GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0028 in Pseudomonas fluorescens FW300-N1B4

Align TM0028, component of β-glucoside porter (Conners et al., 2005). Binds cellobiose, laminaribiose (Nanavati et al. 2006). Regulated by cellobiose-responsive repressor BglR (characterized)
to candidate Pf1N1B4_5104 Oligopeptide transport system permease protein OppB (TC 3.A.1.5.1)

Query= TCDB::Q9WXN5
         (330 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_5104
          Length = 324

 Score =  178 bits (452), Expect = 1e-49
 Identities = 122/326 (37%), Positives = 173/326 (53%), Gaps = 20/326 (6%)

Query: 5   LLKAENVRAYYKLEKVSVKAVDGLSFEILEDEVIGVVGESGCGKTTLSNVIFMNMVKPLT 64
           +LK E +    +  +  V  VD LSF++ E EV+G+VGESG GKT     +   +  P  
Sbjct: 1   VLKVEELSVIVRKGEHEVTLVDRLSFDLAEGEVLGLVGESGSGKTLACRGLMRLLPSPN- 59

Query: 65  LVDGKIFLRVNGEFVELSS---MTRDEV-KRKFWGKEITIIPQAAMNALMPTIRMEKYVR 120
                  LRV G  V+L+    +  DE   R+  G+++ +I Q   + L P +R+ + + 
Sbjct: 60  -------LRVEGTAVQLAGENLLHLDEAGMRRMRGRQLGMIFQNPSSHLDPLMRIGEQIG 112

Query: 121 HLAESH-GIDEEELLDKARRRFEEVGL-DPLW-IKRYPFELSGGMRQRAVIAIATILNPS 177
                H G    E   +A     +VG+ DP   +  YP E SGGMRQRA+IA+A   NP+
Sbjct: 113 EGIRLHQGASRREARAQAIDVLRQVGIPDPQRRVDSYPHEFSGGMRQRAMIAVALGCNPN 172

Query: 178 LLIADEPTSALDVVNQKVLLKVLMQMKRQ-GIVKSIIFITHDIATVRQIADRMIIMYAGK 236
           +LIADEPT+ALDV  Q  +L++L+ ++ Q G+  SII ITHD+  V Q  D + +MYAG+
Sbjct: 173 VLIADEPTTALDVTVQAQILRLLLDLRDQRGL--SIIMITHDLGVVAQTCDSIAVMYAGR 230

Query: 237 IVEFAPVESLLEKPLHPYTQGLFNSVLTPEPEVKKRGITTIPGAPPNLINPPSGCRFHPR 296
           + E      +L  P HPYT GL +    P        + TI G PP L   P GCRF+PR
Sbjct: 231 LCEHGNKHEVLAHPRHPYTAGLID--CQPATSHGHALLNTIAGQPPLLDALPQGCRFNPR 288

Query: 297 CPHAMDVCKEKEPPLTEIEPGRRVAC 322
           C    + C    P L  +  G R+AC
Sbjct: 289 CQQIGNRCTTLMPGLQPVSHGHRIAC 314


Lambda     K      H
   0.321    0.138    0.405 

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: 297
Number of extensions: 13
Number of successful extensions: 4
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: 330
Length of database: 324
Length adjustment: 28
Effective length of query: 302
Effective length of database: 296
Effective search space:    89392
Effective search space used:    89392
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: 48 (23.1 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:

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:

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:

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:

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