GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dsdA in Paraburkholderia bryophila 376MFSha3.1

Align L-serine ammonia-lyase (EC 4.3.1.17); D-Serine ammonia-lyase (EC 4.3.1.18) (characterized)
to candidate H281DRAFT_02886 H281DRAFT_02886 1-aminocyclopropane-1-carboxylate deaminase

Query= BRENDA::O57809
         (325 letters)



>FitnessBrowser__Burk376:H281DRAFT_02886
          Length = 338

 Score =  160 bits (405), Expect = 4e-44
 Identities = 105/323 (32%), Positives = 159/323 (49%), Gaps = 20/323 (6%)

Query: 9   LAKFPRVELIPWETPIQYLPNISREIGADV--YIKRDDL-TGLGIGGNKIRKLEYLLGDA 65
           L +FPR  L    TPIQ L  +S  +G  V  Y KR+D  +G   GGNK RKLEYL+ +A
Sbjct: 3   LQRFPRYPLTFGPTPIQPLKRLSDHLGGKVHLYAKREDCNSGFAFGGNKTRKLEYLIPEA 62

Query: 66  LSKGADVVITVGAVHSNHAFVTGLAAKKLGLDAILVLR-------GKEELKGNYLLDKIM 118
           L++G D ++++G + SN        A  LG+  +LV            +  GN  + +I+
Sbjct: 63  LAQGCDTLVSIGGIQSNQTRQVAAVAAHLGMKCVLVQENWVNYSDAVYDRVGNIQMSRIL 122

Query: 119 GIETRVYDAKDSFELMKYAEEIAEELKREGRKPYVIPPGGAS-PIGTLGYVRAVGEIATQ 177
           G + R+          K  E+  E ++  G KPY IP G +  P+G LG+V    E+  Q
Sbjct: 123 GADVRLVPDGFDIGFRKSWEDALESVRAAGGKPYAIPAGCSDHPLGGLGFVGFAEEVRQQ 182

Query: 178 SE---VKFDSIVVAAGSGGTLAGLSLGLSILNEDIRPVGIAVGRFGEVMTSKLDNLIKEA 234
                 KFD IVV + +G T AG+ +G +      R +GI           ++  +    
Sbjct: 183 EAELGFKFDYIVVCSVTGSTQAGMVVGFAADGRADRVIGIDASAKPAQTREQITRIASRT 242

Query: 235 AELLGV--KVEVRPELYDYSFG--EYGKITGEVAQIIRKVGTREGIILDPVYTGKAFYGL 290
           AE +G+   +     + D  FG  EYG       + IR     EG++ DPVY GK+ +G+
Sbjct: 243 AEKVGLGRDITANDVVLDERFGGPEYGLPNDGTLEAIRLCARLEGVLTDPVYEGKSMHGM 302

Query: 291 VDLARKGEL--GEKILFIHTGGI 311
           +D+ R GE   G ++L+ H GG+
Sbjct: 303 IDMVRNGEFPEGSRVLYAHLGGV 325


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: 283
Number of extensions: 23
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: 325
Length of database: 338
Length adjustment: 28
Effective length of query: 297
Effective length of database: 310
Effective search space:    92070
Effective search space used:    92070
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 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