Aligments for a candidate for frcA in Pseudomonas fluorescens FW300-N2C3

GapMind for catabolism of small carbon sources

Aligments for a candidate for frcA in Pseudomonas fluorescens FW300-N2C3

Align Fructose import ATP-binding protein FrcA; EC 7.5.2.- (characterized)
to candidate AO356_28510 AO356_28510 xylose transporter

Query= SwissProt::Q9F9B0
         (260 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_28510
          Length = 518

 Score =  139 bits (350), Expect = 1e-37
 Identities = 86/247 (34%), Positives = 141/247 (57%), Gaps = 11/247 (4%)

Query: 6   ILTARGLVKRYGRVTALDRADFDLYPGEILAVIGDNGAGKSSMIKAISGAVTPD---EGE 62
           +L   G+VK +G V AL+  D  + PGE + + G+NGAGKS+++K +S AV P    EGE
Sbjct: 5   LLQMNGIVKTFGGVKALNGIDIKVRPGECVGLCGENGAGKSTLMKVLS-AVYPHGTWEGE 63

Query: 63  IRLEGKPIQFRSPMEARQAGIETVYQNLALSPALSIADNMFLGREIRKPGIMGKWFRSLD 122
           I  +G+P++ +S  E   AGI  ++Q L L P LS+A+N+F+G E+  PG        ++
Sbjct: 64  IIWDGQPLKAQSISETEAAGIVIIHQELTLVPDLSVAENIFMGHELTLPG------GRMN 117

Query: 123 RAAMEKQARAKLSELGLMTIQNINQAVETLSGGQRQGVAVARAAAFGSKVVIMDEPTAAL 182
             AM  +A A + EL +  + N++  V    GG +Q V +A+A    ++++I+DEP++AL
Sbjct: 118 YPAMIHRAEALMRELKVPDM-NVSLPVSQYGGGYQQLVEIAKALNKQARLLILDEPSSAL 176

Query: 183 GVKESRRVLELILDVRRRGLPIVLISHNMPHVFEVADRIHIHRLGRRLCVINPKDYTMSD 242
              E   +L++I D++ +G+  V ISH +  V  V D I + R G+ +      D  +  
Sbjct: 177 TRSEIEVLLDIIRDLKAKGVACVYISHKLDEVAAVCDTISVIRDGKHIATTAMTDMDIPK 236

Query: 243 AVAFMTG 249
            +  M G
Sbjct: 237 IITQMVG 243



 Score = 75.1 bits (183), Expect = 3e-18
 Identities = 55/206 (26%), Positives = 105/206 (50%), Gaps = 14/206 (6%)

Query: 22  LDRADFDLYPGEILAVIGDNGAGKSSMIKAISGAVTPD-EGEIRLEGKPIQFRSPMEARQ 80
           +D   F L  GEIL + G  GAG++ ++ A+ GA     EGE+ L G+ I  R+P+++ +
Sbjct: 280 VDDISFVLKRGEILGIAGLVGAGRTELVSALFGAYPGRYEGEVWLNGQQIDTRTPLKSIR 339

Query: 81  AGIETVYQNL---ALSPALSIADNMFLGREIRKPGIMGKWFRSLDRAAMEKQARAKLSEL 137
           AG+  V ++     + P L +  N+ L        ++  + + L R   E +  +   E+
Sbjct: 340 AGLCMVPEDRKRQGIIPDLGVGQNITLA-------VLDNYSK-LTRIDAEAELGSIDKEI 391

Query: 138 GLMTIQNINQ--AVETLSGGQRQGVAVARAAAFGSKVVIMDEPTAALGVKESRRVLELIL 195
             M ++  +    + +LSGG +Q   +A+      +V+I+DEPT  + V     + +L+ 
Sbjct: 392 ARMHLKTASPFLPITSLSGGNQQKAVLAKMLLTKPRVLILDEPTRGVDVGAKYEIYKLMG 451

Query: 196 DVRRRGLPIVLISHNMPHVFEVADRI 221
            +   G+ I+++S  +  V  V+DR+
Sbjct: 452 ALAAEGVSIIMVSSELAEVLGVSDRV 477


Lambda     K      H
   0.321    0.136    0.383 

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: 301
Number of extensions: 16
Number of successful extensions: 6
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 260
Length of database: 518
Length adjustment: 30
Effective length of query: 230
Effective length of database: 488
Effective search space:   112240
Effective search space used:   112240
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 49 (23.5 bits)

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

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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, 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