Alignments for a candidate for citM in Pseudomonas fluorescens FW300-N2C3

GapMind for catabolism of small carbon sources

Alignments for a candidate for citM in Pseudomonas fluorescens FW300-N2C3

Align [Citrate]•M2+ (Ca2+ preferring):H+ symporter, CitH (transports Ca2+, Ba2+ & Sr2+) (characterized)
to candidate AO356_28880 AO356_28880 damage-inducible protein CinA

Query= TCDB::P42308
         (426 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_28880
          Length = 434

 Score =  491 bits (1263), Expect = e-143
 Identities = 248/431 (57%), Positives = 323/431 (74%), Gaps = 6/431 (1%)

Query: 1   MLAILGFVMMIVFMYLIMSNRLSALIALIVVPIVFALISGFGKDLGEMMIQGVTDLAPTG 60
           MLA+LG  M++VF +LIM+ RLS ++AL VVPIVFA++ GFG   G+MM+ G+  +AP+ 
Sbjct: 1   MLALLGLAMVVVFTFLIMTKRLSPIVALTVVPIVFAVLGGFGGTTGKMMLDGLKMVAPSA 60

Query: 61  IMLLFAILYFGIMIDSGLFDPLIAKILSFVKGDPLKIAVGTAVLTMTISLDGDGTTTYMI 120
            +LLFAIL+FG+MID+GLFDPLI KIL  V GDP+KIAVGTA+L++ ++LDGDGTTTYMI
Sbjct: 61  ALLLFAILFFGLMIDAGLFDPLIRKILKRVNGDPMKIAVGTALLSLLVALDGDGTTTYMI 120

Query: 121 TIAAMLPLYKRLGMNRLVLAGIAMLGSGVMN-IIPWGGPTARVLASLKLDTSEVFTPLIP 179
           T AAMLPLYKR+GMN ++LA I+ML   +M+ + PWGGP  R +A+L LD  E F PL+P
Sbjct: 121 TCAAMLPLYKRIGMNPMILATISMLSLSIMSGMTPWGGPATRAIAALGLDAGEYFVPLLP 180

Query: 180 AMIAGILWVIAVAYILGKKERKRLGVISI-----DHAPSSDPEAAPLKRPALQWFNLLLT 234
            MI G +WV+  A++LG+ ERKR+G + +     D   ++  E  P KRP L + NLLL 
Sbjct: 181 TMIGGAMWVVFTAFLLGRAERKRIGNVQLQSGGGDCYINAIIEDTPHKRPKLAYVNLLLV 240

Query: 235 VALMAALITSLLPLPVLFMTAFAVALMVNYPNVKEQQKRISAHAGNALNVVSMVFAAGIF 294
           VA+M AL+  L+   +LF+  F +ALM+NYP +  Q++RI AH+GNA+ VV +VFAAGIF
Sbjct: 241 VAVMVALVMGLMHSAILFLIGFVLALMINYPQLDIQKERILAHSGNAMTVVLLVFAAGIF 300

Query: 295 TGILSGTKMVDAMAHSLVSLIPDAMGPHLPLITAIVSMPFTFFMSNDAFYFGVLPIIAEA 354
            GI SGTKMVDA+A +LV  IP + G   PL+ AI SMP TF +SNDA+YFGV+PI+A A
Sbjct: 301 AGIFSGTKMVDALAQTLVDWIPPSWGHLFPLVVAITSMPLTFVLSNDAYYFGVVPILANA 360

Query: 355 ASAYGIDAAEIGRASLLGQPVHLLSPLVPSTYLLVGMAGVSFGDHQKFTIKWAVGTTIVM 414
           A+AYGID  EI RAS+LGQPVHL+SPLV ST LLVGM     GD QK T+KWAV T++V+
Sbjct: 361 AAAYGIDPVEIARASILGQPVHLMSPLVASTLLLVGMVDRDLGDFQKATVKWAVLTSLVI 420

Query: 415 TIAALLIGIIS 425
           T  ALL G ++
Sbjct: 421 TALALLTGALT 431


Lambda     K      H
   0.328    0.142    0.411 

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: 684
Number of extensions: 37
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: 426
Length of database: 434
Length adjustment: 32
Effective length of query: 394
Effective length of database: 402
Effective search space:   158388
Effective search space used:   158388
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: 51 (24.3 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)
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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 paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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