Alignments for a candidate for mt2d in Escherichia coli BW25113

GapMind for catabolism of small carbon sources

Alignments for a candidate for mt2d in Escherichia coli BW25113

Align mannitol 2-dehydrogenase (EC 1.1.1.67) (characterized)
to candidate 16281 b2172 predicted dehydrogenase, NAD-dependent (NCBI)

Query= BRENDA::O08355
         (493 letters)



>FitnessBrowser__Keio:16281
          Length = 488

 Score =  352 bits (903), Expect = e-101
 Identities = 196/485 (40%), Positives = 278/485 (57%), Gaps = 11/485 (2%)

Query: 11  LAPEVKLPAYTLADTRQGIAHIGVGGFHRAHQAYYTDALMNTGEGLDWSICGVGLRSEDR 70
           L   V  P Y     +  I H G G FHRAHQA  TD ++N  +G DW IC + L S D+
Sbjct: 9   LPHHVHAPRYDRQQLQSRIVHFGFGAFHRAHQALLTDRVLNA-QGGDWGICEISLFSGDQ 67

Query: 71  KARDDLAGQDYLFTLYELGDTDDTEVRVIGSISDMLLAE-DSAQALIDKLASPEIRIVSL 129
                L  Q++L+T+ E G  D  +V ++G++ + L A+ DS  A+I+K   P++ IVSL
Sbjct: 68  -LMSQLRAQNHLYTVLEKG-ADGNQVIIVGAVHECLNAKLDSLAAIIEKFCEPQVAIVSL 125

Query: 130 TITEGGYCIDDSNGEFMAHLPQIQHDLAHPSSPKTVFGFICAALTQRRAAGIPAFTVMSC 189
           TITE GYCID + G      P+I HDL  P  P +  G +  AL +RR  G+  FTV+SC
Sbjct: 126 TITEKGYCIDPATGALDTSNPRIIHDLQTPEEPHSAPGILVEALKRRRERGLTPFTVLSC 185

Query: 190 DNLPHNGAVTRKALLAFAALHNAELHDWIKAHVSFPNAMVDRITPMTSTAHRLQLHDEHG 249
           DN+P NG V + A+L  A   + EL  WIK HVSFP  MVDRI P  +    +++    G
Sbjct: 186 DNIPDNGHVVKNAVLGMAEKRSPELAGWIKEHVSFPGTMVDRIVPAATDESLVEISQHLG 245

Query: 250 IDDAWPVVCEPFVQWVLEDKFVNGRPAWEKVGVQFTDDVTPYEEMKIGLLNGSHLALTYL 309
           ++D   + CEPF+QWV+ED FV GRPAWE  GVQ  +DV P+EEMK+ +LNGSH  L YL
Sbjct: 246 VNDPCAISCEPFIQWVVEDNFVAGRPAWEVAGVQMVNDVLPWEEMKLRMLNGSHSFLAYL 305

Query: 310 GFLKGYRFVHETMNDPLFVAYMRAYMDLDVTPNLAPVPGIDLTDYKQTLVDRFSNQAIAD 369
           G+L G+  + + M D  F    R  M  +  P L  +  +DLT Y   L+ RF+N A+  
Sbjct: 306 GYLSGFAHISDCMQDRAFRHAARTLMLDEQAPTL-QIKDVDLTQYADKLIARFANPALKH 364

Query: 370 QLERVCSDGSSKFPKFTVPTINRLIADGRETERA--ALVVAAWALYLKGVDENGVSYTIP 427
           +  ++  DGS K P+  +  I   I  GRET+ +  AL VA W  Y+ GVD+ G +  + 
Sbjct: 365 KTWQIAMDGSQKLPQRMLAGIR--IHQGRETDWSLLALGVAGWMRYVSGVDDAGNAIDVR 422

Query: 428 DPRAEFCQGLVSDDALISQ--RLLAVEEIFGTAIPNSPEFVAAFERCYGSLRDNGVTTTL 485
           DP ++  + LV+  +   +   LL++ E+FG  +P++P FV A E+ +  +   G    L
Sbjct: 423 DPLSDKIRELVAGSSSEQRVTALLSLREVFGDDLPDNPHFVQAIEQAWQQIVQFGAHQAL 482

Query: 486 KHLLK 490
            + LK
Sbjct: 483 LNTLK 487


Lambda     K      H
   0.321    0.137    0.414 

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: 635
Number of extensions: 33
Number of successful extensions: 6
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: 493
Length of database: 488
Length adjustment: 34
Effective length of query: 459
Effective length of database: 454
Effective search space:   208386
Effective search space used:   208386
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: 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
the source code
instructions for running GapMind on your computer

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