GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Sphingomonas wittichii RW1

Align short-chain acyl-CoA dehydrogenase monomer (EC 1.3.8.1) (characterized)
to candidate WP_011952836.1 SWIT_RS10095 acyl-CoA dehydrogenase

Query= metacyc::MONOMER-17424
         (375 letters)



>NCBI__GCF_000016765.1:WP_011952836.1
          Length = 390

 Score =  258 bits (660), Expect = 1e-73
 Identities = 141/374 (37%), Positives = 222/374 (59%), Gaps = 3/374 (0%)

Query: 4   NDEQQQIADAVRAFAQERLKPF-AEQWDKDHRFPKEAIDEMAELGLFGMLVPEQWGGSDT 62
           ++E +   D+V  F      P     W +     ++      E GL G+ VP ++GG+  
Sbjct: 14  SEELRMFEDSVSRFLAAHAGPDRTRHWREQGFVDRDTWRAAGEAGLLGLSVPVEYGGAGV 73

Query: 63  GYVAYAMALEEIAAGDGACSTIMSVHNSVGCVPILRFGNEQQKEQFLTPLATGAMLGAFA 122
            +   A+ +E++     A +  + +HN+V    I+ + NE+QK ++L  + TG  + A A
Sbjct: 74  DFTFDAVIMEQLGRHH-ALNFAIPLHNAVVAPYIVSYANEEQKRRWLPGVVTGETILAVA 132

Query: 123 LTEPQAGSDASSLKTRARLEGDHYVLNGSKQFITSGQNAGVVIVFAVTDPEAGKRGISAF 182
           ++EP AGSD  ++KT AR EGDHYV+NG K FI++G +A ++IV A TDPEAG RG+S F
Sbjct: 133 MSEPGAGSDLQAMKTSARREGDHYVINGQKTFISNGAHASLIIVAAKTDPEAGARGLSLF 192

Query: 183 IVPTDS-PGYQVARVEDKLGQHASDTCQIVFDNVQVPVANRLGAEGEGYKIALANLEGGR 241
            V TD   G+   R+ DK+GQ   DT ++ F +++VPV NR+G EG G+ + +  L   R
Sbjct: 193 AVETDEVEGFTRGRLLDKIGQEGRDTAELFFSDMRVPVENRIGPEGGGFAMLMEKLPQER 252

Query: 242 IGIASQAVGMARAAFEVARDYANERQSFGKPLIEHQAVAFRLADMATKISVARQMVLHAA 301
           + IA QA+ M  AA +    Y  ER++FG+ +++ Q   F+LA+  T+ ++AR  + H  
Sbjct: 253 LVIAWQALAMMEAAIDHTIAYTAERRAFGRAVLDFQNSQFKLAECKTQATIARVFLDHCT 312

Query: 302 ALRDAGRPALVEASMAKLFASEMAEKVCSDALQTLGGYGYLSDFPLERIYRDVRVCQIYE 361
               AG      ASMAK + +E   KV  + LQ  GGYGY++++P+  +Y+D RV +IY 
Sbjct: 313 QQLLAGTLDAATASMAKYWITEAQGKVIDECLQLFGGYGYMTEYPIAEMYKDARVFRIYG 372

Query: 362 GTSDIQRMVIARNL 375
           GTS+I +++IAR+L
Sbjct: 373 GTSEIMKLLIARSL 386


Lambda     K      H
   0.319    0.134    0.382 

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: 344
Number of extensions: 16
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: 390
Length adjustment: 30
Effective length of query: 345
Effective length of database: 360
Effective search space:   124200
Effective search space used:   124200
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