S-316 and N-437.
- S316 (≠ L311) mutation to N: More active on the (S)-enantiomers of mandelamide and lactamide than the (R)-enantiomers; when associated with H-207 and N-437.
- Q382 (≠ D376) mutation to H: Increases activity on lactamide, does not affect activity on mandelamide; when associated with H-207. Active against lactamide but not against mandelamide; when associated with A-202 and H-207.
- I437 (≠ T437) mutation to N: More active on the (S)-enantiomers of mandelamide and lactamide than the (R)-enantiomers. More active on the (S)-enantiomers of mandelamide and lactamide than the (R)-enantiomers; when associated with I-31. More active on the (S)-enantiomers of mandelamide and lactamide than the (R)-enantiomers; when associated with H-207 and N-316.
Q7XJJ7 Fatty acid amide hydrolase; AtFAAH; N-acylethanolamine amidohydrolase; EC 3.5.1.99 from Arabidopsis thaliana (Mouse-ear cress) (see 2 papers)
29% identity, 87% coverage: 56:484/493 of query aligns to 181:591/607 of Q7XJJ7
- K205 (= K79) mutation to A: Loss of activity.
- SS 281:282 (= SS 159:160) mutation to AA: Loss of activity.
- GGGS 302:305 (≠ TGGS 180:183) binding substrate
- S305 (= S183) mutation to A: Loss of activity.
- R307 (= R185) mutation to A: Loss of activity.
- S360 (≠ V238) mutation to A: No effect.
6diiH Structure of arabidopsis fatty acid amide hydrolase in complex with methyl linolenyl fluorophosphonate (see paper)
29% identity, 87% coverage: 56:484/493 of query aligns to 181:591/616 of 6diiH
- binding methyl-9Z,12Z,15Z-octadecatrienylphosphonofluoridate: G255 (≠ A128), T258 (≠ S131), S281 (= S159), G302 (≠ T180), G303 (= G181), S305 (= S183), S472 (≠ T367), I532 (≠ M428), M539 (vs. gap)
Sites not aligning to the query:
8ey9B Structure of arabidopsis fatty acid amide hydrolase mutant s305a in complex with 9-hydroxy-10,12-octadecadienoyl-ethanolamide
28% identity, 87% coverage: 56:484/493 of query aligns to 181:591/605 of 8ey9B
- binding (9R,10E,12Z)-9-hydroxy-N-(2-hydroxyethyl)octadeca-10,12-dienamide: G255 (≠ A128), G302 (≠ T180), G303 (= G181), G304 (= G182), A305 (≠ S183), V442 (≠ Y315), I475 (≠ L370), M539 (vs. gap)
Sites not aligning to the query:
8ey1D Structure of arabidopsis fatty acid amide hydrolase mutant s305a in complex with n-(3-oxododecanoyl)-l-homoserine lactone
28% identity, 87% coverage: 56:484/493 of query aligns to 181:591/605 of 8ey1D
3a1iA Crystal structure of rhodococcus sp. N-771 amidase complexed with benzamide (see paper)
28% identity, 94% coverage: 26:487/493 of query aligns to 32:503/508 of 3a1iA
- active site: K95 (= K79), S170 (= S159), S171 (= S160), G189 (≠ T178), Q191 (≠ T180), G192 (= G181), G193 (= G182), A194 (≠ S183), I197 (≠ Q186)
- binding benzamide: F145 (≠ M129), S146 (≠ G130), G147 (≠ S131), Q191 (≠ T180), G192 (= G181), G193 (= G182), A194 (≠ S183), W327 (≠ Y314)
4yjiA The crystal structure of a bacterial aryl acylamidase belonging to the amidase signature (as) enzymes family (see paper)
27% identity, 92% coverage: 10:465/493 of query aligns to 9:457/490 of 4yjiA
- active site: K79 (= K79), S158 (= S159), S159 (= S160), G179 (≠ T180), G180 (= G181), G181 (= G182), A182 (≠ S183)
- binding n-(4-hydroxyphenyl)acetamide (tylenol): L81 (= L81), G132 (≠ A128), S158 (= S159), G179 (≠ T180), G180 (= G181), A182 (≠ S183)
5h6sC Crystal structure of hydrazidase s179a mutant complexed with a substrate (see paper)
26% identity, 98% coverage: 5:487/493 of query aligns to 3:450/457 of 5h6sC
- active site: K77 (= K79), S152 (= S159), S153 (= S160), L173 (≠ T180), G174 (= G181), G175 (= G182), S176 (= S183)
- binding 4-oxidanylbenzohydrazide: C126 (≠ A128), R128 (≠ G130), W129 (≠ S131), S152 (= S159), L173 (≠ T180), G174 (= G181), S176 (= S183), W306 (≠ G296), F338 (≠ Y347)
Q936X2 Allophanate hydrolase; EC 3.5.1.54 from Pseudomonas sp. (strain ADP) (see paper)
28% identity, 90% coverage: 26:470/493 of query aligns to 39:450/605 of Q936X2
- K91 (= K79) mutation to A: Loss of activity.
- S165 (≠ L154) mutation to A: Loss of activity.
- S189 (= S183) mutation to A: Loss of activity.
Q9FR37 Amidase 1; AtAMI1; Translocon at the outer membrane of chloroplasts 64-I; AtTOC64-I; EC 3.5.1.4 from Arabidopsis thaliana (Mouse-ear cress) (see paper)
39% identity, 33% coverage: 71:233/493 of query aligns to 28:191/425 of Q9FR37
- K36 (= K79) active site, Charge relay system; mutation to A: Loss of catalytic activity.; mutation to R: Reduces catalytic activity 10-fold.
- S113 (= S159) active site, Charge relay system; mutation S->A,T: Loss of catalytic activity.
- S114 (= S160) mutation to A: Loss of catalytic activity.; mutation to T: Reduces catalytic activity 400-fold.
- D133 (= D179) mutation to A: Loss of catalytic activity.; mutation to E: Reduces catalytic activity 600-fold.
- S137 (= S183) active site, Acyl-ester intermediate; mutation to A: Reduces catalytic activity 170-fold.; mutation to T: Loss of catalytic activity.
- C145 (≠ T191) mutation C->A,S: Reduces catalytic activity 10-fold.
Sites not aligning to the query:
- 214 S→T: Slightly reduces catalytic activity.
6te4A Structural insights into pseudomonas aeruginosa type six secretion system exported effector 8: tse8 in complex with a peptide (see paper)
29% identity, 61% coverage: 3:305/493 of query aligns to 1:341/564 of 6te4A
Sites not aligning to the query:
3a2qA Structure of 6-aminohexanoate cyclic dimer hydrolase complexed with substrate (see paper)
33% identity, 53% coverage: 10:268/493 of query aligns to 7:259/482 of 3a2qA
- active site: K69 (= K79), S147 (= S159), S148 (= S160), N166 (≠ T178), A168 (≠ T180), A169 (≠ G181), G170 (= G182), A171 (≠ S183), I174 (≠ Q186)
- binding 6-aminohexanoic acid: G121 (≠ A128), G121 (≠ A128), N122 (≠ M129), S147 (= S159), A168 (≠ T180), A168 (≠ T180), A169 (≠ G181), A171 (≠ S183)
Sites not aligning to the query:
Query Sequence
>WP_012707665.1 NCBI__GCF_000018545.1:WP_012707665.1
MTDLTRLTIAEARAKLSAKEITAVELTDAYIGAIEAANETINAYVTVTPEKARAMAKASD
ARIAAGKAGALEGIPLGIKDLFGTEGVHTQACSHILDGFRPRYESTVTQNLWNDGAVMLG
KLNMDEFAMGSSNETSYYGPVKNPWRAKGSNMDLVPGGSSGGSAAAVAAYLCAGATATDT
GGSIRQPAAFTGTVGIKPTYGRCSRWGVVAFASSLDQAGPIARDVRDAAILLKSMASVDL
KDTTSVDLPVPDYEASIGQSIKGMKIGIPKEYRVDGMPEEIEALWQQGIAWLKEAGAEIV
DITLPHTKYALPAYYIVAPAEASSNLARYDGVRYGLRVDGKDIVDMYEKTRAAGFGREVK
RRIMIGTYVLSAGYYDAYYLRAQKVRSLIKRDFELAFQAGVDAILTPATPSSAFGIADED
LASDPVKMYLNDIFTVTVNMAGLPGIAVPGGLDHKGLPLGLQLIGKPFDEETLFKTAHVI
EQAAGRFAPSKWW
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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