GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaJ2 in Cupriavidus basilensis 4G11

Align Beta-ketoadipyl-CoA thiolase; 3-oxoadipyl-CoA thiolase; EC 2.3.1.174 (characterized)
to candidate RR42_RS25455 RR42_RS25455 acetyl-CoA acetyltransferase

Query= SwissProt::Q8VPF1
         (401 letters)



>FitnessBrowser__Cup4G11:RR42_RS25455
          Length = 394

 Score =  317 bits (812), Expect = 4e-91
 Identities = 178/402 (44%), Positives = 249/402 (61%), Gaps = 9/402 (2%)

Query: 1   MSREVYICDAVRTPIGRFGGSLAAVRADDLAAVPVKALVERNPQVDWSQLDEVYLGCANQ 60
           M+REV +   VRT IG FGGSL  +    + A+ V+  + R  QV    +  V  G   Q
Sbjct: 1   MTREVVVVSGVRTAIGTFGGSLKDLSPTQMGAMVVREALAR-AQVSGDDVGHVVFGNVIQ 59

Query: 61  AGEDNRNVARMALLLAGLPDSVPGVTLNRLCASGMDAVGTAFRAIASGEAELVIAGGVES 120
               +  + R+A +  G+    P +T+NRLC SG+ A+ +A + I  G+A++ I GG ES
Sbjct: 60  TEPRDMYLGRVAAVEGGVTIDAPALTVNRLCGSGLQAIVSAAQTILLGDADVAIGGGAES 119

Query: 121 MSRAPYVMGKADSAFGRGQKIEDTTIGWRFINPLMKAQYGVDAMPETADNVADDYKVSRA 180
           MSRAPY+   A      G ++ D  +    +  L    +G+  M  TA+NVA +Y +SR 
Sbjct: 120 MSRAPYLAQSARW----GARMGDAKMLDMMLGALHDPFHGIH-MGVTAENVAKEYDISRV 174

Query: 181 DQDAFALRSQQLAGRAQAAGYFAEEIVPVVIKGKKGETVVDADEHLRPDTTLEALAKLKP 240
            QD  AL S + A  A  AG+F ++I+PV +KG+KG+   D DEH+R D  +E + KLKP
Sbjct: 175 QQDEAALESHRRASAAIRAGHFKDQILPVTLKGRKGDVTFDTDEHVRHDAVMEDMTKLKP 234

Query: 241 VNGPDK-TVTAGNASGVNDGSVALILASAEAVKKHGLKARAKVLGMASAGVAPRVMGIGP 299
           V   +  TVTAGNASG+ND + A++L      +K GLK  A+++  A AGV P+ MGIGP
Sbjct: 235 VFVKENGTVTAGNASGLNDAAAAVVLMERAEAEKRGLKPMARLVSYAHAGVDPKTMGIGP 294

Query: 300 VPAVRKLLERLNLSVADFDVIELNEAFAAQGLAVTRELGIADDDARVNPNGGAIALGHPL 359
           VPA +K LER  L+VAD DVIE NEAFAAQ  AVT+ LG+  D A+VNPNG  I+LGHP+
Sbjct: 295 VPATKKALERAGLTVADLDVIEANEAFAAQACAVTKALGL--DPAKVNPNGSGISLGHPI 352

Query: 360 GASGARLVLTAVHQLEKSGGQRGLCTMCVGVGQGVALAVERV 401
           GA+GA + + A+++L++  G+  L TMC+G GQG+A   ERV
Sbjct: 353 GATGALITVKALYELQRVQGRYALVTMCIGGGQGIAAIFERV 394


Lambda     K      H
   0.317    0.134    0.379 

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: 388
Number of extensions: 18
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: 401
Length of database: 394
Length adjustment: 31
Effective length of query: 370
Effective length of database: 363
Effective search space:   134310
Effective search space used:   134310
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 (21.6 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 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