GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livM in Hydrogenophaga taeniospiralis CCUG 15921 NBRC 102512

Align High-affinity branched-chain amino acid transport system permease protein BraE, component of Branched chain amino acid uptake transporter. Transports alanine (characterized)
to candidate WP_218017359.1 HTA01S_RS15250 branched-chain amino acid ABC transporter permease

Query= TCDB::P21628
         (417 letters)



>NCBI__GCF_001592305.1:WP_218017359.1
          Length = 312

 Score =  118 bits (295), Expect = 3e-31
 Identities = 94/317 (29%), Positives = 138/317 (43%), Gaps = 31/317 (9%)

Query: 95  VLALVVVAFVWPFFASRGAVDIATLILIYVMLGIGLNIVVGLAGLLDLGYVGFYAVGAYT 154
           ++ALVVV    P F     V I T    + +   G+  +    G++ L  VG   VG + 
Sbjct: 5   LVALVVV----PMFLGGQWVQILTSTACFALAAAGVGFMYSRLGMVSLAQVGLMGVGGWV 60

Query: 155 YALLAEYAGFGFWTALPIAGMMAALFGFLLGFPVLRLRGDYLAIVTLGFGEIIRILLRNM 214
              +       F   L +A  +  +FG+++  P LR+RG YLA++TL     + I+    
Sbjct: 61  MLRMNHGFNLPFELNLAVAATVTMVFGWVMALPALRMRGLYLALITLMAASGLEIVFSTF 120

Query: 215 TEITGGPNGIGSIPKPTLFGLTFERRAPEGMQTFHEFFGIAYNTNYKVILLYVVALLLVL 274
               GG    G +P      L    R P               T  +  L Y V +LLV 
Sbjct: 121 RFPNGGEGFWGVMPS-----LIAPFRRPW------------LATGNEAYLRYTVVMLLVG 163

Query: 275 LALFVINRLMRMPIGRAWEALREDEVACRALGLNPTIVKLSAFTIGASFAGFAGSFFAAR 334
             L   +R  R   GRAW  +R  E A  A G+N    K  AF +    AG AG   A  
Sbjct: 164 FLLIEAHR--RTAPGRAWAMIRRSEAAAMASGVNVVYYKAWAFGLSGLLAGMAGGLLAGT 221

Query: 335 QGLVTPESFTFIESAMILAIVVLGGMGSQLGVILAAVVMVLLQEMRGFNEY------RML 388
            GL+ P +F   ES M+ A+ V+GG    LG +LAAV+  +L  +  FN +       ++
Sbjct: 222 LGLLDPATFRASESIMLFALAVVGGARHWLGAVLAAVLYRVLPGL--FNNWGLDADLALV 279

Query: 389 IFGLTMIVMMIWRPQGL 405
           IFG  ++  ++  P GL
Sbjct: 280 IFGAALLHALMTAPDGL 296


Lambda     K      H
   0.330    0.146    0.439 

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: 358
Number of extensions: 28
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 417
Length of database: 312
Length adjustment: 29
Effective length of query: 388
Effective length of database: 283
Effective search space:   109804
Effective search space used:   109804
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. 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