GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Psest_0085 in Marinobacter adhaerens HP15

Align alpha-ketoglutarate TRAP transporter, solute receptor component (characterized)
to candidate GFF1091 HP15_1069 TRAP transporter solute receptor, TAXI family protein

Query= reanno::psRCH2:GFF85
         (317 letters)



>FitnessBrowser__Marino:GFF1091
          Length = 327

 Score =  165 bits (417), Expect = 2e-45
 Identities = 106/315 (33%), Positives = 159/315 (50%), Gaps = 8/315 (2%)

Query: 10  LAAAAAFTASTAAVAAPT--FINILTGGTSGVYYPIGVALSQQYN---KIDGAKTSVQAT 64
           +AAA +  A++ +V+A    F+ I TGG +GVYYP G A+ +  N   K  G + SV++T
Sbjct: 12  VAAAVSLGAASTSVSAQEQRFVTIGTGGVTGVYYPAGGAICRLVNMDRKEHGIRCSVEST 71

Query: 65  KASVENLNLLQAGRGELAFSLGDSVEDAWNGVEDAGFKAPLKRLRAIAGTYNNYIQIVAS 124
             SV NLN ++ G  +LA +  D    A+NG          K LRA+   +     +VAS
Sbjct: 72  GGSVYNLNAIRQGELDLAVAQSDWQYHAYNGTSQFKDDGANKDLRAVFSLHPEPFTVVAS 131

Query: 125 AESGIKTLDDLKGKRISVGAPKSGTELNARAIFKAAGLDYKDMGRVEFLPYAESVELIKN 184
             SGIKT +DL+GKR+SVG P SG    A  +    G           +  AE  + + +
Sbjct: 132 KGSGIKTFEDLEGKRVSVGNPGSGQRATAEVLMDEMGWTLDKFSLAAEIKAAEQSQALCD 191

Query: 185 RQLDATLQSSGLGMAAIRDLASTMPVTFVEIPAEVVEKI--ESDAYLAGVIPAGTYDGQD 242
             +DA   + G    AI++  ++     V +     +K+  E+  Y   VIP G Y G D
Sbjct: 192 GNIDAFFYTVGHPSGAIKEATTSCDSVLVNVDNAATQKLIDENPYYRKAVIPGGMYRGSD 251

Query: 243 ADVPTVAITNILVTHEKVSDEVAYQMTKLMFDNLAALGNAHSAAKDI-KLENATKNLPIP 301
            DV T  +    V+   V D+V Y + K +F+N  +    H A  ++ K E  +  L  P
Sbjct: 252 DDVTTFGVAATFVSSTDVPDDVVYAVVKAVFENFDSFKRLHPAFANLNKEEMVSDALSAP 311

Query: 302 LHPGAERFYKEAGVL 316
           LHPGA ++YKEAG++
Sbjct: 312 LHPGAAKYYKEAGLI 326


Lambda     K      H
   0.314    0.131    0.359 

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: 227
Number of extensions: 10
Number of successful extensions: 4
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: 317
Length of database: 327
Length adjustment: 28
Effective length of query: 289
Effective length of database: 299
Effective search space:    86411
Effective search space used:    86411
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 bits)
S2: 48 (23.1 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