GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Desulfatiglans anilini DSM 4660

Align Short-chain acyl-CoA dehydrogenase (EC 1.3.8.1) (characterized)
to candidate WP_028321426.1 H567_RS0110890 acyl-CoA dehydrogenase

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



>NCBI__GCF_000422285.1:WP_028321426.1
          Length = 382

 Score =  348 bits (894), Expect = e-100
 Identities = 174/372 (46%), Positives = 250/372 (67%), Gaps = 1/372 (0%)

Query: 5   DDQQQIRDMARDFAQERLKPFAAEWDREHRFPKEAIGEMAGLGFFGMLVPEQWGGCDTGY 64
           D+QQ +R+MAR FA+  +KP AAE D  H  P   + E+  L   G+ VPE++GG    Y
Sbjct: 7   DEQQMVREMARRFAEAEIKPKAAELDATHAHPAAIVRELGELKMLGIAVPEEYGGGGMDY 66

Query: 65  LAYAMALEEIAAGDGACSTIMSVHNSVGCVPILNYGTDEQKERFLKPLASGAMLGAFALT 124
           ++Y +AL E++    +   IMSV+NS+ C P++ YGT EQK+++L+P ASG  LG + LT
Sbjct: 67  VSYVLALIEVSKACASTGVIMSVNNSLYCFPVMAYGTHEQKKKYLEPCASGEKLGCYGLT 126

Query: 125 EPQAGSDASGLKTRARLEGDHYVLNGCKQFITSGQNAGVVIVFAVTDPSAGKRGISAFIV 184
           E  AGSD S + T A  +GD +++NG K+FIT+G  A   ++ AVTD   G +GIS F+ 
Sbjct: 127 EAGAGSDPSAMLTTAVRDGDQWIINGEKKFITNGNVASYCVLAAVTDKGKGYKGISTFVA 186

Query: 185 PT-DSPGYKVARVEDKLGQHASDTCQILFEDVKVPLANRLGEEGEGYRIALANLEGGRVG 243
              D+PG+KV RVE+KLG  AS T +++FED ++P    LG+EGEG++  L+ L+GGR+G
Sbjct: 187 DLEDTPGFKVGRVEEKLGILASGTAELVFEDARLPADALLGQEGEGFKQMLSTLDGGRIG 246

Query: 244 IASQSVGMARAAFEAARDYARERESFGKPIIEHQAVAFRLADMATQIAVARQMVHYAAAL 303
           IASQ++G+ RA  E +  YAR RE F KPI   QA+ ++LADMAT++  A  +   AA L
Sbjct: 247 IASQAIGIGRAVLEESLAYARTREQFNKPISSFQAIQWKLADMATELDAAELLTLRAAWL 306

Query: 304 RDSGKPALVEASMAKLFASEMAEKVCSSALQTLGGYGYLNDFPVERIYRDVRVCQIYEGT 363
            D   P   EA+MAK+FAS++  +     +Q LGGYGY  ++P+ER  RD ++CQIYEGT
Sbjct: 307 EDHHMPYEKEAAMAKMFASDITMRASIEGVQILGGYGYSREYPMERHMRDAKICQIYEGT 366

Query: 364 SDIQRMVISRNL 375
           ++I R+V++RNL
Sbjct: 367 NEIMRLVVARNL 378


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: 394
Number of extensions: 13
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: 375
Length of database: 382
Length adjustment: 30
Effective length of query: 345
Effective length of database: 352
Effective search space:   121440
Effective search space used:   121440
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: 50 (23.9 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