GapMind for catabolism of small carbon sources

 

Alignments for a candidate for catB in Cupriavidus basilensis 4G11

Align Muconate cycloisomerase (EC 5.5.1.1) (characterized)
to candidate RR42_RS21835 RR42_RS21835 muconate cycloisomerase

Query= reanno::WCS417:GFF4626
         (375 letters)



>FitnessBrowser__Cup4G11:RR42_RS21835
          Length = 373

 Score =  447 bits (1151), Expect = e-130
 Identities = 231/367 (62%), Positives = 276/367 (75%)

Query: 6   IESIDTIIVDLPTLRPHKLAMHTMQNQTLVIIRLRCADGIEGIGEATTIGGLSYGNESPD 65
           + S++ I+VDLPT+R H+LAM TMQ QTLVI+RLRC+DGIEGIGEATTIGGLSYG+ESP+
Sbjct: 5   VTSVEAILVDLPTIRAHQLAMTTMQRQTLVIVRLRCSDGIEGIGEATTIGGLSYGDESPE 64

Query: 66  SIKVNIDRHFAPLLIGQDASNINAAMLRLERSIRGNTFAKSGIESALLDALGKRLNLPVS 125
            IK+ ID + AP L G DA NI+AAM RL    RGN FAKS +ESALLDA GKRL LP+S
Sbjct: 65  GIKLTIDTYLAPALAGIDACNIHAAMQRLASVARGNRFAKSALESALLDAQGKRLGLPLS 124

Query: 126 ELLGGRVRDALPVAWTLASGNTEKDIAEAEKMLDLRRHRLFKLKIGAGEVSHDLAHVIAI 185
           ELLGG VR  L   WTLASG+T +DI EAE +L  RRH  FKLKIG   V  D+AHV AI
Sbjct: 125 ELLGGAVRPNLACLWTLASGDTGRDIEEAETLLAERRHNTFKLKIGRRSVRDDVAHVSAI 184

Query: 186 KKALGDRASVRVDVNQAWDEAVALRACKVLGDNGIDLIEQPISRNNRGGMARLNLSSPAP 245
           K+ALGDRA V VDVNQAW+EA A     +L   GIDL+EQP+ R  RG +ARL      P
Sbjct: 185 KRALGDRARVTVDVNQAWNEADAATGIAMLEAAGIDLVEQPVPREQRGALARLAARFVVP 244

Query: 246 IMADESIECVEDAFNLAREGAASVFALKIAKNGGPRAVLRTAAIAEAAGIGLYGGTMLEG 305
           +MADE++   EDA  LAR   A VFALKI+K+GG   +LRTAA+ +AAGI LYGGTMLEG
Sbjct: 245 VMADEAVCGPEDAMELARIAGADVFALKISKSGGIFEMLRTAAVGDAAGIALYGGTMLEG 304

Query: 306 GIGTLASAHAFLTLNKLAWDTELFGPLLLTEDILTEPPVYRDFQLHVSTAPGLGLAIDEE 365
            +GT+A+AH F TL +LAW TELFGPLLL +D++T  P YRDF LH+   PGLGL +DE+
Sbjct: 305 SVGTIAAAHGFATLPRLAWGTELFGPLLLKDDVVTARPEYRDFALHLPVGPGLGLTLDED 364

Query: 366 RLAFFRR 372
           +LA +RR
Sbjct: 365 KLAHYRR 371


Lambda     K      H
   0.320    0.137    0.394 

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: 433
Number of extensions: 11
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: 375
Length of database: 373
Length adjustment: 30
Effective length of query: 345
Effective length of database: 343
Effective search space:   118335
Effective search space used:   118335
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.

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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