GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etoh-dh-nad in Caulobacter crescentus NA1000

Align alcohol dehydrogenase (EC 1.1.1.1); all-trans-retinol dehydrogenase (NAD+) (EC 1.1.1.105) (characterized)
to candidate CCNA_03124 CCNA_03124 NAD/mycothiol-dependent formaldehyde dehydrogenase

Query= BRENDA::C7R702
         (374 letters)



>FitnessBrowser__Caulo:CCNA_03124
          Length = 366

 Score =  248 bits (634), Expect = 1e-70
 Identities = 143/366 (39%), Positives = 206/366 (56%), Gaps = 6/366 (1%)

Query: 9   KAAVAWEAGKPLSIEEVEVQPPQKGEVRVKIVATGVCHTDAFTLSGDDPEGVFPSILGHE 68
           KAAV  E GKPL IE V +  P   EV ++  A GVCH+D   + G     + P++LGHE
Sbjct: 2   KAAVLREVGKPLQIETVAIGKPGPREVLIRTKAAGVCHSDLHFVEGSYTHAL-PAVLGHE 60

Query: 69  GGGIVESVGEGVTSVKPGDHVIPLYTPECGDCKFCLSGKTNLCQKIRETQGKGLMPDGTT 128
             GIVE+VG  V +VK GDHVI    P CG C+ CL+G  NLC      + K   P    
Sbjct: 61  SAGIVEAVGSEVRTVKVGDHVITCLNPYCGHCEVCLTGHMNLCISPETRRSKSDAPR-LF 119

Query: 129 RFSINGK--PIYHYMGTSTFSEYTVLPEISLAKVNPKAPLEEVCLLGCGVTTGMGAVMNT 186
           +  +NG   P+  ++  S+F+E  ++ E +   +    P +   L+GC V TG+GAVM+T
Sbjct: 120 KEDLNGATGPMAQFLNLSSFAEMMLVHEHACVAIRKDMPFDRAALIGCSVMTGVGAVMHT 179

Query: 187 AKVEEGATVAIFGLGGIGLSAVIGAVMAKASRIIAIDINESKFELAKKLGATDCVNPKDY 246
           + V  G TVA+ G GG+GL+ + GA +A A RIIAID    K ELAK  GATD V+    
Sbjct: 180 SNVRPGETVAVIGCGGVGLATINGAAIAGAGRIIAIDRLAGKLELAKTFGATDVVDASQV 239

Query: 247 DKPIQEVIVEMTDGGVDYSFECIGNVNVMRSALECCHKGWGESVIIGVAGAGQEISTRPF 306
           D  I + +VE+T GGV +SFE IG      ++ +   +G G + +IG+   G +I     
Sbjct: 240 D-DIAKAVVELTGGGVHHSFEAIGLKATAEASFKMLRRG-GTANVIGMIPVGTKIELHGV 297

Query: 307 QLVTGRVWKGTAFGGVKGRSELPDYVERYLAGEFKLDDFITHTMPLEKINDAFDLMHEGK 366
             +  R  +G+  G  +   ++P  V+ Y++G+ KLD+ I+  + LE +N AFD +  G+
Sbjct: 298 DFLGERRIQGSYMGSNRFPVDMPRLVDFYMSGKLKLDELISRRIKLEDVNSAFDELKRGE 357

Query: 367 SIRSVI 372
             RSVI
Sbjct: 358 LARSVI 363


Lambda     K      H
   0.317    0.137    0.413 

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: 375
Number of extensions: 20
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: 374
Length of database: 366
Length adjustment: 30
Effective length of query: 344
Effective length of database: 336
Effective search space:   115584
Effective search space used:   115584
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 (21.6 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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