GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Phaeobacter inhibens BS107

Align UDP-glucose 4-epimerase; UDP-galactose 4-epimerase; Uridine diphosphate galactose 4-epimerase; EC 5.1.3.2 (characterized)
to candidate GFF3921 PGA1_65p00240 dTDP-glucose 4,6-dehydratase RffG

Query= SwissProt::A0R5C5
         (313 letters)



>FitnessBrowser__Phaeo:GFF3921
          Length = 350

 Score =  160 bits (404), Expect = 5e-44
 Identities = 112/329 (34%), Positives = 169/329 (51%), Gaps = 24/329 (7%)

Query: 1   MRTLVTGAAGFIGSTLVDRLLADGHGVVGLDDLSSGRA-ENLHSAENSDKFEFVKADIVD 59
           M+ LVTG AGFIGS +V   +A GH VV LD L+     +N+ +  +S  + F + DI D
Sbjct: 1   MKILVTGGAGFIGSAVVRLAVARGHQVVNLDALTYAACLDNVAAVADSPNYAFEQVDIRD 60

Query: 60  -ADLTGLLAEFKPEVIFHLAAQISVKRSVDDPPFDATVNVVGTVRLAEAARL----AGVR 114
            A L  + A  +P+V+ HLAA+  V RS+D P      N+ GT ++ EAAR     AG  
Sbjct: 61  RAALDTVFARHRPDVVMHLAAESHVDRSIDGPGDFIETNITGTYQMLEAARKYWAEAGRP 120

Query: 115 KV--VHTSSGGSVYGTPPAYPT---SEDMPVNPASPYAAGKVAGEVYLNMYRNLYDLDCS 169
           +    H  S   VYG+ PA P+   +E+   +P SPY+A K A +  +  +   Y L   
Sbjct: 121 EAFRFHHISTDEVYGSLPADPSVMFTEETGYDPRSPYSASKAASDHLVRAWGETYGLPVV 180

Query: 170 HIAPANVYGPRQDPHGEAGVVAIFSEALLAGRTTKIFGDGSDTRDYVFVDDVVDAFVRAG 229
               +N YGP   P     VV + +   LAG+   I+GDGS+ RD+++V+D  DA +   
Sbjct: 181 LTNCSNNYGPYHFPEKLIPVVILNA---LAGKPLPIYGDGSNVRDWLYVEDHADALLLVV 237

Query: 230 GPAGGGQRFNVGTGVETSTRELHTAIAGAV----------GAPDEPEFHPPRLGDLRRSR 279
                G+ +N+G   E +  EL   +   +             D+  F   R G   R  
Sbjct: 238 SKGRVGRSYNIGGENERTNLELVETLCAILDEKRPREDGGSYKDQITFVTDRPGHDARYA 297

Query: 280 LDNTRAREVLGWQPQVALAEGIAKTVEFF 308
           +D +R R+ LGW+P V + EG+A+TV+++
Sbjct: 298 IDPSRIRDELGWRPSVTVEEGLARTVQWY 326


Lambda     K      H
   0.317    0.136    0.396 

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: 262
Number of extensions: 12
Number of successful extensions: 5
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: 313
Length of database: 350
Length adjustment: 28
Effective length of query: 285
Effective length of database: 322
Effective search space:    91770
Effective search space used:    91770
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: 41 (21.6 bits)
S2: 49 (23.5 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