SitesBLAST
Comparing BPHYT_RS05360 FitnessBrowser__BFirm:BPHYT_RS05360 to proteins with known functional sites using BLASTp with E ≤ 0.001.
Or try Sites on a Tree, PaperBLAST, Conserved Domains, or compare to all protein structures
Found 20 (the maximum) 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)
23% identity, 76% coverage: 5:337/439 of query aligns to 65:399/534 of P53322
- K283 (= K225) modified: Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in ubiquitin)
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)
23% identity, 81% coverage: 73:428/439 of query aligns to 113:473/495 of Q9NRA2
- K136 (≠ R101) 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 (≠ I141) 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 (≠ MT 156:157) mutation to AA: Localizes in vesicular structures mainly concentrated in the perinuclear region.
- IL 266:267 (≠ LE 231:232) mutation to LA: Localizes in vesicular structures mainly concentrated in the perinuclear region.
- SSLRN 268:272 (≠ RHVSA 233:237) 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 (= G293) 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 (= P299) 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 (= G331) 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
P0AA76 D-galactonate transporter; D-galactonate/H(+) symporter from Escherichia coli (strain K12) (see paper)
21% identity, 85% coverage: 35:406/439 of query aligns to 20:397/430 of P0AA76
- Y29 (= Y44) binding
- D31 (= D46) mutation to N: Loss of galactonate transport activity.
- R32 (= R47) binding
- Y64 (= Y79) binding
- E118 (= E133) mutation to Q: Loss of galactonate transport activity.
- W358 (= W367) binding
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, 56% coverage: 73:320/439 of query aligns to 113:355/495 of Q8BN82
- H183 (≠ I141) 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.
6e9nA E. Coli d-galactonate:proton symporter in the inward open form (see paper)
21% identity, 85% coverage: 35:407/439 of query aligns to 9:379/409 of 6e9nA
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, 56% coverage: 73:320/439 of query aligns to 113:355/495 of Q5Q0U0
- K136 (≠ R96) mutation to E: Markedly decreases H(+)-coupled sialic acid transporter activity.
- R168 (= R126) mutation to C: Abolishes H(+)-coupled sialic acid transporter activity.
- E171 (≠ L129) mutation to C: Decreases H(+)-coupled sialic acid transporter activity; when associated with C-175.
- G172 (= G130) mutation to C: Decreases protein levels and alters subcellular localization.
- E175 (= E133) mutation to C: Decreases H(+)-coupled sialic acid transporter activity; when associated with C-171.
- G176 (≠ A134) mutation to C: Decreases protein levels and alters subcellular localization.
- F179 (= F137) mutation to C: Decreases the affinity and transport rate for D-glucuronate. Does not affect H(+)-coupled sialic acid transporter activity.
- P180 (= P138) mutation to C: Decreases protein levels and alters subcellular localization.
- H183 (≠ I141) mutation to R: Abolishes H(+)-coupled sialic acid transporter activity.
- W186 (≠ L144) mutation to C: Abolishes H(+)-coupled sialic acid transporter activity.
- SSLKN 268:272 (≠ RHVSA 233:237) mutation Missing: Abolishes H(+)-coupled sialic acid transporter activity.
- P334 (= P299) mutation to R: Abolishes H(+)-coupled sialic acid transporter activity.
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.
- 371 G→V: Remains in the endoplasmic reticulum.
Q5EXK5 3-hydroxybenzoate transporter MhbT from Klebsiella oxytoca (see paper)
27% identity, 46% coverage: 91:293/439 of query aligns to 82:301/452 of Q5EXK5
- D82 (≠ H91) mutation to A: Loss of activity.
Sites not aligning to the query:
- 311 V→W: Loss of activity.
- 314 D→A: Loss of activity.
6e9oA E. Coli d-galactonate:proton symporter mutant e133q in the outward substrate-bound form (see paper)
21% identity, 85% coverage: 35:407/439 of query aligns to 12:363/393 of 6e9oA
Q9JI12 Vesicular glutamate transporter 2; VGluT2; Differentiation-associated BNPI; Differentiation-associated Na(+)-dependent inorganic phosphate cotransporter; Solute carrier family 17 member 6 from Rattus norvegicus (Rat) (see 2 papers)
21% identity, 97% coverage: 1:428/439 of query aligns to 43:492/582 of Q9JI12
- R88 (= R47) mutation to A: Impairs synaptic transmission. Abolishes the chloride ion conductance.
- H128 (≠ A72) mutation to A: Greatly lowers L-glutamate transport.
- R184 (= R126) mutation R->A,E,K: Greatly lowers L-glutamate transport.
- E191 (= E133) mutation to A: Greatly lowers L-glutamate transport.; mutation E->D,Q: Lowers L-glutamate transport.
- R322 (≠ F266) mutation to A: Loss of L-glutamate release. Abolishes the chloride ion conductance.
7t3nA R184q/e191q mutant of rat vesicular glutamate transporter 2 (vglut2)
22% identity, 88% coverage: 42:428/439 of query aligns to 35:434/452 of 7t3nA
- binding (1s,3r)-1-aminocyclopentane-1,3-dicarboxylic acid: Y77 (= Y79), Y137 (≠ F137), Y165 (≠ A165), R264 (≠ F266), S265 (≠ V267), F268 (≠ L270), Y269 (= Y271), N392 (= N387)
- binding (2R)-2-(methoxymethyl)-4-{[(25R)-spirost-5-en-3beta-yl]oxy}butyl 4-O-alpha-D-glucopyranosyl-beta-D-glucopyranoside: E152 (≠ R152), T159 (≠ W159), C162 (≠ T162), G163 (≠ A163), A166 (≠ L166), I170 (= I170), E219 (= E226), E220 (= E227), Y223 (≠ L230)
Sites not aligning to the query:
Q51955 4-hydroxybenzoate transporter PcaK from Pseudomonas putida (Arthrobacter siderocapsulatus) (see 2 papers)
21% identity, 87% coverage: 18:400/439 of query aligns to 16:407/448 of Q51955
- D41 (= D46) mutation D->A,N: Abolishes 4-HBA transport.; mutation to E: Decrease in 4-HBA transport.
- D44 (≠ N49) mutation D->A,N: Abolishes 4-HBA transport.; mutation to E: Decrease in 4-HBA transport.
- G85 (≠ N87) mutation to V: Abolishes 4-HBA transport and chemotaxis.
- D89 (≠ H91) mutation to N: Abolishes 4-HBA transport and chemotaxis.
- G92 (= G94) mutation to A: Decrease in 4-HBA transport and chemotaxis.; mutation to C: No change in 4-HBA transport and chemotaxis.; mutation G->L,V: Abolishes 4-HBA transport and chemotaxis.; mutation to Q: Decrease in 4-HBA transport and strong decrease in chemotaxis.
- R124 (= R126) mutation to A: Abolishes 4-HBA transport.
- E144 (≠ Y146) mutation to A: Strong decrease in 4-HBA transport.
- H183 (≠ Q192) mutation to A: Decrease in 4-HBA transport and chemotaxis.
- D323 (= D315) mutation to N: Abolishes 4-HBA transport and chemotaxis.
- H328 (≠ R320) mutation to A: Decrease in 4-HBA transport and chemotaxis.; mutation to R: Decrease in 4-HBA transport and loss of chemotaxis.
- R386 (≠ A379) mutation to A: Strong decrease in 4-HBA transport.
- R398 (≠ N391) mutation to A: Abolishes 4-HBA transport.
Sites not aligning to the query:
- 444 H→A: No change in 4-HBA transport and chemotaxis.
Q9C0U9 Uncharacterized transporter PB1C11.03 from Schizosaccharomyces pombe (strain 972 / ATCC 24843) (Fission yeast) (see paper)
23% identity, 46% coverage: 27:228/439 of query aligns to 93:296/570 of Q9C0U9
Sites not aligning to the query:
- 14 modified: Phosphoserine
Q8NLB7 Gentisate transporter from Corynebacterium glutamicum (strain ATCC 13032 / DSM 20300 / BCRC 11384 / JCM 1318 / LMG 3730 / NCIMB 10025) (see paper)
24% identity, 65% coverage: 31:316/439 of query aligns to 40:313/444 of Q8NLB7
- D54 (vs. gap) mutation to A: Loss of transport activity.; mutation to E: Retains 50% of its transport activity.
- D57 (= D46) mutation to A: Loss of transport activity.; mutation to E: Retains 50% of its transport activity.
- R103 (≠ K92) mutation to A: Loss of transport activity.
- W309 (≠ R312) mutation to V: Loss of transport activity.
- D312 (= D315) mutation to A: Loss of transport activity.
- R313 (= R316) mutation to A: Loss of transport activity.
Sites not aligning to the query:
- 317 mutation I->H,Y: Loss of transport activity.
- 386 R→A: Loss of transport activity.
7aarA Sugar/h+ symporter stp10 in inward open conformation (see paper)
22% identity, 54% coverage: 86:321/439 of query aligns to 87:334/485 of 7aarA