GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Shewanella loihica PV-4

Align L-threonine dehydrogenase (EC 1.1.1.103) (characterized)
to candidate 5208657 Shew_1166 iron-containing alcohol dehydrogenase (RefSeq)

Query= ecocyc::EG12293-MONOMER
         (383 letters)



>FitnessBrowser__PV4:5208657
          Length = 382

 Score =  514 bits (1324), Expect = e-150
 Identities = 259/381 (67%), Positives = 302/381 (79%)

Query: 3   ASTFFIPSVNVIGADSLTDAMNMMADYGFTRTLIVTDNMLTKLGMAGDVQKALEERNIFS 62
           A+ FFIPSVNV+G +++ DA+  +   GF R LIVTD  L ++G+ G + +      I S
Sbjct: 2   AAKFFIPSVNVLGQNAVDDAIGDIKTLGFQRALIVTDKPLVEIGLVGQIVEKFGAAGITS 61

Query: 63  VIYDGTQPNPTTENVAAGLKLLKENNCDSVISLGGGSPHDCAKGIALVAANGGDIRDYEG 122
            I+DG QPNPT  NV AGL LLK N+CD V+SLGGGSPHDCAKGIALVA NGG+I+DYEG
Sbjct: 62  TIFDGVQPNPTVGNVEAGLALLKANDCDFVVSLGGGSPHDCAKGIALVATNGGNIKDYEG 121

Query: 123 VDRSAKPQLPMIAINTTAGTASEMTRFCIITDEARHIKMAIVDKHVTPLLSVNDSSLMIG 182
           +D SAKPQLP++AINTTAGTASEMTRFCIITDEARHIKMAIVDKH TP+LSVND  LM+ 
Sbjct: 122 LDMSAKPQLPLVAINTTAGTASEMTRFCIITDEARHIKMAIVDKHTTPILSVNDPELMLL 181

Query: 183 MPKSLTAATGMDALTHAIEAYVSIAATPITDACALKAVTMIAENLPLAVEDGSNAKAREA 242
            P  LTAATGMDALTHAIEAYVSIAA PITDACA+KA+ +I  NL  AVE+G + +AR+ 
Sbjct: 182 KPAGLTAATGMDALTHAIEAYVSIAANPITDACAIKAIELIKGNLVEAVENGQSLEARDQ 241

Query: 243 MAYAQFLAGMAFNNASLGYVHAMAHQLGGFYNLPHGVCNAVLLPHVQVFNSKVAAARLRD 302
           MAYAQFLAGMAFNNASLGYVHAMAHQLGGFY+LPHGVCNA+LLPHVQ +N++VAA RL+D
Sbjct: 242 MAYAQFLAGMAFNNASLGYVHAMAHQLGGFYDLPHGVCNALLLPHVQAYNAQVAAPRLKD 301

Query: 303 CAAAMGVNVTGKNDAEGAEACINAIRELAKKVDIPAGLRDLNVKEEDFAVLATNALKDAC 362
            A AMGV+V+   D +GA A I+AI+ L+  V IP  L  L VK ED   LA NALKDAC
Sbjct: 302 VAKAMGVDVSTMTDEQGATAAIDAIKALSVAVKIPENLTKLGVKAEDIPTLADNALKDAC 361

Query: 363 GFTNPIQATHEEIVAIYRAAM 383
           G TNP QATHEEI  I+  A+
Sbjct: 362 GLTNPKQATHEEICQIFTNAL 382


Lambda     K      H
   0.318    0.131    0.373 

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: 538
Number of extensions: 19
Number of successful extensions: 1
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: 383
Length of database: 382
Length adjustment: 30
Effective length of query: 353
Effective length of database: 352
Effective search space:   124256
Effective search space used:   124256
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 (21.8 bits)
S2: 50 (23.9 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:

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