SitesBLAST
Comparing PP_2830 FitnessBrowser__Putida:PP_2830 to proteins with known functional sites using BLASTp with E ≤ 0.001.
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Found 15 hits to proteins with known functional sites (download)
P53322 High-affinity nicotinic acid transporter; Nicotinic acid permease from Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) (see paper)
24% identity, 69% coverage: 10:318/450 of query aligns to 56:374/534 of P53322
- K283 (≠ A238) modified: Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in ubiquitin)
6e9nA E. Coli d-galactonate:proton symporter in the inward open form (see paper)
25% identity, 60% coverage: 48:319/450 of query aligns to 9:273/409 of 6e9nA
Sites not aligning to the query:
P0AA76 D-galactonate transporter; D-galactonate/H(+) symporter from Escherichia coli (strain K12) (see paper)
25% identity, 60% coverage: 48:319/450 of query aligns to 20:292/430 of P0AA76
- Y29 (≠ F57) binding D-galactonate
- D31 (= D59) mutation to N: Loss of galactonate transport activity.
- R32 (= R60) binding D-galactonate
- Y64 (= Y92) binding D-galactonate
- E118 (= E146) mutation to Q: Loss of galactonate transport activity.
Sites not aligning to the query:
- 358 binding D-galactonate
6e9oA E. Coli d-galactonate:proton symporter mutant e133q in the outward substrate-bound form (see paper)
24% identity, 60% coverage: 48:319/450 of query aligns to 12:257/393 of 6e9oA
Sites not aligning to the query:
6zguA Crystal structure of a mfs transporter with bound 3-(2-methylphenyl) propanoic acid at 2.41 angstroem resolution
26% identity, 78% coverage: 73:421/450 of query aligns to 35:366/404 of 6zguA
6zgtA Crystal structure of a mfs transporter with bound 2-naphthoic acid at 2.39 angstroem resolution
26% identity, 78% coverage: 73:421/450 of query aligns to 35:366/404 of 6zgtA
6zgsA Crystal structure of a mfs transporter with bound 3-phenylpropanoic acid at 2.39 angstroem resolution
26% identity, 78% coverage: 73:421/450 of query aligns to 35:366/404 of 6zgsA
Q03567 Uncharacterized transporter slc-17.2 from Caenorhabditis elegans (see paper)
24% identity, 81% coverage: 86:450/450 of query aligns to 84:467/493 of Q03567
Sites not aligning to the query:
- 69 modified: carbohydrate, N-linked (GlcNAc...) asparagine
6g9xA Crystal structure of a mfs transporter at 2.54 angstroem resolution (see paper)
26% identity, 74% coverage: 90:421/450 of query aligns to 49:358/396 of 6g9xA
A0LNN5 L-lactate transporter; SfMCT from Syntrophobacter fumaroxidans (strain DSM 10017 / MPOB) (see paper)
26% identity, 78% coverage: 73:421/450 of query aligns to 41:382/412 of A0LNN5
- Y119 (= Y156) binding (S)-lactate; mutation Y->A,F: Loss of transport activity.
- L145 (≠ V177) mutation to A: Strong decrease in transport activity.
- H250 (≠ F289) mutation to A: Strong decrease in transport activity.; mutation to F: Loss of transport activity.
- R256 (≠ T296) mutation to A: No change in transport activity.; mutation to D: Increases transport activity.
- D257 (≠ Y297) mutation to A: Loss of transport activity.
- N276 (≠ T328) mutation to A: Loss of transport activity.
- R280 (= R332) binding (S)-lactate; mutation to A: Abolishes L-lactate binding and L-lactate transport.
- Y331 (≠ L365) mutation to A: Loss of transport activity.; mutation to F: No change in transport activity.
- F335 (≠ M369) mutation to A: Increases transport activity.
- F359 (≠ V397) mutation to A: Loss of transport activity.
- C362 (= C400) mutation to A: Decrease in transport activity.
- K377 (≠ E416) mutation K->A,D: No change in transport activity.
- D378 (≠ Q417) mutation to A: Loss of transport activity.
Sites not aligning to the query:
- 28 L→A: Loss of transport activity.
- 383 Y→A: Loss of transport activity.; Y→F: Strong decrease in transport activity.
8u3gA Structure of naag-bound sialin
21% identity, 87% coverage: 60:449/450 of query aligns to 22:422/427 of 8u3gA
Sites not aligning to the query:
Q8BN82 Sialin; H(+)/nitrate cotransporter; H(+)/sialic acid cotransporter; AST; Solute carrier family 17 member 5; Vesicular excitatory amino acid transporter; VEAT from Mus musculus (Mouse) (see paper)
20% identity, 56% coverage: 63:313/450 of query aligns to 90:335/495 of Q8BN82
- H183 (≠ M154) mutation to R: Abolishes sialic acid transporter activity. Does not affect L-aspartate and L-glutamate transporter activity.
Sites not aligning to the query:
- 39 R→C: Completely abolishes L-aspartate and L-glutamate transporter activity. Retains appreciable H(+)-coupled sialic acid transporter activity.
Q9NRA2 Sialin; H(+)/nitrate cotransporter; H(+)/sialic acid cotransporter; AST; Membrane glycoprotein HP59; Solute carrier family 17 member 5; Vesicular excitatory amino acid transporter; VEAT from Homo sapiens (Human) (see 8 papers)
20% identity, 86% coverage: 63:449/450 of query aligns to 90:483/495 of Q9NRA2
- K136 (≠ R109) to E: in SD; alters intracellular localization, only partially targeted to lysosomes and mainly detected in LAMP1-negative vesicles and in the Golgi apparatus; completely devoid of L-aspartate and L-glutamate transporter activity, but retains appreciable H(+)-coupled sialic acid transporter activity; dbSNP:rs80338795
- H183 (≠ M154) to R: in ISSD; alters intracellular localization, only partially targeted to lysosomes and mainly detected in LAMP1-negative vesicles and in the Golgi apparatus; abolishes H(+)-coupled sialic acid transporter activity; has normal L-aspartate and L-glutamate transporter activity; dbSNP:rs119491109
- LL 198:199 (≠ AT 169:170) mutation to AA: Localizes in vesicular structures mainly concentrated in the perinuclear region.
- IL 266:267 (≠ IE 243:244) mutation to LA: Localizes in vesicular structures mainly concentrated in the perinuclear region.
- SSLR-N 268:272 (≠ RRLAAE 245:250) natural variant: Missing (in ISSD; alters intracellular localization, only partially targeted to lysosomes and mainly detected in LAMP1-negative vesicles and in the Golgi apparatus; abolishes H(+)-coupled sialic acid transporter activity; has normal L-aspartate and L-glutamate transporter activity)
- G328 (= G306) to E: in ISSD; some patients may manifest a milder phenotype consistent with Salla disease; markedly decreases H(+)-coupled sialic acid transporter activity; abolishes L-aspartate and L-glutamate transporter activity; dbSNP:rs386833996
- P334 (= P312) to R: in ISSD; does not affect intracellular localization, targeted to lysosomes; abolishes H(+)-coupled sialic acid transporter activity; abolishes L-aspartate and L-glutamate transporter activity; dbSNP:rs119491110
- G371 (= G340) to V: in ISSD; abolishes H(+)-coupled sialic acid transporter activity; abolishes L-aspartate and L-glutamate transporter activity; dbSNP:rs777862172
Sites not aligning to the query:
- 22:23 Dileucine internalization motif; LL→AA: Targeted to plasma membrane.; LL→GG: Targeted to plasma membrane; sialic acid uptake strongly activated at acidic pH.
- 39 R → C: in SD; frequent variant in Finland; alters intracellular localization, only partially targeted to lysosomes and mainly detected in LAMP1-negative vesicles and in the Golgi apparatus; completely devoid of L-aspartate and L-glutamate transport activity, but retains appreciable H(+)-coupled sialic acid and nitrate transporter activity; dbSNP:rs80338794
8u3hA Structure of fmoc-leu-oh bound sialin
20% identity, 87% coverage: 60:449/450 of query aligns to 22:420/425 of 8u3hA