GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Halomonas desiderata SP1

Align short-chain acyl-CoA dehydrogenase monomer (EC 1.3.8.1) (characterized)
to candidate WP_086509764.1 BZY95_RS09860 acyl-CoA dehydrogenase

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



>NCBI__GCF_002151265.1:WP_086509764.1
          Length = 383

 Score =  301 bits (772), Expect = 2e-86
 Identities = 164/369 (44%), Positives = 231/369 (62%), Gaps = 2/369 (0%)

Query: 9   QIADAVRAFAQERLKPFAEQWDKDHRFPKEAIDEMAELGLFGMLVPEQWGGSDTGYVAYA 68
           Q+ D +  F +ERL P   +  ++   P E ++EM E+GLFG+ +PE++GG        A
Sbjct: 10  QLIDTISRFVRERLIPNEARLAEEDAVPAELLEEMKEMGLFGLSIPEEYGGLGLTMEEEA 69

Query: 69  MALEEIAAGDGACSTIMSVHNSVGCVPILRFGNEQQKEQFLTPLATGAMLGAFALTEPQA 128
           +   EI     A  +I   +N +G   IL  G  +QK +++  LATG +L +F LTEP A
Sbjct: 70  LVAMEIGKTSPAFRSIFGTNNGIGAQGILIDGTPEQKAKYVPRLATGELLSSFCLTEPDA 129

Query: 129 GSDASSLKTRARLEGDHYVLNGSKQFITSGQNAGVVIVFAVTDP-EAGKRGISAFIVPTD 187
           GSDA+SL+T A  +GDHYVLNG+K+FIT+G  A V  V A TDP   G  GI+AFIV  D
Sbjct: 130 GSDAASLRTTAVRDGDHYVLNGTKRFITNGPEADVFTVMARTDPGNKGAGGITAFIVEGD 189

Query: 188 SPGYQVARVEDKLGQHASDTCQIVFDNVQVPVANRLGA-EGEGYKIALANLEGGRIGIAS 246
           +PG +    + K+GQ  + TC I+F++ +VP  N +G  EG+G+K A+  L+ GR+ I++
Sbjct: 190 TPGLKRGPADSKMGQKGAHTCDIIFEDCRVPAENIIGGVEGKGFKTAMKVLDRGRLHISA 249

Query: 247 QAVGMARAAFEVARDYANERQSFGKPLIEHQAVAFRLADMATKISVARQMVLHAAALRDA 306
             VG+A    E + +YA ER+ FG PL EHQ V   LAD  T+    R MVL AA  +DA
Sbjct: 250 VCVGVAERLVEESLNYAIERKQFGVPLAEHQLVQAMLADSKTEAYAGRTMVLDAARRKDA 309

Query: 307 GRPALVEASMAKLFASEMAEKVCSDALQTLGGYGYLSDFPLERIYRDVRVCQIYEGTSDI 366
           G  A   AS  KLF +EM  +V   A+Q  GG GY++++ +ER YRDVR+ +IYEGT+ I
Sbjct: 310 GENASTLASCCKLFCAEMVGRVADRAVQVHGGAGYMAEYAVERFYRDVRLFRIYEGTTQI 369

Query: 367 QRMVIARNL 375
           Q++VIARN+
Sbjct: 370 QQVVIARNM 378


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: 354
Number of extensions: 21
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: 383
Length adjustment: 30
Effective length of query: 345
Effective length of database: 353
Effective search space:   121785
Effective search space used:   121785
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