GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etoh-dh-c in Dyella japonica UNC79MFTsu3.2

Align alcohol dehydrogenase (cytochrome c) (EC 1.1.2.8) (characterized)
to candidate N515DRAFT_2297 N515DRAFT_2297 Cytochrome c, mono- and diheme variants

Query= BRENDA::C7G3B8
         (472 letters)



>FitnessBrowser__Dyella79:N515DRAFT_2297
          Length = 441

 Score =  231 bits (590), Expect = 3e-65
 Identities = 136/402 (33%), Positives = 200/402 (49%), Gaps = 21/402 (5%)

Query: 32  DLIKKGEYVARLGDCVACHTSLNGQKYAGGLSIKTPIGTIYSTNITPDPTYGIGTYTFKE 91
           D + +GEY+ R  DC ACHT   GQ Y GG++ K P GTIYSTNIT D   GIG ++  E
Sbjct: 51  DPVARGEYLTRAADCAACHTVPGGQPYTGGVAFKMPFGTIYSTNITADKETGIGDWSDDE 110

Query: 92  FDEAVRHGVRKDGATLYPAMPYPSFARMTQDDMKALYAYFMHGAQPIAQKNHPTDISWPM 151
           F  A+  GVRKDG  LYPA PY S+  +++DD+ A+ AY +    P      P ++S+P 
Sbjct: 111 FVRALHAGVRKDGKPLYPAFPYTSYTALSRDDVLAIKAY-LFSLPPKHAPARPNELSFPF 169

Query: 152 SMRWPLSIWRSVFAPAPKDFTPAPGTDAEIARGEYLVTGPGHCGACHTPRGFGMQEKALD 211
             RW LS+W ++F    + + P  G      RG YL T  GHC  CHTPR      K  D
Sbjct: 170 DQRWGLSVWNALFLKKQR-YEPVQGKSQAWNRGAYLATALGHCDECHTPRNAMYALKRGD 228

Query: 212 ASGGPDFLGGGGVIDNWIAPSLRNDPVLGLGRWSDEDLFLFLKSGR-TDHSAAFGGMADV 270
           A  G        V+  W A ++ +D   G+G WS++ L  +L  G  +    A G M +V
Sbjct: 229 ALSGE-------VLQGWKAYNITSDKTYGIGNWSEQQLADYLSKGHASGRGTASGPMGEV 281

Query: 271 VGWSTQYFTDADLHAMVKYIKSLPPVPPARGDYSYD------ASTAQMLDSNNIS-GNAG 323
           V +S QY T  D+ A+V Y++ + P   + G    D      AS+A    +  ++ G  G
Sbjct: 282 VQYSLQYLTPEDIGALVTYLREVKPQQGSAGSEVNDRPALALASSASAPGAEELAQGGLG 341

Query: 324 AKTYVDQCAICHRNDGGGVARMFPPLAGNPVVVSDNPTSVAHIVVDGGVLPPTNWAPSAV 383
              +   C+ CH  +G G       L G          ++  +++ G  L     A    
Sbjct: 342 QHLFQGACSSCHLWNGQGRQSEAAALLGTQAANDPQAHNLTQVILQGSTL---RTAHGET 398

Query: 384 AMPDYKNILSDQQIADVVNFIRSAWGNRAPANTTAADIQKLR 425
           +MP +    +D ++A + NF+ + +G + PA  TA ++ K R
Sbjct: 399 SMPSFGQAYTDAEVAALGNFVLTHFGGK-PATLTADEVAKRR 439


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: 621
Number of extensions: 41
Number of successful extensions: 9
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: 472
Length of database: 441
Length adjustment: 33
Effective length of query: 439
Effective length of database: 408
Effective search space:   179112
Effective search space used:   179112
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: 51 (24.3 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