GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctP in Pseudomonas fluorescens FW300-N2E2

Align C4-dicarboxylate-binding periplasmic protein DctP (characterized)
to candidate Pf6N2E2_3238 TRAP-type C4-dicarboxylate transport system, periplasmic component

Query= SwissProt::Q9HU18
         (331 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_3238
          Length = 331

 Score =  467 bits (1202), Expect = e-136
 Identities = 230/331 (69%), Positives = 273/331 (82%)

Query: 1   MLKHTAKALVCALSLTVAGIVQAADPIVIKFSHVVAEHTPKGQGALLFKKLVEERLPGKV 60
           MLK   K L+C L+L+  G   AA+PIVIKFSHVV E TPKGQGAL+FKKL EERLPGKV
Sbjct: 1   MLKPIWKTLLCTLALSAGGNALAAEPIVIKFSHVVGEQTPKGQGALMFKKLAEERLPGKV 60

Query: 61  KVEVYPNSSLFGDGKEMEALLLGDVQIIAPSLAKFEQYTKKLQIFDLPFLFDNIQAVDRF 120
           KVEVYPNS+L+GD KEMEALLLG+VQIIA SLAKFEQYTK +Q+FDLPFLFD+I AVDRF
Sbjct: 61  KVEVYPNSTLYGDDKEMEALLLGEVQIIARSLAKFEQYTKSVQLFDLPFLFDDIPAVDRF 120

Query: 121 QQSPQGKELLTSMQDKGITGLGYWHNGMKQLSANKPLREPKDARGLKFRVQASKVLEEQF 180
           QQSP+G++LL SM+ K ITGL YWHNGMKQLSANKPLR P+DAR L FR+Q S VLEEQF
Sbjct: 121 QQSPEGQKLLKSMESKNITGLAYWHNGMKQLSANKPLRTPEDARDLTFRIQTSAVLEEQF 180

Query: 181 KAVRANPRKMSFAEVYQGLQTGVVNGTENPWSNIYSQKMHEVQKYITESDHGVLDYMVIT 240
           KAV A  + M F+ VYQGL+TG+VNGTEN +SN Y+QK++EVQKY+TES+HG+LDYM+IT
Sbjct: 181 KAVDAKAKPMIFSVVYQGLRTGLVNGTENTYSNFYNQKLNEVQKYVTESNHGILDYMLIT 240

Query: 241 NTKFWNGLPEDVRGVLAKTMDEVTVEVNKQAEALNQGDKQRIVEAKTSEIIELTPEQRAE 300
            + FW GLP D+R  L K + E T   N++AE  NQ DKQ +++AKT+EII LTPEQR  
Sbjct: 241 TSDFWKGLPPDIRSELDKIVVESTAYANQEAERFNQQDKQHVLDAKTTEIITLTPEQRNA 300

Query: 301 WRKAMQPVWKKFEGEIGADLIKAAEAANQAQ 331
           WR+ M+PVW KFE EIG DLIKAA+A+N+AQ
Sbjct: 301 WREKMKPVWAKFEQEIGPDLIKAAQASNKAQ 331


Lambda     K      H
   0.316    0.132    0.376 

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: 372
Number of extensions: 13
Number of successful extensions: 1
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: 331
Length of database: 331
Length adjustment: 28
Effective length of query: 303
Effective length of database: 303
Effective search space:    91809
Effective search space used:    91809
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 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:

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