GapMind for catabolism of small carbon sources

 

Alignments for a candidate for braE in Shewanella loihica PV-4

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 5210164 Shew_2608 inner-membrane translocator (RefSeq)

Query= TCDB::P21628
         (417 letters)



>FitnessBrowser__PV4:5210164
          Length = 357

 Score =  125 bits (313), Expect = 3e-33
 Identities = 94/311 (30%), Positives = 147/311 (47%), Gaps = 46/311 (14%)

Query: 118 TLILIYVMLGI---GLNIVVGLAGLLDLGYVGFYAVGAYTYALLAEYAGFGFWTALPIAG 174
           TL +    LGI   GLNI+VG  G + LG+  F+  GA+  A L           +P+AG
Sbjct: 52  TLFIQISYLGIAALGLNILVGFTGQISLGHGAFFGFGAFASAWLNTSFNIPVVFCIPLAG 111

Query: 175 MMAALFGFLLGFPVLRLRGDYLAIVTLGFGEIIRILLRNMTEITGGPNGIGSIPKPTLFG 234
            +    G + G P  R++G YLAI TL    II+         +GG +G  + P  +LFG
Sbjct: 112 FLTMGVGMMFGMPAARIKGLYLAIATLAAQFIIQDFFGRAEWFSGGSSGAMAAPV-SLFG 170

Query: 235 LTFERRAPEGMQTFHEFFGIAYNTNYKVILLYVVALLLVLLALFVINRLMRMPIGRAWEA 294
             F+        T   F+ IA    + ++ +Y+               LMR   GRA+ A
Sbjct: 171 FDFD--------TDMSFYFIAL---FALVFMYIWGC-----------NLMRSRDGRAFVA 208

Query: 295 LREDEVACRALGLNPTIVKLSAFTIGASFAGFAGSFFAARQGLVTPESFTFIESAMILAI 354
           +R+  ++   +G+     +L +F I + +AG  G+ +A   G V+ E FT + S   LA+
Sbjct: 209 VRDHYLSAEIMGVKLNKYRLLSFGISSFYAGIGGALYAHYLGYVSSEGFTILMSIQFLAM 268

Query: 355 VVLGGMGSQLGVILAAVVMVLLQE----MRGFNEY----------------RMLIFGLTM 394
           V++GG+GS  G ++  V MVLL E    M G  +Y                + +  GL +
Sbjct: 269 VIIGGLGSIKGTLMGVVFMVLLPEVLEGMVGLMKYTDYGNLPMVTDGLAYIKEMAIGLVI 328

Query: 395 IVMMIWRPQGL 405
           I+ +I+ P+GL
Sbjct: 329 ILFLIFEPEGL 339


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: 427
Number of extensions: 29
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: 417
Length of database: 357
Length adjustment: 30
Effective length of query: 387
Effective length of database: 327
Effective search space:   126549
Effective search space used:   126549
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: 50 (23.9 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