SitesBLAST
Comparing WP_057509355.1 NCBI__GCF_001431535.1:WP_057509355.1 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 18 hits to proteins with known functional sites (download)
P46349 Gamma-aminobutyric acid permease; GABA permease; 4-aminobutyrate permease; Gamma-aminobutyrate permease; Proline transporter GabP from Bacillus subtilis (strain 168) (see paper)
41% identity, 97% coverage: 12:459/460 of query aligns to 4:455/469 of P46349
- G33 (= G41) mutation to D: Lack of activity.
- G42 (= G50) mutation to S: Lack of activity.
- G301 (≠ N308) mutation to V: Lack of activity.
- G338 (≠ S345) mutation to E: Lack of activity.
- F341 (= F348) mutation to S: Lack of activity.
- G414 (≠ L420) mutation to R: Lack of activity.
P24207 Phenylalanine-specific permease; Phenylalanine:H(+) symporter PheP from Escherichia coli (strain K12) (see 3 papers)
37% identity, 98% coverage: 7:458/460 of query aligns to 10:458/458 of P24207
- R26 (= R23) mutation R->G,S,Q: Strong decrease in phenylalanine transport activity.
- P54 (= P51) mutation to A: 50% of wild-type phenylalanine transport activity.; mutation to G: No change in phenylalanine transport activity.; mutation to L: 26% of wild-type phenylalanine transport activity.
- F87 (= F84) mutation to L: No effect on phenylalanine transport activity.
- F90 (≠ Y87) mutation to L: 65% of wild-type phenylalanine transport activity.
- Y92 (≠ A89) mutation to L: 41% of wild-type phenylalanine transport activity.
- Y94 (≠ A91) mutation to L: 69% of wild-type phenylalanine transport activity.
- W95 (≠ L92) mutation to L: 10% of wild-type phenylalanine transport activity.
- F98 (≠ T95) mutation to L: No effect on phenylalanine transport activity.
- F101 (≠ A98) mutation to L: 38% of wild-type phenylalanine transport activity.
- W105 (= W102) mutation to L: 39% of wild-type phenylalanine transport activity.
- Y107 (≠ W104) mutation to L: No effect on phenylalanine transport activity.
- W108 (= W105) mutation to L: 71% of wild-type phenylalanine transport activity.
- F111 (≠ L108) mutation to L: 60% of wild-type phenylalanine transport activity.; mutation to Y: Enables the transport of tryptophan to almost the same steady-state level as that of phenylalanine.
- E118 (= E115) mutation E->G,L,V,N: Loss of activity.
- K168 (= K165) mutation K->L,R: Strong decrease in phenylalanine transport activity.; mutation to N: Loss of activity.
- E226 (= E224) mutation E->A,Q,K,R,W: Loss of activity.
- R252 (= R250) mutation R->D,E,F,W,P: Loss of activity.
- P341 (= P338) mutation to A: 5% of wild-type phenylalanine transport activity.; mutation P->G,Q,K,R: Loss of activity.; mutation to S: 3% of wild-type phenylalanine transport activity.; mutation to T: 17% of wild-type phenylalanine transport activity.
- P442 (≠ T442) mutation to A: 46% of wild-type phenylalanine transport activity.; mutation to G: 52% of wild-type phenylalanine transport activity.; mutation to L: 43% of wild-type phenylalanine transport activity.
Q88CZ8 L-histidine transporter HutT from Pseudomonas putida (strain ATCC 47054 / DSM 6125 / CFBP 8728 / NCIMB 11950 / KT2440) (see paper)
38% identity, 93% coverage: 16:445/460 of query aligns to 7:441/467 of Q88CZ8
- T27 (≠ A36) mutation T->A,S: Retains 60% of wild-type activity.; mutation to N: Retains 20% of wild-type activity.
- E98 (≠ Q107) mutation to A: Retains 80% of wild-type activity.
- K156 (= K165) mutation K->A,Q: Retains less than 10% of wild-type activity.; mutation to R: Retains 40% of wild-type activity.
- F212 (= F218) mutation F->A,Q: Loss of activity.; mutation to Y: No change in activity.
- E218 (= E224) mutation E->A,Q: Loss of activity.; mutation to D: Retains 70% of wild-type activity.
P15993 Aromatic amino acid transport protein AroP; Aromatic amino acid:H(+) symporter AroP; General aromatic amino acid permease; General aromatic transport system from Escherichia coli (strain K12) (see paper)
36% identity, 90% coverage: 15:426/460 of query aligns to 10:421/457 of P15993
- Y103 (≠ L108) Key residue for tryptophan transport; mutation to F: Decreases tryptophan transport to less than 50% of wild-type levels and reduces the ability of tryptophan to inhibit phenylalanine transport from 95 to 62%.
P25737 Lysine-specific permease LysP; Lysine transporter LysP; Trigger transporter LysP from Escherichia coli (strain K12) (see 2 papers)
34% identity, 89% coverage: 14:424/460 of query aligns to 11:433/489 of P25737
- Y102 (≠ W104) mutation to L: Retains 4% of wild-type lysine uptake activity. Increases the capacity to inhibit CadC in the presence of lysine.
- W106 (≠ L108) mutation to L: Retains 20% of wild-type lysine uptake activity. Increases the capacity to inhibit CadC in the presence of lysine.
- K163 (= K165) mutation to A: Retains 24% of wild-type lysine uptake activity. Increases the capacity to inhibit CadC in the presence of lysine.
- F216 (= F218) mutation to L: Retains 13% of wild-type lysine uptake activity. Increases the capacity to inhibit CadC in the presence of lysine.
- E222 (= E224) mutation to A: Abolishes lysine uptake. Strongly inhibits CadC.
- E230 (= E232) mutation to V: Abolishes lysine uptake. Shows significant less inhibition of CadC.
- D275 (vs. gap) Essential for the stimulus-dependent interaction with CadC; mutation to A: Retains 88% of wild-type lysine uptake activity, but can hardly inhibit CadC. Cannot interact with CadC; when associated with A-278.
- D278 (vs. gap) Essential for the stimulus-dependent interaction with CadC; mutation to A: Retains 88% of wild-type lysine uptake activity, but can hardly inhibit CadC. Cannot interact with CadC; when associated with A-275.
Sites not aligning to the query:
- 1 modified: Initiator methionine, Removed
- 438 E→A: Retains 14% of wild-type lysine uptake activity. Is unable to inhibit CadC.
- 443 D→A: Retains 11% of wild-type lysine uptake activity. Is unable to inhibit CadC.
- 446 D→A: Retains 13% of wild-type lysine uptake activity. Is unable to inhibit CadC.
P04817 Arginine permease CAN1; Canavanine resistance protein 1 from Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) (see paper)
33% identity, 88% coverage: 15:421/460 of query aligns to 83:509/590 of P04817
- P113 (≠ G45) mutation to L: In CAN1-343; confers citrulline transport activity in GAP1-deleted cells.
- P148 (= P79) mutation to L: In CAN1-337; confers citrulline transport activity in GAP1-deleted cells and leads to sensitivity to L-glutamic acid alpha-hydroxamate, alpha-aminoisobutyrate, 3-chloro-L-alanine, L-ethionine, L-allylglycine, and D-histidine, but not sensitivity to L-aspartic acid alpha-hydroxamate or p-fluoro-L-phenylalanine.
- V149 (≠ T80) mutation to F: In CAN1-315; confers citrulline transport activity in GAP1-deleted cells.
- S152 (≠ A83) mutation to F: In CAN1-342; confers citrulline transport activity in GAP1-deleted cells.
- Y173 (≠ W104) mutation to D: In CAN1-306; confers citrulline transport activity in GAP1-deleted cells.; mutation to H: In CAN1-327; confers citrulline transport activity in GAP1-deleted cells.
- G308 (≠ A231) mutation to A: In CAN1-341; confers citrulline transport activity in GAP1-deleted cells.
- P313 (= P236) mutation to S: In CAN1-329; confers citrulline transport activity in GAP1-deleted cells and leads to sensitivity to L-glutamic acid alpha-hydroxamate, alpha-aminoisobutyrate, 3-chloro-L-alanine, L-ethionine, L-allylglycine, and D-histidine, L-aspartic acid alpha-hydroxamate and p-fluoro-L-phenylalanine.
- TS 354:355 (= TS 269:270) mutation Missing: In CAN1-318; confers citrulline transport activity in GAP1-deleted cells.
- Y356 (≠ E271) mutation to H: In CAN1-340; confers citrulline transport activity in GAP1-deleted cells.; mutation to N: In CAN1-339; confers citrulline transport activity in GAP1-deleted cells.
- W451 (≠ V366) mutation to C: In CAN1-328; confers citrulline transport activity in GAP1-deleted cells.; mutation to L: In CAN1-316; confers citrulline transport activity in GAP1-deleted cells.; mutation to S: In CAN1-335; confers citrulline transport activity in GAP1-deleted cells.
- F461 (≠ L376) mutation to S: In CAN1-307; confers citrulline transport activity in GAP1-deleted cells.
Q9URZ4 Cationic amino acid transporter 1 from Schizosaccharomyces pombe (strain 972 / ATCC 24843) (Fission yeast) (see paper)
29% identity, 86% coverage: 4:400/460 of query aligns to 68:476/587 of Q9URZ4
Sites not aligning to the query:
- 29 modified: Phosphoserine
- 30 modified: Phosphoserine
- 37 modified: Phosphoserine
P19145 General amino-acid permease GAP1 from Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) (see 3 papers)
33% identity, 74% coverage: 16:354/460 of query aligns to 86:439/602 of P19145
- A297 (≠ G221) mutation to V: Impairs basic amino-acids transport and regulation by these amino-acids.
Sites not aligning to the query:
- 76 modified: Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in ubiquitin)
P48813 High-affinity glutamine permease from Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) (see paper)
28% identity, 88% coverage: 15:421/460 of query aligns to 144:570/663 of P48813
Sites not aligning to the query:
- 132 modified: Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in ubiquitin)
Q03770 SPS-sensor component SSY1; Amino-acid permease homolog SSY1 from Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) (see paper)
23% identity, 90% coverage: 15:427/460 of query aligns to 276:772/852 of Q03770
- T382 (≠ G121) mutation T->H,L: Constitutively active, up-regulates amino acid permease transcription in response to subthreshold concentrations of amino acids.; mutation to K: In SSY1-102; constitutively active, up-regulates amino acid permease transcription in the absence of amino-acids.; mutation to R: Constitutively active, up-regulates amino acid permease transcription in the absence of amino acids.
P30825 High affinity cationic amino acid transporter 1; CAT-1; CAT1; Ecotropic retroviral leukemia receptor homolog; Ecotropic retrovirus receptor homolog; Solute carrier family 7 member 1; System Y+ basic amino acid transporter from Homo sapiens (Human) (see paper)
25% identity, 85% coverage: 15:406/460 of query aligns to 27:445/629 of P30825
- N226 (vs. gap) modified: carbohydrate, N-linked (GlcNAc...) asparagine
6f34A Crystal structure of a bacterial cationic amino acid transporter (cat) homologue bound to arginine. (see paper)
25% identity, 70% coverage: 47:370/460 of query aligns to 55:378/458 of 6f34A
- binding arginine: E115 (≠ Q107), Y116 (≠ L108), A119 (≠ V111), F228 (= F218), A229 (= A219), I231 (≠ G221), V314 (≠ A304)
- binding cholesterol: W201 (= W183), Y202 (≠ L184)
- binding : A178 (≠ G155), R179 (≠ E156), A186 (≠ I163), I187 (≠ L164), A190 (= A167), L194 (≠ G171), Q296 (≠ I286), V299 (≠ A289)
Sites not aligning to the query:
5oqtA Crystal structure of a bacterial cationic amino acid transporter (cat) homologue (see paper)
26% identity, 75% coverage: 47:391/460 of query aligns to 53:394/456 of 5oqtA
Sites not aligning to the query:
O34739 Serine/threonine exchanger SteT from Bacillus subtilis (strain 168) (see paper)
22% identity, 84% coverage: 30:416/460 of query aligns to 22:398/438 of O34739
- C94 (≠ V100) mutation to S: Retains 25% of the transport activity; when associated with S-141; S-168; S-291 and S-415.
- C141 (≠ T144) mutation to S: Retains 25% of the transport activity; when associated with S-94; S-168; S-291 and S-415.
- C168 (≠ G171) mutation to S: Retains 25% of the transport activity; when associated with S-94; S-141; S-291 and S-415.
- C291 (≠ A304) mutation to S: Retains 25% of the transport activity; when associated with S-94; S-141; S-168 and S-415.
Sites not aligning to the query:
- 415 C→S: Retains 25% of the transport activity; when associated with S-94; S-141; S-168 and S-291.
6f2wA Bacterial asc transporter crystal structure in open to in conformation (see paper)
24% identity, 84% coverage: 30:415/460 of query aligns to 14:392/433 of 6f2wA
9h76A Bacterial lat transporter basc in complex with l-ala and nb53 (see paper)
24% identity, 84% coverage: 30:415/460 of query aligns to 12:390/430 of 9h76A
P76037 Putrescine importer PuuP from Escherichia coli (strain K12) (see paper)
24% identity, 76% coverage: 8:358/460 of query aligns to 10:360/461 of P76037
- Y110 (≠ L108) mutation to X: The uptake activity is reduced to one-eighth of that of wild-type.
P0AAF1 Putrescine transporter PotE; Putrescine-proton symporter / putrescine-ornithine antiporter from Escherichia coli (strain K12) (see 2 papers)
23% identity, 68% coverage: 81:394/460 of query aligns to 69:379/439 of P0AAF1
- E77 (≠ A89) mutation E->A,D,N,Q: Strong decrease in both uptake and excretion activities.
- Y78 (≠ D90) mutation to L: Uptake activity decreases more than excretion activity.
- K82 (≠ P94) mutation to A: Slight decrease in both uptake and excretion activities.
- Y90 (≠ W102) mutation to L: Uptake activity decreases more than excretion activity.
- Y92 (≠ W104) mutation to L: Moderate decrease in both uptake and excretion activities.
- W201 (≠ F218) mutation W->F,L,Y: Strong decrease in both uptake and excretion activities.
- E207 (= E224) mutation E->A,D,N,Q: Lack of both uptake and excretion activities.
- C210 (≠ A227) mutation to A: Moderate decrease in both uptake and excretion activities.
- C285 (≠ L301) mutation to A: Moderate decrease in both uptake and excretion activities.
- C286 (≠ L302) mutation to A: Moderate decrease in both uptake and excretion activities.
- W292 (≠ N308) mutation W->F,L,Y: Strong decrease in both uptake and excretion activities.
- K301 (≠ F317) mutation to A: Excretion activity decreases more than uptake activity.
- Y308 (≠ E324) mutation to L: Excretion activity decreases more than uptake activity.
Sites not aligning to the query:
- 62 mutation C->A,T: Strong decrease in both uptake and excretion activities.; C→S: Moderate decrease in both uptake and excretion activities.
- 68 K→A: Slight decrease in both uptake and excretion activities.
- 422 W→L: Uptake activity decreases more than excretion activity.
- 425 Y→F: Moderate decrease in both uptake and excretion activities.; Y→L: Strong decrease in both uptake and excretion activities.
- 433 mutation E->A,D,N,Q: Strong decrease in both uptake and excretion activities.
Query Sequence
>WP_057509355.1 NCBI__GCF_001431535.1:WP_057509355.1
MPANPTPAAPASPPRLGHALKPRQLIMMGLGSAIGAGLFLGSGVGVQLAGPAVLLSYLVA
GALVIIVMNALGEMAANKPTSGAFSVYAADALGPTAGATVGWLWWVQLVIVIAAEAVGAA
GLLATVWTGLSVPMAALAFMLFFTAINLLGVKNFGEFEFWFAILKVAAILGFIAIGAALL
LGWLPDATSPGLSNFTGNGGFAPTGLAGVGAALLVVIFAFGGTEIVAVAAAETEDPERSI
ARAIRTVAWRILVFYIGSLSVIIAVVPWTSEALKSPFAAVLEAANIPGAGTAITLVAVIA
LLSALNANLYGASRMIFSLAQRREAPAVLGWADRRQVPVLAVLASVLFGFAATVMELVFP
DRVLPVLLNIVGSTCLLVWTLSLLSQLVLRRRADRAGVALPFRMAAFPWLTALALAILAL
IFALLLYGDQTRLQFLSMVVLTLFIAGCSAAARRLRSQAG
Or try a new SitesBLAST search
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