GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Teredinibacter turnerae T7901

Align Short-chain acyl-CoA dehydrogenase (EC 1.3.8.1) (characterized)
to candidate WP_015818306.1 TERTU_RS10525 acyl-CoA dehydrogenase

Query= reanno::pseudo13_GW456_L13:PfGW456L13_2983
         (375 letters)



>NCBI__GCF_000023025.1:WP_015818306.1
          Length = 1286

 Score =  157 bits (397), Expect = 2e-42
 Identities = 112/361 (31%), Positives = 178/361 (49%), Gaps = 7/361 (1%)

Query: 15  RDFAQERLKPFAAEWDREHRFPKEAIGEMAGLGFFGMLVPEQWGGCDTGYLAYAMALEEI 74
           R +A+ R+   +A  D     P   + + A  G  GM VPEQ+ G           +E++
Sbjct: 624 RQYAETRIN--SALIDERRCVPPYIVMDFASQGLLGMCVPEQYAGQAMTVSDSLRVIEQL 681

Query: 75  AAGDGACSTIMSVHNSVGCVPILNYGTDEQKERFLKPLASGAMLGAFALTEPQAGSDASG 134
           AA D   + ++SVH+ +G  PILNYG+   K+ FL  +A G +LGA A+TEP AGS+   
Sbjct: 682 AAIDANLAAMVSVHHVLGTRPILNYGSQLTKDVFLPKIAEGRILGALAITEPGAGSNPHA 741

Query: 135 LKTRAR-LEGDHYVLNGCKQFITSGQNAGVVIVFA-VTDPSAGKRGISAFIVPTDSPGYK 192
           +   AR      +++ G K +I +G  +GV+  F  V D     +G++AF +     G  
Sbjct: 742 ISATARPAPQGGWLITGEKCWIGNGSWSGVINTFVQVKDEQGNPKGLTAFAIEQGRSGMW 801

Query: 193 VARVEDKLGQHASDTCQILFEDVKVPLANRLGEEGEGYRIALANLEGGRVGIASQSVGMA 252
           +      +G       +I F+DV V  ++ LG  G+G  IA   +  GR+ IA+ S+G  
Sbjct: 802 MGEEAPTMGMRGMVQNRIHFKDVHVTESDMLGRVGQGMEIAQDAMMHGRLVIAAMSLGGL 861

Query: 253 RAAFEAARDYARERESFGKPIIEHQAVAFRLADMATQIAVARQMVHYAAALRDSGK--PA 310
           + A +    YA+ R+     + E      RL++M   IA  + MV     L D G   P+
Sbjct: 862 KRAAQLMTRYAQRRDVASGKLFESSVSIQRLSEMHATIAAIQAMVRSLGELIDQGVEIPS 921

Query: 311 LVEASMAKLFASEMAEKVCSSALQTLGGYGYLNDFPVERIYRDVRVCQIYEGTSDIQRMV 370
            + A+  K  A E   K     +Q LGG GY  +  V ++ RD+R+ +I+EG ++   + 
Sbjct: 922 EIYAA-CKTSAPEFLWKGVDQLMQMLGGRGYTENNAVPQLMRDLRLFRIFEGPTEALNVF 980

Query: 371 I 371
           I
Sbjct: 981 I 981


Lambda     K      H
   0.320    0.135    0.394 

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: 915
Number of extensions: 36
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: 375
Length of database: 1286
Length adjustment: 39
Effective length of query: 336
Effective length of database: 1247
Effective search space:   418992
Effective search space used:   418992
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: 54 (25.4 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