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_012049788.1 SWIT_RS18220 acyl-CoA dehydrogenase

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



>NCBI__GCF_000016765.1:WP_012049788.1
          Length = 375

 Score =  446 bits (1147), Expect = e-130
 Identities = 233/375 (62%), Positives = 290/375 (77%)

Query: 1   MLVNDEQQQIADAVRAFAQERLKPFAEQWDKDHRFPKEAIDEMAELGLFGMLVPEQWGGS 60
           M++++ Q  I +AVRAFAQE+++P ++ ++    +P    +E+A LGL GM+ PE  GG+
Sbjct: 1   MILSETQSAIQEAVRAFAQEQIRPRSQAFEAAGGYPTGLFEELAGLGLLGMVAPEAAGGA 60

Query: 61  DTGYVAYAMALEEIAAGDGACSTIMSVHNSVGCVPILRFGNEQQKEQFLTPLATGAMLGA 120
              YV+YA++L EIAA DGA STI+S+ NS+    +L+ G+E QK +FL  L  G M+GA
Sbjct: 61  GADYVSYALSLIEIAAADGALSTIVSIQNSLLVGGLLKEGSEAQKARFLPELIGGRMIGA 120

Query: 121 FALTEPQAGSDASSLKTRARLEGDHYVLNGSKQFITSGQNAGVVIVFAVTDPEAGKRGIS 180
           FALTE  AGSDA++L+TRA      +VLNG+KQFITSG+ AGV +VFAVTDP AGK+GIS
Sbjct: 121 FALTEADAGSDAAALRTRATRAEGGWVLNGAKQFITSGKIAGVAMVFAVTDPAAGKKGIS 180

Query: 181 AFIVPTDSPGYQVARVEDKLGQHASDTCQIVFDNVQVPVANRLGAEGEGYKIALANLEGG 240
           AF+VPTDSPGY V +VE KLGQ ASDTC I FD++ V      GAEG GY IALANLE G
Sbjct: 181 AFLVPTDSPGYAVDKVEHKLGQAASDTCAIRFDDLFVEDGLLFGAEGRGYNIALANLEQG 240

Query: 241 RIGIASQAVGMARAAFEVARDYANERQSFGKPLIEHQAVAFRLADMATKISVARQMVLHA 300
           RIGIA+Q VGMA+AA E+A  YA +R+S GKP+IEHQAV FRLAD+AT++  ARQ+VLHA
Sbjct: 241 RIGIAAQCVGMAQAALEIAVAYARDRRSMGKPIIEHQAVGFRLADLATRLEAARQLVLHA 300

Query: 301 AALRDAGRPALVEASMAKLFASEMAEKVCSDALQTLGGYGYLSDFPLERIYRDVRVCQIY 360
           A+++DAG P L EASMAKLFASE AE + S A+QTLGGYGYL +F L +IYRDVRVCQIY
Sbjct: 301 ASVKDAGLPCLKEASMAKLFASEAAEAIVSGAIQTLGGYGYLEEFGLAKIYRDVRVCQIY 360

Query: 361 EGTSDIQRMVIARNL 375
           EGTSDIQRMVIAR L
Sbjct: 361 EGTSDIQRMVIARAL 375


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: 447
Number of extensions: 13
Number of successful extensions: 2
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: 375
Length adjustment: 30
Effective length of query: 345
Effective length of database: 345
Effective search space:   119025
Effective search space used:   119025
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