GapMind for catabolism of small carbon sources

 

Alignments for a candidate for drdehyd-cytc in Phyllobacterium brassicacearum STM 196

Align cytochrome c component of deoxyribose dehydrogenase (characterized)
to candidate WP_106709019.1 CU102_RS00535 cytochrome c

Query= reanno::WCS417:GFF2133
         (447 letters)



>NCBI__GCF_003010955.1:WP_106709019.1
          Length = 308

 Score =  140 bits (353), Expect = 6e-38
 Identities = 101/311 (32%), Positives = 143/311 (45%), Gaps = 20/311 (6%)

Query: 8   RTAGWLALPCLVAAGLLAWYVTREPATPFEQEQAG-ATFEPALVSRGEYVARLSDCVACH 66
           R  G L L   +  G   W++T    TP   + A  A   P    RG  +     C +CH
Sbjct: 3   RKFGLLVLLLALVGGTGFWFLT----TPSHLDPARLAATAPGDPQRGMSIFWQGGCASCH 58

Query: 67  SLAG-----KAPFAGGLEMATPLGAIHATNITPDKSTGIGTYSLADFDRAVRHGVAPGGR 121
           +  G     +   AGG  + TP G   A NI+P K  GIG +S  +   A+  GV+PGGR
Sbjct: 59  AAPGAKGEARLVLAGGRNLVTPFGTFVAPNISPSKQ-GIGDWSFENLANAMMEGVSPGGR 117

Query: 122 RLYPAMPYPSYVKLSDDDIKALYAFFMQGIKPANQPNIPSDIPWPLNMRWPIALWNGVFA 181
             YPA PY SY ++   DI  LYA +++ + P+     P  + +P N+R  + LW  ++ 
Sbjct: 118 HYYPAFPYTSYARMQVQDIADLYA-YLKTLPPSENVAGPHKLSFPFNVRRGLGLWKRLYL 176

Query: 182 -PTATYAAKPDQDALWNRGAYIVQGPGHCGSCHTPR-GLAFNEKALDEAGAPFLAGALLD 239
            P          DA+  RG Y+V+GPGHCG CHTPR  +   +KA   AGA    G    
Sbjct: 177 FPEPVLTIANASDAV-RRGQYLVEGPGHCGECHTPRNAIGGMDKAQWLAGATAAEGK--- 232

Query: 240 GWYAPSLRQDPNTGLGRWSEPQIVQFLKTGRNAHAVVYGSMTEAFNNSTQFMQDDDLAAI 299
               P++      G+  WS   I   L++G        GS       +T  +   D  AI
Sbjct: 233 -GVVPNITGGEG-GIDSWSAQDIAYALESGFTPDFDSLGSSMADVVLNTAHLDAADRDAI 290

Query: 300 ARYLKSLPGDP 310
           + YLK++P  P
Sbjct: 291 SAYLKAVPAHP 301



 Score = 25.4 bits (54), Expect = 0.003
 Identities = 13/32 (40%), Positives = 17/32 (53%)

Query: 300 ARYLKSLPGDPQRDGAPWQYQAVAAVQDAPGA 331
           AR   + PGDPQR  + +     A+   APGA
Sbjct: 32  ARLAATAPGDPQRGMSIFWQGGCASCHAAPGA 63


Lambda     K      H
   0.318    0.133    0.423 

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: 473
Number of extensions: 32
Number of successful extensions: 6
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 447
Length of database: 308
Length adjustment: 30
Effective length of query: 417
Effective length of database: 278
Effective search space:   115926
Effective search space used:   115926
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: 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