GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ligJ in Burkholderia phytofirmans PsJN

Align 2-keto-4-carboxy-3-hexenedioate hydratase; KCH hydratase; EC 4.2.1.- (characterized)
to candidate BPHYT_RS30325 BPHYT_RS30325 4-oxalomesaconate hydratase

Query= SwissProt::G2IQQ5
         (341 letters)



>FitnessBrowser__BFirm:BPHYT_RS30325
          Length = 349

 Score =  462 bits (1188), Expect = e-135
 Identities = 218/335 (65%), Positives = 251/335 (74%), Gaps = 1/335 (0%)

Query: 3   MIIDCHGHYTVLPKAHDEWREQQKAAFKAGQPAPPYPEISDDEIRETIEANQLRLIKERG 62
           MIIDCHGHYT  P  H+ WR QQ AA K G   PP P I+DDEIRE+IE  QLR+  ERG
Sbjct: 1   MIIDCHGHYTTSPPQHEAWRAQQIAALKDGGTTPPRPVITDDEIRESIEGGQLRIQHERG 60

Query: 63  ADMTIFSPRASAMAPHVGDQSVAVPWAQACNNLIARVVDLFPETFAGVCMLPQSPEADMT 122
            D+TIFSPRA+ M  H+        W+  CN+L+ RV +LFP  F GVC LPQ+P     
Sbjct: 61  TDLTIFSPRAAGMGHHLATAEANALWSSECNDLVHRVCELFPRNFVGVCQLPQAPGVAPA 120

Query: 123 SSIAELERCVNELGFIGCNLNPDPGGGHFKHPPLTDRFWYPFYEKMVELDVPAMIHVSGS 182
           + I EL RCV ELGFIGCNLNPDP GGH+   PLTDR WYP YE MVELDVPAMIHVS S
Sbjct: 121 NCIGELRRCVEELGFIGCNLNPDPSGGHWSGLPLTDRCWYPLYEAMVELDVPAMIHVSSS 180

Query: 183 CNPAMHATGAYYLAADTIAFMQLLQGNLFADFPTLRFIIPHGGGAVPYHWGRFRGLADML 242
           CNP  HATGA+Y+  DT AFMQLLQG+LFADFPTLRFIIPHGGGAVPYHWGR+RGLA  +
Sbjct: 181 CNPNFHATGAHYINGDTSAFMQLLQGDLFADFPTLRFIIPHGGGAVPYHWGRYRGLAQDM 240

Query: 243 KQPSLDTLLMNNVFFDTCVYHQPGINLLADVIDNKNILFGSEMVGAVRGIDPTTGHYFDD 302
           K+P L   L+ NVFFDTCVYHQPG  LLA VI  +NILF SE +GAV+GIDP TGHY+DD
Sbjct: 241 KRPLLSEYLLKNVFFDTCVYHQPGAELLAKVIPVENILFASETIGAVQGIDPETGHYYDD 300

Query: 303 TKRYIDALD-ISDQERHAIFEGNTRRVFPRLDAKL 336
           T+RYIDA++ +SD +R  I+E N R V+PRL  +L
Sbjct: 301 TRRYIDAIEWLSDADRQRIYEDNARSVYPRLSRQL 335


Lambda     K      H
   0.323    0.140    0.442 

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: 461
Number of extensions: 22
Number of successful extensions: 2
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: 341
Length of database: 349
Length adjustment: 29
Effective length of query: 312
Effective length of database: 320
Effective search space:    99840
Effective search space used:    99840
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.5 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (22.0 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