GapMind for catabolism of small carbon sources

 

Alignments for a candidate for natA in Azospirillum brasilense Sp245

Align NatA aka BRAF aka SLR0467, component of Leucine/proline/alanine/serine/glycine (and possibly histidine) porter, NatABCDE (characterized)
to candidate AZOBR_RS04130 AZOBR_RS04130 branched-chain amino acid ABC transporter substrate-binding protein

Query= TCDB::Q55164
         (267 letters)



>FitnessBrowser__azobra:AZOBR_RS04130
          Length = 252

 Score =  199 bits (506), Expect = 5e-56
 Identities = 110/249 (44%), Positives = 150/249 (60%), Gaps = 6/249 (2%)

Query: 18  LLLAQGLSKSFGGLRAVDHADIVVKEGSITGLIGPNGAGKTTLFNLLSNFIRPDQGEVLF 77
           LL   GL K FGGL A D   + V EG +  LIGPNGAGKTTL   LS  + PD G + F
Sbjct: 5   LLSTNGLVKRFGGLAATDGLSLSVAEGELHALIGPNGAGKTTLIGQLSGELTPDSGTIRF 64

Query: 78  NGDSIGQLAPHQIALRGSVRTFQVAKVLSRLTVLENMLLADQHQTGEKFLPRLINFRRVQ 137
           +   + +L  H+ A RG  R+FQ+  +    T L+N+ LA Q   G  F      F R  
Sbjct: 65  DRRDVTRLPVHKRAQRGLARSFQITSIFPSFTALDNVALAVQAHAGHSF-----RFWRDA 119

Query: 138 KEERANREKAMAMLESVGLGAKAQDYAGALSGGQRKLLEMARALMSNPKLILLDEPAAGV 197
             +R   + A A+LE VGLGA+A   A AL+ G+++ LE+A AL + P+L+LLDEP AG+
Sbjct: 120 GRDRRLADPARAVLERVGLGARADTRADALAHGEKRQLELAMALATGPRLLLLDEPMAGM 179

Query: 198 NPTLIGQICEHIVNWNRQGITFLVIEHNMDVIMTLCHHVWVLAEGRNLADGTPEQIQSDP 257
            P    ++ E ++   + G+T L++EH+MD +  L   + VL  G+NLA GTPEQI++DP
Sbjct: 180 GPEDSARMVE-LLQELKGGVTILLVEHDMDAVFALADRITVLVRGKNLASGTPEQIRNDP 238

Query: 258 RVLEAYLGD 266
            V EAYLGD
Sbjct: 239 AVREAYLGD 247


Lambda     K      H
   0.319    0.136    0.389 

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: 176
Number of extensions: 9
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: 267
Length of database: 252
Length adjustment: 24
Effective length of query: 243
Effective length of database: 228
Effective search space:    55404
Effective search space used:    55404
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 47 (22.7 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