GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glucosaminate-lyase in Dyella japonica UNC79MFTsu3.2

Align Glucosaminate ammonia-lyase; EC 4.3.1.9; D-glucosaminate dehydratase alpha-subunit; GlcNA-DH alpha subunit; GlcNADH-alpha (uncharacterized)
to candidate N515DRAFT_1348 N515DRAFT_1348 thioredoxin reductase (NADPH)

Query= curated2:Q93HX6
         (320 letters)



>FitnessBrowser__Dyella79:N515DRAFT_1348
          Length = 319

 Score =  421 bits (1081), Expect = e-122
 Identities = 205/310 (66%), Positives = 250/310 (80%), Gaps = 2/310 (0%)

Query: 5   RHSRVIILGSGPAGYSAAVYAARANLKPLLITGMQAGGQLTTTTEVDNWPGDVHGLTGPA 64
           +HSR++ILGSGPAGY+AAVYAARANLKP L+TG+Q GGQL TTT+V+NWPGD   + GP 
Sbjct: 5   KHSRLLILGSGPAGYTAAVYAARANLKPTLVTGLQQGGQLMTTTDVENWPGD-KAVQGPE 63

Query: 65  LMERMREHAERFETEIVFDHINAVDFAAKPYTLTGDSATYTCDALIIATGASARYLGLPS 124
           LM+R+ EHAE FETE+VFDHI++ D   +P+ L GDS  YT DAL+IATGA+A+YLG+ S
Sbjct: 64  LMQRLAEHAEHFETEMVFDHIHSADLGQRPFRLKGDSGEYTADALVIATGATAKYLGIES 123

Query: 125 EEAFMGKGVSACATCDGFFYRNKPVAVVGGGNTAVEEALYLANIASTVTLIHRRETFRAE 184
           E+ F GKGVSACATCDGFF+R + V VVGGGNTAVEEALYL+N+ S VTL+HRR+  RAE
Sbjct: 124 EQHFKGKGVSACATCDGFFFRGQEVVVVGGGNTAVEEALYLSNLCSKVTLVHRRDKLRAE 183

Query: 185 KILIDKLNARVAEGKIILKLNANLDEVLGDNMGVTGARLKN-NDGSFDELKVDGVFIAIG 243
           KI+ DKL  + A GKI L  N  + EVLGDN GVTG R+K+ N G+  +++  G F+AIG
Sbjct: 184 KIMQDKLFEKAAAGKIELVWNHTVAEVLGDNSGVTGVRVKDVNSGATRDIQATGFFVAIG 243

Query: 244 HTPNTSLFEGQLTLKDGYLVVQGGRDGNATATSVEGIFAAGDVADHVYRQAITSAGAGCM 303
           HTPNT +FEGQL + DGY+ +  G++G AT TSV G+FAAGDVADHVYRQAITSAG GCM
Sbjct: 244 HTPNTGIFEGQLDMHDGYIKIHSGQEGMATMTSVPGVFAAGDVADHVYRQAITSAGFGCM 303

Query: 304 AALDTERYLD 313
           AALD ER+LD
Sbjct: 304 AALDAERWLD 313


Lambda     K      H
   0.318    0.135    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: 361
Number of extensions: 17
Number of successful extensions: 3
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: 320
Length of database: 319
Length adjustment: 28
Effective length of query: 292
Effective length of database: 291
Effective search space:    84972
Effective search space used:    84972
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 17 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