GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Teredinibacter turnerae T7901

Align UDP-glucose 4-epimerase (EC 5.1.3.2) (characterized)
to candidate WP_015820631.1 TERTU_RS06260 NAD-dependent epimerase

Query= BRENDA::F6DEY6
         (311 letters)



>NCBI__GCF_000023025.1:WP_015820631.1
          Length = 333

 Score =  114 bits (284), Expect = 4e-30
 Identities = 99/338 (29%), Positives = 155/338 (45%), Gaps = 40/338 (11%)

Query: 1   MRVLVTGGAGFIGSHIVEDLLARGLEVAVLDNLATG-----KRENVPKGVP---FFQV-- 50
           M+ LVTG AGFIG+   + L+  G +V  LDNL +      K   + K +P   + QV  
Sbjct: 1   MKYLVTGSAGFIGAATAKRLVDEGHDVFGLDNLNSYYDPALKHHRLEKLLPCENYHQVTM 60

Query: 51  DLRDKEEVERAFREFRPTHVSHQAAQASVKVSVEDPVLDFEVNLLGGLNLLEACRQYGVE 110
           DL D+E V + F   +   V H  AQA V+ S+  P    + N++G + +LE CR   VE
Sbjct: 61  DLADREGVAKLFANEKFQRVIHLGAQAGVRHSINAPFEYIDGNVVGTMTILEGCRHNNVE 120

Query: 111 KLVFASTGGAIYGEVPEGERAEETWPPRPKSPYAASKAAFEHYLSVYGQSYGLKWVSLRY 170
            L++AS+  ++YG  P+   AE      P S YAA+K + E     Y   Y +    LR+
Sbjct: 121 HLIYASS-SSVYGMNPKVPFAESDNVDHPVSLYAATKKSNELMAHAYSNLYDIPTTGLRF 179

Query: 171 GNVYGPRQDPHGEAGVVAIFAERVLNGLPVTLYARKTPGDEGCVRDYVYVGDVAEAHALA 230
             VYGP   P        +F E +L G P+ ++ +         RD+ Y+ D+ E   L 
Sbjct: 180 FTVYGPAGRPDMAPW---LFTEAILKGEPIKVFNKGK-----MQRDFTYIDDIVEG-ILR 230

Query: 231 LFSL--------EG-----------IYNVGTGEGHTTREVLEAVAEAAGKAPQVQPAPPR 271
           + ++        EG           IYN+G          ++A+ +A GK  +    P +
Sbjct: 231 IQNVIPTPNPDDEGSNPSTSRAPYRIYNIGNNNPVELATFIDAIEQACGKKAEKILLPMQ 290

Query: 272 PGDLERSVLSPLKL-MAHGWRPKVGFQEGIRLTVDHFR 308
            GD+ R+      L  A   +P V   +G+   V+ ++
Sbjct: 291 AGDVVRTYADIDALTKATQHKPAVDIYDGVVQFVNWYK 328


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: 256
Number of extensions: 12
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 311
Length of database: 333
Length adjustment: 28
Effective length of query: 283
Effective length of database: 305
Effective search space:    86315
Effective search space used:    86315
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: 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