SitesBLAST
Comparing BWI76_RS27515 BWI76_RS27515 glycerol kinase 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)
P0A6F3 Glycerol kinase; ATP:glycerol 3-phosphotransferase; Glycerokinase; GK; EC 2.7.1.30 from Escherichia coli (strain K12) (see 8 papers)
94% identity, 100% coverage: 1:502/503 of query aligns to 1:502/502 of P0A6F3
- M1 (= M1) modified: Initiator methionine, Removed
- T14 (= T14) binding
- S59 (= S59) mutation to W: Abolishes inhibition of GK by FBP via disruption of the dimer-tetramer assembly reaction. Inhibition by EIIA-Glc is unchanged compared to wild type. The activity of this mutant is significantly higher than wild-type, and the Michaelis constants are increased slightly compared to wild-type.
- A66 (= A66) mutation to T: Although it completely abolishes FBP regulation and disrupts dimer-tetramer equilibrium, the crystal structure is essentially identical to the symmetric tetramer found in the FBP-bound form of the enzyme.
- Y136 (= Y136) binding
- G231 (= G231) mutation to D: Displays an increased enzymatic activity and a decreased allosteric regulation by FBP compared to wild-type. It displays a dimer form and is resistant to tetramer formation in the presence of FBP, whereas wild-type dimers are converted into inactive tetramers in the presence of FBP.
- K233 (= K233) modified: N6-malonyllysine
- G235 (= G235) binding
- R237 (= R237) binding ; mutation to A: Drastically reduces inhibition of GK by FBP and lowers, but did not eliminate, the ability of FBP to promote tetramer association.
- G305 (= G305) mutation to S: In glpK22; abolishes glucose control of glycerol utilization.
- I475 (= I475) mutation to D: It decreases Vmax to about 10% of the wild-type value and the affinity for substrate is increased about two- to fourfold. This mutation decreases the catalytic activity in a manner that is analogous to that obtained upon EIIA-Glc binding. It increases the affinity for FBP about fivefold.
- R480 (= R480) mutation to D: It decreases Vmax to about 10% of the wild-type value and the affinity for substrate is increased about two- to fourfold. This mutation decreases the catalytic activity in a manner that is analogous to that obtained upon EIIA-Glc binding. Regulation by FBP is not affected by this substitution. No inhibition by EIIA-Glc is observed, which is consistent with a decrease in affinity for EIIA-Glc of about 250-fold.
1bu6Y Crystal structures of escherichia coli glycerol kinase and the mutant a65t in an inactive tetramer: conformational changes and implications for allosteric regulation (see paper)
93% identity, 99% coverage: 3:501/503 of query aligns to 1:499/499 of 1bu6Y
1glfO Crystal structures of escherichia coli glycerol kinase and the mutant a65t in an inactive tetramer: conformational changes and implications for allosteric regulation (see paper)
94% identity, 99% coverage: 3:500/503 of query aligns to 1:498/498 of 1glfO
- binding adenosine-5'-diphosphate: T12 (= T14), R16 (= R18), G265 (= G267), T266 (= T268), G309 (= G311), I312 (= I314), Q313 (= Q315), A325 (= A327), Y326 (≠ F328), G409 (= G411), G410 (= G412), A411 (= A413), N414 (= N416)
- binding glycerol: T12 (= T14), Q81 (= Q83), R82 (= R84), E83 (= E85), W102 (= W104), Y134 (= Y136), D244 (= D246), Q245 (= Q247), F269 (= F271)
- binding phosphate ion: G232 (= G234), G233 (= G235), R235 (= R237)
1bo5O Crystal structure of the complex between escherichia coli glycerol kinase and the allosteric regulator fructose 1,6-bisphosphate. (see paper)
94% identity, 99% coverage: 3:500/503 of query aligns to 1:498/498 of 1bo5O
- binding 1,6-di-O-phosphono-beta-D-fructofuranose: G232 (= G234), G233 (= G235), R235 (= R237)
- binding glycerol: Q81 (= Q83), R82 (= R84), E83 (= E85), W102 (= W104), Y134 (= Y136), D244 (= D246), Q245 (= Q247), F269 (= F271)
1gllO Escherichia coli glycerol kinase mutant with bound atp analog showing substantial domain motion (see paper)
93% identity, 99% coverage: 3:500/503 of query aligns to 1:494/494 of 1gllO
- binding phosphomethylphosphonic acid adenylate ester: G11 (= G13), T12 (= T14), T13 (= T15), G261 (= G267), T262 (= T268), G305 (= G311), I308 (= I314), Q309 (= Q315), A321 (= A327), Y322 (≠ F328), S324 (= S330), G406 (= G412), A407 (= A413), N410 (= N416)
- binding glycerol: Q81 (= Q83), R82 (= R84), E83 (= E85), W102 (= W104), Y134 (= Y136), D240 (= D246), Q241 (= Q247), F265 (= F271)
1gljO Escherichia coli glycerol kinase mutant with bound atp analog showing substantial domain motion (see paper)
93% identity, 99% coverage: 3:500/503 of query aligns to 1:494/494 of 1gljO
- binding gamma-arsono-beta, gamma-methyleneadenosine-5'-diphosphate: G11 (= G13), T12 (= T14), T13 (= T15), G261 (= G267), T262 (= T268), G305 (= G311), A306 (= A312), I308 (= I314), Q309 (= Q315), A321 (= A327), Y322 (≠ F328), S324 (= S330), G406 (= G412), A407 (= A413), N410 (= N416)
- binding glycerol: Q81 (= Q83), R82 (= R84), E83 (= E85), W102 (= W104), Y134 (= Y136), D240 (= D246), Q241 (= Q247), F265 (= F271)
1bwfO Escherichia coli glycerol kinase mutant with bound atp analog showing substantial domain motion (see paper)
93% identity, 99% coverage: 3:500/503 of query aligns to 1:494/494 of 1bwfO
- binding phosphodifluoromethylphosphonic acid-adenylate ester: G11 (= G13), T12 (= T14), T13 (= T15), G261 (= G267), T262 (= T268), G305 (= G311), I308 (= I314), Q309 (= Q315), A321 (= A327), Y322 (≠ F328), S324 (= S330), G405 (= G411), G406 (= G412), A407 (= A413), N410 (= N416)
- binding glycerol: Q81 (= Q83), R82 (= R84), E83 (= E85), W102 (= W104), Y134 (= Y136), D240 (= D246), Q241 (= Q247), F265 (= F271)
1gldG Cation promoted association (cpa) of a regulatory and target protein is controlled by phosphorylation (see paper)
92% identity, 99% coverage: 5:500/503 of query aligns to 1:489/489 of 1gldG
- binding adenosine-5'-diphosphate: G9 (= G13), T11 (= T15), R14 (= R18), Y255 (= Y266), G256 (= G267), T257 (= T268), G300 (= G311), I303 (= I314), Q304 (= Q315), A316 (= A327), Y317 (≠ F328), S319 (= S330), G400 (= G411), G401 (= G412), A402 (= A413), N405 (= N416)
- binding glyceraldehyde-3-phosphate: G9 (= G13), T10 (= T14), Q79 (= Q83), R80 (= R84), E81 (= E85), W100 (= W104), Y132 (= Y136), D235 (= D246), Q236 (= Q247), T257 (= T268), F260 (= F271)
- binding manganese (ii) ion: D7 (= D11), R14 (= R18), D235 (= D246)
1glcG Cation promoted association (cpa) of a regulatory and target protein is controlled by phosphorylation (see paper)
92% identity, 99% coverage: 5:500/503 of query aligns to 1:489/489 of 1glcG