GapMind for catabolism of small carbon sources

 

Alignments for a candidate for put1 in Pseudovibrio axinellae Ad2

Align proline dehydrogenase (EC 1.5.5.2) (characterized)
to candidate WP_068001697.1 PsAD2_RS02455 FAD-dependent oxidoreductase

Query= BRENDA::Q5JFG7
         (386 letters)



>NCBI__GCF_001623255.1:WP_068001697.1
          Length = 814

 Score =  178 bits (451), Expect = 6e-49
 Identities = 122/386 (31%), Positives = 194/386 (50%), Gaps = 21/386 (5%)

Query: 4   RELPEKSEITIIGGGIVGVTIAHELAKRGEEVTVIEKRFIGSGSTFRCGTGIRQQFNDEA 63
           RELP+ ++  I+GGGIVG + A+ LAK G +V ++E++ + SG+TF    G+  Q    A
Sbjct: 2   RELPKTAQAVIVGGGIVGCSTAYHLAKLGWDVVLLERKKLTSGTTFHAA-GLVGQLRSSA 60

Query: 64  NV-QVMKRSVELWKKYSEEYGFP--FQQTGYLFLLYDDEEVETFKRNIAIQNKFGVPTRL 120
           N+ Q++  SV+L+K+  EE G    ++  G L L  + E     +R     + FG+  +L
Sbjct: 61  NITQLLGYSVDLYKRLEEETGQATGWKMNGGLRLACNQERWTEVQRQATTAHSFGLDMQL 120

Query: 121 ITPEEAKEIVPLLDISEVVAASWNPTDGKASPFHSTAKFALHAEEFGAKLVEYTEVKDFI 180
           +TP+EA+++ PL+ + +VV A++ P+DG+A+P   T   A  A+  GA++ E T+V    
Sbjct: 121 LTPKEAQDLWPLMQVDDVVGAAFLPSDGQANPSDITLSLAKGAKMAGAQIFEDTKVLSVD 180

Query: 181 IENGEIKGLKTSRGTIKTGIVVNATNAWAKLINAMAGIRTKIPIEPYKHQAVITQPIKKG 240
           +E G IKG++TS+G I+  +VV     W +      G+   +P+   +HQ V+T+PI  G
Sbjct: 181 VEKGIIKGIETSQGRIECAVVVACCGQWTREFAKSVGV--NVPLVSMQHQYVVTEPI-PG 237

Query: 241 SVKPMVISFRYGHAYLTQTSHGGIIGGVGYEEGPT------------YD-LNPTYEFLRE 287
             K +            +   GG++ G GYE  P             Y  L   YE    
Sbjct: 238 VPKNLPTLRDPDRLTYYKEEVGGLVMG-GYEANPLSWAEDGIPKGFHYSLLGSNYEHFEP 296

Query: 288 VSYYFTKIIPALRELLILRTWAGYYAKTPDSNPAIGKIEELSDYYIAAGFSGHGFMMAPA 347
           +       +PAL    I     G  + TPD N  +G+  EL ++Y+ AGF+  G      
Sbjct: 297 LMELSLGRVPALETAGIKELINGPESFTPDGNLIMGEAPELKNFYVNAGFNAFGIAAGGG 356

Query: 348 VAEMVADLITKGKTDLPAWWYDPYRF 373
               +A  I KG+     W  D  RF
Sbjct: 357 AGMALAQWIAKGEPPFDLWPVDIRRF 382


Lambda     K      H
   0.318    0.137    0.406 

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: 662
Number of extensions: 39
Number of successful extensions: 4
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: 386
Length of database: 814
Length adjustment: 36
Effective length of query: 350
Effective length of database: 778
Effective search space:   272300
Effective search space used:   272300
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 (21.7 bits)
S2: 53 (25.0 bits)

This GapMind analysis is from Sep 24 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