GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcdH in Azorhizobium caulinodans ORS 571

Align glutaryl-CoA dehydrogenase (ETF) (EC 1.3.8.6) (characterized)
to candidate WP_012171357.1 AZC_RS14650 isovaleryl-CoA dehydrogenase

Query= BRENDA::B0EVL5
         (395 letters)



>NCBI__GCF_000010525.1:WP_012171357.1
          Length = 390

 Score =  237 bits (605), Expect = 4e-67
 Identities = 141/376 (37%), Positives = 208/376 (55%), Gaps = 5/376 (1%)

Query: 17  DSQLTDTERMVRDSARAYSQERLLPRVQEAFRHEKTDRAIFNEMGELGLLGATIPEQYGG 76
           D QL +T  ++RDS R +SQ+R+ PR  E  R  +  R ++ E+G LGLLG T+ E+YGG
Sbjct: 10  DFQLGETADLLRDSVRGFSQDRIAPRADEIDRSNQFPRDLWPELGALGLLGLTVEEEYGG 69

Query: 77  SGMNYVCYGLIAREVERVDSGYRSMMSVQSSLVMVPINEFGSEETKQKYLPKLATGEWVG 136
           SG+ Y+ + +   E+ R  +         S+L +  I   GS+E KQ+YLPKL +GE VG
Sbjct: 70  SGLGYLEHVIAMEEISRASASVGLSYGAHSNLCVNQIRRNGSQEQKQRYLPKLISGEHVG 129

Query: 137 CFGLTEPNHGSDPGSMVTRARKVDGGYSLSGAKMWITNSPIADVFVVWAKDD----AGDI 192
              ++EP  GSD  SM TRA K    Y L+G+KMWITN PIA+  VV+AK D    A  I
Sbjct: 130 ALAMSEPGAGSDVVSMRTRAEKKGDRYILNGSKMWITNGPIAETLVVYAKTDPAAGARGI 189

Query: 193 RGFVLEKGWKGLSAPAIHGKVGLRASITGEIVMDEVFCPEENAFPTV-RGLKGPFTCLNS 251
             F++EKG+KG S      K+G+R S TGE+V ++   PEEN    V RG+    + L+ 
Sbjct: 190 TAFLIEKGFKGFSTAQKLDKLGMRGSDTGELVFEDCEVPEENVLGQVGRGVNVLMSGLDY 249

Query: 252 ARYGIAWGALGAAEACYETARQYTMDRKQFGRPLAANQLIQKKLADMLTEITLGLQGCLR 311
            R  +A G +G  +AC +    Y  +RKQFG+P+   QL+Q K+ADM   +         
Sbjct: 250 ERAVLAGGPIGIMQACMDVVIPYVHERKQFGQPIGTFQLMQGKIADMYVAMNSVKAYVYA 309

Query: 312 LGRLKDEGNAPVELTSIMKRNSCGKSLDIARVARDMLGGNGISDEFCIARHLVNLEVVNT 371
           + +  D G    E  +     +  K+  +A  A   LGGNG  +++   R L + ++   
Sbjct: 310 VAKACDRGLTTREDAAGAILIAAEKATWMALEAIQTLGGNGYINDYPTGRLLRDAKLYEI 369

Query: 372 YEGTHDIHALILGRAI 387
             GT +I  +++GR +
Sbjct: 370 GAGTSEIRRMLIGREL 385


Lambda     K      H
   0.319    0.136    0.409 

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: 363
Number of extensions: 13
Number of successful extensions: 4
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: 395
Length of database: 390
Length adjustment: 31
Effective length of query: 364
Effective length of database: 359
Effective search space:   130676
Effective search space used:   130676
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 (21.8 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. 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