GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Stenotrophomonas chelatiphaga DSM 21508

Align short-chain acyl-CoA dehydrogenase monomer (EC 1.3.8.1) (characterized)
to candidate WP_057507944.1 ABB28_RS06925 acyl-CoA dehydrogenase

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



>NCBI__GCF_001431535.1:WP_057507944.1
          Length = 382

 Score =  332 bits (850), Expect = 1e-95
 Identities = 174/371 (46%), Positives = 246/371 (66%), Gaps = 1/371 (0%)

Query: 5   DEQQQIADAVRAFAQERLKPFAEQWDKDHRFPKEAIDEMAELGLFGMLVPEQWGGSDTGY 64
           +EQ  + D  R  AQE++ P AE  D+   FP   I  + E GL G+ VP ++GG+    
Sbjct: 7   EEQLMLQDVARRIAQEKIAPSAEHHDRTGEFPLANIQLLGENGLMGIEVPAEYGGAGMDP 66

Query: 65  VAYAMALEEIAAGDGACSTIMSVHNSVGCVPILRFGNEQQKEQFLTPLATGAMLGAFALT 124
           +AY +A+ E+AAGD A STIMSV+NS+ C  IL  GNE QK++++  +A G  +GAFALT
Sbjct: 67  IAYVLAMVEVAAGDAAHSTIMSVNNSLFCNGILTHGNEAQKQKYVRAIAEGTAIGAFALT 126

Query: 125 EPQAGSDASSLKTRARLEGD-HYVLNGSKQFITSGQNAGVVIVFAVTDPEAGKRGISAFI 183
           EPQ+GSDA++++ RA  + D  YV+NG K +ITSG  A  +++FA+TD + G RGISAF+
Sbjct: 127 EPQSGSDATAMRCRAVKQADGSYVINGKKSWITSGPVAKYIVLFAMTDADKGARGISAFL 186

Query: 184 VPTDSPGYQVARVEDKLGQHASDTCQIVFDNVQVPVANRLGAEGEGYKIALANLEGGRIG 243
           + TD+ G+   + E KLG  AS TC+I F++      + LG EGEG+KIA+  L+ GRIG
Sbjct: 187 IDTDNAGFGRGKTEPKLGIRASATCEIEFNDYVAQAEDLLGQEGEGFKIAMGVLDAGRIG 246

Query: 244 IASQAVGMARAAFEVARDYANERQSFGKPLIEHQAVAFRLADMATKISVARQMVLHAAAL 303
           IASQA+G+ARAA+E   +Y  ER++FG  +   Q    ++ADM  K+  A  + L AA +
Sbjct: 247 IASQAIGIARAAYEATLEYVKERKAFGAAIGTFQMTQAKIADMKCKLDAALLLTLRAAWV 306

Query: 304 RDAGRPALVEASMAKLFASEMAEKVCSDALQTLGGYGYLSDFPLERIYRDVRVCQIYEGT 363
           +  G+    EA++AKL ASE A  +   A+Q  GG GY  + PLER +RD ++ +IYEGT
Sbjct: 307 KGEGKRFSNEAAIAKLTASEAAMWITHQAVQIHGGMGYSKEMPLERYFRDAKITEIYEGT 366

Query: 364 SDIQRMVIARN 374
           S+IQR+VIARN
Sbjct: 367 SEIQRLVIARN 377


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: 352
Number of extensions: 16
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: 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