GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Ch1CoA in Rhodobacter maris JA276

Align cyclohex-1-ene-1-carbonyl-CoA dehydrogenase (EC 1.3.8.10) (characterized)
to candidate WP_097070363.1 CRO22_RS11805 acyl-CoA dehydrogenase

Query= BRENDA::Q39QF5
         (380 letters)



>NCBI__GCF_900217815.1:WP_097070363.1
          Length = 386

 Score =  250 bits (638), Expect = 5e-71
 Identities = 154/378 (40%), Positives = 215/378 (56%), Gaps = 7/378 (1%)

Query: 4   LTEEQKLTLDMVRDVATREIAPRALELDEKSLFPEYARDLFAKLGLLNPLLPAAYGGTEM 63
           L E+     +MVR  A   + P A  +D ++ FP         LGLL   +P  +GG  M
Sbjct: 10  LGEDIAALREMVRGWARDRLGPIAARVDAENAFPNELWPEMGALGLLGVTVPEEFGGAGM 69

Query: 64  GVLTLALILEELGRVCASTALLLIAQTDGMLPIIH-GGSPELKERYLRRFAGESTLLTAL 122
           G L   +  EE+ RV AS +L   A ++  +  +   GS E K +YL       T + AL
Sbjct: 70  GYLAHVVATEEIARVSASISLSYGAHSNLCVNQLKLNGSEEQKRKYLPGLVA-GTQIGAL 128

Query: 123 AATEPAAGSDLLAMKTRAVRQGDKYVINGQKCFITNGSVADVIVVYAYTDPEKGSKGISA 182
           A +E  AGSD++ MK RA ++   Y++NG K +ITNG  AD +VVYA TDPE GSKGI+A
Sbjct: 129 AMSESGAGSDVVGMKLRAEKRDGHYLLNGHKYWITNGCDADTLVVYAKTDPEVGSKGITA 188

Query: 183 FVVEKGTPGLVYGRNESKMGMRGSINSELFFENMEVPAENIIGAEGTGFANLMQTLSTNR 242
           F+VEKG  G    ++  K+GMRGS  ++LFF+N EVP+EN++G EG G   LM  L   R
Sbjct: 189 FIVEKGFKGFSTSQHFDKLGMRGSNTAQLFFDNCEVPSENVLGLEGKGVRVLMSGLDYER 248

Query: 243 VFCAAQAVGIAQGALDIAVRHTQDRVQFGKPIAHLAPVQFMVADMATAVEASRLLTRKAA 302
           V  +    GI    LD  V + Q+R QFG+PI +   +Q  +ADM  A+  +R  T + A
Sbjct: 249 VVLSGIGTGIMMACLDEVVPYAQERQQFGQPIGNFQLMQAKIADMYVAMNTARAYTYEVA 308

Query: 303 ELLDDGDKKAVLYGSMAKTM--ASDTAMRVTTDAVQVLGGSGYMKENGVERMMRDAKLTQ 360
           +  D G    V     A T+  AS+ AM     AVQ LGG+G++ ++ V R+ RDAKL +
Sbjct: 309 KACDRG---RVTRQDAAATVLYASEQAMVQAHQAVQALGGAGFLNDSVVSRLFRDAKLME 365

Query: 361 IYTGTNQITRMVTGRALL 378
           I  GT++I RM+ GR L+
Sbjct: 366 IGAGTSEIRRMLIGRELV 383


Lambda     K      H
   0.319    0.134    0.371 

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: 336
Number of extensions: 11
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: 380
Length of database: 386
Length adjustment: 30
Effective length of query: 350
Effective length of database: 356
Effective search space:   124600
Effective search space used:   124600
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 (21.7 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