Alignments for a candidate for puuC in Escherichia coli BW25113

GapMind for catabolism of small carbon sources

Alignments for a candidate for puuC in Escherichia coli BW25113

Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate 17649 b3588 aldehyde dehydrogenase B (lactaldehyde dehydrogenase) (VIMSS)

Query= metacyc::MONOMER-11560
         (497 letters)



>FitnessBrowser__Keio:17649
          Length = 512

 Score =  364 bits (934), Expect = e-105
 Identities = 207/485 (42%), Positives = 292/485 (60%), Gaps = 14/485 (2%)

Query: 16  LKIEGRA--FINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSG 73
           LK++ R   FI GE+     GE ++ L+PV G+ L +VAS    D + A++ A    +  
Sbjct: 19  LKLKARYDNFIGGEWVAPADGEYYQNLTPVTGQLLCEVASSGKRDIDLALDAAHKVKDK- 77

Query: 74  VWSQLAPAKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAE 133
            W+  +   R A L + AD + +N+E LA  ET D GKPI ++S+ D+P A     + A 
Sbjct: 78  -WAHTSVQDRAAILFKIADRMEQNLELLATAETWDNGKPIRETSAADVPLAIDHFRYFAS 136

Query: 134 AIDKVYDEVAPTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPS 193
            I      ++    + +     EP+GVVG I+PWNFPLLMA WK+ PALA GN VVLKP+
Sbjct: 137 CIRAQEGGISEVDSETVAYHFHEPLGVVGQIIPWNFPLLMASWKMAPALAAGNCVVLKPA 196

Query: 194 EKSPLTAIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLM 253
             +PL+ + + ++  +  +P GV+NV+ G G  +G+ LA    +  + FTGST++ +Q+M
Sbjct: 197 RLTPLSVLLLMEIVGDL-LPPGVVNVVNGAGGVIGEYLATSKRIAKVAFTGSTEVGQQIM 255

Query: 254 VYAGESNMKRIWLEAGGKSPNIVFADAPDLQAA----AEAAASAIAFNQGEVCTAGSRLL 309
            YA + N+  + LE GGKSPNI FAD  D + A    A    +  AFNQGEVCT  SR L
Sbjct: 256 QYATQ-NIIPVTLELGGKSPNIFFADVMDEEDAFFDKALEGFALFAFNQGEVCTCPSRAL 314

Query: 310 VERSIKDKFLPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLA 369
           V+ SI ++F+   +  ++  + GNPLD  T +GA V   Q+ T+L+YI+ G K+GA +L 
Sbjct: 315 VQESIYERFMERAIRRVESIRSGNPLDSVTQMGAQVSHGQLETILNYIDIGKKEGADVLT 374

Query: 370 GGKRTL---EETGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTP 426
           GG+R L   E   G Y+EPTI  G  N MR+ QEEIFGPVL+V  F T EEA+ +ANDT 
Sbjct: 375 GGRRKLLEGELKDGYYLEPTILFGQNN-MRVFQEEIFGPVLAVTTFKTMEEALELANDTQ 433

Query: 427 YGLAAGIWTSDISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEK 486
           YGL AG+W+ + + A+K  R ++AG VW N Y      A FGG+KQSG GR+     LE 
Sbjct: 434 YGLGAGVWSRNGNLAYKMGRGIQAGRVWTNCYHAYPAHAAFGGYKQSGIGRETHKMMLEH 493

Query: 487 YTELK 491
           Y + K
Sbjct: 494 YQQTK 498


Lambda     K      H
   0.316    0.132    0.390 

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: 631
Number of extensions: 34
Number of successful extensions: 7
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 497
Length of database: 512
Length adjustment: 34
Effective length of query: 463
Effective length of database: 478
Effective search space:   221314
Effective search space used:   221314
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 (21.6 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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Protein sequences (fasta format)
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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