GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etoh-dh-nad in Leeuwenhoekiella blandensis MED217

Align alcohol dehydrogenase [NAD(P)+] (EC 1.1.1.71) (characterized)
to candidate WP_009780191.1 MED217_RS08975 NAD(P)-dependent alcohol dehydrogenase

Query= BRENDA::Q8H0L8
         (359 letters)



>NCBI__GCF_000152985.1:WP_009780191.1
          Length = 349

 Score =  342 bits (878), Expect = 7e-99
 Identities = 177/350 (50%), Positives = 240/350 (68%), Gaps = 7/350 (2%)

Query: 11  IKAFGWATRHTSGVLSPFNFSRRVTGEKHVQFKVMYCGICHSDLHQLKNEWGNTKYPMVP 70
           +KA+G A       L   N  RR    + V+ K+ YCG+CHSD+H ++N+WG +KYP+VP
Sbjct: 4   VKAYGAADPKAD--LKQINIERREVTPRDVKIKITYCGVCHSDIHTVRNDWGGSKYPVVP 61

Query: 71  GHEVVGVVIEVGSKVEKFKVGDKVGVGCMVGSCRKCENCTVDLENYCPR-QIPTYNGYSL 129
           GHE++G V+EVGS+V  FKVGD VGVGCMV SCR+CE C  DLE +C +  + TYNG   
Sbjct: 62  GHEIIGKVLEVGSEVSDFKVGDTVGVGCMVDSCRECEPCKHDLEQFCEQGMVGTYNGKDK 121

Query: 130 D-GTLTFGGYSDMMVSDEHFVVRWPENLSMDA-APLLCAGITTYSPLKYFGLDKPGMHIG 187
             G  T+GGYS+ ++ D+++V+  PENL  +A APLLCAGITT+SPL ++ + K G  +G
Sbjct: 122 HLGGHTYGGYSEEIIVDKYYVLSVPENLDENAVAPLLCAGITTFSPLNHWKVGK-GDKVG 180

Query: 188 VVGLGGLGHMAVKFAKAFGTKVTVISTSANKKQEAIERLGADSFLISRDPEQMKAAMNTL 247
           V+GLGGLGHM +KFA A G  V +I+TS  K ++A +RLGAD  LIS+D E MK   N+ 
Sbjct: 181 VIGLGGLGHMGIKFAHAMGAHVVMITTSPGKAEDA-KRLGADEVLISKDEEAMKKHANSF 239

Query: 248 DGIIDTVSAVHPILPLLMLMKSHGKLVMVGAPEKPVELPVFPLLMGRKLVAGSCIGGMKE 307
           D +++TV   H I P L L+K    + MVGA E    +    L+MGRK VAGS IGG+KE
Sbjct: 240 DFLLNTVPVGHDINPYLSLLKIDATMCMVGAVEPLEPVHGGSLIMGRKNVAGSLIGGIKE 299

Query: 308 TQEMLDFAAKHNITPDIEVVPMDYVNTALERLLKSDVKYRFVLDIGNTLN 357
           TQEMLDF  +HNI  DIE++ ++ +N A +R++  DVKYRFV+D+ +  N
Sbjct: 300 TQEMLDFCGEHNIVSDIEMIDINTINDAYDRVVNGDVKYRFVIDMESLRN 349


Lambda     K      H
   0.320    0.137    0.417 

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: 364
Number of extensions: 16
Number of successful extensions: 4
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: 359
Length of database: 349
Length adjustment: 29
Effective length of query: 330
Effective length of database: 320
Effective search space:   105600
Effective search space used:   105600
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 24 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