GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Pseudomonas fluorescens FW300-N2C3

Align D-sorbitol dehydrogenase (EC 1.1.1.14; EC 1.1.1.9) (characterized)
to candidate AO356_00820 AO356_00820 alcohol dehydrogenase

Query= metacyc::MONOMER-13193
         (363 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_00820
          Length = 346

 Score =  115 bits (288), Expect = 2e-30
 Identities = 100/333 (30%), Positives = 157/333 (47%), Gaps = 21/333 (6%)

Query: 26  FEERPK-PTITDP----NDVLVAVNYTGICGSDVHYWVHGAIGHFV-VKDPMVLGHESAG 79
           F + P+  T+ DP    + V+V V  TG+C SD H W     GH   ++ P V GHE AG
Sbjct: 9   FSQPPRLMTVEDPTPERHGVVVQVLGTGVCRSDWHGWK----GHDPDIQLPHVPGHELAG 64

Query: 80  TVVEVGPAVKSLKPGDRVALEPGYPCRRCSFCRAGKYNLCPDMVFAATPPYHGTLTGLWA 139
            V EVG  V   K GDR+ +     C  C  C +G   +C          +      +  
Sbjct: 65  IVAEVGRDVTRWKVGDRITVPFVGGCGACPECNSGNQQVCHSQFQPGFTHWGSFAEYVGI 124

Query: 140 APADF-CYKLPDGVSLQEGALIEPLAVAVH--IVKQARVQPGQSVVVMGAGPVGLLCAAV 196
             AD     LP+ +     A +    V     +V Q +V  GQ V V G G VGL    +
Sbjct: 125 HKADLNLVALPENMDFATAASLGCRFVTSFRAVVDQGKVTAGQWVAVHGCGGVGLSAVMI 184

Query: 197 AKAYGASTIVSVDIVQSKLDFARGFCSTHTYVSQRISAEDNAKAIKELAGLPGGADVVID 256
           A A GA+ ++++DI   KL  A+   +  T  + R++  D  +A+ E+    GGA V +D
Sbjct: 185 AHAIGAN-VIAIDICDDKLKLAQSLGAVATINASRVA--DVTEAVLEIT--KGGAHVSLD 239

Query: 257 ASGAEPSIQTSIHVVRMGGTYVQGGMGKSDITFPIMAM---CLKEVTVRGSFRYGAGDYE 313
           A G   +   SI+ +R  G +VQ G+  +D + P + M      E+ + GS    A  Y 
Sbjct: 240 ALGHPTTCFNSINNLRRRGRHVQVGLMLADHSTPSIPMSKVIAYELEICGSHGMQAHRYG 299

Query: 314 LAVELVRTGRVDVKKLITGTVSFKQAEEAFQKV 346
             +E++ +G++  +KL+  T+S +Q+ +A   +
Sbjct: 300 AMMEMITSGKLAPEKLVGKTISLEQSIDALMNM 332


Lambda     K      H
   0.319    0.136    0.406 

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: 294
Number of extensions: 17
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: 363
Length of database: 346
Length adjustment: 29
Effective length of query: 334
Effective length of database: 317
Effective search space:   105878
Effective search space used:   105878
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: 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