GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Sedimenticola selenatireducens DSM 17993

Align acetyl-CoA:acetyl-CoA C-acetyltransferase / acetyl-CoA:propanoyl-CoA 2-C-acetyltransferase (EC 2.3.1.9; EC 2.3.1.16) (characterized)
to candidate WP_029133985.1 A3GO_RS0114375 acetyl-CoA C-acyltransferase

Query= reanno::pseudo3_N2E3:AO353_25685
         (397 letters)



>NCBI__GCF_000428045.1:WP_029133985.1
          Length = 394

 Score =  502 bits (1293), Expect = e-147
 Identities = 255/392 (65%), Positives = 315/392 (80%), Gaps = 1/392 (0%)

Query: 6   DPIVIVSAVRTPMGGFQGELKSLSAPQLGAAAIRAAVERAGVAADAVEEVLFGCVLSAGL 65
           DPIVIV   RTPMGGFQG L +L+APQLG+AAI AAV RAG++ + V+EVL G VL+AG+
Sbjct: 3   DPIVIVDIARTPMGGFQGALAALTAPQLGSAAIAAAVSRAGISPEDVQEVLMGNVLTAGI 62

Query: 66  GQAPARQAALGAGLDKSTRCTTLNKMCGSGMEAAILAHDMLLAGSADVVVAGGMESMSNA 125
           GQAP RQAALGAG+  ST C  ++K+CGSGM+A +LAHD++ AGS  V+VAGGMESMSNA
Sbjct: 63  GQAPTRQAALGAGIPLSTPCAGISKVCGSGMKAVMLAHDLIKAGSNQVMVAGGMESMSNA 122

Query: 126 PYLLDRARSGYRMGHGKVLDHMFLDGLEDAY-DKGRLMGTFAEDCAEANGFTREAQDEFA 184
           PYLL++AR GYR+GHGKV+DHMFLDGLEDAY D+G LMGTFAE CA+   F+RE QDEFA
Sbjct: 123 PYLLEKARGGYRLGHGKVMDHMFLDGLEDAYFDRGALMGTFAEQCADHFKFSREQQDEFA 182

Query: 185 IASTTRAQQAIKDGSFNAEIVPLQVIVGKEQKLITDDEQPPKAKLDKIASLKPAFRDGGT 244
           IAS +RA  AI+ G F  EIVP+ +        +  DEQP KA+ +KI SL+PAFR  GT
Sbjct: 183 IASLSRANAAIEAGRFEREIVPVTISGRGGDTQVAIDEQPGKARPEKIPSLRPAFRKDGT 242

Query: 245 VTAANSSSISDGAAALLLMRRSEAEKRGLKPLAVIHGHAAFADTPGLFPVAPVGAIKKLL 304
           VT ANSSSISDGAAAL+LMR SEAE+RGL P AVIHGHA +A  P  F  APV A++ LL
Sbjct: 243 VTPANSSSISDGAAALVLMRASEAERRGLSPRAVIHGHAGYAGEPCWFTTAPVYAMQNLL 302

Query: 305 KKTGWSLDEVELFEVNEAFAVVSLVTMTKLEIPHSKVNVHGGACALGHPIGASGARILVT 364
           ++  W+  +V+L+E+NEAFAVV++  M ++ + H KVN++GGACALGHPIGASGARI+VT
Sbjct: 303 QRLEWNKQDVDLWEINEAFAVVTMAAMREMGLDHEKVNINGGACALGHPIGASGARIIVT 362

Query: 365 LLSALRQKGLKRGVAAICIGGGEATAMAVECL 396
           LL+AL ++GLKRGVA++CIGGGEATA+A+E L
Sbjct: 363 LLAALEEQGLKRGVASLCIGGGEATAVAIERL 394


Lambda     K      H
   0.318    0.133    0.378 

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: 482
Number of extensions: 10
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: 397
Length of database: 394
Length adjustment: 31
Effective length of query: 366
Effective length of database: 363
Effective search space:   132858
Effective search space used:   132858
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