GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gyaR in Photobacterium gaetbulicola Gung47

Align Glyoxylate reductase; EC 1.1.1.26 (characterized)
to candidate WP_044623793.1 H744_RS21945 2-hydroxyacid dehydrogenase

Query= SwissProt::Q9C4M5
         (331 letters)



>NCBI__GCF_000940995.1:WP_044623793.1
          Length = 329

 Score =  154 bits (390), Expect = 2e-42
 Identities = 101/328 (30%), Positives = 164/328 (50%), Gaps = 27/328 (8%)

Query: 1   MKPKVFITRQIPENGIKMIEKFYEIEL-WKDPKAPPRGVLLEKVREVDALVTLVTDKVDK 59
           MK  VF T++  +N  ++I + Y   L + D +  P+ V +  V+  DA+   V D + +
Sbjct: 1   MKVAVFSTKKYDQNSFELINQHYNHHLDFYDFRLTPQTVKI--VQGYDAVCAFVNDDLSR 58

Query: 60  ELLEN--APKLKIIAQYAVGYDNIDIEEATKRGIYVTNTPGVLTDATADLAFALLLAVAR 117
            +LE   A ++K+IA    GYD +D+E A   GI V   P    +A A+    L+L++ R
Sbjct: 59  PVLEALAANQVKLIAMRCAGYDKVDLEAAKSLGIQVVRVPAYSPEAIAEHTLGLMLSLNR 118

Query: 118 RIVEADAFVRSGEWKKSEVGWHPLMFLGYGLKGKTLGIVGFGRIGQALAKRAKGFGMKII 177
           RI  A    R   +    +        G+   GKT+G++G G+IG A  +  KG GM I+
Sbjct: 119 RIHRAYQRTRDANFSLEGL-------TGFNFHGKTVGVIGTGKIGIATIRILKGLGMNIL 171

Query: 178 YYSRTRKPEAEEEIGAEYVDFETLLKESDFISLHVPLTKETYHMIGEKELKLMKPNAILI 237
            Y     P A E +G EY + + + +++D I+LH P+T E YHM+  +    M+   ++I
Sbjct: 172 AYDPYHNPVAIE-LGVEYTNLDEIYRQADVITLHCPMTDENYHMLNAEAFGKMRDGVMII 230

Query: 238 NTSRGAVVDTNALIKALKEGWIAGAGLDVFEEE----------PYYNEELFK----LKNV 283
           NTSRG ++++   I+ALK   I   G+DV+E E              +++F+      NV
Sbjct: 231 NTSRGELLNSKDAIEALKNSKIGSLGIDVYENEKDLFFEDKSNDVIKDDVFRRLSACHNV 290

Query: 284 VLAPHIGSATHEAREGMAELVAKNLIAF 311
           +   H    T EA   +A+    N+  F
Sbjct: 291 LFTGHQAFLTEEALGNIADTTLNNIKQF 318


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: 230
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: 331
Length of database: 329
Length adjustment: 28
Effective length of query: 303
Effective length of database: 301
Effective search space:    91203
Effective search space used:    91203
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: 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