Aligments for a candidate for actP in Burkholderia phytofirmans PsJN

GapMind for catabolism of small carbon sources

Aligments for a candidate for actP in Burkholderia phytofirmans PsJN

Align Cation/acetate symporter ActP; Acetate permease; Acetate transporter ActP (characterized)
to candidate BPHYT_RS25605 BPHYT_RS25605 symporter

Query= SwissProt::P32705
         (549 letters)



>lcl|FitnessBrowser__BFirm:BPHYT_RS25605 BPHYT_RS25605 symporter
          Length = 516

 Score =  400 bits (1028), Expect = e-116
 Identities = 222/513 (43%), Positives = 325/513 (63%), Gaps = 22/513 (4%)

Query: 36  IIMFLIFVVFTLGITYWASKRVRSRSDYYTAGGNITGFQNGLAIAGDYMSAASFLGISAL 95
           I++F+I +  TL ITYWA++R R+ S++Y AGGN++  +NG A+AGD+MSAA+FLG S L
Sbjct: 6   IVIFMIILAVTLMITYWAARRTRTTSEFYAAGGNLSARENGFALAGDWMSAAAFLGFSGL 65

Query: 96  VFTSGYDGLIYSLGFLVGWPIILFLIAERLRNLGRYTFADVASYRLKQGPIRILSACGSL 155
           V   G DG +Y++  L  + ++L LIAE +RN GRYTF DV + R+K+   R+ +  G++
Sbjct: 66  VSLYGMDGSLYAVAALAAFLVVLMLIAEPVRNTGRYTFGDVIAERMKRPGARLATIVGTV 125

Query: 156 VVVALYLIAQMVGAGKLIELLFGLNYHIAVVLVGVLMMMYVLFGGMLATTWVQIIKAVLL 215
           VV   Y++ QM GAG LI+L+ G+ Y +AVVLVG+ M++YVLFGGM+ATTWVQI+KA+LL
Sbjct: 126 VVNLAYMVPQMAGAGALIKLMLGVPYDVAVVLVGIGMIVYVLFGGMIATTWVQIVKAMLL 185

Query: 216 LFGASFMAFMVMKHVGFSFNNLFSEAMAVHPKGVDIMKPGGLVKDPISALSLGLGLMFGT 275
           L  A  +  M++  V F+   LF+    ++  G  ++  GG    P+  +SL +  +FG 
Sbjct: 186 LVAACVLVSMLLAAVRFNPLALFASVERLY--GSKMLASGGYFHHPLDTMSLFISFIFGV 243

Query: 276 AGLPHILMRFFTVSDAREARKSVFYATGFMGYFYILTFIIGFGAIMLVGANPEYKDAAGH 335
           AGLPHI+ RF+TV DAR ARKSV +     G F+++T +IGF + + VG     +DA   
Sbjct: 244 AGLPHIMTRFYTVPDARTARKSVLWLMFLAGSFFMVTTLIGFASAVFVG-----QDAIRA 298

Query: 336 LIGGNNMAAVHL-------ANAVGGNLFLGFISAVAFATILAVVAGLTLAGASAVSHDLY 388
              G N+A   L       A ++GG +FL  I A+AFA ILAVVAGLTLA + A++HDLY
Sbjct: 299 ADKGGNLALPLLAQYLGGGAGSLGGQIFLASICAIAFAAILAVVAGLTLASSGAIAHDLY 358

Query: 389 ANVFKKGA-TEREELRVSKITVLILGVIAIILGVLFENQNIAFMVGLAFAIAASCNFPII 447
            NV +KGA ++ E++RV++I  + +G+ AI L +L +  N+  +V LA ++AAS NFPII
Sbjct: 359 VNVLRKGAVSDAEQVRVARIATVAVGIAAIGLSLLAQGLNVGVLVILAISVAASSNFPII 418

Query: 448 LLSMYWSKLTTRGAMMGGWLGLITAVVLMILGPTIWVQILGHEKAIFPYEYPALFSITVA 507
           LLS++W +  T G + G   GL ++V L  +GP           A+FP   PA+ S+ + 
Sbjct: 419 LLSIFWRRFNTAGVIGGVIGGLTSSVALAFVGPAFM-----GSHALFPIVNPAIVSLPIG 473

Query: 508 FLGIWFFSATDNSAEGARERELFRAQFIRSQTG 540
               W    T  S     +   F A ++R+QTG
Sbjct: 474 LFSAWL--CTMLSRPTPTQDGDFEAFYLRAQTG 504


Lambda     K      H
   0.329    0.142    0.424 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 733
Number of extensions: 45
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 549
Length of database: 516
Length adjustment: 35
Effective length of query: 514
Effective length of database: 481
Effective search space:   247234
Effective search space used:   247234
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.8 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see the paper from 2019 on GapMind for amino acid biosynthesis, the preprint on GapMind for carbon sources, or view the source code.

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory

GapMind for catabolism of small carbon sources