GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Ch1CoA in Luteimonas huabeiensis HB2

Align Cyclohex-1-ene-1-carbonyl-CoA dehydrogenase; Ch1CoA; EC 1.3.8.10 (characterized)
to candidate WP_024890485.1 Z164_RS0109600 acyl-CoA dehydrogenase

Query= SwissProt::Q2LQN9
         (414 letters)



>NCBI__GCF_000559025.1:WP_024890485.1
          Length = 382

 Score =  241 bits (614), Expect = 3e-68
 Identities = 139/374 (37%), Positives = 216/374 (57%), Gaps = 4/374 (1%)

Query: 38  TEEQKLLMEMVRNLAVREIAPRAIEIDENHSFPVHARDLFADLGLLSPLVPVEYGGTGMD 97
           +EEQ ++ ++ R +A   IAP A   D +  FP+    L  + GL+   VP EYGG GMD
Sbjct: 6   SEEQLMIQDVARRIAQERIAPSAEAFDRSGEFPLENIRLLGENGLMGIEVPTEYGGAGMD 65

Query: 98  ITTFAMVLEEIGKV-CASTALMLLAQADGMLSIILDGSPALKEKYLPRFGEKSTLMTAFA 156
              + + + EI     A + +M +  +     I+  G+ A K+ Y+    E   +  AFA
Sbjct: 66  PVAYVLAMVEIAAADAAHSTIMSVNNSLFCNGILTHGTEAQKQTYVRAIAEGREI-GAFA 124

Query: 157 ATEPGAGSDLLAMKTRAVKKGD-KYVINGQKCFITNGSVADILTVWAYTDPSKGAKGMST 215
            TEP +GSD  +M+ RAV + D  +V+NG+K +IT+G VA  + ++A TDP++GA+G++ 
Sbjct: 125 LTEPQSGSDATSMRCRAVAQADGSFVVNGKKSWITSGPVARYIVLFATTDPAQGARGITA 184

Query: 216 FVVERGTPGLIYGHNEKKMGMRGCPNSELFFEDLEVPAENLVGEEGKGFAYLMGALSINR 275
           F+V+    G   G  E K+G+R     E+ F+D  V A+ ++G+ G+GF   M  L   R
Sbjct: 185 FLVDTQREGFHRGKTEPKLGIRASATCEIEFQDYVVRADEVLGQPGQGFKIAMSVLDAGR 244

Query: 276 VFCASQAVGIAQGALERAMQHTREREQFGKPIAHLTPIQFMIADMATEVEAARLLVRKAT 335
           +  ASQA+GIA+ A E  + + +ER+ FG+PI      Q  IADM  +++A+ LL  +A 
Sbjct: 245 IGIASQAIGIARAAYEATIAYVKERKAFGQPIGAFQMTQAKIADMKCKLDASLLLTLRA- 303

Query: 336 TLLDAKDKRGPLIGGMAKTFASDTAMKVTTDAVQVMGGSGYMQEYQVERMMREAKLTQIY 395
             L  + +R      +AK  AS+ AM +   AVQ+ GG GY +E  VER  R+AK+T+IY
Sbjct: 304 AWLKRQGQRFTTEASVAKLTASEAAMWIAHQAVQIHGGMGYSKEMPVERYFRDAKITEIY 363

Query: 396 TGTNQITRMVTGRS 409
            GT++I R+V  R+
Sbjct: 364 EGTSEIQRLVIARN 377


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: 365
Number of extensions: 13
Number of successful extensions: 5
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: 382
Length adjustment: 31
Effective length of query: 383
Effective length of database: 351
Effective search space:   134433
Effective search space used:   134433
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 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