GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS00890 in Acidovorax sp. GW101-3H11

Align ABC transporter ATP-binding protein (characterized, see rationale)
to candidate Ac3H11_4628 Branched-chain amino acid transport system permease protein LivM (TC 3.A.1.4.1)

Query= uniprot:A0A165KER0
         (358 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_4628
          Length = 358

 Score =  126 bits (316), Expect = 1e-33
 Identities = 99/299 (33%), Positives = 144/299 (48%), Gaps = 41/299 (13%)

Query: 12  AVALLVLPLILQSFGNAWVRIADLALLYVLLALGLNIVVGYAGLLDLGYVAFYAVGAYLF 71
           AVA + +P++   +    + I    ++  L ALG+N++VGY G + LG  AF AVGAY  
Sbjct: 34  AVAFVAVPMLASDYFFRAILIP--FVIMSLAALGVNVLVGYCGQISLGSGAFMAVGAYG- 90

Query: 72  ALMASPHLADNFAAFAAMFPNGLHTSLWIVIPVAALLAAFFGAMLGAPTLKLRGDYLAIV 131
                   A NF       P      L   + +  L A FFG + G P+L+++G YLA+ 
Sbjct: 91  --------AYNFFVRLPGLP------LIPALILGGLCATFFGILFGLPSLRVKGLYLAVA 136

Query: 132 TLG---FGE--IIRIFLNNLDHPVNLTNGPKGLGQIDSVKVFGLDLGKRLEVFGFDINSV 186
           TL    F +   +RI    LD P              SV V        L+VFG  I S 
Sbjct: 137 TLAAQFFSDWMFLRIRWFTLDTPSG------------SVSV------SNLQVFGMPIESA 178

Query: 187 TLYYYLFLVLVVVSVIICYRLQDSRIGRAWMAIREDEIAAKAMGINTRNMKLLAFGMGAS 246
           T  Y   L ++VV  ++   L    IGR WMAIR+ ++AA  +GI     KL AF + + 
Sbjct: 179 TSKYLFCLAILVVMALMAKNLVRGAIGREWMAIRDMDVAASVIGIRPMYAKLSAFAVSSF 238

Query: 247 FGGVSGAMFG-AFQGFVSPESFSLMESVMIVAMVVLGGIGHIPGVILGAVLLSALPEVL 304
             GV+G ++   + G   P +FS+  S  ++ MV++GG+G I G   GA  +  LP  L
Sbjct: 239 IIGVAGGLWAFVYLGAWEPGAFSVDMSFRLLFMVIIGGMGSIMGSFFGAAFIVVLPIAL 297


Lambda     K      H
   0.328    0.144    0.430 

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: 340
Number of extensions: 21
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: 358
Length of database: 358
Length adjustment: 29
Effective length of query: 329
Effective length of database: 329
Effective search space:   108241
Effective search space used:   108241
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: 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