GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcdH in Cereibacter sphaeroides ATCC 17029

Align glutaryl-CoA dehydrogenase (EC 1.3.8.6) (characterized)
to candidate WP_011840847.1 RSPH17029_RS05935 isovaleryl-CoA dehydrogenase

Query= metacyc::G1G01-166-MONOMER
         (393 letters)



>NCBI__GCF_000015985.1:WP_011840847.1
          Length = 385

 Score =  204 bits (519), Expect = 3e-57
 Identities = 130/378 (34%), Positives = 194/378 (51%), Gaps = 7/378 (1%)

Query: 12  PLLLDQQLTEEERMVRDSAYQFAQDKLAPRVLEAFRHEQTDPAIFREMGEVGLLGATIPE 71
           P+  D  L EE   +R++ + +AQ+++ P      R       ++REMGE+GLLG T+PE
Sbjct: 5   PMTFD--LGEEIAALRETVHAWAQERVKPMAARIDRENVFPAELWREMGELGLLGITVPE 62

Query: 72  QYGGSGLNYVCYGLIAREVERIDSGYRSMMSVQSSLVMVPINEFGTEAQKQKYLPKLASG 131
           ++GGS + Y+ + +   EV R  +         S+L +  I   G+  QK +YLPKL SG
Sbjct: 63  EFGGSDMGYLAHTVAVEEVARASASVSLSYGAHSNLCVNQIRLNGSPEQKARYLPKLVSG 122

Query: 132 EWIGCFGLTEPNHGSDPGSMITRARKVDGGYRLTGSKMWITNSPIADVFVVWAKDD---- 187
           E +G   ++E   GSD  SM  +A K +G Y L G+K WITN P ADV VV+AK D    
Sbjct: 123 EHVGALAMSEAGAGSDVVSMKLKAEKRNGYYVLNGTKYWITNGPDADVLVVYAKTDPEAG 182

Query: 188 AGDIRGFVLEKGWQGLSAPAIHGKVGLRASITGEIVMDNVFVPEENIF-PDVRGLKGPFT 246
           A  I  F++EK   G S      KVG+R S TGE++ +N  VP EN+   D +G++   +
Sbjct: 183 AKGITAFLIEKSMTGFSTSPHFDKVGMRGSNTGELIFENCEVPFENVLGQDGKGVRVLMS 242

Query: 247 CLNSARYGISWGALGAAEACWHTARQYTLDRQQFGRPLAANQLIQKKLADMQTEITLALQ 306
            L+  R  +S    G   AC      Y   RQQFG+P+   QL+Q KLADM   +  A  
Sbjct: 243 GLDYERVVLSGIGTGIMAACLDEVVPYCQSRQQFGQPIGNFQLMQGKLADMYVALNTARA 302

Query: 307 GCLRLGRMKDEGTAAVEITSIMKRNSCGKALDIARMARDMLGGNGISDEFGVARHLVNLE 366
                 R  D G       +     +  +A+  A  A   LGG G  ++  V+R   + +
Sbjct: 303 YVYETARACDAGRVTRADAAGCVLYASEQAMVQAHQAVQALGGAGYLNDSVVSRLFRDAK 362

Query: 367 VVNTYEGTHDVHALILGR 384
           ++    GT ++  +++GR
Sbjct: 363 LMEIGAGTSEIRRMLIGR 380


Lambda     K      H
   0.320    0.137    0.413 

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: 348
Number of extensions: 14
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: 393
Length of database: 385
Length adjustment: 30
Effective length of query: 363
Effective length of database: 355
Effective search space:   128865
Effective search space used:   128865
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 10 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