GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sdaB in Caulobacter crescentus NA1000

Align L-serine ammonia-lyase (EC 4.3.1.17) (characterized)
to candidate CCNA_03203 CCNA_03203 threo-3-hydroxyaspartate ammonia-lyase

Query= BRENDA::A0QY48
         (316 letters)



>FitnessBrowser__Caulo:CCNA_03203
          Length = 325

 Score =  204 bits (520), Expect = 2e-57
 Identities = 133/323 (41%), Positives = 184/323 (56%), Gaps = 13/323 (4%)

Query: 4   VTLDDISGAAARIAADIVRTPLLAADWGDPRCP--LWLKAETLQPIGAFKIRGAFNALGR 61
           V+L DI  AA R+    V TPL+ +   + R    ++LK ETLQ  GAFK RGA+N L +
Sbjct: 3   VSLADIQAAAVRLKGSAVETPLIESPALNDRLGGRIFLKPETLQRAGAFKFRGAYNRLSQ 62

Query: 62  LDTHTRARGVVAYSSGNHAQAVAYAAAAYGVPAHIVMPEETPAVKVEATRRRGAHVVLCG 121
           L    +ARGVVA+SSGNHAQ VA AA   GVPA IVMP ++P+VKVE TR  GA +    
Sbjct: 63  LSDEEKARGVVAFSSGNHAQGVALAARLLGVPALIVMPSDSPSVKVEGTRGFGADIRFYD 122

Query: 122 AGERERTAA--ELVEKTGAVLIPPFDHPDIIAGQGTIGIEI----AEDLPELATVLIPVS 175
               +R A   ++  + G V++P +D P IIAGQGT+G+EI    A     L  ++  V 
Sbjct: 123 RFTEDRVAIADQIAAERGCVVVPSYDDPHIIAGQGTVGLEIVAQAAAQGATLDRLICCVG 182

Query: 176 GGGLASGIGTAIRALRPKAKIFAVEPELAADTAESLALGSIVEWPVAKRNRTIADGLRS- 234
           GGGL +G  TA++AL P  +I+ VEP    +T  SL  G      + K  R+I D L + 
Sbjct: 183 GGGLIAGTSTAVKALSPATEIWGVEPAGFDETRRSLESGR--RETIDKDARSICDALLTP 240

Query: 235 TPSELTFAHLRQVIDDVITVSEDEIRSAVRELALRARLVAEPSGAVSLAGYRKAALP-DG 293
            P +LT+   ++ +  V+ V++ E+  A+R      +LV EP G V+L       +   G
Sbjct: 241 IPGDLTWPINQKNLSGVVAVTDAEVAEAMRYAFSTLKLVVEPGGCVALTAALTGKVDVAG 300

Query: 294 SAVAIV-SGGNIEPAQLAAILAG 315
             VAIV SGGN++P   A +L G
Sbjct: 301 KTVAIVLSGGNVDPGLFAQVLGG 323


Lambda     K      H
   0.318    0.134    0.384 

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: 284
Number of extensions: 10
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: 316
Length of database: 325
Length adjustment: 28
Effective length of query: 288
Effective length of database: 297
Effective search space:    85536
Effective search space used:    85536
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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