GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcdH in Rhizobium leguminosarum bv. trifolii WSM1325

Align glutaryl-CoA dehydrogenase (ETF) (EC 1.3.8.6) (characterized)
to candidate WP_012760741.1 RLEG_RS35135 acyl-CoA dehydrogenase family protein

Query= BRENDA::Q3JP94
         (395 letters)



>NCBI__GCF_000023185.1:WP_012760741.1
          Length = 375

 Score =  211 bits (538), Expect = 2e-59
 Identities = 125/371 (33%), Positives = 194/371 (52%), Gaps = 2/371 (0%)

Query: 18  LADDERMVRDAAHAYAQGKLAPRVTEAFRHETTDAAIFREMGEIGLLGPTIPEQYGGPGL 77
           L+D ++ + D A  +A+ +LAP   +  R         +EMGE+GLLG  +PE YGG   
Sbjct: 3   LSDLQQQISDLARDFARDRLAPGAAKRDREHLFPREELKEMGELGLLGMLVPEAYGGSDT 62

Query: 78  DYVSYGLIAREVERVDSGYRSMMSVQSSLVMVPIFEFGSDAQKEKYLPKLATGEWIGCFG 137
             V+Y     E+   D    ++MSV SS+  VPI +FG++ Q++++LPKLA+GEWIG F 
Sbjct: 63  GVVAYAAALEEIAAGDGTCSTIMSVHSSVGCVPILKFGAEEQRQRFLPKLASGEWIGGFA 122

Query: 138 LTEPNHGSDPGSMVTRARKVPGGYSLSGSKMWITNSPIADVFVVWAKLDED-GRDEIRGF 196
           LTEP  GSD  ++ TRAR+    Y + GSK +IT+    DV +V+A  D D G+  I  F
Sbjct: 123 LTEPQAGSDASNLKTRARRDGDHYVIDGSKQFITSGKNGDVIIVFAVTDLDVGKKGITAF 182

Query: 197 ILEKGCKGLSAPAIHGKVGLRASITGEIVLDEAFVPEE-NILPHVKGLRGPFTCLNSARY 255
           I++    G     +  K+GL +S T +I  +   +P E  +    +G R     L   R 
Sbjct: 183 IVQTDTPGYEVIRVEEKLGLHSSDTCQIAFNSMRIPAELRLGAEGEGYRIALANLEGGRI 242

Query: 256 GIAWGALGAAESCWHIARQYVLDRKQFGRPLAANQLIQKKLADMQTEITLGLQGVLRLGR 315
           GIA  A+G A + +  AR Y  +R  FG+P+  +Q +  +LADM   I    Q V     
Sbjct: 243 GIAAQAVGMARAAFEAARDYARERTAFGKPIFEHQAVAFRLADMAVRIEAARQLVFHAAS 302

Query: 316 MKDEGTAAVEITSIMKRNSCGKALDIARLARDMLGGNGISDEFGVARHLVNLEVVNTYEG 375
           +++ G   +   S+ K  +   A  +   A  + GG G   ++ V R   ++ +   YEG
Sbjct: 303 LREAGLPCLSEASMAKLFASEMAERVCSDAIQIHGGYGYMADYPVERIYRDVRICQIYEG 362

Query: 376 THDIHALILGR 386
           T D+  +++ R
Sbjct: 363 TSDVQRMVIAR 373


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: 356
Number of extensions: 14
Number of successful extensions: 3
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: 375
Length adjustment: 30
Effective length of query: 365
Effective length of database: 345
Effective search space:   125925
Effective search space used:   125925
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