GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Methylocapsa aurea KYG T

Align Short-chain acyl-CoA dehydrogenase (EC 1.3.8.1) (characterized)
to candidate WP_036257156.1 DL86_RS00105 isovaleryl-CoA dehydrogenase

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



>NCBI__GCF_000746085.1:WP_036257156.1
          Length = 387

 Score =  282 bits (721), Expect = 1e-80
 Identities = 147/370 (39%), Positives = 223/370 (60%)

Query: 6   DQQQIRDMARDFAQERLKPFAAEWDREHRFPKEAIGEMAGLGFFGMLVPEQWGGCDTGYL 65
           D   +RDM R FA + + P AAE DR   FP++   +M  LG  G+ V E +GG   GYL
Sbjct: 14  DLDIMRDMVRAFASDNIAPRAAEIDRTDAFPQDLWPQMGALGLLGITVEEDYGGAGLGYL 73

Query: 66  AYAMALEEIAAGDGACSTIMSVHNSVGCVPILNYGTDEQKERFLKPLASGAMLGAFALTE 125
           A+ +A+EEI+    +       H+++    I   GTD QK R+L  L SG  +GA A++E
Sbjct: 74  AHCVAMEEISRASASVGLSYGAHSNLCVNQIRRNGTDAQKRRYLPKLLSGEHVGALAMSE 133

Query: 126 PQAGSDASGLKTRARLEGDHYVLNGCKQFITSGQNAGVVIVFAVTDPSAGKRGISAFIVP 185
             +GSD   ++ RA  +GD YVLNG K +IT+G  A  ++V+A TDP+AG  G++AF++ 
Sbjct: 134 ANSGSDVLSMRLRADRKGDRYVLNGAKLWITNGHYASTLVVYAKTDPAAGGHGVTAFLIE 193

Query: 186 TDSPGYKVARVEDKLGQHASDTCQILFEDVKVPLANRLGEEGEGYRIALANLEGGRVGIA 245
               G++ A+  DKLG   S T +++FED +VP  N LG+  +G  + ++ L+  R  +A
Sbjct: 194 KGFKGFRPAQKLDKLGMRGSPTSELVFEDCEVPEENVLGKVNQGVGVLMSGLDYERAVLA 253

Query: 246 SQSVGMARAAFEAARDYARERESFGKPIIEHQAVAFRLADMATQIAVARQMVHYAAALRD 305
           +  +G+ +A  +    Y RER+ FG+PI E + V  +LADM  +++  R  V+  A   D
Sbjct: 254 AGPIGIMQACLDICLPYTRERKQFGRPIGEFELVQGKLADMYARLSACRAYVYAVAGACD 313

Query: 306 SGKPALVEASMAKLFASEMAEKVCSSALQTLGGYGYLNDFPVERIYRDVRVCQIYEGTSD 365
            G+PA  +A+ A LFA+E A +    A+Q LGG GY+ND+P  R+ RD ++ +I  GTS+
Sbjct: 314 RGQPARKDAAGALLFAAESATQAALDAIQLLGGNGYINDYPAGRLLRDAKLYEIGAGTSE 373

Query: 366 IQRMVISRNL 375
           I+RM+I R L
Sbjct: 374 IRRMLIGREL 383


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: 365
Number of extensions: 13
Number of successful extensions: 1
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: 387
Length adjustment: 30
Effective length of query: 345
Effective length of database: 357
Effective search space:   123165
Effective search space used:   123165
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