GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Novosphingobium aromaticivorans DSM 12444

Align 2-methylbutanoyl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate WP_011445295.1 SARO_RS08250 isovaleryl-CoA dehydrogenase

Query= reanno::pseudo6_N2E2:Pf6N2E2_1146
         (375 letters)



>NCBI__GCF_000013325.1:WP_011445295.1
          Length = 387

 Score =  279 bits (713), Expect = 1e-79
 Identities = 151/372 (40%), Positives = 221/372 (59%)

Query: 4   TEEQTQIRDMARQFAEERLKPFAAEWDREHRFPREAIDEMAELGFFGMLVPEQWGGCDTG 63
           TE    IR+ A +FA+E++ P AAE DR  RFPRE  + M  LG  G+ V E++GG   G
Sbjct: 12  TESALMIREAAGRFADEQIAPLAAEIDRNDRFPRELWEPMGALGLHGITVEEEFGGLGLG 71

Query: 64  YLAYAMTLEEIAAGDGACSTIMSVHNSVGCVPILKFGNDEQKAKFLTPLASGAMLGAFAL 123
           YL + + +EE++   G+       H+++    I ++GNDEQKAK+L  L SG  +G+ A+
Sbjct: 72  YLDHVIAVEEVSRASGSVGLSYGAHSNLCVNQIRRWGNDEQKAKYLPKLISGEHVGSLAM 131

Query: 124 TEPQAGSDASSLKTRARLEGDHYVLNGCKQFITSGQNAGVVIVFAVTDPSAGKRGISAFI 183
           +E  AGSD  S+K RA      + LNG K +IT+G  A  ++V+A T P AG RGISAF+
Sbjct: 132 SEAGAGSDVVSMKLRADAVAGGFRLNGTKFWITNGTYADTLVVYAKTSPEAGSRGISAFL 191

Query: 184 VPTDSPGYSVARVEDKLGQHASDTCQILFEDLKVPVGNRLGEEGEGYKIALANLEGGRVG 243
           +  D PG+S+ +  DK+G   S TC+++F+D  VP  N +G    G  + ++ L+  RV 
Sbjct: 192 IEKDMPGFSIGQKIDKMGLRGSPTCELVFDDCFVPEENVMGPLHGGVGVLMSGLDYERVV 251

Query: 244 IAAQAVGMARAAFEAARDYARERSSFGKPIIEHQAVAFRLADMATQIAVARQMVHYAAAL 303
           +A   +G+ +A  +    Y RER  FG+PI   Q +  ++ADM   I  AR  V+  A  
Sbjct: 252 LAGMQIGIMQACLDTVIPYVRERKQFGQPIGTFQLMQAKVADMYVAIQSARAYVYAVAKA 311

Query: 304 RDSGQPALVEASMAKLFASEMAEKVCSMALQTLGGYGYLNDFPLERIYRDVRVCQIYEGT 363
            D+GQ    +A+ A L ASE A +V   A+Q LGG GY  D+P+ER  RD ++  I  GT
Sbjct: 312 CDAGQTTRFDAAGAILLASENAFRVSGEAVQALGGAGYTKDWPVERYLRDAKLLDIGAGT 371

Query: 364 SDIQRMVISRNL 375
           ++I+RM+I R L
Sbjct: 372 NEIRRMLIGREL 383


Lambda     K      H
   0.320    0.134    0.388 

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: 347
Number of extensions: 16
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