Aligments for a candidate for thuE in Pseudomonas fluorescens FW300-N1B4

GapMind for catabolism of small carbon sources

Aligments for a candidate for thuE in Pseudomonas fluorescens FW300-N1B4

Align Trehalose/maltose-binding protein aka TT_C1627, component of The trehalose/maltose/sucrose/palatinose porter (TTC1627-9) plus MalK1 (ABC protein, shared with 3.A.1.1.24) (Silva et al. 2005; Chevance et al., 2006). The receptor (TTC1627) binds disaccharide alpha-glycosides, namely trehalose (alpha-1,1), sucrose (alpha-1,2), maltose (alpha-1,4), palatinose (alpha-1,6) and glucose (characterized)
to candidate Pf1N1B4_5112 Maltose/maltodextrin ABC transporter, substrate binding periplasmic protein MalE

Query= TCDB::Q72H68
         (429 letters)



>lcl|FitnessBrowser__pseudo1_N1B4:Pf1N1B4_5112 Maltose/maltodextrin
           ABC transporter, substrate binding periplasmic protein
           MalE
          Length = 390

 Score =  353 bits (907), Expect = e-102
 Identities = 175/388 (45%), Positives = 244/388 (62%), Gaps = 1/388 (0%)

Query: 42  VGEGGRWMKEMVEAWGKKTGTRVEYIDSPADTNDRLALYQQYWAARSPDVDVYMIDVIWP 101
           VG   +  KE V+AW K+TG  VE + +P    +RL+ YQQ  +A+S D+D+  ID++WP
Sbjct: 1   VGAELQLCKEAVQAWSKQTGNNVEVVSTPNSATERLSFYQQILSAQSSDIDIIQIDMVWP 60

Query: 102 GIVAPHALDLKPYLTEAELKEFFPRIVQNNTIRGKLTSLPFFTDAGILYYRKDLLEKYGY 161
           G++A H LDL+  L     + +F   V N T+ G+L ++P+FTD+G+LYYRKDLLEKY  
Sbjct: 61  GMLAKHLLDLREVLPANATQGYFQAQVDNATVNGRLVTMPWFTDSGLLYYRKDLLEKYNQ 120

Query: 162 TSPPRTWNELEQMAERVMEGERRAGNRDFWGFVFQGKPYEGLTCDALEWIYSHGGGRIVE 221
              PRTW E+   A  + + ER AGN + WG++FQG+ YEGLTC+ALEWI S   G +V 
Sbjct: 121 -QVPRTWEEMTATARNIQQAERTAGNPNAWGYIFQGRAYEGLTCNALEWISSQPEGGLVN 179

Query: 222 PDGTISVNNGRAALALNRAHGWVGRIAPQGVTSYAEEEARNVWQQGNSLFMRNWPYAYAL 281
             G I VN+  +  AL  A  WVG I+P+GV +Y EEE R V+Q GN+LFMRNWPY +AL
Sbjct: 180 SRGDIVVNSQASRTALTLAKSWVGDISPRGVLNYTEEEGRGVFQSGNALFMRNWPYVWAL 239

Query: 282 GQAEGSPIRGKFGVTVLPKASADAPNAATLGGWQLMVSAYSRYPKEAVDLVKYLASYEVQ 341
            Q + S ++ K GV  LP+      +A+TLGGW L VS YS +PK A +LV YL S + Q
Sbjct: 240 VQGQDSAVKDKVGVAPLPRGGETGTHASTLGGWGLAVSRYSAHPKLAAELVSYLTSAQEQ 299

Query: 342 KDNAVRLSRLPTRPALYTDRDVLARNPWFRDLLPVFQNAVSRPSDVAGARYNQVSEAIWT 401
           K  A+  +  P   +LY D ++LA  P++  L  +  + V RP+ +   RY +VS A + 
Sbjct: 300 KHRALIGAYNPVIESLYQDPELLAAMPYYAQLHSILNDGVMRPASITADRYPRVSNAFFD 359

Query: 402 EVHSVLTGRKKGEQAVRDLEARIRRILR 429
            VH VL G    +QA+ +LE+ + RI R
Sbjct: 360 RVHGVLAGELPVDQALAELESELTRIKR 387


Lambda     K      H
   0.319    0.135    0.418 

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: 461
Number of extensions: 22
Number of successful extensions: 2
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: 429
Length of database: 390
Length adjustment: 31
Effective length of query: 398
Effective length of database: 359
Effective search space:   142882
Effective search space used:   142882
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 (21.7 bits)
S2: 50 (23.9 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 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