GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Dechlorosoma suillum PS

Align 2-methyl-branched-chain-enoyl-CoA reductase (EC 1.3.8.5) (characterized)
to candidate Dsui_2302 Dsui_2302 acyl-CoA dehydrogenase

Query= reanno::acidovorax_3H11:Ac3H11_2996
         (376 letters)



>FitnessBrowser__PS:Dsui_2302
          Length = 597

 Score =  131 bits (329), Expect = 6e-35
 Identities = 117/371 (31%), Positives = 165/371 (44%), Gaps = 43/371 (11%)

Query: 37  KDAHQGLAALGAYGICVPEEFGGANLDYLTLALVLEEIAAGDGGTSTAISVTNCPVNAIL 96
           K+A+   A  G   +    EFGG  L  L    V E   + +   S    +T   + A L
Sbjct: 79  KEAYTQFAENGWTALACSPEFGGQGLPKLISTAVNEMWKSANMAFSLCPMLTTGAIEA-L 137

Query: 97  MRYGNAQQKRDWLTPLARGEMLGAFCLTEPHVGSDASALRTTAVKQGD-EYVINGVKQFI 155
           M  G+   K+ +L  +  GE  G   LTEP  GSD +A+RT A  QGD  Y I G K FI
Sbjct: 138 MTAGSDALKQKFLPKMVSGEWTGTMNLTEPSAGSDLAAVRTRAEPQGDGSYKIFGQKIFI 197

Query: 156 TSGKNGQ----VAIVIA-VTDKGAGKKGMSAFLVP-----------TNNPGYVVARLEDK 199
           T G +      V +V+A + +   G KG+S F+VP             N  Y V+ +E K
Sbjct: 198 TYGDHNMTENIVHLVLARLPNAPEGVKGISLFVVPKFMVKDDGSLGERNDAYCVS-IEHK 256

Query: 200 LGQHSSDTAQINFDNCRIPAENLIGAEGEGYKIALGALEGGRIGIAAQSVGMARSAFDAA 259
           LG H+S TA + F +       L+G E  G +     +   R  +  + V +A  A+  A
Sbjct: 257 LGIHASPTAVMAFGDHGGAVGYLVGEENRGLEYMFIMMNAARFAVGMEGVALAERAYQQA 316

Query: 260 LAYSKERESFGT----------AIFNHQAVGFRLADCATQIEAARQLIWHAAALRDAGKP 309
           + Y+K+R   GT          +I  H  V   L    +Q EAAR L +  AA  DA K 
Sbjct: 317 VWYAKDRIQ-GTELGVRGGPKVSILKHPDVRRLLMSMRSQTEAARALAYVVAAAMDAAKH 375

Query: 310 CLKEAAMA-------------KLFASEMAERVCSAAIQTLGGYGVVNDFPVERIYRDVRV 356
              EA  A             K  ++EM+  V S  +Q  GG G + +    +  RD R+
Sbjct: 376 HPDEAVRAANQAFADLMIPVVKGHSTEMSIEVASEGVQVHGGMGFIEETGAAQHLRDARI 435

Query: 357 CQIYEGTSDVQ 367
             IYEGT+ +Q
Sbjct: 436 TAIYEGTTAIQ 446


Lambda     K      H
   0.319    0.134    0.396 

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: 499
Number of extensions: 26
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: 376
Length of database: 597
Length adjustment: 33
Effective length of query: 343
Effective length of database: 564
Effective search space:   193452
Effective search space used:   193452
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: 51 (24.3 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