Aligments for a candidate for etoh-dh-nad in Pseudomonas putida KT2440

GapMind for catabolism of small carbon sources

Aligments for a candidate for etoh-dh-nad in Pseudomonas putida KT2440

Align alcohol dehydrogenase (EC 1.1.1.1) (characterized)
to candidate PP_0056 PP_0056 choline dehydrogenase

Query= BRENDA::Q76HN6
         (526 letters)



>FitnessBrowser__Putida:PP_0056
          Length = 550

 Score =  438 bits (1127), Expect = e-127
 Identities = 241/530 (45%), Positives = 323/530 (60%), Gaps = 10/530 (1%)

Query: 3   FDYLIVGAGSAGCVLANRLSADPSVTVCLLEAGPEDRSPLIHTPLGLAAILPTRHVNWAF 62
           FDY++VGAG AGC+LANRLSADPS  V LLEAG  D  P IH P+G    +     +W F
Sbjct: 10  FDYVVVGAGPAGCLLANRLSADPSCRVLLLEAGGRDNYPWIHIPVGYLYCIGNPRTDWCF 69

Query: 63  KTTPQPGLGGRVGYQPRGKVLGGSSSINGMIYIRGHQDDFNDWQALGNEGWGFDDVLPYF 122
           KT  QPGLGGR    PRGKVLGG SSINGMIY+RG   D++ W A GN+GW + DVLP F
Sbjct: 70  KTEAQPGLGGRALGYPRGKVLGGCSSINGMIYMRGQAADYDHWAAQGNDGWAWKDVLPLF 129

Query: 123 RKSEMHHGGSSEYHGGDGELYVSPANRHA--ASEAFVESALRAGHSYNPDFNGATQEGAG 180
           + SE H  G+SE+HG +GE  V    R++    +AF ++A ++G     DFN    +G G
Sbjct: 130 KASENHFAGASEHHGAEGEWRVE-RQRYSWPILDAFRDAAEQSGIGKVDDFNTGDNQGCG 188

Query: 181 YYDVTIRDGRRWSTATAFLKPVRHRSNLTVLTHTHVESIVLLGKQATGVQALIKGSRVHL 240
           Y+ V  R G RW+ + AFL+P++ R+NLTVLT   V+ ++L   +A  V+AL +G+    
Sbjct: 189 YFQVNQRSGVRWNASKAFLRPIKDRANLTVLTGVQVDQVLLDNTRARAVKALWQGAWHEF 248

Query: 241 RARKEVILSAGAFGSPHLLMLSGIGSAAELEPQGIAPRHELPGVGQNLQDHADVVLCYKS 300
            AR+E+IL AGA GSP +L  SGIG    LE  GI  RH++PGVG NLQDH  + L Y+ 
Sbjct: 249 AARREIILCAGAVGSPGILQRSGIGPRQLLESLGIGVRHDMPGVGGNLQDHLQLRLIYQI 308

Query: 301 NDTSLL---GFSLSGGVKMGKAMFDYARHRNGPVASNCAEAGAFLKTDPGLERPDIQLHS 357
            +T  L     SL G + MG     Y   R+GP+A   ++ GAF+++ P     ++Q H 
Sbjct: 309 RNTRTLNQMANSLWGKMGMG---LRYLYDRSGPLAMAPSQLGAFVRSSPEQATANLQYHV 365

Query: 358 VIGTVDDHNRKLHWGHGFSCHVCVLRPKSIGSVGLASPDPRKAPRIDPNFLAHDDDVATL 417
              +++     LH    F+  VC LRP S G + + S D    PRIDPN+L+   D+   
Sbjct: 366 QPLSLERFGEPLHQFPAFTASVCNLRPASRGRIDICSTDMNSTPRIDPNYLSAPQDLRVA 425

Query: 418 LKGYRITRDIIAQTPMASFGLRD-MYSAGLHNDEQLIELLRKRTDTIYHPIGTCKMGQDE 476
               R+TR I+    +A+F  ++ +    L ++E L E   K   TI+HP+GTC+MG   
Sbjct: 426 ADAIRLTRRIVQAPALAAFEPKEYLPGPALQSEEDLFEAAGKIGTTIFHPVGTCRMGNGA 485

Query: 477 MAVVDSQLRVHGIEGLRVVDASIMPTLVGGNTNAAAIMIAERAAEWIAHG 526
           M VVD+QLRVHGI GLRV DASIMP +  GNT +  +MIAE+AA+ I  G
Sbjct: 486 MDVVDNQLRVHGIPGLRVADASIMPQITSGNTCSPTLMIAEKAAQLILKG 535


Lambda     K      H
   0.319    0.137    0.419 

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: 789
Number of extensions: 34
Number of successful extensions: 5
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: 526
Length of database: 550
Length adjustment: 35
Effective length of query: 491
Effective length of database: 515
Effective search space:   252865
Effective search space used:   252865
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 (21.7 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

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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