GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mt2d in Dyella japonica UNC79MFTsu3.2

Align mannitol 2-dehydrogenase (NADP+) (EC 1.1.1.138) (characterized)
to candidate N515DRAFT_2489 N515DRAFT_2489 alcohol dehydrogenase, propanol-preferring

Query= BRENDA::Q1ACW3
         (345 letters)



>FitnessBrowser__Dyella79:N515DRAFT_2489
          Length = 343

 Score =  115 bits (288), Expect = 2e-30
 Identities = 103/335 (30%), Positives = 157/335 (46%), Gaps = 21/335 (6%)

Query: 19  AVVEVPLPTLRDNDVLIKVKACGVCGTDLHIHEGEFIA--KFPLIPGHETVGVVAAIGKD 76
           ++ EVP+PT    +VL+K++ACGVC TDLH  +G++    K P IPGHE VG V AIG  
Sbjct: 18  SIDEVPVPTPGLGEVLVKIEACGVCHTDLHAVDGDWPVKPKPPFIPGHEGVGYVVAIGPG 77

Query: 77  VKGFTVGERVCAD-NSELCNECFYCRRGQLLLCEKFEAHGVTMDGGFAEYCAYPAGKVFK 135
           V     G+RV        C  C +C  G   LCE  +  G +++GGFAEY    A  V  
Sbjct: 78  VTHLKEGDRVGIPWLYSACGHCEHCLGGWETLCESQQNTGYSVNGGFAEYALAAADYVG- 136

Query: 136 IHNLSDVDATLLEPASCAA----HGLEKIAPKIGSSVLMFGAGPTGLCLAQLPHNGASHV 191
            H    +    + P  CA      GL+    + G+ V++ G G  G    Q       +V
Sbjct: 137 -HLPDGIGFVEIAPVLCAGVTVYKGLKVTDTRPGNWVVISGIGGLGHMAVQYAAAMGLNV 195

Query: 192 VIAAPEGLKMDLAKKLDCADIYVPLSRSNPQAQFDQIKSDNPYGFDIVVEATGSPKILED 251
                +  K+DLA++L  A + +    ++P A    +K +       +V A  SPK    
Sbjct: 196 AAVDIDDAKLDLARRLG-AQLIINARHADPVA---VVKKEIGGAHGALVTAV-SPKAFGQ 250

Query: 252 AINYVRRGGKLVVYGVYSDAARVSWPPSKIFGDEITIIGSFSETYM-FPATIGYLDTGKV 310
           A+N VRRGG + + G+   +  +S     + G  +T+ GS   T +    ++ +   GKV
Sbjct: 251 AMNMVRRGGTVSLNGLPPGSFDLSIFDMVLNG--VTVRGSIVGTRLDLQESLDFAKAGKV 308

Query: 311 KVEGIVNKTYKLEQWGECLEAMRNKSAIKAAIVFE 345
           K       T +LE   E    M ++  I+  +V +
Sbjct: 309 KA---TVTTDRLENINEVFRRM-HQGQIEGRVVLD 339


Lambda     K      H
   0.320    0.138    0.420 

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: 308
Number of extensions: 19
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: 345
Length of database: 343
Length adjustment: 29
Effective length of query: 316
Effective length of database: 314
Effective search space:    99224
Effective search space used:    99224
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 (21.8 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