GapMind for catabolism of small carbon sources

 

Alignments for a candidate for catB in Billgrantia desiderata SP1

Align muconate cycloisomerase (EC 5.5.1.1) (characterized)
to candidate WP_086511713.1 BZY95_RS20345 muconate/chloromuconate family cycloisomerase

Query= metacyc::MONOMER-14643
         (382 letters)



>NCBI__GCF_002151265.1:WP_086511713.1
          Length = 372

 Score =  440 bits (1131), Expect = e-128
 Identities = 227/371 (61%), Positives = 277/371 (74%)

Query: 2   LATAIESIETIIVDLPTIRPHKLAMHTMQNQTLVIIRVRCADGIEGIGESTTIGGLAYGN 61
           ++  I+SIET++VDLPTIRPHKL+M TM  QTLVI+R+R +DGIEG+GE TTIGGLAYG 
Sbjct: 1   MSATIQSIETLLVDLPTIRPHKLSMTTMACQTLVIVRMRHSDGIEGLGEGTTIGGLAYGP 60

Query: 62  ESPDSIKTNIDKHFAPLLIGQDSGNVNAAMLRLERSIRGNTFAKSGIETALLDAHGKRLG 121
           ESP+SIK NID + APLLIGQ SGNVNA   RLER  RGN  AKS +ETALLDA GKRLG
Sbjct: 61  ESPESIKRNIDTYLAPLLIGQPSGNVNALRARLERHARGNMIAKSALETALLDAQGKRLG 120

Query: 122 LPVSELLGGRVRDALPVAWTLASGDTEKDIAEAEKMLDLRRHRIFKLKIGAGEVNRDLAH 181
           L V+ELLGG  +  LPV WTLASGDT KDI EA+  L+ RRH  FKLKIGA  V  D+ H
Sbjct: 121 LSVAELLGGARQTHLPVLWTLASGDTAKDIEEAQLRLEQRRHGDFKLKIGANPVKHDVRH 180

Query: 182 VIAIKKALGDRASVRVDVNQAWDEAVALRACRILGTNGIDLVEQPISRNNRGGMARLNAM 241
           V AIK+ALGDRA VRVDVNQAWDE+ A+   + L   GI+L+EQ I      G+ RL   
Sbjct: 181 VAAIKEALGDRAGVRVDVNQAWDESTAVYGIQALQDAGIELIEQAIPAREHAGLTRLADR 240

Query: 242 SPAPIMADESIECVEDAFNLAREGAASVFALKIAKNGGPRAVLRTASIAEAAGIALYGGT 301
              P++ADE+++   D  +LAR G +  FALKIAK+GG   VL  A +A+AAGI LYGGT
Sbjct: 241 FNVPMLADEAVQDARDGLDLARGGFSGAFALKIAKSGGINGVLELAHVAQAAGIGLYGGT 300

Query: 302 MLEGGLGTMASAHAFVTLNKLAWDTELFGPLLLTEDILSEPLVYRDFELHVPNTPGLGLS 361
           +LEG +GT AS HA+ TL ++AW TE+FGPLLL +DI+ EPL YR+F + +P  PGLG+S
Sbjct: 301 LLEGTIGTAASLHAWATLPEMAWGTEMFGPLLLKDDIVVEPLHYREFGVDLPVGPGLGIS 360

Query: 362 LDEERLAFFRR 372
           LDE++LA + R
Sbjct: 361 LDEDKLAHYAR 371


Lambda     K      H
   0.319    0.136    0.386 

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: 427
Number of extensions: 25
Number of successful extensions: 1
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: 382
Length of database: 372
Length adjustment: 30
Effective length of query: 352
Effective length of database: 342
Effective search space:   120384
Effective search space used:   120384
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 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. 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