GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etoh-dh-c in Marivita geojedonensis DPG-138

Align alcohol dehydrogenase (cytochrome c) (EC 1.1.2.8) (characterized)
to candidate WP_085635893.1 MGEO_RS06505 cytochrome c

Query= BRENDA::C7G3B8
         (472 letters)



>NCBI__GCF_002115805.1:WP_085635893.1
          Length = 294

 Score =  130 bits (328), Expect = 4e-35
 Identities = 84/265 (31%), Positives = 131/265 (49%), Gaps = 21/265 (7%)

Query: 37  GEYVARLGDCVACHTSLNGQK-----YAGGLSIKTPIGTIYSTNITPDPTYGIGTYTFKE 91
           GE V     C +CH + + +       AGG    +  GT  + N++P P  GIG +T  E
Sbjct: 44  GETVFTAAGCASCHAAPDAEGEAKLVLAGGQRFASDFGTFIAPNVSPHPEAGIGGWTLAE 103

Query: 92  FDEAVRHGVRKDGATLYPAMPYPSFARMTQDDMKALYAYFMHGAQPIAQKNHPTDISWPM 151
           F  AV  GV  +G   YPA PY ++  MT+ D+  L+AY+    Q  A  + P ++ +P 
Sbjct: 104 FASAVTRGVSPEGQHYYPAFPYAAYLHMTEQDVADLWAYWQTLPQD-ATPSEPHEVGFPF 162

Query: 152 SMRWPLSIWRSVFAPAPKDFTPAPGTDAEIARGEYLVTGPGHCGACHTPR-GFGMQEKAL 210
           ++R  + +W+ ++     D+  A     +IARG YLV    HCG CHTPR   G  ++  
Sbjct: 163 NIRRAVGVWKQLY--MTDDWVMASAETDQIARGRYLVEALAHCGECHTPRDALGGLDRDA 220

Query: 211 DASGGPDFLGGGGVIDNWIAPSLRNDPVLGLGRWSDEDLFLFLKSGRT-DHSAAFGGMAD 269
             +G P+  G G +      PSL  D +     W   ++  +L++G T D  +A G M  
Sbjct: 221 WLAGAPNPSGRGTI------PSLTPDDL----TWGSTEIAYYLETGFTPDFDSAGGHMVA 270

Query: 270 VVGWSTQYFTDADLHAMVKYIKSLP 294
           V+   T+    +D  A+  Y+K+LP
Sbjct: 271 VIANFTK-LPASDREAVAAYLKALP 294



 Score = 40.4 bits (93), Expect = 8e-08
 Identities = 29/79 (36%), Positives = 38/79 (48%), Gaps = 7/79 (8%)

Query: 168 PKDFTPAPGTDAEIARGEYLVTGPGHCGACH-TPRGFGMQEKALDASGGPDFLGGGGVID 226
           P D T   G DA+ A GE + T  G C +CH  P   G  E  L  +GG  F    G   
Sbjct: 28  PLDDTALAGIDADPANGETVFTAAG-CASCHAAPDAEG--EAKLVLAGGQRFASDFG--- 81

Query: 227 NWIAPSLRNDPVLGLGRWS 245
            +IAP++   P  G+G W+
Sbjct: 82  TFIAPNVSPHPEAGIGGWT 100


Lambda     K      H
   0.318    0.135    0.430 

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: 465
Number of extensions: 40
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 472
Length of database: 294
Length adjustment: 30
Effective length of query: 442
Effective length of database: 264
Effective search space:   116688
Effective search space used:   116688
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: 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