GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etoh-dh-nad in Rubrivirga marina SAORIC-28

Align alcohol dehydrogenase (EC 1.1.1.1); aryl-alcohol dehydrogenase (EC 1.1.1.90); aryl-alcohol dehydrogenase (NADP+) (EC 1.1.1.91) (characterized)
to candidate WP_095509075.1 BSZ37_RS02760 NAD(P)-dependent alcohol dehydrogenase

Query= BRENDA::W6CX26
         (339 letters)



>NCBI__GCF_002283365.1:WP_095509075.1
          Length = 339

 Score =  357 bits (917), Expect = e-103
 Identities = 171/332 (51%), Positives = 232/332 (69%), Gaps = 2/332 (0%)

Query: 4   IKSYAAKEAGSELELYEYDAGELRPEDVEVQVDYCGICHSDLSMIDNEWGFSQYPLVAGH 63
           + +YA  E+G  LE + Y+AG L  ++VE+ V YCGICHSDLSMI+NEWG +QYPLVAGH
Sbjct: 7   VAAYAVHESGGPLEPFTYEAGPLGADEVEIDVLYCGICHSDLSMIENEWGMTQYPLVAGH 66

Query: 64  EVIGRVAALGSAAQEKGVKVGQRVGVGWTARSCGHCDACISGNQINCLEGAVATILNRGG 123
           EVIGRVAA+GS  +   +  G  VG+GW A  CGHC +C +G+Q  C       + + GG
Sbjct: 67  EVIGRVAAVGSDVES--LAEGAVVGLGWHAGYCGHCGSCKTGDQNLCATAQPTIVGHHGG 124

Query: 124 FAEKLRADWQWVIPLPESIDIESAGPLLCGGITVFKPLLMHHITATSRVGVIGIGGLGHI 183
           FA+ +RA    V+ +P+ +D+E+AGPLLCGGITVF PL+   +  T  V VIGIGGLGH+
Sbjct: 125 FADTVRAQASSVVAIPDGMDLEAAGPLLCGGITVFNPLVQFDVRPTDAVAVIGIGGLGHL 184

Query: 184 AIKLLHAMGCEVTAFSSNPSKEQEVLAMGADKVVNSRDPDALNALAGQFDLIINTVNVDL 243
           A++ L+A GCEVTAF+S+PSK++E L +GA KV++SRDPDA+ + AG FD I++TVNV L
Sbjct: 185 ALQFLNAWGCEVTAFTSSPSKQEEALDLGAHKVLSSRDPDAIASAAGTFDFIVSTVNVKL 244

Query: 244 DWQPYFEALAYGGHFHTVGAVMKPLPVPAFTLIAGDRSISGSATGTPYELRKLMKFAGRS 303
           DW  Y   L   G  H VGA ++PL +  F L+ G RSISGS  G P  + +++ FA   
Sbjct: 245 DWNVYVSTLKPKGRLHFVGATLEPLDLGVFPLMLGQRSISGSPVGAPATIEQMLDFAHLH 304

Query: 304 KVSPTTELFPMSQINEAIQHVRDGKARYRVVL 335
            + P  E+FPMS++N A+  ++ G+ARYR+VL
Sbjct: 305 DIKPQVEVFPMSEVNAALGRLKSGEARYRIVL 336


Lambda     K      H
   0.320    0.137    0.415 

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: 354
Number of extensions: 13
Number of successful extensions: 2
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: 339
Length of database: 339
Length adjustment: 28
Effective length of query: 311
Effective length of database: 311
Effective search space:    96721
Effective search space used:    96721
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