SitesBLAST
Comparing WP_109968169.1 NCBI__GCF_003173355.1:WP_109968169.1 to proteins with known functional sites using BLASTp with E ≤ 0.001.
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Found 11 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)
21% identity, 70% coverage: 4:302/425 of query aligns to 77:377/534 of P53322
- K283 (≠ S211) modified: Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in ubiquitin)
8u3gA Structure of naag-bound sialin
24% identity, 88% coverage: 16:390/425 of query aligns to 4:386/427 of 8u3gA
8u3hA Structure of fmoc-leu-oh bound sialin
24% identity, 88% coverage: 16:390/425 of query aligns to 4:384/425 of 8u3hA
P0AA76 D-galactonate transporter; D-galactonate/H(+) symporter from Escherichia coli (strain K12) (see paper)
21% identity, 91% coverage: 3:390/425 of query aligns to 7:395/430 of P0AA76
- Y29 (≠ F31) binding D-galactonate
- D31 (= D33) mutation to N: Loss of galactonate transport activity.
- R32 (= R34) binding D-galactonate
- Y64 (= Y66) binding D-galactonate
- E118 (= E120) mutation to Q: Loss of galactonate transport activity.
- W358 (= W353) binding D-galactonate
6e9oA E. Coli d-galactonate:proton symporter mutant e133q in the outward substrate-bound form (see paper)
21% identity, 91% coverage: 5:390/425 of query aligns to 1:360/393 of 6e9oA
Q9C0U9 Uncharacterized transporter PB1C11.03 from Schizosaccharomyces pombe (strain 972 / ATCC 24843) (Fission yeast) (see paper)
25% identity, 65% coverage: 25:301/425 of query aligns to 102:393/570 of Q9C0U9
Sites not aligning to the query:
- 14 modified: Phosphoserine
6e9nA E. Coli d-galactonate:proton symporter in the inward open form (see paper)
22% identity, 90% coverage: 8:390/425 of query aligns to 1:376/409 of 6e9nA
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)
24% identity, 80% coverage: 51:390/425 of query aligns to 104:447/495 of Q9NRA2
- K136 (≠ R88) 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 (≠ I128) 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 (≠ SI 143:144) mutation to AA: Localizes in vesicular structures mainly concentrated in the perinuclear region.
- IL 266:267 (≠ LV 217:218) mutation to LA: Localizes in vesicular structures mainly concentrated in the perinuclear region.
- SSLRN 268:272 (≠ SELES 219:223) 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 (= G280) 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 (= P286) 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 (≠ A318) 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
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)
24% identity, 80% coverage: 52:390/425 of query aligns to 105:447/495 of Q8BN82
- H183 (≠ I128) 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.
Q5Q0U0 Sialin; H(+)/nitrate cotransporter; H(+)/sialic acid cotransporter; AST; Solute carrier family 17 (Anion/sugar transporter), member 5; Vesicular excitatory amino acid transporter; VEAT from Rattus norvegicus (Rat) (see 2 papers)
23% identity, 80% coverage: 51:390/425 of query aligns to 104:447/495 of Q5Q0U0
- K136 (≠ R83) mutation to E: Markedly decreases H(+)-coupled sialic acid transporter activity.
- R168 (= R113) mutation to C: Abolishes H(+)-coupled sialic acid transporter activity.
- E171 (≠ L116) mutation to C: Decreases H(+)-coupled sialic acid transporter activity; when associated with C-175.
- G172 (= G117) mutation to C: Decreases protein levels and alters subcellular localization.
- E175 (= E120) mutation to C: Decreases H(+)-coupled sialic acid transporter activity; when associated with C-171.
- G176 (≠ A121) mutation to C: Decreases protein levels and alters subcellular localization.
- F179 (= F124) mutation to C: Decreases the affinity and transport rate for D-glucuronate. Does not affect H(+)-coupled sialic acid transporter activity.
- P180 (= P125) mutation to C: Decreases protein levels and alters subcellular localization.
- H183 (≠ I128) mutation to R: Abolishes H(+)-coupled sialic acid transporter activity.
- W186 (≠ L131) mutation to C: Abolishes H(+)-coupled sialic acid transporter activity.
- SSLKN 268:272 (≠ SELES 219:223) mutation Missing: Abolishes H(+)-coupled sialic acid transporter activity.
- P334 (= P286) mutation to R: Abolishes H(+)-coupled sialic acid transporter activity.
- G371 (≠ A318) mutation to V: Remains in the endoplasmic reticulum.
Sites not aligning to the query:
- 22:23 Dileucine internalization motif; LL→AA: Targeted to plasma membrane; sialic acid uptake strongly activated at acidic pH.
- 39 R→C: Markedly decreases H(+)-coupled sialic acid transporter activity.
Q03567 Uncharacterized transporter slc-17.2 from Caenorhabditis elegans (see paper)
21% identity, 67% coverage: 7:289/425 of query aligns to 6:319/493 of Q03567
- N69 (vs. gap) modified: carbohydrate, N-linked (GlcNAc...) asparagine
Query Sequence
>WP_109968169.1 NCBI__GCF_003173355.1:WP_109968169.1
MLVSQESEKRIISLIRLHIIPFALLLYIVAFLDRVNLGYAAIVMNPDLGISAELFGFISG
IFFIGYLIFEVPSNIIMQKVGARIWIGRIMISWGLVAVLMGFVQSPEHLIILRFLLGIAE
AGFFPGMIWYLGTWFPHRYLARSIALFSTAIVISNIIGAPLSMYILDTVNWGSVASWRWL
FIIEGIPAILFGVLSLFILKNRPADAGWLDSDQKQWLVSELESGTIRMKSHRLGDILTDT
RVLLFSGTYFAVTVGMYAIIFFLPTLSSSFLHDLDMRVIGLILMIPYIVTLICMFLVSSH
SDLRGERLYHIIILFFIAGAGLTLDQLAEDPILSLLGITIALSGILSIIGPFWSYVLSVF
TPDEQPVGVAVINSIGNLGGFVGPVITGYLISLFKTLDSGWPVITFILCLGAVMIFMAGK
KGIRM
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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