GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Halomonas xinjiangensis TRM 0175

Align UDP-glucose 4-epimerase (EC 5.1.3.2) (characterized)
to candidate WP_043532135.1 JH15_RS15945 dTDP-glucose 4,6-dehydratase

Query= BRENDA::F6DEY6
         (311 letters)



>NCBI__GCF_000759345.1:WP_043532135.1
          Length = 353

 Score =  122 bits (306), Expect = 1e-32
 Identities = 101/337 (29%), Positives = 157/337 (46%), Gaps = 46/337 (13%)

Query: 1   MRVLVTGGAGFIGSHIVEDLLARGLEVAV-------LDNLATGKRENVPKGVPFFQVDLR 53
           M++L+TGGAGFIGS ++  ++A   +  +         NL +    +V     F QVD+ 
Sbjct: 1   MKLLITGGAGFIGSAVIRHIIANTDDCVINVDKLTYAGNLESLAAVSVSDRYVFEQVDIC 60

Query: 54  DKEEVERAFREFRPTHVSHQAAQASVKVSVEDPVLDFEVNLLGGLNLLEACRQY-----G 108
           D+ E+ER F E +P  V H AA++ V  S++ P    + N++G   LLE  R Y      
Sbjct: 61  DRAELERVFAEHQPDAVMHLAAESHVDRSIDGPAEFIQTNIVGTYTLLEVARAYWSGLAP 120

Query: 109 VEKLVFA---STGGAIYGEVP-EGERAEETWPPRPKSPYAASKAAFEHYLSVYGQSYGLK 164
             +L F     +   +YG++   GE   E     P SPY+ASKA+ +H +  + ++YGL 
Sbjct: 121 ERRLGFRFHHISTDEVYGDLEGPGELFTENTSYAPSSPYSASKASSDHLVRAWQRTYGLP 180

Query: 165 WVSLRYGNVYGPRQDPHGEAGVVAIFAERVLNGLPVTLYARKTPGDEGCVRDYVYVGDVA 224
            +     N YGP   P     ++ +     L G  + +Y R   G++  +RD++YV D  
Sbjct: 181 TLITNCSNNYGPYHFPE---KLIPLMILNALEGKSLPVYGR---GEQ--IRDWLYVED-- 230

Query: 225 EAHALALFSLEG----IYNVGTGEGHTTREVLEAVAEAAGKAPQVQPA------------ 268
            A AL     EG     YN+G   GH  ++ +E V        ++ P+            
Sbjct: 231 HARALHKVVTEGQVGETYNIG---GHNEKQNIEVVRTICSLLDELSPSEHSPYADLVTYV 287

Query: 269 PPRPGDLERSVLSPLKLMAH-GWRPKVGFQEGIRLTV 304
             RPG   R  +   K+     WRP+  F+ GIR TV
Sbjct: 288 TDRPGHDLRYAIDAGKIERDLSWRPEETFESGIRKTV 324


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: 305
Number of extensions: 18
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: 353
Length adjustment: 28
Effective length of query: 283
Effective length of database: 325
Effective search space:    91975
Effective search space used:    91975
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