GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Pseudomonas benzenivorans DSM 8628

Align UDP-glucose 4-epimerase (EC 5.1.3.2) (characterized)
to candidate WP_090444680.1 BLS63_RS12555 dTDP-glucose 4,6-dehydratase

Query= BRENDA::F6DEY6
         (311 letters)



>NCBI__GCF_900100495.1:WP_090444680.1
          Length = 364

 Score =  139 bits (349), Expect = 1e-37
 Identities = 113/351 (32%), Positives = 172/351 (49%), Gaps = 57/351 (16%)

Query: 1   MRVLVTGGAGFIGSHIVEDLLARGLEVAV-LDNLA-TGKRENV-----PKGVPFFQVDLR 53
           M++LVTGGAGFIGS ++  ++    +  V LD L   G  E++      +   F +VD+ 
Sbjct: 1   MKILVTGGAGFIGSAVIRHIIGSTTDSVVNLDKLTYAGNLESLVEVSASERYAFERVDIC 60

Query: 54  DKEEVERAFREFRPTHVSHQAAQASVKVSVEDPVLDFEVNLLGGLNLLEACRQY--GVE- 110
           D+ EVER FRE +P  V H AA++ V  S++ P    E N++G   LLEA RQY  G++ 
Sbjct: 61  DRIEVERVFREHQPDAVMHLAAESHVDRSIDGPAAFIETNIVGTYTLLEAARQYWQGLDE 120

Query: 111 --KLVFA---STGGAIYGEVPEGERA-EETWPPRPKSPYAASKAAFEHYLSVYGQSYGLK 164
             K  F     +   +YG++ + E    E  P  P SPY+ASKA+ +H +  + ++YGL 
Sbjct: 121 SRKTAFRFHHISTDEVYGDLDDPEELFTEATPYAPSSPYSASKASSDHLVRAWRRTYGLP 180

Query: 165 WVSLRYGNVYGPRQDPHGEAGVVAIFAERVLNGLPVTLYARKTPGDEGCVRDYVYVGDVA 224
            +     N YGP   P     ++ +     L G P+ +Y +   GD+  VRD++YV D  
Sbjct: 181 TLVTNCSNNYGPYHFPE---KLIPLIILNALEGKPLPVYGK---GDQ--VRDWLYVED-- 230

Query: 225 EAHALALFSL--EG----IYNVGTGEGHTTREVLEAVAEAAGKAPQVQP----------- 267
             HA AL+ +  EG     YN+G   GH  ++ +E V        +++P           
Sbjct: 231 --HARALYKVVTEGQIGETYNIG---GHNEKQNIEVVHALCVLLDELRPVRANSFASHLT 285

Query: 268 --------APPRPGDLERSVLSPLKLMAH-GWRPKVGFQEGIRLTVDHFRG 309
                      RPG   R  +   K+    GW P+  F+ GIR TV+ + G
Sbjct: 286 CYKDLITHVQDRPGHDLRYAIDASKIQRELGWTPEETFESGIRKTVEWYLG 336


Lambda     K      H
   0.318    0.138    0.411 

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: 298
Number of extensions: 22
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: 311
Length of database: 364
Length adjustment: 28
Effective length of query: 283
Effective length of database: 336
Effective search space:    95088
Effective search space used:    95088
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 (21.7 bits)
S2: 49 (23.5 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