GapMind for catabolism of small carbon sources

 

Alignments for a candidate for braD in Acidovorax sp. GW101-3H11

Align High-affinity branched-chain amino acid transport system permease protein BraD, component of Branched chain amino acid uptake transporter. Transports alanine (characterized)
to candidate Ac3H11_1432 High-affinity branched-chain amino acid transport system permease protein LivH (TC 3.A.1.4.1)

Query= TCDB::P21627
         (307 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_1432
          Length = 294

 Score =  137 bits (346), Expect = 2e-37
 Identities = 93/296 (31%), Positives = 158/296 (53%), Gaps = 17/296 (5%)

Query: 8   LQQLVNGLTVGSTYALIAIGYTMVYGIIGMINFAHGEVYMIGSYIAFIAITLLAMMGLDS 67
           L QL+ GL  GS YA++++G  +++G++ +INFAHG ++M G+ I ++A+  L   G++ 
Sbjct: 12  LSQLLLGLVNGSFYAILSLGLAVIFGLLNVINFAHGALFMTGALITWMAMNYL---GINY 68

Query: 68  VPLMMLAAFAASIIVTSAFGYSIERVAYRPLRGGNRLIPLISAIGMSIFLQNAV--MLSQ 125
             +++LA      +V   FG  IER+  R +   + L  L+  +G+++ ++     +   
Sbjct: 69  WLMLVLAP-----LVVGLFGVLIERLLLRWIYKLDHLYGLLLTLGLTLLIEGVFRSIYGV 123

Query: 126 DSKEKAIPTLLPGNFVFGESSMNGVVISYMQILIFVVTFLVMFGLTLFISRSRLGRACRA 185
                  P LL      G +++  +++   +  + V + +V       I +++LG   RA
Sbjct: 124 SGLGYDTPELLE-----GATNLGFMIMPNYRAWVVVASIVVCVATWYVIEKTKLGAYLRA 178

Query: 186 CAEDLKMTNLLGINSNNIIALTFVIGAALAAVAAVLLGMQYGVINPGIGFLAGIKAFTAA 245
             E+ ++    GIN   ++ LT+  GAALAA A VL    Y V  P +G    I  F   
Sbjct: 179 GTENPRLVEAFGINVPVMVTLTYAFGAALAAFAGVLAAPVYQV-TPLMGQNLIIVVFAVV 237

Query: 246 VLGGIGSIPGAMLGGLLLGVAEAFGADVFGDQYKDVVAFGLLILVLLFRPTGILGR 301
           V+GG+GSI G++L GL LGV E F   VF  +    V F ++++VLL RP G+ G+
Sbjct: 238 VIGGMGSIMGSILTGLGLGVIEGF-TKVFYPEASSTVVFVIMVIVLLIRPAGLFGK 292


Lambda     K      H
   0.328    0.145    0.413 

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: 305
Number of extensions: 19
Number of successful extensions: 7
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: 307
Length of database: 294
Length adjustment: 27
Effective length of query: 280
Effective length of database: 267
Effective search space:    74760
Effective search space used:    74760
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: 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