GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sdaB in Trichormus variabilis ATCC 29413

Align L-serine ammonia-lyase (EC 4.3.1.17); D-Serine ammonia-lyase (EC 4.3.1.18) (characterized)
to candidate WP_011318199.1 AVA_RS06945 1-aminocyclopropane-1-carboxylate deaminase/D-cysteine desulfhydrase

Query= BRENDA::O57809
         (325 letters)



>NCBI__GCF_000204075.1:WP_011318199.1
          Length = 307

 Score =  129 bits (324), Expect = 9e-35
 Identities = 98/305 (32%), Positives = 152/305 (49%), Gaps = 12/305 (3%)

Query: 23  PIQYLPN-ISREIGADVYIKRDDLTGLGIGGNKIRKLEYLLGDALSKGADVVITVGAVHS 81
           PIQ + + I+   G ++ + R DL    + GNK  KL+Y L +A  KG   ++T G  +S
Sbjct: 9   PIQKINSEIANNAGVEIDVLRLDLMHPWVNGNKWYKLKYNLLEAKEKGYTTLLTFGGAYS 68

Query: 82  NHAFVTGLAAKKLGLDAILVLRGKEELKGNYLLD--KIMGIETRVYDAKDSFELMKYAEE 139
           NH F T  A   LG   I V+RG+E L  N  L      G++  VY  ++++     A  
Sbjct: 69  NHIFATAAAGNLLGFQTIGVIRGEETLPLNPTLSFATKQGMQL-VYVDRETYRQRNSATL 127

Query: 140 IAEELKREGRKPYVIPPGGASPIGTLGYVRAVGEIATQSEVKFDSIVVAAGSGGTLAGLS 199
            A+  KR G + ++IP GG++    L  VR   EI + +   F+ + VA G+  TLAG++
Sbjct: 128 HADLRKRFG-EVFIIPEGGSN----LNGVRGCLEIISAATQAFNIVCVACGTATTLAGIA 182

Query: 200 LGLSILNEDIR-PVGIAVGRFGEVMTSKLDNLIKEAAELLGVKVEVRPELYDYSFGEYGK 258
           L L      I  PV    G   E +T  ++N +     +          + DY FG Y K
Sbjct: 183 LALEAKQRVIGFPVLKNGGFLAEEITQFMNNYVAAGLPISSSSPAHWELVCDYHFGGYAK 242

Query: 259 ITGEVAQIIRKVGTREGIILDPVYTGKAFYGLVDLARKGEL--GEKILFIHTGGISGTFH 316
           +  ++    ++     G+ LD VYT K FYG++DL ++     G++IL IHTGG+ G   
Sbjct: 243 VKDDLIVFSQQFTQTHGVPLDYVYTAKMFYGVMDLLKQRYFTKGDRILMIHTGGLQGNIG 302

Query: 317 YGDKL 321
             ++L
Sbjct: 303 MSERL 307


Lambda     K      H
   0.319    0.142    0.402 

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: 203
Number of extensions: 10
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: 325
Length of database: 307
Length adjustment: 27
Effective length of query: 298
Effective length of database: 280
Effective search space:    83440
Effective search space used:    83440
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 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