GapMind for catabolism of small carbon sources

 

Aligments for a candidate for braE in Marinobacter adhaerens HP15

Align Transmembrane component of a broad range amino acid ABC transporter (characterized, see rationale)
to candidate GFF3114 HP15_3057 leucine/isoleucine/valine transporter permease subunit

Query= uniprot:Q1MCU1
         (463 letters)



>FitnessBrowser__Marino:GFF3114
          Length = 423

 Score =  338 bits (868), Expect = 2e-97
 Identities = 179/305 (58%), Positives = 221/305 (72%), Gaps = 18/305 (5%)

Query: 142 ILIYVMLAWGLNIVVGLAGLLDLGYVAFYAVGAYSYALLSSYFGLSFWVLLPLSGIFAAL 201
           +LIY+MLA GLN+VVGLAGLLDLGYVAFYAVGAY++ALLS Y G+SFW+ LP+  + AAL
Sbjct: 122 VLIYIMLALGLNVVVGLAGLLDLGYVAFYAVGAYTFALLSQYTGISFWLALPIGALLAAL 181

Query: 202 WGVILGFPVLRLRGDYLAIVTLAFGEIIRLVLINWTDVTKGTFGISSIPKATLFGIPF-- 259
           +G++LGFPVLRLRGDYLAIVTL FGEIIR++L NWT +T G  GI  IP  TLFG+ F  
Sbjct: 182 FGLVLGFPVLRLRGDYLAIVTLGFGEIIRILLNNWTTLTGGPNGIGGIPDPTLFGMEFGR 241

Query: 260 ---DATAGGFAKLFHLPISSAYYKIFLFYLILALCMLTAYVTIRLRRMPIGRAWEALRED 316
              +     F + F +  S  +  IFL+ + L L + TA V  R  RMP+GRAWEALRED
Sbjct: 242 RVKEEGNTSFHETFGIAYSGEHKVIFLYLIALVLAVFTALVIRRFMRMPVGRAWEALRED 301

Query: 317 EIACRSLGINTVTTKLTAFATGAMFAGFAGSFFAARQGFVSPESFVFLESAVILAIVVLG 376
           EIA RSLG++    KL+AF  GA FAGFAG+ FA++QGF+SPESFVFLESA+ILAIVVLG
Sbjct: 302 EIAARSLGLSRTAVKLSAFTIGAFFAGFAGTVFASKQGFISPESFVFLESAIILAIVVLG 361

Query: 377 GMGSLTGIAIAAIVMVGGTELLREMSFLKLIFGPDFTPELYRMLIFGLAMVVVMLFKPRG 436
           GMGS  G+ +AAI +    EL RE S              YRMLIFG AMV++M+++P+G
Sbjct: 362 GMGSQIGVVLAAIAVTILPELAREFS-------------EYRMLIFGAAMVLMMVWRPQG 408

Query: 437 FVGSR 441
            +  R
Sbjct: 409 LMPMR 413


Lambda     K      H
   0.330    0.145    0.432 

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: 638
Number of extensions: 41
Number of successful extensions: 3
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: 463
Length of database: 423
Length adjustment: 32
Effective length of query: 431
Effective length of database: 391
Effective search space:   168521
Effective search space used:   168521
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 (21.8 bits)
S2: 51 (24.3 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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