GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glucosaminate-lyase in Caulobacter crescentus NA1000

Align Glucosaminate ammonia-lyase; EC 4.3.1.9; D-glucosaminate dehydratase alpha-subunit; GlcNA-DH alpha subunit; GlcNADH-alpha (uncharacterized)
to candidate CCNA_02964 CCNA_02964 thioredoxin-disulfide reductase

Query= curated2:Q93HX6
         (320 letters)



>FitnessBrowser__Caulo:CCNA_02964
          Length = 335

 Score =  329 bits (843), Expect = 7e-95
 Identities = 179/313 (57%), Positives = 228/313 (72%), Gaps = 12/313 (3%)

Query: 5   RHSRVIILGSGPAGYSAAVYAARANLKPLLITGMQAGGQLTTTTEVDNWPGDVHGLTGPA 64
           R +R +I+GSGPAGY+AA+YAARA LKP+LI G+Q GGQLT TT+V+N+PG    + GP 
Sbjct: 7   RQTRCLIIGSGPAGYTAAIYAARALLKPVLIAGIQPGGQLTITTDVENYPGFADVIQGPW 66

Query: 65  LMERMREHAERFETEIVFDHINAVDFAAKPYTLTGDSAT-YTCDALIIATGASARYLGLP 123
           LM++MR  AE   TE V D + +VD + +P+T+  DS   +  + +IIATGA A++LGL 
Sbjct: 67  LMDQMRAQAEHVGTEFVSDIVTSVDLSKRPFTVKTDSGQDWIAETIIIATGAQAKWLGLE 126

Query: 124 SEEAFMGKGVSACATCDGFFYRNKPVAVVGGGNTAVEEALYLANIASTVTLIHRRETFRA 183
           SE  F G GVSACATCDGFFYRNK V VVGGGNTAVEEAL+L + AS VTL+HR++  RA
Sbjct: 127 SEAKFQGFGVSACATCDGFFYRNKDVIVVGGGNTAVEEALFLTSFASKVTLVHRKDELRA 186

Query: 184 EKILIDKLNARVAEGKIILKLNANLDEVLG--DNMGVTGARLKN-NDGSFDELKVDGVFI 240
           EKIL ++L   +A  KI +  ++ +DEVLG  D MGVTGARLKN   G   E+  DGVFI
Sbjct: 187 EKILQERL---LAHPKIEVIWDSVIDEVLGQTDPMGVTGARLKNVKTGETQEVAADGVFI 243

Query: 241 AIGHTPNTSLFEGQL-TLKDGYLVVQGGRDGNATATSVEGIFAAGDVADHVYRQAITSAG 299
           AIGH P++ LF GQL T   GYL V+ G      +T++EG++AAGDV D VYRQA+T+AG
Sbjct: 244 AIGHAPSSELFAGQLETGSGGYLKVKPG----TASTAIEGVYAAGDVTDDVYRQAVTAAG 299

Query: 300 AGCMAALDTERYL 312
            GCMAAL+  R+L
Sbjct: 300 MGCMAALEAVRFL 312


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: 324
Number of extensions: 15
Number of successful extensions: 5
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: 335
Length adjustment: 28
Effective length of query: 292
Effective length of database: 307
Effective search space:    89644
Effective search space used:    89644
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