GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaD in Pantoea rwandensis LMG 26275

Align alcohol dehydrogenase (EC 1.1.1.1); long-chain-alcohol dehydrogenase (EC 1.1.1.192) (characterized)
to candidate WP_084938278.1 HA51_RS25705 iron-containing alcohol dehydrogenase

Query= BRENDA::A4IP64
         (395 letters)



>NCBI__GCF_002095475.1:WP_084938278.1
          Length = 382

 Score =  202 bits (514), Expect = 1e-56
 Identities = 122/359 (33%), Positives = 193/359 (53%), Gaps = 7/359 (1%)

Query: 30  GAKHILVITDPMLVKIGLVDQVTSPLRQEGYSVHVYTDVVPEPPLETGEKAVAFARDGKF 89
           G +  L++TD  +  I  V  + + L+Q+  S+ +   V PEP        VA       
Sbjct: 23  GKEKALLVTDKNIEGIPAVQSLIAQLKQQISSLSIVNSVPPEPSQHDVAAIVAALPSTDV 82

Query: 90  DLVIGVGGGSALDLAKLAAVLAVHDGSVADYLNLTGTRTLEKKGLPKILIPTTSGTGSEV 149
           DLVIGVGGGS LD+AKL ++L V      D L L G +   +     +LIPTT+GTGSE 
Sbjct: 83  DLVIGVGGGSVLDVAKLLSILCVDGAPTLDAL-LAGEKPQTRT--TSLLIPTTAGTGSEA 139

Query: 150 TNISVLSL---ETTKDVVTHDYLLADVAIVDPQLTVSVPPRVTAATGIDALTHAVEAYVS 206
           T  ++L++   ET   ++T   +L D   + P+LT S+PP + ++TGIDAL H +E + +
Sbjct: 140 TPNAILAIPEKETKVGIIT-PVMLPDYVALVPELTTSMPPHIASSTGIDALCHLIECFTA 198

Query: 207 VNASPTSDGLAVAAIRLISRSLRKAVANGSDKQARIDMANGSYLAGLAFFNAGVAGVHAL 266
             A+P SD  A+  ++ +  SL   +A   + +AR++M   SY  G +  +AG   VHA+
Sbjct: 199 TVANPVSDNYALIGMKKLFASLETTIAEPGNLEARLNMLWASYYGGASIAHAGTHLVHAM 258

Query: 267 AYPLGGQFHIAHGESNAVLLPYVMGYIRQSCTKRMADIFNALGGNSSFLSEVEASYRCVE 326
           +YPLGG++H+ HG +NA+LL   M ++R +   + A  ++ L    + L E   S+  VE
Sbjct: 259 SYPLGGKYHLPHGVANAILLAPCMRFVRPAAVSKFAQAYDLLPDADATLDEEAKSHALVE 318

Query: 327 ELERFVADVGIPKTLGGFGIPESALESLTKDAVQQKRLLARSPLPLLEADIRAIYEAAF 385
                V  + +P +L   GI    L  L + A+  +RL+   P+ +   D+R +Y   F
Sbjct: 319 YFAALVKRLKLPASLEELGIGPDHLPYLVEAALDVQRLMKNVPMKVGADDVRNVYLTLF 377


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: 368
Number of extensions: 21
Number of successful extensions: 3
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 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