GapMind for catabolism of small carbon sources

 

Alignments for a candidate for had in Sulfuritalea hydrogenivorans DSM 22779

Align 6-hydroxycyclohex-1-ene-1-carbonyl-CoA dehydrogenase; EC 1.1.1.368 (characterized)
to candidate WP_041098454.1 SUTH_RS08220 6-hydroxycyclohex-1-ene-1-carbonyl-CoA dehydrogenase

Query= SwissProt::O87871
         (368 letters)



>NCBI__GCF_000828635.1:WP_041098454.1
          Length = 359

 Score =  308 bits (788), Expect = 2e-88
 Identities = 168/354 (47%), Positives = 219/354 (61%), Gaps = 11/354 (3%)

Query: 21  WMMTSPGAPMVRAEFEIGELSADQVVVAVAGCGVCHTDLGYYYDSVRTNHALPLALGHEI 80
           W MT PG  +++       L+A + +V VAGCGVCHTDL Y+Y  V T    PL+LGHE+
Sbjct: 9   WQMTEPGK-LLKTRIPTPALAAGEALVKVAGCGVCHTDLSYFYMGVPTVQKPPLSLGHEV 67

Query: 81  SGRVVQAG-ANAAQWLGRAVIVPAVMPCGTCELCTSGHGTICRDQVMPGND--IQGGFAS 137
           SG VV A  + AA+ LG+ VI+PAV+PC  CELC +G G  C  Q MPGN   I GG++S
Sbjct: 68  SGVVVAAHESTAARVLGKEVIIPAVLPCNKCELCKTGRGNRCLAQKMPGNSMGIYGGYSS 127

Query: 138 HVVVPARGLCPVDEARLAAAGLQLADVSVVADAVTTPYQAVLQAGVEPGDVAVVIGV-GG 196
           H+ VPA  LC V         + L  +SVVADAVTTPYQA ++A +  GD  ++IG  GG
Sbjct: 128 HIPVPAADLCIVGNR----GNIPLEHLSVVADAVTTPYQAAIRARLTAGDRVIIIGAAGG 183

Query: 197 VGGYAVQIANAFGAS-VVAIDVDPAKLEMMSKHGAALTLNAREISGRDLKKAIEAHAKAN 255
           VG +  Q+A   GA+ V+ ID++  KLE M  +GA  T+N R  + +++K+  +A  K  
Sbjct: 184 VGSFMTQVAKGMGAAAVIGIDINEEKLEFMKGYGADFTINPRGKTAKEVKELFKAFCKEK 243

Query: 256 GLRLTR-WKIFECSGTGAGQTSAYGLLTHGATLAVVGFTMDKVEVRLSNLMAFHARALGN 314
           GL     WKIFE +G+  GQ  A  LL+   TL VVG+  D+    LS LMAF A  +G 
Sbjct: 244 GLPSNYGWKIFEVTGSKPGQELALSLLSFTGTLVVVGYGSDETSYMLSKLMAFDAELIGT 303

Query: 315 WGCLPEYYPAALDLVLDKKIDLASFIERHPLDQIGEVFAAAHAHKLTRRAILTP 368
           WGCLPEYYP  LD+ +D +I L  F+E  P+ QI +VF  AH  KL RR ILTP
Sbjct: 304 WGCLPEYYPKVLDMCVDGRIALGPFVETRPMSQIEQVFDEAHHGKLKRRVILTP 357


Lambda     K      H
   0.320    0.134    0.406 

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: 303
Number of extensions: 21
Number of successful extensions: 7
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: 368
Length of database: 359
Length adjustment: 29
Effective length of query: 339
Effective length of database: 330
Effective search space:   111870
Effective search space used:   111870
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: 49 (23.5 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