GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcdH in Sphingomonas histidinilytica UM2

Align glutaryl-CoA dehydrogenase (EC 1.3.8.6) (characterized)
to candidate WP_079646512.1 B5X82_RS02900 acyl-CoA dehydrogenase

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



>NCBI__GCF_900167915.1:WP_079646512.1
          Length = 384

 Score =  134 bits (338), Expect = 3e-36
 Identities = 100/342 (29%), Positives = 165/342 (48%), Gaps = 10/342 (2%)

Query: 19  LTEEERMVRDSAYQFAQDKLAPRVLEAFRHEQTDPAIFREMGEVGLLGATIPEQYGGSGL 78
           LTEE+ M RD+   FAQ  LA   LE    +     + R M E GL+G TIPE+ GG G 
Sbjct: 5   LTEEQSMFRDAVAAFAQRHLAAGALERAHSDDYPWEVARMMAEQGLIGITIPEEKGGLGG 64

Query: 79  NYVCYGLIAREVERIDSGYRSMMSVQSSLVMVPINEFGTEAQKQKYLPKLASGEWIGCFG 138
           + +   +    +  +      ++   +   +    +F ++AQK++YL  L  G+ +    
Sbjct: 65  SLMDAVIAIETIASVCPRSADVVQAGNFGAIRTFAQFASDAQKEQYLAPLLKGDGLISVA 124

Query: 139 LTEPNHGSDPGSMITRARKVDGGYRLTGSKMWITNSPIADVFVVWAK--DDAGDIRGFVL 196
           +TEPN GS    + T A     G+R++G K++ T+   A VF+V+ +     G+I   ++
Sbjct: 125 MTEPNAGSAVTELTTTAVPDGDGFRVSGQKIFTTHGTHATVFLVYVRYGPGTGNIGSVLI 184

Query: 197 EKGWQGLSAPAIHGKVG--LRASITGEIVMDNVFVPEENIFPDVRGLKGPFTCLNSARYG 254
           E+G +G S     GK    L       +  DNV+VP++ +     G K   +  N  R G
Sbjct: 185 ERGQEGFS----FGKPVRFLSGEEWNPLFFDNVYVPKDKVLLGPGGFKQQMSGFNVERIG 240

Query: 255 ISWGALGAAEACWHTARQYTLDRQQFGRPLAANQLIQKKLADMQTEITLALQGCLRLGRM 314
            +  +L      ++ A ++   R+QFGR L   Q +Q K A+M+ ++  A     R    
Sbjct: 241 NTARSLALGRYAFNAAVEHAKTRKQFGRALCEFQGLQWKFAEMKLKLDAAQLLLYRAATN 300

Query: 315 KDEGTAAVEITSIMKRNSCGKA-LDIARMARDMLGGNGISDE 355
            D+G  + + T+I K  +C +A  D A  A  ++GG G S +
Sbjct: 301 ADKGLPSPDETAIAK-VACNRAGFDCANEAMQVMGGAGYSQD 341


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: 345
Number of extensions: 18
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: 393
Length of database: 384
Length adjustment: 30
Effective length of query: 363
Effective length of database: 354
Effective search space:   128502
Effective search space used:   128502
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