GapMind for catabolism of small carbon sources

 

Alignments for a candidate for put1 in Phaeobacter inhibens BS107

Align proline dehydrogenase (EC 1.5.5.2) (characterized)
to candidate GFF2298 PGA1_c23300 putative sarcosine dehydrogenase

Query= BRENDA::Q5JFG2
         (385 letters)



>FitnessBrowser__Phaeo:GFF2298
          Length = 815

 Score =  193 bits (490), Expect = 2e-53
 Identities = 132/386 (34%), Positives = 197/386 (51%), Gaps = 16/386 (4%)

Query: 1   MKSEAKTVIIGGGIIGLSIAYNLAKLGESDIVVLEKGYLGNGSTFRCGTGIRQQFGDEAN 60
           + S AK VIIGGGIIG S AY+LAKLG +D V+LE+  L +G+TF    G+  Q    AN
Sbjct: 4   LPSTAKAVIIGGGIIGCSTAYHLAKLGWTDTVLLERKKLTSGTTFH-AAGLVGQLRSNAN 62

Query: 61  I-RMMKRSVELWKGLKEELGYDVEFTQSGYLFLIYSEEELEAFNNNVRLQNRFGVPSRII 119
           I +++  SV+L+  ++ E G    +  +G L L  +EE            + FG+   ++
Sbjct: 63  ITQLLGYSVDLYNKIETETGLGTGWKMNGGLRLACNEERWTEVKRQATTAHSFGLEMELL 122

Query: 120 TPEEAKEIVPPLNTDGVIAAAWNHTDGKANPFKAVFAYANAAKRLGVEIYEYTEAKDIKV 179
           TP+EA+++ P ++   VI AA+  TDG+ANP     A A  A+  G +I+E T+  DI++
Sbjct: 123 TPKEAQDLWPLMDISDVIGAAFMPTDGQANPSDITQALAKGARMAGAKIFEDTKVIDIEI 182

Query: 180 EDGKIKAVVTNRGEIRTGRVINAANAWAPLINKMAGVPIKIPIEPYKHQSVKTEPIKPGQ 239
           EDG+I+AV+T  G I   +VI  A  W     K  GV   +P+ P +HQ + TEP +   
Sbjct: 183 EDGRIRAVITEHGRIECEKVICCAGQWTRTFAKRFGV--NVPLVPMEHQYMVTEPFEGVP 240

Query: 240 IEPMVISFKHGGVYMTQEANQGGVIGGY----------GLKYGPTYDITPT-YDFLRGVS 288
                +       Y  +E   G V+GGY          G+  G  Y +  + +D    + 
Sbjct: 241 SNLPTLRDPDRLTYYKEEVG-GLVMGGYEPNPIPWATDGIPKGFHYSLLDSNFDHFEQLM 299

Query: 289 YRFAQIIPALKYVNIIRVWGGFYAETPDHNAAIGRINEIDEFYIAAGFSGHGFMLAPVVG 348
            +    +PAL++  I  +  G  + TPD N  IG   E+  FY+ AGF+  G       G
Sbjct: 300 EQALGRVPALEHAGIKTLTNGPESFTPDGNFIIGEAPELSNFYVGAGFNAFGIAAGGGAG 359

Query: 349 EALAELIVDGKTDKPLDFYDPYRFER 374
            ALAE + +G+    L   D  RF R
Sbjct: 360 MALAEWVKNGEPPFDLWSADIRRFGR 385


Lambda     K      H
   0.318    0.139    0.412 

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: 750
Number of extensions: 48
Number of successful extensions: 3
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: 385
Length of database: 815
Length adjustment: 36
Effective length of query: 349
Effective length of database: 779
Effective search space:   271871
Effective search space used:   271871
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: 53 (25.0 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