GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Methylococcus capsulatus Bath

Align UDP-glucose 4-epimerase (EC 5.1.3.2); UDP-N-acetylglucosamine 4-epimerase (EC 5.1.3.7) (characterized)
to candidate WP_010960458.1 MCA_RS05745 NAD-dependent epimerase/dehydratase family protein

Query= BRENDA::Q9WYX9
         (309 letters)



>NCBI__GCF_000008325.1:WP_010960458.1
          Length = 320

 Score =  152 bits (383), Expect = 1e-41
 Identities = 106/316 (33%), Positives = 165/316 (52%), Gaps = 17/316 (5%)

Query: 3   ILVTGGAGFIGSHVVDKLIENGYGVIVVDNLSSGKVENLNRNALFYEQSIEDEEMMERI- 61
           ILVTGGAGF+GSH+ + L+  G+ V+ VDN  +G  +N+    L    +   E +   + 
Sbjct: 9   ILVTGGAGFLGSHLCESLLGLGHDVLCVDNFFTGSRDNI----LHLLGNPHFELLRHDVT 64

Query: 62  FSLH-RPEYVFHLAAQASVAISVREPARDAKTNIIGSLVLLEKSIKYGVKKFIFSSTGGA 120
           F L+   + +++LA  AS      +P +  KT++ G++ +L   +   VK  IF ++   
Sbjct: 65  FPLYVEVDEIYNLACPASPIHYQFDPVQTTKTSVHGAINML--GLAKRVKAKIFQASTSE 122

Query: 121 IYGENVKVFPTPETEIPH--PISP---YGIAKYSTEMYLEFFAREYGLKYTVLRYANVYG 175
           +YG+  +V P  E  + H  PI P   Y   K   E     + R++ L   V R  N YG
Sbjct: 123 VYGDP-EVHPQTEDYVGHVNPIGPRSCYDEGKRCAETLFFDYRRQHNLSIKVARIFNTYG 181

Query: 176 PRQDPYGEAGVVAIFTERMLRGEEVHIFGDGEYVRDYVYVDDVVRANLLAMEKGDNEV-- 233
           PR  P  +  VV+ F  + L+G+ + ++GDGE  R + YV D++   +  M+  D+    
Sbjct: 182 PRMHP-NDGRVVSNFIVQALKGQPITLYGDGEQTRSFCYVSDLIEGFIRLMDSPDDFTGP 240

Query: 234 FNIGTGRGTTVNQLFKLLKEITGYDKEPVYKPPRKGDVRKSILDYTKAKEKLGWEPKVSL 293
            N+G     T+ QL + + E+TG   + VY+P    D R+   D T AKEKL WEP + L
Sbjct: 241 VNLGNPGEFTIRQLAEKIIEMTGSSSKLVYQPLPVDDPRQRRPDITLAKEKLDWEPTIHL 300

Query: 294 EEGLKLTVEYFRKTLE 309
           EEGL  T+ YF   L+
Sbjct: 301 EEGLVHTITYFDDLLQ 316


Lambda     K      H
   0.318    0.139    0.396 

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: 260
Number of extensions: 16
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: 309
Length of database: 320
Length adjustment: 27
Effective length of query: 282
Effective length of database: 293
Effective search space:    82626
Effective search space used:    82626
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: 48 (23.1 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