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Comparing WP_015449135.1 NCBI__GCF_000230695.2:WP_015449135.1 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)
P26276 Phosphomannomutase/phosphoglucomutase; PMM / PGM; EC 5.4.2.2; EC 5.4.2.8 from Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) (see 10 papers)
59% identity, 59% coverage: 316:770/770 of query aligns to 12:463/463 of P26276
- R15 (= R319) mutation to A: KM halves, decreases processivity as dissociation of G1,6P intermediate increases 25-fold.
- Y17 (= Y321) binding alpha-D-glucose 1-phosphate; binding alpha-D-mannose 1-phosphate
- R20 (= R324) mutation to A: No phosphoglucomutase activity.
- S108 (= S412) binding via phosphate group; modified: Phosphoserine; mutation S->A,V: About 5% activity, still subject to substrate inhibition and requires G1,6P as an activator; phosphorylation occurs at a different site.; mutation to C: KM for G1P unchanged, kcat decreases 24-fold; G1,6P stimulates reaction by 2-3 orders of magnitude. No stable protein phosphorylation detected, altered ligation of metal residue.
- N110 (= N414) mutation to A: KM halves, decreases processivity as dissociation of G1,6P intermediate increases 30-fold.
- D242 (= D547) binding Mg(2+)
- D244 (= D549) binding Mg(2+)
- D246 (= D551) binding Mg(2+)
- R247 (= R552) mutation to A: Small reduction in KM, small increase in dissociation of G1,6P intermediate.
- R262 (= R567) mutation to A: Increases KM 2-fold, decreases kcat 9-fold for G1P. Alters flexibility of the hinge region.
- K285 (= K590) binding alpha-D-glucose 1-phosphate
- H308 (= H613) binding alpha-D-glucose 1-phosphate; binding alpha-D-mannose 1-phosphate
- E325 (= E630) mutation to A: Reduces KM and Vmax approximately 2-fold.
- EMSGH 325:329 (= EMSGH 630:634) binding alpha-D-glucose 1-phosphate; binding alpha-D-mannose 1-phosphate
- H329 (= H634) mutation to A: No phosphoglucomutase activity using G1P as substrate, protein is less easily phosphorylated, no significant change in structure.
- P368 (= P675) mutation to G: Increases KM 2-fold, decreases kcat 6-fold for G1P. Alters flexibility of the hinge region, structure is less compact.
- R421 (= R728) mutation to C: Loss of phosphomannomutase activity, very low phosphoglucomutase activity.
- RASNT 421:425 (= RASNT 728:732) binding alpha-D-glucose 1-phosphate; binding alpha-D-mannose 1-phosphate
Sites not aligning to the query:
- 1 modified: Initiator methionine, Removed
Q02E40 Phosphomannomutase/phosphoglucomutase; PMM / PGM; EC 5.4.2.2; EC 5.4.2.8 from Pseudomonas aeruginosa (strain UCBPP-PA14) (see paper)
59% identity, 59% coverage: 316:770/770 of query aligns to 12:463/463 of Q02E40
- S108 (= S412) active site, Non-phosphorylated intermediate; modified: Phosphoserine
1pcjX Enzyme-ligand complex of p. Aeruginosa pmm/pgm (see paper)
59% identity, 59% coverage: 316:770/770 of query aligns to 7:458/458 of 1pcjX
- active site: R15 (= R324), S103 (= S412), H104 (= H413), K113 (= K422), D237 (= D547), D239 (= D549), D241 (= D551), R242 (= R552), H324 (= H634), D335 (= D645)
- binding 1-O-phosphono-alpha-D-mannopyranose: Y12 (= Y321), S103 (= S412), T301 (= T611), G302 (= G612), E320 (= E630), S322 (= S632), H324 (= H634), R416 (= R728), S418 (= S730), N419 (= N731), T420 (= T732)
- binding zinc ion: S103 (= S412), D237 (= D547), D239 (= D549), D241 (= D551)
2h5aX Complex of the enzyme pmm/pgm with xylose 1-phosphate (see paper)
59% identity, 59% coverage: 316:770/770 of query aligns to 4:455/455 of 2h5aX
- active site: H101 (= H413), D234 (= D547), D236 (= D549), D238 (= D551), R239 (= R552), D332 (= D645)
- binding 1-O-phosphono-alpha-D-xylopyranose: Y9 (= Y321), T298 (= T611), G299 (= G612), H300 (= H613), E317 (= E630), S319 (= S632), H321 (= H634), R413 (= R728), S415 (= S730), N416 (= N731), T417 (= T732)
- binding zinc ion: S100 (= S412), D234 (= D547), D236 (= D549), D238 (= D551)
2h4lX Complex of pmm/pgm with ribose 1-phosphate (see paper)
59% identity, 59% coverage: 316:770/770 of query aligns to 4:455/455 of 2h4lX
- active site: H101 (= H413), D234 (= D547), D236 (= D549), D238 (= D551), R239 (= R552), D332 (= D645)
- binding 1-O-phosphono-alpha-D-ribofuranose: Y9 (= Y321), R12 (= R324), S100 (= S412), T298 (= T611), E317 (= E630), R413 (= R728), S415 (= S730), N416 (= N731), T417 (= T732)
- binding zinc ion: S100 (= S412), D234 (= D547), D236 (= D549), D238 (= D551)
2fkfA Phosphomannomutase/phosphoglucomutase from pseudomonas aeruginosa with alpha-d-glucose 1,6-bisphosphate bound (see paper)
59% identity, 59% coverage: 316:770/770 of query aligns to 4:455/455 of 2fkfA
- active site: R12 (= R324), S100 (= S412), H101 (= H413), K110 (= K422), D234 (= D547), D236 (= D549), D238 (= D551), R239 (= R552), H321 (= H634), D332 (= D645)
- binding 1,6-di-O-phosphono-alpha-D-glucopyranose: R7 (= R319), H101 (= H413), S319 (= S632), R413 (= R728), S415 (= S730), N416 (= N731), T417 (= T732)
- binding zinc ion: S100 (= S412), D234 (= D547), D236 (= D549), D238 (= D551)
1pcmX Enzyme-ligand complex of p. Aeruginosa pmm/pgm (see paper)
59% identity, 59% coverage: 316:770/770 of query aligns to 4:455/455 of 1pcmX
- active site: R12 (= R324), S100 (= S412), H101 (= H413), K110 (= K422), D234 (= D547), D236 (= D549), D238 (= D551), R239 (= R552), H321 (= H634), D332 (= D645)
- binding 6-O-phosphono-alpha-D-mannopyranose: Y9 (= Y321), S100 (= S412), T298 (= T611), G299 (= G612), H300 (= H613), E317 (= E630), S319 (= S632), H321 (= H634), R413 (= R728), S415 (= S730)
- binding zinc ion: S100 (= S412), D234 (= D547), D236 (= D549), D238 (= D551)
1p5gX Enzyme-ligand complex of p. Aeruginosa pmm/pgm (see paper)
59% identity, 59% coverage: 316:770/770 of query aligns to 4:455/455 of 1p5gX
- active site: R12 (= R324), S100 (= S412), H101 (= H413), K110 (= K422), D234 (= D547), D236 (= D549), D238 (= D551), R239 (= R552), H321 (= H634), D332 (= D645)
- binding 6-O-phosphono-alpha-D-glucopyranose: Y9 (= Y321), S100 (= S412), K277 (= K590), G299 (= G612), H300 (= H613), E317 (= E630), S319 (= S632), H321 (= H634), R413 (= R728), S415 (= S730), N416 (= N731), T417 (= T732)
- binding zinc ion: S100 (= S412), D234 (= D547), D236 (= D549), D238 (= D551)
1p5dX Enzyme-ligand complex of p. Aeruginosa pmm/pgm (see paper)
59% identity, 59% coverage: 316:770/770 of query aligns to 4:455/455 of 1p5dX
- active site: R12 (= R324), S100 (= S412), H101 (= H413), K110 (= K422), D234 (= D547), D236 (= D549), D238 (= D551), R239 (= R552), H321 (= H634), D332 (= D645)
- binding 1-O-phosphono-alpha-D-glucopyranose: Y9 (= Y321), S100 (= S412), R239 (= R552), T298 (= T611), G299 (= G612), H300 (= H613), E317 (= E630), S319 (= S632), H321 (= H634), R413 (= R728), S415 (= S730), T417 (= T732)
- binding zinc ion: S100 (= S412), D234 (= D547), D236 (= D549), D238 (= D551)
1k2yX Crystal structure of phosphomannomutase/phosphoglucomutase s108a mutant from p. Aeruginosa (see paper)
59% identity, 59% coverage: 316:770/770 of query aligns to 8:459/459 of 1k2yX
4il8A Crystal structure of an h329a mutant of p. Aeruginosa pmm/pgm (see paper)
59% identity, 59% coverage: 316:770/770 of query aligns to 8:459/459 of 4il8A
- active site: R16 (= R324), S104 (= S412), H105 (= H413), K114 (= K422), D238 (= D547), D240 (= D549), D242 (= D551), R243 (= R552), A325 (≠ H634), D336 (= D645)
- binding magnesium ion: S104 (= S412), D238 (= D547), D240 (= D549), D242 (= D551)
3rsmA Crystal structure of s108c mutant of pmm/pgm (see paper)
56% identity, 59% coverage: 316:770/770 of query aligns to 1:436/436 of 3rsmA
- active site: C87 (≠ S412), K91 (= K422), D215 (= D547), D217 (= D549), D219 (= D551), R220 (= R552), H302 (= H634), D313 (= D645)
- binding phosphate ion: C87 (≠ S412), D215 (= D547), D217 (= D549), D219 (= D551), R220 (= R552)
- binding zinc ion: D215 (= D547), D217 (= D549), D219 (= D551)
3uw2A X-ray crystal structure of phosphoglucomutase/phosphomannomutase family protein (bth_i1489)from burkholderia thailandensis (see paper)
55% identity, 59% coverage: 313:770/770 of query aligns to 2:458/458 of 3uw2A
- active site: R13 (= R324), S109 (= S412), H110 (= H413), K119 (= K422), D243 (= D547), D245 (= D549), D247 (= D551), R248 (= R552), H330 (= H634)
- binding zinc ion: D243 (= D547), D245 (= D549), D247 (= D551)
1wqaA Crystal structure of pyrococcus horikoshii phosphomannomutase/phosphoglucomutase complexed with mg2+
32% identity, 55% coverage: 316:742/770 of query aligns to 3:433/455 of 1wqaA
- active site: R11 (= R324), S101 (= S412), H102 (= H413), K111 (= K422), D243 (= D547), D245 (= D549), D247 (= D551), R248 (= R552), G330 (≠ H634), R340 (≠ D645)
- binding magnesium ion: S101 (= S412), D243 (= D547), D245 (= D549), D247 (= D551)
6nqhA Xanthomonas citri dephospho-pgm in complex with xylose-1-phosphate
33% identity, 57% coverage: 318:754/770 of query aligns to 6:442/448 of 6nqhA
- active site: R12 (= R324), S97 (= S412), H98 (= H413), K107 (= K422), D237 (= D547), D239 (= D549), D241 (= D551), R242 (= R552), H324 (= H634)
- binding magnesium ion: D237 (= D547), D239 (= D549), D241 (= D551)
- binding 1-O-phosphono-alpha-D-xylopyranose: R12 (= R324), S97 (= S412), H98 (= H413), K107 (= K422), D239 (= D549), R242 (= R552), R280 (≠ K590), S301 (≠ T611), G302 (= G612), E320 (= E630), S322 (= S632), H324 (= H634), R414 (= R728), S416 (= S730), N417 (= N731), T418 (= T732), R423 (≠ V737)
6np8A Xanthomonas citri phospho-pgm in complex with mannose-6-phosphate (see paper)
33% identity, 57% coverage: 318:754/770 of query aligns to 6:442/448 of 6np8A
- active site: R12 (= R324), S97 (= S412), H98 (= H413), K107 (= K422), D237 (= D547), D239 (= D549), D241 (= D551), R242 (= R552), H324 (= H634)
- binding calcium ion: S97 (= S412), D237 (= D547), D239 (= D549), D241 (= D551)
- binding 6-O-phosphono-alpha-D-mannopyranose: Y9 (= Y321), R280 (≠ K590), G302 (= G612), H303 (= H613), E320 (= E630), S322 (= S632), H324 (= H634), R414 (= R728), S416 (= S730), N417 (= N731), T418 (= T732), R423 (≠ V737)
6nolA Xanthomonas citri dephospho-pgm in complex with mannose-1-phosphate (see paper)
33% identity, 57% coverage: 318:754/770 of query aligns to 6:442/448 of 6nolA
- active site: R12 (= R324), S97 (= S412), H98 (= H413), K107 (= K422), D237 (= D547), D239 (= D549), D241 (= D551), R242 (= R552), H324 (= H634)
- binding 1-O-phosphono-alpha-D-mannopyranose: G302 (= G612), E320 (= E630), S322 (= S632), H324 (= H634), R414 (= R728), S416 (= S730), N417 (= N731), T418 (= T732), R423 (≠ V737)
- binding magnesium ion: S97 (= S412), D237 (= D547), D239 (= D549), D241 (= D551)
6nnpA Xanthomonas citri dephospho-pgm in complex with glucose-6-phosphate (see paper)
33% identity, 57% coverage: 318:754/770 of query aligns to 6:442/448 of 6nnpA
- active site: R12 (= R324), S97 (= S412), H98 (= H413), K107 (= K422), D237 (= D547), D239 (= D549), D241 (= D551), R242 (= R552), H324 (= H634)
- binding 6-O-phosphono-alpha-D-glucopyranose: R280 (≠ K590), G302 (= G612), H303 (= H613), E320 (= E630), H324 (= H634), R414 (= R728), S416 (= S730), N417 (= N731), T418 (= T732), R423 (≠ V737)
- binding magnesium ion: S97 (= S412), D237 (= D547), D239 (= D549), D241 (= D551)
6nn2A Xanthomonas citri pgm apo-phospho (see paper)
33% identity, 57% coverage: 318:754/770 of query aligns to 6:442/448 of 6nn2A
- active site: R12 (= R324), S97 (= S412), H98 (= H413), K107 (= K422), D237 (= D547), D239 (= D549), D241 (= D551), R242 (= R552), H324 (= H634)
- binding calcium ion: S97 (= S412), D237 (= D547), D239 (= D549), D241 (= D551)
6n1eA Crystal structure of x. Citri phosphoglucomutase in complex with 1- methyl-glucose 6-phosphate (see paper)
33% identity, 57% coverage: 318:754/770 of query aligns to 6:442/448 of 6n1eA
Query Sequence
>WP_015449135.1 NCBI__GCF_000230695.2:WP_015449135.1
MALNIANERLRNLRVDWRDLLPLAGGTALLLLGLFCAWQTWLIADEGNAVRRVHLAQDEA
VRALAAEIASQRGAVEKVLASVDPATLMSDPAQSAAALRRQLPQAKKLELYSGELTEVLK
ANYREFGYAKAAQLMAAQSAEGLPLAQSVSYGNGDRRLSLVIPLGPPQRAQAWAWVELPF
APLRQRFDAISPAGGRLDLRQGDDRGYVQLLSHGTRSAEAEATGKPVAGSVFSVGAGLPG
AFIVLPRWWLLSGLLALLGLGGGGYLLRLRQRWKALPEVEEPEVPLPARQTAPARAKPPE
PPEPPAAAPVVGVDPSIFRAYDVRGVVGKTLNKEVAHALGQSIGTLMVEKGLREIVVGRD
GRLSGPELAAALADGLREAGVDVIDIGAVPTPVVYYATYRFNTGCGVAVTGSHNPPDYNG
FKIVVGGQTLAEGAIQDLYQRIAGGALASGGGGGLRQVDVAPDYIEKIIADVLAERRLKV
VVDCGNGIPGAIAPQVLEGVGCEVVPLYCDVDGSFPNHHPDPSDPHNLEDLIIAVRQTGA
DLGLAFDGDGDRLGVVTRSGEIVYPDRLLMLFARDVLSRQPGATVIYDVKCTSHLKGQIL
DAGGSPLMWRTGHSLIKAKMRETQAELAGEMSGHFFFKERWYGFDDGIYAAARLLEILAG
DLQGRSAEQIFATLPKSVSTPELKVELAEGEHYRFMDQLRQQASFEDASLITIDGVRADW
PDGWGLVRASNTTPVLVLRFEADDPVALKRIQQLFRRQLLAVNPGLKLPF
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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