GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galU in Shewanella oneidensis MR-1

Align glucosamine-1-phosphate N-acetyltransferase (EC 2.3.1.157); galactosamine-1-phosphate N-acetyltransferase (EC 2.3.1.276); UDP-N-acetylglucosamine diphosphorylase (EC 2.7.7.23); glucose-1-phosphate thymidylyltransferase (EC 2.7.7.24); aldose-1-phosphate nucleotidyltransferase (EC 2.7.7.37); UDP-N-acetylgalactosamine diphosphorylase (EC 2.7.7.83); UTP-glucose-1-phosphate uridylyltransferase (EC 2.7.7.9) (characterized)
to candidate 202296 SO3186 glucose-1-phosphate-thymidylyltransferase (NCBI ptt file)

Query= BRENDA::Q975F9
         (401 letters)



>FitnessBrowser__MR1:202296
          Length = 304

 Score = 86.3 bits (212), Expect = 1e-21
 Identities = 68/225 (30%), Positives = 103/225 (45%), Gaps = 17/225 (7%)

Query: 2   KAFILAAGSGERLEPITHTRPKAFVPILSKPLIEYQIEYLRKCGIRDITVIVSSKNKEYF 61
           K  ILA GSG RL PIT    K  +P+  KP+I Y I  L   GIRDI +I + +++  F
Sbjct: 16  KGIILAGGSGTRLYPITKGVSKQLLPVYDKPMIYYPISVLMLAGIRDILIITTPEDQSSF 75

Query: 62  EKKLKE-------ISIVTQKDDIKGTGAAILSAKF--NDEALIIYGDLFFSNE--KEICN 110
           ++ L +       +    Q        A I+  +F  ND   +  GD  F  +    I  
Sbjct: 76  QRLLGDGSDFGISLQYAVQVTPDGLAQAFIIGEEFIGNDNVCLALGDNIFWGQGFSPILK 135

Query: 111 IITLKEN--AIIGVKVSNPKDYGVLVLDNQNNLSKIIEKPEIPPSNLINAGIYKLNSDIF 168
               +    ++ G +V +P+ +GV+  D       I EKP  P SN    G+Y  ++ + 
Sbjct: 136 KAAARPTGASVFGYQVKDPERFGVVEFDQDLKAISIEEKPLKPKSNFAVTGLYFYDNRVV 195

Query: 169 TYLDKISISERGELELTDAIN---LMAKDHRVKVIEYEGYWMDIG 210
                +  SERGELE+T +IN   L      V+++     W+D G
Sbjct: 196 NIAKNVKPSERGELEIT-SINQAYLEMGKLNVELLGRGFAWLDTG 239


Lambda     K      H
   0.317    0.139    0.393 

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: 300
Number of extensions: 16
Number of successful extensions: 2
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: 401
Length of database: 304
Length adjustment: 29
Effective length of query: 372
Effective length of database: 275
Effective search space:   102300
Effective search space used:   102300
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