GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gyaR in Phyllobacterium brassicacearum STM 196

Align Glyoxylate reductase; EC 1.1.1.26 (characterized)
to candidate WP_106711063.1 CU102_RS09940 phosphoglycerate dehydrogenase

Query= SwissProt::Q9C4M5
         (331 letters)



>NCBI__GCF_003010955.1:WP_106711063.1
          Length = 531

 Score =  207 bits (528), Expect = 4e-58
 Identities = 121/333 (36%), Positives = 186/333 (55%), Gaps = 17/333 (5%)

Query: 1   MKPKVFITRQIPENGIKM-----IEKFYEIELWKDPKAPPRGVLLEKVREVDALVTLVTD 55
           M P+V ++ ++    +++     ++  Y  +L KD +      LLE + + D L      
Sbjct: 1   MAPRVLVSDKLSPTAVQIFKDRGVDVDYLPDLGKDKEK-----LLEVIGQYDGLAIRSAT 55

Query: 56  KVDKELLENAPKLKIIAQYAVGYDNIDIEEATKRGIYVTNTPGVLTDATADLAFALLLAV 115
           KV ++L+  A  LK+I +  +G DN+DI  A++RGI V NTP   +  TA+ A AL+ AV
Sbjct: 56  KVTEKLIAAAKNLKVIGRAGIGVDNVDIPAASRRGIIVMNTPFGNSITTAEHAVALMFAV 115

Query: 116 ARRIVEADAFVRSGEWKKSEVGWHPLMFLGYGLKGKTLGIVGFGRIGQALAKRAKGFGMK 175
           AR + EAD+  R+G+W+K+        F+G  + GKTLG++G G IG  +A R  G  M 
Sbjct: 116 ARELPEADSSTRAGKWEKNR-------FMGVEITGKTLGVIGCGNIGSIVATRGIGLKMH 168

Query: 176 IIYYSRTRKPEAEEEIGAEYVDFETLLKESDFISLHVPLTKETYHMIGEKELKLMKPNAI 235
           ++ +         EE+G E V+ + LL  +DFISLH P+T +T  +I    +  MK    
Sbjct: 169 VVAFDPFLSEGRAEELGVEKVELDELLTRADFISLHTPMTDKTRGIINADAIAKMKDGVR 228

Query: 236 LINTSRGAVVDTNALIKALKEGWIAGAGLDVFEEEPYYNEELFKLKNVVLAPHIGSATHE 295
           +IN +RG ++    LI  LK G +AGAG+DVFE EP    ELF L NVV  PH+G++T E
Sbjct: 229 IINCARGGLIVEKDLIAGLKSGKVAGAGIDVFEVEPATENELFHLPNVVCTPHLGASTSE 288

Query: 296 AREGMAELVAKNLIAFAKGEIPPNLVNKDVLTS 328
           A+E +A  VA+ +  +       N +N   +T+
Sbjct: 289 AQENVALQVAEQMSDYLIKGAVSNAINMPSITA 321


Lambda     K      H
   0.317    0.137    0.392 

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: 417
Number of extensions: 14
Number of successful extensions: 2
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: 331
Length of database: 531
Length adjustment: 32
Effective length of query: 299
Effective length of database: 499
Effective search space:   149201
Effective search space used:   149201
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 (21.6 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