Aligments for a candidate for Bap2 in Pseudomonas fluorescens FW300-N2E3

GapMind for catabolism of small carbon sources

Aligments for a candidate for Bap2 in Pseudomonas fluorescens FW300-N2E3

Align Arbuscular mycorrhizal fungal proline:H+ symporter, AAP1 (binds and probably transports nonpolar, hydrophobic amino acids) (characterized)
to candidate AO353_24825 AO353_24825 amino acid transporter

Query= TCDB::Q2VQZ4
         (536 letters)



>lcl|FitnessBrowser__pseudo3_N2E3:AO353_24825 AO353_24825 amino acid
           transporter
          Length = 470

 Score =  248 bits (632), Expect = 5e-70
 Identities = 151/483 (31%), Positives = 244/483 (50%), Gaps = 23/483 (4%)

Query: 24  ETGEVKNGGLKQDLKNRHMQMIAIGGAIGAGLFVGSGGALQKGGPAALLIGYLIIGIMLL 83
           E+ E K   L + LK+RH+ M+++GG IG GLF+GSG  + +GGP   ++ YLI G ++ 
Sbjct: 3   ESIERKGIHLTRALKSRHIFMLSLGGVIGTGLFMGSGVTINQGGPVGAILAYLIAGFLMY 62

Query: 84  CTCLALAEMAVLYPVNGAFFTYIVRFVDPSWGFAMGWQYALAWLTVLPFELIAASITIRF 143
              + L E++V  PV+G+F T+  +F+ P+ GF +GW Y ++W + +  E  AA + +  
Sbjct: 63  LVMVCLGELSVQMPVSGSFQTHATKFIGPATGFMIGWVYWMSWASTVGLEFTAAGMLMVR 122

Query: 144 WREDINMAVWVSVFLVVLMGIQIFGVRGYGEVEFVLSIIKICACVGFIILGIVINCGGV- 202
           W   + +  W ++F+VVL G+     R +GE E+  S IK+ A +GFI++G+++  G + 
Sbjct: 123 WFPTVPIWYWSALFVVVLFGLNALATRAFGEAEYWFSGIKVAAILGFIVVGVLVIFGAIP 182

Query: 203 ---GDQGYIGVKYWRDPGAFTSFKGFCAVFVVAAFSFGGTEMVGLAAAESANPRKSIPMA 259
              G    +      D           AV +   ++F G E++G+AA E+  P KSIP A
Sbjct: 183 LTSGAPAPMMSNLIGDSLFPNGLPAVFAVMMTVVYAFQGCEIMGVAAGETDQPEKSIPRA 242

Query: 260 SKQVFWRIAIFYILNLFIVGLILPANDPRLMGASGANTKASPFVLAIQDAGIKVLPSIMN 319
            + V +R+ IFY+L + ++  I+P     LM         SPFV      GI     +MN
Sbjct: 243 VRNVVFRVLIFYVLAIVVLSAIVPWQQAGLM--------ESPFVQVFDMVGIPYAADLMN 294

Query: 320 AVITVAVLSVANSCTFGSTRTIQAMAERNMAPNFFKYIDSKGRPLYCVILQIAFGLLAYI 379
            VI  A+LSV NS  + STR + AM++  MAP     +  +G PL  + + + F L++ +
Sbjct: 295 FVILTAILSVGNSGLYASTRILWAMSKTGMAPKSLSPLSKRGVPLRALSITLCFALVSLM 354

Query: 380 GAAPQGMEIFGWLLALTGLGFLFVWGSICLAHIRMRAGMKAQGINLGLIPYKTPFGVAGS 439
            +      +F  L+A++G+     W  I LA  + R      G  L  + Y+ P+     
Sbjct: 355 TSFIAADTLFMVLMAVSGMSGTVTWIVIALAQYKFRRAYIRDGGKLSDLKYRAPW----- 409

Query: 440 YLGLGLNILALIASFYTALFPASGASPTAEAFFSSYLAFFSVTLLYLGYKACTRKRQMYV 499
           +  L +  +AL  S +  L       P      S Y  F  + L Y  Y    RKRQ  +
Sbjct: 410 FPLLPILCIALCCSLFVFLAMDETQRP------SLYWGFGFMALCYGAYFLIQRKRQAVL 463

Query: 500 RPA 502
            P+
Sbjct: 464 APS 466


Lambda     K      H
   0.327    0.142    0.442 

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: 636
Number of extensions: 36
Number of successful extensions: 3
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: 536
Length of database: 470
Length adjustment: 34
Effective length of query: 502
Effective length of database: 436
Effective search space:   218872
Effective search space used:   218872
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 (21.7 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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Protein sequences (fasta format)
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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