GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pcaF in Pseudomonas fluorescens FW300-N2E3

Align β-ketoadipyl-CoA thiolase (EC 2.3.1.174; EC 2.3.1.223) (characterized)
to candidate AO353_01065 AO353_01065 acetyl-CoA acetyltransferase

Query= metacyc::MONOMER-15952
         (401 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_01065
          Length = 392

 Score =  345 bits (884), Expect = 2e-99
 Identities = 199/401 (49%), Positives = 261/401 (65%), Gaps = 10/401 (2%)

Query: 1   MNEALIIDAVRTPIGRYAGALASVRADDLGAIPLKALIARHPQLDWSAVDDVIYGCANQA 60
           MNE +I+ A RT IG + GAL+++ A +LGA  ++ L+ +   +D + +D+VI G    A
Sbjct: 1   MNEVVIVAATRTAIGSFQGALSAIPATELGAAVIRRLLEQ-TGIDAAQIDEVILGQVLTA 59

Query: 61  GEDNRNVARMAALLAGLPVSVPGTTLNRLCGSGLDAVGSAARALRCGEAGLMLAGGVESM 120
           G   +N AR  A+ AGLP + P  TLN++CGSGL AV  A +A+RCG+A L++AGG E+M
Sbjct: 60  GA-GQNPARQTAIKAGLPHTTPALTLNKVCGSGLKAVHLAVQAIRCGDAELVIAGGQENM 118

Query: 121 SRAPFVMGKSEQAFGRS-AEIFDTTIGWRFVNKLMQQGFGIDSMPETAENVAAQFNISRA 179
           S AP+V+ K+        A++ D+ I     +       GI     TAEN+A ++ ISR 
Sbjct: 119 SLAPYVLPKARTGLRMGHAQLQDSMIQDGLWDAFNDYHMGI-----TAENLAQKYEISRE 173

Query: 180 DQDAFALRSQHKAAAAIANGRLAKEIVAVEIAQRKGPAKIVEHDEHPRGDTTLEQLAKLG 239
            QD FA  SQ KAAAAI  GR   EI  + I QRKG   + + DE PR D+T + LAKL 
Sbjct: 174 AQDTFAAASQQKAAAAIEGGRFQSEITPILIPQRKGEPLVFDTDEQPRIDSTAQALAKLK 233

Query: 240 TPFRQGGSVTAGNASGVNDGACALLLASSEAAQRHGLKARARVVGMATAGVEPRIMGIGP 299
             F++ GSVTAGNAS +NDGA  LLLAS+  AQ  GL   AR+   A+AGV+P IMGIGP
Sbjct: 234 PAFQKDGSVTAGNASTLNDGAAVLLLASAAKAQALGLPVLARIKAYASAGVDPSIMGIGP 293

Query: 300 VPATRKVLELTGLALADMDVIELNEAFAAQGLAVLRELGLADDDERVNPNGGAIALGHPL 359
           VPATR  L+  G  + D+D+IE NEAFAAQ LAV +ELG   D  +VN NGGAIALGHP+
Sbjct: 294 VPATRLTLQKAGWNVEDLDLIEANEAFAAQALAVGKELGW--DTSKVNVNGGAIALGHPI 351

Query: 360 GMSGARLVTTALHELEERQGRYALCTMCIGVGQGIALIIER 400
           G SGAR++ + +HEL  R G+  L T+CIG GQG+ L IER
Sbjct: 352 GASGARILVSLVHELIRRDGKKGLATLCIGGGQGVGLAIER 392


Lambda     K      H
   0.319    0.134    0.384 

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: 415
Number of extensions: 15
Number of successful extensions: 4
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: 401
Length of database: 392
Length adjustment: 31
Effective length of query: 370
Effective length of database: 361
Effective search space:   133570
Effective search space used:   133570
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 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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