GapMind for catabolism of small carbon sources

 

Alignments for a candidate for x5p-reductase in Shewanella loihica PV-4

Align Lmo2663 protein (characterized, see rationale)
to candidate 5211294 Shew_3710 L-threonine 3-dehydrogenase (RefSeq)

Query= uniprot:Q8Y414
         (343 letters)



>FitnessBrowser__PV4:5211294
          Length = 341

 Score =  157 bits (396), Expect = 5e-43
 Identities = 110/348 (31%), Positives = 184/348 (52%), Gaps = 17/348 (4%)

Query: 1   MKAVVKTNPGYDQMELKDVEEPQVYGDKVKIKVAFTGICGSDIHTFKGEYKNPTT---PV 57
           MKA+ K  P  + + + D  +P+V  + + IK+  T ICG+D+H +  +  +  T   P+
Sbjct: 1   MKALSKLKPE-EGIWMVDAPKPEVGHNDLLIKIRKTAICGTDVHIYNWDEWSQNTIPVPM 59

Query: 58  TLGHEFSGVVVEVGPDVTSIKVGDRVTSETTFETCGECIYCKEHDYNLCSNRRGIGTQAN 117
            +GHE+ G VVE+G +V   ++GDRV+ E    TCG C  C+    +LC N  G+G    
Sbjct: 60  VVGHEYVGEVVEIGQEVRGFQIGDRVSGEGHI-TCGHCRNCRAGRTHLCRNTSGVGVNRE 118

Query: 118 GSFAEFVLSREESCHVLDERISLEAAALTEPLACCVHSALEKTTIRPDDTVLVFGPGPIG 177
           G+FAE+++    +   + + IS + A++ +P    VH+AL    +  D  VL+ G GPIG
Sbjct: 119 GAFAEYLVIPAFNAFKIPDDISDDLASIFDPFGNAVHTALSFDLVGED--VLITGAGPIG 176

Query: 178 LLLAQVVKAQGATVIMAGITKDSD-RLRLAKELGMDRIVDTLKEDLAEVV--LGMTGGYG 234
           ++ A V +  GA  ++  IT  ++ RL LAK++G  R V+  KE L +V+  LGMT G+ 
Sbjct: 177 IMAAAVCRHVGARHVV--ITDVNEYRLELAKKMGATRAVNVAKEKLEDVMQDLGMTEGFD 234

Query: 235 AERVFDCSGAVPAVNQGLPLTKKKGDFVQVGLFAEKKNAIDEESIIQREIAYIGSRSQKP 294
                + SG   A +  L      G    +G+      AID   +I + +   G   ++ 
Sbjct: 235 VG--LEMSGVPAAFHSMLDTMNHGGKIAMLGI-PGGDMAIDWSKVIFKGLIIKGIYGREM 291

Query: 295 -SSWILALDLLANGKIDTDKMITKVYGLDDWREAFEAVMAGNEIKVLV 341
             +W     L+ +G +D   +IT  Y +DD++  F+A+ +G   KV++
Sbjct: 292 FETWYKMASLIQSG-LDISPIITHHYNVDDFQAGFDAMRSGQSGKVIL 338


Lambda     K      H
   0.317    0.135    0.392 

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: 299
Number of extensions: 20
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: 343
Length of database: 341
Length adjustment: 29
Effective length of query: 314
Effective length of database: 312
Effective search space:    97968
Effective search space used:    97968
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: 49 (23.5 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