GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcdH in Halomonas desiderata SP1

Align glutaryl-CoA dehydrogenase (ETF) (EC 1.3.8.6) (characterized)
to candidate WP_086510406.1 BZY95_RS13300 isovaleryl-CoA dehydrogenase

Query= BRENDA::Q3JP94
         (395 letters)



>NCBI__GCF_002151265.1:WP_086510406.1
          Length = 389

 Score =  212 bits (540), Expect = 1e-59
 Identities = 132/375 (35%), Positives = 202/375 (53%), Gaps = 2/375 (0%)

Query: 14  LDQQLADDERMVRDAAHAYAQGKLAPRVTEAFRHETTDAAIFREMGEIGLLGPTIPEQYG 73
           LD  L D+  M+RD  +A+A+ ++APR  E          ++++ G++GLLG T+PE+ G
Sbjct: 8   LDFGLDDELNMLRDQVNAFARDEIAPRAAEIDEKNEFPNDLWQKFGDMGLLGITVPEEDG 67

Query: 74  GPGLDYVSYGLIAREVERVDSGYRSMMSVQSSLVMVPIFEFGSDAQKEKYLPKLATGEWI 133
           G G+ Y+++ +   E+ R  +         S+L +  +    +  QK KYLPKL +GE I
Sbjct: 68  GTGMGYLAHCIAMEEISRASASVGLSYGAHSNLCVNQLKINANAEQKAKYLPKLISGEHI 127

Query: 134 GCFGLTEPNHGSDPGSMVTRARKVPGGYSLSGSKMWITNSPIADVFVVWAKLD-EDGRDE 192
           G   ++EP  GSD  SM  RAR+    Y L+G+KMWITN P ADV VV+AK D E G   
Sbjct: 128 GALAMSEPGAGSDVVSMKLRARQEGDKYILNGNKMWITNGPDADVLVVYAKTDPEAGSKG 187

Query: 193 IRGFILEKGCKGLSAPAIHGKVGLRASITGEIVLDEAFVPEENIL-PHVKGLRGPFTCLN 251
           I  FI+EKG  G S      K+G+R S T E+V  +  VP EN+L    KG+R   + L+
Sbjct: 188 ITAFIIEKGMPGFSTAQKLDKLGMRGSNTCELVFQDCEVPVENVLGDEGKGVRVLMSGLD 247

Query: 252 SARYGIAWGALGAAESCWHIARQYVLDRKQFGRPLAANQLIQKKLADMQTEITLGLQGVL 311
             R  +A G +G  ++   +   YV +RKQF + +   QL+Q K+ADM T +      + 
Sbjct: 248 YERTVLAAGPIGIMQAAMDVVVPYVHERKQFNQSIGEFQLVQGKIADMYTTLNACRAYLY 307

Query: 312 RLGRMKDEGTAAVEITSIMKRNSCGKALDIARLARDMLGGNGISDEFGVARHLVNLEVVN 371
            +    D G  + +  + +      KA  +A  A  +LGGNG  +E+   R L + ++  
Sbjct: 308 AVAAACDRGQTSRKDAAGVILYCAEKATQVALDAIQLLGGNGYINEYPTGRLLRDAKLYE 367

Query: 372 TYEGTHDIHALILGR 386
              GT +I  +++GR
Sbjct: 368 IGAGTSEIRRMLIGR 382


Lambda     K      H
   0.320    0.138    0.414 

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: 362
Number of extensions: 20
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: 389
Length adjustment: 31
Effective length of query: 364
Effective length of database: 358
Effective search space:   130312
Effective search space used:   130312
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 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