GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaD in Cupriavidus basilensis 4G11

Align alcohol dehydrogenase (EC 1.1.1.1); long-chain-alcohol dehydrogenase (EC 1.1.1.192) (characterized)
to candidate RR42_RS11005 RR42_RS11005 4-hydroxybutyrate dehydrogenase

Query= BRENDA::A4IP64
         (395 letters)



>FitnessBrowser__Cup4G11:RR42_RS11005
          Length = 382

 Score =  177 bits (449), Expect = 5e-49
 Identities = 118/359 (32%), Positives = 190/359 (52%), Gaps = 24/359 (6%)

Query: 13  HVGWGALDQLVPEVKRLGAKHILVITDPMLVKIGLVDQVTSPLRQEGYSVHVYTDVVPEP 72
           H+ +G + QL  E +R+G +  LV+TD  +V  G+  Q    L   G   H   D  P  
Sbjct: 11  HLDFGTISQLKAECERIGIRRPLVVTDKGVVAAGVAQQAIVAL---GGLPHEIFDETPSN 67

Query: 73  PLETG-EKAVAFARDGKFDLVIGVGGGSALDLAKLAAVLAVHDGSVADYLNLTG-TRTLE 130
           P E   +KA A  RD   D +I VGGGS++DLAK  A+LA H G +  Y  + G +  L 
Sbjct: 68  PTEAMVKKAAAQYRDSGCDGLIAVGGGSSIDLAKGIAILATHPGELTTYATIEGGSARLT 127

Query: 131 KKGLPKILIPTTSGTGSEVTNISVLSLETTKDVVTHDY-LLADVAIVDPQLTVSVPPRVT 189
           ++  P I +PTTSGTGSEV   +++ LE  + +  H + LL   AI DP LT+ +P  +T
Sbjct: 128 ERAAPLIAVPTTSGTGSEVARGAIIILEDGRKLGFHSWHLLPKSAICDPGLTLGLPAGLT 187

Query: 190 AATGIDALTHAVEAYVSVNASPTSDGLAVAAIRLISRSLRKAVANGSDKQARIDMANGSY 249
           AATG+DA+ H VE +++   +P +DG+A+  +    + + +A  +G D+ AR++M + S 
Sbjct: 188 AATGMDAIAHCVETFLAPAFNPPADGIALDGLERGWKHIERATRDGQDRDARLNMMSAS- 246

Query: 250 LAGLAFFNAGVAGVHALAYPLG-----GQFHIAHGESNAVLLPYVMGYIRQSCT----KR 300
           + G   F  G+  VH+L++PLG     G+  + HG  NAV++P V+ +   + +     R
Sbjct: 247 MQGAMAFQKGLGCVHSLSHPLGGLKVDGKTGLHHGTLNAVVMPAVLRFNADAPSVVRDNR 306

Query: 301 MADIFNALGGNSSFLSEVEASYRCVEELERFVADVGIPKTLGGFGIPESALESLTKDAV 359
            A + +A+G        +       + +    A +G+P  L   G+ E   + +   A+
Sbjct: 307 YARLRHAMG--------LPQDADLAQAVHDMTARLGLPTGLRQMGVTEDMFDKVIAGAL 357


Lambda     K      H
   0.318    0.135    0.381 

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: 378
Number of extensions: 16
Number of successful extensions: 6
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: 395
Length of database: 382
Length adjustment: 30
Effective length of query: 365
Effective length of database: 352
Effective search space:   128480
Effective search space used:   128480
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 (21.7 bits)
S2: 50 (23.9 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