GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Ch1CoA in Marinobacter adhaerens HP15

Align Cyclohex-1-ene-1-carbonyl-CoA dehydrogenase; Ch1CoA; EC 1.3.8.10 (characterized)
to candidate GFF928 HP15_907 acyl-CoA dehydrogenase domain protein

Query= SwissProt::Q2LQN9
         (414 letters)



>FitnessBrowser__Marino:GFF928
          Length = 388

 Score =  270 bits (689), Expect = 7e-77
 Identities = 149/376 (39%), Positives = 211/376 (56%), Gaps = 2/376 (0%)

Query: 37  LTEEQKLLMEMVRNLAVREIAPRAIEIDENHSFPVHARDLFADLGLLSPLVPVEYGGTGM 96
           LTE+Q    E  R  A + +AP A + D  H FPV       ++G +    P   GG G+
Sbjct: 5   LTEDQLAFREAARAFAEKSMAPHAAKWDNEHIFPVDMMKEAGEMGFMGMYTPEALGGMGL 64

Query: 97  DITTFAMVLEEIGKVCASTALMLLAQADGMLSIILDGSPALKEKYLPRFGEKSTLMTAFA 156
                ++++EE+   C STA  +         +    S  LK++ +P+      L  ++ 
Sbjct: 65  SRLDTSVIVEELAAACPSTAAFITIHNMATWMVASFASDDLKQEIVPKLASGEWL-ASYC 123

Query: 157 ATEPGAGSDLLAMKTRAVKKGDKYVINGQKCFITNGSVADILTVWAYTD-PSKGAKGMST 215
            TEPGAGSD  +++T+AV+ GD YVING K FI+     DIL + A T  P  G KG+ST
Sbjct: 124 LTEPGAGSDAASLRTKAVRDGDSYVINGSKVFISGAGATDILVLMARTGAPDSGYKGIST 183

Query: 216 FVVERGTPGLIYGHNEKKMGMRGCPNSELFFEDLEVPAENLVGEEGKGFAYLMGALSINR 275
           FV+     G+ YG NE+KMG    P   +  E++ +PA N VG+EG GFA  M  L   R
Sbjct: 184 FVIPADADGISYGKNEEKMGWHSQPTRMISLENVRIPASNRVGDEGDGFAIAMKGLDGGR 243

Query: 276 VFCASQAVGIAQGALERAMQHTREREQFGKPIAHLTPIQFMIADMATEVEAARLLVRKAT 335
           +  A+ ++G AQ AL RA  +  EREQFGKP+A    +QF +ADMAT + AAR +VR   
Sbjct: 244 LNIATCSLGGAQAALLRARNYMHEREQFGKPLAAFQALQFKLADMATNLVAARQMVRLGA 303

Query: 336 TLLDAKDKRGPLIGGMAKTFASDTAMKVTTDAVQVMGGSGYMQEYQVERMMREAKLTQIY 395
             LD  D    L   MAK FA+D   +V  +A+Q+ GG GY++EY +ER +R+ ++ QI 
Sbjct: 304 FKLDNADPEATLHCAMAKRFATDACFEVVNEALQLHGGYGYIREYPLERYLRDLRVHQIL 363

Query: 396 TGTNQITRMVTGRSLL 411
            GTN+I R++  R LL
Sbjct: 364 EGTNEIMRLIVARRLL 379


Lambda     K      H
   0.318    0.133    0.375 

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: 351
Number of extensions: 10
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: 414
Length of database: 388
Length adjustment: 31
Effective length of query: 383
Effective length of database: 357
Effective search space:   136731
Effective search space used:   136731
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 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