GapMind for catabolism of small carbon sources

 

Alignments for a candidate for braE in Desulfacinum infernum DSM 9756

Align Transmembrane component of a broad range amino acid ABC transporter (characterized, see rationale)
to candidate WP_245795194.1 BUB04_RS13185 branched-chain amino acid ABC transporter permease

Query= uniprot:Q1MCU1
         (463 letters)



>NCBI__GCF_900129305.1:WP_245795194.1
          Length = 320

 Score =  192 bits (489), Expect = 1e-53
 Identities = 116/313 (37%), Positives = 170/313 (54%), Gaps = 32/313 (10%)

Query: 144 IYVMLAWGLNIVVGLAGLLDLGYVAFYAVGAYSYALLSSYFGLSFWVLLPLSGIFAALWG 203
           +Y  L   LN++VG AGL +LG+ AFYAVGAY+ A+L++ F +    LLPL  + A ++ 
Sbjct: 36  LYAALGLSLNLIVGHAGLFNLGHAAFYAVGAYTAAILNTMFHIPVLALLPLCALTAGIFA 95

Query: 204 VILGFPVLRLRGDYLAIVTLAFGEIIRLVLINWT-DVTKGTFGISSIPKATLFGIPFDAT 262
           +++  P++ LRGDYL IVT+  GEI+R+ LIN    +T G  GI  I +  LFG+     
Sbjct: 96  LLVAKPIIHLRGDYLCIVTIGVGEIVRIALINNIFGITGGANGIFGISRPNLFGL----- 150

Query: 263 AGGFAKLFHLPISSAYYKIFLFYLILALCMLTAYVTIRLRRMPIGRAWEALREDEIACRS 322
                 +   P          FYLI      TA+   RL     GRA   LREDE A   
Sbjct: 151 ------VIRKPHE-------FFYLIWFFVAATAFFFHRLENSRFGRALNYLREDETAAEG 197

Query: 323 LGINTVTTKLTAFATGAMFAGFAGSFFAARQGFVSPESFVFLESAVILAIVVLGGMGSLT 382
            GI+T   KL AF  GA +AG  G+ +AA+   +SPESF F ES ++  +++LGG GS+ 
Sbjct: 198 SGIDTAHYKLMAFVIGAAWAGMVGNLYAAKMTIISPESFSFWESVLMFTLIILGGSGSIP 257

Query: 383 GIAIAAIVMVGGTELLREMSFLKLIFGPDFTPELYRMLIFGLAMVVVMLFKPRGFVGSRE 442
           G+ + A +++G  E+ R            FT    RM++FG AM+ +M+F+  G + ++ 
Sbjct: 258 GVLLGAFLVIGLPEVFR-----------GFTNA--RMMVFGAAMIAMMIFRTGGILPAKP 304

Query: 443 PTAFLRERKAISG 455
               L  R+   G
Sbjct: 305 RRYILPGREEGQG 317


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: 452
Number of extensions: 27
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: 320
Length adjustment: 30
Effective length of query: 433
Effective length of database: 290
Effective search space:   125570
Effective search space used:   125570
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: 50 (23.9 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