GapMind for catabolism of small carbon sources

 

Alignments for a candidate for catB in Sphingomonas histidinilytica UM2

Align muconate cycloisomerase (EC 5.5.1.1) (characterized)
to candidate WP_079647404.1 B5X82_RS06935 muconate cycloisomerase

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



>NCBI__GCF_900167915.1:WP_079647404.1
          Length = 395

 Score =  413 bits (1062), Expect = e-120
 Identities = 209/374 (55%), Positives = 270/374 (72%)

Query: 6   IESIETIIVDLPTIRPHKLAMHTMQNQTLVIIRVRCADGIEGIGESTTIGGLAYGNESPD 65
           +E I+T IVD+PTIRPH L+M  +  Q +VI+RV C+DGI G GE TTIGGL+YG+ESP+
Sbjct: 13  VEKIDTWIVDIPTIRPHVLSMIAINKQVMVIVRVHCSDGIVGTGEGTTIGGLSYGDESPE 72

Query: 66  SIKTNIDKHFAPLLIGQDSGNVNAAMLRLERSIRGNTFAKSGIETALLDAHGKRLGLPVS 125
            +K  ID + APLLIG+++ N  + M  + + + GN FAK+ +ETALLDA  +R G+P+S
Sbjct: 73  GMKLTIDDYMAPLLIGREATNTASLMTLVRQYVVGNHFAKNAVETALLDAEAQRAGVPLS 132

Query: 126 ELLGGRVRDALPVAWTLASGDTEKDIAEAEKMLDLRRHRIFKLKIGAGEVNRDLAHVIAI 185
           ELLGGR+RD LPV WTLASGDT +DI EAE+ML  RRH +FKLKIG   +  D+AHV AI
Sbjct: 133 ELLGGRLRDRLPVLWTLASGDTGRDIEEAEEMLAQRRHDVFKLKIGKRALADDVAHVAAI 192

Query: 186 KKALGDRASVRVDVNQAWDEAVALRACRILGTNGIDLVEQPISRNNRGGMARLNAMSPAP 245
           K+A+GDRASVRVDVNQAWDE  A R   +L   G+DL+EQP+ R +R GM RL A SP  
Sbjct: 193 KRAMGDRASVRVDVNQAWDEPTARRGAHMLADAGVDLIEQPLPRADREGMRRLTAYSPIA 252

Query: 246 IMADESIECVEDAFNLAREGAASVFALKIAKNGGPRAVLRTASIAEAAGIALYGGTMLEG 305
           IMADE++    DA + AR   A  F++K  + GG  A  + A+IAEA  I +YGGTMLEG
Sbjct: 253 IMADEALRGPSDALDFARNRGADAFSIKPPQAGGLFAGGQLAAIAEAGHIGVYGGTMLEG 312

Query: 306 GLGTMASAHAFVTLNKLAWDTELFGPLLLTEDILSEPLVYRDFELHVPNTPGLGLSLDEE 365
            +GT+A AH + T  KL W TELFGPLL TE+IL+EPL +R+F L +P  PGLG++LD +
Sbjct: 313 SVGTIACAHLYATFAKLEWGTELFGPLLQTEEILTEPLAFREFGLDLPTGPGLGVALDMD 372

Query: 366 RLAFFRRDKTSTAI 379
           ++  FRRD  S  +
Sbjct: 373 KVHHFRRDGPSRTV 386


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: 421
Number of extensions: 14
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: 382
Length of database: 395
Length adjustment: 30
Effective length of query: 352
Effective length of database: 365
Effective search space:   128480
Effective search space used:   128480
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 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