Aligments for a candidate for adhAqn in Pseudomonas fluorescens FW300-N2E2

GapMind for catabolism of small carbon sources

Aligments for a candidate for adhAqn in Pseudomonas fluorescens FW300-N2E2

Align alcohol dehydrogenase (quinone) (EC 1.1.5.5) (characterized)
to candidate Pf6N2E2_1382 Quino(hemo)protein alcohol dehydrogenase, PQQ-dependent (EC 1.1.99.8)

Query= BRENDA::Q44002
         (739 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_1382
          Length = 591

 Score =  346 bits (888), Expect = 2e-99
 Identities = 210/590 (35%), Positives = 304/590 (51%), Gaps = 53/590 (8%)

Query: 21  ICAALISGYATMASADDGQGATGEAIIHADDHPGNWMTYGRTYSEQRYSPLDQINRSNVG 80
           + A L+SG A  A  D       + I+    +P   +T G     QRYSPLD +N  NV 
Sbjct: 16  LSAMLLSGSALAAVTD-------QEILQDPKNPEQIVTNGLGVQGQRYSPLDTLNTDNVK 68

Query: 81  NLKLAWYLDL--DTNRGQEGTPLVIDGVMYATTNWSMMKAVDAATGKLLWSYDPRVPGNI 138
           +L+  W      +  RGQ+  P++ DGVMY T ++S + AVDA TGK LW YD R+P +I
Sbjct: 69  DLRPVWAFSFGGEKQRGQQAQPMIKDGVMYLTGSYSRVFAVDARTGKKLWQYDARLPDDI 128

Query: 139 ADKGCCDTVNRGAAYWNGKVYFGTFDGRLIALDAKTGKLVWSVNTIPPEAELGKQRSYTV 198
             + CCD +NRG A +   V+FGT D +L+AL+  TGK+VWS            +  Y++
Sbjct: 129 --RPCCDVINRGVALYGDLVFFGTLDAKLVALNKDTGKVVWSKKVAD------HKEGYSI 180

Query: 199 DGAPRIAKGRVIIGNGGSEFGARGFVTAFDAETGKVDWRFFTAPNPKNEPDHTASDSVLM 258
             AP I  G++I G  G EFG  G ++A+D + G++ W   T P  +    +   D   +
Sbjct: 181 SAAPLIVNGKLITGVAGGEFGVVGQISAYDPKNGELLW---TRPTVEGHMGYVYKDGKAV 237

Query: 259 N------KAYQTWSPTGAWTRQGGGGTVWDSIVYDPVADLVYLGVGNGSPWNYKYRSEGK 312
                  +A +TW P   W  + GG   W    YDP  +L+  G GN +PWN   R    
Sbjct: 238 ENGISGGEAGKTW-PGDLW--KTGGAAPWLGGYYDPETNLLLFGTGNPAPWNSHLRP--- 291

Query: 313 GDNLFLGSIVALKPETGEYVWHFQETPMDQWDFTSVQQIMTLDLPINGETRHVIVHAPKN 372
           GDNL+  S +AL P+ G   WHFQ TP D WD+  V ++++ +    G+       A +N
Sbjct: 292 GDNLYSSSRLALNPDDGTIKWHFQSTPHDGWDYDGVNELISFNYKEGGKDIKAAATADRN 351

Query: 373 GFFYIIDAKTGEFISGKNYV-YVNWASGLDPKTGRPIYNPDALYTLTGKEWYG-----IP 426
           GFFY++D   G+FI G  +V  + WA+GLD K GRPIYN  +     G E  G      P
Sbjct: 352 GFFYVLDRTNGKFIRGFPFVDKITWATGLD-KDGRPIYNEASRPGAPGSEAKGSSVFVAP 410

Query: 427 GDLGGHNFAAMAFSPKTGLVYIPAQQVPFLYTNQVGGFTPHPDSWNLGLDMNK-VGIPDS 485
             LG  N+  MA++  TGL Y+P+        N+ G      D WN G+   K      +
Sbjct: 411 AFLGAKNWMPMAYNQDTGLFYVPS--------NEWG-----MDIWNEGIAYKKGAAFLGA 457

Query: 486 PEAKQAFVKDLKGWIVAWDPQKQAEAWRVDHKGPWNGGILATGGDLLFQGLANGEFHAYD 545
               +   +D  G + A DP+   E WR  +  P  GG+L T G+L+F G   G   A++
Sbjct: 458 GFTIKPLNEDYIGVLRAIDPKTGKEVWRHKNYAPLWGGVLTTKGNLVFTGTPEGFLQAFN 517

Query: 546 ATNGSDLFHFAADSGIIAPPVTYLANGKQYVAVEVGWGGIYPFFLGGLAR 595
           A  G  ++ F   SG++  P+T+  +G+QYV+V  GWGG  P + G +A+
Sbjct: 518 AKTGEKVWEFQTGSGVLGSPITWEMDGEQYVSVVSGWGGAVPLWGGEVAK 567


Lambda     K      H
   0.318    0.137    0.440 

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: 1832
Number of extensions: 165
Number of successful extensions: 22
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: 739
Length of database: 591
Length adjustment: 38
Effective length of query: 701
Effective length of database: 553
Effective search space:   387653
Effective search space used:   387653
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: 54 (25.4 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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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

GapMind for catabolism of small carbon sources