GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sdaB in Marivita geojedonensis DPG-138

Align L-serine ammonia-lyase (EC 4.3.1.17); D-Serine ammonia-lyase (EC 4.3.1.18) (characterized)
to candidate WP_085641172.1 MGEO_RS18545 D-cysteine desulfhydrase

Query= BRENDA::O57809
         (325 letters)



>NCBI__GCF_002115805.1:WP_085641172.1
          Length = 341

 Score =  203 bits (517), Expect = 4e-57
 Identities = 132/325 (40%), Positives = 175/325 (53%), Gaps = 18/325 (5%)

Query: 10  AKFPRVELIPWETPIQYLPNISREIGAD-VYIKRDDLTGLGIGGNKIRKLEYLLGDALSK 68
           ++FPRV L    T ++ +  +S+E+G   ++IKRDD TG+  GGNK RKLE+L+ +A ++
Sbjct: 4   SRFPRVNLAHLPTALEPMDRLSKELGGPRIWIKRDDCTGMSTGGNKTRKLEFLMAEAQAQ 63

Query: 69  GADVVITVGAVHSNHAFVTGLAAKKLGLDAILVLRGKE-------ELKGNYLLDKIMGIE 121
           GAD+VIT GA  SNHA  T   A KLG+D  ++L  +         L GN  LD + G  
Sbjct: 64  GADLVITQGATQSNHARQTAACAAKLGMDCHILLEDRTGSNDPNYNLNGNVFLDFLHG-A 122

Query: 122 TRVYDAKDSFELMKYAEEIAEELKREGRKPYVIPPGGASPIGTLGYVRAVGEIATQSE-- 179
           T         ++    E +AE+ + EGR  Y IP GG++P G LGY  A  E+ TQ+   
Sbjct: 123 TAEKRPGTGLDMNAAMEVVAEKFRAEGRNVYTIPGGGSNPTGALGYANAAMELVTQANNM 182

Query: 180 -VKFDSIVVAAGSGGTLAGLSLGLSILNEDIRPVGIAVGRFGEVMTSKLDNLIKEAAELL 238
            +K D IV A GS GT AGL +GL  +N +I  +GI V          + NL  + AE L
Sbjct: 183 GLKIDRIVHATGSAGTQAGLVVGLKAINANIPLLGIGVRAPKPKQEENVYNLAVKTAEKL 242

Query: 239 GVKVEVRPE----LYDYSFGEYGKITGEVAQIIRKVGTREGIILDPVYTGKAFYGLVDLA 294
           G    V  E      DY    YG  T E    I      EGI+LDPVY+GK   GL+DL 
Sbjct: 243 GCPGVVSREDVEANTDYVGEGYGIPTKEGLAAIEMFARLEGILLDPVYSGKGAAGLIDLI 302

Query: 295 RKGELG--EKILFIHTGGISGTFHY 317
           RKG     E I+F+HTGG    F Y
Sbjct: 303 RKGAFAGDENIVFVHTGGGVALFGY 327


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: 273
Number of extensions: 15
Number of successful extensions: 6
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: 341
Length adjustment: 28
Effective length of query: 297
Effective length of database: 313
Effective search space:    92961
Effective search space used:    92961
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: 49 (23.5 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