GapMind for catabolism of small carbon sources

 

Alignments for a candidate for braE in Maridesulfovibrio zosterae DSM 11974

Align Transmembrane component of a broad range amino acid ABC transporter (characterized, see rationale)
to candidate WP_051249582.1 H589_RS0101625 branched-chain amino acid ABC transporter permease

Query= uniprot:Q1MCU1
         (463 letters)



>NCBI__GCF_000425265.1:WP_051249582.1
          Length = 390

 Score =  272 bits (695), Expect = 2e-77
 Identities = 147/319 (46%), Positives = 199/319 (62%), Gaps = 20/319 (6%)

Query: 120 MVVVAIKGPQGSLTYVDNFGIQILIYVMLAWGLNIVVGLAGLLDLGYVAFYAVGAYSYAL 179
           ++  AI  P     Y  +  I  ++Y+ L  GLNIVVGLAG+LDLGY+AFY +GAY+YAL
Sbjct: 80  LLAFAIAYPHLFGRYAQDVAINCMVYICLGLGLNIVVGLAGMLDLGYIAFYGLGAYTYAL 139

Query: 180 LSSYFGLSFWVLLPLSGIFAALWGVILGFPVLRLRGDYLAIVTLAFGEIIRLVLINWTDV 239
           LS  + +SFW+ LPLS   A L   I+G+  +R+RGDYLAIVTL F EI+R+V  NW  +
Sbjct: 140 LSVTYKISFWLCLPLSAAVAGLGACIIGYCSMRMRGDYLAIVTLGFAEIVRMVFNNWMSL 199

Query: 240 TKGTFGISSIPKATLFGIPFDATAGGFAKLFHLPISSAYYKIFLFYLILALCMLTAYVTI 299
           T G  GI+ I    ++   F      F  L+   +S       ++Y+ILAL + T     
Sbjct: 200 TNGPNGITGIKAPGIYWPDF-TNGMTFEHLWLKKLS------LIYYVILALVVFTIIAVY 252

Query: 300 RLRRMPIGRAWEALREDEIACRSLGINTVTTKLTAFATGAMFAGFAGSFFAARQGFVSPE 359
           RL    IGRAWEA+REDE A   +GI T   KL A+ TGA F G AG+F+AAR  FVSPE
Sbjct: 253 RLNHSRIGRAWEAIREDETAAEVMGIPTFYMKLLAYCTGACFGGMAGAFYAARMRFVSPE 312

Query: 360 SFVFLESAVILAIVVLGGMGSLTGIAIAAIVMVGGTELLREMSFLKLIFGPDFTPELYRM 419
           SF FLESA++L++VVLGGMGS+ G+ + A+ ++   E+ R+              ELYRM
Sbjct: 313 SFTFLESAMVLSMVVLGGMGSIPGVILGALALIALPEIFRDF-------------ELYRM 359

Query: 420 LIFGLAMVVVMLFKPRGFV 438
           L+FG  M ++MLF+P+G +
Sbjct: 360 LVFGGVMTLMMLFRPQGLL 378


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: 524
Number of extensions: 22
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: 390
Length adjustment: 32
Effective length of query: 431
Effective length of database: 358
Effective search space:   154298
Effective search space used:   154298
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 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