GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaJ1 in Desulfitobacterium hafniense DCB-2

Align 3-ketoacyl-CoA thiolase, peroxisomal; Acetyl-CoA acyltransferase; Beta-ketothiolase; Peroxisomal 3-oxoacyl-CoA thiolase; EC 2.3.1.16 (characterized)
to candidate WP_011461057.1 DHAF_RS22625 acetyl-CoA C-acyltransferase

Query= SwissProt::P09110
         (424 letters)



>NCBI__GCF_000021925.1:WP_011461057.1
          Length = 384

 Score =  318 bits (815), Expect = 2e-91
 Identities = 183/386 (47%), Positives = 238/386 (61%), Gaps = 8/386 (2%)

Query: 37  DVVVVHGRRTAICRAGRGGFKDTTPDELLSAVMTAVLKDV-NLRPEQLGDICVGNVLQPG 95
           +  ++  +RTAI +AGRG      PD+L + V+  VLK   NL    + D  +G     G
Sbjct: 3   EAFIIEAKRTAIGKAGRGSLAHMRPDDLAAFVIQDVLKSAPNLNSADIDDCVIGCSFPEG 62

Query: 96  A-GAIMARIAQFLSDIPETVPLSTVNRQCSSGLQAVASIAGGIRNGSYDIGMACGVESMS 154
             G  MAR+    + +P  V   T+NR CSSGLQA++  A  IR G     +A G ESMS
Sbjct: 63  EQGMNMARVIALRAGLPIDVSGLTINRFCSSGLQAISLAADRIRLGEAHAMLAGGAESMS 122

Query: 155 LADRGNPGNITSRLMEKEKARDCLIPMGITSENVAERFGISREKQDTFALASQQKAARAQ 214
               G  G         E   +  + MG+T+ENVA+++ I+RE+QD FA AS QKA  AQ
Sbjct: 123 AVPMGG-GKPAPNPYMMEHCPEVYLSMGLTAENVAKKYEITREQQDEFAAASHQKAHAAQ 181

Query: 215 SKGCFQAEIVPVTTTVHDDKGTKRSITVTQDEGIRPSTTMEGLAKLKPAFKKDGSTTAGN 274
             G F+ EIVPV        G K  +  ++DEGIR  +T+E L KLKPAFK  G  TAGN
Sbjct: 182 VGGRFEEEIVPVLIA----SGKKGEVWFSKDEGIRADSTVESLGKLKPAFKNGGCVTAGN 237

Query: 275 SSQVSDGAAAILLARRSKAEELGLPILGVLRSYAVVGVPPDIMGIGPAYAIPVALQKAGL 334
           SSQ SDGAAA LL    K +EL L  L + R +AV GV  ++MGIGP  AIP  L++ GL
Sbjct: 238 SSQTSDGAAATLLMSEEKVKELDLKPLALWRGFAVAGVEAELMGIGPIKAIPKVLKQVGL 297

Query: 335 TVSDVDIFEINEAFASQAAYCVEKLRLPPEKVNPLGGAVALGHPLGCTGARQVITLLNEL 394
           T+  +D+FE+NEAFASQ+   ++ L + P KVNP GGA+A GHPLGCTGA+   TLL+E+
Sbjct: 298 TLEQIDLFELNEAFASQSLAIIKTLGIDPAKVNPNGGAIAFGHPLGCTGAKLTATLLHEM 357

Query: 395 KRRGKRAYGVVSMCIGTGMGAAAVFE 420
           KRRG + YG+V+MCIG GMGAA V+E
Sbjct: 358 KRRGLK-YGMVTMCIGGGMGAAGVYE 382


Lambda     K      H
   0.317    0.134    0.385 

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: 425
Number of extensions: 23
Number of successful extensions: 5
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: 424
Length of database: 384
Length adjustment: 31
Effective length of query: 393
Effective length of database: 353
Effective search space:   138729
Effective search space used:   138729
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 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